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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Disease and SLC38A8[original query]
Association between liver-specific gene polymorphisms and their expression levels with nonalcoholic fatty liver disease. GWAS Catalog
Hepatology (Baltimore, Md.) 2013 Feb 57 (2): 590-600.
Adams Leon A, White Scott W, Marsh Julie A, Lye Stephen J, Connor Kristin L, Maganga Richard, Ayonrinde Oyekoya T, Olynyk John K, Mori Trevor A, Beilin Lawrence J, Palmer Lyle J, Hamdorf Jeffrey M, Pennell Craig
Gene-environment interaction effects on lung function- a genome-wide association study within the Framingham heart study.
Environmental health : a global access science source 2013 12 (1): 101.
Liao Shu-Yi, Lin Xihong, Christiani David
Clinical and genetic variability in children with partial albinism.
Scientific reports 2019 11 9 (1): 16576.
Campbell Patrick, Ellingford Jamie M, Parry Neil R A, Fletcher Tracy, Ramsden Simon C, Gale Theodora, Hall Georgina, Smith Katherine, Kasperaviciute Dalia, Thomas Ellen, Lloyd I Chris, Douzgou Sofia, Clayton-Smith Jill, Biswas Susmito, Ashworth Jane L, Black Graeme C M, Sergouniotis Panagiotis
Genetic causes of nystagmus, foveal hypoplasia and subnormal visual acuity- other than albinism.
Ophthalmic genetics 2021 2 42 (3): 243-251.
Ehrenberg Miriam, Bagdonite-Bejarano Laura, Fulton Anne B, Orenstein Naama, Yahalom Claud
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