| Year |
Citation |
Score |
| 2024 |
Rexach JE, Cheng Y, Chen L, Polioudakis D, Lin LC, Mitri V, Elkins A, Han X, Yamakawa M, Yin A, Calini D, Kawaguchi R, Ou J, Huang J, Williams C, ... ... Spina S, et al. Cross-disorder and disease-specific pathways in dementia revealed by single-cell genomics. Cell. PMID 39265576 DOI: 10.1016/j.cell.2024.08.019 |
0.3 |
|
| 2024 |
Pina-Escudero SD, La Joie R, Spina S, Hwang JH, Miller ZA, Huang EJ, Grant H, Mundada NS, Boxer AL, Gorno-Tempini ML, Rosen HJ, Kramer JH, Miller BL, Seeley WW, Rabinovici GD, et al. Comorbid neuropathology and atypical presentation of Alzheimer's disease. Alzheimer's & Dementia (Amsterdam, Netherlands). 16: e12602. PMID 39040464 DOI: 10.1002/dad2.12602 |
0.309 |
|
| 2023 |
Chen Y, Spina S, Callahan P, Grinberg LT, Seeley WW, Rosen HJ, Kramer JH, Miller BL, Rankin KP. Pathology-specific patterns of cerebellar atrophy in neurodegenerative disorders. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 38109286 DOI: 10.1002/alz.13551 |
0.318 |
|
| 2023 |
Valentino RR, Scotton WJ, Roemer SF, Lashley T, Heckman MG, Shoai M, Martinez-Carrasco A, Tamvaka N, Walton RL, Baker MC, Macpherson HL, Real R, Soto-Beasley AI, Mok K, Revesz T, ... ... Spina S, et al. Creating the Pick's disease International Consortium: Association study of H2 haplotype with risk of Pick's disease. Medrxiv : the Preprint Server For Health Sciences. PMID 37163045 DOI: 10.1101/2023.04.17.23288471 |
0.3 |
|
| 2023 |
Ogonowski N, Santamaria-Garcia H, Baez S, Lopez A, Laserna A, Garcia-Cifuentes E, Ayala-Ramirez P, Zarante I, Suarez-Obando F, Reyes P, Kauffman M, Cochran N, Schulte M, Sirkis DW, Spina S, et al. Frontotemporal dementia presentation in patients with heterozygous p.H157Y variant of . Journal of Medical Genetics. PMID 36813542 DOI: 10.1136/jmg-2022-108627 |
0.301 |
|
| 2022 |
Horie K, Barthélemy NR, Spina S, VandeVrede L, He Y, Paterson RW, Wright BA, Day GS, Davis AA, Karch CM, Seeley WW, Perrin RJ, Koppisetti RK, Shaikh F, Lago AL, et al. CSF tau microtubule-binding region identifies pathological changes in primary tauopathies. Nature Medicine. PMID 36424467 DOI: 10.1038/s41591-022-02075-9 |
0.321 |
|
| 2022 |
Theofilas P, Piergies AMH, Oh I, Lee YB, Li SH, Pereira FL, Petersen C, Ehrenberg AJ, Eser RA, Ambrose AJ, Chin B, Yang T, Khan S, Ng R, Spina S, et al. Caspase-6-cleaved tau is relevant in Alzheimer's disease and marginal in four-repeat tauopathies: diagnostic and therapeutic implications. Neuropathology and Applied Neurobiology. e12819. PMID 35508761 DOI: 10.1111/nan.12819 |
0.33 |
|
| 2022 |
Mattsson-Carlgren N, Grinberg LT, Boxer A, Ossenkoppele R, Jonsson M, Seeley W, Ehrenberg A, Spina S, Janelidze S, Rojas-Martinex J, Rosen H, La Joie R, Lesman-Segev O, Iaccarino L, Kollmorgen G, et al. Cerebrospinal Fluid Biomarkers in Autopsy-Confirmed Alzheimer Disease and Frontotemporal Lobar Degeneration. Neurology. PMID 35173015 DOI: 10.1212/WNL.0000000000200040 |
0.309 |
|
| 2021 |
Thijssen EH, La Joie R, Strom A, Fonseca C, Iaccarino L, Wolf A, Spina S, Allen IE, Cobigo Y, Heuer H, VandeVrede L, Proctor NK, Lago AL, Baker S, Sivasankaran R, et al. Plasma phosphorylated tau 217 and phosphorylated tau 181 as biomarkers in Alzheimer's disease and frontotemporal lobar degeneration: a retrospective diagnostic performance study. The Lancet. Neurology. 20: 739-752. PMID 34418401 DOI: 10.1016/S1474-4422(21)00214-3 |
0.331 |
|
| 2021 |
Peet BT, Spina S, Mundada N, La Joie R. Neuroimaging in Frontotemporal Dementia: Heterogeneity and Relationships with Underlying Neuropathology. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 18: 728-752. PMID 34389969 DOI: 10.1007/s13311-021-01101-x |
0.302 |
|
| 2021 |
Spina S, La Joie R, Petersen C, Nolan AL, Cuevas D, Cosme C, Hepker M, Hwang JH, Miller ZA, Huang EJ, Karydas AM, Grant H, Boxer AL, Gorno-Tempini ML, Rosen HJ, et al. Comorbid neuropathological diagnoses in early versus late-onset Alzheimer's disease. Brain : a Journal of Neurology. PMID 33693619 DOI: 10.1093/brain/awab099 |
