Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population

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Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population is …
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scholarly articleQ13442814

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P6179Dimensions Publication ID1014094111
P356DOI10.1186/1471-2350-11-97
P8608Fatcat IDrelease_tuisrmdatffsrndx77srryasmq
P932PMC publication ID2894791
P698PubMed publication ID20550665
P5875ResearchGate publication ID44675687

P50authorYi ShiQ64866311
P2093author name stringYing Li
Yang Yang
Li Wang
Ming Chen
Zhenglin Yang
Xin Tang
Xiaoqi Liu
Yan Yang
Fang Lu
Ben Zhang
Xuejun Zhang
Ying Lin
Li Cai
Jiyun Yang
Shi Ma
Yang Xian
Jichuan Wu
Mingjing Bao
Pengqiu Li
Shaoqin Rao
P2860cites workThe common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetesQ24290189
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Mapping human genetic diversity in AsiaQ28267585
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Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)Q28298538
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetesQ28680760
Genome-wide association studies in type 2 diabetesQ28752564
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variantsQ29547210
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levelsQ29547214
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetesQ29614589
A variant in CDKAL1 influences insulin response and risk of type 2 diabetesQ29614878
Genetic association studies: design, analysis and interpretationQ34760468
Type 2 diabetes whole-genome association study in four populations: the DiaGen consortiumQ35946296
Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 AsiansQ36807593
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 populationQ36906418
Genomic dissection of population substructure of Han Chinese and its implication in association studiesQ37466190
Prevalence of diabetes and impaired fasting glucose in the Chinese adult population: International Collaborative Study of Cardiovascular Disease in Asia (InterASIA).Q39655754
Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemiaQ42459504
Meta-analysis and a large association study confirm a role for calpain-10 variation in type 2 diabetes susceptibilityQ42927967
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 diabetesQ44286433
Replication and identification of novel variants at TCF7L2 associated with type 2 diabetes in Hong Kong ChineseQ46180946
Positive association between variations in CDKAL1 and type 2 diabetes in Han Chinese individualsQ46394498
Zinc transporter-8 gene (SLC30A8) is associated with type 2 diabetes in ChineseQ46482847
Meta-analysis of the association between SNPs in TCF7L2 and type 2 diabetes in East Asian populationQ47689076
A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.Q53780537
Genetic variation in the gene encoding adiponectin is associated with an increased risk of type 2 diabetes in the Japanese population.Q53981339
A Comparison of Tests for Hardy-Weinberg EquilibriumQ56170949
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populationsQ57502502
Association Study of the Genetic Polymorphisms of the Transcription Factor 7-Like 2 (TCF7L2) Gene and Type 2 Diabetes in the Chinese PopulationQ59656748
The E23K variation in the KCNJ11 gene is associated with type 2 diabetes in Chinese and East Asian population.Q64882057
New diagnostic criteria and classification of diabetes--again?Q74827490
Replication study for the association of TCF7L2 with susceptibility to type 2 diabetes in a Japanese populationQ79882491
Exon sequencing and association analysis of polymorphisms in TCF7L2 with type 2 diabetes in a Chinese populationQ81312927
ENPP1/PC-1 K121Q polymorphism and genetic susceptibility to type 2 diabetesQ81580507
P921main subjecttype 2 diabetesQ3025883
P304page(s)97
P577publication date2010-06-15
P1433published inBMC Medical GeneticsQ15759918
P1476titleAssociation study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population
P478volume11

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cites work (P2860)
Q57491983Association Between SLC30A8 rs13266634 Polymorphism and Risk of T2DM and IGR in Chinese Population: A Systematic Review and Meta-Analysis
Q37044783Association between IGF2BP2 Polymorphisms and Type 2 Diabetes Mellitus: A Case-Control Study and Meta-Analysis
Q35715829Association between SLC30A8 rs13266634 Polymorphism and Type 2 Diabetes Risk: A Meta-Analysis
Q43486091Association between type 2 diabetes and CDKN2A/B: a meta-analysis study
Q34486577Association of CDKN2BAS polymorphism rs4977574 with coronary heart disease: a case-control study and a meta-analysis
Q40035575Association of SLC30A8 gene polymorphism with type 2 diabetes, evidence from 46 studies: a meta-analysis
Q31131358Association of genetic variants with isolated fasting hyperglycaemia and isolated postprandial hyperglycaemia in a Han Chinese population
Q34077730Association of six single nucleotide polymorphisms with gestational diabetes mellitus in a Chinese population
Q34878934Association of the rs11196218 polymorphism in TCF7L2 with type 2 diabetes mellitus in Asian population
Q34128452Association of the type 2 diabetes mellitus susceptibility gene, TCF7L2, with schizophrenia in an Arab-Israeli family sample
Q37660145CDKAL1 and HHEX are associated with type 2 diabetes-related traits among Yup'ik people.
Q30932524Can data science inform environmental justice and community risk screening for type 2 diabetes?
Q36663024Common genetic variants in peroxisome proliferator-activated receptor-γ (PPARG) and type 2 diabetes risk among Women's Health Initiative postmenopausal women
Q35083749Contribution of SLC30A8 variants to the risk of type 2 diabetes in a multi-ethnic population: a case control study
Q34960340Cumulative effect and predictive value of genetic variants associated with type 2 diabetes in Han Chinese: a case-control study
Q35606938Genetic determinants for gestational diabetes mellitus and related metabolic traits in Mexican women
Q37522623Genetic variants at 10q23.33 are associated with plasma lipid levels in a Chinese population
Q34233822Genetic variants of IDE-KIF11-HHEX at 10q23.33 associated with type 2 diabetes risk: a fine-mapping study in Chinese population
Q83715974Genetic variants on chromosome 6p21.1 and 6p22.3 are associated with type 2 diabetes risk: a case-control study in Han Chinese
Q64101205Genetic, Functional, and Immunological Study of ZnT8 in Diabetes
Q34529892Genome-wide meta-analysis of genetic susceptible genes for Type 2 Diabetes
Q48329731Hematopoietically expressed homeobox (HHEX) gene polymorphism (rs5015480) is associated with increased risk of gestational diabetes mellitus.
Q34482894Hematopoietically-expressed homeobox gene three widely-evaluated polymorphisms and risk for diabetes: a meta-analysis
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Q28943320Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia
Q34546292Using extreme phenotype sampling to identify the rare causal variants of quantitative traits in association studies
Q35149473Validation of type 2 diabetes risk variants identified by genome-wide association studies in Han Chinese population: a replication study and meta-analysis

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