Year |
Citation |
Score |
2021 |
Ewers M, Luan Y, Frontzkowski L, Neitzel J, Rubinski A, Dichgans M, Hassenstab J, Gordon BA, Chhatwal JP, Levin J, Schofield P, Benzinger TLS, Morris JC, Goate A, Karch CM, ... ... Rossor M, et al. Segregation of functional networks is associated with cognitive resilience in Alzheimer's disease. Brain : a Journal of Neurology. PMID 33725114 DOI: 10.1093/brain/awab112 |
0.332 |
|
2020 |
Weston PSJ, Poole T, Nicholas JM, Toussaint N, Simpson IJA, Modat M, Ryan NS, Liang Y, Rossor MN, Schott JM, Ourselin S, Zhang H, Fox NC. Measuring cortical mean diffusivity to assess early microstructural cortical change in presymptomatic familial Alzheimer's disease. Alzheimer's Research & Therapy. 12: 112. PMID 32943095 DOI: 10.1186/S13195-020-00679-2 |
0.44 |
|
2020 |
Ball HA, McWhirter L, Ballard C, Bhome R, Blackburn DJ, Edwards MJ, Fleming SM, Fox NC, Howard R, Huntley J, Isaacs JD, Larner AJ, Nicholson TR, Pennington CM, Poole N, ... ... Rossor MN, et al. Functional cognitive disorder: dementia's blind spot. Brain : a Journal of Neurology. PMID 32791521 DOI: 10.1093/Brain/Awaa224 |
0.354 |
|
2020 |
O'Connor A, Karikari TK, Poole T, Ashton NJ, Lantero Rodriguez J, Khatun A, Swift I, Heslegrave AJ, Abel E, Chung E, Weston PSJ, Pavisic IM, Ryan NS, Barker S, Rossor MN, et al. Plasma phospho-tau181 in presymptomatic and symptomatic familial Alzheimer's disease: a longitudinal cohort study. Molecular Psychiatry. PMID 32665603 DOI: 10.1038/S41380-020-0838-X |
0.386 |
|
2020 |
Gratwicke J, Zrinzo L, Kahan J, Peters A, Brechany U, McNichol A, Beigi M, Akram H, Hyam J, Oswal A, Day B, Mancini L, Thornton J, Yousry T, Crutch SJ, ... ... Rossor MN, et al. Bilateral Nucleus Basalis of Meynert Deep Brain Stimulation for dementia with Lewy bodies A Randomised Clinical Trial. Brain Stimulation. PMID 32334074 DOI: 10.1016/J.Brs.2020.04.010 |
0.346 |
|
2020 |
Franzmeier N, Koutsouleris N, Benzinger T, Goate A, Karch CM, Fagan AM, McDade E, Duering M, Dichgans M, Levin J, Gordon BA, Lim YY, Masters CL, Rossor M, Fox NC, et al. Predicting sporadic Alzheimer's disease progression via inherited Alzheimer's disease-informed machine-learning. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 32043733 DOI: 10.1002/Alz.12032 |
0.43 |
|
2019 |
Moore KM, Nicholas J, Grossman M, McMillan CT, Irwin DJ, Massimo L, Van Deerlin VM, Warren JD, Fox NC, Rossor MN, Mead S, Bocchetta M, Boeve BF, Knopman DS, Graff-Radford NR, et al. Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study. The Lancet. Neurology. PMID 31810826 DOI: 10.1016/S1474-4422(19)30394-1 |
0.373 |
|
2019 |
Convery RS, Jiao J, Clarke MTM, Moore KM, Koriath CAM, Woollacott IOC, Weston PSJ, Gunn R, Rabiner I, Cash DM, Rossor MN, Warren JD, Fox NC, Ourselin S, Bocchetta M, et al. Longitudinal (F)AV-1451 PET imaging in a patient with frontotemporal dementia due to a Q351R MAPT mutation. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 31439620 DOI: 10.1136/Jnnp-2019-320904 |
0.375 |
|
2019 |
Firth NC, Primativo S, Marinescu RV, Shakespeare TJ, Suarez-Gonzalez A, Lehmann M, Carton A, Ocal D, Pavisic I, Paterson RW, Slattery CF, Foulkes AJM, Ridha BH, Gil-Néciga E, Oxtoby NP, ... ... Rossor MN, et al. Longitudinal neuroanatomical and cognitive progression of posterior cortical atrophy. Brain : a Journal of Neurology. PMID 31219516 DOI: 10.1093/Brain/Awz136 |
0.466 |
|
2019 |
Franzmeier N, Ren J, Damm A, Monté-Rubio G, Boada M, Ruiz A, Ramirez A, Jessen F, Düzel E, Rodríguez Gómez O, Benzinger T, Goate A, Karch CM, Fagan AM, McDade E, ... ... Rossor M, et al. The BDNF SNP modulates the association between beta-amyloid and hippocampal disconnection in Alzheimer's disease. Molecular Psychiatry. PMID 30899092 DOI: 10.1038/S41380-019-0404-6 |
0.393 |
|
2019 |
Vöglein J, Paumier K, Jucker M, Preische O, McDade E, Hassenstab J, Benzinger TL, Noble JM, Berman SB, Graff-Radford NR, Ghetti B, Farlow MR, Chhatwal J, Salloway S, Xiong C, ... ... Rossor M, et al. Clinical, pathophysiological and genetic features of motor symptoms in autosomal dominant Alzheimer's disease. Brain : a Journal of Neurology. PMID 30897203 DOI: 10.1093/Brain/Awz050 |
0.415 |
|
2019 |
Warren-Gash C, Forbes HJ, Williamson E, Breuer J, Hayward AC, Mavrodaris A, Ridha BH, Rossor MN, Thomas SL, Smeeth L. Human herpesvirus infections and dementia or mild cognitive impairment: a systematic review and meta-analysis. Scientific Reports. 9: 4743. PMID 30894595 DOI: 10.1038/S41598-019-41218-W |
0.341 |
|
2019 |
Rossor AM, Jaunmuktane Z, Rossor MN, Hoti G, Reilly MM. TDP43 pathology in the brain, spinal cord, and dorsal root ganglia of a patient with FOSMN Neurology. 92. PMID 30700593 DOI: 10.1212/Wnl.0000000000007008 |
0.365 |
|
2019 |
Preische O, Schultz SA, Apel A, Kuhle J, Kaeser SA, Barro C, Gräber S, Kuder-Buletta E, LaFougere C, Laske C, Vöglein J, Levin J, Masters CL, Martins R, Schofield PR, ... Rossor MN, et al. Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer's disease. Nature Medicine. PMID 30664784 DOI: 10.1038/S41591-018-0304-3 |
0.43 |
|
2019 |
Mackintosh M, Aldridge RW, Rossor M, Gonzalez-Izquierdo A, Whitaker KJ, Ford E, Direk K, Denaxas S. Dementia recognition, diagnosis, and treatment in the UK, 1997–2017: a change-point analysis The Lancet. 394. DOI: 10.1016/S0140-6736(19)32867-3 |
0.353 |
|
2019 |
Weston PSJ, Toussaint N, Poole T, Simpson I, Nicholas JM, Lehmann M, Modat M, Daga P, Ryan NS, Liang Y, Rossor MN, Schott JM, Ourselin S, Zhang H, Fox NC. P3-419: Measuring Cortical Mean Diffusivity To Assess Early Microstructural Cortical Change In Presymptomatic Autosomal Dominant Alzheimer'S Disease Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3453 |
0.374 |
|
2018 |
Vöglein J, Noachtar S, McDade E, Quaid KA, Salloway S, Ghetti B, Noble J, Berman S, Chhatwal J, Mori H, Fox N, Allegri R, Masters CL, Buckles V, Ringman JM, ... Rossor M, et al. Seizures as an early symptom of autosomal dominant Alzheimer's disease. Neurobiology of Aging. 76: 18-23. PMID 30616208 DOI: 10.1016/J.Neurobiolaging.2018.11.022 |
0.322 |
|
2018 |
Suárez-Calvet M, Capell A, Araque Caballero MÁ, Morenas-Rodríguez E, Fellerer K, Franzmeier N, Kleinberger G, Eren E, Deming Y, Piccio L, Karch CM, Cruchaga C, Paumier K, Bateman RJ, Fagan AM, ... ... Rossor MN, et al. CSF progranulin increases in the course of Alzheimer's disease and is associated with sTREM2, neurodegeneration and cognitive decline. Embo Molecular Medicine. PMID 30482868 DOI: 10.15252/Emmm.201809712 |
0.475 |
|
2018 |
Koriath C, Kenny J, Adamson G, Druyeh R, Taylor W, Beck J, Quinn L, Mok TH, Dimitriadis A, Norsworthy P, Bass N, Carter J, Walker Z, Kipps C, Coulthard E, ... ... Rossor MN, et al. Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series. Molecular Psychiatry. PMID 30279455 DOI: 10.1038/S41380-018-0224-0 |
0.361 |
|
2018 |
Müller S, Preische O, Sohrabi HR, Gräber S, Jucker M, Ringman JM, Martins RN, McDade E, Schofield PR, Ghetti B, Rossor M, Fox NN, Graff-Radford NR, Levin J, Danek A, et al. Relationship between physical activity, cognition, and Alzheimer pathology in autosomal dominant Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 30266303 DOI: 10.1016/J.Jalz.2018.06.3059 |
0.438 |
|
2018 |
Araque Caballero MÁ, Suárez-Calvet M, Duering M, Franzmeier N, Benzinger T, Fagan AM, Bateman RJ, Jack CR, Levin J, Dichgans M, Jucker M, Karch C, Masters CL, Morris JC, Weiner M, ... Rossor M, et al. White matter diffusion alterations precede symptom onset in autosomal dominant Alzheimer's disease. Brain : a Journal of Neurology. PMID 30239611 DOI: 10.1093/Brain/Awy229 |
0.43 |
|
2018 |
McDade E, Wang G, Gordon BA, Hassenstab J, Benzinger TLS, Buckles V, Fagan AM, Holtzman DM, Cairns NJ, Goate AM, Marcus DS, Morris JC, Paumier K, Xiong C, Allegri R, ... ... Rossor MN, et al. Longitudinal cognitive and biomarker changes in dominantly inherited Alzheimer disease. Neurology. PMID 30217935 DOI: 10.1212/Wnl.0000000000006277 |
0.435 |
|
2018 |
Woollacott IOC, Bocchetta M, Sudre CH, Ridha BH, Strand C, Courtney R, Ourselin S, Cardoso MJ, Warren JD, Rossor MN, Revesz T, Fox NC, Holton JL, Lashley T, Rohrer JD. Pathological correlates of white matter hyperintensities in a case of progranulin mutation associated frontotemporal dementia. Neurocase. 1-9. PMID 30112957 DOI: 10.1080/13554794.2018.1506039 |
0.365 |
|
2018 |
Ritchie CW, Russ TC, Banerjee S, Barber B, Boaden A, Fox NC, Holmes C, Isaacs JD, Leroi I, Lovestone S, Norton M, O'Brien J, Pearson J, Perry R, Pickett J, ... ... Rossor MN, et al. Correction to: The Edinburgh Consensus: preparing for the advent of disease-modifying therapies for Alzheimer's disease. Alzheimer's Research & Therapy. 10: 73. PMID 30060761 DOI: 10.1186/S13195-018-0372-0 |
0.321 |
|
2018 |
Ridha BH, Crutch S, Cutler D, Frost C, Knight W, Barker S, Epie N, Warrington EK, Kukkastenvehmas R, Douglas J, Rossor MN. A double-blind placebo-controlled cross-over clinical trial of DONepezil In Posterior cortical atrophy due to underlying Alzheimer's Disease: DONIPAD study. Alzheimer's Research & Therapy. 10: 44. PMID 29716655 DOI: 10.1186/S13195-018-0363-1 |
0.434 |
|
2018 |
Hwang YT, Rocchi L, Hammond P, Hardy CJ, Warren JD, Ridha BH, Rothwell J, Rossor MN. Effect of donepezil on transcranial magnetic stimulation parameters in Alzheimer's disease. Alzheimer's & Dementia (New York, N. Y.). 4: 103-107. PMID 29560413 DOI: 10.1016/J.Trci.2018.02.001 |
0.386 |
|
2018 |
Paterson RW, Slattery CF, Poole T, Nicholas JM, Magdalinou NK, Toombs J, Chapman MD, Lunn MP, Heslegrave AJ, Foiani MS, Weston PSJ, Keshavan A, Rohrer JD, Rossor MN, Warren JD, et al. Cerebrospinal fluid in the differential diagnosis of Alzheimer's disease: clinical utility of an extended panel of biomarkers in a specialist cognitive clinic. Alzheimer's Research & Therapy. 10: 32. PMID 29558979 DOI: 10.1186/S13195-018-0361-3 |
0.44 |
|
2018 |
Franzmeier N, Düzel E, Jessen F, Buerger K, Levin J, Duering M, Dichgans M, Haass C, Suárez-Calvet M, Fagan AM, Paumier K, Benzinger T, Masters CL, Morris JC, Perneczky R, ... ... Rossor M, et al. Left frontal hub connectivity delays cognitive impairment in autosomal-dominant and sporadic Alzheimer's disease. Brain : a Journal of Neurology. PMID 29462334 DOI: 10.1093/Brain/Awy008 |
0.455 |
|
2018 |
Weston PSJ, Nicholas JM, Henley SMD, Liang Y, Macpherson K, Donnachie E, Schott JM, Rossor MN, Crutch SJ, Butler CR, Zeman AZ, Fox NC. Accelerated long-term forgetting in presymptomatic autosomal dominant Alzheimer's disease: a cross-sectional study. The Lancet. Neurology. 17: 123-132. PMID 29413314 DOI: 10.1016/S1474-4422(17)30434-9 |
0.39 |
|
2018 |
Gordon BA, Blazey TM, Su Y, Hari-Raj A, Dincer A, Flores S, Christensen J, McDade E, Wang G, Xiong C, Cairns NJ, Hassenstab J, Marcus DS, Fagan AM, Jack CR, ... ... Rossor MN, et al. Spatial patterns of neuroimaging biomarker change in individuals from families with autosomal dominant Alzheimer's disease: a longitudinal study. The Lancet. Neurology. PMID 29397305 DOI: 10.1016/S1474-4422(18)30028-0 |
0.461 |
|
2018 |
Marshall CR, Hardy CJD, Volkmer A, Russell LL, Bond RL, Fletcher PD, Clark CN, Mummery CJ, Schott JM, Rossor MN, Fox NC, Crutch SJ, Rohrer JD, Warren JD. Primary progressive aphasia: a clinical approach. Journal of Neurology. PMID 29392464 DOI: 10.1007/S00415-018-8762-6 |
0.336 |
|
2018 |
Weston PS, Poole T, Ryan NS, Liang Y, O'Connor A, Heslegrave A, Druyeh R, Mead S, Blennow K, Rossor MN, Schott JM, Zetterberg H, Fox NC. O2-04-04: Longitudinal Measurement Of Serum Neurofilament Light Concentration In Familial Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.2660 |
0.36 |
|
2018 |
Molteni E, Veale T, Altmann A, Cardoso MJ, Benzinger TLS, Jack CR, McDade E, Morris JC, Rossor MN, Ourselin S, Fox NC, Cash DM, Modat M. Ic-P-165: Robust Identification Of Brain Structures Most Discriminative In Detecting Early Changes In Autosomal Dominant Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.2232 |
0.374 |
|
2018 |
O'Connor A, Poole T, Weston PSJ, Ryan NS, Liang Y, Macpherson K, Pavisic IM, Collins J, Druyeh R, Mead S, Blennow K, Rossor MN, Schott JM, Zettenberg H, Fox NC. P3-261: Serum Neurofilament Light Concentration And Progression In Familial Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.1621 |
0.388 |
|
2017 |
Cash DM, Bocchetta M, Thomas DL, Dick KM, van Swieten JC, Borroni B, Galimberti D, Masellis M, Tartaglia MC, Rowe JB, Graff C, Tagliavini F, Frisoni GB, Laforce R, Finger E, ... ... Rossor MN, et al. Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study. Neurobiology of Aging. 62: 191-196. PMID 29172163 DOI: 10.1016/J.Neurobiolaging.2017.10.008 |
0.371 |
|
2017 |
Hardy CJD, Hwang YT, Bond RL, Marshall CR, Ridha BH, Crutch SJ, Rossor MN, Warren JD. Donepezil enhances understanding of degraded speech in Alzheimer's disease. Annals of Clinical and Translational Neurology. 4: 835-840. PMID 29159197 DOI: 10.1002/Acn3.471 |
0.387 |
|
2017 |
Weston PSJ, Poole T, Ryan NS, Nair A, Liang Y, Macpherson K, Druyeh R, Malone IB, Ahsan RL, Pemberton H, Klimova J, Mead S, Blennow K, Rossor MN, Schott JM, et al. Serum neurofilament light in familial Alzheimer disease: A marker of early neurodegeneration. Neurology. PMID 29070659 DOI: 10.1212/Wnl.0000000000004667 |
0.396 |
|
2017 |
Ritchie CW, Russ TC, Banerjee S, Barber B, Boaden A, Fox NC, Holmes C, Isaacs JD, Leroi I, Lovestone S, Norton M, O'Brien J, Pearson J, Perry R, Pickett J, ... ... Rossor MN, et al. The Edinburgh Consensus: preparing for the advent of disease-modifying therapies for Alzheimer's disease. Alzheimer's Research & Therapy. 9: 85. PMID 29070066 DOI: 10.1186/S13195-017-0312-4 |
0.445 |
|
2017 |
Kinnunen KM, Cash DM, Poole T, Frost C, Benzinger TLS, Ahsan RL, Leung KK, Cardoso MJ, Modat M, Malone IB, Morris JC, Bateman RJ, Marcus DS, Goate A, Salloway S, ... ... Rossor MN, et al. Presymptomatic atrophy in autosomal dominant Alzheimer's disease: A serial MRI study. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 28738187 DOI: 10.1016/J.Jalz.2017.06.2268 |
0.432 |
|
2017 |
Warren-Gash C, Forbes H, Breuer J, Hayward AC, Mavrodaris A, Ridha BH, Rossor M, Thomas SL, Smeeth L. Association between human herpesvirus infections and dementia or mild cognitive impairment: a systematic review protocol. Bmj Open. 7: e016522. PMID 28645980 DOI: 10.1136/Bmjopen-2017-016522 |
0.31 |
|
2017 |
Kenny J, Woollacott I, Koriath C, Hosszu L, Adamson G, Rudge P, Rossor MN, Collinge J, Rohrer JD, Mead S. A novel prion protein variant in a patient with semantic dementia. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 28572272 DOI: 10.1136/Jnnp-2017-315577 |
0.451 |
|
2017 |
Brown BM, Sohrabi HR, Taddei K, Gardener SL, Rainey-Smith SR, Peiffer JJ, Xiong C, Fagan AM, Benzinger T, Buckles V, Erickson KI, Clarnette R, Shah T, Masters CL, Weiner M, ... ... Rossor M, et al. Habitual exercise levels are associated with cerebral amyloid load in presymptomatic autosomal dominant Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 28501451 DOI: 10.1016/J.Jalz.2017.03.008 |
0.403 |
|
2017 |
Müller S, Preische O, Sohrabi HR, Gräber S, Jucker M, Dietzsch J, Ringman JM, Martins RN, McDade E, Schofield PR, Ghetti B, Rossor M, Graff-Radford NR, Levin J, Galasko D, et al. Decreased body mass index in the preclinical stage of autosomal dominant Alzheimer's disease. Scientific Reports. 7: 1225. PMID 28450713 DOI: 10.1038/S41598-017-01327-W |
0.37 |
|
2017 |
Rossor M. 23 Dementia: thirty years back and forth Journal of Neurology, Neurosurgery, and Psychiatry. 88. DOI: 10.1136/Jnnp-2017-Bnpa.23 |
0.419 |
|
2017 |
Weston PSJ, Poole T, Ryan NS, Nair A, Liang Y, Macpherson K, Druyeh R, Malone IB, Ahsan RL, Pemberton H, Klimova J, Mead S, Blennow K, Rossor MN, Schott JM, et al. Serum Neurofilament Light Concentration In Familial Alzheimer’S Disease And Association With Markers Of Disease Stage And Severity Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.07.427 |
0.342 |
|
2017 |
Fox NC, Ryan NS, Weston PSJ, Chavez-Gutierrez L, Modat M, Cash DM, Ourselin S, Rossor MN. Neuroimaging And Heterogeneity In Familial Alzheimer'S Disease Alzheimers & Dementia. 13: 1211. DOI: 10.1016/J.Jalz.2017.07.377 |
0.442 |
|
2017 |
McDade E, Wang G, Benzinger TL, Buckles VD, Fagan AM, Gordon BA, Hassenstab J, Holtzman DM, Cairns NJ, Goate AM, Marcus DS, Morris JC, Paumier KL, Xiong C, Ricardo A, ... ... Rossor MN, et al. LONGITUDINAL BIOMARKER CHANGES IN AUTOSOMAL DOMINANT ALZHEIMER'S DISEASE FROM THE DIAN STUDY Alzheimer's & Dementia. 13: P879-P880. DOI: 10.1016/J.Jalz.2017.07.265 |
0.436 |
|
2017 |
Woollacott IO, Bocchetta M, Sudre CH, Ridha BH, Strand C, Courtney R, Ourselin S, Cardoso JM, Warren JD, Rossor MN, Fox NC, Revesz T, Lashley T, Holton J, Rohrer JD. Pathological Correlates Of White Matter Hyperintensities On Cadaveric Mri In Progranulin-Associated Frontotemporal Dementia Alzheimers & Dementia. 13: 805. DOI: 10.1016/J.Jalz.2017.06.1097 |
0.359 |
|
2016 |
Ryan NS, Nicholas JM, Weston PS, Liang Y, Lashley T, Guerreiro R, Adamson G, Kenny J, Beck J, Chavez-Gutierrez L, de Strooper B, Revesz T, Holton J, Mead S, Rossor MN, et al. Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case series. The Lancet. Neurology. PMID 27777022 DOI: 10.1016/S1474-4422(16)30193-4 |
0.445 |
|
2016 |
Tang M, Ryman DC, McDade E, Jasielec MS, Buckles VD, Cairns NJ, Fagan AM, Goate A, Marcus DS, Xiong C, Allegri RF, Chhatwal JP, Danek A, Farlow MR, Fox NC, ... ... Rossor MN, et al. Neurological manifestations of autosomal dominant familial Alzheimer's disease: a comparison of the published literature with the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS). The Lancet. Neurology. PMID 27777020 DOI: 10.1016/S1474-4422(16)30229-0 |
0.431 |
|
2016 |
Shah H, Albanese E, Duggan C, Rudan I, Langa KM, Carrillo MC, Chan KY, Joanette Y, Prince M, Rossor M, Saxena S, Snyder HM, Sperling R, Varghese M, Wang H, et al. Research priorities to reduce the global burden of dementia by 2025. The Lancet. Neurology. 15: 1285-1294. PMID 27751558 DOI: 10.1016/S1474-4422(16)30235-6 |
0.313 |
|
2016 |
Weston PS, Nicholas JM, Lehmann M, Ryan NS, Liang Y, Macpherson K, Modat M, Rossor MN, Schott JM, Ourselin S, Fox NC. Presymptomatic cortical thinning in familial Alzheimer disease: A longitudinal MRI study. Neurology. PMID 27733562 DOI: 10.1212/Wnl.0000000000003322 |
