HuGE Literature Finder
Records 1-27
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Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric population.
Scientific reports 2019 Feb 9 (1): 1604. Han Jae Joon, Nguyen Pham Dinh, Oh Doo-Yi, Han Jin Hee, Kim Ah-Reum, Kim Min Young, Park Hye-Rim, Tran Lam Huyen, Dung Nguyen Huu, Koo Ja-Won, Lee Jun Ho, Oh Seung Ha, Anh Vu Hoang, Choi Byung Yo |
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Effect of GRM7 polymorphisms on the development of noise-induced hearing loss in Chinese Han workers: a nested case-control study.
BMC medical genetics 2018 Jan 19 (1): 4. Yu Peipei, Jiao Jie, Chen Guoshun, Zhou Wenhui, Zhang Huanling, Wu Hui, Li Yanhong, Gu Guizhen, Zheng Yuxin, Yu Yue, Yu Shan |
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Recurrent, low-frequency coding variants contributing to colorectal cancer in the Swedish population.
PloS one 2018 13 (3): e0193547. Jiao Xiang, Liu Wen, Mahdessian Hovsep, Bryant Patrick, Ringdahl Jenny, Timofeeva Maria, Farrington Susan M, Dunlop Malcolm, Lindblom Anni |
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Polygenic Profile and Exercise-Induced Muscle Damage by a Competitive Half-Ironman.
Journal of strength and conditioning research 2017 Nov . Del Coso Juan, Salinero Juan J, Lara Beatriz, Gallo-Salazar César, Areces Francisco, Herrero David, Puente Carl |
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Genome-wide analysis of genetic risk factors for rheumatic heart disease in Aboriginal Australians provides support for pathogenic molecular mimicry.
The Journal of infectious diseases 2017 Sep . Gray Lesley-Ann, D'Antoine Heather A, Tong Steven Y C, McKinnon Melita, Bessarab Dawn, Brown Ngaire, Reményi Bo, Steer Andrew, Syn Genevieve, Blackwell Jenefer M, Inouye Michael, Carapetis Jonathan |
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A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.
European heart journal 2017 01 38 (1): 27-34. Gudbjartsson Daniel F, Holm Hilma, Sulem Patrick, Masson Gisli, Oddsson Asmundur, Magnusson Olafur Th, Saemundsdottir Jona, Helgadottir Hafdis Th, Helgason Hannes, Johannsdottir Hrefna, Gretarsdottir Solveig, Gudjonsson Sigurjon A, Njølstad Inger, Løchen Maja-Lisa, Baum Larry, Ma Ronald C W, Sigfusson Gunnlaugur, Kong Augustine, Thorgeirsson Guðmundur, Sverrisson Jon Th, Thorsteinsdottir Unnur, Stefansson Kari, Arnar David |
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A genotypic ascertainment approach to refute the association of MYO1A variants with non-syndromic deafness.
European journal of human genetics : EJHG 2016 Oct . Patton John, Brewer Carmen, Chien Wade, Johnston Jennifer J, Griffith Andrew J, Biesecker Leslie |
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Targeted next-generation sequencing helps to decipher the genetic and phenotypic heterogeneity of hypertrophic cardiomyopathy.
International journal of molecular medicine 2016 Sep . Cecconi Massimiliano, Parodi Maria I, Formisano Francesco, Spirito Paolo, Autore Camillo, Musumeci Maria B, Favale Stefano, Forleo Cinzia, Rapezzi Claudio, Biagini Elena, Davì Sabrina, Canepa Elisabetta, Pennese Loredana, Castagnetta Mauro, Degiorgio Dario, Coviello Domenico |
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Genetic association of MYH genes with hereditary hearing loss in Korea.
Gene 2016 Jul . Kim Sang-Joo, Lee Seokwon, Park Hong-Joon, Kang Tae-Hun, Sagong Borum, Baek Jeong-In, Oh Se-Kyung, Choi Jae Young, Lee Kyu-Yup, Kim Un-Kyu |
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Association of MYH9 rs3752462 and rs5756168 Polymorphisms With Transplanted Kidney Artery Stenosis.
Transplantation proceedings 2016 Jun 48 (5): 1561-5. Pazik J, Lewandowski Z, Oldak M, Ozieblo D, Perkowska Ptasinska A, Sadowska A, Nowacka-Cieciura E, Nowaczyk M, Malejczyk J, Kwiatkowski A, Durlik |
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Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system.
International journal of molecular medicine 2016 Apr . Zhao Yue, Cao Hong, Song Yindi, Feng Yue, Ding Xiaoxue, Pang Mingjie, Zhang Yunmei, Zhang Hong, Ding Jiahuan, Xia Xuesh |
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MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patients.
Orphanet journal of rare diseases 2016 11 (1): 91. Fiorillo C, Astrea G, Savarese M, Cassandrini D, Brisca G, Trucco F, Pedemonte M, Trovato R, Ruggiero L, Vercelli L, D'Amico A, Tasca G, Pane M, Fanin M, Bello L, Broda P, Musumeci O, Rodolico C, Messina S, Vita G L, Sframeli M, Gibertini S, Morandi L, Mora M, Maggi L, Petrucci A, Massa R, Grandis M, Toscano A, Pegoraro E, Mercuri E, Bertini E, Mongini T, Santoro L, Nigro V, Minetti C, Santorelli F M, Bruno C, |
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Spectrum of MYBPC3 Gene Mutations in Patients with Hypertrophic Cardiomyopathy, Reporting Two Novel Mutations from North-West of Iran.
