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Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

Title: Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity
Authors: Hendricks, AE; Bochukova, EG; Marenne, G; Keogh, JM; Atanassova, N; Bounds, R; Wheeler, E; Mistry, V; Henning, E; Koerner, A; Muddyman, D; McCarthy, S; Hinney, A; Hebebrand, J; Scott, RA; Langenberg, C; Wareham, NJ; Surendran, P; Howson, JM; Butterworth, AS; Danesh, J; Nordestgaard, BG; Nielsen, SF; Afzal, S; Papadia, S; Ashford, S; Garg, S; Millhauser, GL; Palomino, RI; Kwasniewska, A; Tachmazidou, I; O'Rahilly, S; Zeggini, E; Barroso, I; Farooqi, IS; Grp, USS; Consortium, EPIC-CVD; Consortium, U
Source: ftqueenmaryuniv
Publication Year: 2018
Subject Terms: edu; info
Description: This work was supported by the Wellcome Trust (ISF, IB) (098497/Z/12/Z; WT098051), Medical Research Council (ISF, SOR) (MRC_MC_UU_12012/5), NIHR Cambridge Biomedical Research Centre (ISF, IB, SOR), Bernard Wolfe Health Neuroscience Endowment (ISF), European Research Council (ISF) and NIH grant DK064265 (GLM), the European Community’s Seventh Framework Programme (FP7/2007–2013) project Beta-JUDO n°279153 (ISF, AK). This study comprises one arm of the UK10K Consortium (WT091310). The UK Household Longitudinal Study is led by the Institute for Social and Economic Research at the University of Essex and funded by the Economic and Social Research Council. The survey was conducted by NatCen and the genome-wide scan data were analysed and deposited by the Wellcome Trust www.nature.com/scientificreports/ Scientific Reports | 7: 4394 | DOI:10.1038/s41598-017-03054-8 1 1 Sanger Institute. Information on how to access the data can be found on the Understanding Society website https://www.understandingsociety.ac.uk/. AH and JH were funded by the German Ministry for Education and Research (National Genome Research Net-Plus 01GS0820), the German Research Foundation (DFG; HI865/2-1), the European Community’s Seventh Framework Programme (FP7/2007-2013) under grant agreements n°245009 and n°262055. We thank participants and staff of the Copenhagen City Heart Study, Copenhagen Ischemic Heart Disease Study, and the Copenhagen General Population Study for their important contributions (CCHS, CGPS, CIHDS). CHD case ascertainment and validation, genotyping, and clinical chemistry assays in EPICCVD were supported by grants awarded to the University of Cambridge from the EU Framework Programme 7 (HEALTH-F2-2012-279233), the UK Medical Research Council (G0800270) and British Heart Foundation (SP/09/002), the European Research Council (268834), the UK National Institute for Health Research Cambridge Biomedical Research Centre, Merck and Pfizer. We thank all EPIC participants and staff for their contribution to the study, the laboratory .
Document Type: article in journal/newspaper
Language: English
Relation: http://qmro.qmul.ac.uk/xmlui/handle/123456789/33964
Availability: http://qmro.qmul.ac.uk/xmlui/handle/123456789/33964
Rights: lic_creative-commons
Accession Number: edsbas.CF01F29
Database: BASE