| Year |
Citation |
Score |
| 2020 |
Prudencio M, Humphrey J, Pickles S, Brown AL, Hill SE, Kachergus J, Shi J, Heckman M, Spiegel M, Cook C, Song Y, Yue M, Daughrity L, Carlomagno Y, Jansen-West K, ... ... Fisher EM, et al. Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia. The Journal of Clinical Investigation. PMID 32790644 DOI: 10.1172/Jci139741 |
0.317 |
|
| 2020 |
Lana-Elola E, Watson-Scales S, Slender A, Gibbins D, Martineau A, Douglas C, Mohun T, Fisher EM, Tybulewicz VL. Correction: Genetic dissection of Down syndrome-associated congenital heart defects using a new mouse mapping panel. Elife. 9. PMID 32692312 DOI: 10.7554/eLife.61021 |
0.51 |
|
| 2019 |
Wiseman FK, Pulford LJ, Barkus C, Liao F, Portelius E, Webb R, Chavez-Gutierrez L, Cleverley K, Noy S, Sheppard O, Collins T, Powell C, Sarell CJ, Rickman M, Choong X, ... ... Fisher EM, et al. Trisomy of human chromosome 21 enhances amyloid-beta 3 deposition independently of an extra copy of APP (vol 141, pg 2457, 2018) Brain. 142. PMID 30879033 DOI: 10.1093/Brain/Awz061 |
0.78 |
|
| 2017 |
Naert G, Ferré V, Keller E, Slender A, Gibbins D, Fisher EM, Tybulewicz VL, Maurice T. In vivo and ex vivo analyses of amyloid toxicity in the Tc1 mouse model of Down syndrome. Journal of Psychopharmacology (Oxford, England). 269881117743484. PMID 29215943 DOI: 10.1177/0269881117743484 |
0.587 |
|
| 2017 |
Holmes HE, Powell NM, Ma D, Ismail O, Harrison IF, Wells JA, Colgan N, O'Callaghan JM, Johnson RA, Murray TK, Ahmed Z, Heggenes M, Fisher A, Cardoso MJ, Modat M, ... ... Fisher EM, et al. Comparison of In Vivo and Ex Vivo MRI for the Detection of Structural Abnormalities in a Mouse Model of Tauopathy. Frontiers in Neuroinformatics. 11: 20. PMID 28408879 DOI: 10.3389/Fninf.2017.00020 |
0.351 |
|
| 2017 |
Wiseman FK, Pulford LJ, Barkus C, Liao F, Portelius E, Webb R, Chavez-Gutierrez L, Cleverley K, Noy S, Rickman M, Tosh J, Whittaker H, Stewart F, Szaruga M, Nizetic D, ... ... Fisher E, et al. TRISOMY 21 CAUSES A DEFICIT IN LYSOSOMAL CATHEPSINS AND ALTERS APP/Aβ PROCESSING, INDEPENDENTLY OF AN EXTRA COPY OF APP Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.06.791 |
0.759 |
|
| 2016 |
Qiu J, McQueen J, Bilican B, Dando O, Magnani D, Punovuori K, Selvaraj BT, Livesey M, Haghi G, Heron S, Burr K, Patani R, Rajan R, Sheppard O, Kind PC, ... ... Fisher EM, et al. Evidence for evolutionary divergence of activity-dependent gene expression in developing neurons. Elife. 5. PMID 27692071 DOI: 10.7554/Elife.20337 |
0.574 |
|
| 2016 |
Powell NM, Modat M, Cardoso MJ, Ma D, Holmes HE, Yu Y, O'Callaghan J, Cleary JO, Sinclair B, Wiseman FK, Tybulewicz VL, Fisher EM, Lythgoe MF, Ourselin S. Fully-Automated μMRI Morphometric Phenotyping of the Tc1 Mouse Model of Down Syndrome. Plos One. 11: e0162974. PMID 27658297 DOI: 10.1371/Journal.Pone.0162974 |
0.749 |
|
| 2016 |
Buss L, Fisher E, Hardy J, Nizetic D, Groet J, Pulford L, Strydom A. Intracerebral haemorrhage in Down syndrome: protected or predisposed? F1000research. 5. PMID 27239286 DOI: 10.12688/F1000Research.7819.1 |
0.4 |
|
| 2016 |
Peiris H, Duffield MD, Fadista J, Jessup CF, Kashmir V, Genders AJ, McGee SL, Martin AM, Saiedi M, Morton N, Carter R, Cousin MA, Kokotos AC, Oskolkov N, Volkov P, ... ... Fisher EM, et al. A Syntenic Cross Species Aneuploidy Genetic Screen Links RCAN1 Expression to β-Cell Mitochondrial Dysfunction in Type 2 Diabetes. Plos Genetics. 12: e1006033. PMID 27195491 DOI: 10.1371/Journal.Pgen.1006033 |
0.571 |
|
| 2016 |
Karmiloff-Smith A, Al-Janabi T, D'Souza H, Groet J, Massand E, Mok K, Startin C, Fisher E, Hardy J, Nizetic D, Tybulewicz V, Strydom A. The importance of understanding individual differences in Down syndrome. F1000research. 5. PMID 27019699 DOI: 10.12688/F1000Research.7506.1 |
0.563 |
|
| 2016 |
Holmes HE, Colgan N, Ismail O, Ma D, Powell NM, O'Callaghan JM, Harrison IF, Johnson RA, Murray TK, Ahmed Z, Heggenes M, Fisher A, Cardoso MJ, Modat M, Walker-Samuel S, ... Fisher EM, et al. Imaging the accumulation and suppression of tau pathology using multiparametric MRI. Neurobiology of Aging. 39: 184-94. PMID 26923415 DOI: 10.1016/J.Neurobiolaging.2015.12.001 |
0.314 |
|
| 2016 |
Hall JH, Wiseman FK, Fisher EM, Tybulewicz VL, Harwood JL, Good MA. Tc1 mouse model of trisomy-21 dissociates properties of short- and long-term recognition memory. Neurobiology of Learning and Memory. PMID 26868479 DOI: 10.1016/J.Nlm.2016.02.002 |
0.729 |
|
| 2016 |
Lana-Elola E, Watson-Scales S, Slender A, Gibbins D, Martineau A, Douglas C, Mohun T, Fisher EM, Tybulewicz VLj. Genetic dissection of Down syndrome-associated congenital heart defects using a new mouse mapping panel. Elife. 5. PMID 26765563 DOI: 10.7554/eLife.11614 |
0.583 |
|
| 2016 |
Hall JH, Good MA, Fisher E, Wiseman FK, Harwood JL, Tybulewicz VL. P1-036: Dissociating Aberrant Memory Processes in Mouse Models of Alzheimer's Disease and Down Syndrome Alzheimer's & Dementia. 12: P414-P415. DOI: 10.1016/J.Jalz.2016.06.783 |
0.741 |
|
| 2015 |
Choong XY, Tosh JL, Pulford LJ, Fisher EM. Dissecting Alzheimer disease in Down syndrome using mouse models. Frontiers in Behavioral Neuroscience. 9: 268. PMID 26528151 DOI: 10.3389/Fnbeh.2015.00268 |
0.394 |
|
