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Human Molecular Genetics|September 8, 2009
A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTABAnna C Need, Deborah K Attix, Jill M McEvoy, et al.Science Advances|November 16, 2022
Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetesAbhishek Nag, Ryan S Dhindsa, Jonathan Mitchell, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 12, 2005
UCHL-1 gene in multiple system atrophy: a haplotype tagging approachDaniel G Healy, Patrick M Abou-Sleiman, Niall Quinn, et al.Cell Reports|October 28, 2020
Reduced GABAergic Neuron Excitability, Altered Synaptic Connectivity, and Seizures in a KCNT1 Gain-of-Function Mouse Model of Childhood EpilepsyAmy N Shore, Sophie Colombo, William F Tobin, et al.Nature Genetics|June 2, 2009
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillinAnn K Daly, Peter T Donaldson, Pallav Bhatnagar, et al.Nature|February 4, 2026
Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomesXueqing Zoe Zou, Fengyuan Hu, Haiyi Lou, et al.Proceedings of the National Academy of Sciences of the United States of America|July 24, 2025
Cell type-specific purifying selection of synonymous mitochondrial DNA variationCaleb A Lareau, Patrick Maschmeyer, Yajie Yin, et al.American Journal of Human Genetics|November 27, 2012
Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesisDanit Oz-Levi, Bruria Ben-Zeev, Elizabeth K Ruzzo, et al.Plos Genetics|January 23, 2008
Discerning the ancestry of European Americans in genetic association studiesAlkes L Price, Johannah Butler, Nick Patterson, et al.Plos Genetics|March 21, 2009
A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility lociSreekumar G Pillai, Dongliang Ge, Guohua Zhu, et al.Pageof 34