| 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 |
0.332 |
|
| 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 |
0.426 |
|
| 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 |
0.35 |
|
| 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 |
0.339 |
|
| 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 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2012 |
Fecto F, Deng H, Chen W, Hong S, Boycott K, Gorrie G, Siddique N, Yang Y, Shi Y, Zhai H, Jiang H, Hirano M, Rampersaud E, Jansen G, Donkervoort S, et al. UBQLN2 Mutations in ALS and ALS/Dementia: A Genetic, Functional and Histopathological Analysis (S05.006) Neurology. 78: S05.006-S05.006. DOI: 10.1212/Wnl.78.1_Meetingabstracts.S05.006 |
0.297 |
|
| 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 DOI: 10.2174/157339908786241179 |
0.295 |
|
| 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 |
0.294 |
|
| 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 |
0.293 |
|
| 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 |
0.289 |
|
| 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 |
0.278 |
|
| 2011 |
Vance DD, Stoutenberg M, Chen G, Myerberg R, Tekin D, Nathanson L, Jacobs K, Clark J, Perry A, Rampersaud E, Goldschmidt-Clermont P, Seo D. Increased eNos Gene Expression Identified Among Marathon Runners With Improved Vo2max Medicine & Science in Sports & Exercise. 43: 150. DOI: 10.1249/01.Mss.0000403124.38547.48 |
0.277 |
|
| 2017 |
Wang Z, Wilson CL, Easton J, Hedges D, Liu Q, Wu G, Rusch M, Edmonson M, Levy S, Lanctot JQ, Caron E, Shelton K, Currie K, Lear M, Mulder HL, ... ... Rampersaud E, et al. Abstract 3001: Germline mutations in cancer predisposition genes and risk for subsequent neoplasms among long-term survivors of childhood cancer in the St. Jude Lifetime Cohort Cancer Research. 77: 3001-3001. DOI: 10.1158/1538-7445.Am2017-3001 |
0.276 |
|
| 2022 |
Flerlage JE, Myers JR, Maciaszek JL, Oak N, Rashkin SR, Hui Y, Wang YD, Chen W, Wu G, Chang TC, Hamilton KV, Goldin LR, Rotunno M, Caporaso NE, Vogt A, ... ... Rampersaud E, et al. Discovery of novel predisposing coding and noncoding variants in familial Hodgkin lymphoma. Blood. PMID 35977101 DOI: 10.1182/blood.2022016056 |
0.276 |
|
| 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 |
0.274 |
|
| 2022 |
Brady SW, Roberts KG, Gu Z, Shi L, Pounds S, Pei D, Cheng C, Dai Y, Devidas M, Qu C, Hill AN, Payne-Turner D, Ma X, Iacobucci I, Baviskar P, ... ... Rampersaud E, et al. The genomic landscape of pediatric acute lymphoblastic leukemia. Nature Genetics. PMID 36050548 DOI: 10.1038/s41588-022-01159-z |
0.266 |
|
| 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 |
0.266 |
|
| 2019 |
Paikari A, Zhang Y, Chang A, Goyal A, Rampersaud E, Flanagan JM, Weiss MJ, Sheehan VA. Regulation of Fetal Hemoglobin through the Insulin Signaling Pathway Blood. 134: 811-811. DOI: 10.1182/Blood-2019-131313 |
0.263 |
|
| 2011 |
Farmer JT, Musto A, Vance DD, Tekin D, Cuccaro M, Vance J, Meshbane K, Belton RL, Dauer R, Seo D, Pericak-Vance MA, Goldschmidt PJ, Rampersaud E. An Effective Exercise Program For Developing Genetic Risk Predictions Of Fitness Response Among Multi-ethnic Employees Medicine & Science in Sports & Exercise. 43: 50-51. DOI: 10.1249/01.Mss.0000402823.51676.94 |
0.262 |
|
| 2019 |
