type 1 diabetes phenotype

Aliases

T1D, type 1 diabetes, type- I diabetes

Related entities (8)

Mentioned in (56)

Papers in which this entity is mentioned.

• Modeling heterogeneity in single-cell perturbation states enhances detection of response eQTLs. (2025)
• Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. (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)
• Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations. (2022)
• Lack of Evidence for a Relationship Between Salivary CRP and Women's Sexual Desire: An Investigation Across Clinical and Healthy Samples. (2022)
• Different FreeSurfer versions might generate different statistical outcomes in case-control comparison studies. (2022)
• Shared genetic architecture across psychiatric disorders. (2021)
• Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data. (2021)
• Studying the Effect of Maternal Pregestational Diabetes on Fetal Neurodevelopment Using Magnetoencephalography. (2020)
• Polygenic risk scores: from research tools to clinical instruments. (2020)
• Relationship of prenatal maternal obesity and diabetes to offspring neurodevelopmental and psychiatric disorders: a narrative review. (2020)
• Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data (2020)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. (2018)
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
• Immune Dysfunction and Autoimmunity as Pathological Mechanisms in Autism Spectrum Disorders. (2018)
• Neonatal Cytokine Profiles Associated With Autism Spectrum Disorder. (2017)
• Human Brain Abnormalities Associated With Prenatal Alcohol Exposure and Fetal Alcohol Spectrum Disorder. (2017)
• The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). (2017)
• Defining Feasibility and Pilot Studies in Preparation for Randomised Controlled Trials: Development of a Conceptual Framework. (2016)
• Integrating basic research with prevention/intervention to reduce risky substance use among college students. (2015)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• A review of the nonpressor and nonantidiuretic actions of the hormone vasopressin. (2015)
• HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data. (2015)
• Maternal periconceptional alcohol consumption and congenital limb deficiencies. (2014)
• Inference of high resolution HLA types using genome-wide RNA or DNA sequencing reads. (2014)
• Maternal obesity and tobacco use modify the impact of genetic variants on the occurrence of conotruncal heart defects. (2014)
• PolymiRTS Database 3.0: linking polymorphisms in microRNAs and their target sites with human diseases and biological pathways. (2014)
• HLA typing from 1000 genomes whole genome and whole exome illumina data. (2013)
• A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines. (2013)
• Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. (2012)
• Vitamin D and its role during pregnancy in attaining optimal health of mother and fetus. (2012)
• Soluble epoxide hydrolase inhibition, epoxygenated fatty acids and nociception. (2011)
• A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. (2011)
• Epigenetics and psychoneuroimmunology: mechanisms and models. (2011)
• Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA. (2011)
• Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants. (2011)
• Risks of overweight and abdominal obesity at age 16 years associated with prenatal exposures to maternal prepregnancy overweight and gestational diabetes mellitus. (2010)
• Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample. (2010)
• Liver and adipose expression associated SNPs are enriched for association to type 2 diabetes. (2010)
• Using public control genotype data to increase power and decrease cost of case-control genetic association studies. (2010)
• Maternal folate-related gene environment interactions and congenital heart defects. (2010)
• The genetic interpretation of area under the ROC curve in genomic profiling. (2010)
• Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy. (2009)
• Finding the missing heritability of complex diseases. (2009)
• Genomewide association studies and human disease. (2009)
• Insulin-like growth factor-I mitigates motor coordination deficits associated with neonatal alcohol exposure in rats. (2009)
• Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk. (2009)
• Potential role for plasma placental growth factor in predicting coronary heart disease risk in women. (2009)
• Common and rare variants in multifactorial susceptibility to common diseases. (2008)
• Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. (2007)
• Coordinate expression of insulin-like growth factor system components by neurons and neuroglia during retinal and cerebellar development. (1992)

Merged raw entities (4)

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