| 2015 |
Colgan N, Siow B, O'Callaghan JM, Harrison IF, Wells JA, Holmes HE, Ismail O, Richardson S, Alexander DC, Collins EC, Fisher EM, Johnson R, Schwarz AJ, Ahmed Z, O'Neill MJ, et al. Application of neurite orientation dispersion and density imaging (NODDI) to a tau pathology model of Alzheimer's disease. Neuroimage. PMID 26505297 DOI: 10.1016/J.Neuroimage.2015.10.043 |
0.308 |
|
| 2015 |
Wiseman FK, Al-Janabi T, Hardy J, Karmiloff-Smith A, Nizetic D, Tybulewicz VL, Fisher EM, Strydom A. A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome. Nature Reviews. Neuroscience. 16: 564-74. PMID 26243569 DOI: 10.1038/Nrn3983 |
0.772 |
|
| 2015 |
Witton J, Padmashri R, Zinyuk LE, Popov VI, Kraev I, Line SJ, Jensen TP, Tedoldi A, Cummings DM, Tybulewicz VL, Fisher EM, Bannerman DM, Randall AD, Brown JT, Edwards FA, et al. Hippocampal circuit dysfunction in the Tc1 mouse model of Down syndrome. Nature Neuroscience. 18: 1291-8. PMID 26237367 DOI: 10.1038/Nn.4072 |
0.56 |
|
| 2015 |
Joyce PI, Mcgoldrick P, Saccon RA, Weber W, Fratta P, West SJ, Zhu N, Carter S, Phatak V, Stewart M, Simon M, Kumar S, Heise I, Bros-Facer V, Dick J, ... ... Fisher EM, et al. A novel SOD1-ALS mutation separates central and peripheral effects of mutant SOD1 toxicity. Human Molecular Genetics. 24: 1883-97. PMID 25468678 DOI: 10.1093/Hmg/Ddu605 |
0.359 |
|
| 2015 |
Fratta P, Polke JM, Newcombe J, Mizielinska S, Lashley T, Poulter M, Beck J, Preza E, Devoy A, Sidle K, Howard R, Malaspina A, Orrell RW, Clarke J, Lu CH, ... ... Fisher EM, et al. Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion. Neurobiology of Aging. 36: 546.e1-7. PMID 25179228 DOI: 10.1016/J.Neurobiolaging.2014.07.037 |
0.341 |
|
| 2014 |
Garrett CA, Barri M, Kuta A, Soura V, Deng W, Fisher EM, Schiavo G, Hafezparast M. DYNC1H1 mutation alters transport kinetics and ERK1/2-cFos signalling in a mouse model of distal spinal muscular atrophy. Brain : a Journal of Neurology. 137: 1883-93. PMID 24755273 DOI: 10.1093/Brain/Awu097 |
0.322 |
|
| 2014 |
Ma D, Cardoso MJ, Modat M, Powell N, Wells J, Holmes H, Wiseman F, Tybulewicz V, Fisher E, Lythgoe MF, Ourselin S. Automatic structural parcellation of mouse brain MRI using multi-atlas label fusion. Plos One. 9: e86576. PMID 24475148 DOI: 10.1371/Journal.Pone.0086576 |
0.715 |
|
| 2014 |
Ricketts T, McGoldrick P, Fratta P, de Oliveira HM, Kent R, Phatak V, Brandner S, Blanco G, Greensmith L, Acevedo-Arozena A, Fisher EM. A nonsense mutation in mouse Tardbp affects TDP43 alternative splicing activity and causes limb-clasping and body tone defects. Plos One. 9: e85962. PMID 24465814 DOI: 10.1371/Journal.Pone.0085962 |
0.37 |
|
| 2014 |
Fratta P, Collins T, Pemble S, Nethisinghe S, Devoy A, Giunti P, Sweeney MG, Hanna MG, Fisher EM. Sequencing analysis of the spinal bulbar muscular atrophy CAG expansion reveals absence of repeat interruptions. Neurobiology of Aging. 35: 443.e1-3. PMID 24041967 DOI: 10.1016/J.Neurobiolaging.2013.07.015 |
0.317 |
|
| 2014 |
Holmes HE, Wiseman F, O'Callaghan JM, Wells J, Tybulewicz VL, Fisher EM, Lythgoe MF. P2-026: HYPOPERFUSION IN THE ABSENCE OF APP GENE TRIPLICATION IN THE TC1 MOUSE MODEL OF DOWN's SYNDROME Alzheimer's & Dementia. 10: P479-P480. DOI: 10.1016/J.Jalz.2014.05.699 |
0.701 |
|
| 2013 |
Schiavo G, Greensmith L, Hafezparast M, Fisher EM. Cytoplasmic dynein heavy chain: the servant of many masters. Trends in Neurosciences. 36: 641-51. PMID 24035135 DOI: 10.1016/J.Tins.2013.08.001 |
0.332 |
|
| 2013 |
Fratta P, Poulter M, Lashley T, Rohrer JD, Polke JM, Beck J, Ryan N, Hensman D, Mizielinska S, Waite AJ, Lai MC, Gendron TF, Petrucelli L, Fisher EM, Revesz T, et al. Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia. Acta Neuropathologica. 126: 401-9. PMID 23818065 DOI: 10.1007/S00401-013-1147-0 |
0.346 |
|
| 2013 |
Saccon RA, Bunton-Stasyshyn RK, Fisher EM, Fratta P. Is SOD1 loss of function involved in amyotrophic lateral sclerosis? Brain : a Journal of Neurology. 136: 2342-58. PMID 23687121 DOI: 10.1093/Brain/Awt097 |
0.302 |
|
| 2013 |
Gribble SM, Wiseman FK, Clayton S, Prigmore E, Langley E, Yang F, Maguire S, Fu B, Rajan D, Sheppard O, Scott C, Hauser H, Stephens PJ, Stebbings LA, Ng BL, ... ... Fisher EM, et al. Massively parallel sequencing reveals the complex structure of an irradiated human chromosome on a mouse background in the Tc1 model of Down syndrome. Plos One. 8: e60482. PMID 23596509 DOI: 10.1371/Journal.Pone.0060482 |
0.799 |
|
| 2013 |
McGoldrick P, Joyce PI, Fisher EM, Greensmith L. Rodent models of amyotrophic lateral sclerosis. Biochimica Et Biophysica Acta. 1832: 1421-36. PMID 23524377 DOI: 10.1016/J.Bbadis.2013.03.012 |
0.301 |
|
| 2013 |
Ahmed MM, Dhanasekaran AR, Tong S, Wiseman FK, Fisher EM, Tybulewicz VL, Gardiner KJ. Protein profiles in Tc1 mice implicate novel pathway perturbations in the Down syndrome brain. Human Molecular Genetics. 22: 1709-24. PMID 23349361 DOI: 10.1093/Hmg/Ddt017 |
0.761 |
|
| 2013 |
Fratta P, Malik B, Gray A, La Spada AR, Hanna MG, Fisher EM, Greensmith L. FUS is not dysregulated by the spinal bulbar muscular atrophy androgen receptor polyglutamine repeat expansion. Neurobiology of Aging. 34: 1516.e17-9. PMID 23062703 DOI: 10.1016/J.Neurobiolaging.2012.09.008 |
