Genetics of diabetes

Genetic ancestry and monogenic disease risk in the Scottish Traveller founder population.

Nature communications·2026

Implementation of exome sequencing for rare undiagnosed diseases in LMICs: the G2MC rare diseases exome sequencing pilot project.

Human genetics·2026

Type 2 diabetes genetics in 125,000 admixed adults from Mexico City.

medRxiv : the preprint server for health sciences·2026

Analysis of 173,303 exomes and genomes in the Pakistan Genome Resource.

Nature·2026

Validation of the Shoebox PureTest audiometry technology for remote data collection in clinical trials.

Scientific reports·2026

Alzheimer's disease-like brain pattern biomarker: capturing risks and predicting disease onset.

Molecular psychiatry·2026

The evolution of thyroid cancer diagnostics: Historical milestones and their impact on contemporary clinical practice.

Reviews in endocrine & metabolic disorders·2026

Weight regain after obesity treatment: mechanisms, predictors, and real-world evidence from the IGOBE program.

Reviews in endocrine & metabolic disorders·2026

Mammary adipocyte plasticity and epithelial crosstalk: roles in development, remodeling, and disease.

Reviews in endocrine & metabolic disorders·2026

Role of thyroid peroxidase in health and disease: A comprehensive update on TPO gene and protein expression, enzymatic activity and pharmacological modulation.

Reviews in endocrine & metabolic disorders·2026

Effect of acute postprandial exercise on continuous glucose monitoring outcomes in type 2 diabetes: A systematic review and meta-analysis of crossover trials.

Reviews in endocrine & metabolic disorders·2026

Natriuretic peptide receptor C in cardiovascular-kidney-liver-metabolic syndrome: from natriuretic peptide deficiency to direct tissue signaling?

Reviews in endocrine & metabolic disorders·2026

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Frontiers in genetics·2026

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

Frontiers in pediatrics·2026

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology·2026

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Human molecular genetics·2026

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Epilepsia·2026

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Seizure·2026

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Genetics of diabetes

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Genetic ancestry and monogenic disease risk in the Scottish Traveller founder population.

Implementation of exome sequencing for rare undiagnosed diseases in LMICs: the G2MC rare diseases exome sequencing pilot project.

Type 2 diabetes genetics in 125,000 admixed adults from Mexico City.

Analysis of 173,303 exomes and genomes in the Pakistan Genome Resource.

Validation of the Shoebox PureTest audiometry technology for remote data collection in clinical trials.

Alzheimer's disease-like brain pattern biomarker: capturing risks and predicting disease onset.

The evolution of thyroid cancer diagnostics: Historical milestones and their impact on contemporary clinical practice.

Weight regain after obesity treatment: mechanisms, predictors, and real-world evidence from the IGOBE program.

Mammary adipocyte plasticity and epithelial crosstalk: roles in development, remodeling, and disease.

Role of thyroid peroxidase in health and disease: A comprehensive update on TPO gene and protein expression, enzymatic activity and pharmacological modulation.

Effect of acute postprandial exercise on continuous glucose monitoring outcomes in type 2 diabetes: A systematic review and meta-analysis of crossover trials.

Natriuretic peptide receptor C in cardiovascular-kidney-liver-metabolic syndrome: from natriuretic peptide deficiency to direct tissue signaling?

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Related Experiment Videos

Genetics of diabetes

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