Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: SLC7A7[original query] |
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Genetic variants in SLC7A7 are associated with risk of glioma in a Chinese population. Experimental biology and medicine (Maywood, N.J.) 2013 Sep 238 (9): 1075-81. Fan Songhua, Zhao Yingjie, Li Xiaoying, Du Yanli, Wang Jingkun, Song Xiao, Zhou Fangfang, Chen Hongyan, Chen Gong, Zhao Yao, Mao Ying, Lan Qi |
Genetic variants associated with methotrexate efficacy and toxicity in early rheumatoid arthritis: results from the treatment of early aggressive rheumatoid arthritis trial. The pharmacogenomics journal 2014 Feb 14 (1): 48-53. Aslibekyan S, Brown E E, Reynolds R J, Redden D T, Morgan S, Baggott J E, Sha J, Moreland L W, O'Dell J R, Curtis J R, Mikuls T R, Bridges S L, Arnett D |
Association of three common single nucleotide polymorphisms of SLC7A7 with the development of glioma in a Chinese population. Genetics and molecular research : GMR 2017 May 16 (2): . Zhang H, Shi W |
Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos.
Human molecular genetics 2017 Mar 26 (6): 1193-1204. Jain Deepti, Hodonsky Chani J, Schick Ursula M, Morrison Jean V, Minnerath Sharon, Brown Lisa, Schurmann Claudia, Liu Yongmei, Auer Paul L, Laurie Cecelia A, Taylor Kent D, Browning Brian L, Papanicolaou George, Browning Sharon R, Loos Ruth J F, North Kari E, Thyagarajan Bharat, Laurie Cathy C, Thornton Timothy A, Sofer Tamar, Reiner Alexander |
Whole exome sequencing in childhood-onset lupus frequently detects single gene etiologies. Pediatric rheumatology online journal 2019 8 17 (1): 52. Tirosh Irit, Spielman Shiri, Barel Ortal, Ram Reut, Stauber Tali, Paret Gideon, Rubinsthein Marina, Pessach Itai M, Gerstein Maya, Anikster Yair, Shukrun Rachel, Dagan Adi, Adler Katerina, Pode-Shakked Ben, Volkov Alexander, Perelman Marina, Greenberger Shoshana, Somech Raz, Lahav Einat, Majmundar Amar J, Padeh Shai, Hildebrandt Friedhelm, Vivante As |
Frequency and spectrum of disease-causing variants in 1892 patients with suspected genetic HLH disorders. Blood advances 2020 Jun 4 (12): 2578-2594. Gadoury-Levesque Vanessa, Dong Lei, Su Rui, Chen Jianjun, Zhang Kejian, Risma Kimberly A, Marsh Rebecca A, Sun Mi |
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- Page last updated:Apr 22, 2024
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