Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Body Weight and POMC[original query] |
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| Sequence analysis of the pro-opiomelanocortin (POMC) gene in obese/diabetic Japanese. International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity 2002 May 26 (5): 730-1. Ohshiro Y, Ueda K, Wakasaki H, Kosaka M, Nishi M, Sasaki H, Takasu N, Nanjo |
| Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study. Diabetes 2005 Aug 54 (8): 2492-6. Baker M, Gaukrodger N, Mayosi BM, Imrie H, Farrall M, Watkins H, Connell JM, Avery PJ, Keavney B |
| Six novel mutations in the proopiomelanocortin and melanocortin receptor 4 genes in severely obese adults living in southern Italy. Clinical chemistry 2005 Aug 51 (8): 1358-64. Buono Pasqualina, Pasanisi Fabrizio, Nardelli Carmela, Ieno Luigi, Capone Silvana, Liguori Rosario, Finelli Carmine, Oriani Giovannangelo, Contaldo Franco, Sacchetti Luc |
| Association of single nucleotide polymorphisms in the promoter region of the pro-opiomelanocortin gene (POMC) with low bone mineral density in adult women. Journal of human genetics 2005 50 (5): 235-40. Sudo Yoshihiro, Ezura Yoichi, Kajita Mitsuko, Yoshida Hideyo, Suzuki Takao, Hosoi Takayuki, Inoue Satoshi, Shiraki Masataka, Ito Hiromoto, Emi Mitsu |
| Proopiomelanocortin gene variants are associated with serum leptin and body fat in a normal female population. European journal of human genetics : EJHG 2005 Jun 13 (6): 772-80. Chen Yuanneng, Snieder Harold, Wang Xiaoling, Kaviya Bhavini, McCaffrey Clare, Spector Tim D, Carter Nicholas D, O'Dell Sandra |
| Mutational analysis of the pro-opiomelanocortin gene in French obese children led to the identification of a novel deleterious heterozygous mutation located in the alpha-melanocyte stimulating hormone domain. Pediatric research 2008 Feb 63 (2): 211-6. Dubern Beatrice, Lubrano-Berthelier Cecile, Mencarelli Monica, Ersoy Baran, Frelut Marie-Laure, Bouglé Dominique, Costes Bruno, Simon Chantal, Tounian Patrick, Vaisse Christian, Clement Kari |
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.
Nature genetics 2010 Oct . Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, Allen HL, Lindgren CM, Luan J, Mägi R, Randall JC, Vedantam S, Winkler TW, Qi L, Workalemahu T, Heid IM, Steinthorsdottir V, Stringham HM, Weedon MN, Wheeler E, Wood AR, Ferreira T, Weyant RJ, Segrè AV, Estrada K, Liang L, Nemesh J, Park JH, Gustafsson S, Kilpeläinen TO, Yang J, Bouatia-Naji N, Esko T, Feitosa MF, Kutalik Z, Mangino M, Raychaudhuri S, Scherag A, Smith AV, Welch R, Zhao JH, Aben KK, Absher DM, Amin N, Dixon AL, Fisher E, Glazer NL, Goddard ME, Heard-Costa NL, Hoesel V, Hottenga JJ, Johansson A, Johnson T, Ketkar S, Lamina C, Li S, Moffatt MF, Myers RH, Narisu N, Perry JR, Peters MJ, Preuss M, Ripatti S, Rivadeneira F, Sandholt