0.413 |
|
2016 |
Meeter LH, Dopper EG, Jiskoot LC, Sanchez-Valle R, Graff C, Benussi L, Ghidoni R, Pijnenburg YA, Borroni B, Galimberti D, Laforce RJ, Masellis M, Vandenberghe R, Ber IL, Otto M, ... ... Rossor MN, et al. Neurofilament light chain: a biomarker for genetic frontotemporal dementia. Annals of Clinical and Translational Neurology. 3: 623-36. PMID 27606344 DOI: 10.1002/Acn3.325 |
0.306 |
|
2016 |
Weston PS, Paterson RW, Dickson J, Barnes A, Bomanji JB, Kayani I, Lunn MP, Mummery CJ, Warren JD, Rossor MN, Fox NC, Zetterberg H, Schott JM. Diagnosing Dementia in the Clinical Setting: Can Amyloid PET Provide Additional Value Over Cerebrospinal Fluid? Journal of Alzheimer's Disease : Jad. PMID 27567830 DOI: 10.3233/Jad-160302 |
0.394 |
|
2016 |
Lim YY, Hassenstab J, Cruchaga C, Goate A, Fagan AM, Benzinger TL, Maruff P, Snyder PJ, Masters CL, Allegri R, Chhatwal J, Farlow MR, Graff-Radford NR, Laske C, Levin J, ... ... Rossor M, et al. BDNF Val66Met moderates memory impairment, hippocampal function and tau in preclinical autosomal dominant Alzheimer's disease. Brain : a Journal of Neurology. PMID 27521573 DOI: 10.1093/Brain/Aww200 |
0.439 |
|
2016 |
Schott JM, Crutch SJ, Carrasquillo MM, Uphill J, Shakespeare TJ, Ryan NS, Yong KX, Lehmann M, Ertekin-Taner N, Graff-Radford NR, Boeve BF, Murray ME, Khan QU, Petersen RC, Dickson DW, ... ... Rossor MN, et al. Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 26993346 DOI: 10.1016/J.Jalz.2016.01.010 |
0.42 |
|
2016 |
Koriath C, Adamson G, Druyeh R, Kenny J, Rossor M, Schott J, Collinge J, Fox N, Rohrer J, Mead S. Probing Ftd Genetics With Next-Generation Sequencing Journal of Neurology, Neurosurgery, and Psychiatry. 87. DOI: 10.1136/Jnnp-2016-315106.61 |
0.351 |
|
2016 |
Weston P, Liang Y, Henley S, Nicholas J, Ryan N, Schott J, Rossor M, Butler C, Zeman A, Fox N. Long-Term Forgetting In Preclinical Familial Alzheimer'S Disease Journal of Neurology, Neurosurgery, and Psychiatry. 87. DOI: 10.1136/Jnnp-2016-315106.18 |
0.361 |
|
2016 |
Mutsaerts HJMM, Rohrer JD, Thomas DL, Cash DM, Vita Ed, Nicholas JM, Swieten JCv, Dopper EGP, Jiskoot LC, Minkelen Rv, Rombouts SARB, Dick KM, Bocchetta M, Cardoso MJ, Espak M, ... ... Rossor MN, et al. Cerebral Perfusion As An Imaging Biomarker Of Presymptomatic Genetic Frontotemporal Dementia: Preliminary Results From The Genetic Frontotemporal Dementia Initiative (Genfi) Alzheimers & Dementia. 12. DOI: 10.1016/J.Jalz.2016.06.772 |
0.415 |
|
2016 |
McDade E, Weng H, Wang G, Xiong C, Fagan AM, Hassenstab J, Marcus DS, Morris JC, Benzinger TL, Cairns NJ, Goate AM, Buckles V, Holtzman DM, Berman S, Ghetti B, ... ... Rossor MN, et al. O5-02-01: Longitudinal Clinical and Biomarker Changes in Dominantly Inherited Alzheimer's Disease: The Dominantly Inherited Alzheimer Network Alzheimer's & Dementia. 12: P378-P379. DOI: 10.1016/J.Jalz.2016.06.710 |
0.409 |
|
2016 |
Lim YY, Hassenstab J, Cruchaga C, Goate AM, Fagan AM, Lee Smith Benzinger T, Maruff P, Snyder PJ, Masters CL, Ricardo A, Chhatwal JP, Farlow MR, Graff-Radford NR, Laske C, Levin J, ... ... Rossor MN, et al. F5-02-03: BDNF VAL66MET Moderates Cognitive Impairment, Neuronal Dysfunction and TAU in Preclinical Autosomal Dominant Alzheimer's Disease Alzheimer's & Dementia. 12: P369-P369. DOI: 10.1016/J.Jalz.2016.06.689 |
0.387 |
|
2016 |
Cash DM, Kinnunen KM, Weston PS, Ryan NS, Modat M, Bateman R, Morris JC, Ourselin S, Rossor MN, Benzinger TLS, Fox NC. Longitudinal Atrophy In Autosomal Dominant Ad And Sporadic Ad: Lessons From Dian Alzheimers & Dementia. 12. DOI: 10.1016/J.Jalz.2016.06.688 |
0.346 |
|
2016 |
Weston PSJ, Henley SMD, Liang Y, Nicholas J, Ryan NS, MacPherson K, Donnachie E, Schott JM, Rossor MN, Crutch SJ, Butler CR, Zeman AZ, Fox NC. Accelerated Long-Term Forgetting In Presymptomatic Familial Alzheimer’S Disease Alzheimers & Dementia. 12: 231. DOI: 10.1016/J.Jalz.2016.06.415 |
0.315 |
|
2016 |
Rossor MN, Richard E, Reiman EM, Leys D, Skoog I, Snyder HM, Amouyel P, Carrillo MC. FTS3-01-04: Setting the Agenda: Prevention Studies for Vascular Contributions to Dementia Alzheimer's & Dementia. 12: P277-P277. DOI: 10.1016/J.Jalz.2016.06.2387 |
0.304 |
|
2016 |
Cash DM, Ridgway GR, Kinnunen KM, Benzinger TLS, Wallon D, Jack CR, Bateman R, Morris JC, Rossor MN, Ourselin S, Fox NC. A Longitudinal Morphometric Study Of Familial Alzheimer’S Disease: Results From Dian Alzheimers & Dementia. 12. DOI: 10.1016/J.Jalz.2016.06.172 |
0.401 |
|
2015 |
Weston PS, Paterson RW, Modat M, Burgos N, Cardoso MJ, Magdalinou N, Lehmann M, Dickson JC, Barnes A, Bomanji JB, Kayani I, Cash DM, Ourselin S, Toombs J, Lunn MP, ... ... Rossor MN, et al. Using florbetapir positron emission tomography to explore cerebrospinal fluid cut points and gray zones in small sample sizes. Alzheimer's & Dementia (Amsterdam, Netherlands). 1: 440-446. PMID 26835507 DOI: 10.1016/J.Dadm.2015.10.001 |
0.305 |
|
2015 |
Ringman JM, Liang LJ, Zhou Y, Vangala S, Teng E, Kremen S, Wharton D, Goate A, Marcus DS, Farlow M, Ghetti B, McDade E, Masters CL, Mayeux RP, Rossor M, et al. Erratum: Early behavioural changes in familial Alzheimers disease in the Dominantly Inherited Alzheimer Network (Brain (2015) 138 (103645) (10.1093/brain/awv004)) Brain. 138. PMID 26598496 DOI: 10.1093/Brain/Awv210 |
0.398 |
|
2015 |
Ryan NS, Rossor MN, Fox NC. Alzheimer's disease in the 100 years since Alzheimer's death. Brain : a Journal of Neurology. 138: 3816-21. PMID 26541346 DOI: 10.1093/Brain/Awv316 |
0.447 |
|
2015 |
Fletcher PD, Downey LE, Golden HL, Clark CN, Slattery CF, Paterson RW, Rohrer JD, Schott JM, Rossor MN, Warren JD. Pain and temperature processing in dementia: a clinical and neuroanatomical analysis. Brain : a Journal of Neurology. PMID 26463677 DOI: 10.1093/Brain/Awv276 |
0.393 |
|
2015 |
Paterson RW, Toombs J, Slattery CF, Nicholas JM, Andreasson U, Magdalinou NK, Blennow K, Warren JD, Mummery CJ, Rossor MN, Lunn MP, Crutch SJ, Fox NC, Zetterberg H, Schott JM. Dissecting IWG-2 typical and atypical Alzheimer's disease: insights from cerebrospinal fluid analysis. Journal of Neurology. PMID 26410752 DOI: 10.1007/S00415-015-7904-3 |
0.406 |
|
2015 |
Ryan NS, Biessels GJ, Kim L, Nicholas JM, Barber PA, Walsh P, Gami P, Morris HR, Bastos-Leite AJ, Schott JM, Beck J, Mead S, Chavez-Gutierrez L, de Strooper B, Rossor MN, et al. Genetic determinants of white matter hyperintensities and amyloid angiopathy in familial Alzheimer's disease. Neurobiology of Aging. PMID 26410308 DOI: 10.1016/J.Neurobiolaging.2015.08.026 |
0.396 |
|
2015 |
Bocchetta M, Gordon E, Manning E, Barnes J, Cash DM, Espak M, Thomas DL, Modat M, Rossor MN, Warren JD, Ourselin S, Frisoni GB, Rohrer JD. Detailed volumetric analysis of the hypothalamus in behavioral variant frontotemporal dementia. Journal of Neurology. PMID 26338813 DOI: 10.1007/S00415-015-7885-2 |
0.322 |
|
2015 |
Wang F, Gordon BA, Ryman DC, Ma S, Xiong C, Hassenstab J, Goate A, Fagan AM, Cairns NJ, Marcus DS, McDade E, Ringman JM, Graff-Radford NR, Ghetti B, Farlow MR, ... ... Rossor MN, et al. Cerebral amyloidosis associated with cognitive decline in autosomal dominant Alzheimer disease. Neurology. PMID 26245925 DOI: 10.1212/Wnl.0000000000001903 |
0.376 |
|
2015 |
Rossor M, Knapp M. Can we model a cognitive footprint of interventions and policies to help to meet the global challenge of dementia? Lancet (London, England). 386: 1008-10. PMID 26233601 DOI: 10.1016/S0140-6736(15)60248-3 |
0.31 |
|
2015 |
Sposito T, Preza E, Mahoney CJ, Setó-Salvia N, Ryan NS, Morris HR, Arber C, Devine MJ, Houlden H, Warner TT, Bushell TJ, Zagnoni M, Kunath T, Livesey FJ, Fox NC, ... Rossor MN, et al. Developmental regulation of tau splicing is disrupted in stem cell-derived neurons from frontotemporal dementia patients with the 10 + 16 splice-site mutation in MAPT. Human Molecular Genetics. PMID 26136155 DOI: 10.1093/Hmg/Ddv246 |
0.356 |
|
2015 |
Lynch DS, Jaunmuktane Z, Sheerin UM, Phadke R, Brandner S, Milonas I, Dean A, Bajaj N, McNicholas N, Costello D, Cronin S, McGuigan C, Rossor M, Fox N, Murphy E, et al. Hereditary leukoencephalopathy with axonal spheroids: a spectrum of phenotypes from CNS vasculitis to parkinsonism in an adult onset leukodystrophy series. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 25935893 DOI: 10.1136/Jnnp-2015-310788 |
0.319 |
|
2015 |
Fletcher PD, Downey LE, Golden HL, Clark CN, Slattery CF, Paterson RW, Schott JM, Rohrer JD, Rossor MN, Warren JD. Auditory hedonic phenotypes in dementia: A behavioural and neuroanatomical analysis. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 67: 95-105. PMID 25929717 DOI: 10.1016/J.Cortex.2015.03.021 |
0.431 |
|
2015 |
Ringman JM, Liang LJ, Zhou Y, Vangala S, Teng E, Kremen S, Wharton D, Goate A, Marcus DS, Farlow M, Ghetti B, McDade E, Masters CL, Mayeux RP, Rossor M, et al. Early behavioural changes in familial Alzheimer's disease in the Dominantly Inherited Alzheimer Network. Brain : a Journal of Neurology. 138: 1036-45. PMID 25688083 DOI: 10.1093/Brain/Awv004 |
0.383 |
|
2015 |
Rohrer JD, Nicholas JM, Cash DM, van Swieten J, Dopper E, Jiskoot L, van Minkelen R, Rombouts SA, Cardoso MJ, Clegg S, Espak M, Mead S, Thomas DL, De Vita E, Masellis M, ... ... Rossor MN, et al. Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis. The Lancet. Neurology. 14: 253-62. PMID 25662776 DOI: 10.1016/S1474-4422(14)70324-2 |
0.407 |
|
2015 |
Rohrer JD, Isaacs AM, Mizielinska S, Mead S, Lashley T, Wray S, Sidle K, Fratta P, Orrell RW, Hardy J, Holton J, Revesz T, Rossor MN, Warren JD. C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis. The Lancet. Neurology. 14: 291-301. PMID 25638642 DOI: 10.1016/S1474-4422(14)70233-9 |
0.36 |
|
2015 |
Witoonpanich P, Crutch SJ, Warren JD, Rossor MN. The undiscovered syndrome: Macdonald Critchley's case of semantic dementia. Neurocase. 21: 408-12. PMID 24818802 DOI: 10.1080/13554794.2014.910307 |
0.359 |
|
2015 |
Fletcher P, Schott J, Rossor M, Warren J. Abnormal Sound And Music Reward Processing In Dementia: A Behavioural And Neuroanatomical Analysis Journal of Neurology, Neurosurgery, and Psychiatry. 86. DOI: 10.1136/Jnnp-2015-312379.46 |
0.407 |
|
2015 |
Weston P, Paterson R, Lehmann M, Modat M, Bomanji J, Kayani I, Dickson J, Barnes A, Cash D, Ourselin S, Zetterberg H, Toombs J, Warren J, Rossor M, Fox N, et al. Using Florbetapir Pet To Increase Diagnostic Certainty In Atypical Dementias Journal of Neurology, Neurosurgery, and Psychiatry. 86. DOI: 10.1136/Jnnp-2015-312379.24 |
0.383 |
|
2015 |
Fletcher P, Rohrer J, Schott J, Rossor M, Warren J. Abnormal Pain And Temperature Processing In Dementia Journal of Neurology, Neurosurgery, and Psychiatry. 86. DOI: 10.1136/Jnnp-2015-312379.13 |
0.389 |
|
2015 |
Ryan NS, Rossor MN, Fox NC. Alzheimer's disease in the 100 years since Alzheimer's death Brain. 138: 3816-3821. DOI: 10.1093/brain/awv316 |
0.307 |
|
2015 |
Paterson RW, Toombs J, Slattery CF, Nicholas J, Blennow K, Andreasson U, Magdalinou NK, Warren JD, Mummery CJ, Rossor MN, Lunn M, Crutch SJ, Fox NC, Zetterberg H, Schott JM. Dissecting IWG-2 typical and atypical Alzheimer's disease: Insights from cerebrospinal fluid analysis Alzheimers & Dementia. 11: 254. DOI: 10.1016/J.Jalz.2015.07.315 |
0.407 |
|
2015 |
Cash DM, Dick KM, Fellows A, Espak M, Swieten JCv, Galimberti D, Borroni B, Masellis M, Tagliavini F, Graff C, Rowe J, Frisoni GB, Laforce R, Finger E, Sorbi S, ... ... Rossor MN, et al. MONDAY, JULY 20, 2015 ORAL SESSIONS O2-01 NEUROIMAGING: IMAGING — AUTOSOMAL DOMINANT ALZHEIMER'S DISEASE AND FTLDGrey matter differences in genetic frontotemporal dementia: Results from the genfi study Alzheimers & Dementia. 11. DOI: 10.1016/J.Jalz.2015.07.130 |
0.415 |
|
2015 |
Agustus JL, Clark CN, Golden HL, Slattery CF, Fletcher PD, Cohen MH, Downey LE, Mummery CJ, Rossor MN, Schott JM, Mead S, Rohrer JD, Fox NC, Warren JD. Dementia and music: fMRI signatures of molecular nexopathies Alzheimers & Dementia. 11: 528. DOI: 10.1016/J.Jalz.2015.06.658 |
0.332 |
|
2015 |
Ryan NS, Walsh P, Gami P, Troakes C, Rossor MN, Fox NC, Revesz T, Lashley T. Genetic influences on amyloid angiopathy and white matter pathology in familial Alzheimer's disease: A comparison of app and PSEN1 mutations Alzheimers & Dementia. 11: 431. DOI: 10.1016/J.Jalz.2015.06.411 |
0.434 |
|
2015 |
Weston PSJ, Lehmann M, Simpson I, Toussaint N, Harper L, Ryan NS, MacPherson K, Woodward F, Zhang H, Schott JM, Ourselin S, Rossor MN, Fox CN. Measurement of cortical mean diffusivity detects early microstructural breakdown of the cerebral cortex in presymptomatic familial Alzheimer’s disease Alzheimers & Dementia. 11: 81. DOI: 10.1016/J.Jalz.2015.06.140 |
0.32 |
|
2015 |
Weston PSJ, Lehmann M, Nicholas JM, Harper L, Ryan NS, MacPherson K, Woodward F, Schott JM, Rossor MN, Fox NC. A cortical signature of familial Alzheimer’s disease: Cross-sectional and longitudinal study of presymptomatic changes Alzheimers & Dementia. 11. DOI: 10.1016/J.Jalz.2015.06.139 |
0.321 |
|
2015 |
Cash DM, Dick KM, Fellows A, Espak M, Swieten JCv, Galimberti D, Borroni B, Masellis M, Tagliavini F, Graff C, Rowe J, Frisoni GB, Laforce R, Finger E, Sorbi S, ... ... Rossor MN, et al. Grey matter differences in genetic frontotemporal dementia: Results from the genfi study Alzheimers & Dementia. 11: 171. DOI: 10.1016/J.Jalz.2015.06.075 |
0.349 |
|
2015 |
Bocchetta M, Cardoso MJ, Cash DM, Rossor MN, Frisoni GB, Ourselin S, Rohrer JD. Volumetry of the cerebellum and its subregions in genetic frontotemporal dementia Alzheimers & Dementia. 11: 532. DOI: 10.1016/J.Jalz.2015.06.070 |
0.343 |
|
2015 |
Bocchetta M, Gordon E, Manning E, Cash DM, Espak M, Modat M, Ourselin S, Rossor MN, Frisoni GB, Rohrer JD. Detailed structural analysis of the hypothalamus in behavioral variant frontotemporal dementia Alzheimers & Dementia. 11. DOI: 10.1016/J.Jalz.2015.06.069 |
0.302 |
|
2014 |
Slattery CF, Beck JA, Harper L, Adamson G, Abdi Z, Uphill J, Campbell T, Druyeh R, Mahoney CJ, Rohrer JD, Kenny J, Lowe J, Leung KK, Barnes J, Clegg SL, ... ... Rossor MN, et al. R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 10: 602-608.e4. PMID 25160042 DOI: 10.1016/J.Jalz.2014.05.1751 |
0.443 |
|
2014 |
Thomas JB, Brier MR, Bateman RJ, Snyder AZ, Benzinger TL, Xiong C, Raichle M, Holtzman DM, Sperling RA, Mayeux R, Ghetti B, Ringman JM, Salloway S, McDade E, Rossor MN, et al. Functional connectivity in autosomal dominant and late-onset Alzheimer disease. Jama Neurology. 71: 1111-22. PMID 25069482 DOI: 10.1001/Jamaneurol.2014.1654 |
0.445 |
|
2014 |
Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JB, Dobson-Stone C, Brooks WS, Schofield PR, Halliday GM, Hodges JR, Piguet O, Bartley L, Thompson E, Haan E, ... ... Rossor MN, et al. Frontotemporal dementia and its subtypes: a genome-wide association study. The Lancet. Neurology. 13: 686-99. PMID 24943344 DOI: 10.1016/S1474-4422(14)70065-1 |
0.343 |
|
2014 |
Fagan AM, Xiong C, Jasielec MS, Bateman RJ, Goate AM, Benzinger TL, Ghetti B, Martins RN, Masters CL, Mayeux R, Ringman JM, Rossor MN, Salloway S, Schofield PR, Sperling RA, et al. Longitudinal change in CSF biomarkers in autosomal-dominant Alzheimer's disease. Science Translational Medicine. 6: 226ra30. PMID 24598588 DOI: 10.1126/Scitranslmed.3007901 |
0.467 |
|
2014 |
Downey LE, Fletcher PD, Golden HL, Mahoney CJ, Agustus JL, Schott JM, Rohrer JD, Beck J, Mead S, Rossor MN, Crutch SJ, Warren JD. Altered body schema processing in frontotemporal dementia with C9ORF72 mutations. Journal of Neurology, Neurosurgery, and Psychiatry. 85: 1016-23. PMID 24521566 DOI: 10.1136/Jnnp-2013-306995 |
0.368 |
|
2014 |
Mahoney CJ, Ridgway GR, Malone IB, Downey LE, Beck J, Kinnunen KM, Schmitz N, Golden HL, Rohrer JD, Schott JM, Rossor MN, Ourselin S, Mead S, Fox NC, Warren JD. Profiles of white matter tract pathology in frontotemporal dementia. Human Brain Mapping. 35: 4163-79. PMID 24510641 DOI: 10.1002/Hbm.22468 |
0.4 |
|
2014 |
Gallagher MD, Suh E, Grossman M, Elman L, McCluskey L, Van Swieten JC, Al-Sarraj S, Neumann M, Gelpi E, Ghetti B, Rohrer JD, Halliday G, Van Broeckhoven C, Seilhean D, Shaw PJ, ... ... Rossor M, et al. TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions. Acta Neuropathologica. 127: 407-18. PMID 24442578 DOI: 10.1007/S00401-013-1239-X |
0.338 |
|
2014 |
Lashley T, Rohrer JD, Mahoney C, Gordon E, Beck J, Mead S, Warren J, Rossor M, Revesz T. A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia. Neuropathology and Applied Neurobiology. 40: 502-13. PMID 24286341 DOI: 10.1111/Nan.12100 |
0.446 |
|
2014 |
Beck J, Pittman A, Adamson G, Campbell T, Kenny J, Houlden H, Rohrer JD, de Silva R, Shoai M, Uphill J, Poulter M, Hardy J, Mummery CJ, Warren JD, Schott JM, ... ... Rossor MN, et al. Validation of next-generation sequencing technologies in genetic diagnosis of dementia. Neurobiology of Aging. 35: 261-5. PMID 23998997 DOI: 10.1016/J.Neurobiolaging.2013.07.017 |
0.316 |
|
2014 |
Liang Y, Gordon E, Rohrer J, Downey L, de Silva R, Jäger HR, Nicholas J, Modat M, Cardoso MJ, Mahoney C, Warren J, Rossor M, Fox N, Caine D. A cognitive chameleon: lessons from a novel MAPT mutation case. Neurocase. 20: 684-94. PMID 23998300 DOI: 10.1080/13554794.2013.826697 |
0.389 |
|
2014 |
Kotting P, Rossor MN, McKeith IG, O'Brien JT. How dementia and neurodegenerative disease clinical research networks have enhanced research delivery in England Clinical Investigation. 4: 687-691. DOI: 10.4155/Cli.14.68 |
0.314 |
|
2014 |
Weston PSJ, Lehmann M, Ryan NS, Liang Y, Woodward FJ, Macpherson K, Rossor M, Fox N. A Cortical Atrophy Signature Of Familial Alzheimer'S Disease: Temporal Evolution Of Presymptomatic Changes Alzheimers & Dementia. 10: 401. DOI: 10.1016/J.Jalz.2014.05.496 |
0.348 |
|
2014 |
Kinnunen KM, Leung KK, Finnegan S, Leite AJB, Lehmann M, Nicholas JM, Cash DM, Ryan NS, Rossor MN, Ourselin S, Fox NC. Automated Segmentation Of Thalamus From Mri: Method Validation And Comparison For Volumetric Measurement In Familial Alzheimer'S Disease Alzheimers & Dementia. 10. DOI: 10.1016/J.Jalz.2014.05.200 |
0.397 |
|
2014 |
Ryan NS, Simpson I, Nicholas JM, Leung KK, Clegg S, Macpherson K, Kinnunen KM, Weston PSJ, Cash DM, Malone IB, Zhang H, Daga P, Toussaint N, Rossor MN, Ourselin S, et al. Longitudinal Volumetric And Diffusion Tensor Imaging In Familial Alzheimer'S Disease Alzheimers & Dementia. 10. DOI: 10.1016/J.Jalz.2014.05.182 |
