Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and ABHD12[original query] |
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Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.
Nature genetics 2011 Nov 43 (11): 1131-8. Chambers John C, Zhang Weihua, Sehmi Joban, Li Xinzhong, Wass Mark N, Van der Harst Pim, Holm Hilma, Sanna Serena, Kavousi Maryam, Baumeister Sebastian E, Coin Lachlan J, Deng Guohong, Gieger Christian, Heard-Costa Nancy L, Hottenga Jouke-Jan, Kühnel Brigitte, Kumar Vinod, Lagou Vasiliki, Liang Liming, Luan Jian'an, Vidal Pedro Marques, Mateo Leach Irene, O'Reilly Paul F, Peden John F, Rahmioglu Nilufer, Soininen Pasi, Speliotes Elizabeth K, Yuan Xin, Thorleifsson Gudmar, Alizadeh Behrooz Z, Atwood Larry D, Borecki Ingrid B, Brown Morris J, Charoen Pimphen, Cucca Francesco, Das Debashish, de Geus Eco J C, Dixon Anna L, Döring Angela, Ehret Georg, Eyjolfsson Gudmundur I, Farrall Martin, Forouhi Nita G, Friedrich Nele, Goessling Wolfram, Gudbjartsson Daniel F, Harris Tamara B, Hartikainen Anna-Liisa, Heath Simon, Hirschfield Gideon M, Hofman Albert, Homuth Georg, Hyppönen Elina, Janssen Harry L A, Johnson Toby, Kangas Antti J, Kema Ido P, Kühn Jens P, Lai Sandra, Lathrop Mark, Lerch Markus M, Li Yun, Liang T Jake, Lin Jing-Ping, Loos Ruth J F, Martin Nicholas G, Moffatt Miriam F, Montgomery Grant W, Munroe Patricia B, Musunuru Kiran, Nakamura Yusuke, O'Donnell Christopher J, Olafsson Isleifur, Penninx Brenda W, Pouta Anneli, Prins Bram P, Prokopenko Inga, Puls Ralf, Ruokonen Aimo, Savolainen Markku J, Schlessinger David, Schouten Jeoffrey N L, Seedorf Udo, Sen-Chowdhry Srijita, Siminovitch Katherine A, Smit Johannes H, Spector Timothy D, Tan Wenting, Teslovich Tanya M, Tukiainen Taru, Uitterlinden Andre G, Van der Klauw Melanie M, Vasan Ramachandran S, Wallace Chris, Wallaschofski Henri, Wichmann H-Erich, Willemsen Gonneke, Würtz Peter, Xu Chun, Yerges-Armstrong Laura M, , , , , , , , Abecasis Goncalo R, Ahmadi Kourosh R, Boomsma Dorret I, Caulfield Mark, Cookson William O, van Duijn Cornelia M, Froguel Philippe, Matsuda Koichi, McCarthy Mark I, Meisinger Christa, Mooser Vincent, Pietiläinen Kirsi H, Schumann Gunter, Snieder Harold, Sternberg Michael J E, Stolk Ronald P, Thomas Howard C, Thorsteinsdottir Unnur, Uda Manuela, Waeber Gérard, Wareham Nicholas J, Waterworth Dawn M, Watkins Hugh, Whitfield John B, Witteman Jacqueline C M, Wolffenbuttel Bruce H R, Fox Caroline S, Ala-Korpela Mika, Stefansson Kari, Vollenweider Peter, Völzke Henry, Schadt Eric E, Scott James, Järvelin Marjo-Riitta, Elliott Paul, Kooner Jaspal |
| Comprehensive Molecular Screening in Chinese Usher Syndrome Patients. Investigative ophthalmology & visual science 2018 Mar 59 (3): 1229-1237. Sun Tengyang, Xu Ke, Ren Yanfan, Xie Yue, Zhang Xiaohui, Tian Lu, Li Ya |
| Genotype-phenotype spectrum and correlation of PHARC Syndrome due to pathogenic ABHD12 variants. BMC medical genomics 2024 8 17 (1): 203. Xicui Long, Wenyu Xiong, Xuegang Wang, Jia Geng, Mingjun Zhong, Yu Huang, Man Liu, Fengxiao Bu, Jing Cheng, Yu Lu, Huijun Yu |
| Comprehensive variant analysis of phospholipase A2 superfamily genes in large Chinese Parkinson' s disease cohorts. Mechanisms of ageing and development 2024 5 219 111940. Jiabin Liu, Yige Wang, Yuwen Zhao, Hongxu Pan, Zhenhua Liu, Qian Xu, Shen Lu, Hong Jiang, Junling Wang, Qiying Sun, Jieqiong Tan, Xinxiang Yan, Jinchen Li, Beisha Tang, Jifeng G |
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