The molecular genetics of non-insulin-dependent diabetes mellitus

The link between family history and risk of type 2 diabetes is not explained by anthropometric, lifestyle or genetic risk factors: the EPIC-InterAct study.

Diabetologia·2012

Common variants in CNDP1 and CNDP2, and risk of nephropathy in type 2 diabetes.

Diabetologia·2011

A family history of diabetes is associated with reduced physical fitness in the Prevalence, Prediction and Prevention of Diabetes (PPP)-Botnia study.

Diabetologia·2010

Interaction between prenatal growth and high-risk genotypes in the development of type 2 diabetes.

Diabetologia·2009

Common variants in the TCF7L2 gene help to differentiate autoimmune from non-autoimmune diabetes in young (15-34 years) but not in middle-aged (40-59 years) diabetic patients.

Diabetologia·2008

HLA-DQB1 genotypes, islet antibodies and beta cell function in the classification of recent-onset diabetes among young adults in the nationwide Diabetes Incidence Study in Sweden.

Diabetologia·2006

Snus, nicotine pouches and cardiovascular disease: Evidence, mechanisms, and the challenge of novel nicotine products.

Journal of internal medicine·2026

Cognitive safety of statin use in the elderly: Evidence from a nationally representative sample.

Journal of internal medicine·2026

AA amyloidosis in the four historical monogenic autoinflammatory diseases: Clinical burden and insights from a retrospective referral-centre study.

Journal of internal medicine·2026

European Consortium for Lipodystrophies consensus definition and classification framework for monogenic lipodystrophy.

Journal of internal medicine·2026

Upcoming therapies for steatotic liver disease: Translating breakthroughs into clinical practice.

Journal of internal medicine·2026

Recent advances in polyendocrine metabolic ovarian syndrome, formerly polycystic ovary syndrome, with emphasis on endocrine and metabolic dysfunction and cardiovascular risk.

Journal of internal medicine·2026

Heterogeneity of azithromycin resistance markers in Neisseria gonorrhoeae and challenges in implementing molecular assays for routine surveillance.

New microbes and new infections·2026

Large-Scale Neuroimaging and Genetic Analyses of the Human Thalamus in Loneliness.

Biological psychiatry global open science·2026

A recurrent CCDC82 frameshift variant associated with syndromic neurodevelopmental disorder in a consanguineous Pakistani family.

Biochemistry and biophysics reports·2026

Clinical and molecular characterization of giant axonal neuropathy due to a homozygous c.851 + 1G>A variant in GAN: A case report and literature review.

Global medical genetics·2026

The genome sequence of the Lesser noctule, Nyctalus leisleri (Kuhl, 1817) (Chiroptera: Vespertilionidae).

Wellcome open research·2026

Additional PAX3 Variants for Dominant Blue Eyes in Cats.

Animal genetics·2026

Related Experiment Videos

The molecular genetics of non-insulin-dependent diabetes mellitus

Related Concept Videos

The link between family history and risk of type 2 diabetes is not explained by anthropometric, lifestyle or genetic risk factors: the EPIC-InterAct study.

Common variants in CNDP1 and CNDP2, and risk of nephropathy in type 2 diabetes.

A family history of diabetes is associated with reduced physical fitness in the Prevalence, Prediction and Prevention of Diabetes (PPP)-Botnia study.

Interaction between prenatal growth and high-risk genotypes in the development of type 2 diabetes.

Common variants in the TCF7L2 gene help to differentiate autoimmune from non-autoimmune diabetes in young (15-34 years) but not in middle-aged (40-59 years) diabetic patients.

HLA-DQB1 genotypes, islet antibodies and beta cell function in the classification of recent-onset diabetes among young adults in the nationwide Diabetes Incidence Study in Sweden.

Snus, nicotine pouches and cardiovascular disease: Evidence, mechanisms, and the challenge of novel nicotine products.

Cognitive safety of statin use in the elderly: Evidence from a nationally representative sample.

AA amyloidosis in the four historical monogenic autoinflammatory diseases: Clinical burden and insights from a retrospective referral-centre study.

European Consortium for Lipodystrophies consensus definition and classification framework for monogenic lipodystrophy.

Upcoming therapies for steatotic liver disease: Translating breakthroughs into clinical practice.

Recent advances in polyendocrine metabolic ovarian syndrome, formerly polycystic ovary syndrome, with emphasis on endocrine and metabolic dysfunction and cardiovascular risk.

Heterogeneity of azithromycin resistance markers in Neisseria gonorrhoeae and challenges in implementing molecular assays for routine surveillance.

Large-Scale Neuroimaging and Genetic Analyses of the Human Thalamus in Loneliness.

A recurrent CCDC82 frameshift variant associated with syndromic neurodevelopmental disorder in a consanguineous Pakistani family.

Clinical and molecular characterization of giant axonal neuropathy due to a homozygous c.851 + 1G>A variant in GAN: A case report and literature review.

The genome sequence of the Lesser noctule, Nyctalus leisleri (Kuhl, 1817) (Chiroptera: Vespertilionidae).

Additional PAX3 Variants for Dominant Blue Eyes in Cats.

Related Experiment Videos

The molecular genetics of non-insulin-dependent diabetes mellitus

Related Concept Videos

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