Publications

2021:2

1. EMBO molecular medic

   Machine learning suggests polygenic risk for cognitive dysfunction in amyotrophic lateral sclerosis

   Placek Katerina, Benatar Michael, Wuu Joanne, Rampersaud Evadnie, Hennessy Laura, Van Deerlin Vivianna M, Grossman Murray, Irwin David J, Elman Lauren, McCluskey Leo, others

   EMBO molecular medicine 2021
2. IBRO Neuroscience Re

   Repeats expansions in ATXN2, NOP56, NIPA1 and ATXN1 are not associated with ALS in Africans

   Nel Melissa, Mavundla Thandeka, Gultig Kayleigh, Botha Gerrit, Mulder Nicola, Benatar Michael, Wuu Joanne, Cooley Anne, Myers Jason, Rampersaud Evadnie, others

   IBRO Neuroscience Reports 2021

2020:5

1. Nature neuroscience

   Publisher correction: exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, dnajc7, encoding a heat-shock protein

   Farhan Sali MK, Howrigan Daniel P, Abbott Liam E, Klim Joseph R, Topp Simon D, Byrnes Andrea E, Churchhouse Claire, Phatnani Hemali, Smith Bradley N, Rampersaud Evadnie, others

   Nature neuroscience 2020
2. medRxiv

   Machine learning suggests polygenic contribution to cognitive dysfunction in amyotrophic lateral sclerosis (ALS)

   Placek Katerina, Benatar Michael, Wuu Joanne, Rampersaud Evadnie, Hennessy Laura, Van Deerlin Vivianna M, Grossman Murray, Irwin David, Elman Lauren, McCluskey Leo, others

   medRxiv 2020
3. Science Advances

   XAF1 as a modifier of p53 function and cancer susceptibility

   Pinto Emilia M, Figueiredo Bonald C, Chen Wenan, Galvao Henrique CR, Formiga Maria Nirvana, Fragoso Maria Candida BV, Ashton-Prolla Patricia, Ribeiro Enilze MSF, Felix Gabriela, Costa Tatiana EB, others

   Science Advances 2020
4. Blood advances

   A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data

   Chang Ti-Cheng, Haupfear Kelly M, Yu Jing, Rampersaud Evadnie, Sheehan Vivien A, Flanagan Jonathan M, Hankins Jane S, Weiss Mitchell J, Wu Gang, Vege Sunitha, others

   Blood advances 2020
5. BookChapter

   Fetal Hemoglobin Mediates the Effect of Beta Globin Gene Polymorphisms on Neurocognitive Functioning in Sickle Cell Disease

   Heitzer Andrew M, Longoria Jennifer, Rampersaud Evadnie, Rashkin Sara, Estepp Jeremie H, Okhomina Victoria, Wang Winfred, Raches Darcy, Potter Brian, King Allison A, others

   In BLOOD 2020

2019:6

1. Genome research

   Pediatric Cancer Variant Pathogenicity Information Exchange (PeCanPIE): a cloud-based platform for curating and classifying germline variants

   Edmonson Michael N, Patel Aman N, Hedges Dale J, Wang Zhaoming, Rampersaud Evadnie, Kesserwan Chimene A, Zhou Xin, Liu Yanling, Newman Scott, Rusch Michael C, others

   Genome research 2019
2. Journal

   Employment Cost Index, Historical Listing–Volume V: Continuous Occupational and Industry Series: September 1975-December 2017. Table 4: employment cost index for total…

   Benjamin Emelia J, Muntner Paul, Alonso Alvaro, Bittencourt Marcio S, Callaway Clifton W, Carson April P, Chamberlain Alanna M, Chang Alexander R, Cheng Susan, Das Sandeep R, others

   2019
3. Blood advances

   Germline deletion of ETV6 in familial acute lymphoblastic leukemia

   Rampersaud Evadnie, Ziegler David S, Iacobucci Ilaria, Payne-Turner Debbie, Churchman Michelle L, Schrader Kasmintan A, Joseph Vijai, Offit Kenneth, Tucker Katherine, Sutton Rosemary, others

   Blood advances 2019
4. Journal

   Regulation of Fetal Hemoglobin through the Insulin Signaling Pathway

   Paikari Alireza, Zhang Yankai, Chang Alicia, Goyal Ankush, Rampersaud Evadnie, Flanagan Jonathan M, Weiss Mitchell J, Sheehan Vivien A

   2019
5. Nature neuroscience

   Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein

   Farhan Sali MK, Howrigan Daniel P, Abbott Liam E, Klim Joseph R, Topp Simon D, Byrnes Andrea E, Churchhouse Claire, Phatnani Hemali, Smith Bradley N, Rampersaud Evadnie, others

   Nature neuroscience 2019
6. haematologica

   Children with sickle cell anemia and APOL1 genetic variants develop albuminuria early in life