C, Scott LJ, Timpson NJ, Tyrer JP, van Wingerden S, Watanabe RM, White CC, Wiklund F, Barlassina C, Chasman DI, Cooper MN, Jansson JO, Lawrence RW, Pellikka N, Prokopenko I, Shi J, Thiering E, Alavere H, Alibrandi MT, Almgren P, Arnold AM, Aspelund T, Atwood LD, Balkau B, Balmforth AJ, Bennett AJ, Ben-Shlomo Y, Bergman RN, Bergmann S, Biebermann H, Blakemore AI, Boes T, Bonnycastle LL, Bornstein SR, Brown MJ, Buchanan TA, Busonero F, Campbell H, Cappuccio FP, Cavalcanti-Proença C, Chen YD, Chen CM, Chines PS, Clarke R, Coin L, Connell J, Day IN, Heijer MD, Duan J, Ebrahim S, Elliott P, Elosua R, Eiriksdottir G, Erdos MR, Eriksson JG, Facheris MF, Felix SB, Fischer-Posovszky P, Folsom AR, Friedrich N, Freimer NB, Fu M, Gaget S, Gejman PV, Geus EJ, Gieger C, Gjesing AP, Goel A, Goyette P, Grallert H, Gräßler J, Greenawalt DM, Groves CJ, Gudnason V, Guiducci C, Hartikainen AL, Hassanali N, Hall AS, Havulinna AS, Hayward C, Heath AC, Hengstenberg C, Hicks AA, Hinney A, Hofman A, Homuth G, Hui J, Igl W, Iribarren C, Isomaa B, Jacobs KB, Jarick I, Jewell E, John U, Jørgensen T, Jousilahti P, Jula A, Kaakinen M, Kajantie E, Kaplan LM, Kathiresan S, Kettunen J, Kinnunen L, Knowles JW, Kolcic I, König IR, Koskinen S, Kovacs P, Kuusisto J, Kraft P, Kvaløy K, Laitinen J, Lantieri O, Lanzani C, Launer LJ, Lecoeur C, Lehtimäki T, Lettre G, Liu J, Lokki ML, Lorentzon M, Luben RN, Ludwig B, Manunta P, Marek D, Marre M, Martin NG, McArdle WL, McCarthy A, McKnight B, Meitinger T, Melander O, Meyre D, Midthjell K, Montgomery GW, Morken MA, Morris AP, Mulic R, Ngwa JS, Nelis M, Neville MJ, Nyholt DR, O'Donnell CJ, O'Rahilly S, Ong KK, Oostra B, Paré G, Parker AN, Perola M, Pichler I, Pietiläinen KH, Platou CG, Polasek O, Pouta A, Rafelt S, Raitakari O, Rayner NW, Ridderstråle M, Rief W, Ruokonen A, Robertson NR, Rzehak P, Salomaa V, Sanders AR, Sandhu MS, Sanna S, Saramies J, Savolainen MJ, Scherag S, Schipf S, Schreiber S, Schunkert H, Silander K, Sinisalo J, Siscovick DS, Smit JH, Soranzo N, Sovio U, Stephens J, Surakka I, Swift AJ, Tammesoo ML, Tardif JC, Teder-Laving M, Teslovich TM, Thompson JR, Thomson B, Tönjes A, Tuomi T, van Meurs JB, van Ommen GJ, Vatin V, Viikari J, Visvikis-Siest S, Vitart V, Vogel CI, Voight BF, Waite LL, Wallaschofski H, Walters GB, Widen E, Wiegand S, Wild SH, Willemsen G, Witte DR, Witteman JC, Xu J, Zhang Q, Zgaga L, Ziegler A, Zitting P, Beilby JP, Farooqi IS, Hebebrand J, Huikuri HV, James AL, Kähönen M, Levinson DF, Macciardi F, Nieminen MS, Ohlsson C, Palmer LJ, Ridker PM, Stumvoll M, Beckmann JS, Boeing H, Boerwinkle E, Boomsma DI, Caulfield MJ, Chanock SJ, Collins FS, Cupples LA, Smith GD, Erdmann J, Froguel P, Grönberg H, Gyllensten U, Hall P, Hansen T, Harris TB, Hattersley AT, Hayes RB, Heinrich J, Hu FB, Hveem K, Illig T, Jarvelin MR, Kaprio J, Karpe F, Khaw