Human Genome Epidemiology Literature Finder
Reproductive and Child Health
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Records 1 - 18 (of 18 Records) |
| Query Trace: Hearing Loss Or Hearing Screening Or Congenital Deafness[original query] |
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A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.
American journal of human genetics 2009 Mar 84 (3): 328-38. Schrauwen Isabelle, Ealy Megan, Huentelman Matthew J, Thys Melissa, Homer Nils, Vanderstraeten Kathleen, Fransen Erik, Corneveaux Jason J, Craig David W, Claustres Mireille, Cremers Cor W R J, Dhooge Ingeborg, Van de Heyning Paul, Vincent Robert, Offeciers Erwin, Smith Richard J H, Van Camp G |
| Genetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise.
PloS one 2015 10 (6): e0130827. Grondin Yohann, Bortoni Magda E, Sepulveda Rosalinda, Ghelfi Elisa, Bartos Adam, Cotanche Douglas, Clifford Royce E, Rogers Rick |
| 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 |
| Variants in WFS1 and Other Mendelian Deafness Genes Are Associated with Cisplatin-Associated Ototoxicity.
Clinical cancer research : an official journal of the American Association for Cancer Research 2016 Dec . Wheeler Heather E, Gamazon Eric R, Frisina Robert D, Perez-Cervantes Carlos, El Charif Omar, Mapes Brandon, Fossa Sophie D, Feldman Darren R, Hamilton Robert J, Vaughn David J, Beard Clair J, Fung Chunkit, Kollmannsberger Christian, Kim Jeri, Mushiroda Taisei, Kubo Michiaki, Ardeshir-Rouhani-Fard Shirin, Einhorn Lawrence H, Cox Nancy J, Dolan M Eileen, Travis Lois |
| Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study.
Journal of neuromuscular diseases 2019 6 (2): 201-211. Tao Feifei, Beecham Gary W, Rebelo Adriana P, Blanton Susan H, Moran John J, Lopez-Anido Camila, Svaren John, Abreu Lisa, Rizzo Devon, Kirk Callyn A, Wu Xingyao, Feely Shawna, Verhamme Camiel, Saporta Mario A, Herrmann David N, Day John W, Sumner Charlotte J, Lloyd Thomas E, Li Jun, Yum Sabrina W, Taroni Franco, Baas Frank, Choi Byung-Ok, Pareyson Davide, Scherer Steven S, Reilly Mary M, Shy Michael E, Züchner Stephan, |
| 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 |
| GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank.
American journal of human genetics 2019 Oct 105 (4): 788-802. Wells Helena R R, Freidin Maxim B, Zainul Abidin Fatin N, Payton Antony, Dawes Piers, Munro Kevin J, Morton Cynthia C, Moore David R, Dawson Sally J, Williams Frances M |
| Genome-wide association study identifies 7q11.22 and 7q36.3 associated with noise-induced hearing loss among Chinese population.
Journal of cellular and molecular medicine 2020 Nov . Niu Yuguang, Xie Chengyong, Du Zhenhua, Zeng Jifeng, Chen Hongxia, Jin Liang, Zhang Qing, Yu Huiying, Wang Yahui, Ping Jie, Yang Chenning, Liu Xinyi, Li Yuanfeng, Zhou Gangqi |
| A Genome-wide Association Study for Concussion Risk.
Medicine and science in sports and exercise 2020 (4): 704-711. Kim Stuart K, Roche Megan D, Fredericson Michael, Dragoo Jason L, Horton Brandon H, Avins Andy L, Belanger Heather G, Ioannidis John P A, Abrams Geoffrey |
| Clinical and Genome-Wide Analysis of Multiple Severe Cisplatin-Induced Neurotoxicities in Adult-Onset Cancer Survivors.
Clinical cancer research : an official journal of the American Association for Cancer Research 2020 (24): 6550-6558. Trendowski Matthew R, Wheeler Heather E, El-Charif Omar, Feldman Darren R, Hamilton Robert J, Vaughn David J, Fung Chunkit, Kollmannsberger Christian, Einhorn Lawrence H, Travis Lois B, Dolan M Eile |
| Novel Risk Loci in Tinnitus and Causal Inference With Neuropsychiatric Disorders Among Adults of European Ancestry.
JAMA otolaryngology-- head & neck surgery 2020 9 146 (11): 1015-1025. Clifford Royce E, Maihofer Adam X, Stein Murray B, Ryan Allen F, Nievergelt Caroline |
| TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study.
