Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: ILDR1[original query] |
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Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort. Genetics in medicine : official journal of the American College of Medical Genetics 2015 Jul . Bademci Guney, Foster Joseph, Mahdieh Nejat, Bonyadi Mortaza, Duman Duygu, Cengiz F Basak, Menendez Ibis, Diaz-Horta Oscar, Shirkavand Atefeh, Zeinali Sirous, Subasioglu Asli, Tokgoz-Yilmaz Suna, Huesca-Hernandez Fabiola, de la Luz Arenas-Sordo Maria, Dominguez-Aburto Juan, Hernandez-Zamora Edgar, Montenegro Paola, Paredes Rosario, Moreta Germania, Vinueza Rodrigo, Villegas Franklin, Mendoza-Benitez Santiago, Guo Shengru, Bozan Nazim, Tos Tulay, Incesulu Armagan, Sennaroglu Gonca, Blanton Susan H, Ozturkmen-Akay Hatice, Yildirim-Baylan Muzeyyen, Tekin Musta |
A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records.
PLoS genetics 2016 Oct 12 (10): e1006371. Hoffmann Thomas J, Keats Bronya J, Yoshikawa Noriko, Schaefer Catherine, Risch Neil, Lustig Lawrence |
A Novel p.G141R Mutation in ILDR1 Leads to Recessive Nonsyndromic Deafness DFNB42 in Two Chinese Han Families. Neural plasticity 2018 6 2018 7272308. Wang Xueling, Wang Longhao, Peng Hu, Yang Tao, Wu H |
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment.
Scientific reports 2019 Oct 9 (1): 15192. Nagtegaal Andries Paul, Broer Linda, Zilhao Nuno R, Jakobsdottir Johanna, Bishop Charles E, Brumat Marco, Christiansen Mark W, Cocca Massimiliano, Gao Yan, Heard-Costa Nancy L, Evans Daniel S, Pankratz Nathan, Pratt Sheila R, Price T Ryan, Spankovich Christopher, Stimson Mary R, Valle Karen, Vuckovic Dragana, Wells Helena, Eiriksdottir Gudny, Fransen Erik, Ikram Mohammad Arfan, Li Chuang-Ming, Longstreth W T, Steves Claire, Van Camp Guy, Correa Adolfo, Cruickshanks Karen J, Gasparini Paolo, Girotto Giorgia, Kaplan Robert C, Nalls Michael, Schweinfurth John M, Seshadri Sudha, Sotoodehnia Nona, Tranah Gregory J, Uitterlinden André G, Wilson James G, Gudnason Vilmundur, Hoffman Howard J, Williams Frances M K, Goedegebure And |
Inherited variants at 3q13.33 and 3p24.1 are associated with risk of diffuse large B-cell lymphoma and implicate immune pathways. Human molecular genetics 2019 10 29 (1): 70-79. Kleinstern Geffen, Yan Huihuang, Hildebrandt Michelle A T, Vijai Joseph, Berndt Sonja I, Ghesquières Hervé, McKay James, Wang Sophia S, Nieters Alexandra, Ye Yuanqing, Monnereau Alain, Brooks-Wilson Angela R, Lan Qing, Melbye Mads, Jackson Rebecca D, Teras Lauren R, Purdue Mark P, Vajdic Claire M, Vermeulen Roel C H, Giles Graham G, Cocco Pier Luigi, Birmann Brenda M, Kraft Peter, Albanes Demetrius, Zeleniuch-Jacquotte Anne, Crouch Simon, Zhang Yawei, Sarangi Vivekananda, Asmann Yan, Offit Kenneth, Salles Gilles, Wu Xifeng, Smedby Karin E, Skibola Christine F, Slager Susan L, Rothman Nathaniel, Chanock Stephen J, Cerhan James |
A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility.
Cancer research 2020 12 81 (7): 1695-1703. Emami Nima C, Cavazos Taylor B, Rashkin Sara R, Cario Clinton L, Graff Rebecca E, Tai Caroline G, Mefford Joel A, Kachuri Linda, Wan Eunice, Wong Simon, Aaronson David, Presti Joseph, Habel Laurel A, Shan Jun, Ranatunga Dilrini K, Chao Chun R, Ghai Nirupa R, Jorgenson Eric, Sakoda Lori C, Kvale Mark N, Kwok Pui-Yan, Schaefer Catherine, Risch Neil, Hoffmann Thomas J, Van Den Eeden Stephen K, Witte John |
Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria. European journal of human genetics : EJHG 2021 Nov . Adeyemo Adebolajo, Faridi Rabia, Chattaraj Parna, Yousaf Rizwan, Tona Risa, Okorie Samuel, Bharadwaj Thashi, Nouel-Saied Liz M, Acharya Anushree, Schrauwen Isabelle, Morell Robert J, Leal Suzanne M, Friedman Thomas B, Griffith Andrew J, Roux Isabel |
Analyses of the expression and prognosis of ILDR1 in human gastric cancer. Heliyon 2022 9 8 (9): e10253. Wang Li, Zhai Rujun, Song Guodong, Wang Yo |
Potential susceptibility genes in patients with stage III and IV periodontitis: A whole-exome sequencing pilot study. Biomolecules & biomedicine 2023 7 . Fan Xue, Jianjiang Zhao, XiaoCui Gao, Xuehai Jiang, Zedong L |
Imputation of SNPs associated with presbycusis through linkage disequilibrium analysis in the ILDR1 gene. Journal of genetics 2023 2 102 . Flores Sergio V, Levi-Monsalve Alejandro, Alvarez-Lobo Juan Pab |
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- Page last updated:Apr 16, 2024
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