Further evidence for a type 2 diabetes susceptibility locus on chromosome 11q

Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.

Human molecular genetics·2021

APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups.

Lipids in health and disease·2021

Population sequencing data reveal a compendium of mutational processes in the human germ line.

Science (New York, N.Y.)·2021

Association of HIV-1 Infection and Antiretroviral Therapy With Type 2 Diabetes in the Hispanic Population of the Rio Grande Valley, Texas, USA.

Frontiers in medicine·2021

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.

Nature communications·2021

Genetic Overlap Profiles of Cognitive Ability in Psychotic and Affective Illnesses: A Multisite Study of Multiplex Pedigrees.

Biological psychiatry·2021

Revealing the Shared Genetic Architecture of Metabolic Dysfunction-Associated Steatotic Liver Disease-Related Traits Through Genomic Structural Equation Modeling.

Genetic epidemiology·2026

Mendelianization: Concentrating Polygenic Signal Into a Single Causal Locus.

Genetic epidemiology·2026

Robust Inference With Ghostknockoffs in Genome-Wide Association Studies With Sample Relatedness.

Genetic epidemiology·2026

The Omnicausal Model Reveals the Highly Polyfactorial Nature of Complex Diseases.

Genetic epidemiology·2026

Applying Bayesian Multivariable Mendelian Randomisation to Prioritise Candidate Causal Traits From High-Dimensional Data: Illustration From Estimation of the Effect of Maternal Metabolites on Offspring Birthweight.

Genetic epidemiology·2026

Individualized Bayesian Inference Identifies Novel Genetic Variants for Parkinson's Disease.

Genetic epidemiology·2026

Bidirectional associations between brain functional networks and sleep disorders: A bidirectional Mendelian randomization study.

Medicine·2026

Duodenal fluid analysis of 13 patients with progressive familial intrahepatic cholestasis type 2 from a single institution.

Medicine·2026

Genetic evidence for CTSH as a potential therapeutic target in sepsis: A Mendelian randomization and colocalization study.

Medicine·2026

Genetic and clinical spectrum of progressive familial intrahepatic cholestasis type 1: novel ATP8B1 variants and genotype-phenotype correlations.

European journal of pediatrics·2026

Genetically supported targets and drug repurposing for sleep disorders: a Mendelian randomization systematic study.

Naunyn-Schmiedeberg's archives of pharmacology·2026

Yeast Knockout Strain Collection: Driving Functional Genomics, Biotechnological Applications and Human Disease Research.

Yeast (Chichester, England)·2026

Related Experiment Videos

Further evidence for a type 2 diabetes susceptibility locus on chromosome 11q

Related Concept Videos

Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.

APOC3 genetic variation, serum triglycerides, and risk of coronary artery disease in Asian Indians, Europeans, and other ethnic groups.

Population sequencing data reveal a compendium of mutational processes in the human germ line.

Association of HIV-1 Infection and Antiretroviral Therapy With Type 2 Diabetes in the Hispanic Population of the Rio Grande Valley, Texas, USA.

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.

Genetic Overlap Profiles of Cognitive Ability in Psychotic and Affective Illnesses: A Multisite Study of Multiplex Pedigrees.

Revealing the Shared Genetic Architecture of Metabolic Dysfunction-Associated Steatotic Liver Disease-Related Traits Through Genomic Structural Equation Modeling.

Mendelianization: Concentrating Polygenic Signal Into a Single Causal Locus.

Robust Inference With Ghostknockoffs in Genome-Wide Association Studies With Sample Relatedness.

The Omnicausal Model Reveals the Highly Polyfactorial Nature of Complex Diseases.

Applying Bayesian Multivariable Mendelian Randomisation to Prioritise Candidate Causal Traits From High-Dimensional Data: Illustration From Estimation of the Effect of Maternal Metabolites on Offspring Birthweight.

Individualized Bayesian Inference Identifies Novel Genetic Variants for Parkinson's Disease.

Bidirectional associations between brain functional networks and sleep disorders: A bidirectional Mendelian randomization study.

Duodenal fluid analysis of 13 patients with progressive familial intrahepatic cholestasis type 2 from a single institution.

Genetic evidence for CTSH as a potential therapeutic target in sepsis: A Mendelian randomization and colocalization study.

Genetic and clinical spectrum of progressive familial intrahepatic cholestasis type 1: novel ATP8B1 variants and genotype-phenotype correlations.

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Related Experiment Videos

Further evidence for a type 2 diabetes susceptibility locus on chromosome 11q

Related Concept Videos

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