Zahr RS, Rampersaud E, Kang G, Weiss MJ, Wu G, Davis RL, Hankins JS, Estepp JH, Lebensburger J. Children with sickle cell anemia and APOL1 genetic variants develop albuminuria early in life. Haematologica. PMID 30890594 DOI: 10.3324/Haematol.2018.212779 |
0.262 |
|
| 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 |
0.259 |
|
| 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, Khleifat AA, et al. Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein. Nature Neuroscience. PMID 31857710 DOI: 10.1038/S41593-019-0570-5 |
0.257 |
|
| 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 |
0.254 |
|
| 2018 |
Rampersaud E, Palmer LE, Hankins JS, Sheehan VA, Bi W, Mulder H, Kang G, Estepp JH, Wang S, Thrasher A, Villavicencio M, Hodges JR, Chen W, Chang T, Cheng Y, et al. Precision Medicine for Sickle Cell Disease through Whole Genome Sequencing Blood. 132: 3641-3641. DOI: 10.1182/Blood-2018-99-117606 |
0.254 |
|
| 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 |
0.252 |
|
| 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 |
0.251 |
|
| 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 |
0.251 |
|
| 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 |
0.248 |
|
| 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 |
0.24 |
|
| 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 |
0.237 |
|
| 2021 |
Rampersaud E, Kang G, Palmer LE, Rashkin SR, Wang S, Bi W, Alberts NM, Anghelescu D, Barton M, Birch K, Boulos N, Brandow AM, Brooke RJ, Chang TC, Chen W, et al. A polygenic score for acute vaso-occlusive pain in pediatric sickle cell disease. Blood Advances. 5: 2839-2851. PMID 34283174 DOI: 10.1182/bloodadvances.2021004634 |
0.237 |
|
| 2017 |
Warner SC, Walsh DA, Laslett LL, Maciewicz RA, Soni A, Hart DJ, Zhang W, Muir KR, Dennison EM, Leaverton P, Rampersaud E, Cooper C, Spector TD, Cicuttini FM, Arden NK, et al. Pain in knee osteoarthritis is associated with variation in the neurokinin 1/substance P receptor (TACR1) gene. European Journal of Pain (London, England). PMID 28493529 DOI: 10.1002/Ejp.1027 |
0.236 |
|
| 2023 |
Dilliott AA, Al Nasser A, Elnagheeb M, Fifita J, Henden L, Keseler IM, Lenz S, Marriott H, Mccann E, Mesaros M, Opie-Martin S, Owens E, Palus B, Ross J, Wang Z, ... ... Rampersaud E, et al. Clinical testing panels for ALS: global distribution, consistency, and challenges. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-16. PMID 36896705 DOI: 10.1080/21678421.2023.2173015 |
0.234 |
|
| 2011 |
Martin ER, Rampersaud E. Family-based genetic association tests Cold Spring Harbor Protocols. 6. DOI: 10.1101/pdb.top96 |
0.231 |
|
| 2013 |
Ahmeti KB, Ajroud-Driss S, Al-Chalabi A, Andersen PM, Armstrong J, Birve A, Blauw HM, Brown RH, Bruijn L, Chen W, Chio A, Comeau MC, Cronin S, Diekstra FP, Soraya Gkazi A, ... ... Rampersaud E, et al. Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. Neurobiology of Aging. 34: 357.e7-19. PMID 22959728 DOI: 10.1016/j.neurobiolaging.2012.07.017 |
0.222 |
|
| 2021 |
Nel M, Mavundla T, Gultig K, Botha G, Mulder N, Benatar M, Wuu J, Cooley A, Myers J, Rampersaud E, Wu G, Heckmann JM. Repeats expansions in , and are not associated with ALS in Africans. Ibro Neuroscience Reports. 10: 130-135. PMID 34179866 DOI: 10.1016/j.ibneur.2021.02.002 |
0.221 |
|
| 2022 |
Nel M, Mahungu AC, Monnakgotla N, Botha GR, Mulder NJ, Wu G, Rampersaud E, van Blitterswijk M, Wuu J, Cooley A, Myers J, Rademakers R, Taylor JP, Benatar M, Heckmann JM. Revealing the Mutational Spectrum in Southern Africans With Amyotrophic Lateral Sclerosis. Neurology. Genetics. 8: e654. PMID 35047667 DOI: 10.1212/NXG.0000000000000654 |
