Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population.
about
Incretin physiology and pathophysiology from an Asian perspectiveNew insights from monogenic diabetes for "common" type 2 diabetesConsistent directions of effect for established type 2 diabetes risk variants across populations: the population architecture using Genomics and Epidemiology (PAGE) ConsortiumTransferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast AsiaIslet biology, the CDKN2A/B locus and type 2 diabetes risk.A statistical method for region-based meta-analysis of genome-wide association studies in genetically diverse populations.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.A population-based cohort study suggests an increased risk of multiple sclerosis incidence in patients with type 2 diabetes mellitusIGF2BP2 and obesity interaction analysis for type 2 diabetes mellitus in Chinese Han population.Association of six single nucleotide polymorphisms with gestational diabetes mellitus in a Chinese population.Association of genetic variation in FTO with risk of obesity and type 2 diabetes with data from 96,551 East and South Asians.Genetic variants of IDE-KIF11-HHEX at 10q23.33 associated with type 2 diabetes risk: a fine-mapping study in Chinese population.No 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.The association between KCNQ1 gene polymorphism and type 2 diabetes risk: a meta-analysis.Hematopoietically-expressed homeobox gene three widely-evaluated polymorphisms and risk for diabetes: a meta-analysis.Rs4074134 near BDNF gene is associated with type 2 diabetes mellitus in Chinese Han population independently of body mass index.Cumulative effect and predictive value of genetic variants associated with type 2 diabetes in Han Chinese: a case-control study.Genetic variant in fat mass and obesity-associated gene associated with type 2 diabetes risk in Han Chinese.Heterogeneity of genetic associations of CDKAL1 and HHEX with susceptibility of type 2 diabetes mellitus by gender.Validation of type 2 diabetes risk variants identified by genome-wide association studies in Han Chinese population: a replication study and meta-analysis.Significance of a common variant in the CDKAL1 gene with susceptibility to type 2 diabetes mellitus in Iranian populationNutrigenomics and personalized diets: What will they mean for food?Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs.Association between Gene Polymorphisms of Seven Newly Identified Loci and Type 2 Diabetes and the Correlate Quantitative Traits in Chinese Dong Populations.Association between SLC30A8 rs13266634 Polymorphism and Type 2 Diabetes Risk: A Meta-Analysis.Positive Association Between Type 2 Diabetes Risk Alleles Near CDKAL1 and Reduced Birthweight in Chinese Han Individuals.Variant rs2237892 of KCNQ1 Is Potentially Associated with Hypertension and Macrovascular Complications in Type 2 Diabetes Mellitus in A Chinese Han Population.Gene Polymorphism Association with Type 2 Diabetes and Related Gene-Gene and Gene-Environment Interactions in a Uyghur Population.Association between IGF2BP2 Polymorphisms and Type 2 Diabetes Mellitus: A Case-Control Study and Meta-AnalysisTrans-ethnic fine mapping identifies a novel independent locus at the 3' end of CDKAL1 and novel variants of several susceptibility loci for type 2 diabetes in a Han Chinese populationKCNQ1 rs2237892 C→T gene polymorphism and type 2 diabetes mellitus in the Asian population: a meta-analysis of 15,736 patients.FTO Genotype and Type 2 Diabetes Mellitus: Spatial Analysis and Meta-Analysis of 62 Case-Control Studies from Different Regions.Synthetic associations in the context of genome-wide association scan signals.Developments in obesity genetics in the era of genome-wide association studies.Association of SLC30A8 gene polymorphism with type 2 diabetes, evidence from 46 studies: a meta-analysis.Replication of genome-wide association signals in Asian Indians with early-onset type 2 diabetes.Common variants in KCNQ1 confer increased risk of type 2 diabetes and contribute to the diabetic epidemic in East Asians: a replication and meta-analysis.Hepatocyte nuclear factor 1b is a novel negative regulator of white adipocyte differentiation.