0.381 |
|
2014 |
Cash DM, Kinnunen KM, Leung KK, Ahsan L, Cardoso J, Modat M, Nicholas J, Malone I, Benzinger T, Jack CR, Thompson P, Saykin AJ, Sperling RR, Villemagne V, Weiner M, ... ... Rossor M, et al. Longitudinal Rates Of Atrophy In Familial Alzheimer'S Disease Alzheimers & Dementia. 10. DOI: 10.1016/J.Jalz.2014.05.112 |
0.427 |
|
2013 |
Benzinger TL, Blazey T, Jack CR, Koeppe RA, Su Y, Xiong C, Raichle ME, Snyder AZ, Ances BM, Bateman RJ, Cairns NJ, Fagan AM, Goate A, Marcus DS, Aisen PS, ... ... Rossor MN, et al. Regional variability of imaging biomarkers in autosomal dominant Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America. 110: E4502-9. PMID 24194552 DOI: 10.1073/Pnas.1317918110 |
0.389 |
|
2013 |
Cash DM, Ridgway GR, Liang Y, Ryan NS, Kinnunen KM, Yeatman T, Malone IB, Benzinger TL, Jack CR, Thompson PM, Ghetti BF, Saykin AJ, Masters CL, Ringman JM, Salloway SP, ... ... Rossor MN, et al. The pattern of atrophy in familial Alzheimer disease: volumetric MRI results from the DIAN study. Neurology. 81: 1425-33. PMID 24049139 DOI: 10.1212/Wnl.0B013E3182A841C6 |
0.45 |
|
2013 |
Mills SM, Mallmann J, Santacruz AM, Fuqua A, Carril M, Aisen PS, Althage MC, Belyew S, Benzinger TL, Brooks WS, Buckles VD, Cairns NJ, Clifford D, Danek A, Fagan AM, ... ... Rossor MN, et al. Preclinical trials in autosomal dominant AD: implementation of the DIAN-TU trial. Revue Neurologique. 169: 737-43. PMID 24016464 DOI: 10.1016/J.Neurol.2013.07.017 |
0.339 |
|
2013 |
Rohrer JD, Warren JD, Fox NC, Rossor MN. Presymptomatic studies in genetic frontotemporal dementia. Revue Neurologique. 169: 820-4. PMID 24012408 DOI: 10.1016/J.Neurol.2013.07.010 |
0.414 |
|
2013 |
Warren JD, Rohrer JD, Rossor MN. Clinical review. Frontotemporal dementia. Bmj (Clinical Research Ed.). 347: f4827. PMID 23920254 DOI: 10.1136/Bmj.F4827 |
0.339 |
|
2013 |
Rohrer JD, Beck J, Plagnol V, Gordon E, Lashley T, Revesz T, Janssen JC, Fox NC, Warren JD, Rossor MN, Mead S, Schott JM. Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia. Journal of Neurology, Neurosurgery, and Psychiatry. 84: 1411-2. PMID 23904625 DOI: 10.1136/Jnnp-2013-306116 |
0.382 |
|
2013 |
Ahmed R, Guerreiro R, Rohrer JD, Guven G, Rossor MN, Hardy J, Fox NC. A novel A781V mutation in the CSF1R gene causes hereditary diffuse leucoencephalopathy with axonal spheroids. Journal of the Neurological Sciences. 332: 141-4. PMID 23816250 DOI: 10.1016/J.Jns.2013.06.007 |
0.313 |
|
2013 |
Guerreiro R, Kara E, Le Ber I, Bras J, Rohrer JD, Taipa R, Lashley T, Dupuits C, Gurunlian N, Mochel F, Warren JD, Hannequin D, Sedel F, Depienne C, Camuzat A, ... ... Rossor MN, et al. Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene. Jama Neurology. 70: 875-82. PMID 23649896 DOI: 10.1001/Jamaneurol.2013.698 |
0.347 |
|
2013 |
Ryan NS, Keihaninejad S, Shakespeare TJ, Lehmann M, Crutch SJ, Malone IB, Thornton JS, Mancini L, Hyare H, Yousry T, Ridgway GR, Zhang H, Modat M, Alexander DC, Rossor MN, et al. Magnetic resonance imaging evidence for presymptomatic change in thalamus and caudate in familial Alzheimer's disease. Brain : a Journal of Neurology. 136: 1399-414. PMID 23539189 DOI: 10.1093/Brain/Awt065 |
0.346 |
|
2013 |
Barnes J, Carmichael OT, Leung KK, Schwarz C, Ridgway GR, Bartlett JW, Malone IB, Schott JM, Rossor MN, Biessels GJ, DeCarli C, Fox NC. Vascular and Alzheimer's disease markers independently predict brain atrophy rate in Alzheimer's Disease Neuroimaging Initiative controls. Neurobiology of Aging. 34: 1996-2002. PMID 23522844 DOI: 10.1016/J.Neurobiolaging.2013.02.003 |
0.441 |
|
2013 |
Witoonpanich P, Cash DM, Shakespeare TJ, Yong KX, Nicholas JM, Omar R, Crutch SJ, Rossor MN, Warren JD. Olfactory impairment in posterior cortical atrophy. Journal of Neurology, Neurosurgery, and Psychiatry. 84: 588-90. PMID 23435114 DOI: 10.1136/Jnnp-2012-304497 |
0.44 |
|
2013 |
Beck J, Poulter M, Hensman D, Rohrer JD, Mahoney CJ, Adamson G, Campbell T, Uphill J, Borg A, Fratta P, Orrell RW, Malaspina A, Rowe J, Brown J, Hodges J, ... ... Rossor MN, et al. Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population. American Journal of Human Genetics. 92: 345-53. PMID 23434116 DOI: 10.1016/J.Ajhg.2013.01.011 |
0.386 |
|
2013 |
Rohrer JD, Caso F, Mahoney C, Henry M, Rosen HJ, Rabinovici G, Rossor MN, Miller B, Warren JD, Fox NC, Ridgway GR, Gorno-Tempini ML. Patterns of longitudinal brain atrophy in the logopenic variant of primary progressive aphasia. Brain and Language. 127: 121-6. PMID 23395096 DOI: 10.1016/J.Bandl.2012.12.008 |
0.382 |
|
2013 |
Scahill RI, Ridgway GR, Bartlett JW, Barnes J, Ryan NS, Mead S, Beck J, Clarkson MJ, Crutch SJ, Schott JM, Ourselin S, Warren JD, Hardy J, Rossor MN, Fox NC. Genetic influences on atrophy patterns in familial Alzheimer's disease: a comparison of APP and PSEN1 mutations. Journal of Alzheimer's Disease : Jad. 35: 199-212. PMID 23380992 DOI: 10.3233/Jad-121255 |
0.448 |
|
2013 |
Mahoney CJ, Malone IB, Ridgway GR, Buckley AH, Downey LE, Golden HL, Ryan NS, Ourselin S, Schott JM, Rossor MN, Fox NC, Warren JD. White matter tract signatures of the progressive aphasias. Neurobiology of Aging. 34: 1687-99. PMID 23312804 DOI: 10.1016/J.Neurobiolaging.2012.12.002 |
0.362 |
|
2013 |
Mahoney C, Yeatman T, Rohrer J, Manning E, Leung K, Rossor M, Warren J, Fox N. The Evolution Of Frontotemporal Dementia Due To The Mapt Mutation: A Seventeen Year Natural History Study Journal of Neurology, Neurosurgery, and Psychiatry. 84. DOI: 10.1136/Jnnp-2013-306573.86 |
0.421 |
|
2013 |
Rossor M, Ahmed R, Liang Y, Douglas J, Mahoney C, Warren J, Schott J, Fox N. Longitudinal Research Into Alzheimer'S Disease, Fronto–Temporal Dementia And Other Dementias Journal of Neurology, Neurosurgery, and Psychiatry. 84. DOI: 10.1136/Jnnp-2013-306573.68 |
0.463 |
|
2013 |
Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, ... ... Rossor M, et al. Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Nature Genetics. 45: 712-712. DOI: 10.1038/Ng0613-712A |
0.351 |
|
2013 |
Mills S, Mallmann J, Santacruz A, Fuqua A, Carril M, Aisen P, Althage M, Belyew S, Benzinger T, Brooks W, Buckles V, Cairns N, Clifford D, Danek A, Fagan A, ... ... Rossor M, et al. Erratum to “Preclinical trials in autosomal dominant AD: Implementation of the DIAN-TU trial” [Rev. Neurol. 169 (10) (2013) 737–743] Revue Neurologique. 169: 1018. DOI: 10.1016/J.Neurol.2013.10.005 |
0.302 |
|
2013 |
Thomas J, Brier M, Bateman R, Snyder A, Benzinger T, Xiong C, Raichle M, Sperling R, Mayeux R, Ghetti B, Ringman J, Salloway S, McDade E, Rossor M, Schofield P, et al. IC-P-184: Resting state functional connectivity in autosomal dominant and sporadic Alzheimer's disease Alzheimer's & Dementia. 9: P105-P105. DOI: 10.1016/J.Jalz.2013.05.181 |
0.364 |
|
2013 |
Blazey T, Jack C, Kantarci K, Preboske G, Ringman J, Brickman A, Raichle M, Hornbeck R, Saykin A, Salloway S, McDade E, Rossor M, Fox N, Thompson P, Correia S, et al. Prevalence and growth of cerebral microhemorrhages in autosomal dominant Alzheimer's disease Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.05.100 |
0.405 |
|
2013 |
Cash D, Ridgway G, Modat M, Ryan N, Kinnunen K, Cardoso J, Benzinger T, Jack CR, Raichle M, Marcus D, Ringman J, Thompson P, Ghetti B, Salloway S, Sperling R, ... ... Rossor M, et al. Dissociating volume and intensity differences in familial Alzheimer's disease Alzheimers & Dementia. 9: 603. DOI: 10.1016/J.Jalz.2013.05.075 |
0.42 |
|
2013 |
Cash D, Ridgway G, Ryan N, Liang Y, Kinnunen K, Mahoney C, Rossor M, Ourselin S, Fox N. Comparison of local grey matter volume in familial and sporadic Alzheimer’s disease Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.05.074 |
0.352 |
|
2013 |
Kinnunen K, Ridgway G, Cash D, Leite AB, Finnegan S, Daga P, Cardoso M, Ryan N, Espak M, Rossor M, Ourselin S, Fox N. Abnormalities of fronto-striato-thalamic tract structure and effective connectivity in familial Alzheimer's disease Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.04.351 |
0.422 |
|
2013 |
Kinnunen K, Ryan N, Cash D, Leite AB, Finnegan S, Cardoso M, Leung K, Modat M, Benzinger T, Jack C, Marcus D, Raichle M, Thompson P, Ringman J, Ghetti B, ... ... Rossor M, et al. Are early atrophy patterns in autosomal dominant familial Alzheimer's disease gene-dependent? Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.04.017 |
0.413 |
|
2012 |
Morris JC, Aisen PS, Bateman RJ, Benzinger TL, Cairns NJ, Fagan AM, Ghetti B, Goate AM, Holtzman DM, Klunk WE, McDade E, Marcus DS, Martins RN, Masters CL, Mayeux R, ... ... Rossor MN, et al. Developing an international network for Alzheimer research: The Dominantly Inherited Alzheimer Network. Clinical Investigation. 2: 975-984. PMID 23139856 DOI: 10.4155/Cli.12.93 |
0.419 |
|
2012 |
Downey LE, Mahoney CJ, Rossor MN, Crutch SJ, Warren JD. Impaired self-other differentiation in frontotemporal dementia due to the C9ORF72 expansion. Alzheimer's Research & Therapy. 4: 42. PMID 23016833 DOI: 10.1186/Alzrt145 |
0.379 |
|
2012 |
Wray S, Self M, Lewis PA, Taanman JW, Ryan NS, Mahoney CJ, Liang Y, Devine MJ, Sheerin UM, Houlden H, Morris HR, Healy D, ... ... Rossor MN, et al. Creation of an open-access, mutation-defined fibroblast resource for neurological disease research. Plos One. 7: e43099. PMID 22952635 DOI: 10.1371/Journal.Pone.0043099 |
0.325 |
|
2012 |
Sorbi S, Hort J, Erkinjuntti T, Fladby T, Gainotti G, Gurvit H, Nacmias B, Pasquier F, Popescu BO, Rektorova I, Religa D, Rusina R, Rossor M, Schmidt R, Stefanova E, et al. EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 19: 1159-79. PMID 22891773 DOI: 10.1111/J.1468-1331.2012.03784.X |
0.422 |
|
2012 |
Bateman RJ, Xiong C, Benzinger TL, Fagan AM, Goate A, Fox NC, Marcus DS, Cairns NJ, Xie X, Blazey TM, Holtzman DM, Santacruz A, Buckles V, Oliver A, Moulder K, ... ... Rossor MN, et al. Clinical and biomarker changes in dominantly inherited Alzheimer's disease. The New England Journal of Medicine. 367: 795-804. PMID 22784036 DOI: 10.1056/Nejmoa1202753 |
0.446 |
|
2012 |
Rohrer JD, Clarkson MJ, Kittus R, Rossor MN, Ourselin S, Warren JD, Fox NC. Rates of hemispheric and lobar atrophy in the language variants of frontotemporal lobar degeneration. Journal of Alzheimer's Disease : Jad. 30: 407-11. PMID 22406442 DOI: 10.3233/Jad-2012-111556 |
0.358 |
|
2012 |
Mahoney CJ, Beck J, Rohrer JD, Lashley T, Mok K, Shakespeare T, Yeatman T, Warrington EK, Schott JM, Fox NC, Rossor MN, Hardy J, Collinge J, Revesz T, Mead S, et al. Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features. Brain : a Journal of Neurology. 135: 736-50. PMID 22366791 DOI: 10.1093/Brain/Awr361 |
0.395 |
|
2012 |
Crutch SJ, Lehmann M, Schott JM, Rabinovici GD, Rossor MN, Fox NC. Posterior cortical atrophy. The Lancet. Neurology. 11: 170-8. PMID 22265212 DOI: 10.1016/S1474-4422(11)70289-7 |
0.431 |
|
2012 |
Gerrish A, Russo G, Richards A, Moskvina V, Ivanov D, Harold D, Sims R, Abraham R, Hollingworth P, Chapman J, Hamshere M, Pahwa JS, Dowzell K, Williams A, Jones N, ... ... Rossor M, et al. The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 28: 377-87. PMID 22027014 DOI: 10.3233/Jad-2011-110824 |
0.415 |
|
2012 |
Ryan NS, Bastos-Leite AJ, Rohrer JD, Werring DJ, Fox NC, Rossor MN, Schott JM. Cerebral microbleeds in familial Alzheimer's disease. Brain : a Journal of Neurology. 135: e201; author reply e. PMID 21685457 DOI: 10.1093/Brain/Awr126 |
0.453 |
|
2012 |
McNaughton D, Knight W, Guerreiro R, Ryan N, Lowe J, Poulter M, Nicholl DJ, Hardy J, Revesz T, Lowe J, Rossor M, Collinge J, Mead S. Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series. Neurobiology of Aging. 33: 426.e13-21. PMID 21193246 DOI: 10.1016/J.Neurobiolaging.2010.10.010 |
0.415 |
|
2012 |
Rohrer JD, Rossor MN, Warren JD. Alzheimer's pathology in primary progressive aphasia. Neurobiology of Aging. 33: 744-52. PMID 20580129 DOI: 10.1016/J.Neurobiolaging.2010.05.020 |
0.427 |
|
2012 |
Mahoney C, Rossor MN, Fox NC, Warren JD. 019 Profiles of white matter degeneration in frontotemporal dementia Journal of Neurology, Neurosurgery, and Psychiatry. 83. DOI: 10.1136/Jnnp-2011-301993.61 |
0.387 |
|
2012 |
Ryan N, Biessels G, Bastos-Leite A, Beck J, Mead S, Morris H, Schott JM, Rossor MN, Fox NC. White Matter Lesions In Familial Alzheimer'S Disease: Evidence For Influence Of Mutation Position On Amyloid Angiopathy? Journal of Neurology, Neurosurgery, and Psychiatry. 83. DOI: 10.1136/Jnnp-2011-301993.1 |
0.373 |
|
2012 |
Ryan N, Liang Y, Beck J, Mead S, Rossor M, Fox N. Clinical spectrum of familial Alzheimer's disease in 100 cases Alzheimers & Dementia. 8: 262. DOI: 10.1016/J.Jalz.2012.05.697 |
0.432 |
|
2012 |
Schott J, Crutch S, Uphill J, Ryan N, Shakespeare T, Lehmann M, Yong K, Rossor M, Fox N, Mead S. Genetic risk factors for posterior cortical atrophy may be distinct from late-onset Alzheimer's disease Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.1810 |
0.394 |
|
2012 |
Kinnunen K, Cash D, Leung K, Liang Y, Cardoso M, Modat M, Malone I, Benzinger T, Koeppe R, Jack C, Raichle M, Marcus D, Ringman J, Thompson P, Saykin A, ... ... Rossor M, et al. Brain and hippocampal rates of atrophy in familial Alzheimer's disease mutation carriers: Preliminary findings from the DIAN study Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.172 |
0.429 |
|
2012 |
Liang Y, Crutch S, Nicholas J, Ryan N, Warrington E, Shakespeare T, Yeatman T, Rossor M, Fox N. Longitudinal presymptomatic cognitive changes in individuals at risk of familial Alzheimer's disease Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.1167 |
0.4 |
|
2012 |
Kinnunen K, Cash D, Liang Y, Leung K, Cardoso M, Modat M, Malone I, Yeatman T, Nicholas J, Benzinger T, Koeppe R, Jack C, Raichle M, Marcus D, Ringman J, ... ... Rossor M, et al. Cross-sectional cerebral volumetric differences and associations with estimated time to age-at-onset in familial Alzheimer's disease: Findings from the DIAN study Alzheimers & Dementia. 8: 23. DOI: 10.1016/J.Jalz.2012.05.064 |
0.395 |
|
2012 |
Cash D, Liang Y, Leung K, Ryan N, Modat M, Cardoso M, Yeatman T, Crutch S, Woodward F, Malone I, Bartlett J, Kinnunen K, Rossor M, Ourselin S, Fox N. Rates of brain and hippocampal atrophy in presymptomatic familial Alzheimer's disease: Acceleration and mutation effects Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.053 |
0.421 |
|
2012 |
Cash D, Ridgway G, Ryan N, Kinnunen K, Yeatman T, Malone I, Benzinger T, Koeppe R, Jack C, Raichle M, Marcus D, Ringman J, Thompson P, Saykin A, Salloway S, ... ... Rossor M, et al. A voxel-based morphometry study of volumetric MRI in familial Alzheimer’s disease Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2012.05.052 |
0.377 |
|
2012 |
Mahoney CJ, Rohrer JD, Beck J, Shakespeare T, Yeatman T, Schot JM, Fox N, Rossor MN, Hardy J, Collinge J, Mead S, Warren JD. The neuroimaging phenotype of frontotemporal dementia with the C9ORF72 hexanucletoide repeat expansion Alzheimers & Dementia. 8: 8. DOI: 10.1016/J.Jalz.2012.05.025 |
0.395 |
|
2012 |
Bateman R, Benzinger T, Cairns N, Fagan A, Goate A, Marcus D, Storandt M, Xiong C, Buckles V, Holtzman D, Moulder K, Oliver A, Santacruz A, Fox N, Ghetti B, ... ... Rossor M, et al. Presymptomatic Alzheimer's disease in the Dominantly Inherited Alzheimer's Network (DIAN) Alzheimers & Dementia. 8: 4. DOI: 10.1016/J.Jalz.2012.05.015 |
0.414 |
|
2011 |
Ryan NS, Rossor MN. Defining and describing the pre-dementia stages of familial Alzheimer's disease. Alzheimer's Research & Therapy. 3: 29. PMID 21952009 DOI: 10.1186/Alzrt91 |
0.465 |
|
2011 |
Schott JM, Warren JD, Barkhof F, Rossor MN, Fox NC. Suspected early dementia. Bmj (Clinical Research Ed.). 343: d5568. PMID 21933826 DOI: 10.1136/Bmj.D5568 |
0.36 |
|
2011 |
Rohrer JD, Lashley T, Schott JM, Warren JE, Mead S, Isaacs AM, Beck J, Hardy J, de Silva R, Warrington E, Troakes C, Al-Sarraj S, King A, Borroni B, Clarkson MJ, ... ... Rossor MN, et al. Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration. Brain : a Journal of Neurology. 134: 2565-81. PMID 21908872 DOI: 10.1093/Brain/Awr198 |
0.459 |
|
2011 |
Brelstaff J, Lashley T, Holton JL, Lees AJ, Rossor MN, Bandopadhyay R, Revesz T. Transportin1: a marker of FTLD-FUS. Acta Neuropathologica. 122: 591-600. PMID 21847626 DOI: 10.1007/S00401-011-0863-6 |
0.328 |
|
2011 |
Sims R, Dwyer S, Harold D, Gerrish A, Hollingworth P, Chapman J, Jones N, Abraham R, Ivanov D, Pahwa JS, Moskvina V, Dowzell K, Thomas C, Stretton A, Lovestone S, ... ... Rossor M, et al. No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 764-71. PMID 21812096 DOI: 10.1002/Ajmg.B.31216 |
0.431 |
|
2011 |
Rascovsky K, Hodges JR, Knopman D, Mendez MF, Kramer JH, Neuhaus J, van Swieten JC, Seelaar H, Dopper EG, Onyike CU, Hillis AE, Josephs KA, Boeve BF, Kertesz A, Seeley WW, ... ... Rossor MN, et al. Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain : a Journal of Neurology. 134: 2456-77. PMID 21810890 DOI: 10.1093/Brain/Awr179 |
0.417 |
|
2011 |
Lashley T, Rohrer JD, Bandopadhyay R, Fry C, Ahmed Z, Isaacs AM, Brelstaff JH, Borroni B, Warren JD, Troakes C, King A, Al-Saraj S, Newcombe J, Quinn N, Ostergaard K, ... ... Rossor MN, et al. A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies. Brain : a Journal of Neurology. 134: 2548-64. PMID 21752791 DOI: 10.1093/Brain/Awr160 |
0.353 |
|
2011 |
Mahoney CJ, Rohrer JD, Goll JC, Fox NC, Rossor MN, Warren JD. Structural neuroanatomy of tinnitus and hyperacusis in semantic dementia. Journal of Neurology, Neurosurgery, and Psychiatry. 82: 1274-8. PMID 21531705 DOI: 10.1136/Jnnp.2010.235473 |
0.334 |
|
2011 |
McKhann GM, Knopman DS, Chertkow H, Hyman BT, Jack CR, Kawas CH, Klunk WE, Koroshetz WJ, Manly JJ, Mayeux R, Mohs RC, Morris JC, Rossor MN, Scheltens P, Carrillo MC, et al. The diagnosis of dementia due to Alzheimer's disease: recommendations from the National Institute on Aging-Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 7: 263-9. PMID 21514250 DOI: 10.1016/J.Jalz.2011.03.005 |
0.449 |
|
2011 |
Rohrer JD, Warren JD, Reiman D, Uphill J, Beck J, Collinge J, Rossor MN, Isaacs AM, Mead S. A novel exon 2 I27V VCP variant is associated with dissimilar clinical syndromes. Journal of Neurology. 258: 1494-6. PMID 21387114 DOI: 10.1007/S00415-011-5966-4 |