0.31 |
|
| 2013 |
De Oliveira H, Ricketts T, Fisher E, Greensmith L, Fratta P, Plagnol V, Baralle F, Buratti E, Herzog J, Gondo Y, Acevedo-Arozena A. A missense mutation in the mouse TDP-43 gene leads to a gain of TDP-43 mediated splicing function: Implications for neurodegeneration Journal of the Neurological Sciences. 333: e438-e439. DOI: 10.1016/J.Jns.2013.07.1571 |
0.328 |
|
| 2013 |
Choong XY, Raha A, Tybulewicz V, Wiseman F, Fisher E. P1-106: Using primary neurons from transgenic mice to identify genes on human chromosome 21 influencing Alzheimer's neuropathology Alzheimer's & Dementia. 9: P189-P189. DOI: 10.1016/J.Jalz.2013.05.328 |
0.779 |
|
| 2012 |
Grizenkova J, Akhtar S, Hummerich H, Tomlinson A, Asante EA, Wenborn A, Fizet J, Poulter M, Wiseman FK, Fisher EM, Tybulewicz VL, Brandner S, Collinge J, Lloyd SE. Overexpression of the Hspa13 (Stch) gene reduces prion disease incubation time in mice. Proceedings of the National Academy of Sciences of the United States of America. 109: 13722-7. PMID 22869728 DOI: 10.1073/Pnas.1208917109 |
0.77 |
|
| 2012 |
Ghazi-Noori S, Froud KE, Mizielinska S, Powell C, Smidak M, Fernandez de Marco M, O'Malley C, Farmer M, Parkinson N, Fisher EM, Asante EA, Brandner S, Collinge J, Isaacs AM. Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic mice. Brain : a Journal of Neurology. 135: 819-32. PMID 22366797 DOI: 10.1093/Brain/Aws006 |
0.344 |
|
| 2012 |
Sheppard O, Wiseman FK, Ruparelia A, Tybulewicz VL, Fisher EM. Mouse models of aneuploidy. Thescientificworldjournal. 2012: 214078. PMID 22262951 DOI: 10.1100/2012/214078 |
0.788 |
|
| 2012 |
Devoy A, Bunton-Stasyshyn RK, Tybulewicz VL, Smith AJ, Fisher EM. Genomically humanized mice: technologies and promises. Nature Reviews. Genetics. 13: 14-20. PMID 22179716 DOI: 10.1038/Nrg3116 |
0.58 |
|
| 2012 |
Sheppard O, Plattner F, Rubin A, Slender A, Linehan JM, Brandner S, Tybulewicz VL, Fisher EM, Wiseman FK. Altered regulation of tau phosphorylation in a mouse model of down syndrome aging. Neurobiology of Aging. 33: 828.e31-44. PMID 21843906 DOI: 10.1016/J.Neurobiolaging.2011.06.025 |
0.749 |
|
| 2011 |
Lana-Elola E, Watson-Scales SD, Fisher EM, Tybulewicz VL. Down syndrome: searching for the genetic culprits. Disease Models & Mechanisms. 4: 586-95. PMID 21878459 DOI: 10.1242/Dmm.008078 |
0.655 |
|
| 2011 |
Joyce PI, Fratta P, Fisher EM, Acevedo-Arozena A. SOD1 and TDP-43 animal models of amyotrophic lateral sclerosis: recent advances in understanding disease toward the development of clinical treatments. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 22: 420-48. PMID 21706386 DOI: 10.1007/S00335-011-9339-1 |
0.347 |
|
| 2011 |
Acevedo-Arozena A, Kalmar B, Essa S, Ricketts T, Joyce P, Kent R, Rowe C, Parker A, Gray A, Hafezparast M, Thorpe JR, Greensmith L, Fisher EM. A comprehensive assessment of the SOD1G93A low-copy transgenic mouse, which models human amyotrophic lateral sclerosis. Disease Models & Mechanisms. 4: 686-700. PMID 21540242 DOI: 10.1242/Dmm.007237 |
0.401 |
|
| 2011 |
Banks GT, Haas MA, Line S, Shepherd HL, Alqatari M, Stewart S, Rishal I, Philpott A, Kalmar B, Kuta A, Groves M, Parkinson N, Acevedo-Arozena A, Brandner S, Bannerman D, ... ... Fisher EM, et al. Behavioral and other phenotypes in a cytoplasmic Dynein light intermediate chain 1 mutant mouse. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 5483-94. PMID 21471385 DOI: 10.1523/Jneurosci.5244-10.2011 |
0.314 |
|
| 2011 |
Stevens JC, Fisher EM, Mead S. How does the genetic assassin select its neuronal target? Mammalian Genome : Official Journal of the International Mammalian Genome Society. 22: 139-47. PMID 21373885 DOI: 10.1007/S00335-011-9319-5 |
0.348 |
|
| 2011 |
Cleary JO, Wiseman FK, Norris FC, Price AN, Choy M, Tybulewicz VL, Ordidge RJ, Brandner S, Fisher EM, Lythgoe MF. Structural correlates of active-staining following magnetic resonance microscopy in the mouse brain. Neuroimage. 56: 974-83. PMID 21310249 DOI: 10.1016/J.Neuroimage.2011.01.082 |
0.728 |
|
| 2011 |
Duchon A, Pothion S, Brault V, Sharp AJ, Tybulewicz VL, Fisher EM, Herault Y. The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndrome. Behavioural Brain Research. 217: 271-81. PMID 21047530 DOI: 10.1016/J.Bbr.2010.10.023 |
0.675 |
|
| 2011 |
McGoldrick P, Dick J, Ricketts T, Joyce P, Fratta P, Acevedo-Arozena A, Fisher E, Greensmith L. P16 Investigating novel mutant mouse models of motor neuron disease Neuromuscular Disorders. 21: S11. DOI: 10.1016/S0960-8966(10)70047-X |
0.341 |
|
| 2010 |
Ruparelia A, Wiseman F, Sheppard O, Tybulewicz VL, Fisher EM. Down syndrome and the molecular pathogenesis resulting from trisomy of human chromosome 21. Journal of Biomedical Research. 24: 87-99. PMID 23554618 DOI: 10.1016/S1674-8301(10)60016-4 |
0.782 |
|
| 2010 |
Wiseman FK, Sheppard O, Linehan JM, Brandner S, Tybulewicz VL, Fisher EM. Generation of a panel of antibodies against proteins encoded on human chromosome 21. Journal of Negative Results in Biomedicine. 9: 7. PMID 20727138 DOI: 10.1186/1477-5751-9-7 |
0.796 |
|
| 2010 |
Dunlevy L, Bennett M, Slender A, Lana-Elola E, Tybulewicz VL, Fisher EM, Mohun T. Down's syndrome-like cardiac developmental defects in embryos of the transchromosomic Tc1 mouse. Cardiovascular Research. 88: 287-95. PMID 20558441 DOI: 10.1093/Cvr/Cvq193 |
