Author details

Full Name

Rongling Li

Affiliation

National Human Genome Research Institute, National Institutes of Health

ORCID

Career Start Year

1994

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35488921	The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review.	Hum Genet	2022
35488921	The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review.	Hum Genet	2022
32964493	Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network.	Genet Epidemiol	2021
32964493	Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network.	Genet Epidemiol	2021
32174366	Machine learning algorithms applied to a prediction of personal overall thermal comfort using skin temperatures and occupants' heating behavior.	Appl Ergon	2020
32174366	Machine learning algorithms applied to a prediction of personal overall thermal comfort using skin temperatures and occupants' heating behavior.	Appl Ergon	2020
32274338	Identification of a dynamic system model for a building and heating system including heat pump and thermal energy storage.	MethodsX	2020
32274338	Identification of a dynamic system model for a building and heating system including heat pump and thermal energy storage.	MethodsX	2020
30298529	The eMERGE genotype set of 83,717 subjects imputed to ~40â¿¿million variants genome wide and association with the herpes zoster medical record phenotype.	Genet Epidemiol	2019
30590688	Enrichment sampling for a multi-site patient survey using electronic health records and census data.	J Am Med Inform Assoc	2019
30298529	The eMERGE genotype set of 83,717 subjects imputed to ~40â¿¿million variants genome wide and association with the herpes zoster medical record phenotype.	Genet Epidemiol	2019
31311600	GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.	BMC Med	2019
31311600	GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network.	BMC Med	2019
30590688	Enrichment sampling for a multi-site patient survey using electronic health records and census data.	J Am Med Inform Assoc	2019
29301385	Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.	J Pers Med	2018
30240342	Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey.	AJOB Empir Bioeth	2018
29301385	Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.	J Pers Med	2018
30240342	Parents' attitudes toward consent and data sharing in biobanks: A multisite experimental survey.	AJOB Empir Bioeth	2018
27867202	Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations.	Int J Obes (Lond)	2017
28391526	Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci.	Hum Genet	2017
28335839	Apolipoprotein L1 VariantsÂ and Blood Pressure Traits inÂ African Americans.	J Am Coll Cardiol	2017
29037375	Modelling hand skin temperature in relation to body composition.	J Therm Biol	2017
28222112	Genome-wide study of resistant hypertension identified from electronic health records.	PLoS One	2017
28203683	Identification of unique venous thromboembolism-susceptibility variants in African-Americans.	Thromb Haemost	2017
27867202	Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations.	Int J Obes (Lond)	2017
28190457	Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.	Am J Hum Genet	2017
28335839	Apolipoprotein L1 VariantsÂ and Blood Pressure Traits inÂ African Americans.	J Am Coll Cardiol	2017
28222112	Genome-wide study of resistant hypertension identified from electronic health records.	PLoS One	2017
28190457	Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.	Am J Hum Genet	2017
28391526	Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci.	Hum Genet	2017
28203683	Identification of unique venous thromboembolism-susceptibility variants in African-Americans.	Thromb Haemost	2017
29037375	Modelling hand skin temperature in relation to body composition.	J Therm Biol	2017
26169577	A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough.	Pharmacogenomics J	2016
26746457	Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.	JAMA	2016
26912863	The phenotypic legacy of admixture between modern humans and Neandertals.	Science	2016
26857349	Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network.	Clin Pharmacol Ther	2016
26169577	A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough.	Pharmacogenomics J	2016
27881091	Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions.	BMC Med Res Methodol	2016
27535653	eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.	BMC Med Genomics	2016
27881091	Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions.	BMC Med Res Methodol	2016
27535653	eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.	BMC Med Genomics	2016
26912863	The phenotypic legacy of admixture between modern humans and Neandertals.	Science	2016
26746457	Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.	JAMA	2016
26857349	Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network.	Clin Pharmacol Ther	2016
25297839	Genetic variation in the HLA region is associated with susceptibility to herpes zoster.	Genes Immun	2015
25297839	Genetic variation in the HLA region is associated with susceptibility to herpes zoster.	Genes Immun	2015
26142422	CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.	J Am Med Inform Assoc	2015
26473487	The Association of Serum Leptin with Mortality in Older Adults.	PLoS One	2015
26473487	The Association of Serum Leptin with Mortality in Older Adults.	PLoS One	2015
26142422	CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.	J Am Med Inform Assoc	2015

1 - 50 of 196

Leo-Pekka Lyytik??inen

Tampere University

Career Start Year 2009

Number of shared co-authors 90

Adam S Butterworth

British Heart Foundation Cardiovascular Epidemiology Unit, University of Cambridge

Career Start Year 2006

Number of shared co-authors 69

Jasmin Divers

Wake Forest School of Medicine.

