Evadnie Rampersaud, Ph.D. - Publications

2005 Duke University, Durham, NC 
Genetics, Statistics, Bioinformatics Biology

46 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Fukuda Y, Cheong PL, Lynch J, Brighton C, Frase S, Kargas V, Rampersaud E, Wang Y, Sankaran VG, Yu B, Ney PA, Weiss MJ, Vogel P, Bond PJ, Ford RC, et al. The severity of hereditary porphyria is modulated by the porphyrin exporter and Lan antigen ABCB6. Nature Communications. 7: 12353. PMID 27507172 DOI: 10.1038/ncomms12353  0.4
2016 Vernon LL, Vance DD, Wang L, Rampersaud E, Vance JM, Pericak-Vance M, Huang CC, Kaplan LD. Regional Differential Genetic Response of Human Articular Cartilage to Impact Injury. Cartilage. 7: 163-173. PMID 27047639 DOI: 10.1177/1947603515618483  0.4
2015 Wang L, Man N, Sun XJ, Tan Y, Garcia Cao M, Liu F, Hatlen M, Xu H, Huang G, Mattlin M, Mehta A, Rampersaud E, Benezra R, Nimer SD. Regulation of AKT signaling by Id1 controls t(8;21) leukemia initiation and progression. Blood. PMID 26084673 DOI: 10.1182/blood-2015-03-635532  0.4
2014 András IE, Rampersaud E, Eum SY, Toborek M. Transcriptional profile of HIV-induced nuclear translocation of amyloid β in brain endothelial cells. Archives of Medical Research. 45: 744-52. PMID 25446617 DOI: 10.1016/j.arcmed.2014.11.003  0.4
2014 Veerapen MK, Pelaez L, Potter JE, Duthely L, Birusingh R, Rampersaud E, Bodamer OA, Rodriguez MM. Bridging the gaps between the histopathological and demographic risk factors of preterm birth in a unique Miami inner-city population. Fetal and Pediatric Pathology. 33: 226-33. PMID 24833307 DOI: 10.3109/15513815.2014.913749  0.4
2014 Vance DD, Chen GL, Stoutenberg M, Myerburg RJ, Jacobs K, Nathanson L, Perry A, Seo D, Goldschmidt-Clermont PJ, Rampersaud E. Cardiac performance, biomarkers and gene expression studies in previously sedentary men participating in half-marathon training. Bmc Sports Science, Medicine and Rehabilitation. 6: 6. PMID 24552436 DOI: 10.1186/2052-1847-6-6  0.4
2013 Graff M, Fernández-Rhodes L, Liu S, Carlson C, Wassertheil-Smoller S, Neuhouser M, Reiner A, Kooperberg C, Rampersaud E, Manson JE, Kuller LH, Howard BV, Ochs-Balcom HM, Johnson KC, Vitolins MZ, et al. Generalization of adiposity genetic loci to US Hispanic women. Nutrition & Diabetes. 3: e85. PMID 23978819 DOI: 10.1038/nutd.2013.26  0.4
2013 Liu CT, Monda KL, Taylor KC, Lange L, Demerath EW, Palmas W, Wojczynski MK, Ellis JC, Vitolins MZ, Liu S, Papanicolaou GJ, Irvin MR, Xue L, Griffin PJ, Nalls MA, ... ... Rampersaud E, et al. Genome-wide association of body fat distribution in African ancestry populations suggests new loci. Plos Genetics. 9: e1003681. PMID 23966867 DOI: 10.1371/journal.pgen.1003681  0.4
2013 Choi JJ, Eum SY, Rampersaud E, Daunert S, Abreu MT, Toborek M. Exercise attenuates PCB-induced changes in the mouse gut microbiome. Environmental Health Perspectives. 121: 725-30. PMID 23632211 DOI: 10.1289/ehp.1306534  0.4
2013 Brodt C, Siegfried JD, Hofmeyer M, Martel J, Rampersaud E, Li D, Morales A, Hershberger RE. Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy. Journal of Cardiac Failure. 19: 233-9. PMID 23582089 DOI: 10.1016/j.cardfail.2013.03.001  0.4
2013 Norton N, Li D, Rampersaud E, Morales A, Martin ER, Zuchner S, Guo S, Gonzalez M, Hedges DJ, Robertson PD, Krumm N, Nickerson DA, Hershberger RE. Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy. Circulation. Cardiovascular Genetics. 6: 144-53. PMID 23418287 DOI: 10.1161/CIRCGENETICS.111.000062  0.4