0.636 |
|
| 2010 |
Reynolds LE, Watson AR, Baker M, Jones TA, D'Amico G, Robinson SD, Joffre C, Garrido-Urbani S, Rodriguez-Manzaneque JC, Martino-Echarri E, Aurrand-Lions M, Sheer D, Dagna-Bricarelli F, Nizetic D, McCabe CJ, ... ... Fisher EM, et al. Tumour angiogenesis is reduced in the Tc1 mouse model of Down's syndrome. Nature. 465: 813-7. PMID 20535211 DOI: 10.1038/Nature09106 |
0.607 |
|
| 2010 |
Chia R, Tattum MH, Jones S, Collinge J, Fisher EM, Jackson GS. Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis. Plos One. 5: e10627. PMID 20498711 DOI: 10.1371/Journal.Pone.0010627 |
0.334 |
|
| 2010 |
van de Leemput J, Wavrant-De Vrièze F, Rafferty I, Bras JM, Giunti P, Fisher EM, Hardy JA, Singleton AB, Houlden H. Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series. Movement Disorders : Official Journal of the Movement Disorder Society. 25: 771-3. PMID 20437544 DOI: 10.1002/Mds.22970 |
0.333 |
|
| 2010 |
El-Kadi AM, Bros-Facer V, Deng W, Philpott A, Stoddart E, Banks G, Jackson GS, Fisher EM, Duchen MR, Greensmith L, Moore AL, Hafezparast M. The legs at odd angles (Loa) mutation in cytoplasmic dynein ameliorates mitochondrial function in SOD1G93A mouse model for motor neuron disease. The Journal of Biological Chemistry. 285: 18627-39. PMID 20382740 DOI: 10.1074/Jbc.M110.129320 |
0.3 |
|
| 2010 |
Urwin H, Authier A, Nielsen JE, Metcalf D, Powell C, Froud K, Malcolm DS, Holm I, Johannsen P, Brown J, Fisher EM, van der Zee J, Bruyland M, Van Broeckhoven C, et al. Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations. Human Molecular Genetics. 19: 2228-38. PMID 20223751 DOI: 10.1093/Hmg/Ddq100 |
0.341 |
|
| 2010 |
Miller G, Neilan M, Chia R, Gheryani N, Holt N, Charbit A, Wells S, Tucci V, Lalanne Z, Denny P, Fisher EM, Cheeseman M, Askew GN, Dear TN. ENU mutagenesis reveals a novel phenotype of reduced limb strength in mice lacking fibrillin 2. Plos One. 5: e9137. PMID 20161761 DOI: 10.1371/Journal.Pone.0009137 |
0.324 |
|
| 2010 |
Alford KA, Slender A, Vanes L, Li Z, Fisher EM, Nizetic D, Orkin SH, Roberts I, Tybulewicz VL. Perturbed hematopoiesis in the Tc1 mouse model of Down syndrome. Blood. 115: 2928-37. PMID 20154221 DOI: 10.1182/Blood-2009-06-227629 |
0.632 |
|
| 2010 |
Haas M, Fisher E, Tybulewicz V, Guillemot F. [P2.56]: Cortical projection neuron dendrite morphology in the Tc1 mouse model of Down Syndrome International Journal of Developmental Neuroscience. 28: 706-706. DOI: 10.1016/J.Ijdevneu.2010.07.186 |
0.546 |
|
| 2009 |
Banks GT, Bros-Facer V, Williams HP, Chia R, Achilli F, Bryson JB, Greensmith L, Fisher EM. Mutant glycyl-tRNA synthetase (Gars) ameliorates SOD1(G93A) motor neuron degeneration phenotype but has little affect on Loa dynein heavy chain mutant mice. Plos One. 4: e6218. PMID 19593442 DOI: 10.1371/Journal.Pone.0006218 |
0.307 |
|
| 2009 |
Achilli F, Bros-Facer V, Williams HP, Banks GT, AlQatari M, Chia R, Tucci V, Groves M, Nickols CD, Seburn KL, Kendall R, Cader MZ, Talbot K, van Minnen J, Burgess RW, ... ... Fisher EM, et al. An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy. Disease Models & Mechanisms. 2: 359-73. PMID 19470612 DOI: 10.1242/Dmm.002527 |
0.315 |
|
| 2009 |
Becker EB, Oliver PL, Glitsch MD, Banks GT, Achilli F, Hardy A, Nolan PM, Fisher EM, Davies KE. A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice. Proceedings of the National Academy of Sciences of the United States of America. 106: 6706-11. PMID 19351902 DOI: 10.1073/Pnas.0810599106 |
0.339 |
|
| 2009 |
Wiseman FK, Alford KA, Tybulewicz VL, Fisher EM. Down syndrome--recent progress and future prospects. Human Molecular Genetics. 18: R75-83. PMID 19297404 DOI: 10.1093/Hmg/Ddp010 |
0.775 |
|
| 2009 |
Galante M, Jani H, Vanes L, Daniel H, Fisher EM, Tybulewicz VL, Bliss TV, Morice E. Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome. Human Molecular Genetics. 18: 1449-63. PMID 19181682 DOI: 10.1093/Hmg/Ddp055 |
0.619 |
|
| 2009 |
Wang Y, Mulligan C, Denyer G, Delom F, Dagna-Bricarelli F, Tybulewicz VL, Fisher EM, Griffiths WJ, Nizetic D, Groet J. Quantitative proteomics characterization of a mouse embryonic stem cell model of Down syndrome. Molecular & Cellular Proteomics : McP. 8: 585-95. PMID 19001410 DOI: 10.1074/Mcp.M800256-Mcp200 |
0.644 |
|
| 2008 |
Wilson MD, Barbosa-Morais NL, Schmidt D, Conboy CM, Vanes L, Tybulewicz VL, Fisher EM, Tavaré S, Odom DT. Species-specific transcription in mice carrying human chromosome 21. Science (New York, N.Y.). 322: 434-8. PMID 18787134 DOI: 10.1126/Science.1160930 |
0.611 |
|
| 2008 |
Canzonetta C, Mulligan C, Deutsch S, Ruf S, O'Doherty A, Lyle R, Borel C, Lin-Marq N, Delom F, Groet J, Schnappauf F, De Vita S, Averill S, Priestley JV, Martin JE, ... ... Fisher EM, et al. DYRK1A-dosage imbalance perturbs NRSF/REST levels, deregulating pluripotency and embryonic stem cell fate in Down syndrome. American Journal of Human Genetics. 83: 388-400. PMID 18771760 DOI: 10.1016/J.Ajhg.2008.08.012 |
0.601 |
|
| 2008 |
