blood drug
Evidence from:
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Related entities (10)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| blood | biomarker_for | addiction | — | 1 |
| blood | associated_with | GTEx | — | 1 |
| blood | associated_with | schizophrenia | — | 1 |
| eQTLGen Consortium | expressed_in | blood | — | 1 |
| eQTLGen Consortium | associated_with | blood | — | 1 |
| ethanol group | expressed_in | blood | — | 1 |
| GENEVA consortium | associated_with | blood | — | 1 |
| genomic DNA | associated_with | blood | — | 1 |
| monocytes | associated_with | blood | — | 1 |
| study cohort | associated_with | blood | — | 1 |
Mentioned in (112)
Papers in which this entity is mentioned.
- Whole genome sequencing approach to assess homologous recombination deficiency in a pan-cancer cohort. (2026)
- Nanopore-based cell-free DNA fragmentation and methylation profiles from the cerebral spinal fluid of patients with lung cancer brain metastases. (2025)
- Stratified Medicine Pediatrics: Cell-Free DNA and Serial Tumor Sequencing Identifies Subtype-Specific Cancer Evolution and Epigenetic States. (2025)
- Transcription start sites experience a high influx of heritable variants fueled by early development. (2025)
- Machine learning approaches to the identification of children affected by prenatal alcohol exposure: A narrative review. (2024)
- An overview of DNA methylation-derived trait score methods and applications. (2023)
- Association between the timing of childhood adversity and epigenetic patterns across childhood and adolescence: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) prospective cohort. (2023)
- A DNA methylation atlas of normal human cell types. (2023)
- Combined low-pass whole genome and targeted sequencing in liquid biopsies for pediatric solid tumors. (2023)
- Validation of the new EPIC DNA methylation microarray (900K EPIC v2) for high-throughput profiling of the human DNA methylome. (2023)
- Single-molecule methylation profiles of cell-free DNA in cancer with nanopore sequencing. (2023)
- A systematic review of neuroimaging epigenetic research: calling for an increased focus on development. (2023)
- mutations, genetic mosaicism and human disease. (2022)
- At the dawn: cell-free DNA fragmentomics and gene regulation. (2022)
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022)
- Circulating Tumor DNA as a Biomarker in Patients With Stage III and IV Wilms Tumor: Analysis From a Children's Oncology Group Trial, AREN0533. (2022)
- Genetic variants associated with longitudinal changes in brain structure across the lifespan. (2022)
- Epigenome-wide change and variation in DNA methylation in childhood: trajectories from birth to late adolescence. (2021)
- Autosomal sex-associated co-methylated regions predict biological sex from DNA methylation. (2021)
- Application of third-generation sequencing in cancer research. (2021)
- Infant circulating MicroRNAs as biomarkers of effect in fetal alcohol spectrum disorders. (2021)
- Best practices for variant calling in clinical sequencing. (2020)
- Immune network dysregulation associated with child neurodevelopmental delay: modulatory role of prenatal alcohol exposure. (2020)
- Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring. (2020)
- Patterns of Reliability: Assessing the Reproducibility and Integrity of DNA Methylation Measurement. (2020)
- Pan-cancer analysis of whole genomes. (2020)
- Association between DNA methylation and ADHD symptoms from birth to school age: a prospective meta-analysis. (2020)
- DNA methylation and brain structure and function across the life course: A systematic review. (2020)
- Genome-wide DNA methylation comparison between live human brain and peripheral tissues within individuals. (2019)
- Sensitive Periods for the Effect of Childhood Adversity on DNA Methylation: Results From a Prospective, Longitudinal Study. (2019)
- Alcohol Use in Pregnancy. (2019)
- Epigenetics and depression . (2019)
- Serial liquid biopsies for detection of treatment failure and profiling of resistance mechanisms in -rearranged lung cancer. (2019)
- Genome-wide cell-free DNA fragmentation in patients with cancer. (2019)
- RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues. (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)
- Pan-cancer whole-genome analyses of metastatic solid tumours. (2019)
- Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
- Circular DNA elements of chromosomal origin are common in healthy human somatic tissue. (2018)
- Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. (2018)
- What Should a Psychiatrist Know About Genetics? Review and Recommendations From the Residency Education Committee of the International Society of Psychiatric Genetics. (2018)
- The Immune Landscape of Cancer. (2018)
- Detection of circulating tumour DNA is associated with inferior outcomes in Ewing sarcoma and osteosarcoma: a report from the Children's Oncology Group. (2018)
- Human Genetics of Addiction: New Insights and Future Directions. (2018)
- Extending the Human Connectome Project across ages: Imaging protocols for the Lifespan Development and Aging projects. (2018)
- Elevated polygenic burden for autism is associated with differential DNA methylation at birth. (2018)
- Tumor fraction in cell-free DNA as a biomarker in prostate cancer. (2018)
- Interactive effects of prenatal alcohol exposure and chronic stress in adulthood on anxiety-like behavior and central stress-related receptor mRNA expression: Sex- and time-dependent effects. (2018)
- Annotation-free quantification of RNA splicing using LeafCutter. (2018)
- Case-control meta-analysis of blood DNA methylation and autism spectrum disorder. (2018)
- Copy number signatures and mutational processes in ovarian carcinoma. (2018)
- Universal Patterns of Selection in Cancer and Somatic Tissues. (2017)
- Postnatal choline supplementation selectively attenuates hippocampal microRNA alterations associated with developmental alcohol exposure. (2017)
- Sexual Dimorphism of miRNAs Secreted by Bovine -produced Embryos. (2017)
