whole blood anatomy

Aliases

blood

Related entities (14)

Mentioned in (53)

Papers in which this entity is mentioned.

• Integrative epigenetics and transcriptomics identify aging genes in human blood. (2026)
• An overview of DNA methylation-derived trait score methods and applications. (2023)
• Multiomic prioritisation of risk genes for anorexia nervosa. (2023)
• Single-molecule methylation profiles of cell-free DNA in cancer with nanopore sequencing. (2023)
• Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease. (2022)
• Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022)
• Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. (2021)
• Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (2021)
• Detection and characterization of lung cancer using cell-free DNA fragmentomes. (2021)
• Klotho gene polymorphism, brain structure and cognition in early-life development. (2020)
• Transcriptomic signatures across human tissues identify functional rare genetic variation. (2020)
• Liquid versus tissue biopsy for detecting acquired resistance and tumor heterogeneity in gastrointestinal cancers. (2019)
• Hypermethylation of Proopiomelanocortin and Period 2 Genes in Blood Are Associated with Greater Subjective and Behavioral Motivation for Alcohol in Humans. (2019)
• RNA-Seq Signatures Normalized by mRNA Abundance Allow Absolute Deconvolution of Human Immune Cell Types. (2019)
• Comparison of Illumina 450K and EPIC arrays in placental DNA methylation. (2019)
• Elimination Characteristics of the Alcohol Biomarker Phosphatidylethanol (PEth) in Blood during Alcohol Detoxification. (2019)
• Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
• A SNP panel for identification of DNA and RNA specimens. (2018)
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
• Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility. (2018)
• Comparison of DNA methylation measured by Illumina 450K and EPIC BeadChips in blood of newborns and 14-year-old children. (2018)
• Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
• Elevated polygenic burden for autism is associated with differential DNA methylation at birth. (2018)
• Genetic effects on gene expression across human tissues. (2017)
• Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors. (2017)
• A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
• The impact of structural variation on human gene expression. (2017)
• 2D Representation of Transcriptomes by t-SNE Exposes Relatedness between Human Tissues. (2016)
• Fragment Length of Circulating Tumor DNA. (2016)
• Presence of an epigenetic signature of prenatal cigarette smoke exposure in childhood. (2016)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• Systematic pan-cancer analysis of tumour purity. (2015)
• Interindividual methylomic variation across blood, cortex, and cerebellum: implications for epigenetic studies of neurological and neuropsychiatric phenotypes. (2015)
• Robust enumeration of cell subsets from tissue expression profiles. (2015)
• Prenatal ethanol exposure alters adult hippocampal VGLUT2 expression with concomitant changes in promoter DNA methylation, H3K4 trimethylation and miR-467b-5p levels. (2015)
• Reconstructing A/B compartments as revealed by Hi-C using long-range correlations in epigenetic data. (2015)
• Maternal and neonatal plasma microRNA biomarkers for fetal alcohol exposure in an ovine model. (2014)
• Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine. (2014)
• DNA methylation signatures link prenatal famine exposure to growth and metabolism. (2014)
• DNA methylation contributes to natural human variation. (2013)
• Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. (2012)
• Blood cell origin of circulating microRNAs: a cautionary note for cancer biomarker studies. (2012)
• The majority of microRNAs detectable in serum and saliva is concentrated in exosomes. (2012)
• Argonaute2 complexes carry a population of circulating microRNAs independent of vesicles in human plasma. (2011)
• Identification of recent cannabis use: whole-blood and plasma free and glucuronidated cannabinoid pharmacokinetics following controlled smoked cannabis administration. (2011)
• Significant differences in global genomic DNA methylation by gender and race/ethnicity in peripheral blood. (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)
• Haemolysis during sample preparation alters microRNA content of plasma. (2011)
• Effects of moderate drinking during pregnancy on placental gene expression. (2010)
• A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. (2009)
• A haplotype containing quantitative trait loci for SLC1A1 gene expression and its association with obsessive-compulsive disorder. (2009)

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