Morice E, Andreae LC, Cooke SF, Vanes L, Fisher EM, Tybulewicz VL, Bliss TV. Preservation of long-term memory and synaptic plasticity despite short-term impairments in the Tc1 mouse model of Down syndrome. Learning & Memory (Cold Spring Harbor, N.Y.). 15: 492-500. PMID 18626093 DOI: 10.1101/Lm.969608 |
0.574 |
|
| 2007 |
Mensah A, Mulligan C, Linehan J, Ruf S, O'Doherty A, Grygalewicz B, Shipley J, Groet J, Tybulewicz V, Fisher E, Brandner S, Nizetic D. An additional human chromosome 21 causes suppression of neural fate of pluripotent mouse embryonic stem cells in a teratoma model. Bmc Developmental Biology. 7: 131. PMID 18047653 DOI: 10.1186/1471-213X-7-131 |
0.636 |
|
| 2007 |
Filimonenko M, Stuffers S, Raiborg C, Yamamoto A, Malerød L, Fisher EM, Isaacs A, Brech A, Stenmark H, Simonsen A. Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease. The Journal of Cell Biology. 179: 485-500. PMID 17984323 DOI: 10.1083/Jcb.200702115 |
0.316 |
|
| 2007 |
van de Leemput J, Chandran J, Knight MA, Holtzclaw LA, Scholz S, Cookson MR, Houlden H, Gwinn-Hardy K, Fung HC, Lin X, Hernandez D, Simon-Sanchez J, Wood NW, Giunti P, Rafferty I, ... ... Fisher EM, et al. Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans. Plos Genetics. 3: e108. PMID 17590087 DOI: 10.1371/Journal.Pgen.0030108 |
0.399 |
|
| 2007 |
Hough TA, Polewski M, Johnson K, Cheeseman M, Nolan PM, Vizor L, Rastan S, Boyde A, Pritzker K, Hunter AJ, Fisher EM, Terkeltaub R, Brown SD. Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 22: 1397-407. PMID 17539739 DOI: 10.1359/Jbmr.070515 |
0.368 |
|
| 2007 |
Kasperaviciute D, Weale ME, Shianna KV, Banks GT, Simpson CL, Hansen VK, Turner MR, Shaw CE, Al-Chalabi A, Pall HS, Goodall EF, Morrison KE, Orrell RW, Beck M, Jablonka S, ... ... Fisher EM, et al. Large-scale pathways-based association study in amyotrophic lateral sclerosis. Brain : a Journal of Neurology. 130: 2292-301. PMID 17439985 DOI: 10.1093/Brain/Awm055 |
0.311 |
|
| 2006 |
Tybulewicz VL, Fisher EM. New techniques to understand chromosome dosage: mouse models of aneuploidy. Human Molecular Genetics. 15: R103-9. PMID 16987872 DOI: 10.1093/Hmg/Ddl179 |
0.681 |
|
| 2005 |
Pfister KK, Fisher EM, Gibbons IR, Hays TS, Holzbaur EL, McIntosh JR, Porter ME, Schroer TA, Vaughan KT, Witman GB, King SM, Vallee RB. Cytoplasmic dynein nomenclature. The Journal of Cell Biology. 171: 411-3. PMID 16260502 DOI: 10.1083/Jcb.200508078 |
0.303 |
|
| 2005 |
Chia R, Achilli F, Festing MF, Fisher EM. The origins and uses of mouse outbred stocks. Nature Genetics. 37: 1181-6. PMID 16254564 DOI: 10.1038/Ng1665 |
0.302 |
|
| 2005 |
O'Doherty A, Ruf S, Mulligan C, Hildreth V, Errington ML, Cooke S, Sesay A, Modino S, Vanes L, Hernandez D, Linehan JM, Sharpe PT, Brandner S, Bliss TV, Henderson DJ, ... ... Fisher EM, et al. An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes. Science (New York, N.Y.). 309: 2033-7. PMID 16179473 DOI: 10.1126/science.1114535 |
0.612 |
|
| 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, ... ... Fisher EM, et al. Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nature Genetics. 37: 806-8. PMID 16041373 DOI: 10.1038/Ng1609 |
0.328 |
|
| 2005 |
Achilli F, Boyle S, Kieran D, Chia R, Hafezparast M, Martin JE, Schiavo G, Greensmith L, Bickmore W, Fisher EM. The SOD1 transgene in the G93A mouse model of amyotrophic lateral sclerosis lies on distal mouse chromosome 12. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group On Motor Neuron Diseases. 6: 111-4. PMID 16036435 DOI: 10.1080/14660820510035351 |
0.444 |
|
| 2005 |
Kieran D, Hafezparast M, Bohnert S, Dick JR, Martin J, Schiavo G, Fisher EM, Greensmith L. A mutation in dynein rescues axonal transport defects and extends the life span of ALS mice. The Journal of Cell Biology. 169: 561-7. PMID 15911875 DOI: 10.1083/Jcb.200501085 |
0.3 |
|
| 2005 |
Hafezparast M, Brandner S, Linehan J, Martin JE, Collinge J, Fisher EM. Prion disease incubation time is not affected in mice heterozygous for a dynein mutation. Biochemical and Biophysical Research Communications. 326: 18-22. PMID 15567146 DOI: 10.1016/J.Bbrc.2004.10.206 |
0.334 |
|
| 2004 |
Tsipouri V, Curtin JA, Nolan PM, Vizor L, Parsons CA, Clapham CM, Latham ID, Rooke LJ, Martin JE, Peters J, Hunter AJ, Rogers D, Rastan S, Brown SD, Fisher EM, et al. Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse. Comparative and Functional Genomics. 5: 123-7. PMID 18629060 DOI: 10.1002/Cfg.382 |
0.358 |
|
| 2004 |
Rastan S, Hough T, Kierman A, Hardisty R, Erven A, Gray IC, Voeling S, Isaacs A, Tsai H, Strivens M, Washbourne R, Thornton C, Greenaway S, Hewitt M, McCormick S, ... ... Fisher EM, et al. Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disorders. Genetica. 122: 47-9. PMID 15619960 DOI: 10.1007/S10709-004-1930-X |
0.354 |
|
| 2004 |
Brown J, Gydesen S, Johannsen P, Gade A, Skibinski G, Chakrabarti L, Brun A, Spillantini M, Yancopoulou D, Thusgaard T, Sorensen A, Fisher E, Collinge J. Frontotemporal dementia linked to chromosome 3. Dementia and Geriatric Cognitive Disorders. 17: 274-6. PMID 15178935 DOI: 10.1159/000077153 |
0.419 |
|
| 2004 |
Lloyd SE, Thompson SR, Beck JA, Linehan JM, Wadsworth JD, Brandner S, Collinge J, Fisher EM. Identification and characterization of a novel mouse prion gene allele. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 15: 383-9. PMID 15170227 DOI: 10.1007/S00335-004-3041-5 |