KT, Kiemeney LA, Krude H, Laakso M, Lawlor DA, Metspalu A, Munroe PB, Ouwehand WH, Pedersen O, Penninx BW, Peters A, Pramstaller PP, Quertermous T, Reinehr T, Rissanen A, Rudan I, Samani NJ, Schwarz PE, Shuldiner AR, Spector TD, Tuomilehto J, Uda M, Uitterlinden A, Valle TT, Wabitsch M, Waeber G, Wareham NJ, Watkins H, Wilson JF, Wright AF, Zillikens MC, Chatterjee N, McCarroll SA, Purcell S, Schadt EE, Visscher PM, Assimes TL, Borecki IB, Deloukas P, Fox CS, Groop LC, Haritunians T, Hunter DJ, Kaplan RC, Mohlke KL, O'Connell JR, Peltonen L, Schlessinger D, Strachan DP, van Duijn CM, Wichmann HE, Frayling TM, Thorsteinsdottir U, Abecasis GR, Barroso I, Boehnke M, Stefansson K, North KE, I McCarthy M, Hirschhorn JN, Ingelsson E, Loos RJ |
| Melanocortin 4 Receptor Pathway Dysfunction in Obesity: Patient Stratification Aimed at MC4R Agonist Treatment. The Journal of clinical endocrinology and metabolism 2018 5 103 (7): 2601-2612. Ayers Kristin L, Glicksberg Benjamin S, Garfield Alastair S, Longerich Simonne, White Joseph A, Yang Pengwei, Du Lei, Chittenden Thomas W, Gulcher Jeffery R, Roy Sophie, Fiedorek Fred, Gottesdiener Keith, Cohen Sarah, North Kari E, Schadt Eric E, Li Shuyu D, Chen Rong, Van der Ploeg Lex H |
| Ciliary gene RPGRIP1L is required for hypothalamic arcuate neuron development. JCI insight 2019 2 4 (3): . Wang Liheng, De Solis Alain J, Goffer Yossef, Birkenbach Kathryn E, Engle Staci E, Tanis Ross, Levenson Jacob M, Li Xueting, Rausch Richard, Purohit Manika, Lee Jen-Yi, Tan Jerica, De Rosa Maria Caterina, Doege Claudia A, Aaron Holly L, Martins Gabriela J, Brüning Jens C, Egli Dieter, Costa Rui, Berbari Nicolas, Leibel Rudolph L, Stratigopoulos Geor |
| Genetic Obesity and Bariatric Surgery Outcome in 1014 Patients with Morbid Obesity. Obesity surgery 2019 Oct . Cooiman M I, Kleinendorst L, Aarts E O, Janssen I M C, van Amstel H K Ploos, Blakemore A I, Hazebroek E J, Meijers-Heijboer H J, van der Zwaag B, Berends F J, van Haelst M |
| Effects of Heterozygous Variants in the Leptin-Melanocortin Pathway on Roux-en-Y Gastric Bypass Outcomes: a 15-Year Case-Control Study. Obesity surgery 2022 6 32 (8): 2632-2640. Campos Alejandro, Cifuentes Lizeth, Hashem Anas, Busebee Bradley, Hurtado-Andrade Maria D, Ricardo-Silgado Maria L, McRae Alison, De la Rosa Alan, Feris Fauzi, Bublitz Joshua T, Hensrud Donald, Camilleri Michael, Kellogg Todd A, Eckel-Passow Jeanette E, Olson Janet, Acosta Andr |
| Heterozygous Genetic Variants in Autosomal Recessive Genes of the Leptin-Melanocortin Signalling Pathway Are Associated With the Development of Childhood Obesity. Frontiers in endocrinology 2022 13 832911. Šket Robert, Kotnik Primož, Bizjan Barbara Jenko, Kocen Valentina, Mlinari? Matej, Tesovnik Tine, Debeljak Maruša, Battelino Tadej, Kova? Jern |
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