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Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease JM Lee, VC Wheeler, MJ Chao, JPG Vonsattel, RM Pinto, D Lucente, ... Cell 162 (3), 516-526, 2015 | 461 | 2015 |
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion JM Lee, EM Ramos, JH Lee, T Gillis, JS Mysore, MR Hayden, SC Warby, ... Neurology 78 (10), 690-695, 2012 | 454 | 2012 |
Integrated genomics and proteomics define huntingtin CAG length-dependent networks in mice P Langfelder, JP Cantle, D Chatzopoulou, N Wang, F Gao, I Al-Ramahi, ... Nature neuroscience 19 (4), 623-633, 2016 | 388 | 2016 |
CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset JM Lee, K Correia, J Loupe, KH Kim, D Barker, EP Hong, MJ Chao, ... Cell 178 (4), 887-900. e14, 2019 | 343 | 2019 |
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study KM Moore, J Nicholas, M Grossman, CT McMillan, DJ Irwin, L Massimo, ... The Lancet Neurology 19 (2), 145-156, 2020 | 296 | 2020 |
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export A Legati, D Giovannini, G Nicolas, U López-Sánchez, B Quintáns, ... Nature genetics 47 (6), 579-581, 2015 | 296 | 2015 |
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome AY Huang, D Yu, LK Davis, JH Sul, F Tsetsos, V Ramensky, I Zelaya, ... Neuron 94 (6), 1101-1111. e7, 2017 | 196 | 2017 |
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Plasma Tau and Neurofilament Light in Frontotemporal Lobar Degeneration and Alzheimer Disease I Illán-Gala, A Lleo, A Karydas, AM Staffaroni, H Zetterberg, ... Neurology 96 (5), e671-e683, 2021 | 123 | 2021 |
Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium T Miyagawa, D Brushaber, J Syrjanen, W Kremers, J Fields, LK Forsberg, ... Alzheimer's & Dementia 16 (1), 106-117, 2020 | 119 | 2020 |
Genomic Analysis Reveals Disruption of Striatal Neuronal Development and Therapeutic Targets in Human Huntington’s Disease Neural Stem Cells KL Ring, MC An, N Zhang, RN O’Brien, EM Ramos, F Gao, R Atwood, ... Stem Cell Reports 5 (6), 1023-1038, 2015 | 117 | 2015 |
A152T tau allele causes neurodegeneration that can be ameliorated in a zebrafish model by autophagy induction A Lopez, SE Lee, K Wojta, EM Ramos, E Klein, J Chen, AL Boxer, ... Brain, 0 | 114 | |
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Common SNP-based haplotype analysis of the 4p16. 3 Huntington disease gene region JM Lee, T Gillis, JS Mysore, EM Ramos, RH Myers, MR Hayden, ... The American Journal of Human Genetics 90 (3), 434-444, 2012 | 84 | 2012 |
Primary familial brain calcification EM Ramos, J Oliveira, MJ Sobrido, G Coppola University of Washington, Seattle, 2017 | 81* | 2017 |
Plasma neurofilament light for prediction of disease progression in familial frontotemporal lobar degeneration JC Rojas, P Wang, AM Staffaroni, C Heller, Y Cobigo, A Wolf, SYM Goh, ... Neurology 96 (18), e2296-e2312, 2021 | 78 | 2021 |
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Large normal and reduced penetrance alleles in Huntington disease: instability in families and frequency at the laboratory, at the clinic and in the population J Sequeiros, EM Ramos, J Cerqueira, MC Costa, A Sousa, J Pinto‐Basto, ... Clinical genetics 78 (4), 381-387, 2010 | 75 | 2010 |