0.345 |
|
| 2003 |
Hafezparast M, Ahmad-Annuar A, Hummerich H, Shah P, Ford M, Baker C, Bowen S, Martin JE, Fisher EM. Paradigms for the identification of new genes in motor neuron degeneration. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group On Motor Neuron Diseases. 4: 249-57. PMID 14753659 DOI: 10.1080/14660820310016084 |
0.398 |
|
| 2003 |
Doherty AM, Fisher EM. Microcell-mediated chromosome transfer (MMCT): small cells with huge potential. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 14: 583-92. PMID 14629108 DOI: 10.1007/S00335-003-4002-0 |
0.369 |
|
| 2003 |
Ahmad-Annuar A, Shah P, Hafezparast M, Hummerich H, Witherden AS, Morrison KE, Shaw PJ, Kirby J, Warner TT, Crosby A, Proukakis C, Wilkinson P, Orrell RW, Bradley L, Martin JE, ... Fisher EM, et al. No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group On Motor Neuron Diseases. 4: 150-7. PMID 13129801 DOI: 10.1080/14660820310011737 |
0.349 |
|
| 2003 |
Hafezparast M, Klocke R, Ruhrberg C, Marquardt A, Ahmad-Annuar A, Bowen S, Lalli G, Witherden AS, Hummerich H, Nicholson S, Morgan PJ, Oozageer R, Priestley JV, Averill S, King VR, ... ... Fisher EM, et al. Mutations in dynein link motor neuron degeneration to defects in retrograde transport. Science (New York, N.Y.). 300: 808-12. PMID 12730604 DOI: 10.1126/Science.1083129 |
0.325 |
|
| 2003 |
Mead S, Stumpf MP, Whitfield J, Beck JA, Poulter M, Campbell T, Uphill JB, Goldstein D, Alpers M, Fisher EM, Collinge J. Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics. Science (New York, N.Y.). 300: 640-3. PMID 12690204 DOI: 10.1126/Science.1083320 |
0.337 |
|
| 2002 |
Lloyd SE, Uphill JB, Targonski PV, Fisher EM, Collinge J. Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in mice. Neurogenetics. 4: 77-81. PMID 12481985 DOI: 10.1007/S10048-002-0133-9 |
0.441 |
|
| 2002 |
Ramos VC, Vidal-Taboada J, Bergoñon S, Egeo A, Fisher EM, Scartezzini P, Oliva R. Characterisation and expression analysis of the WDR9 gene, located in the Down critical region-2 of the human chromosome 21. Biochimica Et Biophysica Acta. 1577: 377-83. PMID 12359327 DOI: 10.1016/S0167-4781(02)00421-9 |
0.388 |
|
| 2002 |
Hafezparast M, Ball S, Nicholson SJ, Witherden A, Arac D, Broadway N, Saggerson D, Cooper E, Naase M, Gokhale S, Quant P, Lascelles C, Nickols C, Baker CS, Peters J, ... ... Fisher EM, et al. A new mouse mutant, skijumper. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 13: 359-364. PMID 12152619 DOI: 10.1007/Pl00021068 |
0.345 |
|
| 2002 |
Witherden AS, Hafezparast M, Nicholson SJ, Ahmad-Annuar A, Bermingham N, Arac D, Rankin J, Iravani M, Ball S, Peters J, Martin JE, Huntley D, Hummerich H, Sergot M, Fisher EM. An integrated genetic, radiation hybrid, physical and transcription map of a region of distal mouse chromosome 12, including an imprinted locus and the 'Legs at odd angles' (Loa) mutation. Gene. 283: 71-82. PMID 11867214 DOI: 10.1016/S0378-1119(01)00853-8 |
0.388 |
|
| 2001 |
Mead S, Mahal SP, Beck J, Campbell T, Farrall M, Fisher E, Collinge J. Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1. American Journal of Human Genetics. 69: 1225-35. PMID 11704923 DOI: 10.1086/324710 |
0.367 |
|
| 2001 |
Lloyd SE, Onwuazor ON, Beck JA, Mallinson G, Farrall M, Targonski P, Collinge J, Fisher EM. Identification of multiple quantitative trait loci linked to prion disease incubation period in mice. Proceedings of the National Academy of Sciences of the United States of America. 98: 6279-83. PMID 11353827 DOI: 10.1073/Pnas.101130398 |
0.449 |
|
| 2000 |
Mead S, Beck J, Dickinson A, Fisher EM, Collinge J. Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease. Neuroscience Letters. 290: 117-20. PMID 10936691 DOI: 10.1016/S0304-3940(00)01319-7 |
0.382 |
|
| 2000 |
Nolan PM, Peters J, Strivens M, Rogers D, Hagan J, Spurr N, Gray IC, Vizor L, Brooker D, Whitehill E, Washbourne R, Hough T, Greenaway S, Hewitt M, Liu X, ... ... Fisher EM, et al. A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse. Nature Genetics. 25: 440-3. PMID 10932191 DOI: 10.1038/78140 |
0.368 |
|
| 2000 |
Isaacs AM, Davies KE, Hunter AJ, Nolan PM, Vizor L, Peters J, Gale DG, Kelsell DP, Latham ID, Chase JM, Fisher EM, Bouzyk MM, Potter A, Masih M, Walsh FS, et al. Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy. Human Molecular Genetics. 9: 1865-71. PMID 10915775 DOI: 10.1046/J.1529-8027.2001.01008-19.X |
0.393 |
|
| 2000 |
Nolan PM, Peters J, Vizor L, Strivens M, Washbourne R, Hough T, Wells C, Glenister P, Thornton C, Martin J, Fisher E, Rogers D, Hagan J, Reavill C, Gray I, et al. Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 500-6. PMID 10886012 DOI: 10.1007/S003350010096 |
0.342 |
|
| 1999 |
Hafezparast M, Witherden A, Nicholson S, Bermingham N, Mackin J, ten Asbroek A, Ball S, Peters J, Baas F, Martin JE, Fisher EM. The kinesin light chain gene: its mapping and exclusion in mouse and human forms of inherited motor neuron degeneration. Neuroscience Letters. 273: 49-52. PMID 10505649 DOI: 10.1016/S0304-3940(99)00620-5 |
0.387 |
|
| 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, ... ... Fisher EM, 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 |
