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Biorxiv : the Preprint Server for Biology|January 3, 2024
Population-scale skeletal muscle single-nucleus multi-omic profiling reveals extensive context specific genetic regulationArushi Varshney, Nandini Manickam, Peter Orchard, et al.JAMA Psychiatry|September 29, 2021
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association StudyOlga Giannakopoulou, Kuang Lin, Xiangrui Meng, et al.Science (New York, N.Y.)|April 28, 2007
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variantsLaura J Scott, Karen L Mohlke, Lori L Bonnycastle, 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.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.Diabetes|February 28, 2004
A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14Kaisa Silander, Laura J Scott, Timo T Valle, et al.Genetics|March 15, 2021
Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestriesAlan M Kwong, Thomas W Blackwell, Jonathon LeFaive, et al.Nature Genetics|January 15, 2008
Newly identified loci that influence lipid concentrations and risk of coronary artery diseaseCristen J Willer, Serena Sanna, Anne U Jackson, et al.The Journal of Clinical Investigation|June 4, 2008
Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levelsWei-Min Chen, Michael R Erdos, Anne U Jackson, et al.Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophreniaRunjia Li, Sarah A Gagliano Taliun, Kevin Liao, et al.Pageof 14