Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: FREQ[original query] |
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CCR5 genotyping in an Australian and New Zealand type 1 diabetes cohort. Autoimmunity 2002 Nov 35 (7): 457-61. Buhler M M, Craig M, Donaghue K C, Badhwar P, Willis J, Manolios N, Tait B D, Silink M, Bennetts B H, Stewart G |
Proopiomelanocortin gene variants are associated with serum leptin and body fat in a normal female population. European journal of human genetics : EJHG 2005 Jun 13 (6): 772-80. Chen Yuanneng, Snieder Harold, Wang Xiaoling, Kaviya Bhavini, McCaffrey Clare, Spector Tim D, Carter Nicholas D, O'Dell Sandra |
Gene polymorphisms in the Quebec population: a risk to develop hypertriglyceridemia. Biochemical and biophysical research communications 2006 Jun 344 (2): 588-96. Garenc Christophe, Aubert Samuel, Laroche Jerôme, Bergeron Jean, Gagné Claude, Rousseau François, Julien Pier |
Interaction between variation in the D2 dopamine receptor (DRD2) and the neuronal calcium sensor-1 (FREQ) genes in predicting response to nicotine replacement therapy for tobacco dependence. The pharmacogenomics journal 0 6 (3): 194-9. Dahl J P, Jepson C, Levenson R, Wileyto E P, Patterson F, Berrettini W H, Lerman |
Microsomal glutathione S-transferase gene polymorphisms and colorectal cancer risk in a Han Chinese population. International journal of colorectal disease 2007 Oct 22 (10): 1185-94. Zhang Hao, Liao Ling-Hong, Liu Shuk-Ming, Lau Kwok-Wai, Lai Albert Kai-Cheong, Zhang Jin-Hui, Wang Qi, Chen Xiao-Qian, Wei Wei, Liu Hua, Cai Jian-Hua, Lung Maria Li, Tai Susan S W, Wu Madeli |
Association of common promoter polymorphisms of MCP1 with hepatitis B virus clearance. Experimental & molecular medicine 2006 Dec 38 (6): 694-702. Park Byung Lae, Kim Yoon Jun, Cheong Hyun Sub, Kim Lyoung Hyo, Choi Yoo Hyun, Lee Hyo-Suk, Shin Hyoung D |
Functional polymorphism in aldehyde dehydrogenase-2 gene associated with risk of tuberculosis. BMC medical genetics 2014 15 40. Park Seung Kyu, Park Choon-Sik, Lee Hyo-Suk, Park Kyong Soo, Park Byung Lae, Cheong Hyun Sub, Shin Hyoung D |
Haplotypes at LBX1 have distinct inheritance patterns with opposite effects in adolescent idiopathic scoliosis. PloS one 2015 10 (2): e0117708. Chettier Rakesh, Nelson Lesa, Ogilvie James W, Albertsen Hans M, Ward Kenne |
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures.
Nature communications 2016 Jan 7 10129. Styrkarsdottir Unnur, Thorleifsson Gudmar, Gudjonsson Sigurjon A, Sigurdsson Asgeir, Center Jacqueline R, Lee Seung Hun, Nguyen Tuan V, Kwok Timothy C Y, Lee Jenny S W, Ho Suzanne C, Woo Jean, Leung Ping-C, Kim Beom-Jun, Rafnar Thorunn, Kiemeney Lambertus A, Ingvarsson Thorvaldur, Koh Jung-Min, Tang Nelson L S, Eisman John A, Christiansen Claus, Sigurdsson Gunnar, Thorsteinsdottir Unnur, Stefansson Ka |
Evaluation of the Iranian panel reactive antibody calculator and potential usefulness: A retrospective study. Clinical transplantation 2022 8 36 (11): e14789. Mohammadzadeh Sahand, Jaladat Abdul Reza, Mohammadi Maryam, Geramizadeh Bita, Anbardar Mohammad Hossein, Soleimani Neda, Amirinezhad Fard Elahe, Tehrani Narges Jamshidi |
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- Page last updated:Apr 22, 2024
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