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

di András, Ibolya E., Rampersaud, Evadnie, Eum, Sung Yong, Toborek, Michal
Pubblicato in Arch Med Res (2014)

Investigating parent of origin effects in studies of Type 2 Diabetes and Obesity

di Rampersaud, Evadnie, Mitchell, Braxton D., Naj, Adam C., Pollin, Toni I.
Pubblicazione 2008

Rare variant mutations identified in pediatric patients with dilated cardiomyopathy

di Rampersaud, Evadnie, Siegfried, Jill D, Norton, Nadine, Li, Duanxiang, Martin, Eden, Hershberger, Ray E
Pubblicazione 2011

Exercise Attenuates PCB-Induced Changes in the Mouse Gut Microbiome

di Choi, Jeong June, Eum, Sung Yong, Rampersaud, Evadnie, Daunert, Sylvia, Abreu, Maria T., Toborek, Michal
Pubblicazione 2013

Defining a molecular portrait of physical fitness

di Clouse, Adam, Deo, Sapna, Rampersaud, Evadnie, Farmer, Jeff, Goldschmidt-Clermont, Pascal J., Daunert, Sylvia
Pubblicazione 2013

Common susceptibility variants examined for association with dilated cardiomyopathy

di Rampersaud, Evadnie, Kinnamon, Daniel D., Hamilton, Kara, Khuri, Sawsan, Hershberger, Ray E., Martin, Eden R.
Pubblicazione 2010

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

di Brodt, Chad, Siegfried, Jill D., Hofmeyer, Mark, Martel, Jose, Rampersaud, Evadnie, Li, Duanxiang, Morales, Ana, Hershberger, Ray E.
Pubblicazione 2013

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

di Veerapen, Muthu Kumar, Pelaez, Liset, Potter, JoNell Efantis, Duthely, Lunthita, Birusingh, Rhea, Rampersaud, Evadnie, Bodamer, Olaf A, Rodriguez, Maria Matilde
Pubblicazione 2014

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

di Zahr, Rima S., Rampersaud, Evadnie, Kang, Guolian, Weiss, Mitchell J., Wu, Gang, Davis, Robert L., Hankins, Jane S., Estepp, Jeremie H., Lebensburger, Jeffrey
Pubblicato in Haematologica (2019)

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

di Norton, Nadine, Robertson, Peggy D., Rieder, Mark J., Zuchner, Stephan, Rampersaud, Evadnie, Martin, Eden, Li, Duanxiang, Nickerson, Deborah A., Hershberger, Ray E.
Pubblicazione 2012

Regional Differential Genetic Response of Human Articular Cartilage to Impact Injury

di Vernon, Lauren L., Vance, Danica D., Wang, Liyong, Rampersaud, Evadnie, Vance, Jeffery M., Pericak-Vance, Margaret, Huang, C.-Y. Charles, Kaplan, Lee D.
Pubblicato in Cartilage (2015)

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

di Rampersaud, Evadnie, Allen, Andrew, Li, Yi-Ju, Shao, Yujun, Bass, Meredyth, Haynes, Carol, Ashley-Koch, Allison, Martin, Eden R, Schmidt, Silke, Hauser, Elizabeth R
Pubblicazione 2003

Extent and Distribution of Linkage Disequilibrium in the Old Order Amish

di Van Hout, Cristopher V, Levin, Albert M, Rampersaud, Evadnie, Shen, Haiqing, O'Connell, Jeffrey R, Mitchell, Braxton D, Shuldiner, Alan R, Douglas, Julie A
Pubblicazione 2010

Generalization of a genetic risk score for time to first albuminuria in children with sickle cell anemia: SCCRIP cohort study results

di Rashkin, Sara R., Rampersaud, Evadnie, Kang, Guolian, Ataga, Kenneth I., Hankins, Jane S., Wang, Winfred, Estepp, Jeremie H., Weiss, Mitchell J., Lebensburger, Jeffrey, Zahr, Rima S.
Pubblicato in Br J Haematol (2021)

Serum 25-hydroxyvitamin D levels are not associated with subclinical vascular disease or C-reactive protein in the Old Order Amish

di 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
Pubblicazione 2009

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

di 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
Pubblicazione 2014

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

di Nel, Melissa, Mavundla, Thandeka, Gultig, Kayleigh, Botha, Gerrit, Mulder, Nicola, Benatar, Michael, Wuu, Joanne, Cooley, Anne, Myers, Jason, Rampersaud, Evadnie, Wu, Gang, Heckmann, Jeannine M.
Pubblicato in IBRO Neurosci Rep (2021)

A Duplication in Chromosome 4q35 Is Associated with Hereditary Benign Intraepithelial Dyskeratosis

di Allingham, R. Rand, Seo, Ben, Rampersaud, Evadnie, Bembe, MaryLou, Challa, Pratap, Liu, Ningpu, Parrish, Tanisha, Karolak, Linda, Gilbert, John, Pericak-Vance, Margaret A., Klintworth, Gordon K., Vance, Jeffery M.
Pubblicazione 2001

Physical Activity and the Association of Common FTO Gene Variants With Body Mass Index and Obesity

di 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, Shuldiner, Alan R., Snitker, Soren
Pubblicazione 2008

Genetic Characterization and Influence on Inflammatory Bowel Disease Expression in a Diverse Hispanic South Florida Cohort

di 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, McCauley, Jacob L
Pubblicato in Clin Transl Gastroenterol (2017)