Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 8 (of 8 Records)

Query Trace: Disease and ERLIN1[original query]
The ERLIN1-CHUK-CWF19L1 gene cluster influences liver fat deposition and hepatic inflammation in the NHLBI Family Heart Study.
Atherosclerosis 2013 May 228 (1): 175-80.
Feitosa Mary F, Wojczynski Mary K, North Kari E, Zhang Qunyuan, Province Michael A, Carr Jeffrey J, Borecki Ingrid
Association of polymorphisms in GCKR and TRIB1 with nonalcoholic fatty liver disease and metabolic syndrome traits.
Endocrine journal 2014 61 (7): 683-9.
Kitamoto Aya, Kitamoto Takuya, Nakamura Takahiro, Ogawa Yuji, Yoneda Masato, Hyogo Hideyuki, Ochi Hidenori, Mizusawa Seiho, Ueno Takato, Nakao Kazuwa, Sekine Akihiro, Chayama Kazuaki, Nakajima Atsushi, Hotta Kiku
Genetic analysis of nonalcoholic fatty liver disease within a Caribbean-Hispanic population.
Molecular genetics & genomic medicine 2015 Nov 3 (6): 558-69.
Edelman Deborah, Kalia Harmit, Delio Maria, Alani Mustafa, Krishnamurthy Karthik, Abd Mortadha, Auton Adam, Wang Tao, Wolkoff Allan W, Morrow Bernice
Targeted resequencing identifies genes with recurrent variation in cerebral palsy.
NPJ genomic medicine 2019 4 27.
van Eyk C L, Corbett M A, Frank M S B, Webber D L, Newman M, Berry J G, Harper K, Haines B P, McMichael G, Woenig J A, MacLennan A H, Gecz
Validating a non-invasive, ALT-based non-alcoholic fatty liver phenotype in the million veteran program.
PloS one 2020 15 (8): e0237430.
Serper Marina, Vujkovic Marijana, Kaplan David E, Carr Rotonya M, Lee Kyung Min, Shao Qing, Miller Donald R, Reaven Peter D, Phillips Lawrence S, O'Donnell Christopher J, Meigs James B, Wilson Peter W F, Vickers-Smith Rachel, Kranzler Henry R, Justice Amy C, Gaziano John M, Muralidhar Sumitra, Pyarajan Saiju, DuVall Scott L, Assimes Themistocles L, Lee Jennifer S, Tsao Philip S, Rader Daniel J, Damrauer Scott M, Lynch Julie A, Saleheen Danish, Voight Benjamin F, Chang Kyong-Mi,
Association of Genetic Risk Score With NAFLD in An Ethnically Diverse Cohort.
Hepatology communications 2021 Jun .
Wang Jun, Conti David V, Bogumil David, Sheng Xin, Noureddin Mazen, Wilkens Lynne R, Le Marchand Loic, Rosen Hugo R, Haiman Christopher A, Setiawan Veronica Wen
Causal Relationship and Shared Genetic Loci between Psoriasis and Type 2 Diabetes through Trans-Disease Meta-Analysis. GWAS Catalog
The Journal of investigative dermatology 2021 1 141 (6): 1493-1502.
Patrick Matthew T, Stuart Philip E, Zhang Haihan, Zhao Qingyuan, Yin Xianyong, He Kevin, Zhou Xu-Jie, Mehta Nehal N, Voorhees John J, Boehnke Michael, Gudjonsson Johann E, Nair Rajan P, Handelman Samuel K, Elder James T, Liu Dajiang J, Tsoi Lam
The common p.Ile291Val variant of ERLIN1 enhances TM6SF2 function and is associated with protection against MASLD.
Med (New York, N.Y.) 2024 5 .
Miriam Daphne Rendel, Cecilia Vitali, Kate Townsend Creasy, David Zhang, Eleonora Scorletti, Helen Huang, Katharina Sophie Seeling, Joseph Park, Leonida Hehl, Mara Sophie Vell, Donna Conlon, Sikander Hayat, , Michael C Phillips, Kai Markus Schneider, Daniel J Rader, Carolin Victoria Schneid
TOP