0.428 |
|
2011 |
Mahoney CJ, Rohrer JD, Omar R, Rossor MN, Warren JD. Neuroanatomical profiles of personality change in frontotemporal lobar degeneration. The British Journal of Psychiatry : the Journal of Mental Science. 198: 365-72. PMID 21372059 DOI: 10.1192/Bjp.Bp.110.082677 |
0.313 |
|
2011 |
Knight WD, Okello AA, Ryan NS, Turkheimer FE, RodrÃguez Martinez de Llano S, Edison P, Douglas J, Fox NC, Brooks DJ, Rossor MN. Carbon-11-Pittsburgh compound B positron emission tomography imaging of amyloid deposition in presenilin 1 mutation carriers. Brain : a Journal of Neurology. 134: 293-300. PMID 21084313 DOI: 10.1093/Brain/Awq310 |
0.303 |
|
2011 |
Rohrer JD, Paviour D, Vandrovcova J, Hodges J, de Silva R, Rossor MN. Novel L284R MAPT mutation in a family with an autosomal dominant progressive supranuclear palsy syndrome. Neuro-Degenerative Diseases. 8: 149-52. PMID 20838030 DOI: 10.1159/000319454 |
0.33 |
|
2011 |
Rohrer JD, Lashley T, Holton J, Revesz T, Urwin H, Isaacs AM, Fox NC, Rossor MN, Warren J. The clinical and neuroanatomical phenotype of FUS associated frontotemporal lobar degeneration. Journal of Neurology, Neurosurgery, and Psychiatry. 82: 1405-7. PMID 20639383 DOI: 10.1136/Jnnp.2010.214437 |
0.403 |
|
2011 |
Knight WD, Kim LG, Douiri A, Frost C, Rossor MN, Fox NC. Acceleration of cortical thinning in familial Alzheimer's disease. Neurobiology of Aging. 32: 1765-73. PMID 20005601 DOI: 10.1016/J.Neurobiolaging.2009.11.013 |
0.44 |
|
2011 |
Lehmann M, Crutch SJ, Ridgway GR, Ridha BH, Barnes J, Warrington EK, Rossor MN, Fox NC. Cortical thickness and voxel-based morphometry in posterior cortical atrophy and typical Alzheimer's disease. Neurobiology of Aging. 32: 1466-76. PMID 19781814 DOI: 10.1016/J.Neurobiolaging.2009.08.017 |
0.405 |
|
2011 |
Lehmann M, Rohrer JD, Clarkson MJ, Ridgway GR, Scahill RI, Modat M, Warren JD, Ourselin S, Barnes J, Rossor MN, Fox NC. Patterns of cortical thickness in pathologically-confirmed typical and atypical Alzheimer's disease Advances in Alzheimer's Disease. 2: 57-67. DOI: 10.3233/978-1-60750-793-2-57 |
0.313 |
|
2011 |
Ryan NS, Okello A, Knight WD, Lehmann M, Malone I, Clarkson M, Bartlett J, Ridgway G, Mancini L, Thornton J, Ourselin S, Brooks D, Rossor M, Fox N. Early subcortical amyloid deposition in familial Alzheimer's disease is accompanied by changes in tissue volume and diffusivity Journal of Neurology, Neurosurgery, and Psychiatry. 82. DOI: 10.1136/Jnnp.2010.235572.6 |
0.347 |
|
2011 |
Ryan N, Rossor MN, Fox NC. P.01 Characterising the clinical phenotype of familial Alzheimer's disease (FAD) Journal of Neurology, Neurosurgery, and Psychiatry. 82. DOI: 10.1136/Jnnp-2011-300645.1 |
0.401 |
|
2011 |
Ryan N, Biessels G, Bastos-Leite A, Mead S, Rossor M, Fox N. White matter lesions in familial Alzheimer's disease: evidence for influence of mutation position on amyloid angiopathy? Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.666 |
0.407 |
|
2011 |
Rohrer J, Clarkson M, Kittus R, Rossor M, Ourselin S, Warren J, Fox N. Tracking progression with serial MRI in the language variants of frontotemporal lobar degeneration Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.623 |
0.346 |
|
2011 |
Rascovsky K, Hodges JR, Knopman D, Mendez MF, Kramer JH, Xie S, van Swieten JC, Seelaar H, Dopper EG, Onyike CU, Hillis A, Josephs KA, Boeve BF, Kertesz A, Seeley WW, ... ... Rossor M, et al. P4-166: Determinants of survival in autopsy-confirmed patients with behavioral variant frontotemporal dementia (bvFTD): Second Report of the international bvFTD criteria consortium (FTDC) Alzheimer's & Dementia. 7: S761-S762. DOI: 10.1016/J.Jalz.2011.05.2188 |
0.329 |
|
2011 |
Rossor M. Dominantly Inherited Alzheimer Network (DIAN): History genetic and pathology overview and update Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.1959 |
0.331 |
|
2011 |
Barnes J, Carmichael O, Leung K, Schwarz C, Ridgway G, Bartlett J, Malone I, Schott J, Rossor M, Biessels G, DeCarli C, Fox N. The independent effects of white matter hyperintensity volume and cerebrospinal fluid amyloid levels on brain atrophy Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.014 |
0.419 |
|
2010 |
Jones L, Holmans PA, Hamshere ML, Harold D, Moskvina V, Ivanov D, Pocklington A, Abraham R, Hollingworth P, Sims R, Gerrish A, Pahwa JS, Jones N, Stretton A, Morgan AR, ... ... Rossor M, et al. Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease. Plos One. 5: e13950. PMID 21085570 DOI: 10.1371/Journal.Pone.0013950 |
0.35 |
|
2010 |
Dubois B, Feldman HH, Jacova C, Cummings JL, Dekosky ST, Barberger-Gateau P, Delacourte A, Frisoni G, Fox NC, Galasko D, Gauthier S, Hampel H, Jicha GA, Meguro K, O'Brien J, ... ... Rossor M, et al. Revising the definition of Alzheimer's disease: a new lexicon. The Lancet. Neurology. 9: 1118-27. PMID 20934914 DOI: 10.1016/S1474-4422(10)70223-4 |
0.433 |
|
2010 |
Rohrer JD, Rossor MN, Warren JD. Syndromes of nonfluent primary progressive aphasia: a clinical and neurolinguistic analysis. Neurology. 75: 603-10. PMID 20713949 DOI: 10.1212/Wnl.0B013E3181Ed9C6B |
0.337 |
|
2010 |
Rossor MN, Fox NC, Mummery CJ, Schott JM, Warren JD. The diagnosis of young-onset dementia. The Lancet. Neurology. 9: 793-806. PMID 20650401 DOI: 10.1016/S1474-4422(10)70159-9 |
0.455 |
|
2010 |
Urwin H, Josephs KA, Rohrer JD, Mackenzie IR, Neumann M, Authier A, Seelaar H, Van Swieten JC, Brown JM, Johannsen P, Nielsen JE, Holm IE, Dickson DW, Rademakers R, ... ... Rossor MN, et al. FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration. Acta Neuropathologica. 120: 33-41. PMID 20490813 DOI: 10.1007/S00401-010-0698-6 |
0.356 |
|
2010 |
Ryan NS, Rossor MN. Correlating familial Alzheimer's disease gene mutations with clinical phenotype. Biomarkers in Medicine. 4: 99-112. PMID 20387306 DOI: 10.2217/Bmm.09.92 |
0.452 |
|
2010 |
Guerreiro RJ, Beck J, Gibbs JR, Santana I, Rossor MN, Schott JM, Nalls MA, Ribeiro H, Santiago B, Fox NC, Oliveira C, Collinge J, Mead S, Singleton A, Hardy J. Genetic variability in CLU and its association with Alzheimer's disease. Plos One. 5: e9510. PMID 20209083 DOI: 10.1371/Journal.Pone.0009510 |
0.35 |
|
2010 |
Barnes J, Mitchell LA, Kennedy J, Bastos-Leite AJ, Barker S, Lehmann M, Nordstrom RC, Frost C, Smith JR, Garde E, Rossor MN, Fox NC. Does registration of serial MRI improve diagnosis of dementia? Neuroradiology. 52: 987-95. PMID 20195590 DOI: 10.1007/S00234-010-0665-X |
0.352 |
|
2010 |
Rinne JO, Brooks DJ, Rossor MN, Fox NC, Bullock R, Klunk WE, Mathis CA, Blennow K, Barakos J, Okello AA, Rodriguez Martinez de Liano S, Liu E, Koller M, Gregg KM, Schenk D, et al. 11C-PiB PET assessment of change in fibrillar amyloid-beta load in patients with Alzheimer's disease treated with bapineuzumab: a phase 2, double-blind, placebo-controlled, ascending-dose study. The Lancet. Neurology. 9: 363-72. PMID 20189881 DOI: 10.1016/S1474-4422(10)70043-0 |
0.331 |
|
2010 |
Lehmann M, Rohrer JD, Clarkson MJ, Ridgway GR, Scahill RI, Modat M, Warren JD, Ourselin S, Barnes J, Rossor MN, Fox NC. Reduced cortical thickness in the posterior cingulate gyrus is characteristic of both typical and atypical Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 20: 587-98. PMID 20182057 DOI: 10.3233/Jad-2010-1401 |
0.431 |
|
2010 |
Gordon E, Rohrer JD, Kim LG, Omar R, Rossor MN, Fox NC, Warren JD. Measuring disease progression in frontotemporal lobar degeneration: a clinical and MRI study. Neurology. 74: 666-73. PMID 20177120 DOI: 10.1212/Wnl.0B013E3181D1A879 |
0.394 |
|
2010 |
Archer HA, Kennedy J, Barnes J, Pepple T, Boyes R, Randlesome K, Clegg S, Leung KK, Ourselin S, Frost C, Rossor MN, Fox NC. Memory complaints and increased rates of brain atrophy: risk factors for mild cognitive impairment and Alzheimer's disease. International Journal of Geriatric Psychiatry. 25: 1119-26. PMID 20084620 DOI: 10.1002/Gps.2440 |
0.366 |
|
2010 |
Rohrer JD, Ridgway GR, Modat M, Ourselin S, Mead S, Fox NC, Rossor MN, Warren JD. Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations. Neuroimage. 53: 1070-6. PMID 20045477 DOI: 10.1016/J.Neuroimage.2009.12.088 |
0.373 |
|
2010 |
Petzold A, Chapman MD, Schraen S, Verwey NA, Pasquier F, Bombois S, Brettschneider J, Fox NC, von Arnim CA, Teunissen C, Pijnenburg Y, Riepe MW, Otto M, Tumani H, Scheltens P, ... ... Rossor MN, et al. An unbiased, staged, multicentre, validation strategy for Alzheimer's disease CSF tau levels. Experimental Neurology. 223: 432-8. PMID 20005225 DOI: 10.1016/J.Expneurol.2009.11.010 |
0.363 |
|
2010 |
Rohrer JD, Rossor MN, Warren JD. Apraxia in progressive nonfluent aphasia. Journal of Neurology. 257: 569-74. PMID 19908082 DOI: 10.1007/S00415-009-5371-4 |
0.377 |
|
2010 |
Bird CM, Chan D, Hartley T, Pijnenburg YA, Rossor MN, Burgess N. Topographical short-term memory differentiates Alzheimer's disease from frontotemporal lobar degeneration. Hippocampus. 20: 1154-69. PMID 19852032 DOI: 10.1002/Hipo.20715 |
0.394 |
|
2010 |
Rohrer JD, Ridgway GR, Crutch SJ, Hailstone J, Goll JC, Clarkson MJ, Mead S, Beck J, Mummery C, Ourselin S, Warrington EK, Rossor MN, Warren JD. Progressive logopenic/phonological aphasia: erosion of the language network. Neuroimage. 49: 984-93. PMID 19679189 DOI: 10.1016/J.Neuroimage.2009.08.002 |
0.362 |
|
2010 |
Mahoney C, Rossor MN, Rohrer JD, Warren JD, Fox NC, Goll JC. POD07 Tinnitus and hyperacusis in semantic dementia Journal of Neurology, Neurosurgery, and Psychiatry. 81. DOI: 10.1136/Jnnp.2010.226340.107 |
0.337 |
|
2010 |
Ryan NS, Okello A, Knight WD, Lehmann M, Malone I, Clarkson MJ, Bartlett J, Ridgway GR, Mancini L, Thornton J, Ourselin S, Brooks DJ, Rossor MN, Fox NC. Early subcortical amyloid deposition in familial Alzheimer's disease is accompanied by changes in tissue volume and diffusivity Alzheimers & Dementia. 6. DOI: 10.1016/J.Jalz.2010.05.429 |
0.392 |
|
2009 |
Knight WD, Ahsan RL, Jackson J, Cipolotti L, Warrington EK, Fox NC, Rossor MN. Pure progressive amnesia and the APPV717G mutation. Alzheimer Disease and Associated Disorders. 23: 410-4. PMID 19950418 DOI: 10.1097/Wad.0B013E31819Cb7F3 |
0.439 |
|
2009 |
Rohrer JD, Guerreiro R, Vandrovcova J, Uphill J, Reiman D, Beck J, Isaacs AM, Authier A, Ferrari R, Fox NC, Mackenzie IR, Warren JD, de Silva R, Holton J, Revesz T, ... ... Rossor MN, et al. The heritability and genetics of frontotemporal lobar degeneration. Neurology. 73: 1451-6. PMID 19884572 DOI: 10.1212/Wnl.0B013E3181Bf997A |
0.404 |
|
2009 |
Lloyd SE, Rossor M, Fox N, Mead S, Collinge J. HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q. Bmc Medical Genetics. 10: 90. PMID 19754925 DOI: 10.1186/1471-2350-10-90 |
0.394 |
|
2009 |
Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, ... ... Rossor M, et al. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Nature Genetics. 41: 1088-93. PMID 19734902 DOI: 10.1038/Ng.440 |
0.322 |
|
2009 |
Okello A, Koivunen J, Edison P, Archer HA, Turkheimer FE, NÃ¥gren K, Bullock R, Walker Z, Kennedy A, Fox NC, Rossor MN, Rinne JO, Brooks DJ. Conversion of amyloid positive and negative MCI to AD over 3 years: an 11C-PIB PET study. Neurology. 73: 754-60. PMID 19587325 DOI: 10.1212/Wnl.0B013E3181B23564 |
0.389 |
|
2009 |
Rohrer JD, Warren JD, Rossor MN. Abnormal laughter-like vocalisations replacing speech in primary progressive aphasia. Journal of the Neurological Sciences. 284: 120-3. PMID 19435636 DOI: 10.1016/J.Jns.2009.04.021 |
0.323 |
|
2009 |
Rohrer JD, Warren JD, Modat M, Ridgway GR, Douiri A, Rossor MN, Ourselin S, Fox NC. Patterns of cortical thinning in the language variants of frontotemporal lobar degeneration. Neurology. 72: 1562-9. PMID 19414722 DOI: 10.1212/Wnl.0B013E3181A4124E |
0.34 |
|
2009 |
Kolstoe SE, Ridha BH, Bellotti V, Wang N, Robinson CV, Crutch SJ, Keir G, Kukkastenvehmas R, Gallimore JR, Hutchinson WL, Hawkins PN, Wood SP, Rossor MN, Pepys MB. Molecular dissection of Alzheimer's disease neuropathology by depletion of serum amyloid P component. Proceedings of the National Academy of Sciences of the United States of America. 106: 7619-23. PMID 19372378 DOI: 10.1073/Pnas.0902640106 |
0.393 |
|
2009 |
Omar R, Sampson EL, Loy CT, Mummery CJ, Fox NC, Rossor MN, Warren JD. Delusions in frontotemporal lobar degeneration. Journal of Neurology. 256: 600-7. PMID 19365594 DOI: 10.1007/S00415-009-0128-7 |
0.391 |
|
2009 |
Chan D, Anderson V, Pijnenburg Y, Whitwell J, Barnes J, Scahill R, Stevens JM, Barkhof F, Scheltens P, Rossor MN, Fox NC. The clinical profile of right temporal lobe atrophy. Brain : a Journal of Neurology. 132: 1287-98. PMID 19297506 DOI: 10.1093/Brain/Awp037 |
0.326 |
|
2009 |
Collinge J, Gorham M, Hudson F, Kennedy A, Keogh G, Pal S, Rossor M, Rudge P, Siddique D, Spyer M, Thomas D, Walker S, Webb T, Wroe S, Darbyshire J. Safety and efficacy of quinacrine in human prion disease (PRION-1 study): a patient-preference trial. The Lancet. Neurology. 8: 334-44. PMID 19278902 DOI: 10.1016/S1474-4422(09)70049-3 |
0.357 |
|
2009 |
Rollinson S, Rizzu P, Sikkink S, Baker M, Halliwell N, Snowden J, Traynor BJ, Ruano D, Cairns N, Rohrer JD, Mead S, Collinge J, Rossor M, Akay E, Guerreiro R, et al. Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration. Neurobiology of Aging. 30: 656-65. PMID 19217189 DOI: 10.1016/J.Neurobiolaging.2009.01.009 |
0.338 |
|
2009 |
Rohrer JD, Ahsan RL, Isaacs AM, Nielsen JE, Ostergaard L, Scahill R, Warren JD, Rossor MN, Fox NC, Johannsen P. Presymptomatic generalized brain atrophy in frontotemporal dementia caused by CHMP2B mutation. Dementia and Geriatric Cognitive Disorders. 27: 182-6. PMID 19202337 DOI: 10.1159/000200466 |
0.388 |
|
2009 |
Okello A, Edison P, Archer HA, Turkheimer FE, Kennedy JC, Bullock R, Walker Z, Kennedy A, Fox NCI, Rossor M, Brooks DJ. Microglial activation and amyloid deposition in mild cognitive impairment A PET study Neurology. 72: 56-62. PMID 19122031 DOI: 10.1212/01.Wnl.0000338622.27876.0D |
0.371 |
|
2009 |
Harold D, Abraham R, Hollingworth P, Sims R, Gerrish A, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Williams A, Jones N, Thomas C, Stretton A, Morgan AR, Lovestone S, ... ... Rossor M, et al. Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Nature Genetics. 41: 1156-1156. DOI: 10.1038/Ng1009-1156D |
0.351 |
|
2009 |
Lehmann M, Clarkson MJ, Rohrer JD, Scahill RI, Modat M, Warren JD, Ourselin S, Rossor MN, Barnes J, Fox NC. Characteristic patterns of cortical thickness in pathologically-confirmed Alzheimer's disease and frontotemporal lobar degeneration Alzheimers & Dementia. 5. DOI: 10.1016/J.Jalz.2009.05.561 |
0.433 |
|
2009 |
Chan D, Bird C, Hartley T, Pijnenburg Y, Rossor M, Burgess N. O4-05-05: Short-term spatial memory is impaired in early Alzheimer's disease but not in temporal variant frontotemporal lobar degeneration Alzheimer's & Dementia. 5: P160-P160. DOI: 10.1016/J.Jalz.2009.05.553 |
0.356 |
|
2009 |
Ryan N, McNaughton D, Knight W, Guerreiro R, Poulter M, Nicholl D, Hardy J, Rossor M, Collinge J, Mead S. Duplications of APP—but not PRNP—are a significant cause of early-onset dementia in a large UK referral series Alzheimers & Dementia. 5: 460. DOI: 10.1016/J.Jalz.2009.04.869 |
0.379 |
|
2008 |
Rohrer JD, McNaught E, Foster J, Clegg SL, Barnes J, Omar R, Warrington EK, Rossor MN, Warren JD, Fox NC. Tracking progression in frontotemporal lobar degeneration: serial MRI in semantic dementia. Neurology. 71: 1445-51. PMID 18955688 DOI: 10.1212/01.Wnl.0000327889.13734.Cd |
0.374 |
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2008 |
Edison P, Archer HA, Gerhard A, Hinz R, Pavese N, Turkheimer FE, Hammers A, Tai YF, Fox N, Kennedy A, Rossor M, Brooks DJ. Microglia, amyloid, and cognition in Alzheimer's disease: An [11C](R)PK11195-PET and [11C]PIB-PET study. Neurobiology of Disease. 32: 412-9. PMID 18786637 DOI: 10.1016/J.Nbd.2008.08.001 |
0.337 |
|
2008 |
Rohrer JD, Warren JD, Barnes J, Mead S, Beck J, Pepple T, Boyes R, Omar R, Collinge J, Stevens JM, Warrington EK, Rossor MN, Fox NC. Mapping the progression of progranulin-associated frontotemporal lobar degeneration. Nature Clinical Practice. Neurology. 4: 455-60. PMID 18648346 DOI: 10.1038/Ncpneuro0869 |
0.408 |
|
2008 |
Rohrer JD, Warren JD, Omar R, Mead S, Beck J, Revesz T, Holton J, Stevens JM, Al-Sarraj S, Pickering-Brown SM, Hardy J, Fox NC, Collinge J, Warrington EK, Rossor MN. Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene. Archives of Neurology. 65: 506-13. PMID 18413474 DOI: 10.1001/Archneur.65.4.506 |
0.378 |
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2008 |
Schott JM, Crutch SJ, Frost C, Warrington EK, Rossor MN, Fox NC. Neuropsychological correlates of whole brain atrophy in Alzheimer's disease. Neuropsychologia. 46: 1732-7. PMID 18395233 DOI: 10.1016/J.Neuropsychologia.2008.02.015 |
0.413 |
|
2008 |
Ridha BH, Anderson VM, Barnes J, Boyes RG, Price SL, Rossor MN, Whitwell JL, Jenkins L, Black RS, Grundman M, Fox NC. Volumetric MRI and cognitive measures in Alzheimer disease : comparison of markers of progression. Journal of Neurology. 255: 567-74. PMID 18274807 DOI: 10.1007/S00415-008-0750-9 |
0.422 |
|
2008 |
Beck J, Rohrer JD, Campbell T, Isaacs A, Morrison KE, Goodall EF, Warrington EK, Stevens J, Revesz T, Holton J, Al-Sarraj S, King A, Scahill R, Warren JD, Fox NC, ... Rossor MN, et al. A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series. Brain : a Journal of Neurology. 131: 706-20. PMID 18234697 DOI: 10.1093/Brain/Awm320 |
0.393 |
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2008 |
Wild EJ, Mudanohwo EE, Sweeney MG, Schneider SA, Beck J, Bhatia KP, Rossor MN, Davis MB, Tabrizi SJ. Huntington's disease phenocopies are clinically and genetically heterogeneous. Movement Disorders : Official Journal of the Movement Disorder Society. 23: 716-20. PMID 18181206 DOI: 10.1002/Mds.21915 |
0.35 |
|
2008 |
Rohrer JD, Knight WD, Warren JE, Fox NC, Rossor MN, Warren JD. Word-finding difficulty: a clinical analysis of the progressive aphasias. Brain : a Journal of Neurology. 131: 8-38. PMID 17947337 DOI: 10.1093/Brain/Awm251 |
0.348 |
|
2008 |
Barnes J, Scahill RI, Frost C, Schott JM, Rossor MN, Fox NC. Increased hippocampal atrophy rates in AD over 6 months using serial MR imaging. Neurobiology of Aging. 29: 1199-203. PMID 17368654 DOI: 10.1016/J.Neurobiolaging.2007.02.011 |
0.34 |
|
2008 |