P2860
Q26784623-EDE719A6-D081-4BFF-849E-5ED2D8DFF4FAQ26795455-6D681D0D-BCDC-4983-B547-7296D165DE61Q28384670-A98B193B-951A-4ABD-8D75-B704674D7DB6Q28943320-D3911271-26B3-4405-A260-DEF1751805ACQ30251397-45984EEE-C906-4AED-A4D1-83228CBD0E96Q30511184-3C30E62B-0546-4F25-AD03-A4CEFB2FA237Q30932524-2D4E9339-A8A9-47F2-A59A-3D6CB82C5E0CQ31131358-C48C346B-50D3-4D85-A728-01DD446D3332Q33571827-7433DC67-97AD-4380-B733-E7F802045530Q33998893-9A0ADA20-71C2-4337-8A7F-4C20870640DAQ34077730-2C4E3505-778C-494A-80F5-5ED77534DD8FQ34080885-5BDCD95C-B0AF-4649-A968-B08A04EA2090Q34233822-DD06B8B0-5EFB-4135-BBE1-9EDBABD6711DQ34380447-1FEE014F-2B56-4BE4-8F3B-BD795220F5D3Q34429467-B0E9C894-7BAE-4008-BA57-CCC59846F9A2Q34469768-29B8F180-4E56-4ECE-BE2C-30B6DA5296B7Q34482894-3BB4D62A-9E62-40AC-B3DF-FC4B5F17E044Q34595193-DC3C8E00-F54E-43C9-880A-5228E884474EQ34960340-F41926CE-B888-4ADD-BE42-21FFCF5EA751Q34992839-F70B034E-A837-4B8C-B346-DC3761F66700Q35031022-32CC4354-518C-4677-A5D4-4750C0ED911AQ35149473-1519DAC2-04E7-44A5-8882-867650A11E10Q35172426-DEC99AB3-62B5-4B7D-8A8B-FB7AFF555CAAQ35551472-9EF3591E-14C4-496C-AC90-EF79D09657FEQ35633247-46431E10-4E6E-4943-9CFB-66E575DD60B7Q35639108-A194D82D-CD18-4057-AA67-64E043B2AF40Q35715829-4FDA7CAA-277D-4C47-9967-89958BB26656Q36477163-2691C915-7CBE-4E33-8676-C6A1E2FEAA2EQ36562961-ABBF3AC8-FA34-455B-A997-5CCDBE7AE338Q36585672-436F3058-493A-4EBD-ABD4-5DA066FB7817Q37044783-813E43D4-28E8-4E05-8884-0EC5F28BE706Q37301380-BB73E6C6-EBD5-4F8D-89E4-666FDAE6EC93Q37595304-F7F3039C-6B2C-4289-B57A-7DEAD4B23CB9Q37676251-F025201D-EB58-476C-9530-79C2911C7CD0Q37784094-31F0BA32-C892-420E-AA53-F693E653FFBAQ37953145-D8E017B6-0DD9-46EB-86AA-9AE4E102C62AQ40035575-D719CA67-D919-40EA-AF4C-2514BFB0B95DQ40637158-4153533A-55AC-4CF6-B466-B6228A2FF53FQ42258090-81FA0518-DFE0-4B18-AE93-2207E5C09892Q42799800-91DCF563-B8DC-4C67-AD72-4D485A28AC8E
P2860
Implication of genetic variants near SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, FTO, TCF2, KCNQ1, and WFS1 in type 2 diabetes in a Chinese population.
description
2010 nî lūn-bûn
@nan
2010 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Implication of genetic variant ...... betes in a Chinese population.
@ast
Implication of genetic variant ...... betes in a Chinese population.
@en
type
label
Implication of genetic variant ...... betes in a Chinese population.
@ast
Implication of genetic variant ...... betes in a Chinese population.
@en
prefLabel
Implication of genetic variant ...... betes in a Chinese population.
@ast
Implication of genetic variant ...... betes in a Chinese population.
@en
P2093
P2860
P356
P1433
P1476
Implication of genetic variant ...... betes in a Chinese population.
@en
P2093
Xianghai Zhou
Xiuqin Sun
Xiuying Zhang
Xueyao Han
Yingying Luo
P2860
P2888
P356
10.1186/1471-2350-11-81
P577
2010-05-28T00:00:00Z
P5875
P6179
1017186675