Author
23andMe (United States)ORCID 0000-0001-5191-1099Unclaimed ORCID profile · follow to get notified of new preprints
5 papers
Recent·Most cited
Joël Becker, Casper A.P. Burik, Grant Goldman…·Aysu Okbay
The paper constructs polygenic indexes for 47 phenotypes across 11 datasets and provides a tool to correct errors-in-variables bias when using PGIs as proxies for the additive SNP factor.
Padhraig Gormley, Mitja Kurki, Marjo Eveliina Hiekkala…·George McMahon
This study shows common genetic variants significantly contribute to migraine family clustering, with higher burden in familial cases compared to population-based cases.
David M. Howard, Mark J. Adams, Masoud Shirali…·Andrew Mark McIntosh
This study conducts a GWAS on depression phenotypes in UK Biobank, identifying genetic variants enriched in excitatory synaptic pathways.
Joanna Martin, Raymond Kenney Walters, Ditte Demontis…·Gerd Lehmkuhl
This study investigates genetic mechanisms underlying sex bias in ADHD prevalence using genome-wide data and finds no mean polygenic burden difference across sexes but increased risk in female siblings and comorbid conditions.
Brian B. Boutwell, David A. Hinds, Jorim J. Tielbeek…·Catherine H. Wilson
This study replicates and extends findings of CADM2 and MSRA gene associations with personality traits using data from 23andMe.