type 2 diabetes phenotype

Aliases

NIDDM, T2D, T2DM, diabetes, non-insulin-dependent diabetes, type 2 diabetes, type 2 diabetes mellitus, type II diabetes

Related entities (5)

Mentioned in (35)

Papers in which this entity is mentioned.

• Cardiovascular and Metabolic Outcomes in Adults with Fetal Alcohol Spectrum Disorders: A Retrospective Cohort Study. (2026)
• Modeling heterogeneity in single-cell perturbation states enhances detection of response eQTLs. (2025)
• Associations between common genetic variants and income provide insights about the socio-economic health gradient. (2025)
• Concordance between male- and female-specific GWAS results helps define underlying genetic architecture of complex traits. (2025)
• Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders. (2025)
• Genome-wide association testing beyond SNPs. (2025)
• Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
• Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. (2024)
• Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
• Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. (2024)
• Principles and methods for transferring polygenic risk scores across global populations. (2024)
• CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods. (2024)
• Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
• Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
• Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
• Variant interpretation using population databases: Lessons from gnomAD. (2022)
• Med-BERT: pretrained contextualized embeddings on large-scale structured electronic health records for disease prediction. (2021)
• Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies. (2021)
• Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data. (2021)
• Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. (2021)
• Macrophage Polarization States in the Tumor Microenvironment. (2021)
• Polygenic risk scores: from research tools to clinical instruments. (2020)
• Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (2020)
• The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
• Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data (2020)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
• Determining cell type abundance and expression from bulk tissues with digital cytometry. (2019)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• What Happens When Children with Fetal Alcohol Spectrum Disorders Become Adults? (2015)
• Effects of alcohol on the endocrine system. (2013)
• Dosage transmission disequilibrium test (dTDT) for linkage and association detection. (2013)
• Maternal ethanol consumption alters the epigenotype and the phenotype of offspring in a mouse model. (2010)
• 3' end mRNA processing: molecular mechanisms and implications for health and disease. (2008)

Merged raw entities (7)

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