Schott JM, MacManus DG, Frost C, Rossor MN, Waldman AD, Fox NC. P1-287: Proton spectroscopy in Alzheimer's disease: A longitudinal multiple time point study Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.877 |
0.394 |
|
2008 |
Rohrer JD, McNaught E, Foster J, Clegg S, Barnes J, Omar R, Rossor M, Warren J, Fox N. O3-06-03: Profiles of longitudinal brain atrophy in semantic dementia Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.452 |
0.338 |
|
2008 |
Williams J, Abraham R, Morgan A, Sims R, Hollingworth P, O'Donovan M, Owen M, Holmans P, Nikolov I, Moskvina V, Lovestone S, Rubinsztein D, Brayne C, Gill M, Lawlor B, ... ... Rossor M, et al. O2-06-01: A powerful, genome-wide association scan for susceptibility genes for late-onset Alzheimer's disease Alzheimer's & Dementia. 4: T143-T143. DOI: 10.1016/J.Jalz.2008.05.349 |
0.34 |
|
2008 |
Lehmann M, Douiri A, Barnes J, Chan D, Rossor MN, Fox NC. IC-P3-195: Atrophy patterns in Alzheimer's disease and semantic dementia: A comparison of FreeSurfer and manual measurements Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.139 |
0.404 |
|
2008 |
Ridha BH, Rossor MN, Crutch SJ, Keir G, Gallimore JR, Hutchinson WL, Hawkins PN, Pepys MB. P2-307: CPHPC depletes serum amyloid P component from the cerebrospinal fluid in Alzheimer's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1384 |
0.361 |
|
2008 |
McNaught E, Rohrer JD, Omar R, Ahsan L, Rossor MN, Warren JD, Fox NC. P2‐189: Longitudinal atrophy rate as a biomarker of disease progression in frontotemporal lobar degeneration Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1263 |
0.373 |
|
2008 |
Ahsan L, Rohrer JD, Isaacs A, Nielsen JE, Ostergaard L, Scahill R, Rossor MN, Warren JD, Fox NC, Johannsen P. P2‐183: Generalised brain atrophy predates symptom onset in frontotemporal dementia caused by CHMP2B mutation Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1257 |
0.351 |
|
2008 |
Rohrer JD, Warren JD, Rossor MN. P2-182: Gelastic dementia: Laughter replacing speech in frontotemporal lobar degeneration Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1256 |
0.338 |
|
2008 |
Lehmann M, Douiri A, Barnes J, Chan D, Rossor MN, Fox NC. P2-038: Atrophy patterns in Alzheimer's disease and semantic dementia: A comparison of FreeSurfer and manual measurements Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1119 |
0.436 |
|
2008 |
Knight W, Foster J, Ahsan L, Warrington E, Fox N, Rossor M. IC-P3-190: An unusual, APPV717G-associated familial Alzheimer's disease phenotype: Neuropsychological and radiological data Alzheimer's & Dementia. 4: T83-T83. DOI: 10.1016/J.Jalz.2008.05.1113 |
0.399 |
|
2008 |
Kennedy J, Barnes J, Archer H, Pepple T, Sluimer JD, Henneman WJP, Rossor MN, Fox NC. IC-P2-109: Medial temporal lobe atrophy and rate of loss predicts future cognitive decline in patients with memory complaints with or without memory deficits: A comparison of methods Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.102 |
0.408 |
|
2008 |
Barnes J, Mitchell LA, Kennedy J, Barker S, Lehmann M, Nordstrom RC, Frost C, Smith JR, Garde E, Rossor MN, Fox NC. AbstractPoster presentation: Imaging posterIC-P1-003: Registration of serial MRI improves diagnosis of dementia Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.016 |
0.322 |
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2007 |
Crutch SJ, Rossor MN, Warrington EK. A novel technique for the quantitative assessment of apraxic deficits: application to individuals with mild cognitive impairment. Journal of Neuropsychology. 1: 237-57. PMID 19331019 DOI: 10.1348/174866407X209943 |
0.383 |
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2007 |
Omar R, Warren JD, Ron MA, Lees AJ, Rossor MN, Kartsounis LD. The neuro-behavioural syndrome of brainstem disease. Neurocase. 13: 452-65. PMID 18781444 DOI: 10.1080/13554790802001403 |
0.329 |
|
2007 |
Crutch SJ, Rossor MN, Warrington EK. The quantitative assessment of apraxic deficits in Alzheimer's disease. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 43: 976-86. PMID 17941354 DOI: 10.1016/S0010-9452(08)70695-6 |
0.366 |
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2007 |
Barnes J, Lewis EB, Scahill RI, Bartlett JW, Frost C, Schott JM, Rossor MN, Fox NC. Automated measurement of hippocampal atrophy using fluid-registered serial MRI in AD and controls. Journal of Computer Assisted Tomography. 31: 581-7. PMID 17882036 DOI: 10.1097/Rct.0B013E31802F4139 |
0.312 |
|
2007 |
Ridha BH, Tozer DJ, Symms MR, Stockton KC, Lewis EB, Siddique MM, MacManus DG, Rossor MN, Fox NC, Tofts PS. Quantitative magnetization transfer imaging in Alzheimer disease. Radiology. 244: 832-7. PMID 17709831 DOI: 10.1148/Radiol.2443061128 |
0.373 |
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2007 |
Dubois B, Feldman HH, Jacova C, Dekosky ST, Barberger-Gateau P, Cummings J, Delacourte A, Galasko D, Gauthier S, Jicha G, Meguro K, O'brien J, Pasquier F, Robert P, Rossor M, et al. Research criteria for the diagnosis of Alzheimer's disease: revising the NINCDS-ADRDA criteria. The Lancet. Neurology. 6: 734-46. PMID 17616482 DOI: 10.1016/S1474-4422(07)70178-3 |
0.421 |
|
2007 |
Petzold A, Keir G, Warren J, Fox N, Rossor MN. A systematic review and meta-analysis of CSF neurofilament protein levels as biomarkers in dementia. Neuro-Degenerative Diseases. 4: 185-94. PMID 17596713 DOI: 10.1159/000101843 |
0.327 |
|
2007 |
Knight WD, Kennedy J, Mead S, Rossor MN, Beck J, Collinge J, Mummery C. A novel presenilin 1 deletion (p.L166del) associated with early onset familial Alzheimer's disease. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 14: 829-31. PMID 17594345 DOI: 10.1111/J.1468-1331.2007.01857.X |
0.463 |
|
2007 |
Ridha BH, Barnes J, van de Pol LA, Schott JM, Boyes RG, Siddique MM, Rossor MN, Scheltens P, Fox NC. Application of automated medial temporal lobe atrophy scale to Alzheimer disease. Archives of Neurology. 64: 849-54. PMID 17562933 DOI: 10.1001/Archneur.64.6.849 |
0.346 |
|
2007 |
Whitwell JL, Sampson EL, Loy CT, Warren JE, Rossor MN, Fox NC, Warren JD. VBM signatures of abnormal eating behaviours in frontotemporal lobar degeneration. Neuroimage. 35: 207-13. PMID 17240166 DOI: 10.1016/J.Neuroimage.2006.12.006 |
0.357 |
|
2007 |
Waldemar G, Dubois B, Emre M, Georges J, McKeith IG, Rossor M, Scheltens P, Tariska P, Winblad B. Recommendations for the diagnosis and management of Alzheimer's disease and other disorders associated with dementia: EFNS guideline. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 14: e1-26. PMID 17222085 DOI: 10.1111/J.1468-1331.2006.01605.X |
0.416 |
|
2007 |
Edison P, Archer HA, Hinz R, Hammers A, Pavese N, Tai YF, Hotton G, Cutler D, Fox N, Kennedy A, Rossor M, Brooks DJ. Amyloid, hypometabolism, and cognition in Alzheimer disease: an [11C]PIB and [18F]FDG PET study. Neurology. 68: 501-8. PMID 17065593 DOI: 10.1212/01.Wnl.0000244749.20056.D4 |
0.374 |
|
2007 |
Barnes J, Godbolt AK, Frost C, Boyes RG, Jones BF, Scahill RI, Rossor MN, Fox NC. Atrophy rates of the cingulate gyrus and hippocampus in AD and FTLD. Neurobiology of Aging. 28: 20-8. PMID 16406154 DOI: 10.1016/J.Neurobiolaging.2005.11.012 |
0.393 |
|
2006 |
Barnes J, Whitwell JL, Frost C, Josephs KA, Rossor M, Fox NC. Measurements of the amygdala and hippocampus in pathologically confirmed Alzheimer disease and frontotemporal lobar degeneration. Archives of Neurology. 63: 1434-9. PMID 17030660 DOI: 10.1001/Archneur.63.10.1434 |
0.434 |
|
2006 |
Schott JM, Frost C, Whitwell JL, Macmanus DG, Boyes RG, Rossor MN, Fox NC. Combining short interval MRI in Alzheimer's disease: Implications for therapeutic trials. Journal of Neurology. 253: 1147-53. PMID 16998650 DOI: 10.1007/S00415-006-0173-4 |
0.388 |
|
2006 |
Ridha BH, Barnes J, Bartlett JW, Godbolt A, Pepple T, Rossor MN, Fox NC. Tracking atrophy progression in familial Alzheimer's disease: a serial MRI study. The Lancet. Neurology. 5: 828-34. PMID 16987729 DOI: 10.1016/S1474-4422(06)70550-6 |
0.46 |
|
2006 |
Archer HA, Macfarlane F, Price S, Moore EK, Pepple T, Cutler D, Frost C, Fox NC, Rossor MN. Do symptoms of memory impairment correspond to cognitive impairment: a cross sectional study of a clinical cohort. International Journal of Geriatric Psychiatry. 21: 1206-12. PMID 16977678 DOI: 10.1002/Gps.1644 |
0.308 |
|
2006 |
Archer HA, Edison P, Brooks DJ, Barnes J, Frost C, Yeatman T, Fox NC, Rossor MN. Amyloid load and cerebral atrophy in Alzheimer's disease: an 11C-PIB positron emission tomography study. Annals of Neurology. 60: 145-7. PMID 16802294 DOI: 10.1002/Ana.20889 |
0.396 |
|
2006 |
Crutch SJ, Rossor MN. Artistic changes in Alzheimer's disease. International Review of Neurobiology. 74: 147-61. PMID 16730513 DOI: 10.1016/S0074-7742(06)74012-0 |
0.452 |
|
2006 |
Waldman AD, Cordery RJ, MacManus DG, Godbolt A, Collinge J, Rossor MN. Regional brain metabolite abnormalities in inherited prion disease and asymptomatic gene carriers demonstrated in vivo by quantitative proton magnetic resonance spectroscopy. Neuroradiology. 48: 428-33. PMID 16598479 DOI: 10.1007/S00234-006-0068-1 |
0.39 |
|
2006 |
Godbolt AK, Waldman AD, MacManus DG, Schott JM, Frost C, Cipolotti L, Fox NC, Rossor MN. MRS shows abnormalities before symptoms in familial Alzheimer disease. Neurology. 66: 718-22. PMID 16534109 DOI: 10.1212/01.Wnl.0000201237.05869.Df |
0.371 |
|
2006 |
Godbolt AK, Beck JA, Collinge JC, Cipolotti L, Fox NC, Rossor MN. A second family with familial AD and the V717L APP mutation has a later age at onset. Neurology. 66: 611-2. PMID 16505331 DOI: 10.1212/01.Wnl.0000197791.53828.2C |
0.323 |
|
2006 |
Cordery RJ, MacManus D, Godbolt A, Rossor MN, Waldman AD. Short TE quantitative proton magnetic resonance spectroscopy in variant Creutzfeldt-Jakob disease. European Radiology. 16: 1692-8. PMID 16408201 DOI: 10.1007/S00330-005-0090-4 |
0.367 |
|
2006 |
Schott JM, Ridha BH, Crutch SJ, Healy DG, Uphill JB, Warrington EK, Rossor MN, Fox NC. Apolipoprotein e genotype modifies the phenotype of Alzheimer disease. Archives of Neurology. 63: 155-6. PMID 16401755 DOI: 10.1001/Archneur.63.1.155 |
0.378 |
|
2006 |
Schott JM, Ridha BH, Crutch SJ, Warrington EK, Rossor MN, Fox NC. P1-282: Apolipoprotein E genotype in biparietal Alzheimer's disease Alzheimer's & Dementia. 2: S179-S179. DOI: 10.1016/J.Jalz.2006.05.659 |
0.381 |
|
2006 |
Scahill RI, Godbolt AK, Whitwell JL, Knight WD, Schott JM, Warren JD, Rossor MN, Fox NC. P2-306: Patterns of atrophy in confirmed cases of sporadic and familial Alzheimer's disease: A voxel-based morphometric study Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1146 |
0.425 |
|
2006 |
Ridha BH, Symms MR, Tozer DJ, Stockton KC, Siddique MM, Lewis EB, MacManus DG, Kukkastenvehmas RH, Boulby PA, Barker GJ, Rossor MN, Fox NC, Tofts PS. P2-294: Magnetization transfer ratio in Alzheimer's disease: Comparison with volumetric measurements Alzheimer's & Dementia. 2: S325-S326. DOI: 10.1016/J.Jalz.2006.05.1133 |
0.358 |
|
2006 |
Barnes J, Lewis EB, Scahill RI, Bartlett JW, Frost C, Schott JM, Rossor MN, Fox NC. P2-250: Automated measurement of hippocampal atrophy using fluid-registered serial MRI in AD and controls Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1089 |
0.319 |
|
2005 |
Pariente J, Cole S, Henson R, Clare L, Kennedy A, Rossor M, Cipoloti L, Puel M, Demonet JF, Chollet F, Frackowiak RS. Alzheimer's patients engage an alternative network during a memory task. Annals of Neurology. 58: 870-9. PMID 16315273 DOI: 10.1002/Ana.20653 |
0.352 |
|
2005 |
Likeman M, Anderson VM, Stevens JM, Waldman AD, Godbolt AK, Frost C, Rossor MN, Fox NC. Visual assessment of atrophy on magnetic resonance imaging in the diagnosis of pathologically confirmed young-onset dementias. Archives of Neurology. 62: 1410-5. PMID 16157748 DOI: 10.1001/Archneur.62.9.1410 |
0.44 |
|
2005 |
Whitwell JL, Josephs KA, Rossor MN, Stevens JM, Revesz T, Holton JL, Al-Sarraj S, Godbolt AK, Fox NC, Warren JD. Magnetic resonance imaging signatures of tissue pathology in frontotemporal dementia. Archives of Neurology. 62: 1402-8. PMID 16157747 DOI: 10.1001/Archneur.62.9.1402 |
0.405 |
|
2005 |
Whitwell JL, Sampson EL, Watt HC, Harvey RJ, Rossor MN, Fox NC. A volumetric magnetic resonance imaging study of the amygdala in frontotemporal lobar degeneration and Alzheimer's disease. Dementia and Geriatric Cognitive Disorders. 20: 238-44. PMID 16088140 DOI: 10.1159/000087343 |
0.39 |
|
2005 |
Ridha BH, Josephs KA, Rossor MN. Delusions and hallucinations in dementia with Lewy bodies: worsening with memantine. Neurology. 65: 481-2. PMID 16087923 DOI: 10.1212/01.Wnl.0000172351.95783.8E |
0.334 |
|
2005 |
Skibinski G, Parkinson NJ, Brown JM, Chakrabarti L, Lloyd SL, Hummerich H, Nielsen JE, Hodges JR, Spillantini MG, Thusgaard T, Brandner S, Brun A, Rossor MN, Gade A, Johannsen P, et al. Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nature Genetics. 37: 806-8. PMID 16041373 DOI: 10.1038/Ng1609 |
0.358 |
|
2005 |
Schott JM, Price SL, Frost C, Whitwell JL, Rossor MN, Fox NC. Measuring atrophy in Alzheimer disease: a serial MRI study over 6 and 12 months. Neurology. 65: 119-24. PMID 16009896 DOI: 10.1212/01.Wnl.0000167542.89697.0F |
0.374 |
|
2005 |
Godbolt AK, Josephs KA, Revesz T, Warrington EK, Lantos P, King A, Fox NC, Al Sarraj S, Holton J, Cipolotti L, Khan MN, Rossor MN. Sporadic and familial dementia with ubiquitin-positive tau-negative inclusions: clinical features of one histopathological abnormality underlying frontotemporal lobar degeneration. Archives of Neurology. 62: 1097-101. PMID 16009765 DOI: 10.1001/Archneur.62.7.1097 |
0.416 |
|
2005 |
Warren JD, Schott JM, Fox NC, Thom M, Revesz T, Holton JL, Scaravilli F, Thomas DG, Plant GT, Rudge P, Rossor MN. Brain biopsy in dementia. Brain : a Journal of Neurology. 128: 2016-25. PMID 15901648 DOI: 10.1093/Brain/Awh543 |
0.432 |
|
2005 |
Fox NC, Black RS, Gilman S, Rossor MN, Griffith SG, Jenkins L, Koller M. Effects of Abeta immunization (AN1792) on MRI measures of cerebral volume in Alzheimer disease. Neurology. 64: 1563-72. PMID 15883317 DOI: 10.1212/01.Wnl.0000159743.08996.99 |
0.358 |
|
2005 |
Klünemann HH, Ridha BH, Magy L, Wherrett JR, Hemelsoet DM, Keen RW, De Bleecker JL, Rossor MN, Marienhagen J, Klein HE, Peltonen L, Paloneva J. The genetic causes of basal ganglia calcification, dementia, and bone cysts: DAP12 and TREM2. Neurology. 64: 1502-7. PMID 15883308 DOI: 10.1212/01.Wnl.0000160304.00003.Ca |
0.352 |
|
2005 |
Godbolt AK, Cipolotti L, Anderson VM, Archer H, Janssen JC, Price S, Rossor MN, Fox NC. A decade of pre-diagnostic assessment in a case of familial Alzheimer's disease: tracking progression from asymptomatic to MCI and dementia. Neurocase. 11: 56-64. PMID 15804925 DOI: 10.1080/13554790490896866 |
0.484 |
|
2005 |
Archer HA, Schott JM, Barnes J, Fox NC, Holton JL, Revesz T, Cipolotti L, Rossor MN. Knight's move thinking? Mild cognitive impairment in a chess player. Neurocase. 11: 26-31. PMID 15804921 DOI: 10.1080/13554790490896875 |
0.388 |
|
2005 |
Barnes J, Scahill RI, Schott JM, Frost C, Rossor MN, Fox NC. Does Alzheimer's disease affect hippocampal asymmetry? Evidence from a cross-sectional and longitudinal volumetric MRI study. Dementia and Geriatric Cognitive Disorders. 19: 338-44. PMID 15785035 DOI: 10.1159/000084560 |
0.413 |
|
2005 |
Cordery RJ, Alner K, Cipolotti L, Ron M, Kennedy A, Collinge J, Rossor MN. The neuropsychology of variant CJD: a comparative study with inherited and sporadic forms of prion disease. Journal of Neurology, Neurosurgery, and Psychiatry. 76: 330-6. PMID 15716521 DOI: 10.1136/Jnnp.2003.030320 |
0.373 |
|
2005 |
Janssen JC, Schott JM, Cipolotti L, Fox NC, Scahill RI, Josephs KA, Stevens JM, Rossor MN. Mapping the onset and progression of atrophy in familial frontotemporal lobar degeneration. Journal of Neurology, Neurosurgery, and Psychiatry. 76: 162-8. PMID 15654025 DOI: 10.1136/Jnnp.2003.032201 |
0.425 |
|
2005 |
Edison P, Archer H, Hinz R, Hammers A, Gerhard A, Pavese N, Tai Y, Hotton G, Cuttler D, Fox N, Rossor M, Brooks DJ. Correlation of regional cerebral amyloid load in Alzheimer's disease, measured with [11C]-PIB PET using spectral analysis and tissue uptake ratios, with performance on recognition memory tests. Journal of Cerebral Blood Flow and Metabolism. 25. DOI: 10.1038/Sj.Jcbfm.9591524.0591 |
0.35 |
|
2005 |
Edison P, Archer H, Hinz R, Gerhard A, Turkheimer F, Hammers A, Pavese N, Tai YF, Rossor M, Brooks DJ. Correlations between the distribution of microglial activation and amyloid plaque load in Alzheimer’s disease: An 11C-PK11195 and 11C-PIB PET study Alzheimers & Dementia. 1. DOI: 10.1016/J.Jalz.2005.06.298 |
0.301 |
|
2005 |
Godbolt AK, MacManus DG, Waldman AD, Schott JM, Cipolotti L, Frost C, Fox NC, Rossor MN. MR spectroscopy demonstrates presymptomatic changes in familial Alzheimer’s disease Alzheimers & Dementia. 1. DOI: 10.1016/J.Jalz.2005.06.206 |
0.35 |
|
2005 |
Edison P, Archer H, Hinz R, Gerhard A, Hammers A, Pavese N, Tai YF, Fox N, Rossor M, Brooks DJ. Amyloid load in mild cognitive impairment compared to Alzheimer patients and normal subjects: An 11C-PIB PET study Alzheimers & Dementia. 1. DOI: 10.1016/J.Jalz.2005.06.185 |
0.346 |
|
2005 |
Brooks D, Edison P, Archer H, Hinz R, Gerhard A, Hammers A, Pavese N, Tai Y, Cuttler D, Fox N, Rossor M, Brooks D. The relationship between amyloid load, microglial activation, and cognition in Alzheimer’s disease: PET findings Alzheimers & Dementia. 1. DOI: 10.1016/J.Jalz.2005.06.053 |
0.342 |
|
2005 |
Godbolt AK, Cipolotti L, Watt H, Janssen JC, Fox NC, Rossor MN. Survival in Alzheimer Disease—Reply Archives of Neurology. 62: 689. DOI: 10.1001/Archneur.62.4.689-B |
0.325 |
|
2004 |
Whitwell JL, Warren JD, Josephs KA, Godbolt AK, Revesz T, Fox NC, Rossor MN. Voxel-based morphometry in tau-positive and tau-negative frontotemporal lobar degenerations. Neuro-Degenerative Diseases. 1: 225-30. PMID 16908994 DOI: 10.1159/000080990 |
0.379 |
|
2004 |
Cagnin A, Rossor M, Sampson EL, Mackinnon T, Banati RB. In vivo detection of microglial activation in frontotemporal dementia. Annals of Neurology. 56: 894-7. PMID 15562429 DOI: 10.1002/Ana.20332 |
0.348 |
|
2004 |
Paviour DC, Schott JM, Stevens JM, Revesz T, Holton JL, Rossor MN, Lees AJ, Fox NC. Pathological substrate for regional distribution of increased atrophy rates in progressive supranuclear palsy. Journal of Neurology, Neurosurgery, and Psychiatry. 75: 1772-5. PMID 15548504 DOI: 10.1136/Jnnp.2003.033472 |