0.326 |
|
| 2021 |
Naasan G, Shdo SM, Rodriguez EM, Spina S, Grinberg L, Lopez L, Karydas A, Seeley WW, Miller BL, Rankin KP. Psychosis in neurodegenerative disease: differential patterns of hallucination and delusion symptoms. Brain : a Journal of Neurology. PMID 33501939 DOI: 10.1093/brain/awaa413 |
0.324 |
|
| 2020 |
Soleimani-Meigooni DN, Iaccarino L, La Joie R, Baker S, Bourakova V, Boxer AL, Edwards L, Eser R, Gorno-Tempini ML, Jagust WJ, Janabi M, Kramer JH, Lesman-Segev OH, Mellinger T, Miller BL, ... ... Spina S, et al. 18F-flortaucipir PET to autopsy comparisons in Alzheimer's disease and other neurodegenerative diseases. Brain : a Journal of Neurology. PMID 33141172 DOI: 10.1093/brain/awaa276 |
0.334 |
|
| 2020 |
Borghesani V, Battistella G, Mandelli ML, Welch A, Weis E, Younes K, Neuhaus J, Grinberg LT, Seeley WM, Spina S, Miller B, Miller Z, Gorno-Tempini ML. Regional and hemispheric susceptibility of the temporal lobe to FTLD-TDP type C pathology. Neuroimage. Clinical. 28: 102369. PMID 32798912 DOI: 10.1016/J.Nicl.2020.102369 |
0.361 |
|
| 2020 |
Kim KH, Seo JD, Kim ES, Kim HS, Jeon S, Pak K, Lee MJ, Lee JH, Lee YM, Lee K, Shin JH, Ko JK, Jung NY, Lee JM, Yoon JA, ... ... Spina S, et al. Comparison of Amyloid in Cerebrospinal Fluid, Brain Imaging, and Autopsy in a Case of Progressive Supranuclear Palsy. Alzheimer Disease and Associated Disorders. PMID 32520735 DOI: 10.1097/Wad.0000000000000396 |
0.383 |
|
| 2020 |
Pasquini L, Nana AL, Toller G, Brown JA, Deng J, Staffaroni A, Kim EJ, Hwang JL, Li L, Park Y, Gaus SE, Allen I, Sturm VE, Spina S, Grinberg LT, et al. Salience Network Atrophy Links Neuron Type-Specific Pathobiology to Loss of Empathy in Frontotemporal Dementia. Cerebral Cortex (New York, N.Y. : 1991). PMID 32500143 DOI: 10.1093/Cercor/Bhaa119 |
0.321 |
|
| 2020 |
Thijssen EH, La Joie R, Wolf A, Strom A, Wang P, Iaccarino L, Bourakova V, Cobigo Y, Heuer H, Spina S, VandeVrede L, Chai X, Proctor NK, Airey DC, Shcherbinin S, et al. Diagnostic value of plasma phosphorylated tau181 in Alzheimer's disease and frontotemporal lobar degeneration. Nature Medicine. PMID 32123386 DOI: 10.1038/S41591-020-0762-2 |
0.413 |
|
| 2020 |
Liu AJ, Chang JE, Naasan G, Boxer AL, Miller BL, Spina S. Progressive supranuclear palsy and primary lateral sclerosis secondary to globular glial tauopathy: a case report and a practical theoretical framework for the clinical prediction of this rare pathological entity. Neurocase. 1-7. PMID 32090696 DOI: 10.1080/13554794.2020.1732427 |
0.383 |
|
| 2020 |
Resende EPF, Nolan AL, Petersen C, Ehrenberg AJ, Spina S, Allen IE, Rosen HJ, Kramer J, Miller BL, Seeley WW, Gorno-Tempini ML, Miller Z, Grinberg LT. Language and spatial dysfunction in Alzheimer disease with white matter thorn-shaped astrocytes: Astrocytic tau, cognitive function, and Alzheimer disease. Neurology. PMID 32001514 DOI: 10.1212/Wnl.0000000000008937 |
0.446 |
|
| 2020 |
Mantyh WG, Spina S, Lee A, Iaccarino L, Soleimani-Meigooni D, Tsoy E, Mellinger TJ, Grant H, Vandevrede L, La Joie R, Lesman-Segev O, Gaus S, Possin KL, Grinberg LT, Miller BL, et al. Tau Positron Emission Tomographic Findings in a Former US Football Player With Pathologically Confirmed Chronic Traumatic Encephalopathy. Jama Neurology. PMID 31904765 DOI: 10.1001/Jamaneurol.2019.4509 |
0.342 |
|
| 2019 |
Miller ZA, Spina S, Pakvasa M, Rosenberg L, Watson C, Mandelli ML, Paredes MF, Joie R, Rabinovici GD, Rosen HJ, Grinberg LT, Huang EJ, Miller BL, Seeley WW, Gorno-Tempini ML. Cortical developmental abnormalities in logopenic variant primary progressive aphasia with dyslexia. Brain Communications. 1: fcz027. PMID 32699834 DOI: 10.1093/braincomms/fcz027 |
0.36 |
|
| 2019 |
