Cross-atlas neuronal localization amid fragile common–rare convergence in attention-deficit/hyperactivity disorder

Code, distributable derived inputs, machine-readable results, figures, tables, and provenance records supporting an evidence-calibrated analysis of common-variant, rare-variant, and developmental-cell evidence in ADHD. The archive reproduces the reported derived-input analyses and explicitly does not claim a replicated ADHD-specific molecular mechanism. Raw third-party GWAS, FinnGen, CELLxGENE, GEO, publisher supplements, MAGMA, and LD-reference resources are not redistributed; source links, hashes, and retrieval instructions are provided.