   Zahr Rima S, Rampersaud Evadnie, Kang Guolian, Weiss Mitchell J, Wu Gang, Davis Robert L, Hankins Jane S, Estepp Jeremie H, Lebensburger Jeffrey

   haematologica 2019

2018:10

1. Neuron

   Genome-wide analyses identify KIF5A as a novel ALS gene

   Nicolas Aude, Kenna Kevin P, Renton Alan E, Ticozzi Nicola, Faghri Faraz, Chia Ruth, Dominov Janice A, Kenna Brendan J, Nalls Mike A, Keagle Pamela, others

   Neuron 2018
2. Amyotrophic Lateral

   Identification of compound heterozygous variants in OPTN in an ALS-FTD patient from the CReATe consortium: a case report

   Pottier Cyril, Rampersaud Evadnie, Baker Matt, Wu Gang, Wuu Joanne, McCauley Jacob L, Zuchner Stephan, Schule Rebecca, Bermudez Christin, Hussain Sumaira, others

   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 2018
3. BioRxiv

   Enrichment of rare protein truncating variants in amyotrophic lateral sclerosis patients

   Farhan Sali MK, Howrigan Daniel P, Abbott Liam E, Byrnes Andrea E, Churchhouse Claire, Phatnani Hemali, Smith Bradley N, Topp Simon D, Rampersaud Evadnie, Wu Gang, others

   BioRxiv 2018
4. Journal of Clinical

   Genetic risk for subsequent neoplasms among long-term survivors of childhood cancer

   Wang Zhaoming, Wilson Carmen L, Easton John, Thrasher Andrew, Mulder Heather, Liu Qi, Hedges Dale J, Wang Shuoguo, Rusch Michael C, Edmonson Michael N, others

   Journal of Clinical Oncology 2018
5. Journal

   Monogenic and polygenic associations with subsequent breast cancer risk in survivors of childhood cancer: The St. Jude Lifetime Cohort Study (SJLIFE)

   Wang Zhaoming, Wilson Carmen L, Liu Qi, Easton John, Mulder Heather L, Rusch Michael, Edmonson Michael, Levy Shawn, Patel Aman, Shao Ying, others

   2018
6. Circulation

   Forecasting the future of cardiovascular disease in the United States: a policy statement from the American Heart Association

   Benjamin EJ, Virani SS, Callaway CW, Chamberlain AM, Chang AR, Cheng S, Deo R

   Circulation 2018
7. Blood

   Insulin-like Growth Factor Binding Protein-3 (IGFBP3) Induces Fetal Hemoglobin in Hematopoietic Stem and Progenitor Cells from Patients with Sickle Cell Anemia

   Paikari Alireza, Mi Tian, Zhang Yankai, Rampersaud Evadnie, Kang Guolian, Wu Gang, Hankins Jane S, Estepp Jeremie H, Sumazin Pavel, Weiss Mitchell J, others

   Blood 2018
8. Blood

   Children with Sickle Cell Anemia and APOL1 Gene Variants Develop Albuminuria Early in Life

   Zahr Rima, Lebensburger Jeffrey, Rampersaud Evadnie, Hankins Jane S, Estepp Jeremie H

   Blood 2018
9. Blood

   Precision medicine for sickle cell disease through whole genome sequencing

   Rampersaud Evadnie, Palmer Lance E, Hankins Jane S, Sheehan Vivien A, Bi Wenjian, Mulder Heather, Kang Guolian, Estepp Jeremie H, Wang Shuoguo, Thrasher Andrew, others

   Blood 2018
10. Blood

    Data access and interactive visualization of whole genome sequence of sickle cell patients within the St. Jude Cloud

    Palmer Lance E, Zhou Xin, McLeod Clay, Rampersaud Evadnie, Estepp Jeremie H, Tang Xing, Wang Jian, Siosan Edgar, Michael J Robert, Birch Kirby, others

    Blood 2018

2017:4

1. European Journal of

   Pain in knee osteoarthritis is associated with variation in the neurokinin 1/substance P receptor (TACR1) gene

   Warner Sophie C, Walsh David A, Laslett Laura L, Maciewicz Rose A, Soni Anushka, Hart Deborah J, Zhang Weiya, Muir Kenneth R, Dennison Elaine M, Leaverton Paul, others

   European Journal of Pain 2017
2. Clinical and transla

   Genetic characterization and influence on inflammatory bowel disease expression in a diverse Hispanic South Florida Cohort

   Damas Oriana M, Gomez Lissette, Quintero Maria A, Rampersaud Evadnie, Slifer Susan, Beecham Gary W, Kerman David H, Deshpande Amar R, Sussman Daniel A, Abreu Maria T, others

   Clinical and translational gastroenterology 2017
3. Journal

   Germline mutations in cancer predisposition genes and risk for subsequent neoplasms among long-term survivors of childhood cancer in the St. Jude Lifetime Cohort

   Wang Zhaoming, Wilson Carmen L, Easton John, Hedges Dale, Liu Qi, Wu Gang, Rusch Michael, Edmonson Michael, Levy Shawn, Lanctot Jennifer Q, others

