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Prevalence and risk factors of gestational diabetes in Punjab, North India: results from a population screening program

European journal of endocrinology, 2015-08, Vol.173 (2), p.257-267

2015

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A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes

PloS one, 2018-12, Vol.13 (12), p.e0208654-e0208654

2018

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Cohort profile: Epigenetics in Pregnancy (EPIPREG) - population-based sample of European and South Asian pregnant women with epigenome-wide DNA methylation (850k) in peripheral blood leukocytes

PloS one, 2021-01, Vol.16 (8), p.e0256158-e0256158

2021

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Blood-based epigenetic estimators of chronological age in human adults using DNA methylation data from the Illumina MethylationEPIC array

BMC genomics, 2020-10, Vol.21 (1), p.747-13, Article 747

2020

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Automated pathway and reaction prediction facilitates in silico identification of unknown metabolites in human cohort studies

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2017-12, Vol.1071, p.58-67

2017

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Relationship between insulin sensitivity and gene expression in human skeletal muscle

BMC endocrine disorders, 2021-02, Vol.21 (1), p.32-32, Article 32

2021

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The genetics of diabetic complications

Nature reviews. Nephrology, 2015-05, Vol.11 (5), p.277-287

2015

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Prioritizing genes for follow-up from genome wide association studies using information on gene expression in tissues relevant for type 2 diabetes mellitus

BMC medical genomics, 2009-12, Vol.2 (1), p.72-72, Article 72

2009

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Common genetic variants highlight the role of insulin resistance and body fat distribution in type 2 diabetes, independent of obesity

Diabetes (New York, N.Y.), 2014-12, Vol.63 (12), p.4378-4387

2014

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A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY

Diabetologia, 2022-04, Vol.65 (4), p.632-643

2022

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Sulfonylureas in NIDDM

Diabetes care, 1992-06, Vol.15 (6), p.737-754

Groop, L C

1992

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PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

Nature genetics, 2003-07, Vol.34 (3), p.267-273

2003

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Demonstrating stratification in a European American population

Nature genetics, 2005-08, Vol.37 (8), p.868-872

2005

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Correction to: A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY

Diabetologia, 2022-05, Vol.65 (5), p.912-912

2022

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Interaction between the obesity-risk gene FTO and the dopamine D2 receptor gene ANKK1/TaqIA on insulin sensitivity

Diabetologia, 2016-12, Vol.59 (12), p.2622-2631

2016

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Genotype-based treatment of type 2 diabetes with an α2A-adrenergic receptor antagonist

Science translational medicine, 2014-10, Vol.6 (257), p.257ra139

2014

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TXNIP regulates peripheral glucose metabolism in humans

PLoS medicine, 2007-05, Vol.4 (5), p.e158

2007

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Whole grain, bran, and germ intake and risk of type 2 diabetes: a prospective cohort study and systematic review

PLoS medicine, 2007-08, Vol.4 (8), p.e261

2007

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HAPT2D: high accuracy of prediction of T2D with a model combining basic and advanced data depending on availability

European journal of endocrinology, 2018-04, Vol.178 (4), p.331-341

2018

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Inhibition of the Rise in FFA by Acipimox Partially Prevents GH-Induced Insulin Resistance in GH-Deficient Adults

The journal of clinical endocrinology and metabolism, 2001-12, Vol.86 (12), p.5813-5818

2001

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Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene

PLoS medicine, 2007-04, Vol.4 (4), p.e118-e118

2007

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Prevalence and risk factors of gestational diabetes in Punjab, North India: results from a population screening program

A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes

Cohort profile: Epigenetics in Pregnancy (EPIPREG) - population-based sample of European and South Asian pregnant women with epigenome-wide DNA methylation (850k) in peripheral blood leukocytes

Blood-based epigenetic estimators of chronological age in human adults using DNA methylation data from the Illumina MethylationEPIC array

Automated pathway and reaction prediction facilitates in silico identification of unknown metabolites in human cohort studies

Relationship between insulin sensitivity and gene expression in human skeletal muscle

Genome-wide association analysis of type 2 diabetes in the EPIC-InterAct study

The genetics of diabetic complications

Prioritizing genes for follow-up from genome wide association studies using information on gene expression in tissues relevant for type 2 diabetes mellitus

Identification of ten loci associated with height highlights new biological pathways in human growth

Common genetic variants highlight the role of insulin resistance and body fat distribution in type 2 diabetes, independent of obesity

A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY

Sulfonylureas in NIDDM

A common variant of HMGA2 is associated with adult and childhood height in the general population

PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

Demonstrating stratification in a European American population

Correction to: A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY

Interaction between the obesity-risk gene FTO and the dopamine D2 receptor gene ANKK1/TaqIA on insulin sensitivity

Genotype-based treatment of type 2 diabetes with an α2A-adrenergic receptor antagonist

TXNIP regulates peripheral glucose metabolism in humans

Whole grain, bran, and germ intake and risk of type 2 diabetes: a prospective cohort study and systematic review

HAPT2D: high accuracy of prediction of T2D with a model combining basic and advanced data depending on availability

HbA1c measured in stored erythrocytes is positively linearly associated with mortality in individuals with diabetes mellitus

Inhibition of the Rise in FFA by Acipimox Partially Prevents GH-Induced Insulin Resistance in GH-Deficient Adults

Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene

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