(Q38078821)

28 August 2017

1 reference

title

Genetics of type 2 diabetes and potential clinical implications (English)

1 reference

28 August 2017

1 reference

1

1 reference

28 August 2017

Kyong Soo Park

2

1 reference

28 August 2017

publication date

2 February 2013

1 reference

Archives of Pharmacal Research

28 August 2017

published in

1 reference

28 August 2017

volume

36

1 reference

28 August 2017

issue

2

1 reference

28 August 2017

page(s)

167-177

1 reference

https://scigraph.springernature.com/pub.10.1007/s12272-013-0021-x

28 August 2017

exact match

0 references

cites work

Diagnosis and classification of diabetes mellitus

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Clinical assessment incorporating a personal genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Genetic variation in the multidrug and toxin extrusion 1 transporter protein influences the glucose-lowering effect of metformin in patients with diabetes: a preliminary study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Personal omics profiling reveals dynamic molecular and medical phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Genetics of type 2 diabetes in East Asian populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Genetic risk reclassification for type 2 diabetes by age below or above 50 years using 40 type 2 diabetes risk single nucleotide polymorphisms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Ser1369Ala variant in sulfonylurea receptor gene ABCC8 is associated with antidiabetic efficacy of gliclazide in Chinese type 2 diabetic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Inactivation of the Fto gene protects from obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

The Correlation between Relatives on the Supposition of Mendelian Inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Association testing of novel type 2 diabetes risk alleles in the JAZF1, CDC123/CAMK1D, TSPAN8, THADA, ADAMTS9, and NOTCH2 loci with insulin release, insulin sensitivity, and obesity in a population-based sample of 4,516 glucose-tolerant middle-aged D

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Studies of association of variants near the HHEX, CDKN2A/B, and IGF2BP2 genes with type 2 diabetes and impaired insulin release in 10,705 Danish subjects: validation and extension of genome-wide association studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Variants of CDKAL1 and IGF2BP2 affect first-phase insulin secretion during hyperglycaemic clamps

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Antioxidative Protection by Melatonin: Multiplicity of Mechanisms from Radical Detoxification to Radical Avoidance

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Isomers of the TCF1 gene encoding hepatocyte nuclear factor-1 alpha show differential expression in the pancreas and define the relationship between mutation position and clinical phenotype in monogenic diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Lack of TCF2/vHNF1 in mice leads to pancreas agenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Familial risks for type 2 diabetes in Sweden

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Impact of CYP2C9 amino acid polymorphisms on glyburide kinetics and on the insulin and glucose response in healthy volunteers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Polymorphisms in the TCF7L2, CDKAL1 and SLC30A8 genes are associated with impaired proinsulin conversion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Parental origin of sequence variants associated with complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Glucose: a vital toxin and potential utility of melatonin in protecting against the diabetic state

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

A genome-wide association study of gestational diabetes mellitus in Korean women

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Association of genetic variation in FTO with risk of obesity and type 2 diabetes with data from 96,551 East and South Asians.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Common variants near MC4R are associated with fat mass, weight and risk of obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Clinical risk factors, DNA variants, and the development of type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Parental transmission of type 2 diabetes: the Framingham Offspring Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Genotype score in addition to common risk factors for prediction of type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

A genome-wide association search for type 2 diabetes genes in African Americans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

The search for genetic risk factors of type 2 diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Common variants of the novel type 2 diabetes genes CDKAL1 and HHEX/IDE are associated with decreased pancreatic beta-cell function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

How to interpret a genome-wide association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Common vs. rare allele hypotheses for complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

The E23K variant of KCNJ11 encoding the pancreatic beta-cell adenosine 5'-triphosphate-sensitive potassium channel subunit Kir6.2 is associated with an increased risk of secondary failure to sulfonylurea in patients with type 2 diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Effect of genetic variation in the organic cation transporter 1 (OCT1) on metformin action

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Gene variants in the novel type 2 diabetes loci CDC123/CAMK1D, THADA, ADAMTS9, BCL11A, and MTNR1B affect different aspects of pancreatic beta-cell function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

A genome-wide association study identifies novel risk loci for type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Diabetes-associated common genetic variation and its association with GLP-1 concentrations and response to exogenous GLP-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Impact of polymorphisms in WFS1 on prediabetic phenotypes in a population-based sample of middle-aged people with normal and abnormal glucose regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Genetic variation in KCNQ1 associates with fasting glucose and beta-cell function: a study of 3,734 subjects comprising three ethnicities living in Singapore

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Substrate specificity of MATE1 and MATE2-K, human multidrug and toxin extrusions/H(+)-organic cation antiporters

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Is genetic testing useful to predict type 2 diabetes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

TCF7L2 variant rs7903146 affects the risk of type 2 diabetes by modulating incretin action.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Involvement of organic cation transporter 1 in hepatic and intestinal distribution of metformin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Deficit of tRNA(Lys) modification by Cdkal1 causes the development of type 2 diabetes in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

The Krüppel-like zinc finger protein GLIS3 transactivates neurogenin 3 for proper fetal pancreatic islet differentiation in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

Loss-of-function CYP2C9 variants improve therapeutic response to sulfonylureas in type 2 diabetes: a Go-DARTS study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12272-013-0021-X

10.1007/S12272-013-0021-X

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

28 August 2017

1005867903

0 references

1 reference