Author details

Full Name

Jennifer A Brody

Affiliation

ORCID

Career Start Year

2012

Papers

167

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37916415	Polygenic Risk Score Associates With Atherosclerotic Plaque Characteristics at Autopsy.	Arterioscler Thromb Vasc Biol	2024
37546893	Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus.	medRxiv	2023
35943854	Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI.	Brain	2023
36444934	Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.	Hum Mol Genet	2023
37936531	Proteomic prediction of incident heart failure and its main subtypes.		2023
38028628	Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.	Front Genet	2023
37662265	WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.	medRxiv	2023
38014529	Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis.	Circ Genom Precis Med	2023
37923804	Identification of circulating proteins associated with general cognitive function among middle-aged and older adults.	Commun Biol	2023
37904051	Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.	Nat Genet	2023
37961350	A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.	bioRxiv	2023
37868038	The functional impact of rare variation across the regulatory cascade.	Cell Genom	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
36778386	Structural variation across 138,134 samples in the TOPMed consortium.	Res Sq	2023
37399490	Polygenic risk of major depressive disorder as a risk factor for venous thromboembolism.	Blood Adv	2023
36960714	Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program.	Circ Genom Precis Med	2023
37461703	Polygenic Risk Score Associates with Atherosclerotic Plaque Characteristics at Autopsy.	bioRxiv	2023
37398003	Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.	medRxiv	2023
37126548	The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.	Sci Adv	2023
36747810	Structural variation across 138,134 samples in the TOPMed consortium.	bioRxiv	2023
37046083	Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.	Nature	2023
36791419	Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.	Diabetes	2023
36918541	Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.	Nat Commun	2023
34553764	Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.	Hum Mol Genet	2022
36180445	Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.	Nat Commun	2022
36050321	Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.	Nat Commun	2022
35592775	The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.	Front Endocrinol (Lausanne)	2022
36042188	Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.	Nat Commun	2022
35652341	Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.	Hypertension	2022
35446786	Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases.	JCI Insight	2022
36097025	Clonal hematopoiesis of indeterminate potential, DNA methylation, and risk for coronary artery disease.	Nat Commun	2022
35822943	Targeted Genome Sequencing Identifies Multiple Rare Variants inÂ Caveolin-1 Associated with Obstructive Sleep Apnea.	Am J Respir Crit Care Med	2022
35504910	DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases.	Nat Commun	2022
36220816	Whole genome sequence analysis of blood lipid levels in >66,000 individuals.	Nat Commun	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
35995843	Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populations.	Commun Biol	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
36267918	Genome-wide analyses identify <i>SCN5A</i> as a susceptibility locus for premature atrial contraction frequency.	iScience	2022
35927319	Rare genetic variants explain missing heritability in smoking.	Nat Hum Behav	2022
35790642	Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing.	Eur J Epidemiol	2022
35546478	Integrative analysis of clinical and epigenetic biomarkers of mortality.	Aging Cell	2022
35536696	Pulmonary Function and Blood DNA Methylation: A Multiancestry Epigenome-Wide Association Meta-analysis.	Am J Respir Crit Care Med	2022
36568030	Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants.	HGG Adv	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
34789503	Obesity Partially Mediates the Diabetogenic Effect of Lowering LDL Cholesterol.	Diabetes Care	2022
34582791	Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.	Am J Hum Genet	2021
34230475	Publisher Correction: A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids.	Nat Commun	2021
33846329	Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.	Nat Commun	2021
33887194	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.	Am J Hum Genet	2021