2013 Rampersaud E, Nathanson L, Farmer J, Meshbane K, Belton RL, Dressen A, Cuccaro M, Musto A, Daunert S, Deo S, Hudson N, Vance JM, Seo D, Mendez A, Dykxhoorn DM, et al. Genomic signatures of a global fitness index in a multi-ethnic cohort of women. Annals of Human Genetics. 77: 147-57. PMID 23289938 DOI: 10.1111/ahg.12006  0.4
2013 Clouse A, Deo S, Rampersaud E, Farmer J, Goldschmidt-Clermont PJ, Daunert S. Defining a molecular portrait of physical fitness. Analytical and Bioanalytical Chemistry. 405: 21-6. PMID 23196749 DOI: 10.1007/s00216-012-6533-2  0.4
2013 Velez Edwards DR, Naj AC, Monda K, North KE, Neuhouser M, Magvanjav O, Kusimo I, Vitolins MZ, Manson JE, O'Sullivan MJ, Rampersaud E, Edwards TL. Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study. Human Genetics. 132: 323-36. PMID 23192594 DOI: 10.1007/s00439-012-1246-3  0.4
2012 Norton N, Robertson PD, Rieder MJ, Züchner S, Rampersaud E, Martin E, Li D, Nickerson DA, Hershberger RE. Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era Circulation: Cardiovascular Genetics. 5: 167-174. PMID 22337857 DOI: 10.1161/CIRCGENETICS.111.961805  0.4
2012 Rampersaud E, Ciliberti MA. Genomics of pediatric metabolic syndrome Pediatric Metabolic Syndrome: Comprehensive Clinical Review and Related Health Issues. 241-266. DOI: 10.1007/978-1-4471-2366-8_13  0.4
2011 Deng HX, Chen W, Hong ST, Boycott KM, Gorrie GH, Siddique N, Yang Y, Fecto F, Shi Y, Zhai H, Jiang H, Hirano M, Rampersaud E, Jansen GH, Donkervoort S, et al. Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Nature. 477: 211-5. PMID 21857683 DOI: 10.1038/nature10353  0.4
2011 Rampersaud E, Siegfried JD, Norton N, Li D, Martin E, Hershberger RE. Rare variant mutations identified in pediatric patients with dilated cardiomyopathy. Progress in Pediatric Cardiology. 31: 39-47. PMID 21483645 DOI: 10.1016/j.ppedcard.2010.11.008  0.4
2011 Norton N, Li D, Rieder MJ, Siegfried JD, Rampersaud E, Züchner S, Mangos S, Gonzalez-Quintana J, Wang L, McGee S, Reiser J, Martin E, Nickerson DA, Hershberger RE. Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy American Journal of Human Genetics. 88: 273-282. PMID 21353195 DOI: 10.1016/j.ajhg.2011.01.016  0.4
2011 Valdes AM, Arden NK, Vaughn FL, Doherty SA, Leaverton PE, Zhang W, Muir KR, Rampersaud E, Dennison EM, Edwards MH, Jameson KA, Javaid MK, Spector TD, Cooper C, Maciewicz RA, et al. Role of the Nav1.7 R1150W amino acid change in susceptibility to symptomatic knee osteoarthritis and multiple regional pain. Arthritis Care & Research. 63: 440-4. PMID 21031562 DOI: 10.1002/acr.20375  0.4
2011 Martin ER, Rampersaud E. Family-based genetic association tests Cold Spring Harbor Protocols. 6. DOI: 10.1101/pdb.top96  0.4
2010 Shen H, Damcott CM, Rampersaud E, Pollin TI, Horenstein RB, McArdle PF, Peyser PA, Bielak LF, Post WS, Chang YP, Ryan KA, Miller M, Rumberger JA, Sheedy PF, Shelton J, et al. Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish. Archives of Internal Medicine. 170: 1850-5. PMID 21059979 DOI: 10.1001/archinternmed.2010.384  0.4
2010 Köttgen A, Pattaro C, Böger CA, Fuchsberger C, Olden M, Glazer NL, Parsa A, Gao X, Yang Q, Smith AV, O'Connell JR, Li M, Schmidt H, Tanaka T, Isaacs A, ... ... Rampersaud E, et al. New loci associated with kidney function and chronic kidney disease. Nature Genetics. 42: 376-84. PMID 20383146 DOI: 10.1038/ng.568  0.4