NPJ precision oncology 2021 7 5 (1): 64. Meijer A J M, Diepstraten F A, Langer T, Broer L, Domingo I K, Clemens E, Uitterlinden A G, de Vries A C H, van Grotel M, Vermeij W P, Ozinga R A, Binder H, Byrne J, van Dulmen-den Broeder E, Garrè M L, Grabow D, Kaatsch P, Kaiser M, Kenborg L, Winther J F, Rechnitzer C, Hasle H, Kepak T, Kepakova K, Tissing W J E, van der Kooi A L F, Kremer L C M, Kruseova J, Pluijm S M F, Kuehni C E, van der Pal H J H, Parfitt R, Spix C, Tillmanns A, Deuster D, Matulat P, Calaminus G, Hoetink A E, Elsner S, Gebauer J, Haupt R, Lackner H, Blattmann C, Neggers S J C M M, Rassekh S R, Wright G E B, Brooks B, Nagtegaal A P, Drögemöller B I, Ross C J D, Bhavsar A P, Am Zehnhoff-Dinnesen A G, Carleton B C, Zolk O, van den Heuvel-Eibrink M M, , |
| Genome-wide association study suggests that variation at the RCOR1 locus is associated with tinnitus in UK Biobank.
Scientific reports 2021 (1): 6470. Wells Helena R R, Abidin Fatin N Zainul, Freidin Maxim B, Williams Frances M K, Dawson Sally |
| Glucose hypometabolism in the Auditory Pathway in Age Related Hearing Loss in the ADNI cohort.
NeuroImage. Clinical 2021 Sep 32 102823. Zainul Abidin Fatin N, Scelsi Marzia A, Dawson Sally J, Altmann Andre, |
| A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo.
Communications biology 2021 Oct 4 (1): 1148. Skuladottir Astros Th, Bjornsdottir Gyda, Nawaz Muhammad Sulaman, Petersen Hannes, Rognvaldsson Solvi, Moore Kristjan Helgi Swerford, Olafsson Pall I, Magnusson Sigurður H, Bjornsdottir Anna, Sveinsson Olafur A, Sigurdardottir Gudrun R, Saevarsdottir Saedis, Ivarsdottir Erna V, Stefansdottir Lilja, Gunnarsson Bjarni, Muhlestein Joseph B, Knowlton Kirk U, Jones David A, Nadauld Lincoln D, Hartmann Annette M, Rujescu Dan, Strupp Michael, Walters G Bragi, Thorgeirsson Thorgeir E, Jonsdottir Ingileif, Holm Hilma, Thorleifsson Gudmar, Gudbjartsson Daniel F, Sulem Patrick, Stefansson Hreinn, Stefansson Ka |
| Population-scale analysis of common and rare genetic variation associated with hearing loss in adults.
Communications biology 2022 06 5 (1): 540. Praveen Kavita, Dobbyn Lee, Gurski Lauren, Ayer Ariane H, Staples Jeffrey, Mishra Shawn, Bai Yu, Kaufman Alexandra, Moscati Arden, Benner Christian, Chen Esteban, Chen Siying, Popov Alexander, Smith Janell, , , , Melander Olle, Jones Marcus B, Marchini Jonathan, Balasubramanian Suganthi, Zambrowicz Brian, Drummond Meghan C, Baras Aris, Abecasis Goncalo R, Ferreira Manuel A, Stahl Eli A, Coppola Giovan |
| Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure.
Nature communications 2023 1 14 (1): 157. Rämö Joel T, Kiiskinen Tuomo, Seist Richard, Krebs Kristi, Kanai Masahiro, Karjalainen Juha, Kurki Mitja, Hämäläinen Eija, Häppölä Paavo, Havulinna Aki S, Hautakangas Heidi, , Mägi Reedik, Palta Priit, Esko Tõnu, Metspalu Andres, Pirinen Matti, Karczewski Konrad J, Ripatti Samuli, Milani Lili, Stankovic Konstantina M, Mäkitie Antti, Daly Mark J, Palotie Aar |
| Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort.
PLoS genetics 2023 1 19 (1): e1010584. Hui Daniel, Mehrabi Shadi, Quimby Alexandra E, Chen Tingfang, Chen Sixing, Park Joseph, Li Binglan, , , Ruckenstein Michael J, Rader Daniel J, Ritchie Marylyn D, Brant Jason A, Epstein Douglas J, Mathieson Ia |
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