Contributions of rare coding variants in hypotension syndrome genes to population blood pressure variation

por Nandakumar, Priyanka, Morrison, Alanna C., Grove, Megan L., Boerwinkle, Eric, Chakravarti, Aravinda
Publicado 2018

MicroRNAs in the miR-17 and miR-15 families are downregulated in chronic kidney disease with hypertension

por Nandakumar, Priyanka, Tin, Adrienne, Grove, Megan L., Ma, Jianzhong, Boerwinkle, Eric, Coresh, Josef, Chakravarti, Aravinda
Publicado 2017

Imputation of missing covariate values in epigenome-wide analysis of DNA methylation data

por Wu, Chong, Demerath, Ellen W., Pankow, James S., Bressler, Jan, Fornage, Myriam, Grove, Megan L., Chen, Wei, Guan, Weihua
Publicado 2016

Rare coding TTN variants are associated with electrocardiographic QT interval in the general population

por Kapoor, Ashish, Bakshy, Kiranmayee, Xu, Linda, Nandakumar, Priyanka, Lee, Dongwon, Boerwinkle, Eric, Grove, Megan L., Arking, Dan E., Chakravarti, Aravinda
Publicado 2016

Medical implications of technical accuracy in genome sequencing

por Goldfeder, Rachel L., Priest, James R., Zook, Justin M., Grove, Megan E., Waggott, Daryl, Wheeler, Matthew T., Salit, Marc, Ashley, Euan A.
Publicado 2016

Cerebral white matter hyperintensities on MRI and acceleration of epigenetic aging: the atherosclerosis risk in communities study

por Raina, Abhay, Zhao, Xiaoping, Grove, Megan L., Bressler, Jan, Gottesman, Rebecca F., Guan, Weihua, Pankow, James S., Boerwinkle, Eric, Mosley, Thomas H., Fornage, Myriam
Publicado 2017

Detoxification Role of Metabolic Glutathione S-Transferase (GST) Genes in Blood Lead Concentrations of Jamaican Children with and without Autism Spectrum Disorder

por Rahbar, Mohammad H., Samms-Vaughan, Maureen, Kim, Sori, Saroukhani, Sepideh, Bressler, Jan, Hessabi, Manouchehr, Grove, Megan L., Shakspeare-Pellington, Sydonnie, Loveland, Katherine A.
Publicado 2022

Interactions between Environmental Factors and Glutathione S-Transferase (GST) Genes with Respect to Detectable Blood Aluminum Concentrations in Jamaican Children

por Rahbar, Mohammad H., Samms-Vaughan, Maureen, Zhao, Yuansong, Saroukhani, Sepideh, Bressler, Jan, Hessabi, Manouchehr, Grove, Megan L., Shakespeare-Pellington, Sydonnie, Loveland, Katherine A.
Publicado 2022

Associations of Metabolic Genes (GSTT1, GSTP1, GSTM1) and Blood Mercury Concentrations Differ in Jamaican Children with and without Autism Spectrum Disorder

por Rahbar, Mohammad H., Samms-Vaughan, Maureen, Saroukhani, Sepideh, Bressler, Jan, Hessabi, Manouchehr, Grove, Megan L., Shakspeare-Pellington, Sydonnie, Loveland, Katherine A., Beecher, Compton, McLaughlin, Wayne
Publicado 2021

Additive and Interactive Associations of Environmental and Sociodemographic Factors with the Genotypes of Three Glutathione S-Transferase Genes in Relation to the Blood Arsenic Con...

por Rahbar, Mohammad H., Samms-Vaughan, Maureen, Zhao, Yuansong, Saroukhani, Sepideh, Zaman, Sheikh F., Bressler, Jan, Hessabi, Manouchehr, Grove, Megan L., Shakspeare-Pellington, Sydonnie, Loveland, Katherine A.
Publicado 2022

Blood manganese concentrations in Jamaican children with and without autism spectrum disorders

por Rahbar, Mohammad H, Samms-Vaughan, Maureen, Dickerson, Aisha S, Loveland, Katherine A, Ardjomand-Hessabi, Manouchehr, Bressler, Jan, Shakespeare-Pellington, Sydonnie, Grove, Megan L, Pearson, Deborah A, Boerwinkle, Eric
Publicado 2014