Clinical laboratory 2016 62 (5): 757-64. Emrahi Leila, Tabrizi Mehrnoush Toufan, Gharehsouran Jalal, Ardebili Seyyed Mojtaba Mohaddes, Estiar Mehrdad Asgha |
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Updated field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma: the MelGene database.
The Journal of investigative dermatology 2015 Apr 135 (4): 1074-9. Antonopoulou Kyriaki, Stefanaki Irene, Lill Christina M, Chatzinasiou Foteini, Kypreou Katerina P, Karagianni Fani, Athanasiadis Emmanouil, Spyrou George M, Ioannidis John P A, Bertram Lars, Evangelou Evangelos, Stratigos Alexander |
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Evaluation of genetic variants in miRNAs in patients with colorectal cancer.
Cancer biomarkers : section A of Disease markers 2015 15 (2): 157-62. Dikaiakos Panagiotis, Gazouli Maria, Rizos Spyros, Zografos George, Theodoropoulos George |
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Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss.
BMC genomics 2014 15 (1): 1155. Haraksingh Rajini R, Jahanbani Fereshteh, Rodriguez-Paris Juan, Gelernter Joel, Nadeau Kari C, Oghalai John S, Schrijver Iris, Snyder Michael |
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Pathway-based analysis of genetic susceptibility to cervical cancer in situ: HLA-DPB1 affects risk in Swedish women.
Genes and immunity 2011 Dec 12 (8): 605-14. Ivansson E L, Juko-Pecirep I, Erlich H A, Gyllensten U |
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Association between single-nucleotide polymorphisms in pre-miRNAs and the risk of asthma in a Chinese population.
DNA and cell biology 2011 Nov 30 (11): 919-23. Su Xiao-Wei, Yang Yan, Lv Mei-Li, Li Li-Juan, Dong Wei, Miao-Liao , Gao Lin-Bo, Luo Hai-Bo, Yun-Liu , Cong Rui-Juan, Liang Wei-Bo, Li Ying- |
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Comprehensive Field Synopsis and Systematic Meta-analyses of Genetic Association Studies in Cutaneous Melanoma.
Journal of the National Cancer Institute 2011 Jun . Chatzinasiou F, Lill CM, Kypreou K, Stefanaki I, Nicolaou V, Spyrou G, Evangelou E, Roehr JT, Kodela E, Katsambas A, Tsao H, Ioannidis JP, Bertram L, Stratigos AJ |
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Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
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Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care 2010 Oct 33 (10): 2250-3. Bailey Swneke D, Xie Changchun, Do Ron, Montpetit Alexandre, Diaz Rafael, Mohan Viswanathan, Keavney Bernard, Yusuf Salim, Gerstein Hertzel C, Engert James C, Anand Sonia, |
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Common genetic variants in pre-microRNAs and risk of gallbladder cancer in North Indian population.
Journal of human genetics 2010 Aug 55 (8): 495-9. Srivastava Kshitij, Srivastava Anvesha, Mittal Balr |
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Genetic variations of ?-MYH7 in hypertrophic cardiomyopathy and dilated cardiomyopathy.
Indian journal of human genetics 2010 May 16 (2): 67-71. Tanjore Reena, Rangaraju Advithi, Vadapalli Shivani, Remersu Sushant, Narsimhan Calambur, Nallari Pratib |
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Modest association of malignant melanoma with the rs910873 and rs1885120 markers on chromosome 20: a population-based study.
Melanoma research 2010 Apr 20 (2): 159-60. Debniak Tadeusz, Gapska Paulina, Serrano-Fernandez Pablo, Rassoud Ibrahim, Cybulski Cezary, Maleszka Romuald, Sulikowski Mieczys?aw, Narod Steven, Lubi?ski J |
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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
American journal of human genetics 2009 Nov 85 (5): 628-42. Talmud Philippa J, Drenos Fotios, Shah Sonia, Shah Tina, Palmen Jutta, Verzilli Claudio, Gaunt Tom R, Pallas Jacky, Lovering Ruth, Li Kawah, Casas Juan Pablo, Sofat Reecha, Kumari Meena, Rodriguez Santiago, Johnson Toby, Newhouse Stephen J, Dominiczak Anna, Samani Nilesh J, Caulfield Mark, Sever Peter, Stanton Alice, Shields Denis C, Padmanabhan Sandosh, Melander Olle, Hastie Claire, Delles Christian, Ebrahim Shah, Marmot Michael G, Smith George Davey, Lawlor Debbie A, Munroe Patricia B, Day Ian N, Kivimaki Mika, Whittaker John, Humphries Steve E, Hingorani Aroon D, , , |
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Common genetic variants in pre-microRNAs were associated with increased risk of breast cancer in Chinese women.
Human mutation 2009 Jan 30 (1): 79-84. Hu Zhibin, Liang Jie, Wang Zhanwei, Tian Tian, Zhou Xiaoyi, Chen Jiaping, Miao Ruifen, Wang Yan, Wang Xinru, Shen Hongbi |
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Investigation of MYH14 as a candidate gene in cleft lip with or without cleft palate.
European journal of oral sciences 2008 Jun 116 (3): 287-90. Martinelli Marcella, Arlotti Marzia, Palmieri Annalisa, Scapoli Luca, Savoia Anna, Di Stazio Mariateresa, Pezzetti Furio, Masiero Elena, Carinci Frances |
- Page last reviewed:Jul 30, 2019
- Page last updated:Jan 23, 2020
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