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Keng‐Han Lin

23andMe (United States) · US
Area of research
Genetics · Neurology
Research interest
Research interests include Genetic Associations and Epidemiology, Parkinson's Disease Mechanisms and Treatments, Substance Abuse Treatment and Outcomes, and Genomic variations and chromosomal abnormalities.
h-index
35
citations
12,167
works
78
NIH funding
primary concept
Biology
email

Recent publications

Genomics yields biological and phenotypic insights into bipolar disorder
Nature 2025cited by 144position: middledoi
Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores
npj Parkinson s Disease 2025cited by 5position: middledoi
A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals
EBioMedicine 2024cited by 13position: middledoi
Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
Nature Genetics 2023cited by 246position: middledoi
CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice
Translational Psychiatry 2023cited by 77position: middledoi
The genetic legacy of African Americans from Catoctin Furnace
Science 2023cited by 21position: middledoi
Discovery of genomic loci associated with sleep apnea risk through multi-trait GWAS analysis with snoring
SLEEP 2022cited by 39position: middledoi
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Nature 2021cited by 2,264position: middledoi
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease
Nature Genetics 2021cited by 1,074position: middledoi
Genetic determinants of daytime napping and effects on cardiometabolic health
Nature Communications 2021cited by 569position: middledoi
Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
Nature Genetics 2021cited by 274position: middledoi
Genetic analyses identify widespread sex-differential participation bias
Nature Genetics 2021cited by 266position: middledoi
Fox Insight collects online, longitudinal patient-reported outcomes and genetic data on Parkinson’s disease
Scientific Data 2020cited by 110position: middledoi
Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure
Nature Communications 2020cited by 86position: middledoi
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
bioRxiv (Cold Spring Harbor Laboratory) 2019cited by 423position: middledoi
The genetic architecture of type 2 diabetes
Nature 2016cited by 1,107position: middledoi

Grants

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Frequent collaborators

No co-authors indexed yet.