bioRxiv / medRxiv
open access
CC BY 4.0
Investigating the Y chromosome in complex disease: Phenome-wide scan across 104,334 Finnish men
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- THRB splice site variants lead to exon 4 skipping and TRβ1 gain-of-function syndrome#214809
- The YTHDF proteins shape the brain gene signatures of Alzheimer's disease#290724
- The YTHDF proteins modulate Alzheimer's disease-associated brain gene signatures.#1158694
- G protein-coupled receptor 17 is regulated by WNT pathway during oligodendrocyte precursor cell differentiation#1146087
- Novel Postzygotic Variants Associated With Hypomelanosis of Ito Expand the ACTB-Related Neurocutaneous Disease Spectrum#254084
Record · ID 373560
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive