Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: MYCT1[original query] |
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Novel genes and variants associated with IgA nephropathy by co-segregating with the disease phenotypes in 10 IgAN families. Gene 2015 Oct 571 (1): 43-51. Liu Ruihong, Hu Bin, Li Qibin, Jing Xiangyi, Zhong Cheng, Chang Yu, Liao Qijun, Lam Man F, Leung Joseph C K, Lai Kar N, Wang Yimi |
Founder Mutations for Early Onset Melanoma as Revealed by Whole Exome Sequencing Suggests That This is Not Associated with the Increasing Incidence of Melanoma in Poland. Cancer research and treatment 2018 May . D?bniak Tadeusz, Scott Rodney J, Lea Rodney A, Górski Bohdan, Masoj? Bart?omiej, Cybulski Cezary, Kram Andrzej, Maleszka Romuald, Gromowski Tomasz, Paszkowska-Szczur Katarzyna, Kashyap Aniruddh, Lener Marcin R, Mali?ska Karolina, Rogo?a Emilia, Murawa Dawid, Rudnicka Helena, Deptu?a Jakub, Lubi?ski J |
Identification of novel genes by targeted exome sequencing in Retinoblastoma. Ophthalmic genetics 2022 8 43 (6): 771-788. Bisht Shilpa, Chawla Bhavna, Kumar Amit, Vijayan Viswanathan, Kumar Manoj, Sharma Pradeep, Dada Ri |
Genetic variants associated with circulating liver injury markers in Mexican Americans, a population at risk for non-alcoholic fatty liver disease. Frontiers in genetics 2022 11 13 995488. Sabotta Caroline M, Kwan Suet-Ying, Petty Lauren E, Below Jennifer E, Joon Aron, Wei Peng, Fisher-Hoch Susan P, McCormick Joseph B, Beretta Lau |
Identification of Genetic Risk Factors for Keratinocyte Cancer in Immunosuppressed Solid Organ Transplant Recipients: A Case-Control Study. Cancers 2023 7 15 (13): . Raute Sunder-Plassmann, Alexandra Geusau, Georg Endler, Wolfgang Weninger, Matthias Wielsch |
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