X chromosome drug
Evidence from:
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all sources
Related entities (5)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| DNA methylation | associated_with | X chromosome | — | 1 |
| pluripotent cells | associated_with | X chromosome | — | 1 |
| X chromosome | risk_factor_for | obsessive-compulsive disorder | — | 1 |
| X chromosome | associated_with | Post-Traumatic Stress Disorder | — | 1 |
| X chromosome | associated_with | sex | — | 1 |
Mentioned in (22)
Papers in which this entity is mentioned.
- ChromoGen: Diffusion model predicts single-cell chromatin conformations. (2025)
- Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
- Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
- Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. (2024)
- The complete sequence of a human genome. (2022)
- Sex differences in the genetic architecture of obsessive-compulsive disorder. (2019)
- Sex and gender differences in developmental programming of metabolism. (2018)
- Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line. (2018)
- The fractured landscape of RNA-seq alignment: the default in our STARs. (2018)
- BECon: a tool for interpreting DNA methylation findings from blood in the context of brain. (2017)
- Methylomic trajectories across human fetal brain development. (2015)
- Interindividual methylomic variation across blood, cortex, and cerebellum: implications for epigenetic studies of neurological and neuropsychiatric phenotypes. (2015)
- Heritability and genomics of gene expression in peripheral blood. (2014)
- Recurrent variations in DNA methylation in human pluripotent stem cells and their differentiated derivatives. (2012)
- cn.MOPS: mixture of Poissons for discovering copy number variations in next-generation sequencing data with a low false discovery rate. (2012)
- DNA copy number, including telomeres and mitochondria, assayed using next-generation sequencing. (2010)
- Genetics and beyond--the transcriptome of human monocytes and disease susceptibility. (2010)
- Recurring mutations found by sequencing an acute myeloid leukemia genome. (2009)
- A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. (2009)
- Can we identify genes for alcohol consumption in samples ascertained for heterogeneous purposes? (2009)
- The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus). (2008)
- Rapid Sex Determination Using PCR Technique Compared to Classic Cytogenetics - PMC
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 |
|---|---|---|---|
| x chromosome | drug | 7 | 9 |
| chromosome x | drug | 6 | 6 |
| x chromosome | variant | 4 | 4 |
| x chromosome genes | gene | 4 | 5 |
| chromosome x | variant | 3 | 3 |