Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: GPR50[original query] |
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Sex-specific association between bipolar affective disorder in women and GPR50, an X-linked orphan G protein-coupled receptor. Molecular psychiatry 2005 May 10 (5): 470-8. Thomson P A, Wray N R, Thomson A M, Dunbar D R, Grassie M A, Condie A, Walker M T, Smith D J, Pulford D J, Muir W, Blackwood D H R, Porteous D |
Lack of association of an insertion/deletion polymorphism in the G protein-coupled receptor 50 with bipolar disorder in a Northern Swedish population. Psychiatric genetics 2006 Dec 16 (6): 235-6. Alaerts Maaike, Venken Tine, Lenaerts An-Sofie, De Zutter Sonia, Norrback Karl-Fredrik, Adolfsson Rolf, Del-Favero Jurg |
Sequence variants in the melatonin-related receptor gene (GPR50) associate with circulating triglyceride and HDL levels. Journal of lipid research 2006 Apr 47 (4): 761-6. Bhattacharyya Sumit, Luan Jian'an, Challis Benjamin, Keogh Julia, Montague Carl, Brennand John, Morten John, Lowenbeim Sarah, Jenkins Suzanne, Farooqi I Sadaf, Wareham Nicholas J, O'Rahilly Steph |
GPR50 is not associated with childhood-onset mood disorders in a large sample of Hungarian families. Psychiatric genetics 2007 Dec 17 (6): 347-50. Feng Yu, Wigg Karen, King Nicole, Vetró Agnes, Kiss Eniko, Kapornai Krisztina, Mayer László, Gádoros Júlia, Kennedy James L, Kovacs Maria, Barr Cathy L, |
Evaluation of GPR50, hMel-1B, and ROR-alpha melatonin-related receptors and the etiology of adolescent idiopathic scoliosis. Journal of pediatric orthopedics 2010 Sep 30 (6): 539-43. Shyy William, Wang Kai, Gurnett Christina A, Dobbs Matthew B, Miller Nancy H, Wise Carol, Sheffield Val C, Morcuende Jose |
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population. PloS one 2010 5 (7): e11495. Chaste Pauline, Clement Nathalie, Mercati Oriane, Guillaume Jean-Luc, Delorme Richard, Botros Hany Goubran, Pagan Cécile, Périvier Samuel, Scheid Isabelle, Nygren Gudrun, Anckarsäter Henrik, Rastam Maria, Ståhlberg Ola, Gillberg Carina, Serrano Emilie, Lemière Nathalie, Launay Jean Marie, Mouren-Simeoni Marie Christine, Leboyer Marion, Gillberg Christopher, Jockers Ralf, Bourgeron Thom |
Association of GPR50, an X-linked orphan G protein-coupled receptor, and affective disorder in an independent sample of the Scottish population. Neuroscience letters 2010 May 475 (3): 169-73. Macintyre Donald J, McGhee Kevin A, Maclean Alan W, Afzal Maryam, Briffa Katy, Henry Brian, Thomson Pippa A, Muir Walter J, Blackwood Douglas H |
Mutation screening of melatonin-related genes in patients with autism spectrum disorders. BMC medical genomics 2010 Apr 3 (1): 1. Jonsson L, Ljunggren E, Bremer A, Pedersen C, Landen M, Thuresson K, Giacobini M, Melke J |
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders. Journal of pineal research 2011 Nov 51 (4): 394-9. Chaste Pauline, Clement Nathalie, Botros Hany Goubran, Guillaume Jean-Luc, Konyukh Marina, Pagan Cécile, Scheid Isabelle, Nygren Gudrun, Anckarsäter Henrik, Rastam Maria, Ståhlberg Ola, Gillberg I Carina, Melke Jonas, Delorme Richard, Leblond Claire, Toro Roberto, Huguet Guillaume, Fauchereau Fabien, Durand Christelle, Boudarene Lydia, Serrano Emilie, Lemière Nathalie, Launay Jean Marie, Leboyer Marion, Jockers Ralf, Gillberg Christopher, Bourgeron Thom |
Association of the intronic rs2072621 polymorphism of the X-linked GPR50 gene with affective disorder with seasonal pattern. European psychiatry : the journal of the Association of European Psychiatrists 2012 Jul 27 (5): 369-71. Delavest M, Even C, Benjemaa N, Poirier M-F, Jockers R, Krebs M |
Involvement of GPR50 polymorphisms in depression: independent replication in a prospective elderly cohort. Brain and behavior 2015 Mar 5 (3): e00313. Ryan Joanne, Carrière Isabelle, Ritchie Karen, Ancelin Marie-Lau |
Rapid response of stage IV colorectal cancer with APC/TP53/KRAS mutations to FOLFIRI and Bevacizumab combination chemotherapy: a case report of use of liquid biopsy. BMC medical genetics 2020 1 21 (1): 3. Hendricks Alexander, Rosenstiel Philip, Hinz Sebastian, Burmeister Greta, Röcken Christoph, Boersch Kathrin, Schafmayer Clemens, Becker Thomas, Franke Andre, Forster Micha |
A missense mutation in zinc finger homeobox-3 (ZFHX3) impedes growth and alters metabolism and hypothalamic gene expression in mice. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2023 9 37 (10): e23189. Patrick M Nolan, Gareth Banks, Nora Bourbia, Ashleigh G Wilcox, Liz Bentley, Lee Moir, Lee Kent, Rosie Hillier, Dana Wilson, Perry Barrett, Rebecca Dumbe |
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- Page last updated:Apr 16, 2024
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