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Jump to: Article Number of items: 1. ArticleJackson, Victoria E. and Ntalla, Ioanna and Sayers, Ian and Morris, Richard and Whincup, Peter and Casas, Juan-Pablo and Amuzu, Antoinette and Choi, Minkyoung and Dale, Caroline and Kumari, Meena and Engmann, Jorgen and Kalsheker, Noor and Chappell, Sally and Guetta-Baranes, Tamar and McKeever, Tricia M. and Palmer, Colin N.A. and Tavendale, Roger and Holloway, John W. and Sayer, Avan A. and Dennison, Elaine M. and Cooper, Cyrus and Bafadhel, Mona and Barker, Bethan and Brightling, Chris and Bolton, Charlotte E. and John, Michelle E. and Parker, Stuart G. and Moffat, Miriam F. and Wardlaw, Andrew J. and Connolly, Martin J. and Porteous, David J. and Smith, Blair H. and Padmanabhan, Sandosh and Hocking, Lynne and Stirrups, Kathleen E. and Deloukas, Panos and Strachan, David P. and Hall, Ian P. and Tobin, Martin D. and Wain, Louise V. (2016) Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12. Thorax, 71 (6). pp. 501-509. ISSN 1468-3296 |