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Cancer Research|March 22, 2018
Germline Lysine-Specific Demethylase 1 (LSD1/KDM1A) Mutations Confer Susceptibility to Multiple MyelomaXiaomu Wei, M Nieves Calvo-Vidal, Siwei Chen, et al.
Lancet (London, England)|October 23, 2015
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association studyIsabelle Cleynen, Gabrielle Boucher, Luke Jostins, et al.
American Journal of Human Genetics|June 5, 2018
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic SpectrumAndrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, et al.
Nature Genetics|January 26, 2023
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domainsDitte Demontis, G Bragi Walters, Georgios Athanasiadis, et al.
Nature Genetics|November 18, 2014
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsyMikko Muona, Samuel F Berkovic, Leanne M Dibbens, et al.
Human Molecular Genetics|June 14, 2011
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degenerationYi Yu, Tushar R Bhangale, Jesen Fagerness, et al.
Gastroenterology|January 4, 2017
Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association StudyPaola Nicoletti, Guruprasad P Aithal, Einar S Bjornsson, et al.
Nature|May 29, 2020
A structural variation reference for medical and population geneticsRyan L Collins, Harrison Brand, Konrad J Karczewski, et al.
Nature Genetics|April 28, 2018
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorderDonna M Werling, Harrison Brand, Joon-Yong An, et al.
Science Translational Medicine|January 12, 2018
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's diseaseKen Y Hui, Heriberto Fernandez-Hernandez, Jianzhong Hu, et al.
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