Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: DCLRE1C[original query] |
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Recurrent CYP2C19 deletion allele is associated with triple-negative breast cancer. BMC cancer 2014 14 (1): 902. Tervasmäki Anna, Winqvist Robert, Jukkola-Vuorinen Arja, Pylkäs Kat |
A genome-wide analysis of gene-caffeine consumption interaction on basal cell carcinoma. Carcinogenesis 2016 Dec 37 (12): 1138-1143. Li Xin, Cornelis Marilyn C, Liang Liming, Song Fengju, De Vivo Immaculata, Giovannucci Edward, Tang Jean Y, Han Jia |
Identification of 12 novel loci that confer susceptibility to early-onset dyslipidemia. International journal of molecular medicine 2019 Jan 43 (1): 57-82. Yamada Yoshiji, Kato Kimihiko, Oguri Mitsutoshi, Horibe Hideki, Fujimaki Tetsuo, Yasukochi Yoshiki, Takeuchi Ichiro, Sakuma J |
Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer families. BMC cancer 2019 Apr 19 (1): 313. Shahi Rajendra Bahadur, De Brakeleer Sylvia, Caljon Ben, Pauwels Ingrid, Bonduelle Maryse, Joris Sofie, Fontaine Christel, Vanhoeij Marian, Van Dooren Sonia, Teugels Erik, De Grève Jacqu |
Polymorphisms of the DNA repair gene EXO1 modulate cognitive aging in old adults in a Taiwanese population. DNA repair 2019 Mar 78 1-6. Lin Eugene, Kuo Po-Hsiu, Liu Yu-Li, Yang Albert C, Tsai Shih-J |
[Analysis of a child with severe combined immunodeficiency due to variants of DCLRE1C gene]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 7 39 (7): 743-748. Xu Xiaowei, Yan Dandan, Yin Jing, Zheng Jie, Wang Xuetao, Shu Jian |
Polymorphisms Within DNA Double-Strand Breaks Repair-Related Genes Contribute to Structural Chromosome Abnormality in Recurrent Pregnancy Loss. Frontiers in genetics 2022 1 12 787718. Cheng Zhenbo, Cheng Dehua, Li Jiancheng, Guo Lihuang, Zhang Wei, Zhang Conghui, Liu Yangxu, Huang Yue, Xu Keqi |
Case report: Artemis deficiency and 3M syndrome-coexistence of two distinct genetic disorders. Frontiers in pediatrics 2023 7 11 1211254. Ayca Ceylan, Ilyas Emre Tekdemir, Nadir Kocak, Ivan Kingyue Chinn, Jordan Scott Orange, Hasibe Art |
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- Page last updated:Apr 22, 2024
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