Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: SOS2[original query] |
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Candidate gene association study of insulin signaling genes and Alzheimer's disease: evidence for SOS2, PCK1, and PPARgamma as susceptibility loci. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Jun 144B (4): 508-16. Hamilton Gillian, Proitsi Petra, Jehu Luke, Morgan Angharad, Williams Julie, O'Donovan Michael C, Owen Michael J, Powell John F, Lovestone Sim |
A pharmacogenomic approach to the treatment of children with GH deficiency or Turner syndrome. European journal of endocrinology / European Federation of Endocrine Societies 2013 Sep 169 (3): 277-89. Clayton P, Chatelain P, Tatò L, Yoo H W, Ambler G R, Belgorosky A, Quinteiro S, Deal C, Stevens A, Raelson J, Croteau P, Destenaves B, Olivier |
Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years.
G3 (Bethesda, Md.) 2014 Feb 4 (2): 307-14. Shaffer John R, Polk Deborah E, Wang Xiaojing, Feingold Eleanor, Weeks Daniel E, Lee Myoung-Keun, Cuenco Karen T, Weyant Robert J, Crout Richard J, McNeil Daniel W, Marazita Mary |
Exome sequencing of desmoplastic melanoma identifies recurrent NFKBIE promoter mutations and diverse activating mutations in the MAPK pathway. Nature genetics 2015 Sep . Shain A Hunter, Garrido Maria, Botton Thomas, Talevich Eric, Yeh Iwei, Sanborn J Zachary, Chung Jongsuk, Wang Nicholas J, Kakavand Hojabr, Mann Graham J, Thompson John F, Wiesner Thomas, Roy Ritu, Olshen Adam B, Gagnon Alexander, Gray Joe W, Huh Nam, Hur Joe S, Busam Klaus J, Scolyer Richard A, Cho Raymond J, Murali Rajmohan, Bastian Boris |
Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications. European journal of human genetics : EJHG 2020 8 29 (1): 51-60. Lissewski Christina, Chune Valérie, Pantaleoni Francesca, De Luca Alessandro, Capri Yline, Brinkmann Julia, Lepri Francesca, Daniele Paola, Leenders Erika, Mazzanti Laura, Scarano Emanuela, Radio Francesca Clementina, Kutsche Kerstin, Kuechler Alma, Gérard Marion, Ranguin Kara, Legendre Marine, Vial Yoann, van der Burgt Ineke, Rinne Tuula, Andreucci Elena, Mastromoro Gioia, Digilio Maria Cristina, Cave Hélène, Tartaglia Marco, Zenker Mart |
A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population. PLoS genetics 2020 Nov 16 (11): e1008802. Tcheandjieu Catherine, Aguirre Matthew, Gustafsson Stefan, Saha Priyanka, Potiny Praneetha, Haendel Melissa, Ingelsson Erik, Rivas Manuel A, Priest James |
Identification of Rare Variants in Right Ventricular Outflow Tract Obstruction Congenital Heart Disease by Whole-Exome Sequencing. Frontiers in cardiovascular medicine 2022 2 8 811156. Zhou Yue, Bai Kai, Wang Yu, Meng Zhuo, Zhou Shuang, Jiang Shiwei, Wang Hualin, Wang Jian, Yang Mei, Wang Qingjie, Sun Kun, Chen S |
Genetic variants of SOS2, MAP2K1 and RASGRF2 in the RAS pathway genes predict survival of HBV-related hepatocellular carcinoma patients. Archives of toxicology 2023 4 . Lin Qiuling, Qiu Moqin, Wei Xueyan, Xiang Zhouyun, Zhou Zihan, Ji Iiangyan, Liang Xiumei, Zhou Xianguo, Wen Qiuping, Liu Yingchun, Yu Hongpi |
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- Page last updated:Apr 29, 2024
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