Author details

Full Name

Yuki Bradford

Affiliation

University of Pennsylvania

ORCID

Career Start Year

2001

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36540980	Leveraging Multi-Ancestry Polygenic Risk Scores for Body Mass Index to Predict Antiretroviral Therapy-Induced Weight Gain.	Pac Symp Biocomput	2023
37099271	Pharmacogenetics of tenofovir renal toxicity in HIV-positive Southern Africans.	Pharmacogenet Genomics	2023
37098852	Pharmacogenetics of tenofovir clearance among Southern Africans living with HIV.	Pharmacogenet Genomics	2023
35091749	Pharmacogenetics of Between-Individual Variability in Plasma Clearance of Bedaquiline and Clofazimine in South Africa.	J Infect Dis	2022
35512135	Pharmacogenetics of Dolutegravir Plasma Exposure Among Southern Africans With Human Immunodeficiency Virus.	J Infect Dis	2022
36441943	Quality Control Procedures for Genome-Wide Association Studies.	Curr Protoc	2022
36513072	Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank.	Cell Rep Med	2022
36556195	The Penn Medicine BioBank: Towards a Genomics-Enabled Learning Healthcare System to Accelerate Precision Medicine in a Diverse Population.	J Pers Med	2022
36376295	Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure.	Nat Commun	2022
32829410	Efavirenz Pharmacogenetics and Weight Gain Following Switch to Integrase Inhibitor-Containing Regimens.	Clin Infect Dis	2021
33625064	Genetic Associations with Weight Gain among South Africans who Initiated Dolutegravir-Containing and Tenofovir-Containing Regimens.	J Acquir Immune Defic Syndr	2021
33901188	Tissue specificity-aware TWAS (TSA-TWAS) framework identifies novel associations with metabolic, immunologic, and virologic traits in HIV-positive adults.	PLoS Genet	2021
34140684	A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts.	Nat Genet	2021
34086673	Novel EDGE encoding method enhances ability to identify genetic interactions.	PLoS Genet	2021
33432171	Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations.	Nat Med	2021
32472697	Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium.	Clin Pharmacol Ther	2020
31822125	Mitochondrial DNA Haplogroups and Frailty in Adults Living with HIV.	AIDS Res Hum Retroviruses	2020
33031386	Genetics of height and risk of atrial fibrillation: A Mendelian randomization study.	PLoS Med	2020
30864331	Influence of tissue context on gene prioritization for predicted transcriptome-wide association studies.	Pac Symp Biocomput	2019
31891604	A phenome-wide association study (PheWAS) in the Population Architecture using Genomics and Epidemiology (PAGE) study reveals potential pleiotropy in African Americans.	PLoS One	2019
30894353	Cross-Cancer Pleiotropic Associations with Lung Cancer Risk in African Americans.	Cancer Epidemiol Biomarkers Prev	2019
29216383	Genetic Susceptibility to Postdiarrheal Hemolytic-Uremic Syndrome After Shiga Toxin-Producing Escherichia coli Infection: A Centers for Disease Control and Prevention FoodNet Study.	J Infect Dis	2018
30046033	PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity.	Nat Commun	2018
29847509	Brain neurotransmitter transporter/receptor genomics and efavirenz central nervous system adverse events.	Pharmacogenet Genomics	2018
29618318	A simulation study investigating power estimates in phenome-wide association studies.	BMC Bioinformatics	2018
29218904	Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression.	Pac Symp Biocomput	2018
28099408	Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202.	Pharmacogenet Genomics	2017
28222112	Genome-wide study of resistant hypertension identified from electronic health records.	PLoS One	2017
26169577	A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough.	Pharmacogenomics J	2016
27623284	Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium.	PLoS Genet	2016
27508393	Phenome-Wide Association Study to Explore Relationships between Immune System Related Genetic Loci and Complex Traits and Diseases.	PLoS One	2016
27535653	eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.	BMC Med Genomics	2016
27168765	Identification of genetic interaction networks via an evolutionary algorithm evolved Bayesian network.	BioData Min	2016
26776200	BIOFILTER AS A FUNCTIONAL ANNOTATION PIPELINE FOR COMMON AND RARE COPY NUMBER BURDEN.	Pac Symp Biocomput	2016
26030142	Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.	PLoS One	2015
25969697	The effects of electronic medical record phenotyping details on genetic association studies: HDL-C as a case study.	BioData Min	2015
24952745	Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.	Nat Genet	2014
25414722	Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records.	Front Genet	2014
25436638	Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network.	PLoS One	2014
25566314	Imputation and quality control steps for combining multiple genome-wide datasets.	Front Genet	2014
25177340	Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index.	Front Genet	2014
23463857	Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.	Circulation	2013
24349219	KIAA1462, a coronary artery disease associated gene, is a candidate gene for late onset Alzheimer disease in APOE carriers.	PLoS One	2013
23838604	Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema.	Pharmacogenet Genomics	2013
23755828	Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study.	Lancet	2013
22100668	A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes.	Circ Cardiovasc Genet	2012
21234875	Quality control procedures for genome-wide association studies.	Curr Protoc Hum Genet	2011
22125226	Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.	Genet Epidemiol	2011
21981779	Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.	Am J Hum Genet	2011
19626040	Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.	Genes Immun	2009

1 - 50 of 62

John J Connolly

Center for Applied Genomics, Children's Hospital of Philadelphia

Career Start Year 2012

Number of shared co-authors 77

Emily R Holzinger

National Human Genome Research Institute, National Institutes of Health

Career Start Year 2010

Number of shared co-authors 24

Elizabeth T Cirulli

Duke University

Career Start Year 2007

Number of shared co-authors 7

Jennifer E Below

Vanderbilt Genetics Institute, Vanderbilt University Medical Center

Career Start Year 2007

Number of shared co-authors 83

Ian B Stanaway

Kidney Research Institute and Division of Nephrology, University of Washington

Career Start Year 2006

Number of shared co-authors 65

Steven J Schrodi

University of Wisconsin Madison

Career Start Year 2004

Number of shared co-authors 24

Zolt??n Kutalik

University of Lausanne

Career Start Year 2004

Number of shared co-authors 99

Tushar Bhangale

Genentech Inc.

