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Evadnie Rampersaud
Evadnie Rampersaud
Principal Scientist - Group Lead, St. Jude Children's Research Hospital
在 stjude.org 的电子邮件经过验证
标题
引用次数
引用次数
年份
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
CKDGen Consortium, KidneyGen Consortium, EchoGen consortium, ...
Nature 478 (7367), 103-109, 2011
23202011
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
14102011
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
9032010
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
6162018
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
3962011
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
3832008
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
3532009
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
3522001
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
3332013
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
3242013
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
2042007
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
1882022
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
1642008
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
1542013
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
1422014
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), 2078-2087, 2018
1352018
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
1322012
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
1262013
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
1172019
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
1062009
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