Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: UNC13B[original query] |
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G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes. Diabetes 2008 Oct 57 (10): 2843-50. Trégouet David-Alexandre, Groop Per-Henrik, McGinn Steven, Forsblom Carol, Hadjadj Samy, Marre Michel, Parving Hans-Henrik, Tarnow Lise, Telgmann Ralph, Godefroy Tiphaine, Nicaud Viviane, Rousseau Rachel, Parkkonen Maikki, Hoverfält Anna, Gut Ivo, Heath Simon, Matsuda Fumihiko, Cox Roger, Kazeem Gbenga, Farrall Martin, Gauguier Dominique, Brand-Herrmann Stefan-Martin, Cambien François, Lathrop Mark, Vionnet Nathalie, |
Genetic associations in diabetic nephropathy: a meta-analysis. Diabetologia 2010 Dec . Mooyaart AL, Valk EJ, van Es LA, Bruijn JA, de Heer E, Freedman BI, Dekkers OM, Baelde HJ |
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.
BMC medical genetics 2011 12 (1): 104. Liu Xinmin, Cheng Rong, Verbitsky Miguel, Kisselev Sergey, Browne Andrew, Mejia-Sanatana Helen, Louis Elan D, Cote Lucien J, Andrews Howard, Waters Cheryl, Ford Blair, Frucht Steven, Fahn Stanley, Marder Karen, Clark Lorraine N, Lee Joseph |
Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2016 Mar . Egawa Jun, Hoya Satoshi, Watanabe Yuichiro, Nunokawa Ayako, Shibuya Masako, Ikeda Masashi, Inoue Emiko, Okuda Shujiro, Kondo Kenji, Saito Takeo, Kaneko Naoshi, Muratake Tatsuyuki, Igeta Hirofumi, Iwata Nakao, Someya Toshiyu |
The Association of UNC13B Gene Polymorphisms and Diabetic Kidney Disease in a Chinese Han Population. Medical science monitor : international medical journal of experimental and clinical research 2019 Nov 25 8527-8533. Wang Ya, Tan Jie, Liu Dan, Yang Yameng, Wu Hongy |
Going Deep into Synaptic Vesicle Machinery Genes and Migraine Susceptibility - A Case-Control Association Study. Headache 2020 9 60 (10): 2152-2165. Quintas Marlene, Neto João Luís, Sequeiros Jorge, Sousa Alda, Pereira-Monteiro José, Lemos Carolina, Alonso Isab |
Development and clinical validation of a novel 9-gene prognostic model based on multi-omics in pancreatic adenocarcinoma. Pharmacological research 2020 Dec 105370. Xu Dafeng, Wang Yu, Liu Xiangmei, Zhou Kailun, Wu Jincai, Chen Jiacheng, Chen Cheng, Chen Liang, Zheng Jinfa |
The genetic map of diabetic nephropathy: evidence from a systematic review and meta-analysis of genetic association studies. Clinical kidney journal 2020 10 13 (5): 768-781. Tziastoudi Maria, Stefanidis Ioannis, Zintzaras Eli |
Linkage of Alzheimer disease families with Puerto Rican ancestry identifies a chromosome 9 locus. Neurobiology of aging 2021 4 104 115.e1-115.e7. Rajabli Farid, Feliciano-Astacio Briseida E, Cukier Holly N, Wang Liyong, Griswold Anthony J, Hamilton-Nelson Kara L, Adams Larry D, Rodriguez Vanessa C, Mena Pedro R, Tejada Sergio, Celis Katrina, Whitehead Patrice L, Van Booven Derek J, Hofmann Natalia K, Bussies Parker L, Prough Michael, Chinea Angel, Feliciano Nereida I, Vardarajan Badri N, Reitz Christiane, Lee Joseph H, Prince Martin J, Jimenez Ivonne Z, Mayeux Richard P, Acosta Heriberto, Dalgard Clifton L, Haines Jonathan L, Vance Jeffery M, Cuccaro Michael L, Beecham Gary W, Pericak-Vance Margaret |
UNC13B variants associated with partial epilepsy with favourable outcome. Brain : a journal of neurology 2021 4 144 (10): 3050-3060. Wang Jie, Qiao Jing-Da, Liu Xiao-Rong, Liu De-Tian, Chen Yan-Hui, Wu Yi, Sun Yan, Yu Jing, Ren Rong-Na, Mei Zhen, Liu Yu-Xi, Shi Yi-Wu, Jiang Mi, Lin Si-Mei, He Na, Li Bin, Bian Wen-Jun, Li Bing-Mei, Yi Yong-Hong, Su Tao, Liu Han-Kui, Gu Wei-Yue, Liao Wei-Pi |
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- Page last updated:Apr 16, 2024
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