Common variants in CDKAL1, CDKN2A/B, IGF2BP2, SLC30A8, and HHEX/IDE genes are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population.
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Singapore Genome Variation Project: a haplotype map of three Southeast Asian populationsNew insights from monogenic diabetes for "common" type 2 diabetesTransferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast AsiaA genome-wide association study identifies susceptibility variants for type 2 diabetes in Han ChineseA genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans.Genome-wide meta-analyses identify novel loci associated with n-3 and n-6 polyunsaturated fatty acid levels in Chinese and European-ancestry populations.Acute cytokine-mediated downregulation of the zinc transporter ZnT8 alters pancreatic beta-cell function.Individualized therapy for type 2 diabetes: clinical implications of pharmacogenetic data.Can data science inform environmental justice and community risk screening for type 2 diabetes?Association of genetic variants with isolated fasting hyperglycaemia and isolated postprandial hyperglycaemia in a Han Chinese population.PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese populationInvestigation of type 2 diabetes risk alleles support CDKN2A/B, CDKAL1, and TCF7L2 as susceptibility genes in a Han Chinese cohort.Common genetic variants on chromosome 9p21 are associated with myocardial infarction and type 2 diabetes in an Italian population.Interaction of iron status with single nucleotide polymorphisms on incidence of type 2 diabetes.Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population.Genetics of type 2 diabetes: insights into the pathogenesis and its clinical application.Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population.Exploring the Association Between Demographics, SLC30A8 Genotype, and Human Islet Content of Zinc, Cadmium, Copper, Iron, Manganese and NickelConsistent association of type 2 diabetes risk variants found in europeans in diverse racial and ethnic groups.The longitudinal association of common susceptibility variants for type 2 diabetes and obesity with fasting glucose level and BMI.Impact of common variants of PPARG, KCNJ11, TCF7L2, SLC30A8, HHEX, CDKN2A, IGF2BP2, and CDKAL1 on the risk of type 2 diabetes in 5,164 Indians.Genetics of type 2 diabetes in European populations.Association of six single nucleotide polymorphisms with gestational diabetes mellitus in a Chinese population.Globalization of diabetes: the role of diet, lifestyle, and genes.Two isoforms of the mRNA binding protein IGF2BP2 are generated by alternative translational initiation.Genetic variants of IDE-KIF11-HHEX at 10q23.33 associated with type 2 diabetes risk: a fine-mapping study in Chinese population.Associations of type 2 diabetes with common variants in PPARD and the modifying effect of vitamin D among middle-aged and elderly ChineseNo detectable association of IGF2BP2 and SLC30A8 genes with type 2 diabetes in the population of Hyderabad, India.IGF2BP2 alternative variants associated with glutamic acid decarboxylase antibodies negative diabetes in Malaysian subjects.Genetic predisposition to long-term nondiabetic deteriorations in glucose homeostasis: Ten-year follow-up of the GLACIER study.Hematopoietically-expressed homeobox gene three widely-evaluated polymorphisms and risk for diabetes: a meta-analysis.The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han populationAntiretroviral therapy modifies the genetic effect of known type 2 diabetes-associated risk variants in HIV-infected women.Four pairs of gene-gene interactions associated with increased risk for type 2 diabetes (CDKN2BAS-KCNJ11), obesity (SLC2A9-IGF2BP2, FTO-APOA5), and hypertension (MC4R-IGF2BP2) in Chinese women.Cumulative effect and predictive value of genetic variants associated with type 2 diabetes in Han Chinese: a case-control study.An FTO variant is associated with Type 2 diabetes in South Asian populations after accounting for body mass index and waist circumferenceHeterogeneity of genetic associations of CDKAL1 and HHEX with susceptibility of type 2 diabetes mellitus by gender.Elite athletes' genetic predisposition for altered risk of complex metabolic traitsUse of net reclassification improvement (NRI) method confirms the utility of combined genetic risk score to predict type 2 diabetes.Contribution of SLC30A8 variants to the risk of type 2 diabetes in a multi-ethnic population: a case control study.
P2860
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P2860
Common variants in CDKAL1, CDKN2A/B, IGF2BP2, SLC30A8, and HHEX/IDE genes are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Common variants in CDKAL1, CDK ...... e in a Chinese Han population.
@en
type
label
Common variants in CDKAL1, CDK ...... e in a Chinese Han population.
@en
prefLabel
Common variants in CDKAL1, CDK ...... e in a Chinese Han population.
@en
P2093
P2860
P50
P356
P1433
P1476
Common variants in CDKAL1, CDK ...... e in a Chinese Han population.
@en
P2093
P2860
P304
P356
10.2337/DB08-0047
P407
P577
2008-07-15T00:00:00Z