   2017
4. circulation

   Heart disease and stroke statistics—2017 update: a report from the American Heart Association

   Benjamin Emelia J, Blaha Michael J, Chiuve Stephanie E, Cushman Mary, Das Sandeep R, Deo Rajat, De Ferranti Sarah D, Floyd James, Fornage Myriam, Gillespie Cathleen, others

   circulation 2017

2016:2

1. Cartilage

   Regional differential genetic response of human articular cartilage to impact injury

   Vernon Lauren L, Vance Danica D, Wang Liyong, Rampersaud Evadnie, Vance Jeffery M, Pericak-Vance Margaret, Huang C-Y Charles, Kaplan Lee D

   Cartilage 2016
2. Nature communication

   The severity of hereditary porphyria is modulated by the porphyrin exporter and Lan antigen ABCB6

   Fukuda Yu, Cheong Pak Leng, Lynch John, Brighton Cheryl, Frase Sharon, Kargas Vasileios, Rampersaud Evadnie, Wang Yao, Sankaran Vijay G, Yu Bing, others

   Nature communications 2016

2015:4

1. Gastroenterology

   942 Racial/Ethnic Groupings Influence Methylation Signatures of Colorectal Cancers

   Sussman Daniel A, McCauley Jacob L, Konidari Ioanna, Griswold Anthony J, Young Juan I, Hulme William F, Berera Shivali, Kobetz-Kerman Erin N, Rampersaud Evadnie

   Gastroenterology 2015
2. Blood, The Journal o

   Regulation of AKT signaling by Id1 controls t (8; 21) leukemia initiation and progression

   Wang Lan, Man Na, Sun Xiao-Jian, Tan Yurong, Garcı́a-Cao Marta, Liu Fan, Hatlen Megan, Xu Haiming, Huang Gang, Mattlin Meredith, others

   Blood, The Journal of the American Society of Hematology 2015
3. BookChapter

   Gene expression changes associated with HIV-induced nuclear translocation of amyloid beta in brain endothelium

   Andras IE, Rampersaud E, Eum SY, Toborek M

   In JOURNAL OF NEUROIMMUNE PHARMACOLOGY 2015
4. Journal

   Blood First Edition Paper, prepublished online June 17, 2015; DOI 10.1182/blood-2015-03-635532

   Wang Lan, Man Na, Sun Xiao-Jian, Tan Yurong, Cao Marta Garcia, Liu Fan, Hatlen Megan, Xu Haiming, Huang Gang, Mattlin Meredith, others

   2015

2014:6

1. BMC sports science,

   Cardiac performance, biomarkers and gene expression studies in previously sedentary men participating in half-marathon training

   Vance Danica D, Chen Gordon L, Stoutenberg Mark, Myerburg Robert J, Jacobs Kevin, Nathanson Lubov, Perry Arlette, Seo David, Goldschmidt-Clermont Pascal J, Rampersaud Evadnie

   BMC sports science, medicine and rehabilitation 2014
2. Fetal and pediatric

   Bridging the Gaps Between the Histopathological and Demographic Risk Factors of Preterm Birth in a Unique Miami Inner-City Population

   Veerapen Muthu Kumar, Pelaez Liset, Potter JoNell Efantis, Duthely Lunthita, Birusingh Rhea, Rampersaud Evadnie, Bodamer Olaf A, Rodriguez Maria Matilde

   Fetal and pediatric pathology 2014
3. Archives of medical

   Transcriptional Profile of HIV-induced Nuclear Translocation of Amyloid βin Brain Endothelial Cells

   András Ibolya E, Rampersaud Evadnie, Eum Sung Yong, Toborek Michal

   Archives of medical research 2014
4. BookChapter

   A New Method to Identify Podocyte-specific Gene Expression Profiles Associated with Progression of Diabetic Kidney Disease in Type 2 Diabetes

   Correa-Medina Mayrin, Rampersaud Evadnie, Nair Christopher Pedigo Viji, Leak-Johnson Tennille, Kretzler Matthias, Nelson Robert G, Merscher-Gomez Sandra, Fornoni Alessia

   In DIABETES 2014
5. J Exerc Sports Ortho

   Dynamic gene expression profile changes in synovial fluid following meniscal injury; osteoarthritis (OA) markers found

   Vance DD, Wang L, Rampersaud E, Lesniak P, Vance JM, Pericak-Vance MA, Kaplan L

   J Exerc Sports Orthop 2014
6. Human molecular gene

   A genome-wide association meta-analysis identifies a novel locus at 17q11. 2 associated with sporadic amyotrophic lateral sclerosis

   Fogh Isabella, Ratti Antonia, Gellera Cinzia, Lin Kuang, Tiloca Cinzia, Moskvina Valentina, Corrado Lucia, Sorarù Gianni, Cereda Cristina, Corti Stefania, others

   Human molecular genetics 2014

2013:11

1. Human genetics

   Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women’s Health Initiative SHARe Study