2010 Rampersaud E, Kinnamon DD, Hamilton K, Khuri S, Hershberger RE, Martin ER. Common susceptibility variants examined for association with dilated cardiomyopathy. Annals of Human Genetics. 74: 110-6. PMID 20201937 DOI: 10.1111/j.1469-1809.2010.00566.x  0.4
2010 Van Hout CV, Levin AM, Rampersaud E, Shen H, O'Connell JR, Mitchell BD, Shuldiner AR, Douglas JA. Extent and distribution of linkage disequilibrium in the Old Order Amish. Genetic Epidemiology. 34: 146-50. PMID 19697356 DOI: 10.1002/gepi.20444  0.4
2009 Michos ED, Streeten EA, Ryan KA, Rampersaud E, Peyser PA, Bielak LF, Shuldiner AR, Mitchell BD, Post W. Serum 25-hydroxyvitamin d levels are not associated with subclinical vascular disease or C-reactive protein in the old order amish. Calcified Tissue International. 84: 195-202. PMID 19148561 DOI: 10.1007/s00223-008-9209-3  0.4
2009 Wang Y, O'Connell JR, McArdle PF, Wade JB, Dorff SE, Shah SJ, Shi X, Pan L, Rampersaud E, Shen H, Kim JD, Subramanya AR, Steinle NI, Parsa A, Ober CC, et al. From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene. Proceedings of the National Academy of Sciences of the United States of America. 106: 226-31. PMID 19114657 DOI: 10.1073/pnas.0808358106  0.4
2008 Rampersaud E, Mitchell BD, Naj AC, Pollin TI. Investigating parent of origin effects in studies of type 2 diabetes and obesity. Current Diabetes Reviews. 4: 329-39. PMID 18991601  0.4
2008 Rampersaud E, Bielak LF, Parsa A, Shen H, Post W, Ryan KA, Donnelly P, Rumberger JA, Sheedy PF, Peyser PA, Shuldiner AR, Mitchell BD. The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults. American Journal of Epidemiology. 168: 1016-23. PMID 18805900 DOI: 10.1093/aje/kwn211  0.4
2008 Rampersaud E, Mitchell BD, Pollin TI, Fu M, Shen H, O'Connell JR, Ducharme JL, Hines S, Sack P, Naglieri R, Shuldiner AR, Snitker S. Physical activity and the association of common FTO gene variants with body mass index and obesity. Archives of Internal Medicine. 168: 1791-7. PMID 18779467 DOI: 10.1001/archinte.168.16.1791  0.4
2008 Köttgen A, Hwang SJ, Rampersaud E, Coresh J, North KE, Pankow JS, Meigs JB, Florez JC, Parsa A, Levy D, Boerwinkle E, Shuldiner AR, Fox CS, Kao WH. TCF7L2 variants associate with CKD progression and renal function in population-based cohorts. Journal of the American Society of Nephrology : Jasn. 19: 1989-99. PMID 18650481 DOI: 10.1681/ASN.2007121291  0.4
2008 Mitchell BD, McArdle PF, Shen H, Rampersaud E, Pollin TI, Bielak LF, Jaquish C, Douglas JA, Roy-Gagnon MH, Sack P, Naglieri R, Hines S, Horenstein RB, Chang YP, Post W, et al. The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study. American Heart Journal. 155: 823-8. PMID 18440328 DOI: 10.1016/j.ahj.2008.01.019  0.4
2007 Rampersaud E, Damcott CM, Fu M, Shen H, McArdle P, Shi X, Shelton J, Yin J, Chang YP, Ott SH, Zhang L, Zhao Y, Mitchell BD, O'Connell J, Shuldiner AR. 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 quantitative traits and from independent populations. Diabetes. 56: 3053-62. PMID 17846126 DOI: 10.2337/db07-0457  0.4
2007 Rampersaud E, Morris RW, Weinberg CR, Speer MC, Martin ER. Power calculations for likelihood ratio tests for offspring genotype risks, maternal effects, and parent-of-origin (POO) effects in the presence of missing parental genotypes when unaffected siblings are available. Genetic Epidemiology. 31: 18-30. PMID 17096358 DOI: 10.1002/gepi.20189  0.4
