List of works - Cheng Hu

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

scientific article published on 24 March 2017

A causal relationship between uric acid and diabetic macrovascular disease in Chinese type 2 diabetes patients: A Mendelian randomization analysis.

scientific article published on 31 March 2016

A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans

scientific article

An evaluation of the performance of HapMap SNP data in a Shanghai Chinese population: analyses of allele frequency, linkage disequilibrium pattern and tagging SNPs transferability on chromosome 1q21-q25

scientific article

Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels

scientific article

Association between KCNQ1 genetic variants and obesity in Chinese patients with type 2 diabetes

scientific article

Association of KCNJ11 and ABCC8 genetic polymorphisms with response to repaglinide in Chinese diabetic patients.

scientific article published in August 2008

Association of PAX4 genetic variants with oral antidiabetic drugs efficacy in Chinese type 2 diabetes patients

scientific article published on 22 April 2014

Association of adiposity indices with bone density and bone turnover in the Chinese population

scientific article

Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population

scientific article

Association of serum uric acid levels with osteoporosis and bone turnover markers in a Chinese population

scientific article published on 14 December 2017

Association of the POU class 2 homeobox 1 gene (POU2F1) with susceptibility to Type 2 diabetes in Chinese populations

article

Causal Association of Overall Obesity and Abdominal Obesity with Type 2 Diabetes: A Mendelian Randomization Analysis

scientific article published on 06 April 2018

Circulating Unsaturated Fatty Acids Delineate the Metabolic Status of Obese Individuals

scientific article published on 6 September 2015

Circulating miR-29b positively correlates with non-alcoholic fatty liver disease in a Chinese population

scientific article published on 03 April 2019

Common variants in or near ZNRF1, COLEC12, SCYL1BP1 and API5 are associated with diabetic retinopathy in Chinese patients with type 2 diabetes.

scientific article published on 28 March 2015

Common variants of hepatocyte nuclear factor 1beta are associated with type 2 diabetes in a Chinese population.

scientific article published on 23 January 2009

Diabetes in China: Epidemiology and Genetic Risk Factors and Their Clinical Utility in Personalized Medication.

scientific article

Discovery of potential biomarkers for osteoporosis using LC-MS/MS metabolomic methods

scientific article published on 18 February 2019

Effects of ABCA1 variants on rosiglitazone monotherapy in newly diagnosed type 2 diabetes patients.

scientific article published in February 2008

Effects of GCK, GCKR, G6PC2 and MTNR1B variants on glucose metabolism and insulin secretion

scientific article

FADS1-FADS2 genetic polymorphisms are associated with fatty acid metabolism through changes in DNA methylation and gene expression

article

Genetic Variants Flanking the FGF21 Gene Were Associated with Renal Function in Chinese Patients with Type 2 Diabetes.

scientific article published on 7 May 2019

Genetic and clinical variables identify predictors for chronic kidney disease in type 2 diabetes

scientific article

Genetic variants of PLA2G6 are associated with Type 2 diabetes mellitus and triglyceride levels in a Chinese population

scientific article published on 11 October 2014

Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians

scientific article

Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes

scientific article published on 28 January 2016

Genome-wide association study identifies three novel loci for type 2 diabetes

scientific article

Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4.

scientific article published on 27 March 2013

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

scientific article

Impaired pancreatic beta cell compensatory function is the main cause of type 2 diabetes in individuals with high genetic risk: a 9 year prospective cohort study in the Chinese population.

scientific article

Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits

scientific article published on 11 September 2011

Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1q

scientific article (publication date: July 2009)

Linking MTNR1B Variants to Diabetes: The Role of Circadian Rhythms

scientific article published on 01 June 2016

Mendelian randomization analysis to assess a causal effect of haptoglobin on macroangiopathy in Chinese type 2 diabetes patients

scientific article published on 16 January 2018

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

scientific article

Monogenic Obesity Mutations Lead to Less Weight Loss After Bariatric Surgery: a 6-Year Follow-Up Study

scientific article published on 01 April 2019

Nerve growth factor is closely related to glucose metabolism, insulin sensitivity and insulin secretion in the second trimester: a case-control study in Chinese

scientific article published on 19 November 2020

No association of vascular endothelial growth factor A gene rs9369425 polymorphism with glucose metabolism in Chinese Han population

scientific article published on August 1, 2010

Overall and central obesity with insulin sensitivity and secretion in a Han Chinese population: a Mendelian randomization analysis.

scientific article

PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population

scientific article

Pharmacogenomics of glinides.

scientific article published on January 2015

Phenotypic heterogeneity in Chinese patients with hepatocyte nuclear factor-1β mutations.

scientific article

Polymorphisms of the KCNQ1 gene are associated with the therapeutic responses of sulfonylureas in Chinese patients with type 2 diabetes

scientific article published on 03 October 2016

Rapid Elevation in CMPF May Act As a Tipping Point in Diabetes Development.

scientific article published on 16 March 2016

Role of gut microbiota, bile acids and their cross-talk in the effects of bariatric surgery on obesity and type 2 diabetes.

scientific article

Roux-en-Y Gastric Bypass Surgery Suppresses Hepatic Gluconeogenesis and Increases Intestinal Gluconeogenesis in a T2DM Rat Model

scientific article published on 01 November 2016

SNPs in PRKCA-HIF1A-GLUT1 are associated with diabetic kidney disease in a Chinese Han population with type 2 diabetes

scientific article published on 11 May 2020

Sodium-glucose co-transporter (SGLT) and glucose transporter (GLUT) expression in the kidney of type 2 diabetic subjects.