Career Start Year 2004

Number of shared co-authors 49

Sarah S Murray

University of California San Diego Health System

Career Start Year 2004

Number of shared co-authors 65

Benjamin M Neale

Massachusetts General Hospital

Career Start Year 2002

Number of shared co-authors 85

Andrew S Allen

Duke University School of Medicine

Career Start Year 2001

Number of shared co-authors 5

Chunyu Liu

Boston University School of Public Health

Career Start Year 2001

Number of shared co-authors 89

Andrew D Skol

The University of Chicago

Career Start Year 2001

Number of shared co-authors 15

Weihua Zhang

Imperial College London

Career Start Year 2001

Number of shared co-authors 107

Nathan Pankratz

University of Minnesota

Career Start Year 2001

Number of shared co-authors 84

Jo Knight

Data Science Institute and Lancaster University Medical School

Career Start Year 2000

Number of shared co-authors 49

Elizabeth E Blue

University of Washington

Career Start Year 2000

Number of shared co-authors 11

Nicole Soranzo

Wellcome Sanger Institute

Career Start Year 1998

Number of shared co-authors 96

Andrew P Morris

The University of Manchester

Career Start Year 1997

Number of shared co-authors 126

Michael M Barmada

Graduate School of Public Health, University of Pittsburgh

Career Start Year 1996

Number of shared co-authors 13

Hemant K Tiwari

University of Alabama at Birmingham

Career Start Year 1995

Number of shared co-authors 58

Heather J Cordell

Population Health Sciences Institute, Newcastle University

Career Start Year 1993

Number of shared co-authors 56

William C L Stewart

Middle Tennessee State University

Career Start Year 1992

Number of shared co-authors 3

David B Goldstein

Institute for Genomic Medicine, Columbia University Irving Medical Center

Career Start Year 1992

Number of shared co-authors 45

David Altshuler

Broad Institute of Harvard and Massachusetts Institute of Technology (MIT)

Career Start Year 1992

Number of shared co-authors 94

David A Hinds

23andMe Inc.

Career Start Year 1992

Number of shared co-authors 54

Elizabeth R Hauser

Duke University School of Medicine

Career Start Year 1989

Number of shared co-authors 34

Joel N Hirschhorn

Broad Institute of MIT and Harvard

Career Start Year 1988

Number of shared co-authors 116

Nicholas J Schork

University of California San Diego

Career Start Year 1987

Number of shared co-authors 81

Deborah A Nickerson

University of Washington

Career Start Year 1976

Number of shared co-authors 129

row(s) 1 - 30 of 30

Marylyn D Ritchie

Center for Systems Genomics, Pennsylvania State University, University Park

Co-authored papers 43

Jonathan L Haines

Cleveland Institute for Computational Biology, Case Western Reserve University

Co-authored papers 18

Dana C Crawford

Cleveland Institute for Computational Biology, Case Western Reserve University

Co-authored papers 17

Shefali S Verma

University of Pennsylvania

Co-authored papers 16

Dan M Roden

Vanderbilt University Medical Center

Co-authored papers 13

David W Haas

Vanderbilt University Medical Center

Co-authored papers 13

Iftikhar J Kullo

Mayo Clinic

Co-authored papers 12

Anurag Verma

Corporal Michael J Crescenz VA Medical Center Philadelphia

Co-authored papers 12

Catherine A McCarty

University of Minnesota Medical School, 1035 University Drive duluth

Co-authored papers 11

Gail P Jarvik

University of Washington Medical Center

Co-authored papers 10

Joshua C Denny

Vanderbilt University

Co-authored papers 10

Peggy L Peissig

Center for Precision Medicine Research, Marshfield Clinic Research Institute

Co-authored papers 9

Rongling Li

National Human Genome Research Institute, National Institutes of Health

Co-authored papers 9

Mariza de Andrade

Mayo Clinic

Co-authored papers 8

Rebecca L Zuvich

Center for Human Genetics Research, Vanderbilt University School of Medicine

Co-authored papers 7

Gerard Tromp

Biomedical Research Institute, Stellenbosch University.

Co-authored papers 7

Sarah A Pendergrass

Biomedical and Translational Informatics Institute

Co-authored papers 7

Murray H Brilliant

Marshfield Clinic Research Institute

Co-authored papers 7

Eric B Larson

University of Washington

Co-authored papers 6

Rex L Chisholm

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

Co-authored papers 6

David R Crosslin

University of Washington Medical Center

Co-authored papers 6

Suzette J Bielinski

Mayo Clinic

Co-authored papers 6

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 6

Luke V Rasmussen

Northwestern University Feinberg School of Medicine

Co-authored papers 6

Margaret A Pericak-Vance

Co-authored papers 6

Helena Kuivaniemi

Biomedical Research Institute, Stellenbosch University.

Co-authored papers 5

Daniel J Rader

Co-authored papers 5

David S Carrell