| Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk CKDGen Consortium, KidneyGen Consortium, EchoGen consortium, ... Nature 478 (7367), 103-109, 2011 | 2285 | 2011 |
| 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 | 1373 | 2011 |
| New loci associated with kidney function and chronic kidney disease A Köttgen, C Pattaro, CA Böger, C Fuchsberger, M Olden, NL Glazer, ... Nature genetics 42 (5), 376-384, 2010 | 880 | 2010 |
| 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), 1268-1283. e6, 2018 | 578 | 2018 |
| Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy N Norton, D Li, MJ Rieder, JD Siegfried, E Rampersaud, S Züchner, ... The American Journal of Human Genetics 88 (3), 273-282, 2011 | 387 | 2011 |
| 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 | 379 | 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 | 352 | 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 | 349 | 2001 |
| A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry KL Monda, GK Chen, KC Taylor, C Palmer, TL Edwards, LA Lange, ... Nature genetics 45 (6), 690-696, 2013 | 319 | 2013 |
| Exercise attenuates PCB-induced changes in the mouse gut microbiome JJ Choi, SY Eum, E Rampersaud, S Daunert, MT Abreu, M Toborek Environmental health perspectives 121 (6), 725-730, 2013 | 316 | 2013 |
| 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 | 202 | 2007 |
| 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 | 161 | 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 | 150 | 2013 |
| 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 | 146 | 2022 |
| A genome-wide association meta-analysis identifies a novel locus at 17q11. 2 associated with sporadic amyotrophic lateral sclerosis I Fogh, A Ratti, C Gellera, K Lin, C Tiloca, V Moskvina, L Corrado, ... Human molecular genetics 23 (8), 2220-2231, 2014 | 138 | 2014 |
| 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 | 133 | 2012 |
| Genetic risk for subsequent neoplasms among long-term survivors of childhood cancer Z Wang, CL Wilson, J Easton, A Thrasher, H Mulder, Q Liu, DJ Hedges, ... Journal of Clinical Oncology 36 (20), 2078, 2018 | 127 | 2018 |
| Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy N Norton, D Li, E Rampersaud, A Morales, ER Martin, S Zuchner, S Guo, ... Circulation: Cardiovascular Genetics 6 (2), 144-153, 2013 | 124 | 2013 |
| 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 | 111 | 2019 |
| Serum 25-hydroxyvitamin d levels are not associated with subclinical vascular disease or C-reactive protein in the old order amish ED Michos, EA Streeten, KA Ryan, E Rampersaud, PA Peyser, LF Bielak, ... Calcified tissue international 84, 195-202, 2009 | 103 | 2009 |
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