A new highly penetrant form of obesity due to deletions on chromosome 16p11.2

Walters, RG; Jacquemont, S; Valsesia, A; de Smith, AJ; Martinet, D; Andersson, J; Falchi, M; Chen, F; Andrieux, J; Lobbens, S; Delobel, B; Stutzmann, F; Moustafa, JSE-S; Chevre, J-C; Lecoeur, C; Vatin, V; Bouquillon, S; Buxton, JL; Boute, O; Holder-Espinasse, M; Cuisset, J-M; Lemaitre, M-P; Ambresin, A-E; Brioschi, A; Gaillard, M; Giusti, V; Fellmann, F; Ferrarini, A; Hadjikhani, N; Campion, D; Guilmatre, A; Goldenberg, A; Calmels, N; Mandel, J-L; Le Caignec, C; David, A; Isidor, B; Cordier, M-P; Dupuis-Girod, S; Labalme, A; Sanlaville, D; Beri-Dexheimer, M; Jonveaux, P; Leheup, B; Ounap, K; Bochukova, EG; Henning, E; Keogh, J; Ellis, RJ; MacDermot, KD; van Haelst, MM; Vincent-Delorme, C; Plessis, G; Touraine, R; Philippe, A; Malan, V; Mathieu-Dramard, M; Chiesa, J; Blaumeiser, B; Kooy, RF; Caiazzo, R; Pigeyre, M; Balkau, B; Sladek, R; Bergmann, S; Mooser, V; Waterworth, D; Reymond, A; Vollenweider, P; Waeber, G; Kurg, A; Palta, P; Esko, T; Metspalu, A; Nelis, M; Elliott, P; Hartikainen, A-L; McCarthy, MI; Peltonen, L; Carlsson, L; Jacobson, P; Sjostrom, L; Huang, N; Hurles, ME; O'Rahilly, S; Farooqi, IS; Maennik, K; Jarvelin, M-R; Pattou, F; Meyre, D; Walley, AJ; Coin, LJM; Blakemore, AIF; Froguel, P; Beckmann, JS

Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/14661

Title:	A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
Authors:	Walters, RG Jacquemont, S Valsesia, A de Smith, AJ Martinet, D Andersson, J Falchi, M Chen, F Andrieux, J Lobbens, S Delobel, B Stutzmann, F Moustafa, JSE-S Chevre, J-C Lecoeur, C Vatin, V Bouquillon, S Buxton, JL Boute, O Holder-Espinasse, M Cuisset, J-M Lemaitre, M-P Ambresin, A-E Brioschi, A Gaillard, M Giusti, V Fellmann, F Ferrarini, A Hadjikhani, N Campion, D Guilmatre, A Goldenberg, A Calmels, N Mandel, J-L Le Caignec, C David, A Isidor, B Cordier, M-P Dupuis-Girod, S Labalme, A Sanlaville, D Beri-Dexheimer, M Jonveaux, P Leheup, B Ounap, K Bochukova, EG Henning, E Keogh, J Ellis, RJ MacDermot, KD van Haelst, MM Vincent-Delorme, C Plessis, G Touraine, R Philippe, A Malan, V Mathieu-Dramard, M Chiesa, J Blaumeiser, B Kooy, RF Caiazzo, R Pigeyre, M Balkau, B Sladek, R Bergmann, S Mooser, V Waterworth, D Reymond, A Vollenweider, P Waeber, G Kurg, A Palta, P Esko, T Metspalu, A Nelis, M Elliott, P Hartikainen, A-L McCarthy, MI Peltonen, L Carlsson, L Jacobson, P Sjostrom, L Huang, N Hurles, ME O'Rahilly, S Farooqi, IS Maennik, K Jarvelin, M-R Pattou, F Meyre, D Walley, AJ Coin, LJM Blakemore, AIF Froguel, P Beckmann, JS
Keywords:	Science & Technology;Multidisciplinary Sciences;Science & Technology - Other Topics;MULTIDISCIPLINARY SCIENCES;GENOME-WIDE ASSOCIATION;CIRCULAR BINARY SEGMENTATION;COPY NUMBER VARIATION;FRAMESHIFT MUTATION;MENTAL-RETARDATION;CHILDHOOD OBESITY;RISK LOCI;AUTISM;MICRODELETION;INDIVIDUALS
Issue Date:	2010
Publisher:	NATURE PUBLISHING GROUP
Citation:	NATURE, 463 (7281): pp. 671 - U104 (7), (2010)
URI:	http://bura.brunel.ac.uk/handle/2438/14661
DOI:	http://dx.doi.org/10.1038/nature08727
ISSN:	http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000274193900038&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=f12c8c83318cf2733e615e54d9ed7ad5 http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000274193900038&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=f12c8c83318cf2733e615e54d9ed7ad5 0028-0836
Appears in Collections:	Dept of Life Sciences Research Papers

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