0.428 |
|
| 1999 |
Hernandez D, Fisher EM. Mouse autosomal trisomy: two's company, three's a crowd. Trends in Genetics : Tig. 15: 241-7. PMID 10354585 DOI: 10.1016/S0168-9525(99)01743-6 |
0.463 |
|
| 1999 |
Hernandez D, Mee PJ, Martin JE, Tybulewicz VL, Fisher EM. Transchromosomal mouse embryonic stem cell lines and chimeric mice that contain freely segregating segments of human chromosome 21. Human Molecular Genetics. 8: 923-33. PMID 10196383 DOI: 10.1093/Hmg/8.5.923 |
0.668 |
|
| 1998 |
Katsanis N, Fisher EM. Identification, expression, and chromosomal localization of ubiquitin conjugating enzyme 7 (UBE2G2), a human homologue of the Saccharomyces cerevisiae ubc7 gene. Genomics. 51: 128-31. PMID 9693041 DOI: 10.1006/Geno.1998.5263 |
0.391 |
|
| 1998 |
Hafezparast M, Fisher E. Wasted by an elongation factor. Trends in Genetics. 14: 215-217. PMID 9635401 DOI: 10.1016/S0168-9525(98)01478-4 |
0.387 |
|
| 1998 |
Prasher VP, Farrer MJ, Kessling AM, Fisher EM, West RJ, Barber PC, Butler AC. Molecular mapping of Alzheimer-type dementia in Down's syndrome. Annals of Neurology. 43: 380-3. PMID 9506555 DOI: 10.1002/Ana.410430316 |
0.423 |
|
| 1998 |
Bermingham NA, Rauf S, Katsanis N, Martin JE, Hunter AJ, Fisher EM. The immunophilin FKBP4 (FKBP52/FKBP59) maps to the distal short arm of human chromosome 12. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 268. PMID 9501323 DOI: 10.1007/S003359900746 |
0.394 |
|
| 1998 |
Vidal-Taboada JM, Bergoñón S, Sánchez M, López-Acedo C, Groet J, Nizetic D, Egeo A, Scartezzini P, Katsanis N, Fisher EM, Delabar JM, Oliva R. High resolution physical mapping and identification of transcribed sequences in the Down syndrome region-2. Biochemical and Biophysical Research Communications. 243: 572-8. PMID 9480850 DOI: 10.1006/Bbrc.1998.8141 |
0.385 |
|
| 1998 |
Katsanis N, Fisher EM. A novel C-terminal binding protein (CTBP2) is closely related to CTBP1, an adenovirus E1A-binding protein, and maps to human chromosome 21q21.3. Genomics. 47: 294-9. PMID 9479502 DOI: 10.1006/Geno.1997.5115 |
0.374 |
|
| 1997 |
Fisher EM. The contribution of the mouse to advances in human genetics. Advances in Genetics. 35: 155-205. PMID 9348648 DOI: 10.1016/S0065-2660(08)60450-2 |
0.413 |
|
| 1997 |
Hoyle J, Tan KH, Fisher EM. Mapping the valosin-containing protein (VCP) gene on human chromosome 9 and mouse chromosome 4, and a likely pseudogene on the mouse X chromosome. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 778-80. PMID 9321476 DOI: 10.1007/S003359900566 |
0.451 |
|
| 1997 |
Rogers DC, Fisher EM, Brown SD, Peters J, Hunter AJ, Martin JE. Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 711-3. PMID 9321461 DOI: 10.1007/S003359900551 |
0.329 |
|
| 1997 |
Katsanis N, Beck JA, Fisher EM. Mapping of a novel SH3 domain protein and two proteins of unknown function to human chromosome 21. Human Genetics. 100: 477-80. PMID 9272176 DOI: 10.1007/S004390050537 |
0.44 |
|
| 1997 |
Martin JE, Fisher EM. Phenotypic analysis--making the most of your mouse. Trends in Genetics : Tig. 13: 254-6. PMID 9242043 DOI: 10.1016/S0168-9525(97)01193-1 |
0.326 |
|
| 1997 |
Katsanis N, Yaspo ML, Fisher EM. Identification and mapping of a novel human gene, HRMT1L1, homologous to the rat protein arginine N-methyltransferase 1 (PRMT1) gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 526-9. PMID 9196002 DOI: 10.1007/S003359900491 |
0.329 |
|
| 1997 |
Hoyle J, Tan KH, Fisher EM. Localization of genes encoding two human one-domain members of the AAA family: PSMC5 (the thyroid hormone receptor-interacting protein, TRIP1) and PSMC3 (the Tat-binding protein, TBP1). Human Genetics. 99: 285-8. PMID 9048938 DOI: 10.1007/S004390050356 |
0.365 |
|
| 1997 |
Hernandez D, Fisher EM. Down syndrome genetics: unravelling a multifactorial disorder. Human Molecular Genetics. 1411-6. PMID 8875245 DOI: 10.1093/Hmg/5.Supplement_1.1411 |
0.444 |
|
| 1997 |
Bermingham NA, Martin JE, Fisher EM. The mouse lysosomal membrane protein 1 gene as a candidate for the motorneuron degeneration (mnd) locus. Genomics. 32: 266-71. PMID 8833154 DOI: 10.1006/Geno.1996.0114 |
0.487 |
|
| 1997 |
Bermingham N, Hernandez D, Balfour A, Gilmour F, Martin JE, Fisher EM. Mapping TNNC1, the gene that encodes cardiac troponin I in the human and the mouse. Genomics. 30: 620-2. PMID 8825654 DOI: 10.1006/Geno.1995.1288 |
0.394 |
|
| 1996 |
Matthews D, Fry L, Powles A, Weber J, McCarthy M, Fisher E, Davies K, Williamson R. Evidence that a locus for familial psoriasis maps to chromosome 4q Nature Genetics. 14: 231-233. PMID 8841203 DOI: 10.1038/Ng1096-231 |
0.358 |
|
| 1996 |
Hoyle J, Fisher EM. Genomic organization and mapping of the mouse P26s4 ATPase gene: a member of the remarkably conserved AAA gene family. Genomics. 31: 115-8. PMID 8808288 DOI: 10.1006/Geno.1996.0017 |
0.365 |
|
| 1996 |
Katsanis N, Fisher EM. The gene encoding the p60 subunit of chromatin assembly factor I (CAF1P60) maps to human chromosome 21q22.2, a region associated with some of the major features of Down syndrome. Human Genetics. 98: 497-9. PMID 8792829 DOI: 10.1007/S004390050246 |
0.463 |
|
| 1996 |