   Edwards Digna R Velez, Naj Adam C, Monda Keri, North Kari E, Neuhouser Marian, Magvanjav Oyunbileg, Kusimo Ibukun, Vitolins Mara Z, Manson JoAnn E, O’Sullivan Mary Jo, others

   Human genetics 2013
2. Journal

   Defining a molecular portrait of physical fitness

   Clouse Adam, Deo Sapna, Rampersaud Evadnie, Farmer Jeff, Goldschmidt-Clermont Pascal J, Daunert Sylvia

   2013
3. Circulation: Cardiov

   Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy

   Norton Nadine, Li Duanxiang, Rampersaud Evadnie, Morales Ana, Martin Eden R, Zuchner Stephan, Guo Shengru, Gonzalez Michael, Hedges Dale J, Robertson Peggy D, others

   Circulation: Cardiovascular Genetics 2013
4. Annals of human gene

   Genomic Signatures of a Global Fitness Index in a Multi-Ethnic Cohort of Women

   Rampersaud Evadnie, Nathanson Lubov, Farmer Jeffrey, Meshbane Karyn, Belton Richard L, Dressen Amy, Cuccaro Michael, Musto Anthony, Daunert Sylvia, Deo Sapna, others

   Annals of human genetics 2013
5. Journal of cardiac f

   Temporal relationship of conduction system disease and ventricular dysfunction in LMNA cardiomyopathy

   Brodt Chad, Siegfried Jill D, Hofmeyer Mark, Martel Jose, Rampersaud Evadnie, Li Duanxiang, Morales Ana, Hershberger Ray E

   Journal of cardiac failure 2013
6. Environmental health

   Exercise attenuates PCB-induced changes in the mouse gut microbiome

   Choi Jeong June, Eum Sung Yong, Rampersaud Evadnie, Daunert Sylvia, Abreu Maria T, Toborek Michal

   Environmental health perspectives 2013
7. PLoS Genet

   Genome-wide association of body fat distribution in African ancestry populations suggests new loci

   Liu Ching-Ti, Monda Keri L, Taylor Kira C, Lange Leslie, Demerath Ellen W, Palmas Walter, Wojczynski Mary K, Ellis Jaclyn C, Vitolins Mara Z, Liu Simin, others

   PLoS Genet 2013
8. Nutrition & diabetes

   Generalization of adiposity genetic loci to US Hispanic women

   Graff M, Fernandez-Rhodes Lindsay, Liu S, Carlson C, Wassertheil-Smoller S, Neuhouser M, Reiner A, Kooperberg C, Rampersaud E, Manson JE, others

   Nutrition & diabetes 2013
9. Journal

   Abstract P296: Genome Wide Association Study of Weight Change Among Post-Menopausal African Americans: The Women’s Health Initiative Study

   Yoneyama Sachiko, Justice Anne, Monda Keri, North Kari E, Wassertheil-Smoller Sylvia, Neuhouser Marian, Rampersaud Evadnie, Liu Simin, Howard Barbara V, Manson Joanne E, others

   2013
10. BookChapter

    Genome Wide Association Study of Weight Change Among Post-Menopausal African Americans: The Women’s Health Initiative Study

    Yoneyama Sachiko, Justice Anne, Monda Keri, North Kari E, Wassertheil-Smoller Sylvia, Neuhouser Marian, Rampersaud Evadnie, Liu Simin, Howard Barbara V, Manson Joanne E, others

    In CIRCULATION 2013
11. Nature genetics

    A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

    Monda Keri L, Chen Gary K, Taylor Kira C, Palmer Cameron, Edwards Todd L, Lange Leslie A, Ng Maggie CY, Adeyemo Adebowale A, Allison Matthew A, Bielak Lawrence F, others

    Nature genetics 2013

2012:6

1. Circulation: Cardiov

   Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era

   Norton Nadine, Robertson Peggy D, Rieder Mark J, Züchner Stephan, Rampersaud Evadnie, Martin Eden, Li Duanxiang, Nickerson Deborah A, Hershberger Ray E

   Circulation: Cardiovascular Genetics 2012
2. BookChapter

   Genomics of Pediatric Metabolic Syndrome

   Rampersaud Evadnie, Ciliberti Maria A

   2012
3. Journal

   UBQLN2 Mutations in ALS and ALS/Dementia: A Genetic, Functional and Histopathological Analysis (S05. 006)

   Fecto Faisal, Deng Han-Xiang, Chen Wenjie, Hong Seong-Tshool, Boycott Kym, Gorrie George, Siddique Nailah, Yang Yi, Shi Yong, Zhai Hong, others

   2012
4. Journal

   Exome Sequencing and Genome-Wide Linkage Analysis in 17 Families with Dilated Cardiomyopathy Confirms TTN Truncating Variants as a Major Cause

   Hershberger Ray E, Norton Nadine, Li Duanxiang, Rampersaud Evadnie, Morales Ana, Martin Eden R, Guo Shengru, Gonzalez Michael, Zuchner Stephan, Robertson Peggy D, others

