The utility of genome‐wide association studies in hepatology
暂无分享,去创建一个
[1] S. Kashiwagi,et al. Contribution of HLA class I and class II alleles to the regulation of antibody production to hepatitis B surface antigen in humans. , 1996, International immunology.
[2] N Risch,et al. The Future of Genetic Studies of Complex Human Diseases , 1996, Science.
[3] K. Weiss,et al. Linkage disequilibrium mapping of complex disease: fantasy or reality? , 1998, Current opinion in biotechnology.
[4] J. Nadeau,et al. Finding Genes That Underlie Complex Traits , 2002, Science.
[5] S. Liu-Cordero. Patterns of linkage disequilibrium in the human genome , 2002 .
[6] C. O'Morain,et al. CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease. , 2002, American journal of human genetics.
[7] P. Donaldson,et al. Genetic factors in the pathogenesis of primary biliary cirrhosis. , 2003, Clinics in liver disease.
[8] Jack Satsangi,et al. New genes in inflammatory bowel disease: lessons for complex diseases? , 2006, The Lancet.
[9] E. Carlsson,et al. Variation in the adiponutrin gene influences its expression and associates with obesity. , 2006, Diabetes.
[10] D. Reich,et al. Principal components analysis corrects for stratification in genome-wide association studies , 2006, Nature Genetics.
[11] A. Morris,et al. Fine mapping versus replication in whole-genome association studies. , 2007, American journal of human genetics.
[12] T. Wienker,et al. Increased gallstone risk in humans conferred by common variant of hepatic ATP‐binding cassette transporter for cholesterol , 2007, Hepatology.
[13] P. Donnelly,et al. Replicating genotype–phenotype associations , 2007, Nature.
[14] Michael Krawczak,et al. A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease , 2007, Nature Genetics.
[15] M. McCarthy,et al. Genome-wide association studies for complex traits: consensus, uncertainty and challenges , 2008, Nature Reviews Genetics.
[16] Christopher G. Mathew,et al. New links to the pathogenesis of Crohn disease provided by genome-wide association scans , 2008, Nature Reviews Genetics.
[17] A. Morris,et al. Evaluating the effects of imputation on the power, coverage, and cost efficiency of genome-wide SNP platforms. , 2008, American journal of human genetics.
[18] L. Naldi,et al. A European study of HLA-B in Stevens–Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs , 2008, Pharmacogenetics and genomics.
[19] Nicholas J Schork,et al. Methods for handling multiple testing. , 2008, Advances in genetics.
[20] Alexander Pertsemlidis,et al. Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease , 2008, Nature Genetics.
[21] Judy H. Cho,et al. Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease , 2008, Nature Genetics.
[22] Luigi Ferrucci,et al. Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. , 2008, American journal of human genetics.
[23] Judy H. Cho,et al. Finding the missing heritability of complex diseases , 2009, Nature.
[24] Peter Kraft,et al. Genetic risk prediction--are we there yet? , 2009, The New England journal of medicine.
[25] Joseph T. Glessner,et al. From Disease Association to Risk Assessment: An Optimistic View from Genome-Wide Association Studies on Type 1 Diabetes , 2009, PLoS genetics.
[26] Ming-Huei Chen,et al. Genome-wide association meta-analysis for total serum bilirubin levels. , 2009, Human molecular genetics.
[27] Thomas Berg,et al. IL28B is associated with response to chronic hepatitis C interferon-α and ribavirin therapy , 2009, Nature Genetics.
[28] A. Zhernakova,et al. Detecting shared pathogenesis from the shared genetics of immune-related diseases , 2009, Nature Reviews Genetics.
[29] Common disorders are quantitative traits , 2009, Nature Reviews Genetics.
[30] R. Plomin,et al. Common disorders are quantitative traits , 2009, Nature Reviews Genetics.
[31] John P. A. Ioannidis,et al. Validating, augmenting and refining genome-wide association signals , 2009, Nature Reviews Genetics.
[32] M. Daly,et al. HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin , 2009, Nature Genetics.
[33] Pauline C Ng,et al. An agenda for personalized medicine. , 2009, Nature.
[34] Karen L. Mohlke,et al. Genetic Risk Prediction — Are We There Yet? , 2009 .
[35] K. Siminovitch,et al. Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants. , 2009, The New England journal of medicine.
[36] A. Koike,et al. Genome-wide association of IL28B with response to pegylated interferon-α and ribavirin therapy for chronic hepatitis C , 2009, Nature Genetics.
[37] D. Clayton. Prediction and Interaction in Complex Disease Genetics: Experience in Type 1 Diabetes , 2009, PLoS genetics.
[38] Jacques Fellay,et al. Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance , 2009, Nature.
[39] G. Abecasis,et al. Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. , 2009, Human Molecular Genetics.
[40] F. Collins,et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits , 2009, Proceedings of the National Academy of Sciences.
[41] J. Hirschhorn. Genomewide association studies--illuminating biologic pathways. , 2009, The New England journal of medicine.
[42] David B. Goldstein,et al. Genetic variation in IL28B and spontaneous clearance of hepatitis C virus , 2009, Nature.
[43] Y. Kamatani,et al. A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians , 2009, Nature Genetics.
[44] David B. Goldstein,et al. Rare Variants Create Synthetic Genome-Wide Associations , 2010, PLoS biology.
[45] David Kershenobich,et al. Variant in PNPLA3 is associated with alcoholic liver disease , 2010, Nature Genetics.
[46] Nancy R Cook,et al. Association between a literature-based genetic risk score and cardiovascular events in women. , 2010, JAMA.
[47] D. Clayton,et al. Genome-wide association study and meta-analysis finds over 40 loci affect risk of type 1 diabetes , 2009, Nature Genetics.
[48] T. Karlsen,et al. Genetics of cholestatic liver disease in 2010 , 2010, Current opinion in gastroenterology.
[49] C. Wijmenga,et al. Genome-wide association analysis in primary sclerosing cholangitis. , 2010, Gastroenterology.
[50] C. Rui. Genetic variation in IL-28B and spontaneous clearance of hepatitis C virus , 2012 .