0.219 |
|
| 2023 |
Monnakgotla NR, Mahungu AC, Heckmann JM, Botha G, Mulder NJ, Wu G, Rampersaud E, Myers J, Van Blitterswijk M, Rademakers R, Taylor JP, Wuu J, Benatar M, Nel M. Analysis of Structural Variants Previously Associated With ALS in Europeans Highlights Genomic Architectural Differences in Africans. Neurology. Genetics. 9: e200077. PMID 37346932 DOI: 10.1212/NXG.0000000000200077 |
0.217 |
|
| 2021 |
Rashkin SR, Rampersaud E, Kang G, Ataga KI, Hankins JS, Wang W, Estepp JH, Weiss MJ, Lebensburger J, Zahr RS. Generalization of a genetic risk score for time to first albuminuria in children with sickle cell anaemia: SCCRIP cohort study results. British Journal of Haematology. PMID 34137022 DOI: 10.1111/bjh.17647 |
0.214 |
|
| 2015 |
Sussman DA, McCauley JL, Konidari I, Griswold AJ, Young JI, Hulme WF, Berera S, Kobetz-Kerman EN, Rampersaud E. 942 Racial/Ethnic Groupings Influence Methylation Signatures of Colorectal Cancers Gastroenterology. 148: S-181-S-182. DOI: 10.1016/S0016-5085(15)30605-3 |
0.198 |
|
| 2022 |
Heitzer AM, Longoria J, Rampersaud E, Rashkin SR, Estepp JH, Okhomina VI, Wang WC, Raches D, Potter B, Steinberg MH, King AA, Kang G, Hankins JS. Fetal hemoglobin modulates neurocognitive performance in sickle cell anemia. Current Research in Translational Medicine. 70: 103335. PMID 35303690 DOI: 10.1016/j.retram.2022.103335 |
0.189 |
|
| 2022 |
Umeda M, Ma J, Huang BJ, Hagiwara K, Westover T, Abdelhamed S, Barajas JM, Thomas ME, Walsh MP, Song G, Tian L, Liu Y, Chen X, Kolekar P, Tran Q, ... ... Rampersaud E, et al. Integrated genomic analysis identifies UBTF tandem duplications as a recurrent lesion in pediatric acute myeloid leukemia. Blood Cancer Discovery. PMID 35176137 DOI: 10.1158/2643-3230.BCD-21-0160 |
0.189 |
|
| 2023 |
Heitzer AM, Rashkin SR, Trpchevska A, Longoria JN, Rampersaud E, Olufadi Y, Wang WC, Raches D, Potter B, Steinberg MH, King AA, Kang G, Takemoto CM, Hankins JS. Catechol-O-methyltransferase gene (COMT) is associated with neurocognitive functioning in patients with sickle cell disease. Current Research in Translational Medicine. 72: 103433. PMID 38244277 DOI: 10.1016/j.retram.2023.103433 |
0.178 |
|
| 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 |
0.154 |
|
| 2012 |
Klatte T, Kroeger N, Rampersaud EN, Birkhäuser FD, Logan JE, Sonn G, Riss J, Rao PN, Kabbinavar FF, Belldegrun AS, Pantuck AJ. Gain of chromosome 8q is associated with metastases and poor survival of patients with clear cell renal cell carcinoma. Cancer. 118: 5777-82. PMID 22605478 DOI: 10.1002/cncr.27607 |
0.136 |
|
| 2020 |
Placek K, Benatar M, Wuu J, Rampersaud E, Hennessy L, Van Deerlin VM, Grossman M, Irwin DJ, Elman L, McCluskey L, Quinn C, Granit V, Statland JM, Burns TM, Ravits J, et al. Machine learning suggests polygenic risk for cognitive dysfunction in amyotrophic lateral sclerosis. Embo Molecular Medicine. e12595. PMID 33270986 DOI: 10.15252/emmm.202012595 |
0.135 |
|
| 2013 |
Abern MR, Owusu RA, Anderson MR, Rampersaud EN, Inman BA. Perioperative intravesical chemotherapy in non-muscle-invasive bladder cancer: a systematic review and meta-analysis. Journal of the National Comprehensive Cancer Network : Jnccn. 11: 477-84. PMID 23584348 |
0.135 |
|
| 2008 |