   2012
5. Journal

   Abstract P233: Generalization of Adiposity-Related Common Genetic Variants among US Hispanic Women in WHI-SHARe

   Fernández-Rhodes Lindsay, Graff Mariaelisa, Liu Simin, Carlson Christopher, Wassertheil-Smoller Sylvia, Neuhouser Marian, Reiner Alexander, Kooperberg Charles, Rampersaud Evadnie, Manson JoAnn E, others

   2012
6. Circ Cardiovasc Gene

   National Heart, Lung and Blood Institute GO Exome Sequencing Project. Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era

   Norton N, Robertson PD, Rieder MJ, Züchner S, Rampersaud E, Martin E, Li D, Nickerson DA, Hershberger RE

   Circ Cardiovasc Genet 2012

2011:12

1. Nature

   Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

   Deng Han-Xiang, Chen Wenjie, Hong Seong-Tshool, Boycott Kym M, Gorrie George H, Siddique Nailah, Yang Yi, Fecto Faisal, Shi Yong, Zhai Hong, others

   Nature 2011
2. Nature

   Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

   Ehret Georg B, Munroe Patricia B, Rice Kenneth M, Bochud Murielle, Johnson Andrew D, Chasman Daniel I, Smith Albert V, Tobin Martin D, Verwoert Germaine C, Hwang Shih-Jen, others

   Nature 2011
3. The American Journal

   Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy

   Norton Nadine, Li Duanxiang, Rieder Mark J, Siegfried Jill D, Rampersaud Evadnie, Züchner Stephan, Mangos Steve, Gonzalez-Quintana Jorge, Wang Libin, McGee Sean, others

   The American Journal of Human Genetics 2011
4. Arthritis care & res

   Role of the Nav1. 7 R1150W amino acid change in susceptibility to symptomatic knee osteoarthritis and multiple regional pain

   Valdes Ana M, Arden Nigel K, Vaughn Frances L, Doherty Sally A, Leaverton Paul E, Zhang Weiya, Muir Kenneth R, Rampersaud Evadnie, Dennison Elaine M, Edwards Mark H, others

   Arthritis care & research 2011
5. Progress in pediatri

   Rare variant mutations identified in pediatric patients with dilated cardiomyopathy

   Rampersaud Evadnie, Siegfried Jill D, Norton Nadine, Li Duanxiang, Martin Eden, Hershberger Ray E

   Progress in pediatric cardiology 2011
6. Medicine & Science i

   An Effective Exercise Program For Developing Genetic Risk Predictions Of Fitness Response Among Multi-ethnic Employees: 691Board# 3 3: 15 PM-5: 15 PM

   Farmer Jeffrey T, Musto Anthony, Vance Danica D, Tekin Demet, Cuccaro Michael, Vance Jeffery, Meshbane Karyn, Belton Richard L, Dauer Ryan, Seo David, others

   Medicine & Science in Sports & Exercise 2011
7. Journal

   Role of the NaV1. 7 R1150W Amino Acid Change in Susceptibility to Symptomatic Knee

   VALDES ANAM, ARDEN NIGEL K, VAUGHN FRANCES L, DOHERTY SALLY A, LEAVERTON PAUL E, MUIR WEIYA ZHANGI‘KENNETH R, RAMPERSAUD EVADNIE

   2011
8. Medicine & Science i

   Increased eNos Gene Expression Identified Among Marathon Runners With Improved Vo2max: 995June 3 2: 00 PM-2: 15 PM

   Vance Danica D, Stoutenberg Mark, Chen Gordon, Myerberg Robert, Tekin Demet, Nathanson Lubov, Jacobs Kevin, Clark Jennifer, Perry Arlette, Rampersaud Evadnie, others

   Medicine & Science in Sports & Exercise 2011
9. Cold Spring Harbor P

   Family-based genetic association tests

   Martin Eden R, Rampersaud Evadnie

   Cold Spring Harbor Protocols 2011
10. BookChapter

    Whole Exome Sequencing Identifies a Mutation in Transportin 3 as a Cause of Dilated Cardiomyopathy

    Li Duanxiang, Norton Nadine, Xu Yan, Wiley David J, Luo Chunyan, Ouyang Ping, Siegfried Jill D, Rampersaud Evadnie, Zchner Stephan, Mangos Steve, others

    In CIRCULATION RESEARCH 2011
11. Journal

    Gene expression signatures of left ventricular mass and stroke volume change in response to endurance training

    Vance DD, Nathanson Lubov, Stoutenberg M, Chen G, Myerberg R, Jacobs K, Clarke J, Perry A, Seo D, Rampersaud E, others

    2011
12. Journal

    A prescription for personalized wellness: Identification of genomic signatures of VO2max responsiveness among individuals undergoing combined aerobic and resistance training

    Rampersaud E, Nathanson Lubov, Musto T, Mendez A, Belton RL, Meshbane K, Dressen A, Hudson N, Cuccaro M, Vance JM, others