Arrant AE, Roth JR, Boyle NR, Kashyap SN, Hoffmann MQ, Murchison CF, Ramos EM, Nana AL, Spina S, Grinberg LT, Miller BL, Seeley WW, Roberson ED. Impaired β-glucocerebrosidase activity and processing in frontotemporal dementia due to progranulin mutations. Acta Neuropathologica Communications. 7: 218. PMID 31870439 DOI: 10.1186/S40478-019-0872-6 |
0.362 |
|
| 2019 |
Saijo E, Metrick MA, Koga S, Parchi P, Litvan I, Spina S, Boxer A, Rojas JC, Galasko D, Kraus A, Rossi M, Newell K, Zanusso G, Grinberg LT, Seeley WW, et al. Correction to: 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration. Acta Neuropathologica. PMID 31748840 DOI: 10.1007/S00401-019-02092-Y |
0.311 |
|
| 2019 |
Lin LC, Nana AL, Hepker M, Hwang JL, Gaus SE, Spina S, Cosme CG, Gan L, Grinberg LT, Geschwind DH, Coppola G, Rosen HJ, Miller BL, Seeley WW. Preferential tau aggregation in von Economo neurons and fork cells in frontotemporal lobar degeneration with specific MAPT variants. Acta Neuropathologica Communications. 7: 159. PMID 31640778 DOI: 10.1186/S40478-019-0809-0 |
0.428 |
|
| 2019 |
Karch CM, Kao AW, Karydas A, Onanuga K, Martinez R, Argouarch A, Wang C, Huang C, Sohn PD, Bowles KR, Spina S, Silva MC, Marsh JA, Hsu S, Pugh DA, et al. A Comprehensive Resource for Induced Pluripotent Stem Cells from Patients with Primary Tauopathies. Stem Cell Reports. PMID 31631020 DOI: 10.1016/J.Stemcr.2019.09.006 |
0.43 |
|
| 2019 |
Nolan A, De Paula Franca Resende E, Petersen C, Neylan K, Spina S, Huang E, Seeley W, Miller Z, Grinberg LT. Astrocytic Tau Deposition Is Frequent in Typical and Atypical Alzheimer Disease Presentations. Journal of Neuropathology and Experimental Neurology. PMID 31626288 DOI: 10.1093/Jnen/Nlz094 |
0.457 |
|
| 2019 |
Brown JA, Deng J, Neuhaus J, Sible IJ, Sias AC, Lee SE, Kornak J, Marx GA, Karydas AM, Spina S, Grinberg LT, Coppola G, Geschwind DH, Kramer JH, Gorno-Tempini ML, et al. Patient-Tailored, Connectivity-Based Forecasts of Spreading Brain Atrophy. Neuron. PMID 31623919 DOI: 10.1016/J.Neuron.2019.08.037 |
0.371 |
|
| 2019 |
Saijo E, Metrick MA, Koga S, Parchi P, Litvan I, Spina S, Boxer A, Rojas JC, Galasko D, Kraus A, Rossi M, Newell K, Zanusso G, Grinberg LT, Seeley WW, et al. 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration. Acta Neuropathologica. PMID 31616982 DOI: 10.1007/S00401-019-02080-2 |
0.356 |
|
| 2019 |
Kim EJ, Hwang JL, Gaus SE, Nana AL, Deng J, Brown JA, Spina S, Lee MJ, Ramos EM, Grinberg LT, Kramer JH, Boxer AL, Gorno-Tempini ML, Rosen HJ, Miller BL, et al. Evidence of corticofugal tau spreading in patients with frontotemporal dementia. Acta Neuropathologica. PMID 31542807 DOI: 10.1007/S00401-019-02075-Z |
0.399 |
|
| 2019 |
Oh J, Eser RA, Ehrenberg AJ, Morales D, Petersen C, Kudlacek J, Dunlop SR, Theofilas P, Resende EDPF, Cosme C, Alho EJL, Spina S, Walsh CM, Miller BL, Seeley WW, et al. Profound degeneration of wake-promoting neurons in Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 31416793 DOI: 10.1016/J.Jalz.2019.06.3916 |
0.394 |
|
| 2019 |
Petersen C, Nolan AL, de Paula França Resende E, Miller Z, Ehrenberg AJ, Gorno-Tempini ML, Rosen HJ, Kramer JH, Spina S, Rabinovici GD, Miller BL, Seeley WW, Heinsen H, Grinberg LT. Alzheimer's disease clinical variants show distinct regional patterns of neurofibrillary tangle accumulation. Acta Neuropathologica. PMID 31250152 DOI: 10.1007/S00401-019-02036-6 |
0.436 |
|
| 2019 |
Spina S, Brown JA, Deng J, Gardner RC, Nana AL, Hwang JL, Gaus SE, Huang EJ, Kramer JH, Rosen HJ, Kornak J, Neuhaus J, Miller BL, Grinberg LT, Boxer AL, et al. Neuropathological correlates of structural and functional imaging biomarkers in 4-repeat tauopathies. Brain : a Journal of Neurology. PMID 31081015 DOI: 10.1093/Brain/Awz122 |
0.353 |
|
| 2019 |
Spina S, Laws SM. Insights into the pathogenesis of normal-pressure hydrocephalus. Neurology. PMID 31004073 DOI: 10.1212/Wnl.0000000000007495 |
0.309 |
|
| 2019 |