Rampersaud EN, Sun L, Moul JW, Madden J, Freedland SJ. Percent Tumor Involvement and Risk of Biochemical Progression After Radical Prostatectomy Journal of Urology. 180: 571-576. PMID 18554662 DOI: 10.1016/j.juro.2008.04.017 |
0.11 |
|
| 2012 |
Kroeger N, Seligson DB, Klatte T, Rampersaud EN, Birkhäuser FD, Rao PN, Leppert JT, Zomorodian N, Kabbinavar FF, Belldegrun AS, Pantuck AJ. Clinical, molecular, and genetic correlates of lymphatic spread in clear cell renal cell carcinoma. European Urology. 61: 888-95. PMID 22269604 DOI: 10.1016/j.eururo.2012.01.012 |
0.105 |
|
| 2012 |
Kroeger N, Klatte T, Birkhäuser FD, Rampersaud EN, Seligson DB, Zomorodian N, Kabbinavar FF, Belldegrun AS, Pantuck AJ. Smoking negatively impacts renal cell carcinoma overall and cancer-specific survival Cancer. 118: 1795-1802. PMID 21997347 DOI: 10.1002/cncr.26453 |
0.1 |
|
| 2012 |
Kroeger N, Rampersaud EN, Patard JJ, Klatte T, Birkhäuser FD, Shariat SF, Lang H, Rioux-Leclerq N, Remzi M, Zomorodian N, Kabbinavar FF, Belldegrun AS, Pantuck AJ. Prognostic value of microvascular invasion in predicting the cancer specific survival and risk of metastatic disease in renal cell carcinoma: A multicenter investigation Journal of Urology. 187: 418-423. PMID 22177164 DOI: 10.1016/j.juro.2011.10.024 |
0.089 |
|
| 2010 |
Rampersaud EN, Vujaskovic Z, Inman BA. Hyperthermia as a treatment for bladder cancer. Oncology (Williston Park, N.Y.). 24: 1149-55. PMID 21141697 |
0.088 |
|
| 2010 |
Rampersaud EN, Vujaskovic Z, Inman BA. Hyperthermia as a treatment for bladder cancer Oncology. 24. |
0.088 |
|
| 2023 |
McHutchison CA, Wuu J, McMillan CT, Rademakers R, Statland J, Wu G, Rampersaud E, Myers J, Hernandez JP, Abrahams S, Benatar M. Temporal course of cognitive and behavioural changes in motor neuron diseases. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 37827570 DOI: 10.1136/jnnp-2023-331697 |
0.085 |
|
| 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 |
0.085 |
|
| 2014 |
Motzer RJ, Jonasch E, Agarwal N, Beard C, Bhayani S, Bolger GB, Chang SS, Choueiri TK, Derweesh IH, Gupta S, Hancock SL, Kim JJ, Kuzel TM, Lam ET, Lau C, ... ... Rampersaud EN, et al. Kidney cancer, version 2.2014. Journal of the National Comprehensive Cancer Network : Jnccn. 12: 175-82. PMID 24586079 DOI: 10.6004/Jnccn.2014.0018 |
0.082 |
|
| 2014 |
Tsivian M, Rampersaud EN, del Pilar Laguna Pes M, Joniau S, Leveillee RJ, Shingleton WB, Aron M, Kim CY, DeMarzo AM, Desai MM, Meler JD, Donovan JF, Klingler HC, Sopko DR, Madden JF, et al. Small renal mass biopsy--how, what and when: report from an international consensus panel. Bju International. 113: 854-63. PMID 24119037 DOI: 10.1111/bju.12470 |
0.082 |
|
| 2009 |
Ferrandino MN, Bagrodia A, Pierre SA, Scales CD, Rampersaud E, Pearle MS, Preminger GM. Radiation Exposure in the Acute and Short-Term Management of Urolithiasis at 2 Academic Centers Journal of Urology. 181: 668-673. PMID 19100573 DOI: 10.1016/j.juro.2008.10.012 |
0.073 |
|
| 2015 |
Motzer RJ, Jonasch E, Agarwal N, Beard C, Bhayani S, Bolger GB, Chang SS, Choueiri TK, Costello BA, Derweesh IH, Gupta S, Hancock SL, Kim JJ, Kuzel TM, Lam ET, ... ... Rampersaud EN, et al. Kidney cancer, version 3.2015. Journal of the National Comprehensive Cancer Network : Jnccn. 13: 151-9. PMID 25691606 DOI: 10.6004/Jnccn.2015.0022 |
0.072 |
|
| 2015 |