    2011

2010:7

1. Nature genetics

   New loci associated with kidney function and chronic kidney disease

   Köttgen Anna, Pattaro Cristian, Böger Carsten A, Fuchsberger Christian, Olden Matthias, Glazer Nicole L, Parsa Afshin, Gao Xiaoyi, Yang Qiong, Smith Albert V, others

   Nature genetics 2010
2. Annals of human gene

   Common susceptibility variants examined for association with dilated cardiomyopathy

   Rampersaud Evadnie, Kinnamon Daniel D, Hamilton Kara, Khuri Sawsan, Hershberger Ray E, Martin Eden R

   Annals of human genetics 2010
3. Archives of internal

   Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish

   Shen Haiqing, Damcott Coleen M, Rampersaud Evadnie, Pollin Toni I, Horenstein Richard B, McArdle Patrick F, Peyser Patricia A, Bielak Lawrence F, Post Wendy S, Chang Yen-Pei C, others

   Archives of internal medicine 2010
4. Genetic epidemiology

   Extent and distribution of linkage disequilibrium in the Old Order Amish

   Van Hout Cristopher V, Levin Albert M, Rampersaud Evadnie, Shen Haiqing, O’Connell Jeffrey R, Mitchell Braxton D, Shuldiner Alan R, Douglas Julie A

   Genetic epidemiology 2010
5. Journal

   www. archinternmed. com/instructions

   Ho P Michael, Zeng Chan, Tavel Heather M, Selby Joe V, O’Connor Patrick J, Margolis Karen L, Magid David J, Ooi Peng Lim, Low Chew Ling, Lin Raymond, others

   2010
6. Journal

   www. archinternmed. com/instructions

   Ting Henry H, Chen Anita Y, Roe Matthew T, Chan Paul S, Spertus John A, Nallamothu Brahmajee K, Sullivan Mark D, DeLong Elizabeth R, Bradley Elizabeth H, Krumholz Harlan M, others

   2010
7. Journal

   Gene expression analyses in marathon runners

   Vance DD, Stoutenberg M, Chen G, Myerberg R, Tekin D, Nathanson Lubov, Jacobs K, Clarke J, Perry A, Goldschmidt-Clermont PJ, others

   2010

2009:3

1. Proceedings of the N

   Whole-genome association study identifies STK39 as a hypertension susceptibility gene

   Wang Ying, O’Connell Jeffrey R, McArdle Patrick F, Wade James B, Dorff Sarah E, Shah Sanjiv J, Shi Xiaolian, Pan Lin, Rampersaud Evadnie, Shen Haiqing, others

   Proceedings of the National Academy of Sciences 2009
2. Calcified tissue int

   Serum 25-hydroxyvitamin d levels are not associated with subclinical vascular disease or C-reactive protein in the old order amish

   Michos Erin D, Streeten Elizabeth A, Ryan Kathleen A, Rampersaud Evadnie, Peyser Patricia A, Bielak Lawrence F, Shuldiner Alan R, Mitchell Braxton D, Post Wendy

   Calcified tissue international 2009
3. Archives of internal

   Errors in Funding/Support, Role of the Sponsor, and Additional Contributionsin: Physical Activity and the Association of Common FTO Gene Variants With Body Mass Index and Obesity

   RAMPERSAUD Evadnie, MITCHELL Braxton D, POLLIN Toni I, MAO FU, HAIQING SHEN, O’CONNELL Jeffery R, DUCHARME Julie L, HINES Scott, SACK Paul, NAGLIERI Rosalie, others

   Archives of internal medicine 2009

2008:9

1. Archives of internal

   Physical activity and the association of common FTO gene variants with body mass index and obesity

   Rampersaud Evadnie, Mitchell Braxton D, Pollin Toni I, Fu Mao, Shen Haiqing, O’Connell Jeffery R, Ducharme Julie L, Hines Scott, Sack Paul, Naglieri Rosalie, others

   Archives of internal medicine 2008
2. American heart journ

   The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study

   Mitchell Braxton D, McArdle Patrick F, Shen Haiqing, Rampersaud Evadnie, Pollin Toni I, Bielak Lawrence F, Jaquish Cashell, Douglas Julie A, Roy-Gagnon Marie-Hélène, Sack Paul, others

   American heart journal 2008
3. Journal of the Ameri

   TCF7L2 variants associate with CKD progression and renal function in population-based cohorts

   Köttgen Anna, Hwang Shih-Jen, Rampersaud Evadnie, Coresh Josef, North Kari E, Pankow James S, Meigs James B, Florez Jose C, Parsa Afshin, Levy Daniel, others

   Journal of the American Society of Nephrology 2008
4. American journal of

   The association of coronary artery calcification and carotid artery intima-media thickness with distinct, traditional coronary artery disease risk factors in asymptomatic adults

   Rampersaud Evadnie, Bielak Lawrence F, Parsa Afshin, Shen Haiqing, Post Wendy, Ryan Kathleen A, Donnelly Patrick, Rumberger John A, Sheedy Patrick F, Peyser Patricia A, others

