Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: GTF2H4[original query] |
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Variation within DNA repair pathway genes and risk of multiple sclerosis. American journal of epidemiology 2010 Jul 172 (2): 217-24. Briggs Farren B S, Goldstein Benjamin A, McCauley Jacob L, Zuvich Rebecca L, De Jager Philip L, Rioux John D, Ivinson Adrian J, Compston Alastair, Hafler David A, Hauser Stephen L, Oksenberg Jorge R, Sawcer Stephen J, Pericak-Vance Margaret A, Haines Jonathan L, Barcellos Lisa F, |
Common genetic variants and risk for HPV persistence and progression to cervical cancer. PloS one 2010 1 5 (1): e8667. Wang Sophia S, Gonzalez Paula, Yu Kai, Porras Carolina, Li Qizhai, Safaeian Mahboobeh, Rodriguez Ana Cecilia, Sherman Mark E, Bratti Concepcion, Schiffman Mark, Wacholder Sholom, Burk Robert D, Herrero Rolando, Chanock Stephen J, Hildesheim All |
Genetic variability in DNA repair and cell cycle control pathway genes and risk of smoking-related lung cancer. Molecular carcinogenesis 2012 Oct 51 Suppl 1 E11-20. Buch Shama C, Diergaarde Brenda, Nukui Tomoko, Day Roger S, Siegfried Jill M, Romkes Marjorie, Weissfeld Joel |
Lack of association between GTF2H4 genetic variants and AERD development and FEV1 decline by aspirin provocation. International journal of immunogenetics 2012 Dec 39 (6): 486-91. Kim J Y, Kim J-H, Bae J S, Park B-L, Uh S-T, Kim M-K, Choi I S, Cho S H, Park C-S, Shin H |
Genetic variant in DNA repair gene GTF2H4 is associated with lung cancer risk: a large-scale analysis of six published GWAS datasets in the TRICL consortium. Carcinogenesis 2016 Jun . Wang Meilin, Liu Hongliang, Liu Zhensheng, Yi Xiaohua, Bickeboller Heike, Hung Rayjean J, Brennan Paul, Landi Maria Teresa, Caporaso Neil, Christiani David C, Doherty Jennifer Anne, , Amos Christopher I, Wei Qing |
Single nucleotide polymorphisms of nucleotide excision repair pathway are significantly associated with outcomes of platinum-based chemotherapy in lung cancer. Scientific reports 2017 Sep 7 (1): 11785. Song Xiao, Wang Shiming, Hong Xuan, Li Xiaoying, Zhao Xueying, Huai Cong, Chen Hongyan, Gao Zhiqiang, Qian Ji, Wang Jiucun, Han Baohui, Bai Chunxue, Li Qiang, Wu Junjie, Lu Da |
Genetic variations in the SULF1 gene alter the risk of cervical cancer and precancerous lesions. Oncology letters 2018 Sep 16 (3): 3833-3841. Dardiotis Efthimios, Siokas Vasileios, Garas Antonios, Paraskevaidis Evangelos, Kyrgiou Maria, Xiromerisiou Georgia, Deligeoroglou Efthimios, Galazios Georgios, Kontomanolis Emmanuel N, Spandidos Demetrios A, Tsatsakis Aristidis, Daponte Alexandr |
Genetic variants of genes in the NER pathway associated with risk of breast cancer: A large-scale analysis of 14 published GWAS datasets in the DRIVE study. International journal of cancer 2019 Apr . Ge Jie, Liu Hongliang, Qian Danwen, Wang Xiaomeng, Moorman Patricia G, Luo Sheng, Hwang Shelley, Wei Qing |
Fine mapping of the major histocompatibility complex (MHC) in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) suggests involvement of both HLA class I and class II loci. Brain, behavior, and immunity 2021 Aug 98 101-109. Hajdarevic Riad, Lande Asgeir, Rekeland Ingrid, Rydland Anne, Strand Elin B, Sosa Daisy D, Creary Lisa E, Mella Olav, Egeland Torstein, Saugstad Ola D, Fluge Øystein, Lie Benedicte A, Viken Marte |
Somatic Variants in DNA Damage Response Genes in Ovarian Cancer Patients Using Whole-exome Sequencing. Anticancer research 2023 4 43 (5): 1891-1900. Joanna Lopacinska-Joergensen, Douglas V N P Oliveira, Tim Svenstrup Poulsen, Claus K Hoegdall, Estrid V Hoegda |
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- Page last updated:Apr 29, 2024
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