0.367 |
|
2004 |
Godbolt AK, Beck JA, Collinge J, Garrard P, Warren JD, Fox NC, Rossor MN. A presenilin 1 R278I mutation presenting with language impairment. Neurology. 63: 1702-4. PMID 15534260 DOI: 10.1212/01.Wnl.0000143060.98164.1A |
0.392 |
|
2004 |
Brooks WS, Kwok JB, Halliday GM, Godbolt AK, Rossor MN, Creasey H, Jones AO, Schofield PR. Hemorrhage is uncommon in new Alzheimer family with Flemish amyloid precursor protein mutation. Neurology. 63: 1613-7. PMID 15534244 DOI: 10.1212/01.Wnl.0000142965.10778.C7 |
0.391 |
|
2004 |
Godbolt AK, Cipolotti L, Watt H, Fox NC, Janssen JC, Rossor MN. The natural history of Alzheimer disease: a longitudinal presymptomatic and symptomatic study of a familial cohort. Archives of Neurology. 61: 1743-8. PMID 15534185 DOI: 10.1001/Archneur.61.11.1743 |
0.442 |
|
2004 |
Price S, Paviour D, Scahill RI, Stevens J, Rossor M, Lees A, Fox NC. Voxel-based morphometry detects patterns of atrophy that help differentiate progressive supranuclear palsy and Parkinson's disease. Neuroimage. 23: 663-669. PMID 15488416 DOI: 10.1016/J.Neuroimage.2004.06.013 |
0.356 |
|
2004 |
Barnes J, Scahill RI, Boyes RG, Frost C, Lewis EB, Rossor CL, Rossor MN, Fox NC. Differentiating AD from aging using semiautomated measurement of hippocampal atrophy rates. Neuroimage. 23: 574-81. PMID 15488407 DOI: 10.1016/J.Neuroimage.2004.06.028 |
0.367 |
|
2004 |
Schott JM, Lees AJ, Rossor MN. Dementia in dementia with Lewy bodies may not be attributable to Alzheimer pathology. Annals of Neurology. 56: 604; author reply 60. PMID 15455442 DOI: 10.1002/Ana.20271 |
0.406 |
|
2004 |
Josephs KA, Holton JL, Rossor MN, Godbolt AK, Ozawa T, Strand K, Khan N, Al-Sarraj S, Revesz T. Frontotemporal lobar degeneration and ubiquitin immunohistochemistry. Neuropathology and Applied Neurobiology. 30: 369-73. PMID 15305982 DOI: 10.1111/J.1365-2990.2003.00545.X |
0.331 |
|
2004 |
Whitwell JL, Anderson VM, Scahill RI, Rossor MN, Fox NC. Longitudinal patterns of regional change on volumetric MRI in frontotemporal lobar degeneration. Dementia and Geriatric Cognitive Disorders. 17: 307-10. PMID 15178942 DOI: 10.1159/000077160 |
0.366 |
|
2004 |
Chan D, Walters RJ, Sampson EL, Schott JM, Smith SJ, Rossor MN. EEG abnormalities in frontotemporal lobar degeneration. Neurology. 62: 1628-30. PMID 15136699 DOI: 10.1212/01.Wnl.0000123103.89419.B7 |
0.397 |
|
2004 |
Chen K, Reiman EM, Alexander GE, Bandy D, Renaut R, Crum WR, Fox NC, Rossor MN. An automated algorithm for the computation of brain volume change from sequential MRIs using an iterative principal component analysis and its evaluation for the assessment of whole-brain atrophy rates in patients with probable Alzheimer's disease. Neuroimage. 22: 134-43. PMID 15110003 DOI: 10.1016/J.Neuroimage.2004.01.002 |
0.394 |
|
2004 |
Sampson EL, Warren JD, Rossor MN. Young onset dementia. Postgraduate Medical Journal. 80: 125-39. PMID 15016933 DOI: 10.1136/Pgmj.2003.011171 |
0.392 |
|
2004 |
Janssen JC, Godbolt AK, Ioannidis P, Thompson EJ, Rossor MN. The prevalence of oligoclonal bands in the CSF of patients with primary neurodegenerative dementia. Journal of Neurology. 251: 184-8. PMID 14991353 DOI: 10.1007/S00415-004-0296-4 |
0.414 |
|
2004 |
Vincent A, Buckley C, Schott JM, Baker I, Dewar BK, Detert N, Clover L, Parkinson A, Bien CG, Omer S, Lang B, Rossor MN, Palace J. Potassium channel antibody-associated encephalopathy: a potentially immunotherapy-responsive form of limbic encephalitis. Brain : a Journal of Neurology. 127: 701-12. PMID 14960497 DOI: 10.1093/Brain/Awh077 |
0.323 |
|
2004 |
Pickering-Brown S, Baker M, Bird T, Trojanowski J, Lee V, Morris H, Rossor M, Janssen JC, Neary D, Craufurd D, Richardson A, Snowden J, Hardy J, Mann D, Hutton M. Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 125: 79-82. PMID 14755449 DOI: 10.1002/Ajmg.B.20083 |
0.36 |
|
2004 |
Brooks WS, Kwok JB, Halliday GM, Godbolt AK, Rossor MN, Creasey HM, Jones AO, Schofield PR. P4-087 Familial Alzheimer's disease and cerebral haemorrhage: a second family with the flemish APP ALA692GLY mutation Neurobiology of Aging. 25: S499. DOI: 10.1016/S0197-4580(04)81645-2 |
0.398 |
|
2004 |
Henley SM, Warrington EK, Warner TT, Stevens JM, Ashburner J, Rossor MN, Fox NC, Tabrizi SJ. P3-375 Correlation between patterns of atrophy and psychomotor task performance in early huntington's disease Neurobiology of Aging. 25: S462. DOI: 10.1016/S0197-4580(04)81524-0 |
0.309 |
|
2004 |
Schott JM, Frost C, Crutch SJ, Boyes RG, Whitwell JL, Scahill RI, Rossor MN, Warrington EK, Fox NC. P3-062 Predictors and correlates of inter-individual variation in MRI derived atrophy rates in Alzheimer's disease Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81214-4 |
0.395 |
|
2004 |
Barnes J, Godbolt AK, Frost C, Boyes RG, Jones BF, Rossor MN, Fox NC. P2-226 Measurement of rates of atrophy in the cingulate gyrus and its subdivisions in a group of patients with confirmed Alzheimer's disease (ad) and frontotemporal lobar degeneration (FTLD) Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)80972-2 |
0.438 |
|
2004 |
Ridha BH, Anderson VM, Barnes J, Boyes RG, Price SL, Rossor MN, Whitwell JL, Black RS, Griffith SG, Jenkins L, Koller M, Fox NC. P2-196 Rates of hippocampal and brain atrophy, and ventricular enlargement, in Alzheimer's disease: a comparison of markers of progression Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)80942-4 |
0.411 |
|
2004 |
Whitwell JL, Godbolt AK, Josephs KA, Stevens JM, Rossor MN, Fox NC. P2-170 Patterns of atrophy on MRI in histologically-proven sporadic Alzheimer's disease and genetically-proven familial Alzheimer's disease Neurobiology of Aging. 25: S274-S275. DOI: 10.1016/S0197-4580(04)80917-5 |
0.456 |
|
2004 |
Ridha BH, Symms MR, Lewis EB, MacManus DG, Boulby PA, Barker GJ, Tofts PS, Rossor MN, Fox NC. P2-157 Magnetization transfer imaging of the hippocampal formation: application to Alzheimer's disease Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)80904-7 |
0.354 |
|
2004 |
Anderson VM, Godbolt AK, Price SL, Janssen JC, Rossor MN, Fox NC. P2-150 Tracking change on MRI in a case of familial Alzheimer's disease: 11 years of imaging spanning pre-symptomatic to Alzheimer's disease Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)80897-2 |
0.449 |
|
2004 |
Fox NC, Black RS, Gilman S, Rossor MN, Griffith SG, Jenkins L, Koller M. O4-05-08 Effects of A-beta immunotherapy (AN1792) on MRI measures of brain, ventricle and hippocampal volumes in Alzheimer's disease Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)80287-2 |
0.352 |
|
2003 |
Cordery RJ, Hall M, Cipolotti L, Al-Sarraj S, O'Donovan DG, Davidson L, Adlard P, Rossor MN. Early cognitive decline in Creutzfeldt-Jakob disease associated with human growth hormone treatment. Journal of Neurology, Neurosurgery, and Psychiatry. 74: 1412-6. PMID 14570836 DOI: 10.1136/Jnnp.74.10.1412 |
0.343 |
|
2003 |
Chan D, Janssen JC, Whitwell JL, Watt HC, Jenkins R, Frost C, Rossor MN, Fox NC. Change in rates of cerebral atrophy over time in early-onset Alzheimer's disease: longitudinal MRI study. Lancet. 362: 1121-2. PMID 14550701 DOI: 10.1016/S0140-6736(03)14469-8 |
0.471 |
|
2003 |
Harvey RJ, Skelton-Robinson M, Rossor MN. The prevalence and causes of dementia in people under the age of 65 years. Journal of Neurology, Neurosurgery, and Psychiatry. 74: 1206-9. PMID 12933919 DOI: 10.1136/Jnnp.74.9.1206 |
0.329 |
|
2003 |
Schott JM, Simon JE, Fox NC, King AP, Khan MN, Cipolotti L, Paviour DC, Stevens JM, Rossor MN. Delineating the sites and progression of in vivo atrophy in multiple system atrophy using fluid-registered MRI. Movement Disorders : Official Journal of the Movement Disorder Society. 18: 955-8. PMID 12889090 DOI: 10.1002/Mds.10468 |
0.311 |
|
2003 |
Josephs KA, Holton JL, Rossor MN, Braendgaard H, Ozawa T, Fox NC, Petersen RC, Pearl GS, Ganguly M, Rosa P, Laursen H, Parisi JE, Waldemar G, Quinn NP, Dickson DW, et al. Neurofilament inclusion body disease: a new proteinopathy? Brain : a Journal of Neurology. 126: 2291-303. PMID 12876145 DOI: 10.1093/Brain/Awg231 |
0.398 |
|
2003 |
Scahill RI, Frost C, Jenkins R, Whitwell JL, Rossor MN, Fox NC. A longitudinal study of brain volume changes in normal aging using serial registered magnetic resonance imaging. Archives of Neurology. 60: 989-94. PMID 12873856 DOI: 10.1001/Archneur.60.7.989 |
0.305 |
|
2003 |
Cairns NJ, Brännström T, Khan MN, Rossor MN, Lantos PL. Neuronal loss in familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions. Experimental Neurology. 181: 319-26. PMID 12782004 DOI: 10.1016/S0014-4886(03)00095-5 |
0.323 |
|
2003 |
Schott JM, Rossor MN. The grasp and other primitive reflexes. Journal of Neurology, Neurosurgery, and Psychiatry. 74: 558-60. PMID 12700289 DOI: 10.1136/Jnnp.74.5.558 |
0.335 |
|
2003 |
Cairns NJ, Perry RH, Jaros E, Burn D, McKeith IG, Lowe JS, Holton J, Rossor MN, Skullerud K, Duyckaerts C, Cruz-Sanchez FF, Lantos PL. Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions. Neuroscience Letters. 341: 177-80. PMID 12697277 DOI: 10.1016/S0304-3940(03)00100-9 |
0.416 |
|
2003 |
King A, Doey L, Rossor M, Mead S, Collinge J, Lantos P. Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene. Neuropathology and Applied Neurobiology. 29: 98-105. PMID 12662318 DOI: 10.1046/J.1365-2990.2003.00423.X |
0.374 |
|
2003 |
Schott JM, Fox NC, Frost C, Scahill RI, Janssen JC, Chan D, Jenkins R, Rossor MN. Assessing the onset of structural change in familial Alzheimer's disease. Annals of Neurology. 53: 181-8. PMID 12557284 DOI: 10.1002/Ana.10424 |
0.41 |
|
2003 |
Janssen JC, Beck JA, Campbell TA, Dickinson A, Fox NC, Harvey RJ, Houlden H, Rossor MN, Collinge J. Early onset familial Alzheimer's disease: Mutation frequency in 31 families. Neurology. 60: 235-9. PMID 12552037 DOI: 10.1212/01.Wnl.0000042088.22694.E3 |
0.393 |
|
2003 |
Walters RJ, Fox NC, Schott JM, Crum WR, Stevens JM, Rossor MN, Thomas DJ. Transient ischaemic attacks are associated with increased rates of global cerebral atrophy. Journal of Neurology, Neurosurgery, and Psychiatry. 74: 213-6. PMID 12531953 DOI: 10.1136/Jnnp.74.2.213 |
0.367 |
|
2003 |
Petzold A, Jenkins R, Watt HC, Green AJ, Thompson EJ, Keir G, Fox NC, Rossor MN. Cerebrospinal fluid S100B correlates with brain atrophy in Alzheimer's disease. Neuroscience Letters. 336: 167-70. PMID 12505619 DOI: 10.1016/S0304-3940(02)01257-0 |
0.424 |
|
2003 |
Pijnenburg YA, Sampson EL, Harvey RJ, Fox NC, Rossor MN. Vulnerability to neuroleptic side effects in frontotemporal lobar degeneration. International Journal of Geriatric Psychiatry. 18: 67-72. PMID 12497558 DOI: 10.1002/Gps.774 |
0.331 |
|
2002 |
Schott JM, Fox NC, Rossor MN. Genetics of the dementias. Journal of Neurology, Neurosurgery, and Psychiatry. 73: II27-31. PMID 12536157 DOI: 10.1136/Jnnp.73.Suppl_2.Ii27 |
0.441 |
|
2002 |
Good CD, Scahill RI, Fox NC, Ashburner J, Friston KJ, Chan D, Crum WR, Rossor MN, Frackowiak RS. Automatic differentiation of anatomical patterns in the human brain: validation with studies of degenerative dementias. Neuroimage. 17: 29-46. PMID 12482066 DOI: 10.1006/Nimg.2002.1202 |
0.385 |
|
2002 |
Gydesen S, Brown JM, Brun A, Chakrabarti L, Gade A, Johannsen P, Rossor M, Thusgaard T, Grove A, Yancopoulou D, Spillantini MG, Fisher EM, Collinge J, Sorensen SA. Chromosome 3 linked frontotemporal dementia (FTD-3). Neurology. 59: 1585-94. PMID 12451202 DOI: 10.1212/01.Wnl.0000034763.54161.1F |
0.402 |
|
2002 |
O'Riordan S, McMonagle P, Janssen JC, Fox NC, Farrell M, Collinge J, Rossor MN, Hutchinson M. Presenilin-1 mutation (E280G), spastic paraparesis, and cranial MRI white-matter abnormalities. Neurology. 59: 1108-10. PMID 12370477 DOI: 10.1212/Wnl.59.7.1108 |
0.363 |
|
2002 |
Morris HR, Baker M, Yasojima K, Houlden H, Khan MN, Wood NW, Hardy J, Grossman M, Trojanowski J, Revesz T, Bigio EH, Bergeron C, Janssen JC, McGeer PL, Rossor MN, et al. Analysis of tau haplotypes in Pick's disease. Neurology. 59: 443-5. PMID 12177383 DOI: 10.1212/Wnl.59.3.443 |
0.364 |
|
2002 |
Lantos PL, Cairns NJ, Khan MN, King A, Revesz T, Janssen JC, Morris H, Rossor MN. Neuropathologic variation in frontotemporal dementia due to the intronic tau 10(+16) mutation. Neurology. 58: 1169-75. PMID 11971082 DOI: 10.1212/Wnl.58.8.1169 |
0.406 |
|
2002 |
Janssen JC, Warrington EK, Morris HR, Lantos P, Brown J, Revesz T, Wood N, Khan MN, Cipolotti L, Fox NC, Rossor MN. Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation. Neurology. 58: 1161-8. PMID 11971081 DOI: 10.1212/Wnl.58.8.1161 |
0.413 |
|
2002 |
Scahill RI, Schott JM, Stevens JM, Rossor MN, Fox NC. Mapping the evolution of regional atrophy in Alzheimer's disease: unbiased analysis of fluid-registered serial MRI. Proceedings of the National Academy of Sciences of the United States of America. 99: 4703-7. PMID 11930016 DOI: 10.1073/Pnas.052587399 |
0.451 |
|
2002 |
Chan D, Fox N, Rossor M. Differing patterns of temporal atrophy in Alzheimer's disease and semantic dementia. Neurology. 58: 838. PMID 11889267 DOI: 10.1212/wnl.58.5.838 |
0.329 |
|
2002 |
Morris HR, Katzenschlager R, Janssen JC, Brown JM, Ozansoy M, Quinn N, Revesz T, Rossor MN, Daniel SE, Wood NW, Lees AJ. Sequence analysis of tau in familial and sporadic progressive supranuclear palsy. Journal of Neurology, Neurosurgery, and Psychiatry. 72: 388-90. PMID 11861703 DOI: 10.1136/Jnnp.72.3.388 |
0.398 |
|
2002 |
Høgh P, Smith SJ, Scahill RI, Chan D, Harvey RJ, Fox NC, Rossor MN. Epilepsy presenting as AD: neuroimaging, electroclinical features, and response to treatment. Neurology. 58: 298-301. PMID 11805262 DOI: 10.1212/Wnl.58.2.298 |
0.317 |
|
2001 |
George-Hyslop PS, Rossor M. Unravelling the disease process The Lancet. 358. PMID 11784550 DOI: 10.1016/S0140-6736(01)07014-3 |
0.415 |
|
2001 |
Petersen RC, Doody R, Kurz A, Mohs RC, Morris JC, Rabins PV, Ritchie K, Rossor M, Thal L, Winblad B. Current concepts in mild cognitive impairment. Archives of Neurology. 58: 1985-92. PMID 11735772 DOI: 10.1001/Archneur.58.12.1985 |
0.372 |
|
2001 |
Chan D, Fox NC, Jenkins R, Scahill RI, Crum WR, Rossor MN. Rates of global and regional cerebral atrophy in AD and frontotemporal dementia. Neurology. 57: 1756-63. PMID 11723259 DOI: 10.1212/Wnl.57.10.1756 |
0.401 |
|
2001 |
Morris HR, Khan MN, Janssen JC, Brown JM, Perez-Tur J, Baker M, Ozansoy M, Hardy J, Hutton M, Wood NW, Lees AJ, Revesz T, Lantos P, Rossor MN. The genetic and pathological classification of familial frontotemporal dementia. Archives of Neurology. 58: 1813-6. PMID 11708988 DOI: 10.1001/Archneur.58.11.1813 |
0.412 |
|
2001 |
Mann DM, Takeuchi A, Sato S, Cairns NJ, Lantos PL, Rossor MN, Haltia M, Kalimo H, Iwatsubo T. Cases of Alzheimer's disease due to deletion of exon 9 of the presenilin-1 gene show an unusual but characteristic beta-amyloid pathology known as 'cotton wool' plaques. Neuropathology and Applied Neurobiology. 27: 189-96. PMID 11489138 DOI: 10.1046/J.1365-2990.2001.00316.X |
0.344 |
|
2001 |
Fox NC, Crum WR, Scahill RI, Stevens JM, Janssen JC, Rossor MN. Imaging of onset and progression of Alzheimer's disease with voxel-compression mapping of serial magnetic resonance images. Lancet. 358: 201-5. PMID 11476837 DOI: 10.1016/S0140-6736(01)05408-3 |
0.441 |
|
2001 |
Crutch SJ, Isaacs R, Rossor MN. Some workmen can blame their tools: artistic change in an individual with Alzheimer's disease. Lancet. 357: 2129-33. PMID 11445128 DOI: 10.1016/S0140-6736(00)05187-4 |
0.412 |
|
2001 |
Houlden H, Baker M, Morris HR, MacDonald N, Pickering-Brown S, Adamson J, Lees AJ, Rossor MN, Quinn NP, Kertesz A, Khan MN, Hardy J, Lantos PL, St George-Hyslop P, Munoz DG, et al. Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype. Neurology. 56: 1702-6. PMID 11425937 DOI: 10.1212/Wnl.56.12.1702 |
0.338 |
|
2001 |
Janssen JC, Lantos PL, Fox NC, Harvey RJ, Beck J, Dickinson A, Campbell TA, Collinge J, Hanger DP, Cipolotti L, Stevens JM, Rossor MN. Autopsy-confirmed familial early-onset Alzheimer disease caused by the l153V presenilin 1 mutation. Archives of Neurology. 58: 953-8. PMID 11405810 DOI: 10.1001/Archneur.58.6.953 |
0.421 |
|
2001 |
Rossor MN. Can the physician predict the neuropathologist? Advances in Experimental Medicine and Biology. 487: 1-4. PMID 11403150 DOI: 10.1007/978-1-4615-1249-3_1 |
0.348 |
|
2001 |
Rossor MN. Pick's disease: a clinical overview. Neurology. 56: S3-5. PMID 11402142 DOI: 10.1212/Wnl.56.Suppl_4.S3 |
0.386 |
|
2001 |
Ishii K, Lippa C, Tomiyama T, Miyatake F, Ozawa K, Tamaoka A, Hasegawa T, Fraser PE, Shoji S, Nee LE, Pollen DA, St George-Hyslop PH, Ii K, Ohtake T, Kalaria RN, ... Rossor MN, et al. Distinguishable effects of presenilin-1 and APP717 mutations on amyloid plaque deposition. Neurobiology of Aging. 22: 367-76. PMID 11378241 DOI: 10.1016/S0197-4580(01)00216-0 |
0.371 |
|
2001 |
O'Brien JT, Paling S, Barber R, Williams ED, Ballard C, McKeith IG, Gholkar A, Crum WR, Rossor MN, Fox NC. Progressive brain atrophy on serial MRI in dementia with Lewy bodies, AD, and vascular dementia. Neurology. 56: 1386-8. PMID 11376193 DOI: 10.1212/Wnl.56.10.1386 |
0.354 |
|
2001 |
Chan D, Fox NC, Scahill RI, Crum WR, Whitwell JL, Leschziner G, Rossor AM, Stevens JM, Cipolotti L, Rossor MN. Patterns of temporal lobe atrophy in semantic dementia and Alzheimer's disease. Annals of Neurology. 49: 433-42. PMID 11310620 DOI: 10.1002/Ana.92 |
0.424 |
|
2001 |
Warrington EK, Agnew SK, Kennedy AM, Rossor MN. Neuropsychological profiles of familial Alzheimer's disease associated with mutations in the presenilin 1 and amyloid precursor protein genes. Journal of Neurology. 248: 45-50. PMID 11266019 DOI: 10.1007/S004150170268 |
0.466 |
|
2001 |
Cordery RJ, Tyrrell PJ, Lantos PL, Rossor MN. Dementia with Lewy bodies studied with positron emission tomography. Archives of Neurology. 58: 505-8. PMID 11255457 DOI: 10.1001/Archneur.58.3.505 |
0.427 |
|
2001 |
Good CD, Scahill RI, Fox NC, Fox NC, Ashburner J, Chan DC, Crum WR, Rossor MN, Frackowiak RS. Patterns of cerebral atrophy in Alzheimer's disease and semantic dementia: A comparison of voxel based morphometry and region of interest measurements Neuroimage. 13: 317. DOI: 10.1016/S1053-8119(01)91660-X |