   American journal of epidemiology 2008
5. Current diabetes rev

   Investigating parent of origin effects in studies of type 2 diabetes and obesity

   Rampersaud Evadnie, Mitchell Braxton D, Naj Adam C, Pollin Toni I

   Current diabetes reviews 2008
6. BookChapter

   Variants in the transcription factor 7-like 2 gene region are associated with incident kidney disease and markers of kidney function in the atherosclerosis risk in communities study, the framingham heart study offspring cohort, and the heredity and phenotype intervention (HAPI) heart study

   Kottgen Anna, Hwang Shih-Jen, Rampersaud Evadnie, Coresh Josef, North Kari E, Pankow James S, Meigs James B, Levy Daniel, Boerwinkle Eric, Shuldiner Alan R, others

   In CIRCULATION 2008
7. BookChapter

   Genome-wide association scan in the old order Amish identifies BQ231042 as a novel susceptibility gene for type 2 diabetes

   Zhang Li, Fu Mao, Rampersaud Evadnie, Damcott Coleen, Shi Xiaolian, Tanner Keith, Ott Sandra H, Shelton John, O’Connell Jeffery, Mitchell Braxton D, others

   In DIABETES 2008
8. Journal

   This issue will be available online September 8, 2008.

   Weinberger Myron H, Goldstein Nathan E, Back Anthony L, Morrison R Sean, Chen Jing, Gu Dongfeng, Jaquish Cashell E, Chen Chung-Shiuan, Rao DC, Liu Depei, others

   2008
9. Pediatr Nephrol

   PMCID: PMC2720772.

   Rampersaud E, Shen H, Kim JD, Subramanya AR, Steinle NI, Parsa A, Ober CC

   Pediatr Nephrol 2008

2007:7

1. Diabetes

   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

   Rampersaud Evadnie, Damcott Coleen M, Fu Mao, Shen Haiqing, McArdle Patrick, Shi Xiaolian, Shelton John, Yin Jing, Chang Yen-Pei C, Ott Sandra H, others

   Diabetes 2007
2. Genetic Epidemiology

   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

   Rampersaud E, Morris RW, Weinberg CR, Speer MC, Martin Eden R

   Genetic Epidemiology: The Official Publication of the International Genetic Epidemiology Society 2007
3. Diabetes

   Genome-Wide Association Scan in the Amish: Identification of GRB10 as a Susceptibility Gene for Type 2 Diabetes.

   Damcott Coleen M, Rampersaud Evadnie, Ott Sandra H, Shi Xiaolian, Fu Mao, Zhang Li, Shelton John, Ying Jing, O’Connell Jeffrey R, Mitchell Braxton D, others

   Diabetes 2007
4. BookChapter

   Genome-wide association (GWA) scan of type 2 diabetes MD) in the Old Order Amish

   Rampersaud E, Damcott CM, Mitchell BD, Shelton J, Ying J, Fu M, Shi J, Zhao Y, Ott S, O’Connell J, others

   In GENETIC EPIDEMIOLOGY 2007
5. Diabetes

   Genome-Wide Association Scan of Type 2 Diabetes (T2D) and Related Traits in the Old Order Amish (OOA) Reveals Novel Candidate Genes.

   Rampersaud Evadnie, Damcott Coleen M, O’Connell Jeffery, Fu Mao, Shelton John, Ying Jing, Shi Xiaolian, Ott Sandra H, McArdle Patrick, Zhang Li, others

   Diabetes 2007
6. Journal

   The APOB R3500Q Polymorphism Is Common In The Old Order Amish And Is Associated With Low Density Lipoprotein Cholesterol Concentrations And Coronary Artery Calcification

   Shen Haiqing, Damcott Coleen M, Rampersaud Evadnie, Pollin Toni I, O’Connell Jeff R, McArdle Patrick, Peyser Patricia A, Bielak Lawrence F, Ryan Kathleen A, Miller Michael, others

   2007
7. Diabetes

   Evidence for replication from diabetes-related quantitative traits and from independent populations

   Rampersaud E, Damcott CM, Fu M, Shen H, McArdle P, Shi X, Shelton J, Yin J, Chang YPC, Ott SH, others

   Diabetes 2007

2006:2

1. Birth Defects Resear

   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

   Stamm Demetra S, Rampersaud Evadnie, Slifer Susan H, Mehltretter Lorraine, Siegel Deborah G, Xie Jianzhen, Hu-Lince Diane, Craig David W, Stephan Dietrich A, George Timothy M, others

   Birth Defects Research Part A: Clinical and Molecular Teratology 2006
2. BookChapter

   Nonsyndromic neural tube defects: genetic basis and genetic investigations

   Rampersaud EVADNIE, Melvin ELIZABETH C, Speer MC

   2006

2005:3

1. Journal of medical g

   Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10

   Rampersaud Evadnie, Bassuk Alexander G, Enterline David S, George TM, Siegel Deborah G, Melvin Elizabeth C, Aben Joanna, Allen Jacqui, Aylsworth Arthur, Brei Timothy, others

