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Translational Psychiatry|February 26, 2020
Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolatesJae Hoon Sul, Susan K Service, Alden Y Huang, et al.Nature|November 6, 2019
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.Nature|August 2, 2019
Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.Medrxiv : the Preprint Server for Health Sciences|November 6, 2024
Phenotype harmonization and analysis for The Populations Underrepresented in Mental illness Association Studies (the PUMAS Project)Ana M Ramirez-Diaz, Ana M Diaz-Zuluaga, Rocky E Stroud, et al.Nature Genetics|July 8, 2026
A blended genome and exome sequencing method captures genetic variation in an unbiased and cost-effective mannerToni A Boltz, Benjamin B Chu, Matthew DeFelice, et al.The American Journal of Psychiatry|August 27, 2014
Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCDDongmei Yu, Carol A Mathews, Jeremiah M Scharf, et al.Nature Genetics|October 8, 2013
Discovery and refinement of loci associated with lipid levelsCristen J Willer, Ellen M Schmidt, Sebanti Sengupta, et al.Nature Genetics|October 8, 2013
Common variants associated with plasma triglycerides and risk for coronary artery diseaseRon Do, Cristen J Willer, Ellen M Schmidt, et al.Pageof 5