Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12
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16/06/2016
16/06/2016
01/06/2016
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| Resumo |
Funding: British Women’s Heart and Health Study is funded by the Department of Health grant no. 90049 and the British Heart Foundation grant no. PG/09/022. British Regional Heart Study is supported by the British Heart Foundation (grant RG/ 13/16/30528). CB (COPDBEAT) received funding from the Medical Research Council UK (grant no. G0601369), CB (COPDBEAT) and AJW (UKCOPD) were supported by the National Institute for Health Research (NIHR Leicester Biomedical Research Unit). MB (COPDBEAT) received funding from the NIHR (grant no. PDF-2013-06-052). Hertfordshire Cohort Study received support from the Medical Research Council, Arthritis Research UK, the International Osteoporosis Foundation and the British Heart Foundation; NIHR Biomedical Research Centre in Nutrition, University of Southampton; NIHR Musculoskeletal Biomedical Research Unit, University of Oxford. Generation Scotland: Scottish Family Health Study is funded by the Chief Scientist Office, Scottish Government Health Directorates, grant number CZD/16/6 and the Scottish Funding Council grant HR03006. EU COPD Gene Scan is funded by the European Union, grant no. QLG1-CT-2001-01012. English Longitudinal Study of Aging is funded by the Institute of Aging, NIH grant No. AG1764406S1. GoDARTs is funded by the Wellcome Trust grants 072960, 084726 and 104970. MDT has been supported by MRC fellowship G0902313. UK Biobank Lung Exome Variant Evaluation study was funded by a Medical Research Council strategic award to MDT, IPH, DPS and LVW (MC_PC_12010) Peer reviewed Publisher PDF |
| Formato |
9 |
| Identificador |
Jackson , V E , Ntalla , I , Sayers , I , Morris , R , Whincup , P , Casas , J-P , Amuzu , A , Choi , M , Dale , C , Kumari , M , Engmann , J , Kalsheker , N , Chappell , S , Guetta-Baranes , T , McKeever , T M , Palmer , C N A , Tavendale , R , Holloway , J W , Sayer , A A , Dennison , E M , Cooper , C , Bafadhel , M , Barker , B , Brightling , C , Bolton , C E , John , M E , Parker , S G , Moffat , M F , Wardlaw , A J , Connolly , M J , Porteous , D J , Smith , B H , Padmanabhan , S , Hocking , L , Stirrups , K E , Deloukas , P , Strachan , D P , Hall , I P , Tobin , M D & Wain , L V 2016 , ' Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12 ' Thorax , vol 71 , no. 6 , pp. 501-509 . , 10.1136/thoraxjnl-2015-207876 0040-6376 PURE: 64326435 PURE UUID: e2777948-4d07-4832-b744-881186193ca5 PubMed: 26917578 |
| Idioma(s) |
eng |
| Relação |
Thorax |
| Direitos |
This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/ |
| Palavras-Chave | #R Medicine #British Heart Foundation #PG/09/022 #RG/ 13/16/30528 #Medical Research Council (MRC) #G0601369 #G0902313 #MC_PC_12010 #National Institute for Health Research (NIHR) #PDF-2013-06-052 #Chief Scientist Office (CSO) #CZD/16/6 #Scottish Funding Council #HR03006 #Wellcome Trust #072960 #084726 #104970 #R |
| Tipo |
Journal article |
| Contribuinte(s) |
University of Aberdeen, Medicine, Medical Sciences & Nutrition, Applied Medicine |
