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American Journal of Respiratory and Critical Care Medicine|July 31, 2023
A Polygenic Risk Score for Idiopathic Pulmonary Fibrosis and Interstitial Lung AbnormalitiesMatthew Moll, Anna L Peljto, John S Kim, et al.
Thorax|February 27, 2016
Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12Victoria E Jackson, Ioanna Ntalla, Ian Sayers, et al.
The European Respiratory Journal|May 11, 2019
Epigenome-wide association study of lung function level and its changeMedea Imboden, Matthias Wielscher, Faisal I Rezwan, et al.
Medrxiv : the Preprint Server for Health Sciences|June 22, 2026
Genome-wide association and multi-omics functional screens reveal the genetic architecture of foveal developmentCallum Hunt, Manjiri Patil, Hammad Syed, et al.
Circulation. Cardiovascular Genetics|October 4, 2011
Four genetic loci influencing electrocardiographic indices of left ventricular hypertrophySonia Shah, Christopher P Nelson, Tom R Gaunt, et al.
Plos Genetics|August 31, 2013
Causal and synthetic associations of variants in the SERPINA gene cluster with alpha1-antitrypsin serum levelsGian Andri Thun, Medea Imboden, Ilaria Ferrarotti, et al.
The Lancet. Respiratory Medicine|July 11, 2020
Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohortsMatthew Moll, Phuwanat Sakornsakolpat, Nick Shrine, et al.
Human Molecular Genetics|August 6, 2010
A large genome scan for rare CNVs in amyotrophic lateral sclerosisHylke M Blauw, Ammar Al-Chalabi, Peter M Andersen, et al.
The Lancet. Respiratory Medicine|December 16, 2018
Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association studyNick Shrine, Michael A Portelli, Catherine John, et al.
The Journal of Allergy and Clinical Immunology|May 23, 2020
Phenotypic and functional translation of IL33 genetics in asthmaMaria E Ketelaar, Michael A Portelli, F Nicole Dijk, et al.
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