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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia HX Deng, W Chen, ST Hong, KM Boycott, GH Gorrie, N Siddique, Y Yang, ... Nature 477 (7363), 211-215, 2011 | 1410 | 2011 |
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Genome-wide analyses identify KIF5A as a novel ALS gene A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ... Neuron 97 (6), 1267-1288, 2018 | 616 | 2018 |
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Physical activity and the association of common FTO gene variants with body mass index and obesity E Rampersaud, BD Mitchell, TI Pollin, M Fu, H Shen, JR O’Connell, ... Archives of internal medicine 168 (16), 1791-1797, 2008 | 383 | 2008 |
Whole-genome association study identifies STK39 as a hypertension susceptibility gene Y Wang, JR O'Connell, PF McArdle, JB Wade, SE Dorff, SJ Shah, X Shi, ... Proceedings of the National Academy of Sciences 106 (1), 226-231, 2009 | 353 | 2009 |
Complete genomic screen in Parkinson disease: evidence for multiple genes WK Scott, MA Nance, RL Watts, JP Hubble, WC Koller, K Lyons, R Pahwa, ... Jama 286 (18), 2239-2244, 2001 | 352 | 2001 |
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Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related … E Rampersaud, CM Damcott, M Fu, H Shen, P McArdle, X Shi, J Shelton, ... Diabetes 56 (12), 3053-3062, 2007 | 204 | 2007 |
The genomic landscape of pediatric acute lymphoblastic leukemia SW Brady, KG Roberts, Z Gu, L Shi, S Pounds, D Pei, C Cheng, Y Dai, ... Nature genetics 54 (9), 1376-1389, 2022 | 188 | 2022 |
The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study BD Mitchell, PF McArdle, H Shen, E Rampersaud, TI Pollin, LF Bielak, ... American heart journal 155 (5), 823-828, 2008 | 164 | 2008 |
Genome-wide association of body fat distribution in African ancestry populations suggests new loci CT Liu, KL Monda, KC Taylor, L Lange, EW Demerath, W Palmas, ... PLoS genetics 9 (8), e1003681, 2013 | 154 | 2013 |
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Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era N Norton, PD Robertson, MJ Rieder, S Züchner, E Rampersaud, E Martin, ... Circulation: Cardiovascular Genetics 5 (2), 167-174, 2012 | 132 | 2012 |
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Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein SMK Farhan, DP Howrigan, LE Abbott, JR Klim, SD Topp, AE Byrnes, ... Nature neuroscience 22 (12), 1966-1974, 2019 | 117 | 2019 |
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