   Journal of medical genetics 2005
2. Journal of medical g

   Potential for expanded power in linkage studies using the ALLEGRO and MERLIN software programs

   Rampersaud E, Scott WK, Hauser ER, Speer MC

   Journal of medical genetics 2005
3. Journal

   Genetic Investigations of a Complex Disorder: Neural Tube Defects

   Rampersaud Evadnie

   2005

2004:1

1. Genetics in Medicine

   No evidence for heterozygote advantage at MTHFR in patients with lumbosacral myelomeningocele or their relatives

   Rampersaud E, Brusato C, Melvin EC, Speer MC, Metcalf K

   Genetics in Medicine 2004

2003:4

1. Clinical genetics

   Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects

   Rampersaud E, Melvin EC, Siegel D, Mehltretter L, Dickerson ME, George TM, Enterline D, Nye JS, Speer Marcy C, Group NTD Collaborative

   Clinical genetics 2003
2. Genetic Epidemiology

   Effects of covariates: a summary of Group 5 contributions

   Hauser Elizabeth R, Hsu Fang-Chi, Daley Denise, Olson Jane M, Rampersaud Evadnie, Lin Jing-Ping, Paterson Andrew D, Poisson Laila M, Chase Gary A, Dahmen Gerlinde, others

   Genetic Epidemiology: The Official Publication of the International Genetic Epidemiology Society 2003
3. BookChapter

   Adjusting for covariates on a slippery slope: linkage analysis of change over time

   Rampersaud Evadnie, Allen Andrew, Li Yi-Ju, Shao Yujun, Bass Meredyth, Haynes Carol, Ashley-Koch Allison, Martin Eden R, Schmidt Silke, Hauser Elizabeth R

   In BMC genetics 2003
4. BookChapter

   Improved inference of missing parental data in a log-linear test of association by inclusion of unaffected siblings.

   Rampersaud E, Speer MC, Martin ER

   In AMERICAN JOURNAL OF HUMAN GENETICS 2003

2002:2

1. American journal of

   T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families

   Speer Marcy C, Melvin Elizabeth C, Viles Kristi D, Bauer Kim A, Rampersaud Evadnie, Drake Courtney, George Timothy M, Enterline David S, Mackey Joanne F, Worley Gordon, others

   American journal of medical genetics 2002
2. BookChapter

   No evidence for heterozygote advantage at MTHFR in patients with lumbosacral myelomeningocele or their relatives.

   Rampersaud E, Brusata C, Metcalf K, Melvin E, Speer MC

   In AMERICAN JOURNAL OF HUMAN GENETICS 2002

2001:3

1. Jama

   Complete genomic screen in Parkinson disease: evidence for multiple genes

   Scott William K, Nance Martha A, Watts Ray L, Hubble Jean P, Koller William C, Lyons Kelly, Pahwa Rajesh, Stern Matthew B, Colcher Amy, Hiner Bradley C, others

   Jama 2001
2. The American Journal

   A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis

   Allingham R Rand, Seo Ben, Rampersaud Evadnie, Bembe MaryLou, Challa Pratap, Liu Ningpu, Parrish Tanisha, Karolak Linda, Gilbert John, Pericak-Vance Margaret A, others

   The American Journal of Human Genetics 2001
3. Journal of clinical

   Clinical studies in non-chromosome 4-linked facioscapulohumeral muscular dystrophy

   Tim Richard W, Gilbert John R, Stajich Jeffrey M, Rampersaud Evadnie, Viles Kristi D, Tawil Rabi, Padberg George W, Frants Rune, Van Der Maarel Silvère, Bossen Edward H, others

   Journal of clinical neuromuscular disease 2001

2000:3

1. BookChapter

   A small duplication of the terminal region of chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis.

   Vance JM, Allingham RR, Seo B, Rampersaud E, Bembe ML, Challa P, Parrish T, Gilbert JR, Pericak-Vance MA, Klintworth GK

   In AMERICAN JOURNAL OF HUMAN GENETICS 2000
2. BookChapter

   Phenotypic characteristics of hereditary benign intraepithelial dyskeratosis (HBID).

   Challa P, Klintworth GK, Seo B, Bembe M, Rampersaud E, Parrish T, Gilbert J, Pericak-Vance MA, Vance JM, Allingham RR

   In AMERICAN JOURNAL OF HUMAN GENETICS 2000
3. BookChapter

   Parkin mutations and idiopathic Parkinson disease (PD).

   Scott WK, Rogala AR, Rampersaud E, Stajich JM, Nance MA, Watts RL, Hubble JP, Scott BL, Haines JL, Koller WC, others

   In AMERICAN JOURNAL OF HUMAN GENETICS 2000

1998:1

1. Journal

   A retrospective cohort analysis investigating the role of calcium channel blockers on cancer incidence

   Rampersaud Evadnie

   1998