MétaCan
Menu
Back to cohort
Record W4415165121 · doi:10.1101/2025.10.10.25337672

Rare coding mutations identify 36 large-effect risk genes in obsessive-compulsive disorder and chronic tic disorders

2025· preprint· en· W4415165121 on OpenAlexaff
Belinda Wang, Matthew N. Tran, Sheng Wang, Yuting Liu, Emily Olfson, Nawei Sun, Jeanselle Dea, Charles Ochieng’ Olwal, Lyvia Bertolace, Michael H. Bloch, Carolina Cappi, Yi-Chieh Chang, Denise A. Chavira, Barbara J. Coffey, Martha J. Falkenstein, Adam C. Frank, Martin E. Franklin, Stephanie Garayalde, Helena Garrido, Marco A. Grados, Rami Hatem, Allyna-London Howell, Starlette Khim, Jennie M. Kuckertz, Mindy M. Le, Allison Libby, Ryan J. McCarty, Mary McNamara, Daniel McNeil, Eurı́pedes Constantino Miguel, Cara Nasello, Tenzin Norbu, Lixian Oh, Ashley Ordway, Catherine Paciotti, Viviana A. Peskin, Christopher Pittenger, H. Blair Simpson, H Martin, Max A. Tischfield, Jinchuan Xing, Jessica Zakrzewski, Andrea Dietrich, Donald L. Gilbert, Pieter J. Hoekstra, Young S. Kim, Samuel Kuperman, Alyssa Rosen, Samuel H. Zinner, Mehdi Bouhaddou, Robert A. King, Guy Rouleau, Kerry J. Ressler, Carol A. Mathews, Nevan J. Krogan, Nenad Šestan, Jay A. Tischfield, A. Moses Lee, Gary A. Heiman, Thomas Fernandez, A. Jeremy Willsey, Matthew W. State

Bibliographic record

VenuemedRxiv · 2025
Typepreprint
Languageen
FieldPsychology
TopicObsessive-Compulsive Spectrum Disorders
Canadian institutionsMcGill UniversityMontreal Neurological Institute and Hospital
Fundersnot available
KeywordsGeneGenome-wide association studyTranscriptomeAutismNeurodevelopmental disorderAutism spectrum disorderGenomics

Abstract

fetched live from OpenAlex

Abstract Obsessive-compulsive disorder (OCD) and chronic tic disorders (CTD) are highly heritable. Recent progress in OCD genomics has highlighted small-effect common alleles. Rare mutations have previously been found to carry large risks for OCD and CTD but only four high-confidence (hc) genes have been identified. We analyzed whole-exome sequencing data from 3,964 individuals with OCD, CTD, or both, including 2,418 trios. We find an excess in cases of de novo and rare protein-damaging mutations and identify 36 hc genes (false discovery rate [FDR] < 0.1), four of which overlap with OCD GWAS loci. Risk genes are shared among OCD, CTD, autism spectrum disorder, and other neurodevelopmental conditions. Transcriptomic and network analyses highlight mechanistic convergence and increased risk gene expression in postnatal cerebellum and pre- and postnatal cortex and striatum. Dozens of large-effect OCDCTD genes offer insights into pathogenesis and a path forward for illuminating pathophysiology and identifying novel treatment targets.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow), Research integrity, Insufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.039
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0000.000
Open science0.0010.001
Research integrity0.0010.002
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.011
GPT teacher head0.317
Teacher spread0.306 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations2
Published2025
Admission routes1
Has abstractyes

Explore more

Same venuemedRxivSame topicObsessive-Compulsive Spectrum DisordersFrench-language works237,207