Blood Lead Concentrations in Jamaican Children with and without Autism Spectrum Disorder

por Rahbar, Mohammad H., Samms-Vaughan, Maureen, Dickerson, Aisha S., Loveland, Katherine A., Ardjomand-Hessabi, Manouchehr, Bressler, Jan, Shakespeare-Pellington, Sydonnie, Grove, Megan L., Pearson, Deborah A., Boerwinkle, Eric
Publicado 2014

Clinical utility of genomic sequencing: a measurement toolkit

por Hayeems, Robin Z., Dimmock, David, Bick, David, Belmont, John W., Green, Robert C., Lanpher, Brendan, Jobanputra, Vaidehi, Mendoza, Roberto, Kulkarni, Shashi, Grove, Megan E., Taylor, Stacie L., Ashley, Euan
Publicado 2020

An epigenome-wide study of obesity in African American youth and young adults: novel findings, replication in neutrophils, and relationship with gene expression

por Wang, Xiaoling, Pan, Yue, Zhu, Haidong, Hao, Guang, Huang, Yisong, Barnes, Vernon, Shi, Huidong, Snieder, Harold, Pankow, James, North, Kari, Grove, Megan, Guan, Weihua, Demerath, Ellen, Dong, Yanbin, Su, Shaoyong
Publicado 2018

Role of Metabolic Genes in Blood Arsenic Concentrations of Jamaican Children with and without Autism Spectrum Disorder

por Rahbar, Mohammad H., Samms-Vaughan, Maureen, Ma, Jianzhong, Bressler, Jan, Loveland, Katherine A., Ardjomand-Hessabi, Manouchehr, Dickerson, Aisha S., Grove, Megan L., Shakespeare-Pellington, Sydonnie, Beecher, Compton, McLaughlin, Wayne, Boerwinkle, Eric
Publicado 2014

Concentration of Lead, Mercury, Cadmium, Aluminum, Arsenic and Manganese in Umbilical Cord Blood of Jamaican Newborns

por Rahbar, Mohammad H., Samms-Vaughan, Maureen, Dickerson, Aisha S., Hessabi, Manouchehr, Bressler, Jan, Coore Desai, Charlene, Shakespeare-Pellington, Sydonnie, Reece, Jody-Ann, Morgan, Renee, Loveland, Katherine A., Grove, Megan L., Boerwinkle, Eric
Publicado 2015

Hypertensive APOL1 risk allele carriers demonstrate greater blood pressure reduction with angiotensin receptor blockade compared to low risk carriers

por Cunningham, Patrick N., Wang, Zhiying, Grove, Megan L., Cooper-DeHoff, Rhonda M., Beitelshees, Amber L., Gong, Yan, Gums, John G., Johnson, Julie A., Turner, Stephen T., Boerwinkle, Eric, Chapman, Arlene B.
Publicado 2019

Evaluation of microarray-based DNA methylation measurement using technical replicates: the Atherosclerosis Risk In Communities (ARIC) Study

por Bose, Maitreyee, Wu, Chong, Pankow, James S, Demerath, Ellen W, Bressler, Jan, Fornage, Myriam, Grove, Megan L, Mosley, Thomas H, Hicks, Chindo, North, Kari, Hong Kao, Wen, Zhang, Yu, Boerwinkle, Eric, Guan, Weihua
Publicado 2014

A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data

por Battle, Stephanie L, Puiu, Daniela, Verlouw, Joost, Broer, Linda, Boerwinkle, Eric, Taylor, Kent D, Rotter, Jerome I, Rich, Stephan S, Grove, Megan L, Pankratz, Nathan, Fetterman, Jessica L, Liu, Chunyu, Arking, Dan E
Publicado 2022

Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome

por Polfus, Linda M., Boerwinkle, Eric, Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Grove, Megan, Shete, Sanjay, Wallace, Stephanie, Milewicz, Dianna, Hanchard, Neil, Lupski, James R., Hashmi, Syed Shahrukh, Gupta-Malhotra, Monesha
Publicado 2016