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Evadnie Rampersaud, Ph.D. - Publications

Affiliations: 
2005 Duke University, Durham, NC 
Area:
Genetics, Statistics, Bioinformatics Biology
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39 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
2020 Chang TC, Haupfear KM, Yu J, Rampersaud E, Sheehan VA, Flanagan JM, Hankins JS, Weiss MJ, Wu G, Vege S, Westhoff CM, Chou ST, Zheng Y. A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data. Blood Advances. 4: 4347-4357. PMID 32915977 DOI: 10.1182/Bloodadvances.2020002148  0.376
2020 Pinto EM, Figueiredo BC, Chen W, Galvao HCR, Formiga MN, Fragoso MCBV, Ashton-Prolla P, Ribeiro EMSF, Felix G, Costa TEB, Savage SA, Yeager M, Palmero EI, Volc S, Salvador H, ... ... Rampersaud E, et al. XAF1 as a modifier of p53 function and cancer susceptibility. Science Advances. 6: eaba3231. PMID 32637605 DOI: 10.1126/Sciadv.Aba3231  0.352
2019 Farhan SMK, Howrigan DP, Abbott LE, Klim JR, Topp SD, Byrnes AE, Churchhouse C, Phatnani H, Smith BN, Rampersaud E, Wu G, Wuu J, Shatunov A, Iacoangeli A, Al Khleifat A, et al. Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein. Nature Neuroscience. PMID 31768050 DOI: 10.1038/S41593-019-0530-0  0.32
2019 Edmonson MN, Patel AN, Hedges DJ, Wang Z, Rampersaud E, Kesserwan CA, Zhou X, Liu Y, Newman S, Rusch MC, McLeod CL, Wilkinson MR, Rice SV, Soussi T, Taylor JP, et al. Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants. Genome Research. PMID 31439692 DOI: 10.1101/Gr.250357.119  0.36
2019 Rampersaud E, Ziegler DS, Iacobucci I, Payne-Turner D, Churchman ML, Schrader KA, Joseph V, Offit K, Tucker K, Sutton R, Warby M, Chenevix-Trench G, Huntsman DG, Tsoli M, Mead RS, et al. Germline deletion of in familial acute lymphoblastic leukemia. Blood Advances. 3: 1039-1046. PMID 30940639 DOI: 10.1182/Bloodadvances.2018030635  0.373
2018 Wang Z, Wilson CL, Easton J, Thrasher A, Mulder H, Liu Q, Hedges DJ, Wang S, Rusch MC, Edmonson MN, Levy S, Lanctot JQ, Caron E, Shelton K, Currie K, ... ... Rampersaud E, et al. Genetic Risk for Subsequent Neoplasms Among Long-Term Survivors of Childhood Cancer. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. JCO2018778589. PMID 29847298 DOI: 10.1200/Jco.2018.77.8589  0.325
2018 Nicolas A, Kenna KP, Renton AE, Ticozzi N, Faghri F, Chia R, Dominov JA, Kenna BJ, Nalls MA, Keagle P, Rivera AM, van Rheenen W, Murphy NA, van Vugt JJFA, Geiger JT, ... ... Rampersaud E, et al. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene. Neuron. 97: 1268-1283.e6. PMID 29566793 DOI: 10.1016/J.Neuron.2018.02.027  0.35
2018 Pottier C, Rampersaud E, Baker M, Wu G, Wuu J, McCauley JL, Zuchner S, Schule R, Bermudez C, Hussain S, Cooley A, Wallace M, Zhang J, Taylor JP, Benatar M, et al. Identification of compound heterozygous variants in OPTN in an ALS-FTD patient from the CReATe consortium: a case report. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-3. PMID 29558868 DOI: 10.1080/21678421.2018.1452947  0.333
2018 Palmer LE, Zhou X, McLeod C, Rampersaud E, Estepp JH, Tang X, Wang J, Siosan E, Michael JR, Birch K, Hodges JR, Villavicencio M, Rusch M, Newman S, Mulder H, et al. Data Access and Interactive Visualization of Whole Genome Sequence of Sickle Cell Patients within the St. Jude Cloud Blood. 132: 723-723. DOI: 10.1182/Blood-2018-99-116597  0.308
2018 Paikari A, Mi T, Zhang Y, Rampersaud E, Kang G, Wu G, Hankins JS, Estepp JH, Sumazin P, Weiss MJ, Sheehan VA. Insulin-like Growth Factor Binding Protein-3 (IGFBP3) Induces Fetal Hemoglobin in Hematopoietic Stem and Progenitor Cells from Patients with Sickle Cell Anemia Blood. 132: 722-722. DOI: 10.1182/Blood-2018-99-115383  0.335
2018 Wang Z, Wilson CL, Liu Q, Easton J, Mulder HL, Rusch M, Edmonson M, Levy S, Patel A, Shao Y, Chang T, Rice SV, Sapkota Y, Brooke RJ, Moon W, ... Rampersaud E, et al. Abstract 3007: Monogenic and polygenic associations with subsequent breast cancer risk in survivors of childhood cancer: The St. Jude Lifetime Cohort Study (SJLIFE) Cancer Research. 78: 3007-3007. DOI: 10.1158/1538-7445.Am2018-3007  0.334
2017 Damas OM, Gomez L, Quintero MA, Rampersaud E, Slifer S, Beecham GW, Kerman DH, Deshpande AR, Sussman DA, Abreu MT, McCauley JL. Genetic Characterization and Influence on Inflammatory Bowel Disease Expression in a Diverse Hispanic South Florida Cohort. Clinical and Translational Gastroenterology. 8: e87. PMID 28406493 DOI: 10.1038/Ctg.2017.13  0.312
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  0.352
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  0.327
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  0.425
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  0.324
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  0.306
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  0.349
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  0.405
2011 Martin ER, Rampersaud E. Family-based genetic association tests. Cold Spring Harbor Protocols. 2011: pdb.top96. PMID 21285276 DOI: 10.1101/Pdb.Top96  0.349
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  0.307
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  0.412
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  0.335
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  0.379
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  0.338
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  0.335
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  0.57
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  0.602
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  0.545
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  0.603
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  0.512
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  0.301
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  0.35
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  0.585
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  0.599
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 DOI: 10.1097/00131402-200109000-00001  0.553
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 DOI: 10.1001/Jama.286.18.2239  0.353
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  0.395
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.  0.568
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