0.442 |
|
2000 |
Bell K, Cairns NJ, Lantos PL, Rossor MN. Immunohistochemistry distinguishes: between Pick's disease and corticobasal degeneration. Journal of Neurology, Neurosurgery, and Psychiatry. 69: 835-6. PMID 11185644 DOI: 10.1136/Jnnp.69.6.835 |
0.47 |
|
2000 |
Rossor MN. Dementia and driving: European national guidelines. EFNS Scientist Panel on Dementia. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 7: 745. PMID 11136368 DOI: 10.1111/J.1468-1331.2006.01586.X-I1 |
0.366 |
|
2000 |
Spillantini MG, Yoshida H, Rizzini C, Lantos PL, Khan N, Rossor MN, Goedert M, Brown J. A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies. Annals of Neurology. 48: 939-43. PMID 11117553 DOI: 10.1002/1531-8249(200012)48:6<939::Aid-Ana17>3.0.Co;2-1 |
0.393 |
|
2000 |
Pickering-Brown S, Baker M, Yen SH, Liu WK, Hasegawa M, Cairns N, Lantos PL, Rossor M, Iwatsubo T, Davies Y, Allsop D, Furlong R, Owen F, Hardy J, Mann D, et al. Pick's disease is associated with mutations in the tau gene. Annals of Neurology. 48: 859-67. PMID 11117542 DOI: 10.1002/1531-8249(200012)48:6<859::Aid-Ana6>3.0.Co;2-1 |
0.396 |
|
2000 |
Wang T, Sharma SD, Fox N, Rossor M, Brown MJ, Sharma P. Description of a simple test for CADASIL disease and determination of mutation frequencies in sporadic ischaemic stroke and dementia patients. Journal of Neurology, Neurosurgery, and Psychiatry. 69: 652-4. PMID 11032621 DOI: 10.1136/Jnnp.69.5.652 |
0.357 |
|
2000 |
Thomas NJ, Morris CM, Scaravilli F, Johansson J, Rossor M, De Lange R, St Clair D, Nicoll J, Blank C, Coulthard A, Bushby K, Ince PG, Burn D, Kalaria RN. Hereditary vascular dementia linked to notch 3 mutations. CADASIL in British families. Annals of the New York Academy of Sciences. 903: 293-8. PMID 10818518 DOI: 10.1111/J.1749-6632.2000.Tb06379.X |
0.401 |
|
2000 |
Waldemar G, Dubois B, Emre M, Scheltens P, Tariska P, Rossor M. Diagnosis and management of Alzheimer's disease and other disorders associated with dementia. The role of neurologists in Europe. European Federation of Neurological Societies. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 7: 133-44. PMID 10809933 DOI: 10.1046/J.1468-1331.2000.00030.X |
0.391 |
|
2000 |
Janssen JC, Hall M, Fox NC, Harvey RJ, Beck J, Dickinson A, Campbell T, Collinge J, Lantos PL, Cipolotti L, Stevens JM, Rossor MN. Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological study. Brain : a Journal of Neurology. 123: 894-907. PMID 10775535 DOI: 10.1093/Brain/123.5.894 |
0.386 |
|
2000 |
Rossor MN, Fox NC. Mere forgetfulness or early Alzheimer's disease? Annals of Neurology. 47: 419-20. PMID 10762150 |
0.324 |
|
2000 |
Fox NC, Cousens S, Scahill R, Harvey RJ, Rossor MN. Using serial registered brain magnetic resonance imaging to measure disease progression in Alzheimer disease: power calculations and estimates of sample size to detect treatment effects. Archives of Neurology. 57: 339-44. PMID 10714659 DOI: 10.1001/Archneur.57.3.339 |
0.39 |
|
2000 |
Janssen JC, Lantos PL, Al-Sarraj S, Rossor MN. Thalamic degeneration with negative prion protein immunostaining. Journal of Neurology. 247: 48-51. PMID 10701897 DOI: 10.1007/S004150050009 |
0.329 |
|
2000 |
Fox NC, Jenkins R, Leary SM, Stevenson VL, Losseff NA, Crum WR, Harvey RJ, Rossor MN, Miller DH, Thompson AJ. Progressive cerebral atrophy in MS: a serial study using registered, volumetric MRI. Neurology. 54: 807-12. PMID 10690967 DOI: 10.1212/Wnl.54.4.807 |
0.308 |
|
2000 |
Jenkins R, Fox NC, Rossor AM, Harvey RJ, Rossor MN. Intracranial volume and Alzheimer disease: evidence against the cerebral reserve hypothesis. Archives of Neurology. 57: 220-4. PMID 10681081 DOI: 10.1001/Archneur.57.2.220 |
0.429 |
|
2000 |
Fox NC, Rossor MN. Seeing what Alzheimer saw--with magnetic resonance microscopy. Nature Medicine. 6: 20-1. PMID 10671077 DOI: 10.1038/71481 |
0.332 |
|
2000 |
Rossor MN, Revesz T, Lantos PL, Warrington EK. Semantic dementia with ubiquitin-positive tau-negative inclusion bodies. Brain : a Journal of Neurology. 123: 267-76. PMID 10648435 DOI: 10.1093/Brain/123.2.267 |
0.383 |
|
2000 |
Warrington EK, Rossor MN. Neuropsychological profiles of familial Alzheimer's disease associated with mutation in the presenilin 1 gene Neurobiology of Aging. 21: 234. DOI: 10.1016/S0197-4580(00)83390-4 |
0.416 |
|
2000 |
Jenkins R, Fox NC, Rossor MN. Registration of serial magnetic resonance imaging scans in Alzheimer's disease: Sensitivity and specificity of rates of atrophy Neurobiology of Aging. 21: 39. DOI: 10.1016/S0197-4580(00)82851-1 |
0.355 |
|
2000 |
Chan D, Fox NC, Scahill R, Cipolotti L, Rossor M. Different patterns of cerebral atrophy in semantic dementia and Alzheimer's disease: A volumetric MRI study Neurobiology of Aging. 21: 144-145. DOI: 10.1016/S0197-4580(00)82451-3 |
0.456 |
|
2000 |
Rossor MN. MRI as a longitudinal measure in MCI and AD Neurobiology of Aging. 21: 142. DOI: 10.1016/S0197-4580(00)82439-2 |
0.338 |
|
2000 |
Scaravilli F, Cordery RJ, Kretzschmar H, Gambetti P, Brink B, Fritz V, Temlett J, Kaplan C, Fish D, An SF, Schulz-Schaeffer WJ, Rossor MN. Sporadic fatal insomnia: A case study Annals of Neurology. 48: 665-669. DOI: 10.1002/1531-8249(200010)48:4<665::Aid-Ana15>3.0.Co;2-D |
0.326 |
|
2000 |
Rossor MN, Fox NC. Mere forgetfulness or early Alzheimer's disease? Annals of Neurology. 47: 419-420. DOI: 10.1002/1531-8249(200004)47:4<419::Aid-Ana2>3.0.Co;2-2 |
0.435 |
|
1999 |
Fox NC, Rossor MN. Diagnosis of early Alzheimer's disease. Revue Neurologique. 155: S33-7. PMID 10637936 |
0.315 |
|
1999 |
Jacob J, Revesz T, Thom M, Rossor MN. A case of sporadic Pick disease with onset at 27 years. Archives of Neurology. 56: 1289-91. PMID 10520947 DOI: 10.1001/Archneur.56.10.1289 |
0.418 |
|
1999 |
Rossor MN, Tyrrell PJ, Warrington EK, Thompson PD, Marsden CD, Lantos P. Progressive frontal gait disturbance with atypical Alzheimer's disease and corticobasal degeneration. Journal of Neurology, Neurosurgery, and Psychiatry. 67: 345-52. PMID 10449557 DOI: 10.1136/Jnnp.67.3.345 |
0.399 |
|
1999 |
Robinson G, Rossor M, Cipolotti L. Selective sparing of verb naming in a case of severe Alzheimer's disease. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 35: 443-50. PMID 10440081 DOI: 10.1016/S0010-9452(08)70812-8 |
0.415 |
|
1999 |
Ashworth A, Lloyd S, Brown J, Gydesen S, Sorensen SA, Brun A, Englund E, Humphreys C, Housman D, Badura M, Stanton V, Taylor K, Cameron J, Munroe D, Johansson J, ... Rossor M, et al. Molecular genetic characterisation of frontotemporal dementia on chromosome 3. Dementia and Geriatric Cognitive Disorders. 10: 93-101. PMID 10436350 DOI: 10.1159/000051222 |
0.326 |
|
1999 |
Rossor MN. Differential diagnosis of frontotemporal dementia: Pick's disease. Dementia and Geriatric Cognitive Disorders. 10: 43-5. PMID 10436339 DOI: 10.1159/000051211 |
0.402 |
|
1999 |
Fox NC, Warrington EK, Rossor MN. Serial magnetic resonance imaging of cerebral atrophy in preclinical Alzheimer's disease. Lancet. 353: 2125. PMID 10382699 DOI: 10.1016/S0140-6736(99)00496-1 |
0.427 |
|
1999 |
Fox NC, Scahill RI, Crum WR, Rossor MN. Correlation between rates of brain atrophy and cognitive decline in AD. Neurology. 52: 1687-9. PMID 10331700 DOI: 10.1212/Wnl.52.8.1687 |
0.369 |
|
1999 |
Burns A, Rossor M, Hecker J, Gauthier S, Petit H, Möller HJ, Rogers SL, Friedhoff LT. The effects of donepezil in Alzheimer's disease - results from a multinational trial. Dementia and Geriatric Cognitive Disorders. 10: 237-44. PMID 10325453 DOI: 10.1159/000017126 |
0.368 |
|
1999 |
Morris HR, Janssen JC, Bandmann O, Daniel SE, Rossor MN, Lees AJ, Wood NW. The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases. Journal of Neurology, Neurosurgery, and Psychiatry. 66: 665-7. PMID 10209184 DOI: 10.1136/Jnnp.66.5.665 |
0.372 |
|
1999 |
Palmer MS, Beck JA, Campbell TA, Humphries CB, Roques PK, Fox NC, Harvey R, Rossor MN, Collinge J. Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK. Mutations in brief no. 223. Online. Human Mutation. 13: 256. PMID 10090481 DOI: 10.1002/(Sici)1098-1004(1999)13:3<256::Aid-Humu11>3.0.Co;2-P |
0.407 |
|
1999 |
Houlden H, Rizzu P, Stevens M, de Knijff P, van Duijn CM, van Swieten JC, Heutink P, Perez-Tur J, Thomas V, Baker M, Morris H, Rossor M, Jannsen JC, Petersen RC, Dodd P, et al. Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations. Neuroscience Letters. 260: 193-5. PMID 10076900 DOI: 10.1016/S0304-3940(98)00931-8 |
0.446 |
|
1999 |
Green AJ, Harvey RJ, Thompson EJ, Rossor MN. Increased tau in the cerebrospinal fluid of patients with frontotemporal dementia and Alzheimer's disease. Neuroscience Letters. 259: 133-5. PMID 10025576 DOI: 10.1016/S0304-3940(98)00904-5 |
0.422 |
|
1999 |
Rossor MN. Early diagnosis of dementia. Journal of Neurology. 246: 4-5. PMID 9987707 DOI: 10.1007/S004150050298 |
0.352 |
|
1999 |
Hill AF, Butterworth RJ, Joiner S, Jackson G, Rossor MN, Thomas DJ, Frosh A, Tolley N, Bell JE, Spencer M, King A, Al-Sarraj S, Ironside JW, Lantos PL, Collinge J. Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples. Lancet. 353: 183-9. PMID 9923873 DOI: 10.1016/S0140-6736(98)12075-5 |
0.346 |
|
1999 |
Lantos PL, Cairns NJ, Harvev R, Rossor MN. Familial Alzheimer's disease and Lewy body pathology Journal of Neuropathology and Experimental Neurology. 58: 514. DOI: 10.1097/00005072-199905000-00031 |
0.433 |
|
1998 |
Whitehouse PJ, Kittner B, Roessner M, Rossor M, Sano M, Thal L, Winblad B. Clinical trial designs for demonstrating disease-course-altering effects in dementia. Alzheimer Disease and Associated Disorders. 12: 281-94. PMID 9876956 DOI: 10.1097/00002093-199812000-00007 |
0.429 |
|
1998 |
Harvey RJ, Whitehouse PJ, Rossor MN. Report of the European Working Group on Dementia Drug Guidelines Meeting--Brussels, November 1997. Alzheimer Disease and Associated Disorders. 12: 259-61. PMID 9876953 DOI: 10.1097/00002093-199812000-00003 |
0.39 |
|
1998 |
Lovat LB, O'Brien AA, Armstrong SF, Madhoo S, Bulpitt CJ, Rossor MN, Pepys MB, Hawkins PN. Scintigraphy with 123I-serum amyloid P component in Alzheimer disease. Alzheimer Disease and Associated Disorders. 12: 208-10. PMID 9772025 DOI: 10.1097/00002093-199809000-00014 |
0.368 |
|
1998 |
Brown J, Lantos PL, Rossor MN. Familial dementia lacking specific pathological features presenting with clinical features of corticobasal degeneration. Journal of Neurology, Neurosurgery, and Psychiatry. 65: 600-3. PMID 9771798 DOI: 10.1136/Jnnp.65.4.600 |
0.375 |
|
1998 |
Fox NC, Warrington EK, Seiffer AL, Agnew SK, Rossor MN. Presymptomatic cognitive deficits in individuals at risk of familial Alzheimer's disease. A longitudinal prospective study. Brain : a Journal of Neurology. 121: 1631-9. PMID 9762953 DOI: 10.1093/Brain/121.9.1631 |
0.449 |
|
1998 |
Houlden H, Crook R, Backhovens H, Prihar G, Baker M, Hutton M, Rossor M, Martin JJ, Van Broeckhoven C, Hardy J. ApoE genotype is a risk factor in nonpresenilin early-onset Alzheimer's disease families. American Journal of Medical Genetics. 81: 117-21. PMID 9514597 DOI: 10.1002/(Sici)1096-8628(19980207)81:1<117::Aid-Ajmg19>3.0.Co;2-M |
0.398 |
|
1998 |
Harvey RJ, Ellison D, Hardy J, Hutton M, Roques PK, Collinge J, Fox NC, Rossor MN. Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucine-->serine (L250S) substitution at codon 250 of the presenilin 1 gene. Journal of Neurology, Neurosurgery, and Psychiatry. 64: 44-9. PMID 9436726 DOI: 10.1136/Jnnp.64.1.44 |
0.421 |
|
1997 |
Revesz T, McLaughlin JL, Rossor MN, Lantos PL. Pathology of familial Alzheimer's disease with Lewy bodies. Journal of Neural Transmission. Supplementum. 51: 121-35. PMID 9470133 DOI: 10.1007/978-3-7091-6846-2_10 |
0.443 |
|
1997 |
Reisberg B, Burns A, Brodaty H, Eastwood R, Rossor M, Sartorius N, Winblad B. Report of an International Psychogeriatric Association Special Meeting Work Group; Under the Cosponsorship of Alzheimer's Disease International, the European Federation of Neurological Societies, the World Health Organization, and the World Psychiatric Association International Psychogeriatrics. 9: 11-38. PMID 9447425 DOI: 10.1017/S1041610297004675 |
0.329 |
|
1997 |
Green AJ, Harvey RJ, Thompson EJ, Rossor MN. Increased S100beta in the cerebrospinal fluid of patients with frontotemporal dementia. Neuroscience Letters. 235: 5-8. PMID 9389582 DOI: 10.1016/S0304-3940(97)00701-5 |
0.429 |
|
1997 |
Fox NC, Freeborough PA, Mekkaoui KF, Stevens JM, Rossor MN. Cerebral and cerebellar atrophy on serial magnetic resonance imaging in an initially symptom free subject at risk of familial prion disease. Bmj (Clinical Research Ed.). 315: 856-7. PMID 9353507 DOI: 10.1136/Bmj.315.7112.856 |
0.43 |
|
1997 |
Rossor MN, Fox NC, Freeborough PA, Roques PK. Slowing the progression of Alzheimer disease: monitoring progression. Alzheimer Disease and Associated Disorders. 11: S6-9. PMID 9348422 |
0.311 |
|
1997 |
Fukutani Y, Cairns NJ, Rossor MN, Lantos PL. Cerebellar pathology in sporadic and familial Alzheimer's disease including APP 717 (Val-->Ile) mutation cases: a morphometric investigation. Journal of the Neurological Sciences. 149: 177-84. PMID 9171327 DOI: 10.1016/S0022-510X(97)05399-9 |
0.374 |
|
1997 |
Fox NC, Kennedy AM, Harvey RJ, Lantos PL, Roques PK, Collinge J, Hardy J, Hutton M, Stevens JM, Warrington EK, Rossor MN. Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factor. Brain : a Journal of Neurology. 120: 491-501. PMID 9126060 DOI: 10.1093/Brain/120.3.491 |
0.432 |
|
1997 |
Larner AJ, Rossor MN. Alzheimer’s disease: towards therapeutic manipulation of the amyloid precursor protein and amyloid β-peptides Expert Opinion On Therapeutic Patents. 7: 1115-1127. DOI: 10.1517/13543776.7.10.1115 |
0.358 |
|
1997 |
Harvey RJ, Summerfield J, Fox N, Warrington E, Rossor M. Dementia associated with haemochromatosis: a report of two cases European Journal of Neurology. 4: 318-322. DOI: 10.1111/J.1468-1331.1997.Tb00354.X |
0.401 |
|
1997 |
Lantos P, Rossor M. A prospective clinicopathological study of familial dementias: A neuropathological review of 56 cases. Journal of Neuropathology and Experimental Neurology. 56: 605. DOI: 10.1097/00005072-199705000-00149 |
0.351 |
|
1997 |
Fox NC, Freeborough PA, Mekkaoui KF, Rossor MN. 1-12-21 Registration of serial MRI detects pre-symptomatic brain atrophy in familial Alzheimer's disease Journal of the Neurological Sciences. 150. DOI: 10.1016/S0022-510X(97)84921-0 |
0.425 |
|
1996 |
Rossor MN, Fox NC, Freeborough PA, Harvey RJ. Clinical features of sporadic and familial Alzheimer's disease. Neurodegeneration : a Journal For Neurodegenerative Disorders, Neuroprotection, and Neuroregeneration. 5: 393-7. PMID 9117552 DOI: 10.1006/Neur.1996.0052 |
0.463 |
|
1996 |
Fox NC, Warrington EK, Freeborough PA, Hartikainen P, Kennedy AM, Stevens JM, Rossor MN. Presymptomatic hippocampal atrophy in Alzheimer's disease. A longitudinal MRI study. Brain : a Journal of Neurology. 119: 2001-7. PMID 9010004 DOI: 10.1093/Brain/119.6.2001 |
0.471 |
|
1996 |
Thal LJ, Schwartz G, Sano M, Weiner M, Knopman D, Harrell L, Bodenheimer S, Rossor M, Philpot M, Schor J, Goldberg A. A multicenter double-blind study of controlled-release physostigmine for the treatment of symptoms secondary to Alzheimer's disease. Physostigmine Study Group. Neurology. 47: 1389-95. PMID 8960716 DOI: 10.1212/Wnl.47.6.1389 |
0.334 |
|
1996 |
Brown J, Lantos PL, Roques P, Fidani L, Rossor MN. Familial dementia with swollen achromatic neurons and corticobasal inclusion bodies: a clinical and pathological study. Journal of the Neurological Sciences. 135: 21-30. PMID 8926492 DOI: 10.1016/0022-510X(95)00236-U |
0.401 |
|
1996 |
Fukutani Y, Cairns NJ, Rossor MN, Lantos PL. Purkinje cell loss and astrocytosis in the cerebellum in familial and sporadic Alzheimer's disease. Neuroscience Letters. 214: 33-6. PMID 8873125 DOI: 10.1016/0304-3940(96)12875-5 |
0.355 |
|
1996 |
Harvey RJ, Roques P, Fox NC, Rossor MN. Non-Alzheimer dementias in young patients. The British Journal of Psychiatry : the Journal of Mental Science. 168: 384-5. PMID 8833704 DOI: 10.1192/Bjp.168.3.384B |
0.408 |
|
1996 |
Mann DM, Iwatsubo T, Cairns NJ, Lantos PL, Nochlin D, Sumi SM, Bird TD, Poorkaj P, Hardy J, Hutton M, Prihar G, Crook R, Rossor MN, Haltia M. Amyloid beta protein (Abeta) deposition in chromosome 14-linked Alzheimer's disease: predominance of Abeta42(43). Annals of Neurology. 40: 149-56. PMID 8773595 DOI: 10.1002/Ana.410400205 |
0.354 |
|
1996 |
Fox N, Harvey RJ, Rossor MN. Protein folding, nucleation phenomena and delayed neurodegeneration in Alzheimer's disease. Reviews in the Neurosciences. 7: 21-8. PMID 8736676 DOI: 10.1515/Revneuro.1996.7.1.21 |
0.407 |
|
1996 |
Armstrong RA, Cairns NJ, Patel R, Lantos PL, Rossor MN. Relationships between beta-amyloid (A beta) deposits and blood vessels in patients with sporadic and familial Alzheimer's disease. Neuroscience Letters. 207: 171-4. PMID 8728477 DOI: 10.1016/0304-3940(96)12525-8 |
0.319 |
|
1996 |
Rossor MN, Fox NC, Beck J, Campbell TC, Collinge J. Incomplete penetrance of familial Alzheimer's disease in a pedigree with a novel presenilin-1 gene mutation. Lancet. 347: 1560. PMID 8684135 DOI: 10.1016/S0140-6736(96)90715-1 |
0.407 |
|
1996 |
Fox NC, Freeborough PA, Rossor MN. Visualisation and quantification of rates of atrophy in Alzheimer's disease. Lancet. 348: 94-7. PMID 8676724 DOI: 10.1016/S0140-6736(96)05228-2 |
0.465 |
|
1996 |
Rossor MN, Kennedy AM, Frackowiak RS. Clinical and neuroimaging features of familial Alzheimer's disease. Annals of the New York Academy of Sciences. 777: 49-56. PMID 8624126 DOI: 10.1111/J.1749-6632.1996.Tb34400.X |
0.437 |
|
1996 |
Fox NC, Warrington EK, Stevens JM, Rossor MN. Atrophy of the hippocampal formation in early familial Alzheimer's disease. A longitudinal MRI study of at-risk members of a family with an amyloid precursor protein 717Val-Gly mutation. Annals of the New York Academy of Sciences. 777: 226-32. PMID 8624089 DOI: 10.1111/J.1749-6632.1996.Tb34423.X |
0.444 |
|
1996 |
Tabrizi SJ, Howard RS, Collinge J, Rossor MN, Scaravilli F. Creutzfeldt-Jakob disease in a young woman Lancet. 347: 945-948. PMID 8598761 DOI: 10.1016/S0140-6736(96)91419-1 |
0.352 |
|
1996 |
Collinge J, Rossor M. A new variant of prion disease. Lancet. 347: 916-7. PMID 8598749 DOI: 10.1016/S0140-6736(96)91407-5 |
0.325 |
|
1996 |