Pottier C, Ren Y, Perkerson RB, Baker M, Jenkins GD, van Blitterswijk M, DeJesus-Hernandez M, van Rooij JGJ, Murray ME, Christopher E, McDonnell SK, Fogarty Z, Batzler A, Tian S, Vicente CT, ... ... Spina S, et al. Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD. Acta Neuropathologica. PMID 30739198 DOI: 10.1007/S00401-019-01962-9 |
0.362 |
|
| 2019 |
Tsai RM, Bejanin A, Lesman-Segev O, LaJoie R, Visani A, Bourakova V, O'Neil JP, Janabi M, Baker S, Lee SE, Perry DC, Bajorek L, Karydas A, Spina S, Grinberg LT, et al. F-flortaucipir (AV-1451) tau PET in frontotemporal dementia syndromes. Alzheimer's Research & Therapy. 11: 13. PMID 30704514 DOI: 10.1186/S13195-019-0470-7 |
0.397 |
|
| 2019 |
Staffaroni AM, Ljubenkov PA, Kornak J, Cobigo Y, Datta S, Marx G, Walters SM, Chiang K, Olney N, Elahi FM, Knopman DS, Dickerson BC, Boeve BF, Gorno-Tempini ML, Spina S, et al. Longitudinal multimodal imaging and clinical endpoints for frontotemporal dementia clinical trials. Brain : a Journal of Neurology. 142: 443-459. PMID 30698757 DOI: 10.1093/Brain/Awy319 |
0.326 |
|
| 2019 |
Vinceti G, Olney N, Mandelli ML, Spina S, Hubbard HI, Santos-Santos MA, Watson C, Miller ZA, Lomen-Hoerth C, Nichelli P, Miller BL, Grinberg LT, Seeley WW, Gorno-Tempini ML. Primary progressive aphasia and the FTD-MND spectrum disorders: clinical, pathological, and neuroimaging correlates. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-13. PMID 30668155 DOI: 10.1080/21678421.2018.1556695 |
0.402 |
|
| 2019 |
Mattsson N, Grinberg LT, Jonsson M, Seeley WW, Spina S, Janelidze S, Rosen HJ, Boxer AL, La Joie R, Lesman-Segev OH, Iaccarino L, Kollmorgen G, Eichenlaub U, Miller BL, Hansson O, et al. P4-536: CEREBROSPINAL FLUID BIOMARKERS FOR AMYLOID AND TAU USING FULLY AUTOMATED ASSAYS: ASSOCIATIONS WITH NEUROPATHOLOGY Alzheimer's & Dementia. 15: P1521-P1521. DOI: 10.1016/J.Jalz.2019.08.083 |
0.366 |
|
| 2019 |
Kim E, Deng J, Brown J, Spina S, Miller BL, Seeley WW. P1-379: HEMISPHERIC ASYMMETRY IN NEURODEGENERATIVE DISEASES Alzheimer's & Dementia. 15: P400-P400. DOI: 10.1016/J.Jalz.2019.06.934 |
0.346 |
|
| 2019 |
Arrant AE, Boyle NR, Roth JR, Li AN, Spina S, Grinberg LT, Miller BL, Seeley WW, Roberson ED. P1-186: IMPAIRED β-GLUCOCEREBROSIDASE ACTIVITY AND PROCESSING IN FRONTOTEMPORAL DEMENTIA DUE TO PROGRANULIN MUTATIONS Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.741 |
0.36 |
|
| 2019 |
Petersen C, Robbins CM, Ehrenberg AJ, Coppola G, Wojta K, Karydas AM, Spina S, Seeley WW, Miller BL, Grinberg LT. P3-442: Individuals With Bdnf Val66Met Polymorphism Show Lower Tau Burden At Matched Cognitive Impairment In Alzheimer'S Disease Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3476 |
0.397 |
|
| 2019 |
Oh JY, Eser R, Ehrenberg A, Morales D, Petersen C, Kudlacek J, Dunlop SR, Mejia MB, Resende EdPF, Cosme CG, Theofilas P, Seeley WW, Spina S, Walsh C, Neylan T, et al. P3-441: Early Degeneration Of Arousal System In Alzheimer'S Disease May Underlie Sleep Disturbances In Precognitive Stages Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3475 |
0.32 |
|
| 2019 |
Spina S, Miller ZA, Pakvasa M, Rosenberg LM, Rabinovici GD, Rosen HJ, Grinberg LT, Miller BL, Seeley WW, Tempini MLG. P3-439: Neuropathological Evidence Of Focal Cortical Dysplasia In Logopenic Variant Primary Progressive Aphasia With Dyslexia And Alzheimer'S Disease Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3473 |
0.42 |
|
| 2019 |
Soleimani-Meigooni DN, Iaccarino L, La Joie R, Lesman-Segev OH, Bourakova V, Strom A, Edwards L, Baker SL, Janabi M, Eser R, Larsen E, Spina S, Seeley WW, Grinberg LT, Jagust WJ, et al. P2-439: [18
F]FLORTAUCIPIR PET AND PATHOLOGY CORRELATIONS IN ALZHEIMER'S DISEASE, NON-ALZHEIMER'S TAUOPATHIES, AND OTHER NEURODEGENERATIVE DISEASES Alzheimer's & Dementia. 15: P782-P782. DOI: 10.1016/J.Jalz.2019.06.2846 |
0.41 |
|
| 2018 |