Hoyle J, Yulug IG, Johnstone K, Scambler PJ, Fisher EM. Characterisation of a short interspersed repeat (Mermaid) that has family members on human chromosome 21 and elsewhere in the human genome. Human Genetics. 97: 117-20. PMID 8557251 DOI: 10.1007/Bf00218845 |
0.386 |
|
| 1996 |
Bermingham N, Hillermann R, Gilmour F, Martin JE, Fisher EM. Human glial cell line-derived neurotrophic factor (GDNF) maps to chromosome 5. Human Genetics. 96: 671-3. PMID 8522325 DOI: 10.1007/Bf00210297 |
0.37 |
|
| 1995 |
Yulug IG, Killary AM, Sandhu AK, Athwal RS, Fox M, Fisher EM. Gene expression in response to retinoic acid in novel human chromosome 21 monochromosomal cell hybrids. Somatic Cell and Molecular Genetics. 21: 357-65. PMID 8619133 DOI: 10.1007/Bf02257471 |
0.372 |
|
| 1995 |
Hernandez D, Egan SE, Yulug IG, Fisher EM. Mapping the gene that encodes phosphatidylinositol-specific phospholipase C-gamma 2 in the human and the mouse. Genomics. 23: 504-7. PMID 7835906 DOI: 10.1006/Geno.1994.1533 |
0.418 |
|
| 1995 |
Yulug IG, Egan SE, See CG, Fisher EM. Mapping GRB2, a signal transduction gene in the human and the mouse. Genomics. 22: 313-8. PMID 7806216 DOI: 10.1006/Geno.1994.1389 |
0.424 |
|
| 1995 |
Hernandez D, Pannett AA, Tybulewicz V, Fisher EM. Highly polymorphic sequence at D21S1448 mapping close to D21S55, within the Down syndrome critical region. Human Genetics. 95: 721-2. PMID 7789964 DOI: 10.1007/Bf00209498 |
0.621 |
|
| 1995 |
Yulug IG, Hillermann R, Fisher EM. The SHB adaptor protein maps to human chromosome 9. Genomics. 24: 615-7. PMID 7713524 DOI: 10.1006/Geno.1994.1681 |
0.339 |
|
| 1995 |
Hoyle J, Yulug IG, Egan SE, Fisher EM. The gene that encodes the phosphatidylinositol-3 kinase regulatory subunit (p85 alpha) maps to chromosome 13 in the mouse. Genomics. 24: 400-2. PMID 7698770 DOI: 10.1006/Geno.1994.1638 |
0.358 |
|
| 1995 |
Yulug IG, Egan SE, See CG, Fisher EM. A human SHC-related sequence maps to chromosome 17, the SHC gene maps to chromosome 1. Human Genetics. 96: 245-8. PMID 7635484 DOI: 10.1007/Bf00207393 |
0.41 |
|
| 1995 |
Yulug IG, See CG, Fisher EM, Ylug IG. The DAD1 protein, whose defect causes apoptotic cell death, maps to human chromosome 14. Genomics. 26: 433-5. PMID 7601483 DOI: 10.1016/0888-7543(95)80241-D |
0.351 |
|
| 1994 |
Yulug IG, Egan SE, Pollock PM, Fisher EM. A homologue of the Drosophila Son of sevenless gene maps to mouse chromosome 17. Genomics. 18: 733-4. PMID 8307589 DOI: 10.1016/S0888-7543(05)80389-1 |
0.414 |
|
| 1993 |
Zinn AR, Page DC, Fisher EM. Turner syndrome: the case of the missing sex chromosome. Trends in Genetics : Tig. 9: 90-3. PMID 8488568 DOI: 10.1016/0168-9525(93)90230-F |
0.598 |
|
| 1991 |
Fisher EM, Beer-Romero P, Brown LG, Ridley A, McNeil JA, Lawrence JB, Willard HF, Bieber FR, Page DC. Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome. Cell. 63: 1205-18. PMID 2124517 DOI: 10.1016/0092-8674(90)90416-C |
0.584 |
|
| 1990 |
Fisher EM, Alitalo T, Luoh SW, de la Chapelle A, Page DC. Human sex-chromosome-specific repeats within a region of pseudoautosomal/Yq homology. Genomics. 7: 625-8. PMID 2387589 DOI: 10.1016/0888-7543(90)90209-D |
0.557 |
|
| 1990 |
Nasir J, Fisher EM, Brockdorff N, Disteche CM, Lyon MF, Brown SD. Unusual molecular characteristics of a repeat sequence island within a Giemsa-positive band on the mouse X chromosome. Proceedings of the National Academy of Sciences of the United States of America. 87: 399-403. PMID 2296595 DOI: 10.1073/Pnas.87.1.399 |
0.588 |
|
| 1990 |
Page DC, Fisher EM, McGillivray B, Brown LG. Additional deletion in sex-determining region of human Y chromosome resolves paradox of X,t(Y;22) female. Nature. 346: 279-81. PMID 1973823 DOI: 10.1038/346279A0 |
0.529 |
|
| 1989 |
Brockdorff N, Fisher EM, Orkin SH, Lyon MF, Brown SD. Localization of the human X-linked gene for chronic granulomatous disease to the mouse X chromosome: implications for X-chromosome evolution. Cytogenetics and Cell Genetics. 48: 124-5. PMID 3197451 DOI: 10.1159/000132605 |
0.636 |
|
| 1988 |
Brown SD, Brockdorff N, Cavanna JS, Fisher EM, Greenfield AJ, Lyon MF, Nasir J. The long-range mapping of mammalian chromosomes. Current Topics in Microbiology and Immunology. 137: 3-12. PMID 3416640 DOI: 10.1007/978-3-642-50059-6_1 |
0.568 |
|
| 1987 |
Page DC, Mosher R, Simpson EM, Fisher EM, Mardon G, Pollack J, McGillivray B, de la Chapelle A, Brown LG. The sex-determining region of the human Y chromosome encodes a finger protein. Cell. 51: 1091-104. PMID 3690661 DOI: 10.1016/0092-8674(87)90595-2 |
0.579 |
|
| 1987 |
Brockdorff N, Cross GS, Cavanna JS, Fisher EM, Lyon MF, Davies KE, Brown SD. The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome. Nature. 328: 166-8. PMID 3600793 DOI: 10.1038/328166A0 |
0.736 |
|
| 1987 |
Brockdorff N, Fisher EM, Cavanna JS, Lyon MF, Brown SD. Construction of a detailed molecular map of the mouse X chromosome by microcloning and interspecific crosses. The Embo Journal. 6: 3291-3297. DOI: 10.1002/J.1460-2075.1987.Tb02648.X |
0.581 |
|
| 1985 |
Fisher EM, Cavanna JS, Brown SD. Microdissection and microcloning of the mouse X chromosome. Proceedings of the National Academy of Sciences of the United States of America. 82: 5846-9. PMID 3862102 DOI: 10.1073/Pnas.82.17.5846 |
0.406 |
|
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