Keng‐Han Lin

23andMe (United States) — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

35h-index11.7kcitations78works15.32yr avg
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Research Topics

Genetic Associations and Epidemiology(24), Parkinson's Disease Mechanisms and Treatments(8), Genomic variations and chromosomal abnormalities(5), Genetics and Neurodevelopmental Disorders(5), Substance Abuse Treatment and Outcomes(4)

Publications72 total

Dyslexia Polygenic Index and Socio-Economic Status Interaction Effects on Reading Skills in Australia and the United Kingdom
Behavior Genetics·2025Open Access
Association between polygenic risk and survival in breast cancer patients
BMC Cancer·2025· 1 citedOpen Access
Multivariate genome-wide association analysis of dyslexia and quantitative reading skill improves gene discovery
Translational Psychiatry·2025· 1 citedOpen Access
Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores
npj Parkinson s Disease·2025· 4 citedOpen Access
Genomics yields biological and phenotypic insights into bipolar disorder
Nature·2025· 107 citedOpen Access
Bidirectional relationship between olfaction and Parkinson’s disease
npj Parkinson s Disease·2024· 2 citedOpen Access
The shared genetic architecture and evolution of human language and musical rhythm
Nature Human Behaviour·2024· 25 citedOpen Access
Risk of Pregnancy-Associated Venous Thromboembolism in Sickle Cell Trait
Blood·2024Open Access
Oral and gut microbiome profiles in people with early idiopathic Parkinson’s disease
Communications Medicine·2024· 7 citedOpen Access
Ancestry-independent risk of venous thromboembolism in individuals with sickle cell trait vs factor V Leiden
Blood Advances·2024· 3 citedOpen Access
Genetic neurodevelopmental clustering and dyslexia
Molecular Psychiatry·2024· 9 citedOpen Access
Genome-wide association studies of coffee intake in UK/US participants of European ancestry uncover cohort-specific genetic associations
Neuropsychopharmacology·2024· 11 citedOpen Access
The genetic architecture of dog ownership: large-scale genome-wide association study in 97,552 European-ancestry individuals
G3 Genes Genomes Genetics·2024· 3 citedOpen Access
Genetic analysis and natural history of Parkinson’s disease due to the <i>LRRK2</i> G2019S variant
Brain·2024· 41 citedOpen Access
A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals
EBioMedicine·2024· 10 citedOpen Access
MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups
Cell Genomics·2024· 23 citedOpen Access
Analysis of rare Parkinson’s disease variants in millions of people
npj Parkinson s Disease·2024· 35 citedOpen Access
Multi-ancestry genome-wide meta-analysis identifies novel basal cell carcinoma loci and shared genetic effects with squamous cell carcinoma
Communications Biology·2024· 12 citedOpen Access
Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
Nature Genetics·2023· 209 citedOpen Access
Correlations in sleeping patterns and circadian preference between spouses
Communications Biology·2023· 10 citedOpen Access
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Frequent Co-authors

Pierre Fontanillas(38), Janie F. Shelton(37), Barry Hicks(36), Ethan M. Jewett(36), Yunxuan Jiang(36), Matthew H. McIntyre(36), G. David Poznik(36), Suyash Shringarpure(36), David A. Hinds(35), Karl Heilbron(33), Elizabeth S. Noblin(33), Robert K. Bell(32), Aaron A. Petrakovitz(30), Anjali J. Shastri(29), Adam Auton(28), Kipper Fletez‐Brant(28), Joanna L. Mountain(28), Katarzyna Bryc(26), Jingchunzi Shi(26), Sayantan Das(25)