Geier EG, Bourdenx M, Storm NJ, Cochran JN, Sirkis DW, Hwang JH, Bonham LW, Ramos EM, Diaz A, Van Berlo V, Dokuru D, Nana AL, Karydas A, Balestra ME, Huang Y, ... ... Spina S, et al. Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia. Acta Neuropathologica. PMID 30382371 DOI: 10.1007/S00401-018-1925-9 |
0.421 |
|
| 2018 |
Ljubenkov PA, Staffaroni AM, Rojas JC, Allen IE, Wang P, Heuer H, Karydas A, Kornak J, Cobigo Y, Seeley WW, Grinberg LT, Spina S, Fagan AM, Jerome G, Knopman D, et al. Cerebrospinal fluid biomarkers predict frontotemporal dementia trajectory. Annals of Clinical and Translational Neurology. 5: 1250-1263. PMID 30349860 DOI: 10.1002/Acn3.643 |
0.35 |
|
| 2018 |
Joie R, Ayakta N, Seeley WW, Borys E, Boxer AL, DeCarli C, Doré V, Grinberg LT, Huang E, Hwang JH, Ikonomovic MD, Jack C, Jagust WJ, Jin LW, Klunk WE, ... ... Spina S, et al. Multisite study of the relationships between antemortem [C]PIB-PET Centiloid values and postmortem measures of Alzheimer's disease neuropathology. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 30347188 DOI: 10.1016/J.Jalz.2018.09.001 |
0.305 |
|
| 2018 |
Kim EJ, Brown JA, Deng J, Hwang JL, Spina S, Miller ZA, DeMay MG, Valcour V, Karydas A, Ramos EM, Coppola G, Miller BL, Rosen HJ, Seeley WW, Grinberg LT. Mixed TDP-43 proteinopathy and tauopathy in frontotemporal lobar degeneration: nine case series. Journal of Neurology. PMID 30324308 DOI: 10.1007/S00415-018-9086-2 |
0.414 |
|
| 2018 |
Pottier C, Zhou X, Perkerson RB, Baker M, Jenkins GD, Serie DJ, Ghidoni R, Benussi L, Binetti G, López de Munain A, Zulaica M, Moreno F, Le Ber I, Pasquier F, Hannequin D, ... ... Spina S, et al. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. The Lancet. Neurology. PMID 29724592 DOI: 10.1016/S1474-4422(18)30126-1 |
0.422 |
|
| 2018 |
Petersen C, Nolan AL, Resende EdPF, Ehrenberg AJ, Miller ZA, Spina S, Miller BL, Seeley WW, Grinberg LT. P1-494: Regional Neurofibrillary Tangle Distribution As A Contributor To Clinical Heterogeneity In Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.504 |
0.41 |
|
| 2018 |
Resende EdPF, Nolan AL, Petersen C, Ehrenberg AJ, Miller ZA, Spina S, Miller BL, Seeley WW, Rosen HJ, Grinberg LT. O1-13-04: Regional Accumulation Of Argyrophilic Thorny-Shaped Astrocyte Clusters (Atac) Correlates With Worse Visuospatial And Language Functions In Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.3044 |
0.315 |
|
| 2017 |
Schonhaut DR, McMillan CT, Spina S, Dickerson BC, Siderowf A, Devous MD, Tsai R, Winer J, Russell DS, Litvan I, Roberson ED, Seeley WW, Grinberg LT, Kramer JH, Miller BL, et al. (18) F-flortaucipir tau PET distinguishes established progressive supranuclear palsy from controls and Parkinson's disease: A multicenter study. Annals of Neurology. PMID 28980714 DOI: 10.1002/Ana.25060 |
0.357 |
|
| 2017 |
Shi Y, Yamada K, Liddelow SA, Smith ST, Zhao L, Luo W, Tsai RM, Spina S, Grinberg LT, Rojas JC, Gallardo G, Wang K, Roh J, Robinson G, Finn MB, et al. ApoE4 markedly exacerbates tau-mediated neurodegeneration in a mouse model of tauopathy. Nature. 549: 523-527. PMID 28959956 DOI: 10.1038/Nature24016 |
0.39 |
|
| 2017 |
Brown JA, Hua AY, Trujllo A, Attygalle S, Binney RJ, Spina S, Lee SE, Kramer JH, Miller BL, Rosen HJ, Boxer AL, Seeley WW. Advancing functional dysconnectivity and atrophy in progressive supranuclear palsy. Neuroimage. Clinical. 16: 564-574. PMID 28951832 DOI: 10.1016/J.Nicl.2017.09.008 |
0.324 |
|
| 2017 |
Kim EJ, Lee MJ, Lee JH, Lee YM, Shin JH, Shin MJ, Choi KU, Jung NY, Pak K, Hwang C, Ahn JW, Sung S, Spina S, Grinberg LT, Seeley WW, et al. Globular glial tauopathy presenting as non-fluent/agrammatic variant primary progressive aphasia with chorea. Parkinsonism & Related Disorders. PMID 28923295 DOI: 10.1016/J.Parkreldis.2017.09.006 |
0.312 |
|
| 2017 |
Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, ... ... Spina S, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics. PMID 28714976 DOI: 10.1038/Ng.3916 |