Motzer RJ, Jonasch E, Agarwal N, Beard C, Bhayani S, Bolger GB, Chang SS, Choueiri TK, Costello BA, Derweesh IH, Gupta S, Hancock SL, Kim JJ, Kuzel TM, Lam ET, ... ... Rampersaud EN, et al. Testicular cancer, version 2.2015: Clinical pactice guidelines in oncology Jnccn Journal of the National Comprehensive Cancer Network. 13: 772-799. DOI: 10.1007/978-3-642-54859-8_57 |
0.062 |
|
| 2014 |
Lu TY, Rampersaud EN. Pazopanib-the latest first-line standard of care targeted kinase inhibitor for the treatment of advanced renal cell carcinoma Clinical Medicine Insights: Therapeutics. 6: 25-32. DOI: 10.4137/CMT.S9280 |
0.059 |
|
| 2004 |
Williams ML, Hata JA, Schroder J, Rampersaud E, Petrofski J, Jakoi A, Milano CA, Koch WJ. Targeted beta-adrenergic receptor kinase (betaARK1) inhibition by gene transfer in failing human hearts. Circulation. 109: 1590-3. PMID 15051637 DOI: 10.1161/01.CIR.0000125521.40985.28 |
0.058 |
|
| 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 |
0.056 |
|
| 2014 |
Rampersaud EN, Klatte T, Bass G, Patard JJ, Bensaleh K, Böhm M, Allhoff EP, Cindolo L, De La Taille A, Mejean A, Soulie M, Bellec L, Christophe Bernhard J, Pfister C, Colombel M, et al. The effect of gender and age on kidney cancer survival: younger age is an independent prognostic factor in women with renal cell carcinoma. Urologic Oncology. 32: 30.e9-13. PMID 23422777 DOI: 10.1016/j.urolonc.2012.10.012 |
0.053 |
|
| 2023 |
Gose T, Aitken HM, Wang Y, Lynch J, Rampersaud E, Fukuda Y, Wills M, Baril SA, Ford RC, Shelat A, Mara MLO, Schuetz JD. The net electrostatic potential and hydration of ABCG2 affect substrate transport. Nature Communications. 14: 5035. PMID 37596258 DOI: 10.1038/s41467-023-40610-5 |
0.052 |
|
| 2013 |
Birkhäuser FD, Pantuck AJ, Rampersaud EN, Wang X, Kroeger N, Pouliot F, Zomorodian N, Riss J, Li G, Kabbinavar FF, Belldegrun AS. Salvage-targeted kidney cancer therapy in patients progressing on high-dose interleukin-2 immunotherapy: the UCLA experience. Cancer Journal (Sudbury, Mass.). 19: 189-96. PMID 23708063 DOI: 10.1097/Ppo.0B013E318292E8A4 |
0.049 |
|
| 2013 |
Birkhäuser FD, Koya RC, Neufeld C, Rampersaud EN, Lu X, Micewicz ED, Chodon T, Atefi M, Kroeger N, Chandramouli GV, Li G, Said JW, McBride WH, Kabbinavar FF, Ribas A, et al. Dendritic cell-based immunotherapy in prevention and treatment of renal cell carcinoma: efficacy, safety, and activity of Ad-GM·CAIX in immunocompetent mouse models. Journal of Immunotherapy (Hagerstown, Md. : 1997). 36: 102-11. PMID 23377663 DOI: 10.1097/Cji.0B013E31827Bec97 |
0.04 |
|
| 2007 |
Sun L, Moul JW, Hotaling JM, Rampersaud E, Dahm P, Robertson C, Fitzsimons N, Albala D, Polascik TJ. Prostate-specific antigen (PSA) and PSA velocity for prostate cancer detection in men aged <50 years. Bju International. 99: 753-7. PMID 17244286 DOI: 10.1111/j.1464-410X.2006.06682.x |
0.035 |
|
| 2022 |
Upadhyaya SA, Campagne O, Billups CA, Orr BA, Onar-Thomas A, Tatevossian RG, Mostafavi R, Myers JR, Vinitsky A, Moreira DC, Lindsay HB, Kilburn L, Baxter P, Smith A, Crawford JR, ... ... Rampersaud E, et al. Phase II study of alisertib as a single agent for treating recurrent or progressive atypical teratoid/rhabdoid tumor. Neuro-Oncology. PMID 35652336 DOI: 10.1093/neuonc/noac151 |
0.032 |
|
| 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 |
0.025 |
|
| 2004 |
Williams ML, Rampersaud E, Wolfe WG. A man with saphenous vein graft aneurysms after bypass surgery. The Annals of Thoracic Surgery. 77: 1815-7. PMID 15111195 DOI: 10.1016/S0003-4975(03)01144-5 |
0.01 |
|
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