Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: GNPAT[original query] |
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A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention. Biological psychiatry 2006 Sep 60 (6): 554-62. Liu Yu-Li, Fann Cathy Shen-Jang, Liu Chih-Min, Chen Wei J, Wu Jer-Yuarn, Hung Shuen-Iu, Chen Chun-Houh, Jou Yuh-Shan, Liu Shih-Kai, Hwang Tzung-Jeng, Hsieh Ming H, Ouyang Wen-Chen, Chan Hung-Yu, Chen Jiann-Jyh, Yang Wei-Chih, Lin Chin-Yu, Lee Sandy F C, Hwu Hai-G |
The role of genetic factors in patients with hepatocellular carcinoma and iron overload - a prospective series of 234 patients. Liver international : official journal of the International Association for the Study of the Liver 2015 Oct . Funakoshi Natalie, Chaze Iphigénie, Alary Anne-Sophie, Tachon Gaëlle, Cunat Séverine, Giansily-Blaizot Muriel, Bismuth Michael, Larrey Dominique, Pageaux Georges-Philippe, Schved Jean-François, Donnadieu-Rigole Hélène, Blanc Pierre, Aguilar-Martinez Patric |
Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload. Hepatology (Baltimore, Md.) 2015 Aug 62 (2): 429-39. McLaren Christine E, Emond Mary J, Subramaniam V Nathan, Phatak Pradyumna D, Barton James C, Adams Paul C, Goh Justin B, McDonald Cameron J, Powell Lawrie W, Gurrin Lyle C, Allen Katrina J, Nickerson Deborah A, Louie Tin, Ramm Grant A, Anderson Gregory J, McLaren Gordon |
The D519G Polymorphism of Glyceronephosphate O-Acyltransferase Is a Risk Factor for Familial Porphyria Cutanea Tarda. PloS one 0 11 (9): e0163322. Farrell Colin P, Overbey Jessica R, Naik Hetanshi, Nance Danielle, McLaren Gordon D, McLaren Christine E, Zhou Luming, Desnick Robert J, Parker Charles J, Phillips John |
GNPAT polymorphism rs11558492 is not associated with increased severity in a large cohort of HFE p.Cys282Tyr homozygous patients. Hepatology (Baltimore, Md.) 2016 Jul . Tchernitchko Dimitri, Scotet Virginie, Lefebvre Thibaud, L'hostis Carine, Gourlaouen Isabelle, Merour Marie-Christine, Rebah Khadidja, Peoc'h Katell, Assari Suzanne, Ferec Claude, Puy Hervé, Le Gac Géra |
GNPAT variant is associated with iron phenotype in healthy Taiwanese women: A population without the HFE C282Y mutation. Hepatology (Baltimore, Md.) 2016 Feb . Hsiao Shu-Chen, Lee Chien-Te, Pei Sung-N |
GNPAT variant (D519G) is not associated with an elevated serum ferritin or iron removed by phlebotomy in patients referred for C282Y-linked hemochromatosis. Annals of hepatology 0 15 (6): 907-910. Levstik Alexander, Stuart Alan, Adams Paul |
GNPAT rs11558492 is not a Major Modifier of Iron Status: Study of Italian Hemochromatosis Patients and Blood Donors. Annals of hepatology 0 16 (3): 451-456. Greni Federico, Valenti Luca, Mariani Raffaella, Pelloni Irene, Rametta Raffaela, Busti Fabiana, Ravasi Giulia, Girelli Domenico, Fargion Silvia, Galimberti Stefania, Piperno Alberto, Pelucchi Sa |
Increased frequency of GNPAT p.D519G in compound HFE p.C282Y/p.H63D heterozygotes with elevated serum ferritin levels. Blood cells, molecules & diseases 2020 Jul 85 102463. Secondes Eriza S, Wallace Daniel F, Rishi Gautam, McLaren Gordon D, McLaren Christine E, Chen Wen-Pin, Ramm Louise E, Powell Lawrie W, Ramm Grant A, Barton James C, Subramaniam V Nath |
Genetic adaptation of skin pigmentation in highland Tibetans. Proceedings of the National Academy of Sciences of the United States of America 2022 9 119 (40): e2200421119. Yang Zhaohui, Bai Caijuan, Pu Youwei, Kong Qinghong, Guo Yongbo, , , Liu Xuyang, Zhao Qi, Qiu Zhichao, Zheng Wangshan, He Yaoxi, Lin Yihan, Deng Lian, Zhang Chao, Xu Shuhua, Peng Yi, Xiang Kun, Zhang Xiaoming, , , Cui Chaoying, , , , Pan Yongyue, Xin Jingxue, Wang Yong, Liu Shiming, Wang Liangbang, Guo Hengliang, Feng Zhenzhen, Wang Shaobo, Shi Hong, Jiang Binghua, Wu Tianyi, Qi Xuebin, Su Bi |
Anatomical characteristics and potential gene mutation sites of a familial recurrent patellar dislocation. BMC medical genomics 2022 8 15 (1): 176. Zhang Qi-Hao, Zhang Yan, He Rui-Xuan, Guo Han-Ming, Wang Xin-Gua |
Multi-ancestry GWAS reveals excitotoxicity associated with outcome after ischaemic stroke.
Brain : a journal of neurology 2022 2 145 (7): 2394-2406. Ibanez Laura, Heitsch Laura, Carrera Caty, Farias Fabiana H G, Del Aguila Jorge L, Dhar Rajat, Budde John, Bergmann Kristy, Bradley Joseph, Harari Oscar, Phuah Chia Ling, Lemmens Robin, Viana Oliveira Souza Alessandro A, Moniche Francisco, Cabezas-Juan Antonio, Arenillas Juan Francisco, Krupinksi Jerzy, Cullell Natalia, Torres-Aguila Nuria, Muiño Elena, Cárcel-Márquez Jara, Marti-Fabregas Joan, Delgado-Mederos Raquel, Marin-Bueno Rebeca, Hornick Alejandro, Vives-Bauza Cristofol, Navarro Rosa Diaz, Tur Silvia, Jimenez Carmen, Obach Victor, Segura Tomas, Serrano-Heras Gemma, Chung Jong Won, Roquer Jaume, Soriano-Tarraga Carol, Giralt-Steinhauer Eva, Mola-Caminal Marina, Pera Joanna, Lapicka-Bodzioch Katarzyna, Derbisz Justyna, Davalos Antoni, Lopez-Cancio Elena, Muñoz Lucia, Tatlisumak Turgut, Molina Carlos, Ribo Marc, Bustamante Alejandro, Sobrino Tomas, Castillo-Sanchez Jose, Campos Francisco, Rodriguez-Castro Emilio, Arias-Rivas Susana, Rodríguez-Yáñez Manuel, Herbosa Christina, Ford Andria L, Gutierrez-Romero Alonso, Uribe-Pacheco Rodrigo, Arauz Antonio, Lopes-Cendes Iscia, Lowenkopf Theodore, Barboza Miguel A, Amini Hajar, Stamova Boryana, Ander Bradley P, Sharp Frank R, Kim Gyeong Moon, Bang Oh Young, Jimenez-Conde Jordi, Slowik Agnieszka, Stribian Daniel, Tsai Ellen A, Burkly Linda C, Montaner Joan, Fernandez-Cadenas Israel, Lee Jin Moo, Cruchaga Carl |
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- Page last updated:Apr 22, 2024
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