Author details

Full Name

Jennifer E Huffman

Affiliation

ORCID

Career Start Year

2009

Papers

142

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37425708	Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program.	medRxiv	2023
37601974	Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries.	Cell Genom	2023
37777856	GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors.	Am J Psychiatry	2023
36716967	DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood.	J Thromb Haemost	2023
37268629	Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups.	Nat Commun	2023
37398003	Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.	medRxiv	2023
36696182	Novel genetic regulators of fibrinogen synthesis identified by an in vitro experimental platform.	J Thromb Haemost	2023
36940203	Genome-wide association study identifies four pan-ancestry loci for suicidal ideation in the Million Veteran Program.	PLoS Genet	2023
37429843	Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure.	Nat Commun	2023
35138379	Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits.	Hum Mol Genet	2022
35771531	A <i>MUC5B</i> Gene Polymorphism, rs35705950-T, Confers Protective Effects Against COVID-19 Hospitalization but Not Severe Disease or Mortality.	Am J Respir Crit Care Med	2022
35654975	A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.	Nat Genet	2022
35653334	A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program.	PLoS Genet	2022
35759254	Association of Kidney Comorbidities and Acute Kidney Failure With Unfavorable Outcomes After COVID-19 in Individuals With the Sickle Cell Trait.	JAMA Intern Med	2022
36154123	Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.	Circulation	2022
35552711	Whole-exome sequencing of 14â¿¿389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.	Hum Mol Genet	2022
35482673	A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program.	PLoS Genet	2022
35915156	Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.	Nat Med	2022
35027740	Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19.	Nat Genet	2022
35228297	Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin.	J Am Soc Nephrol	2022
35347246	A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci.	Mol Psychiatry	2022
35222515	Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program.	Front Genet	2022
32847391	Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease-Brief Report.	Arterioscler Thromb Vasc Biol	2021
33791713	Alternative splicing of OAS1 alters the risk for severe COVID-19.	medRxiv	2021
33837377	Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19.	Nat Med	2021
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2021
34210154	Effects of Thyroid Function on Hemostasis, Coagulation, and Fibrinolysis: A Mendelian Randomization Study.	Thyroid	2021
33984066	Phenome-wide association of 1809 phenotypes and COVID-19 disease progression in the Veterans Health Administration Million Veteran Program.	PLoS One	2021
32989287	Genome-wide association study identifies 48 common genetic variants associated with handedness.	Nat Hum Behav	2021
32888493	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Cell	2020
32336198	Platelet Reactivity in Individuals Over 65 Years Old Is Not Modulated by Age.	Circ Res	2020
33230300	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2020
33166319	PCSK9 loss of function is protective against extra-coronary atherosclerotic cardiovascular disease in a large multi-ethnic cohort.	PLoS One	2020
32661250	The choline transporter Slc44a2 controls platelet activation and thrombosis by regulating mitochondrial function.	Nature Communications	2020
32888494	The Polygenic and Monogenic Basis of Blood Traits and Diseases.	Cell	2020
31160809	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2019
31613361	High-throughput multimodal automated phenotyping (MAP) with application to PheWAS.	J Am Med Inform Assoc	2019
30642921	A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology.	Blood	2019
29185836	Exome-chip meta-analysis identifies association between variation in ANKRD26 and platelet aggregation.	Platelets	2019
31285632	Genome-wide association study of peripheral artery disease in the Million Veteran Program.	Nat Med	2019
31420334	Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.	Blood	2019
29273807	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
30315176	Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels.	Nat Commun	2018
29892015	Multi-ethnic genome-wide association study for atrial fibrillation.	Nat Genet	2018
30498205	Examining the current standards for genetic discovery and replication in the era of mega-biobanks.	Nature Communications	2018
29874175	ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals.	Circ Genom Precis Med	2018
30429575	Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.	Nat Genet	2018
30042098	DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis.	Blood	2018
30275531	Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.	Nat Genet	2018
30224653	Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.	Nat Genet	2018