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Sakornsakolpat, P.* et al.: Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. Nat. Genet. 51, 494-505 (2019)
Shrine, N.* et al.: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Nat. Genet. 51, 481-493 (2019)
Shrine, N.* et al.: Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries (Nature Genetics, (2019), 51, 3, (481-493), 10.1038/s41588-018-0321-7). Nat. Genet., accepted (2019)
Jackson, V.E.* et al.: Meta-analysis of exome array data identifies six novel genetic loci for lung function. Wellcome Open Res. 3:4 (2018)
Teumer, A.* et al.: Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. Nat. Commun. 9:4455 (2018)
Aschard, H.* et al.: Evidence for large-scale gene-by-smoking interaction effects on pulmonary function. Int. J. Epidemiol. 46, 894-904 (2017)
Graff, M.* et al.: Genome-wide physical activity interactions in adiposity ― A meta-analysis of 200,452 adults. PLoS Genet. 13:e1006528 (2017)
Justice, A.E.* et al.: Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Nat. Commun. 8:14977 (2017)
Shungin, D.* et al.: Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions. PLoS Genet. 13:e1006812 (2017)
Wain, L.V.* et al.: Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. Nat. Genet. 49, 416-425 (2017)
Andlauer, T.F.* et al.: Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. Sci. Adv. 2:e1501678 (2016)
Kettunen, J.* et al.: Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Nat. Commun. 7:11122 (2016)
Okbay, A.* et al.: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nat. Genet. 48, 624-633 (2016)
Schumann, G.* et al.: KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference. Proc. Natl. Acad. Sci. U.S.A. 113, 14372-14377 (2016)
Coffee and Caffeine Genetics Consortium et al.: Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. Mol. Psychiatry 20, 647-656 (2015)
Artigas, M.S.* et al.: Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. Nat. Commun. 6:8658 (2015)
Gharib, S.A.* et al.: Integrative pathway genomics of lung function and airflow obstruction. Hum. Mol. Genet. 24, 6836-6848 (2015)
Hägg, S.* et al.: Adiposity as a cause of cardiovascular disease: A Mendelian randomization study. Int. J. Epidemiol. 44, 578-586 (2015)
Horikoshi, M.* et al.: Discovery and fine-mapping of glycaemic and obesity-related trait loci using high-density imputation. PLoS Genet. 11:e1005230 (2015)
Jansen, H.* et al.: Genetic variants primarily associated with type 2 diabetes are related to coronary artery disease risk. Atherosclerosis 241, 419-426 (2015)