- BECon: a tool for interpreting DNA methylation findings from blood in the context of brain. (2017)
- Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors. (2017)
- Puberty and structural brain development in humans. (2017)
- Longitudinal epigenetic predictors of amygdala:hippocampus volume ratio. (2017)
- Epigenetic profiling of ADHD symptoms trajectories: a prospective, methylome-wide study. (2017)
- Prenatal alcohol exposure and prenatal stress differentially alter glucocorticoid signaling in the placenta and fetal brain. (2017)
- An open access pilot freely sharing cancer genomic data from participants in Texas. (2016)
- Correspondence of DNA Methylation Between Blood and Brain Tissue and Its Application to Schizophrenia Research. (2016)
- Maternal choline supplementation in a sheep model of first trimester binge alcohol fails to protect against brain volume reductions in peripubertal lambs. (2016)
- Integrated digital error suppression for improved detection of circulating tumor DNA. (2016)
- The Ontology for Biomedical Investigations. (2016)
- Fragment Length of Circulating Tumor DNA. (2016)
- Epigenomic profiling of preterm infants reveals DNA methylation differences at sites associated with neural function. (2016)
- Genetic and environmental influences interact with age and sex in shaping the human methylome. (2016)
- Glymphatic distribution of CSF-derived apoE into brain is isoform specific and suppressed during sleep deprivation. (2016)
- Genomic Characterization of Brain Metastases Reveals Branched Evolution and Potential Therapeutic Targets. (2015)
- Investigating the early-life determinants of illness in Africa: the Drakenstein Child Health Study. (2015)
- DNA methylation and healthy human aging. (2015)
- DR-BUDDI (Diffeomorphic Registration for Blip-Up blip-Down Diffusion Imaging) method for correcting echo planar imaging distortions. (2015)
- Interindividual methylomic variation across blood, cortex, and cerebellum: implications for epigenetic studies of neurological and neuropsychiatric phenotypes. (2015)
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. (2014)
- Common DNA methylation alterations in multiple brain regions in autism. (2014)
- New therapeutic approaches for Alzheimer's disease and cerebral amyloid angiopathy. (2014)
- Role of prefrontal cortex glucocorticoid receptors in stress and emotion. (2013)
- Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder. (2013)
- The Finnish Twin Cohort Study: an update. (2013)
- ACMG clinical laboratory standards for next-generation sequencing. (2013)
- Zebrafish models of human liver development and disease. (2013)
- Recurrent variations in DNA methylation in human pluripotent stem cells and their differentiated derivatives. (2012)
- Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. (2012)
- Dissociable effects of methylphenidate, atomoxetine and placebo on regional cerebral blood flow in healthy volunteers at rest: a multi-class pattern recognition approach. (2012)
- Detectable clonal mosaicism from birth to old age and its relationship to cancer. (2012)
- Argonaute2 complexes carry a population of circulating microRNAs independent of vesicles in human plasma. (2011)
- Recruitment and retention strategies for minority or poor clinical research participants: lessons from the Healthy Aging in Neighborhoods of Diversity across the Life Span study. (2011)
- Reexamination of testosterone, dihydrotestosterone, estradiol and estrone levels across the menstrual cycle and in postmenopausal women measured by liquid chromatography-tandem mass spectrometry. (2011)
- Epigenetics and psychoneuroimmunology: mechanisms and models. (2011)
- Diffusion tensor imaging of the cerebellum and eyeblink conditioning in fetal alcohol spectrum disorder. (2011)
- Genome wide association for addiction: replicated results and comparisons of two analytic approaches. (2010)
- Genetics and beyond--the transcriptome of human monocytes and disease susceptibility. (2010)
- Interaction between GSTM1/GSTT1 polymorphism and blood mercury on birth weight. (2010)
- TumorBoost: normalization of allele-specific tumor copy numbers from a single pair of tumor-normal genotyping microarrays. (2010)
- Role of testosterone in mediating prenatal ethanol effects on hypothalamic-pituitary-adrenal activity in male rats. (2009)
- Dense genomewide linkage scan for alcohol dependence in African Americans: significant linkage on chromosome 10. (2009)
- Effects of prenatal ethanol exposure on hypothalamic-pituitary-adrenal function across the estrous cycle. (2009)
- An exploration of attitudes among black Americans towards psychiatric genetic research. (2009)
- Neurotoxic effects and biomarkers of lead exposure: a review. (2009)
- Interaction between two independent CNR1 variants increases risk for cocaine dependence in European Americans: a replication study in family-based sample and population-based sample. (2009)
- In utero ethanol exposure impairs defenses against experimental group B streptococcus in the term Guinea pig lung. (2009)
- Chronic binge ethanol-mediated acidemia reduces availability of glutamine and related amino acids in maternal plasma of pregnant sheep. (2008)
- Circulating microRNAs as stable blood-based markers for cancer detection. (2008)
- Elevated fatty acid ethyl esters in meconium of sheep fetuses exposed in utero to ethanol--a new animal model. (2008)
- Elevated inflammation levels in depressed adults with a history of childhood maltreatment. (2008)
- Adolescent but not adult rats exhibit ethanol-mediated appetitive second-order conditioning. (2008)
- Negative BOLD fMRI response in the visual cortex carries precise stimulus-specific information. (2007)
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
- Genetic variation of folate-mediated one-carbon transfer pathway predicts susceptibility to choline deficiency in humans. (2005)
Merged raw entities (5)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| blood | drug | 93 | 133 |
| blood | cohort | 22 | 50 |
| blood | anatomy | 10 | 15 |
| blood sample | drug | 2 | 2 |
| blood tissue | drug | — | — |