Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: CHD1L[original query] |
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Human gene copy number spectra analysis in congenital heart malformations. Physiological genomics 2012 Feb . Tomita-Mitchell A, Mahnke DK, Struble CA, Tuffnell ME, Stamm KD, Hidestrand M, Harris SE, Goetsch MA, Simpson PM, Bick DP, Broeckel U, Pelech AN, Tweddell JS, Mitchell ME |
Mechanistic phenotypes: an aggregative phenotyping strategy to identify disease mechanisms using GWAS data. PloS one 2013 8 (12): e81503. Mosley Jonathan D, Van Driest Sara L, Larkin Emma K, Weeke Peter E, Witte John S, Wells Quinn S, Karnes Jason H, Guo Yan, Bastarache Lisa, Olson Lana M, McCarty Catherine A, Pacheco Jennifer A, Jarvik Gail P, Carrell David S, Larson Eric B, Crosslin David R, Kullo Iftikhar J, Tromp Gerard, Kuivaniemi Helena, Carey David J, Ritchie Marylyn D, Denny Josh C, Roden Dan |
Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary Tract. Journal of clinical medicine 2020 3 9 (3): . Ahn Yo Han, Lee Chung, Kim Nayoung K D, Park Eujin, Kang Hee Gyung, Ha Il-Soo, Park Woong-Yang, Cheong Hae |
Systematic analyses of genetic variants in chromatin interaction regions identified four novel lung cancer susceptibility loci. Journal of Cancer 2020 11 (5): 1075-1081. Ji Pei, Ding Dongsheng, Qin Na, Wang Cheng, Zhu Meng, Li Yuancheng, Dai Juncheng, Jin Guangfu, Hu Zhibin, Shen Hongbing, Chen Liang, Ma Hongx |
Host genetic variation at a locus near CHD1L impacts HIV sequence diversity in a South African population. Journal of virology 2023 9 e0095423. Vanessa E Schulz, Jeffrey F Tuff, Riley H Tough, Lara Lewis, Benjamin Chimukangara, Nigel Garrett, Quarraisha Abdool Karim, Salim S Abdool Karim, Lyle R McKinnon, Ayesha B M Kharsany, Paul J McLar |
Copy number variants and fetal structural abnormalities in stillborn fetuses: A secondary analysis of the Stillbirth Collaborative Research Network study. BJOG : an international journal of obstetrics and gynaecology 2023 6 . T Workalemahu, S Dalton, S L Son, A Allshouse, A Z Carey, J M Page, N R Blue, V Thorsten, R L Goldenberg, H Pinar, U M Reddy, R M Silv |
[Analysis of clinical characteristics and molecular genetics in eighteen patients with 1q21.1 microdeletion syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 4 41 (4): 480-485. Xiaojin Luo, Hongyan Niu, Fei Zhou, Shuangwu Li, Zhenming Li, Yanyun G |
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- Page last updated:Apr 22, 2024
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