0.389 |
|
| 2017 |
Spina S, Schonhaut DR, Boeve BF, Seeley WW, Ossenkoppele R, O'Neil JP, Lazaris A, Rosen HJ, Boxer AL, Perry DC, Miller BL, Dickson DW, Parisi JE, Jagust WJ, Murray ME, et al. Frontotemporal dementia with the V337M MAPT mutation: Tau-PET and pathology correlations. Neurology. PMID 28130473 DOI: 10.1212/Wnl.0000000000003636 |
0.433 |
|
| 2016 |
Ghetti B, Dlouhy SR, Dupree B, Epperson F, Murrell JR, Oblak AL, Piccardo P, Richardson RM, Spina S, Takao M, Vidal R, Yamaguchi K, Young K. Contribution Of The Neuropathology Laboratory At Indiana University To The Deciphering Of Dominantly Inherited Dementias: 1976-2016 Alzheimers & Dementia. 12. DOI: 10.1016/J.Jalz.2016.06.1553 |
0.379 |
|
| 2015 |
Bang J, Spina S, Miller BL. Frontotemporal dementia. Lancet (London, England). 386: 1672-82. PMID 26595641 DOI: 10.1016/S0140-6736(15)00461-4 |
0.32 |
|
| 2015 |
Wang LS, Naj AC, Graham RR, Crane PK, Kunkle BW, Cruchaga C, Murcia JD, Cannon-Albright L, Baldwin CT, Zetterberg H, Blennow K, Kukull WA, Faber KM, Schupf N, Norton MC, ... ... Spina S, et al. Rarity of the Alzheimer disease-protective APP A673T variant in the United States. Jama Neurology. 72: 209-16. PMID 25531812 DOI: 10.1001/Jamaneurol.2014.2157 |
0.405 |
|
| 2014 |
Naj AC, Jun G, Reitz C, Kunkle BW, Perry W, Park YS, Beecham GW, Rajbhandary RA, Hamilton-Nelson KL, Wang LS, Kauwe JS, Huentelman MJ, Myers AJ, Bird TD, Boeve BF, ... ... Spina S, et al. Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. Jama Neurology. 71: 1394-404. PMID 25199842 DOI: 10.1001/Jamaneurol.2014.1491 |
0.362 |
|
| 2014 |
Boyd CD, Tierney M, Wassermann EM, Spina S, Oblak AL, Ghetti B, Grafman J, Huey E. Visuoperception test predicts pathologic diagnosis of Alzheimer disease in corticobasal syndrome. Neurology. 83: 510-9. PMID 24991033 DOI: 10.1212/Wnl.0000000000000667 |
0.413 |
|
| 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, ... ... Spina S, 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 |
0.383 |
|
| 2013 |
Ahmed Z, Bigio EH, Budka H, Dickson DW, Ferrer I, Ghetti B, Giaccone G, Hatanpaa KJ, Holton JL, Josephs KA, Powers J, Spina S, Takahashi H, White CL, Revesz T, et al. Globular glial tauopathies (GGT): consensus recommendations. Acta Neuropathologica. 126: 537-44. PMID 23995422 DOI: 10.1007/S00401-013-1171-0 |
0.385 |
|
| 2013 |
Sundal C, Fujioka S, Van Gerpen JA, Wider C, Nicholson AM, Baker M, Shuster EA, Aasly J, Spina S, Ghetti B, Roeber S, Garbern J, Tselis A, Swerdlow RH, Miller BB, et al. Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations. Parkinsonism & Related Disorders. 19: 869-77. PMID 23787135 DOI: 10.1016/J.Parkreldis.2013.05.013 |
0.376 |
|
| 2013 |
Spina S, Van Laar AD, Murrell JR, Hamilton RL, Kofler JK, Epperson F, Farlow MR, Lopez OL, Quinlan J, DeKosky ST, Ghetti B. Phenotypic variability in three families with valosin-containing protein mutation. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 20: 251-8. PMID 22900631 DOI: 10.1111/J.1468-1331.2012.03831.X |
0.378 |
|
| 2012 |
Sundal C, Van Gerpen JA, Nicholson AM, Wider C, Shuster EA, Aasly J, Spina S, Ghetti B, Roeber S, Garbern J, Borjesson-Hanson A, Tselis A, Swerdlow RH, Miller BB, Fujioka S, et al. MRI characteristics and scoring in HDLS due to CSF1R gene mutations. Neurology. 79: 566-74. PMID 22843259 DOI: 10.1212/Wnl.0B013E318263575A |
0.372 |
|
| 2012 |
Coppola G, Chinnathambi S, Lee JJ, Dombroski BA, Baker MC, Soto-Ortolaza AI, Lee SE, Klein E, Huang AY, Sears R, Lane JR, Karydas AM, Kenet RO, Biernat J, Wang LS, ... ... Spina S, et al. Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases. Human Molecular Genetics. 21: 3500-12. PMID 22556362 DOI: 10.1093/Hmg/Dds161 |
0.478 |
|
| 2012 |
Rademakers R, Baker M, Nicholson AM, Rutherford NJ, Finch N, Soto-Ortolaza A, Lash J, Wider C, Wojtas A, DeJesus-Hernandez M, Adamson J, Kouri N, Sundal C, Shuster EA, Aasly J, ... ... Spina S, et al. Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids. Nature Genetics. 44: 200-5. PMID 22197934 DOI: 10.1038/Ng.1027 |