Career Start Year 2006

Number of shared co-authors 51

Amit Patki

School of Public Health, University of Alabama at Birmingham

Career Start Year 2005

Number of shared co-authors 32

Venkata Saroja Voruganti

University of North Carolina Gillings School of Global Public Health

Career Start Year 2005

Number of shared co-authors 21

Todd L Edwards

Vanderbilt University Medical Center

Career Start Year 2004

Number of shared co-authors 119

Bamidele O Tayo

Loyola University Medical Center.

Career Start Year 2002

Number of shared co-authors 67

Jeanette J McCarthy

Fabric Genomics Inc.

Career Start Year 2000

Number of shared co-authors 2

Scott M Damrauer

Perelman School of Medicine, University of Pennsylvania

Career Start Year 1999

Number of shared co-authors 72

Murielle Bochud

University of Lausanne

Career Start Year 1999

Number of shared co-authors 64

Erik Ingelsson

Stanford University School of Medicine

Career Start Year 1998

Number of shared co-authors 97

Kenneth J Mukamal

Beth Israel Deaconess Medical Center

Career Start Year 1998

Number of shared co-authors 41

John C Chambers

Lee Kong Chian School of Medicine, Nanyang Technological University

Career Start Year 1997

Number of shared co-authors 83

Sharon L R Kardia

School of Public Health, University of Michigan ann arbor

Career Start Year 1997

Number of shared co-authors 96

Harold Snieder

University of Groningen, University Medical Center Groningen

Career Start Year 1997

Number of shared co-authors 82

Hemant K Tiwari

University of Alabama at Birmingham

Career Start Year 1995

Number of shared co-authors 82

Nicholas L Smith

University of Washington

Career Start Year 1994

Number of shared co-authors 86

Joanne M Murabito

Boston University School of Medicine

Career Start Year 1990

Number of shared co-authors 68

Yuling Hong

and Blood Institute

Career Start Year 1990

Number of shared co-authors 10

Carl D Langefeld

Wake Forest University School of Medicine

Career Start Year 1990

Number of shared co-authors 83

Terho Lehtim??ki

Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University

Career Start Year 1990

Number of shared co-authors 104

Elizabeth R Hauser

Duke University School of Medicine

Career Start Year 1989

Number of shared co-authors 24

Shih-Jen Hwang

and Blood Institute

Career Start Year 1988

Number of shared co-authors 57

Peter Kraft

Harvard T. H. Chan School of Public Health

Career Start Year 1988

Number of shared co-authors 106

Daniel I Chasman

Harvard Medical School, Harvard University

Career Start Year 1987

Number of shared co-authors 120

Vincent Mooser

McGill University

Career Start Year 1987

Number of shared co-authors 46

Stephen T Turner

Mayo Clinic

Career Start Year 1984

Number of shared co-authors 62

John Beilby

University of Western Australia

Career Start Year 1980

Number of shared co-authors 54

Charles N Rotimi

Center for Research on Genomics and Global Health, National Institutes of Health

Career Start Year 1980

Number of shared co-authors 82

Albert Hofman

Harvard T.H. Chan School of Public Health

Career Start Year 1952

Number of shared co-authors 128

row(s) 1 - 30 of 30

Marylyn D Ritchie

Center for Systems Genomics, Pennsylvania State University, University Park

Co-authored papers 32

Gail P Jarvik

University of Washington Medical Center

Co-authored papers 31

Iftikhar J Kullo

Mayo Clinic

Co-authored papers 28

Tamara B Harris

National Institute on Aging

Co-authored papers 27

Joshua C Denny

Vanderbilt University

Co-authored papers 25

Catherine A McCarty

University of Minnesota Medical School, 1035 University Drive duluth

Co-authored papers 24

Dana C Crawford

Cleveland Institute for Computational Biology, Case Western Reserve University

Co-authored papers 20

David R Crosslin

University of Washington Medical Center

Co-authored papers 20

Eric B Larson

University of Washington

Co-authored papers 19

Rex L Chisholm

Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University

Co-authored papers 18

Dan M Roden

Vanderbilt University Medical Center

Co-authored papers 17

Christopher G Chute

Brown University, Brown University Warren Alpert Medical School, Dartmouth-Hitchcock Medical Center, Harvard School of Public Health, Johns Hopkins Medicine, Mayo Clinic Minnesota

Co-authored papers 17

David S Carrell

Kaiser Permanente Washington Health Research Institute

Co-authored papers 17

Jennifer A Pacheco

University of Pennsylvania

Co-authored papers 14

Abel N Kho

Northwestern University Feinberg School of Medicine

Co-authored papers 14

Mariza de Andrade

Mayo Clinic