Author details

Full Name

Jeffrey Haessler

Affiliation

ORCID

Career Start Year

2007

Papers

102

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37546893	Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus.	medRxiv	2023
37841955	A Type 1 Diabetes Polygenic Score Is Not Associated With Prevalent Type 2 Diabetes in Large Population Studies.	J Endocr Soc	2023
37648373	Ancestral diversity in lipoprotein(a) studies helps address evidence gaps.	Open Heart	2023
37804200	Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk.	J Am Heart Assoc	2023
38076909	Evidence of survival bias in the association between and age of ischemic stroke onset.		2023
37875120	Estimating heritability explained by local ancestry and evaluating stratification bias in admixture mapping from summary statistics.	Am J Hum Genet	2023
37034613	Unraveling Neuro-Proteogenomic Landscape and Therapeutic Implications for Human Behaviors and Psychiatric Disorders.	Res Sq	2023
36824751	Genetic mechanisms of 184 neuro-related proteins in human plasma.	medRxiv	2023
37131817	Estimating heritability explained by local ancestry and evaluating stratification bias in admixture mapping from summary statistics.	bioRxiv	2023
36918541	Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.	Nat Commun	2023
35263625	Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits.	Am J Hum Genet	2022
36050321	Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.	Nat Commun	2022
35387486	Genetic Landscape of the ACE2 Coronavirus Receptor.	Circulation	2022
36154123	Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.	Circulation	2022
35927319	Rare genetic variants explain missing heritability in smoking.	Nat Hum Behav	2022
35729114	A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood.	Nat Commun	2022
35915156	Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.	Nat 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
34743536	Clonal Hematopoiesis Is Associated With Higher Risk of Stroke.	Stroke	2022
34727735	Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project.	Stroke	2022
34376796	Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.	J Hum Genet	2022
34415308	Epigenome-wide association study of mitochondrial genome copy number.	Hum Mol Genet	2021
34107879	Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.	BMC Genomics	2021
34337551	BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion.	HGG Adv	2021
34517814	Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study.	BMC Genomics	2021
30617275	Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci.	Mol Psychiatry	2020
32226016	Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.	PLoS Genet	2020
32439900	Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.	Nat Commun	2020
32822252	Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation.	Circ Genom Precis Med	2020
32693751	Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke.	Stroke	2020
32888494	The Polygenic and Monogenic Basis of Blood Traits and Diseases.	Cell	2020
32888493	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	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
30604766	Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.	Nat Commun	2019
31420334	Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.	Blood	2019
31217584	Genetic analyses of diverse populations improves discovery for complex traits.	Nature	2019
29273807	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29878111	Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study.	Hum Mol Genet	2018
30012220	Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.	Genome Biol	2018
29874175	ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals.	Circ Genom Precis Med	2018
29531354	Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.	Nat Genet	2018
29381148	Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI.	Int J Obes (Lond)	2018
29748316	Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval.	Circ Genom Precis Med	2018
29549330	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29549329	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	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
28346479	Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.	PLoS Genet	2017
28905132	Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium.	Diabetologia	2017