Author details

Full Name

Cristen J Willer

Affiliation

ORCID

Career Start Year

1994

Papers

195

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36723951	Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart Disease.	JAMA Cardiol	2023
36322199	Using Genomic Structural Equation Modeling to Partition the Genetic Covariance Between Birthweight and Cardiometabolic Risk Factors into Maternal and Offspring Components in the Norwegian HUNT Study.	Behav Genet	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
37749248	Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.	Nat Genet	2023
36519469	Bicuspid Aortic Valve-Associated Regulatory Regions Reveal Regulation and Function During Human-Induced Pluripotent Stem Cell-Based Endothelial-Mesenchymal Transition-Brief Report.		2023
36580301	Sex-Specific Survival Bias and Interaction Modeling in Coronary Artery Disease Risk Prediction.		2023
37316478	Unravelling the genetic architecture of human complex traits through whole genome sequencing.		2023
37308786	Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program.	Nat Genet	2023
37186683	Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease.	Circulation	2023
36739617	A fast linkage method for population GWAS cohorts with related individuals.	Genet Epidemiol	2023
35092149	Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility.	American Journal of Medical Genetics, Part A	2022
35710628	Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT.	Commun Biol	2022
36220816	Whole genome sequence analysis of blood lipid levels in >66,000 individuals.	Nat Commun	2022
35697829	Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.	Commun Biol	2022
36154123	Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.	Circulation	2022
35876838	Incorporating family disease history and controlling case-control imbalance for population-based genetic association studies.		2022
35862132	Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association.	Circulation	2022
35546142	Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits.	Nature Communications	2022
36194491	Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis.	J Clin Invest	2022
35726068	Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease.	Nat Genet	2022
35918347	Author Correction: Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits.	Nature Communications	2022
35534559	Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects.	Nat Genet	2022
36777998	The HUNT study: A population-based cohort for genetic research.	Cell Genom	2022
36477530	Genetic diversity fuels gene discovery for tobacco and alcohol use.	Nature	2022
34102292	Cardiorespiratory Fitness After Open Repair for Acute Type A Aortic Dissection - A Prospective Study.	Seminars in Thoracic and Cardiovascular Surgery	2022
32684393	Gait speed is a preoperative indicator of postoperative events after elective proximal aortic surgery.	Journal of Thoracic and Cardiovascular Surgery	2022
34793753	Differences in Inflammation, Treatment, and Outcomes Between Black and Non-Black Patients Hospitalized for COVID-19: A Prospective Cohort Study.	American Journal of Medicine	2022
35231079	Identification of cell type specific ACE2 modifiers by CRISPR screening.	PLoS Pathogens	2022
35195259	A polygenic risk score improves risk stratification of coronary artery disease: a large-scale prospective Chinese cohort study.	Eur Heart J	2022
34773122	Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease.	Nat Genet	2021
36282123	Genetic insight into sick sinus syndrome.	Eur Heart J	2021
32199657	Aortic progression and reintervention in patients with pathogenic variants after a thoracic aortic dissection.	Journal of Thoracic and Cardiovascular Surgery	2021
34127970	Identification of ACE2 modifiers by CRISPR screening.		2021
33693786	An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population.	Hum Mol Genet	2021
33961016	Genome-wide association study of cardiac troponin I in the general population.	Hum Mol Genet	2021
33580673	Genetic insight into sick sinus syndrome.	Eur Heart J	2021
33846329	Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.	Nat Commun	2021
34272381	Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals.	Nat Commun	2021
34265237	Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm.	Am J Hum Genet	2021
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2021
34151951	The causal effects of serum lipids and apolipoproteins on kidney function: multivariable and bidirectional Mendelian-randomization analyses.	Int J Epidemiol	2021
33662382	GWAS Identifies LINC01184/SLC12A2 as a Risk Locus for Skin and Soft Tissue Infections.	J Invest Dermatol	2021
33513160	Genome-scale CRISPR screening for modifiers of cellular LDL uptake.	PLoS Genet	2021
33604704	Translating genetic association of lipid levels for biological and clinical application.	Cardiovascular Drugs and Therapy	2021
34031205	Development and Validation of a Polygenic Risk Score for Stroke in the Chinese Population.	Neurology	2021
33556117	Exposure and risk factors for COVID-19 and the impact of staying home on Michigan residents.	PLoS ONE	2021
33597122	Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.	J Am Soc Nephrol	2021
33648514	Disclosure of clinically actionable genetic variants to thoracic aortic dissection biobank participants.	BMC Med Genomics	2021
33319384	A survey of aortic disease biorepository participants' preferences for return of research genetic results.	J Genet Couns	2021
32822663	Complex and Potentially Harmful Medication Patterns in Heart Failure with Preserved Ejection Fraction.	American Journal of Medicine	2021