0.357 |
|
| 2011 |
Chen-Plotkin AS, Martinez-Lage M, Sleiman PM, Hu W, Greene R, Wood EM, Bing S, Grossman M, Schellenberg GD, Hatanpaa KJ, Weiner MF, White CL, Brooks WS, Halliday GM, Kril JJ, ... ... Spina S, et al. Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration. Archives of Neurology. 68: 488-97. PMID 21482928 DOI: 10.1001/Archneurol.2011.53 |
0.377 |
|
| 2011 |
Espay AJ, Spina S, Houghton DJ, Murrell JR, de Courten-Myers GM, Ghetti B, Litvan I. Rapidly progressive atypical parkinsonism associated with frontotemporal lobar degeneration and motor neuron disease. Journal of Neurology, Neurosurgery, and Psychiatry. 82: 751-3. PMID 20587488 DOI: 10.1136/Jnnp.2009.201608 |
0.425 |
|
| 2011 |
Ghetti B, Wszolek ZK, Boeve BF, Spina S, Goedert M. Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17 Neurodegeneration: the Molecular Pathology of Dementia and Movement Disorders: Second Edition. 110-134. DOI: 10.1002/9781444341256.Ch14 |
0.463 |
|
| 2010 |
Van Deerlin VM, Sleiman PM, Martinez-Lage M, Chen-Plotkin A, Wang LS, Graff-Radford NR, Dickson DW, Rademakers R, Boeve BF, Grossman M, Arnold SE, Mann DM, Pickering-Brown SM, Seelaar H, Heutink P, ... ... Spina S, et al. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nature Genetics. 42: 234-9. PMID 20154673 DOI: 10.1038/Ng.536 |
0.367 |
|
| 2010 |
Mackenzie IR, Neumann M, Bigio EH, Cairns NJ, Alafuzoff I, Kril J, Kovacs GG, Ghetti B, Halliday G, Holm IE, Ince PG, Kamphorst W, Revesz T, Rozemuller AJ, Kumar-Singh S, ... ... Spina S, et al. Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update. Acta Neuropathologica. 119: 1-4. PMID 19924424 DOI: 10.1007/S00401-009-0612-2 |
0.332 |
|
| 2010 |
Ghetti B, Hagen MC, Murrell JR, Takao M, Piccardo P, Glazier BS, Epperson F, Spina S, Rentz C. P4-140: Alzheimer's Disease Associated with the F105L Mutation in the Presenilin 1 (PSEN1) Gene Alzheimer's & Dementia. 6: e64-e65. DOI: 10.1016/J.Jalz.2010.08.199 |
0.436 |
|
| 2009 |
Huey ED, Pardini M, Cavanagh A, Wassermann EM, Kapogiannis D, Spina S, Ghetti B, Grafman J. Association of ideomotor apraxia with frontal gray matter volume loss in corticobasal syndrome. Archives of Neurology. 66: 1274-80. PMID 19822784 DOI: 10.1001/Archneurol.2009.218 |
0.306 |
|
| 2009 |
Kovacs GG, Murrell JR, Horvath S, Haraszti L, Majtenyi K, Molnar MJ, Budka H, Ghetti B, Spina S. TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 1843-7. PMID 19609911 DOI: 10.1002/Mds.22697 |
0.417 |
|
| 2009 |
Mackenzie IR, Neumann M, Bigio EH, Cairns NJ, Alafuzoff I, Kril J, Kovacs GG, Ghetti B, Halliday G, Holm IE, Ince PG, Kamphorst W, Revesz T, Rozemuller AJ, Kumar-Singh S, ... ... Spina S, et al. Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations. Acta Neuropathologica. 117: 15-8. PMID 19015862 DOI: 10.1007/S00401-008-0460-5 |
0.336 |
|
| 2009 |
Kovacs GG, Murrell JR, Horvath S, Haraszti L, Majtenyi K, Budka H, Ghetti B, Spina S. Novel TARDBP mutation associated with frontotemporal dementia and movement disorder but not motor neuron disease Alzheimers & Dementia. 5: 501. DOI: 10.1016/J.Jalz.2009.04.707 |
0.383 |
|
| 2008 |
Maarouf CL, Daugs ID, Spina S, Vidal R, Kokjohn TA, Patton RL, Kalback WM, Luehrs DC, Walker DG, Castaño EM, Beach TG, Ghetti B, Roher AE. Histopathological and molecular heterogeneity among individuals with dementia associated with Presenilin mutations. Molecular Neurodegeneration. 3: 20. PMID 19021905 DOI: 10.1186/1750-1326-3-20 |
0.436 |
|
| 2008 |
Kovacs GG, Majtenyi K, Spina S, Murrell JR, Gelpi E, Hoftberger R, Fraser G, Crowther RA, Goedert M, Budka H, Ghetti B. White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration. Journal of Neuropathology and Experimental Neurology. 67: 963-75. PMID 18800011 DOI: 10.1097/Nen.0B013E318187A80F |
