HuGE Literature Finder
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Records 1-11
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DNA sequencing and copy number variation analysis of MCHR2 in a cohort of Prader Willi like (PWL) patients.
Obesity research & clinical practice 2017 Oct . Geets Ellen, Aerts Evi, Verrijken An, Van Hoorenbeeck Kim, Verhulst Stijn, Van Gaal Luc, Van Hul W |
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Copy number variations in "classical" obesity candidate genes are not frequently associated with severe early-onset obesity in children.
Journal of pediatric endocrinology & metabolism : JPEM 2017 May 30 (5): 507-515. Windholz Jan, Kovacs Peter, Schlicke Marina, Franke Christin, Mahajan Anubha, Morris Andrew P, Lemke Johannes R, Klammt Jürgen, Kiess Wieland, Schöneberg Torsten, Pfäffle Roland, Körner Ant |
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Copy number variation (CNV) analysis and mutation analysis of the 6q14.1-6q16.3 genes SIM1 and MRAP2 in Prader Willi like patients.
Molecular genetics and metabolism 2016 Jan . Geets Ellen, Zegers Doreen, Beckers Sigri, Verrijken An, Massa Guy, Van Hoorenbeeck Kim, Verhulst Stijn, Van Gaal Luc, Van Hul W |
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Exome sequencing in Thai patients with familial obesity.
Genetics and molecular research : GMR 2016 15 (2): . Kaewsutthi S, Santiprabhob J, Phonrat B, Tungtrongchitr A, Lertrit P, Tungtrongchitr |
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Mutation screen of the SIM1 gene in pediatric patients with early-onset obesity.
International journal of obesity (2005) 2014 Jul 38 (7): 1000-4. Zegers D, Beckers S, Hendrickx R, Van Camp J K, de Craemer V, Verrijken A, Van Hoorenbeeck K, Verhulst S L, Rooman R P, Desager K N, Massa G, Van Gaal L F, Van Hul |
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Rare variants in single-minded 1 (SIM1) are associated with severe obesity.
The Journal of clinical investigation 2013 Jul 123 (7): 3042-50. Ramachandrappa Shwetha, Raimondo Anne, Cali Anna M G, Keogh Julia M, Henning Elana, Saeed Sadia, Thompson Amanda, Garg Sumedha, Bochukova Elena G, Brage Soren, Trowse Victoria, Wheeler Eleanor, Sullivan Adrienne E, Dattani Mehul, Clayton Peter E, Datta Vipan, Datta Vippan, Bruning John B, Wareham Nick J, O'Rahilly Stephen, Peet Daniel J, Barroso Ines, Whitelaw Murray L, Farooqi I Sad |
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Replication and extension of association between common genetic variants in SIM1 and human adiposity.
Obesity (Silver Spring, Md.) 2011 Dec 19 (12): 2394-403. Swarbrick Michael M, Evans Daniel S, Valle Maria I, Favre Hélène, Wu Shi-Hsuan, Njajou Omer T, Li Rongling, Zmuda Joseph M, Miljkovic Iva, Harris Tamara B, Kwok Pui-Yan, Vaisse Christian, Hsueh Wen-C |
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A large-scale candidate gene association study of age at menarche and age at natural menopause.
Human genetics 2010 Nov 128 (5): 515-27. He Chunyan, Kraft Peter, Chasman Daniel I, Buring Julie E, Chen Constance, Hankinson Susan E, Paré Guillaume, Chanock Stephen, Ridker Paul M, Hunter David |
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Analysis of the SIM1 contribution to polygenic obesity in the French population.
Obesity (Silver Spring, Md.) 2010 Aug 18 (8): 1670-5. Ghoussaini Maya, Stutzmann Fanny, Couturier Cyril, Vatin Vincent, Durand Emmanuelle, Lecoeur Cécile, Degraeve Franck, Heude Barbara, Tauber Maithé, Hercberg Serge, Levy-Marchal Claire, Tounian Patrick, Weill Jacques, Traurig Michael, Bogardus Clifton, Baier Leslie J, Michaud Jacques L, Froguel Philippe, Meyre Dav |
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Common variation in SIM1 is reproducibly associated with BMI in Pima Indians.
Diabetes 2009 Jul 58 (7): 1682-9. Traurig Michael, Mack Janel, Hanson Robert L, Ghoussaini Maya, Meyre David, Knowler William C, Kobes Sayuko, Froguel Philippe, Bogardus Clifton, Baier Leslie |
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Studies of the SIM1 gene in relation to human obesity and obesity-related traits.
International journal of obesity (2005) 2007 Mar 31 (3): 429-34. Hung C-C C, Luan J, Sims M, Keogh J M, Hall C, Wareham N J, O'Rahilly S, Farooqi I |
- Page last reviewed:Jul 30, 2019
- Page last updated:Aug 15, 2019
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