{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"institution":[{"name":"bioRxiv"}],"indexed":{"date-parts":[[2026,10,26]],"date-time":"2026-10-26T16:48:32Z","timestamp":1793033312874,"version":"4.5.0"},"posted":{"date-parts":[[2025,11,5]]},"group-title":"Neuroscience","reference-count":88,"publisher":"openRxiv","license":[{"start":{"date-parts":[[2025,11,5]],"date-time":"2025-11-05T00:00:00Z","timestamp":1762300800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.biorxiv.org\/about\/FAQ#license"}],"funder":[{"name":"NIH","award":["R01 NS102371"],"award-info":[{"award-number":["R01 NS102371"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"accepted":{"date-parts":[[2025,11,5]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                <jats:p>\n                  Tourette syndrome (TS) is a highly heritable childhood-onset neuropsychiatric disorder characterized by persistent motor and vocal tics. While both common and rare variants contribute to TS susceptibility, the role of rare\n                  <jats:italic>de novo<\/jats:italic>\n                  mutations (DNMs) remains incompletely characterized. Here, we report findings from the largest TS whole-exome sequencing study to date, analyzing 1,466 TS trios alongside 6,714 autism spectrum disorder (ASD) trios and 5,880 unaffected sibling controls from the Simons Simplex Collection (SSC) and SPARK cohorts. Leveraging a trio-based design across these cohorts enabled calibrated assessment of DNM burden while controlling for background mutation rates. We observed a significant exome-wide enrichment of protein-truncating DNMs in TS probands, particularly within genes intolerant to loss-of-function variation (pLI \u2265 0.9), with little contribution from damaging missense variants. Notably, TS probands did not exhibit enrichment in previously implicated ASD or developmental delay (DD) genes, but elsewhere in the genome, suggesting a distinct rare variant architecture. Using a Bayesian statistical framework that integrates both\n                  <jats:italic>de novo<\/jats:italic>\n                  and rare inherited coding variants, we identified three candidate TS risk genes with FDR \u2264 0.05:\n                  <jats:italic>PPP5C<\/jats:italic>\n                  ,\n                  <jats:italic>EXOC1<\/jats:italic>\n                  , and\n                  <jats:italic>GXYLT1<\/jats:italic>\n                  . Literature shows that they have prior links to neurodevelopmental and psychiatric disorders. These findings reveal a rare variant burden in TS that is genetically distinguishable from ASD, underscore the importance of loss-of-function mutations in TS risk, and nominate novel candidate genes for future functional investigation.\n                <\/jats:p>","DOI":"10.1101\/2025.11.04.686570","type":"posted-content","created":{"date-parts":[[2025,11,5]],"date-time":"2025-11-05T23:40:12Z","timestamp":1762386012000},"source":"Crossref","is-referenced-by-count":3,"title":["Distinct patterns of\n                  <i>de novo<\/i>\n                  coding variants contribute to Tourette Syndrome etiology"],"prefix":"10.64898","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6718-878X","authenticated-orcid":false,"given":"Lingyu","family":"Zhan","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7901-4365","authenticated-orcid":false,"given":"Dongmei","family":"Yu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6776-8626","authenticated-orcid":false,"given":"Franjo","family":"Ivankovic","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8855-7393","authenticated-orcid":false,"given":"Maria","family":"Niarchou","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2265-0824","authenticated-orcid":false,"given":"Laura","family":"Domenech-Salgado","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cathy 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