0.446 |
|
| 2008 |
Ghetti B, Spina S, Murrell JR, Huey ED, Pietrini P, Sweeney B, Wassermann EM, Keohane C, Farlow MR, Grafman J. In vivo and postmortem clinicoanatomical correlations in frontotemporal dementia and parkinsonism linked to chromosome 17. Neuro-Degenerative Diseases. 5: 215-7. PMID 18322394 DOI: 10.1159/000113706 |
0.44 |
|
| 2008 |
Spina S, Farlow MR, Unverzagt FW, Kareken DA, Murrell JR, Fraser G, Epperson F, Crowther RA, Spillantini MG, Goedert M, Ghetti B. The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family. Brain : a Journal of Neurology. 131: 72-89. PMID 18065436 DOI: 10.1093/Brain/Awm280 |
0.477 |
|
| 2008 |
Spina S, Laar ADV, Murrell JR, Courten-Myers Gd, Hamilton RL, Vidal R, Farlow MR, Quinlan J, DeKosky ST, Ghetti B. O2-05-03: Inclusion body myopathy with paget disease of the bone and frontotemporal dementia: New families, a novel mutation, and a new clinical presentation Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.342 |
0.361 |
|
| 2008 |
Ghetti B, Hake AM, Murrell JR, Epperson F, Farlow MR, Vidal R, Spina S. P3-221: Familial Alzheimer's disease associated with the V717L amyloid precursor protein gene mutation: Neuropathological characterization Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1788 |
0.448 |
|
| 2008 |
Spina S, Murrell JR, Vidal R, Ghetti B. P2-205: Neuropathologic and genetic characterization of frontotemporal lobar degeneration with ubiquitin- and/or TDP-43-positive inclusions: A large series Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1280 |
0.325 |
|
| 2007 |
Spina S, Murrell JR, Huey ED, Wassermann EM, Pietrini P, Grafman J, Ghetti B. Corticobasal syndrome associated with the A9D Progranulin mutation. Journal of Neuropathology and Experimental Neurology. 66: 892-900. PMID 17917583 DOI: 10.1097/Nen.0B013E3181567873 |
0.472 |
|
| 2007 |
Rademakers R, Baker M, Gass J, Adamson J, Huey ED, Momeni P, Spina S, Coppola G, Karydas AM, Stewart H, Johnson N, Hsiung GY, Kelley B, Kuntz K, Steinbart E, et al. Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. The Lancet. Neurology. 6: 857-68. PMID 17826340 DOI: 10.1016/S1474-4422(07)70221-1 |
0.353 |
|
| 2007 |
Spina S, Murrell JR, Huey ED, Wassermann EM, Pietrini P, Baraibar MA, Barbeito AG, Troncoso JC, Vidal R, Ghetti B, Grafman J. Clinicopathologic features of frontotemporal dementia with progranulin sequence variation. Neurology. 68: 820-7. PMID 17202431 DOI: 10.1212/01.Wnl.0000254460.31273.2D |
0.365 |
|
| 2007 |
Spina S, Murrell JR, Yoshida H, Ghetti B, Bermingham N, Sweeney B, Dlouhy SR, Crowther RA, Goedert M, Keohane C. The novel Tau mutation G335S: clinical, neuropathological and molecular characterization. Acta Neuropathologica. 113: 461-70. PMID 17186252 DOI: 10.1007/S00401-006-0182-5 |
0.442 |
|
| 2006 |
Huey ED, Grafman J, Wassermann EM, Pietrini P, Tierney MC, Ghetti B, Spina S, Baker M, Hutton M, Elder JW, Berger SL, Heflin KA, Hardy J, Momeni P. Characteristics of frontotemporal dementia patients with a Progranulin mutation. Annals of Neurology. 60: 374-80. PMID 16983677 DOI: 10.1002/Ana.20969 |
0.385 |
|
| 2006 |
Schweitzer K, Decker E, Zhu L, Miller RE, Mirra SS, Spina S, Ghetti B, Wang M, Murrell J. Aberrantly regulated proteins in frontotemporal dementia. Biochemical and Biophysical Research Communications. 348: 465-72. PMID 16890190 DOI: 10.1016/J.Bbrc.2006.07.113 |
0.394 |
|
| 2006 |
Spina S, Murrell JR, Farlow MR, Ghetti B. P4-109: Clinical symptoms and brainstem pathology in FTDP-17 associated with the EXON 10 +3 intronic Tau mutation Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1848 |
0.405 |
|
| 2006 |
Spina S, Murrell JR, Sweeney B, Bermingham N, Ghetti B, Keohane C. P3-156: Early onset frontotemporal dementia and parkinsonism associated with the G335S Tau mutation Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1424 |
0.437 |
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