Genome wide association studies for diabetes: perspective on results and challenges
暂无分享,去创建一个
N J Cox | N. Cox | L H Philipson | J M Torres | L. Philipson | JM Torres
[1] L. Peltonen,et al. HLA haplotypes in Type 1 (insulin-dependent) diabetes mellitus: molecular analysis of the HLA-DQ locus , 1992, Diabetologia.
[2] M. Olivier. A haplotype map of the human genome , 2003, Nature.
[3] Christian Gieger,et al. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk , 2010, Nature Genetics.
[4] P. McKeigue,et al. Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas , 2011, Diabetologia.
[5] C. Graver. Statistical Genetics: Gene Mapping Through Linkage and Association , 2008 .
[6] E. Zeggini,et al. A new era for Type 2 diabetes genetics , 2007, Diabetic medicine : a journal of the British Diabetic Association.
[7] S. Gabriel,et al. The Structure of Haplotype Blocks in the Human Genome , 2002, Science.
[8] P. Visscher,et al. Five years of GWAS discovery. , 2012, American journal of human genetics.
[9] D. Nicolae,et al. Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals , 2011, Diabetologia.
[10] P. Poulsen,et al. Heritability of Type II (non-insulin-dependent) diabetes mellitus and abnormal glucose tolerance – a population-based twin study , 1999, Diabetologia.
[11] Philippe Froguel,et al. Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight , 2010, Nature Genetics.
[12] Chaeyoung Lee,et al. Association of glycosylated hemoglobin with the gene encoding CDKAL1 in the Korean Association Resource (KARE) study , 2012, Human mutation.
[13] G I Bell,et al. Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young. , 2001, The New England journal of medicine.
[14] Lu Qi,et al. Variant of Transcription Factor 7-Like 2 (TCF7L2) Gene and the Risk of Type 2 Diabetes in Large Cohorts of U.S. Women and Men , 2006, Diabetes.
[15] C. Amos. Successful design and conduct of genome-wide association studies. , 2007, Human molecular genetics.
[16] Geoffrey B. Nilsen,et al. Whole-Genome Patterns of Common DNA Variation in Three Human Populations , 2005, Science.
[17] M. Olivier. A haplotype map of the human genome. , 2003, Nature.
[18] D. Botstein,et al. Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease , 2003, Nature Genetics.
[19] A. Bradwell,et al. Identification of susceptibility loci for Type 1 (insulin-dependent) diabetes by trans-racial gene mapping , 1990, Diabetologia.
[20] Jeffrey Ross-Ibarra,et al. Genetic Data Analysis II. Methods for Discrete Population Genentic Data , 2002 .
[21] E S Lander,et al. The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. , 2000, Nature genetics.
[22] P. Donnelly,et al. Designing Genome-Wide Association Studies: Sample Size, Power, Imputation, and the Choice of Genotyping Chip , 2009, PLoS genetics.
[23] M. McCarthy,et al. Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes , 2007, Science.
[24] A. Favier,et al. Identification and cloning of a beta-cell-specific zinc transporter, ZnT-8, localized into insulin secretory granules. , 2004, Diabetes.
[25] Ingo Ruczinski,et al. Hypothesis-driven candidate gene association studies: practical design and analytical considerations. , 2009, American journal of epidemiology.
[26] F. Collins,et al. The HapMap and genome-wide association studies in diagnosis and therapy. , 2009, Annual review of medicine.
[27] R. Collins,et al. Common variants at 30 loci contribute to polygenic dyslipidemia , 2009, Nature Genetics.
[28] Y. Taniguchi,et al. Dual Functions of ASCIZ in the DNA Base Damage Response and Pulmonary Organogenesis , 2010, PLoS genetics.
[29] G. Eisenbarth,et al. Type-I diabetes: a chronic autoimmune disease of human, mouse, and rat. , 1990, Annual review of immunology.