2006 Stamm DS, Rampersaud E, Slifer SH, Mehltretter L, Siegel DG, Xie J, Hu-Lince D, Craig DW, Stephan DA, George TM, Gilbert JR, Speer MC. High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35. Birth Defects Research. Part a, Clinical and Molecular Teratology. 76: 499-505. PMID 16933213 DOI: 10.1002/bdra.20272  0.4
2005 Rampersaud E, Scott WK, Hauser ER, Speer MC. Potential for expanded power in linkage studies using the ALLEGRO and MERLIN software programs. Journal of Medical Genetics. 42: e68. PMID 16326825 DOI: 10.1136/jmg.2005.032029  0.4
2005 Rampersaud E, Bassuk AG, Enterline DS, George TM, Siegel DG, Melvin EC, Aben J, Allen J, Aylsworth A, Brei T, Bodurtha J, Buran C, Floyd LE, Hammock P, Iskandar B, et al. Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10. Journal of Medical Genetics. 42: 940-6. PMID 15831595 DOI: 10.1136/jmg.2005.031658  0.4
2004 Rampersaud E, Brusato C, Melvin EC, Speer MC, Metcalf K. No evidence for heterozygote advantage at MTHFR in patients with lumbosacral myelomeningocele or their relatives. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 6: 69-70. PMID 14726815 DOI: 10.1097/01.GIM.0000106162.27561.68  0.4
2003 Rampersaud E, Allen A, Li YJ, Shao Y, Bass M, Haynes C, Ashley-Koch A, Martin ER, Schmidt S, Hauser ER. Adjusting for covariates on a slippery slope: linkage analysis of change over time. Bmc Genetics. 4: S50. PMID 14975118 DOI: 10.1186/1471-2156-4-S1-S50  0.4
2003 Hauser ER, Hsu FC, Daley D, Olson JM, Rampersaud E, Lin JP, Paterson AD, Poisson LM, Chase GA, Dahmen G, Ziegler A. Effects of covariates: a summary of Group 5 contributions. Genetic Epidemiology. 25: S43-9. PMID 14635168 DOI: 10.1002/gepi.10283  0.4
2003 Rampersaud E, Melvin EC, Siegel D, Mehltretter L, Dickerson ME, George TM, Enterline D, Nye JS, Speer MC. Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects. Clinical Genetics. 63: 210-4. PMID 12694231 DOI: 10.1034/j.1399-0004.2003.00043.x  0.4
2002 Speer MC, Melvin EC, Viles KD, Bauer KA, Rampersaud E, Drake C, George TM, Enterline DS, Mackey JF, Worley G, Gilbert JR, Nye JS. T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families. American Journal of Medical Genetics. 110: 215-8. PMID 12116228 DOI: 10.1002/ajmg.10436  0.4
2001 Tim RW, Gilbert JR, Stajich JM, Rampersaud E, Viles KD, Tawil R, Padberg GW, Frants R, van der Maarel S, Bossen EH, Friedman AH, Pericak-Vance MA, Speer MC. Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy. Journal of Clinical Neuromuscular Disease. 3: 1-7. PMID 19078645  0.4
2001 Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH, Goetz CG, Small GW, ... ... Rampersaud E, et al. Complete genomic screen in Parkinson disease: evidence for multiple genes. Jama. 286: 2239-44. PMID 11710888  0.4
2001 Allingham RR, Seo B, Rampersaud E, Bembe M, Challa P, Liu N, Parrish T, Karolak L, Gilbert J, Pericak-Vance MA, Klintworth GK, Vance JM. A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis. American Journal of Human Genetics. 68: 491-4. PMID 11170897 DOI: 10.1086/318194  0.4
2001 Tim RW, Gilbert JR, Stajich JM, Rampersaud E, Viles KD, Tawil R, Padberg GW, Frants R, Van Der Maarel S, Bossen EH, Friedman AH, Pericak-Vance MA, Speer MC. Clinical studies in non-chromosome 4-linked facioscapulohumeral muscular dystrophy Journal of Clinical Neuromuscular Disease. 3: 1-7.  0.4
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