Janie F. Shelton

23andMe (United States) — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

55h-index14.8kcitations125works11.52yr avg
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Research Topics

Genetic Associations and Epidemiology(27), Parkinson's Disease Mechanisms and Treatments(14), Autism Spectrum Disorder Research(6), Genetics and Neurodevelopmental Disorders(6), COVID-19 Clinical Research Studies(5)

Publications109 total

Dyslexia Polygenic Index and Socio-Economic Status Interaction Effects on Reading Skills in Australia and the United Kingdom
Behavior Genetics·2025Open Access
Large-scale genome-wide analyses of stuttering
Nature Genetics·2025· 5 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
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
Oral and gut microbiome profiles in people with early idiopathic Parkinson’s disease
Communications Medicine·2024· 7 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
Genetic Analysis and Natural History of LRRK2 G2019S Parkinson’s Disease (P11-3.006)
Neurology·2024
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
Multi-ancestry GWAS of diarrhea during acute SARS-CoV2 infection identifies multiple novel loci and contrasting etiological roles of irritable bowel syndrome subtypes
2024· 1 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
Genetic Analysis and Natural History of Parkinson’s Disease Due to the LRRK2 G2019S Variant
2023· 1 citedOpen Access
A new method for multiancestry polygenic prediction improves performance across diverse populations
Nature Genetics·2023· 86 citedOpen Access
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Frequent Co-authors

Pierre Fontanillas(38), Suyash Shringarpure(38), Matthew H. McIntyre(35), David A. Hinds(34), Joanna L. Mountain(34), Robert K. Bell(33), Katarzyna Bryc(33), Michelle Agee(32), Adam Auton(31), Karen E. Huber(31), Aaron Kleinman(31), Elizabeth S. Noblin(31), Nadia K. Litterman(31), Carrie A. M. Northover(30), J. Fah Sathirapongsasuti(30), Babak Alipanahi(23), Catherine H. Wilson(23), Nicholas A. Furlotte(22), Steven J. Pitts(22), Sarah L. Elson(20)