Rossor MN, Fox NC, Freeborough PA, Roques PK. 595 Rates of brain atrophy measured by registration and subtraction of serial 3D MR scans correlate with clinical decline in Alzheimer's disease and related disorders Neurobiology of Aging. 17. DOI: 10.1016/S0197-4580(96)80597-5 |
0.387 |
|
1996 |
McKeith G, Morris C, Lovestone S, Wilcock G, Rossor M, Cayton H, Ragan I, Humphries S, Betteridge D, Durrington P, Galton D, Nicholls P. Apolipoprotein E genotyping in Alzheimer's disease The Lancet. 347: 1775-1776. DOI: 10.1016/S0140-6736(96)90857-0 |
0.39 |
|
1995 |
Brown J, Ashworth A, Gydesen S, Sorensen A, Rossor M, Hardy J, Collinge J. Familial non-specific dementia maps to chromosome 3. Human Molecular Genetics. 4: 1625-8. PMID 8541850 DOI: 10.1093/Hmg/4.9.1625 |
0.412 |
|
1995 |
Kennedy AM, Newman SK, Frackowiak RS, Cunningham VJ, Roques P, Stevens J, Neary D, Bruton CJ, Warrington EK, Rossor MN. Chromosome 14 linked familial Alzheimer's disease. A clinico-pathological study of a single pedigree. Brain : a Journal of Neurology. 118: 185-205. PMID 7895004 DOI: 10.1093/Brain/118.1.185 |
0.427 |
|
1995 |
Jendroska K, Rossor MN, Mathias CJ, Daniel SE. Morphological overlap between corticobasal degeneration and Pick's disease: a clinicopathological report. Movement Disorders : Official Journal of the Movement Disorder Society. 10: 111-4. PMID 7885345 DOI: 10.1002/Mds.870100118 |
0.383 |
|
1995 |
Lannfelt L, Lilius L, Viitanen M, Houlden H, Rossor M, Hardy J, Winblad B, Basun H. Microsatellite D21S210 (GT-12) allele frequencies in sporadic Alzheimer's disease. Acta Neurologica Scandinavica. 91: 145-8. PMID 7785426 DOI: 10.1111/J.1600-0404.1995.Tb00422.X |
0.447 |
|
1995 |
Kennedy AM, Frackowiak RS, Newman SK, Bloomfield PM, Seaward J, Roques P, Lewington G, Cunningham VJ, Rossor MN. Deficits in cerebral glucose metabolism demonstrated by positron emission tomography in individuals at risk of familial Alzheimer's disease. Neuroscience Letters. 186: 17-20. PMID 7783942 DOI: 10.1016/0304-3940(95)11270-7 |
0.4 |
|
1995 |
Orrell RW, James-Galton M, Stevens JM, Rossor MN. Cerebral achromatopsia as a presentation of Trousseau's syndrome. Postgraduate Medical Journal. 71: 44-6. PMID 7708594 DOI: 10.1136/Pgmj.71.831.44 |
0.306 |
|
1995 |
Ashworth A, Brown J, Gydesen S, Sorensen SA, Rossor MN, Hardy J, Collinge J. Frontal lobe or 'nonspecific' dementias are genetically heterogeneous. Neurology. 45: 1781. PMID 7675248 DOI: 10.1212/Wnl.45.9.1781 |
0.476 |
|
1995 |
Rossor MN, Brown J. Progressive supranuclear palsy: neuropathologically based diagnostic clinical criteria. Journal of Neurology, Neurosurgery, and Psychiatry. 59: 343. PMID 7673978 DOI: 10.1136/Jnnp.59.3.343 |
0.305 |
|
1995 |
Houlden H, Crook R, Duff K, Hutton M, Collinge J, Roques P, Rossor M, Hardy J. Apolipoprotein E alleles but neither apolipoprotein B nor apolipoprotein AI/CIII alleles are associated with late onset, familial Alzheimer's disease. Neuroscience Letters. 188: 202-4. PMID 7609909 DOI: 10.1016/0304-3940(95)11422-S |
0.364 |
|
1995 |
Kennedy AM, Rossor MN, Frackowiak RS. Positron emission tomography in familial Alzheimer disease. Alzheimer Disease and Associated Disorders. 9: 17-20. PMID 7605617 DOI: 10.1097/00002093-199505000-00005 |
0.42 |
|
1995 |
Harvey RJ, Rossor MN. Does early-onset Alzheimer disease constitute a distinct subtype? The contribution of molecular genetics. Alzheimer Disease and Associated Disorders. 9: S7-13. PMID 7546599 DOI: 10.1097/00002093-199500091-00003 |
0.461 |
|
1995 |
Bennett C, Crawford F, Osborne A, Diaz P, Hoyne J, Lopez R, Roques P, Duara R, Rossor M, Mullan M. Evidence that the APOE locus influences rate of disease progression in late onset familial Alzheimer's Disease but is not causative. American Journal of Medical Genetics. 60: 1-6. PMID 7485228 DOI: 10.1002/Ajmg.1320600102 |
0.423 |
|
1995 |
Ferris SH, Hasegawa K, Homma A, Khachaturian ZS, Post S, Rossor M, Whitehouse PJ. International efforts to improve Alzheimer disease treatment Alzheimer Disease & Associated Disorders. 9: 181. DOI: 10.1097/00002093-199500940-00001 |
0.385 |
|
1995 |
Perez-Tur J, Froelich S, Prihar G, Crook R, Baker M, Duff K, Wragg M, Busfield F, Lendon C, Clark RF, Roques P, Fuldner RA, Johnston J, Cowburn R, Forsell C, ... ... Rossor M, et al. A mutation in Alzheimer's disease destroying a splice acceptor site in the presenilin-1 gene. Neuroreport. 7: 297-301. DOI: 10.1097/00001756-199512000-00071 |
0.355 |
|
1995 |
Harvey R, Fraser D, Bonner D, Warnes A, Warrington E, Rossor M. Dementia and driving: Results of a semi-realistic simulator study International Journal of Geriatric Psychiatry. 10: 859-864. DOI: 10.1002/Gps.930101008 |
0.364 |
|
1994 |
Lawrence RM, Ronca MA, Tyrrell P, Rossor MN. Psychiatric symptoms in patients with focal cortical degeneration. Behavioural Neurology. 7: 153-8. PMID 24487329 DOI: 10.3233/Ben-1994-73-407 |
0.355 |
|
1994 |
Lantos PL, Ovenstone IM, Johnson J, Clelland CA, Roques P, Rossor MN. Lewy bodies in the brain of two members of a family with the 717 (Val to Ile) mutation of the amyloid precursor protein gene. Neuroscience Letters. 172: 77-9. PMID 8084541 DOI: 10.1016/0304-3940(94)90666-1 |
0.431 |
|
1994 |
Newman SK, Warrington EK, Kennedy AM, Rossor MN. The earliest cognitive change in a person with familial Alzheimer's disease: presymptomatic neuropsychological features in a pedigree with familial Alzheimer's disease confirmed at necropsy. Journal of Neurology, Neurosurgery, and Psychiatry. 57: 967-72. PMID 8057122 DOI: 10.1136/Jnnp.57.8.967 |
0.443 |
|
1994 |
Houlden H, Crook R, Hardy J, Roques P, Collinge J, Rossor M. Confirmation that familial clustering and age of onset in late onset Alzheimer's disease are determined at the apolipoprotein E locus. Neuroscience Letters. 174: 222-4. PMID 7970184 DOI: 10.1016/0304-3940(94)90026-4 |
0.415 |
|
1994 |
Hawkins PN, Rossor MN, Gallimore JR, Miller B, Moore EG, Pepys MB. Concentration of serum amyloid P component in the CSF as a possible marker of cerebral amyloid deposits in Alzheimer's disease. Biochemical and Biophysical Research Communications. 201: 722-6. PMID 7516157 DOI: 10.1006/Bbrc.1994.1760 |
0.386 |
|
1994 |
Karlinsky H, Lennox A, Rossor M. Alzheimer's disease and genetic testing. Alzheimer Disease & Associated Disorders. 8: 63-65. DOI: 10.1097/00002093-199408020-00001 |
0.387 |
|
1993 |
Rossor MN. Molecular pathology of Alzheimer's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 56: 583-6. PMID 8509767 DOI: 10.1136/Jnnp.56.6.583 |
0.43 |
|
1993 |
Brown J, Lantos P, Stratton M, Roques P, Rossor M. Familial progressive supranuclear palsy. Journal of Neurology, Neurosurgery, and Psychiatry. 56: 473-476. PMID 8505637 DOI: 10.1136/Jnnp.56.5.473 |
0.33 |
|
1993 |
Cairns NJ, Chadwick A, Lantos PL, Levy R, Rossor MN. Beta A4 protein deposition in familial Alzheimer's disease with the mutation in codon 717 of the beta A4 amyloid precursor protein gene and sporadic Alzheimer's disease. Neuroscience Letters. 149: 137-40. PMID 8474686 DOI: 10.1016/0304-3940(93)90755-A |
0.409 |
|
1993 |
Brown J, Gydesen S, Sorensen SA, Brun A, Smith S, Houlden H, Twells R, Mullan M, Rossor M, Collinge J. Genetic characterization of a familial non-specific dementia originating in Jutland, Denmark. Journal of the Neurological Sciences. 114: 138-43. PMID 8445394 DOI: 10.1016/0022-510X(93)90288-A |
0.466 |
|
1993 |
Ball JA, Lantos PL, Jackson M, Marsden CD, Scadding JW, Rossor MN. Alien hand sign in association with Alzheimer's histopathology. Journal of Neurology, Neurosurgery, and Psychiatry. 56: 1020-3. PMID 8410026 DOI: 10.1136/Jnnp.56.9.1020 |
0.438 |
|
1993 |
Houlden H, Crawford F, Rossor M, Mullan M. Screening for the APP codon 670/671 mutations in Alzheimer's disease. Neuroscience Letters. 154: 161-2. PMID 8395665 DOI: 10.1016/0304-3940(93)90196-R |
0.435 |
|
1993 |
Parfitt M, Crook R, Roques P, Rossor M, Chartier-Harlin M. The Cystatin-C gene is not linked to early onset familial Alzheimer's disease Neuroscience Letters. 154: 81-83. PMID 8361651 DOI: 10.1016/0304-3940(93)90176-L |
0.417 |
|
1993 |
Ball JA, Kennedy AM, Roques P, Stevens J, Rossor MN. MRI findings in an individual at risk for familial Alzheimer's disease. Dementia (Basel, Switzerland). 4: 120. PMID 8358513 DOI: 10.1159/000107308 |
0.41 |
|
1993 |
Mullan M, Houlden H, Crawford F, Kennedy A, Rogues P, Rossor M. Age of onset in familial early onset Alzheimer's disease correlates with genetic aetiology. American Journal of Medical Genetics. 48: 129-30. PMID 8291565 DOI: 10.1002/Ajmg.1320480303 |
0.405 |
|
1993 |
Rossor MN, Newman S, Frackowiak RS, Lantos P, Kennedy AM. Alzheimer's disease families with amyloid precursor protein mutations. Annals of the New York Academy of Sciences. 695: 198-202. PMID 8239283 DOI: 10.1111/J.1749-6632.1993.Tb23052.X |
0.442 |
|
1992 |
Lantos PL, Luthert PJ, Hanger D, Anderton BH, Mullan M, Rossor M. Familial Alzheimer's disease with the amyloid precursor protein position 717 mutation and sporadic Alzheimer's disease have the same cytoskeletal pathology. Neuroscience Letters. 137: 221-4. PMID 1584463 DOI: 10.1016/0304-3940(92)90408-Y |
0.419 |
|
1992 |
Collinge J, Brown J, Hardy J, Mullan M, Rossor MN, Baker H, Crow TJ, Lofthouse R, Poulter M, Ridley R. Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features. Brain : a Journal of Neurology. 115: 687-710. PMID 1352725 DOI: 10.1093/Brain/115.3.687 |
0.445 |
|
1992 |
Rossor MN. Familial Alzheimer's disease. Bailliã¨Re's Clinical Neurology. 1: 517-34. PMID 1344201 |
0.318 |
|
1992 |
Mullan M, Houlden H, Windelspecht M, Fidani L, Lombardi C, Diaz P, Rossor M, Crook R, Hardy J, Duff K. A locus for familial early-onset Alzheimer's disease on the long arm of chromosome 14, proximal to the alpha 1-antichymotrypsin gene. Nature Genetics. 2: 340-2. PMID 1303291 DOI: 10.1038/Ng1292-340 |
0.375 |
|
1992 |
Fidani L, Rooke K, Chartier-Harlin MC, Hughes D, Tanzi R, Mullan M, Roques P, Rossor M, Hardy J, Goate A. Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->Ile. Human Molecular Genetics. 1: 165-8. PMID 1303172 DOI: 10.1093/Hmg/1.3.165 |
0.364 |
|
1992 |
Anderton B, Hanger D, Lantos P, Mullan M, Rossor M, Luthert P. Familial Alzheimer's disease with an APP717 point mutation and sporadic Alzheimer's disease have the same cytoskeletal pathology Neurobiology of Aging. 13: S57. DOI: 10.1016/0197-4580(92)90352-X |
0.459 |
|
1991 |
Lange KW, Wells FR, Rossor MN, Jenner P, Marsden CD. Cortical nicotinic receptors in Alzheimer's disease and Parkinson's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 54: 373-4. PMID 2056331 DOI: 10.1136/Jnnp.54.4.373-A |
0.385 |
|
1991 |
Tyrrell PJ, Kartsounis LD, Frackowiak RS, Findley LJ, Rossor MN. Progressive loss of speech output and orofacial dyspraxia associated with frontal lobe hypometabolism. Journal of Neurology, Neurosurgery, and Psychiatry. 54: 351-7. PMID 2056322 DOI: 10.1136/Jnnp.54.4.351 |
0.321 |
|
1991 |
van Duijn CM, van Broeckhoven C, Hardy JA, Goate AM, Rossor MN, Vandenberghe A, Martin JJ, Hofman A, Mullan MJ. Evidence for allelic heterogeneity in familial early-onset Alzheimer's disease. The British Journal of Psychiatry : the Journal of Mental Science. 158: 471-4. PMID 2054561 DOI: 10.1192/Bjp.158.4.471 |
0.372 |
|
1991 |
Chartier-Harlin MC, Crawford F, Houlden H, Warren A, Hughes D, Fidani L, Goate A, Rossor M, Roques P, Hardy J. Early-onset Alzheimer's disease caused by mutations at codon 717 of the beta-amyloid precursor protein gene. Nature. 353: 844-6. PMID 1944558 DOI: 10.1038/353844A0 |
0.414 |
|
1991 |
Ewins DL, Rossor MN, Butler J, Roques PK, Mullan MJ, McGregor AM. Association between autoimmune thyroid disease and familial Alzheimer's disease. Clinical Endocrinology. 35: 93-6. PMID 1889144 DOI: 10.1111/J.1365-2265.1991.Tb03502.X |
0.417 |
|
1991 |
Crawford F, Hardy J, Mullan M, Goate A, Hughes D, Fidani L, Roques P, Rossor M, Chartier-Harlin MC. Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene in 14 families with early onset Alzheimer's disease fails to reveal mutations in the beta-amyloid sequence. Neuroscience Letters. 133: 1-2. PMID 1791986 DOI: 10.1016/0304-3940(91)90042-R |
0.365 |
|
1990 |
St George-Hyslop PH, Haines JL, Farrer LA, Polinsky R, Van Broeckhoven C, Goate A, McLachlan DR, Orr H, Bruni AC, Sorbi S, Rainero I, Foncin JF, Pollen D, Cantu JM, Tupler R, ... ... Rossor M, et al. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature. 347: 194-7. PMID 2395471 DOI: 10.1038/347194A0 |
0.413 |
|
1990 |
Farrer LA, Myers RH, Cupples LA, St George-Hyslop PH, Bird TD, Rossor MN, Mullan MJ, Polinsky R, Nee L, Heston L. Transmission and age-at-onset patterns in familial Alzheimer's disease: evidence for heterogeneity. Neurology. 40: 395-403. PMID 2314579 DOI: 10.1097/00002093-199100510-00015 |
0.372 |
|
1990 |
Tyrrell PJ, Sawle GV, Ibanez V, Bloomfield PM, Leenders KL, Frackowiak RS, Rossor MN. Clinical and positron emission tomographic studies in the 'extrapyramidal syndrome' of dementia of the Alzheimer type. Archives of Neurology. 47: 1318-23. PMID 2252449 DOI: 10.1001/Archneur.1990.00530120062011 |
0.461 |
|
1990 |
Tyrrell PJ, Warrington EK, Frackowiak RS, Rossor MN. Heterogeneity in progressive aphasia due to focal cortical atrophy. A clinical and PET study. Brain : a Journal of Neurology. 113: 1321-36. PMID 2245299 DOI: 10.1093/Brain/113.5.1321 |
0.349 |
|
1990 |
Collinge J, Owen F, Poulter M, Leach M, Crow TJ, Rossor MN, Hardy J, Mullan MJ, Janota I, Lantos PL. Prion dementia without characteristic pathology. Lancet. 336: 7-9. PMID 1973256 DOI: 10.1016/0140-6736(90)91518-F |
0.417 |
|
1989 |
Hardy JA, Goate AM, Owen MJ, Mullan MJ, Rossor MN, Pearson RC. Modelling the occurrence and pathology of Alzheimer's disease. Neurobiology of Aging. 10: 429-31; discussion 4. PMID 2812201 DOI: 10.1016/0197-4580(89)90084-5 |
0.409 |
|
1989 |
Wilcock GK, Hope RA, Brooks DN, Lantos PL, Oppenheimer C, Reynolds GP, Rossor MN, Davies MB. Recommended minimum data to be collected in research studies on Alzheimer's disease. The MRC (UK) Alzheimer's Disease Workshop Steering Committee. Journal of Neurology, Neurosurgery, and Psychiatry. 52: 693-700. PMID 2664087 DOI: 10.1136/Jnnp.52.6.693 |
0.428 |
|
1989 |
Rossor M. Alzheimer's disease: the entity and its cause. Biochemical Society Transactions. 17: 67-69. PMID 2653921 DOI: 10.1042/Bst0170067 |
0.44 |
|
1989 |
Lange KW, Wells FR, Rossor MN, Jenner P, Marsden CD. Brain muscarinic receptors in Alzheimer's and Parkinson's diseases. Lancet. 2: 1279. PMID 2573791 DOI: 10.1016/S0140-6736(89)91886-2 |
0.384 |
|
1989 |
Tyrrell PJ, Rossor MN. Extrapyramidal signs in dementia of Alzheimer type. Lancet. 2: 920. PMID 2571838 DOI: 10.1016/S0140-6736(89)91580-8 |
0.403 |
|
1989 |
Hardy J, Goate A, Owen MJ, Rossor M. Presenile dementia associated with mosaic trisomy 21 in a patient with a Down syndrome child. The Lancet. 334: 743. PMID 2570989 DOI: 10.1016/S0140-6736(89)90805-2 |
0.325 |
|
1988 |
Tyrrell P, Rossor M. Recent advances in the understanding of dementia. Postgraduate Medical Journal. 64: 99-106. PMID 3050939 DOI: 10.1136/Pgmj.64.748.99 |
0.331 |
|
1988 |
Waters CM, Peck R, Rossor M, Reynolds GP, Hunt SP. Immunocytochemical studies on the basal ganglia and substantia nigra in Parkinson's disease and Huntington's chorea. Neuroscience. 25: 419-38. PMID 2456487 DOI: 10.1016/0306-4522(88)90249-7 |
0.318 |
|
1987 |
Quinn NP, Rossor MN, Marsden CD. Olfactory threshold in Parkinson's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 50: 88-9. PMID 3819760 DOI: 10.1136/Jnnp.50.1.88 |
0.326 |
|
1987 |
Bondareff W, Mountjoy CQ, Roth M, Rossor MN, Iversen LL, Reynolds GP, Hauser DL. Neuronal degeneration in locus ceruleus and cortical correlates of Alzheimer disease. Alzheimer Disease and Associated Disorders. 1: 256-62. PMID 3453748 DOI: 10.1097/00002093-198701040-00005 |
0.392 |
|
1987 |
Gramsbergen JB, Mountjoy CQ, Rossor MN, Reynolds GP, Roth M, Korf J. A correlative study on hippocampal cation shifts and amino acids and clinico-pathological data in Alzheimer's disease. Neurobiology of Aging. 8: 487-94. PMID 3431623 DOI: 10.1016/0197-4580(87)90122-9 |
0.385 |
|
1987 |
Bondareff W, Mountjoy CQ, Roth M, Rossor MN, Iversen LL, Reynolds GP. Age and histopathologic heterogeneity in Alzheimer's disease. Evidence for subtypes. Archives of General Psychiatry. 44: 412-7. PMID 2883954 DOI: 10.1001/Archpsyc.1987.01800170026005 |
0.413 |
|
1987 |
Katona CE, O'Brien C, Tyrrell P, Hardy J, Rossor M, Walshe JM. Tetrahydroaminoacridine And Alzheimer'S Disease The Lancet. 329: 444-445. DOI: 10.1016/S0140-6736(87)90142-5 |
0.437 |
|
1986 |
Quinn NP, Rossor MN, Marsden CD. Dementia And Parkinson'S Disease — Pathhological And Neurochemical Considerations British Medical Bulletin. 42: 86-90. PMID 3006860 DOI: 10.1093/Oxfordjournals.Bmb.A072104 |
0.433 |
|
1986 |
Rossor M, Mountjoy CQ. Post-mortem neurochemical changes in Alzheimer's disease compared with normal ageing. Canadian Journal of Neurological Sciences. 13: 499-502. PMID 2878713 DOI: 10.1017/S0317167100037203 |
0.394 |
|
1986 |
Dawbarn D, Rossor MN, Mountjoy CQ, Roth M, Emson PC. Decreased somatostatin immunoreactivity but not neuropeptide Y immunoreactivity in cerebral cortex in senile dementia of Alzheimer type. Neuroscience Letters. 70: 154-9. PMID 2877420 DOI: 10.1016/0304-3940(86)90455-6 |
0.376 |
|
1986 |
Rossor M, Iversen LL. Non-cholinergic neurotransmitter abnormalities in Alzheimer's disease British Medical Bulletin. 42: 70-74. PMID 2869818 DOI: 10.1093/Oxfordjournals.Bmb.A072101 |
0.437 |
|
1986 |
Rossor M. Dementia: A Clinical Approach Journal of Neurology, Neurosurgery, and Psychiatry. 49: 851-851. DOI: 10.1136/Jnnp.49.7.851 |
0.328 |
|
1986 |
Rossor MN, Emson PC, Dawbarn D, Mountjoy CQ, Roth M. Chapter 8 Neuropeptides and dementia Progress in Brain Research. 66: 143-159. DOI: 10.1016/S0079-6123(08)64603-8 |
0.369 |
|
1985 |
Rossor MN. Transmitter deficits in Alzheimer's disease Neurochemistry International. 7: 567-570. PMID 20492961 DOI: 10.1016/0197-0186(85)90052-X |
0.432 |
|
1985 |
Emson PC, Horsfield PM, Goedert M, Rossor MN, Hawkes CH. Neurotensin in human brain: regional distribution and effects of neurological illness. Brain Research. 347: 239-44. PMID 2933123 DOI: 10.1016/0006-8993(85)90182-9 |
0.387 |
|
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