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Nature Communications|April 21, 2015
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cellsJin Li, Silje F Jørgensen, S Melkorka Maggadottir, et al.
European Journal of Human Genetics : EJHG|April 8, 2010
A sequence variant on 17q21 is associated with age at onset and severity of asthmaEva Halapi, Daniel F Gudbjartsson, Gudrun M Jonsdottir, et al.
Archives of Neurology|August 11, 2010
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypesGyungah Jun, Adam C Naj, Gary W Beecham, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Elucidating the clinical spectrum and molecular basis of HYAL2 deficiencyJames Fasham, Siying Lin, Promita Ghosh, et al.
American Journal of Human Genetics|January 28, 2014
Causal effects of body mass index on cardiometabolic traits and events: a Mendelian randomization analysisMichael V Holmes, Leslie A Lange, Tom Palmer, et al.
Gastroenterology|August 6, 2016
A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome CompositionDalin Li, Jean-Paul Achkar, Talin Haritunians, et al.
Human Molecular Genetics|August 26, 2016
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathwaysMariona Bustamante, Marie Standl, Quique Bassat, et al.
The American Journal of Psychiatry|April 20, 2013
High loading of polygenic risk for ADHD in children with comorbid aggressionMarian L Hamshere, Kate Langley, Joanna Martin, et al.
American Journal of Human Genetics|October 26, 2023
Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencingJodell E Linder, Ran Tao, Wendy K Chung, et al.
The American Journal of Psychiatry|August 14, 2012
Genome-wide association study of multiplex schizophrenia pedigreesDouglas F Levinson, Jianxin Shi, Kai Wang, et al.
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