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The New England Journal of Medicine|August 8, 2022
Germline Mutations in <i>CIDEB</i> and Protection against Liver DiseaseNiek Verweij, Mary E Haas, Jonas B Nielsen, et al.Nature Genetics|February 27, 2019
Biological and clinical insights from genetics of insomnia symptomsJacqueline M Lane, Samuel E Jones, Hassan S Dashti, et al.Nature Communications|August 15, 2019
Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypesHeming Wang, Jacqueline M Lane, Samuel E Jones, et al.American Journal of Human Genetics|January 2, 2018
Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac DevelopmentJonas B Nielsen, Lars G Fritsche, Wei Zhou, et al.Nature Communications|May 26, 2017
Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valveBo Yang, Wei Zhou, Jiao Jiao, et al.Nature Genetics|August 1, 2018
Biobank-driven genomic discovery yields new insight into atrial fibrillation biologyJonas B Nielsen, Rosa B Thorolfsdottir, Lars G Fritsche, et al.Circulation|August 16, 2014
Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillationMoritz F Sinner, Nathan R Tucker, Kathryn L Lunetta, et al.Nature Communications|August 10, 2020
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancerWei Zhou, Ben Brumpton, Omer Kabil, et al.Nature Communications|August 23, 2022
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetesParsa Akbari, Olukayode A Sosina, Jonas Bovijn, et al.Nature Genetics|October 31, 2017
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biologyManuel A Ferreira, Judith M Vonk, Hansjörg Baurecht, et al.Pageof 8