scientific article published on 6 May 2017

The effect of glucose-dependent insulinotropic polypeptide (GIP) variants on visceral fat accumulation in Han Chinese populations

scientific article

The genetic architecture of type 2 diabetes

scientific article (publication date: 11 July 2016)

Variants from GIPR, TCF7L2, DGKB, MADD, CRY2, GLIS3, PROX1, SLC30A8 and IGF1 Are Associated with Glucose Metabolism in the Chinese ⬇️

scientific article published on November 17, 2010

Variations in KCNQ1 are associated with type 2 diabetes and beta cell function in a Chinese population.

scientific article

Whole-exome sequencing identifies a novel INS mutation causative of maturity-onset diabetes of the young 10.

scientific article

List of works by Cheng Hu

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

A causal relationship between uric acid and diabetic macrovascular disease in Chinese type 2 diabetes patients: A Mendelian randomization analysis.

A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans

An evaluation of the performance of HapMap SNP data in a Shanghai Chinese population: analyses of allele frequency, linkage disequilibrium pattern and tagging SNPs transferability on chromosome 1q21-q25

Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels

Association between KCNQ1 genetic variants and obesity in Chinese patients with type 2 diabetes

Association of KCNJ11 and ABCC8 genetic polymorphisms with response to repaglinide in Chinese diabetic patients.

Association of PAX4 genetic variants with oral antidiabetic drugs efficacy in Chinese type 2 diabetes patients

Association of adiposity indices with bone density and bone turnover in the Chinese population

Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population

Association of serum uric acid levels with osteoporosis and bone turnover markers in a Chinese population

Association of the POU class 2 homeobox 1 gene (POU2F1) with susceptibility to Type 2 diabetes in Chinese populations

Causal Association of Overall Obesity and Abdominal Obesity with Type 2 Diabetes: A Mendelian Randomization Analysis

Circulating Unsaturated Fatty Acids Delineate the Metabolic Status of Obese Individuals

Circulating miR-29b positively correlates with non-alcoholic fatty liver disease in a Chinese population

Common variants in or near ZNRF1, COLEC12, SCYL1BP1 and API5 are associated with diabetic retinopathy in Chinese patients with type 2 diabetes.

Common variants of hepatocyte nuclear factor 1beta are associated with type 2 diabetes in a Chinese population.

Diabetes in China: Epidemiology and Genetic Risk Factors and Their Clinical Utility in Personalized Medication.

Discovery of potential biomarkers for osteoporosis using LC-MS/MS metabolomic methods

Effects of ABCA1 variants on rosiglitazone monotherapy in newly diagnosed type 2 diabetes patients.

Effects of GCK, GCKR, G6PC2 and MTNR1B variants on glucose metabolism and insulin secretion

FADS1-FADS2 genetic polymorphisms are associated with fatty acid metabolism through changes in DNA methylation and gene expression

Genetic Variants Flanking the FGF21 Gene Were Associated with Renal Function in Chinese Patients with Type 2 Diabetes.

Genetic and clinical variables identify predictors for chronic kidney disease in type 2 diabetes

Genetic variants of PLA2G6 are associated with Type 2 diabetes mellitus and triglyceride levels in a Chinese population

Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians

Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes

Genome-wide association study identifies three novel loci for type 2 diabetes

Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4.

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

Impaired pancreatic beta cell compensatory function is the main cause of type 2 diabetes in individuals with high genetic risk: a 9 year prospective cohort study in the Chinese population.

Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits

Linkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1q

Linking MTNR1B Variants to Diabetes: The Role of Circadian Rhythms

Mendelian randomization analysis to assess a causal effect of haptoglobin on macroangiopathy in Chinese type 2 diabetes patients

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

Monogenic Obesity Mutations Lead to Less Weight Loss After Bariatric Surgery: a 6-Year Follow-Up Study

Nerve growth factor is closely related to glucose metabolism, insulin sensitivity and insulin secretion in the second trimester: a case-control study in Chinese

No association of vascular endothelial growth factor A gene rs9369425 polymorphism with glucose metabolism in Chinese Han population

Overall and central obesity with insulin sensitivity and secretion in a Han Chinese population: a Mendelian randomization analysis.

PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population

Pharmacogenomics of glinides.

Phenotypic heterogeneity in Chinese patients with hepatocyte nuclear factor-1β mutations.

Polymorphisms of the KCNQ1 gene are associated with the therapeutic responses of sulfonylureas in Chinese patients with type 2 diabetes

Rapid Elevation in CMPF May Act As a Tipping Point in Diabetes Development.

Role of gut microbiota, bile acids and their cross-talk in the effects of bariatric surgery on obesity and type 2 diabetes.

Roux-en-Y Gastric Bypass Surgery Suppresses Hepatic Gluconeogenesis and Increases Intestinal Gluconeogenesis in a T2DM Rat Model

SNPs in PRKCA-HIF1A-GLUT1 are associated with diabetic kidney disease in a Chinese Han population with type 2 diabetes

Sodium-glucose co-transporter (SGLT) and glucose transporter (GLUT) expression in the kidney of type 2 diabetic subjects.

The effect of glucose-dependent insulinotropic polypeptide (GIP) variants on visceral fat accumulation in Han Chinese populations

The genetic architecture of type 2 diabetes

Variants from GIPR, TCF7L2, DGKB, MADD, CRY2, GLIS3, PROX1, SLC30A8 and IGF1 Are Associated with Glucose Metabolism in the Chinese ⬇️

Variations in KCNQ1 are associated with type 2 diabetes and beta cell function in a Chinese population.

Whole-exome sequencing identifies a novel INS mutation causative of maturity-onset diabetes of the young 10.