[30] J. Florez,et al. The genetics of type 2 diabetes: what have we learned from GWAS? , 2010, Annals of the New York Academy of Sciences.
[31] F. Collins,et al. The Human Genome Project: Lessons from Large-Scale Biology , 2003, Science.
[32] Steven Wiltshire,et al. Association Analysis of 6,736 U.K. Subjects Provides Replication and Confirms TCF7L2 as a Type 2 Diabetes Susceptibility Gene With a Substantial Effect on Individual Risk , 2006, Diabetes.
[33] D. Dries. STATISTICAL GENETICS: GENE MAPPING THROUGH LINKAGE AND ASSOCIATION , 2008 .
[34] Inês Barroso,et al. Genome-wide association studies and type 2 diabetes. , 2011, Briefings in functional genomics.
[35] E. Gamazon,et al. Genetic risk factors for type 2 diabetes: a trans-regulatory genetic architecture? , 2012, American journal of human genetics.
[36] M. McCarthy,et al. Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes. , 2003, Diabetes.
[37] L. Peltonen,et al. Classical twin studies and beyond , 2002, Nature Reviews Genetics.
[38] D. Goldstein,et al. Uncovering the roles of rare variants in common disease through whole-genome sequencing , 2010, Nature Reviews Genetics.
[39] H. Stefánsson,et al. Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes , 2006, Nature Genetics.
[40] K. Narayan,et al. Clinical risk factors, DNA variants, and the development of type 2 diabetes. , 2009, The New England journal of medicine.
[41] A. Scheinfeld,et al. Women and men , 1945 .
[42] Judy H. Cho,et al. Finding the missing heritability of complex diseases , 2009, Nature.
[43] L. Scott,et al. What Will Diabetes Genomes Tell Us? , 2012, Current Diabetes Reports.
[44] S. Maeda,et al. Genetics of type 2 diabetes: the GWAS era and future perspectives [Review]. , 2011, Endocrine journal.
[45] Inês Barroso,et al. Variants in MTNR1B influence fasting glucose levels , 2009, Nature Genetics.
[46] G. Abecasis,et al. A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants , 2007, Science.
[47] J. Petrie,et al. Implications of genome wide association studies for the understanding of type 2 diabetes pathophysiology. , 2011, Biochemical pharmacology.
[48] J. Gulcher,et al. Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2. , 2003, American journal of human genetics.
[49] B. Stranger,et al. Progress and Promise of Genome-Wide Association Studies for Human Complex Trait Genetics , 2011, Genetics.
[50] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.
[51] R. D'Agostino,et al. Genotype score in addition to common risk factors for prediction of type 2 diabetes. , 2008, The New England journal of medicine.
[52] B. Neale. Statistical genetics : gene mapping through linkage and association , 2007 .
[53] L. Groop,et al. Metabolic Consequences of a Family History of NIDDM (The Botnia Study): Evidence for Sex-Specific Parental Effects , 1996, Diabetes.
[54] T. Hudson,et al. A genome-wide association study identifies novel risk loci for type 2 diabetes , 2007, Nature.
[55] Simon C. Potter,et al. A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans , 2012, PLoS ONE.
[56] Marcia M. Nizzari,et al. Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels , 2007, Science.
[57] Dharambir K Sanghera,et al. Type 2 Diabetes Genetics: Beyond GWAS. , 2012, Journal of diabetes & metabolism.
[58] R. Wu,et al. Designs for linkage analysis and association studies of complex diseases. , 2010, Methods in molecular biology.
[59] N. Cox,et al. Trait-Associated SNPs Are More Likely to Be eQTLs: Annotation to Enhance Discovery from GWAS , 2010, PLoS genetics.
[60] Tom H. Lindner,et al. Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus , 2000, Nature Genetics.
[61] J. Aerts,et al. Exome Sequencing and Genetic Testing for MODY , 2012, PloS one.
[62] D. Posthuma,et al. Single Locus Association Models , 2007 .