Author details

Full Name

Henry J Lin

Affiliation

ORCID

Career Start Year

1985

Papers

105

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36918541	Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.	Nat Commun	2023
37868038	The functional impact of rare variation across the regulatory cascade.	Cell Genom	2023
37268629	Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups.	Nat Commun	2023
35287717	Glucose-6-phosphate dehydrogenase deficiency presenting with rhabdomyolysis in a patient with coronavirus disease 2019 pneumonia: aÂ case report.	Journal of Medical Case Reports	2022
36180445	Publisher Correction: Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.	Nat Commun	2022
35594314	Resting heart rate and incident atrial fibrillation: A stratified Mendelian randomization in the AFGen consortium.	PLoS One	2022
36042188	Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.	Nat Commun	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
35389749	Monogenic and Polygenic Contributions to QTc Prolongation in the Population.	Circulation	2022
35952728	Association of polygenic risk scores with incident atherosclerotic cardiovascular disease events among individuals with coronary artery calcium score of zero: The multi-ethnic study of atherosclerosis.	Prog Cardiovasc Dis	2022
36334310	Association of a Multiancestry Genome-Wide Blood Pressure Polygenic Risk Score With Adverse Cardiovascular Events.	Circ Genom Precis Med	2022
35995843	Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populations.	Commun Biol	2022
35738636	Pediatric Patients With Sickle Cell Disease at a Public Hospital: Nutrition, Compliance and Early Experience With L-Glutamine Therapy.	In Vivo	2022
36267918	Genome-wide analyses identify <i>SCN5A</i> as a susceptibility locus for premature atrial contraction frequency.	iScience	2022
35729114	A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood.	Nat Commun	2022
36050321	Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.	Nat Commun	2022
34732054	Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation.	Circ Genom Precis Med	2021
33536627	Author Correction: A structural variation reference for medical and population genetics.	Nature	2021
34319147	Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis.	Circ Genom Precis Med	2021
34405853	Conserved L464 in p97 D1-D2 linker is critical for p97 cofactor regulated ATPase activity.	Biochemical Journal	2021
32602732	Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits.	Circ Genom Precis Med	2020
32439900	Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.	Nat Commun	2020
32933497	Mitochondrial DNA copy number and incident atrial fibrillation.	BMC Med	2020
32822252	Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation.	Circ Genom Precis Med	2020
32498805	An Outbreak of Polygenic Scores for Coronary Artery Disease.	Journal of the American College of Cardiology	2020
31251759	GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations.	PLoS One	2019
30166628	De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathy.	Genet Med	2019
31221261	Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals.	J Am Coll Cardiol	2019
27958378	Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.	Pharmacogenomics J	2018
28719597	Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology.	Pharmacogenomics J	2018
29892015	Multi-ethnic genome-wide association study for atrial fibrillation.	Nat Genet	2018
29874175	ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals.	Circ Genom Precis Med	2018
30202204	Community Partnership in Precision Medicine: Themes from a Community Engagement Conference.	Ethn Dis	2018
30057031	IRF2BPL Is Associated with Neurological Phenotypes.	Am J Hum Genet	2018
30012220	Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.	Genome Biol	2018
30193138	IRF2BPL Is Associated with Neurological Phenotypes.	Am J Hum Genet	2018
30046033	PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity.	Nat Commun	2018
29715082	Efficacy of Asparaginase With and Without Temozolomide Against Glioma Cells and Intracranial Mouse Medulloblastoma.	Anticancer Research	2018
29618737	Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy.	Sci Rep	2018
29127183	Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at <i>ID2</i>.	Heart	2018
29748316	Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval.	Circ Genom Precis Med	2018
29105928	Lego bricks and the octet rule: Molecular models for biochemical pathways with plastic, interlocking toy bricks.	Biochemistry and Molecular Biology Education	2018
28039329	A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	J Med Genet	2017
28767105	Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk.	Nat Commun	2017
28900195	Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium.	Sci Rep	2017
28379579	Discovery of novel heart rate-associated loci using the Exome Chip.	Hum Mol Genet	2017
28416818	Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.	Nat Genet	2017
28334935	Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?	Human Molecular Genetics	2017
28747752	Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.	Nat Genet	2017
28711408	Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in California.	Mol Genet Metab	2017