{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,5]],"date-time":"2025-12-05T14:17:07Z","timestamp":1764944227294,"version":"3.46.0"},"reference-count":64,"publisher":"Oxford University Press (OUP)","issue":"6","license":[{"start":{"date-parts":[[2025,11,25]],"date-time":"2025-11-25T00:00:00Z","timestamp":1764028800000},"content-version":"vor","delay-in-days":328,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"Simons Foundation Bridge to Independence"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2025,10,30]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Sensory processing as a neurological construct is the perception and interpretation of sensory information from both the body and the environment. Disruptions to sensory processing adversely impact daily functioning. One type of disruption that is particularly interesting is altered sensory modulation, leading to hypersensitivity or hyposensitivity, which are common in many neurodevelopmental and psychiatric conditions such as autism spectrum disorder, attention-deficit\/hyperactivity disorder, Alzheimer\u2019s, and schizophrenia. Here we aim to identify modality-specific and cross-modality brain networks involved in altered auditory and somatosensory processing. A systematic review identified 61 patients with new-onset sensory alterations following focal brain injury. Lesions were traced and combined with resting-state data from 1000 healthy controls to generate normative lesion connectivity maps. The specificity of our cohort\u2019s lesion-connectivity compared to lesions associated with 22 other neuropsychiatric symptoms was assessed with voxel-wise two-sample t-tests performed with the FSL Permutation Analysis of Linear Models tool (family-wise error P &amp;lt; 0.05). A conjunction analysis against lesions associated with hallucination was conducted by binarizing and multiplying one-sample T-test maps to identify common lesion-connections between the conditions. Modality-specific networks were connected to their unimodal cortices and the cerebellum. Overall, lesions associated with cross-modality sensitivity changes had convergent connections to the substantia nigra, medial orbitofrontal cortex, and cerebellum (Lobule V, medial Lobule VIIIa). Subgroup analysis by direction revealed that lesions causing decreased sensitivity were connected to lobule X, in addition to the aforementioned cerebellar regions, while those causing increased sensitivity were only connected to medial V and bilateral V. Regardless of directionality, 90% of lesions exhibited connections to bilateral Lobule V. Conjunction analysis with hallucinations revealed common lesion-connections to cerebellar vermis and frontal pole. Our analysis identified significant lesion-connections to the substantia nigra, medial orbitofrontal cortex, and cerebellum\u2014highlighting these key regions in cross-modality sensory processing. These findings emphasize the role of higher cognitive functions in sensory integration and suggest potential targets for neuromodulation to improve sensory processing.<\/jats:p>","DOI":"10.1093\/braincomms\/fcaf463","type":"journal-article","created":{"date-parts":[[2025,11,21]],"date-time":"2025-11-21T13:15:31Z","timestamp":1763730931000},"source":"Crossref","is-referenced-by-count":0,"title":["Network localization of altered auditory and somatosensory sensitivity based on causal brain lesions"],"prefix":"10.1093","volume":"7","author":[{"ORCID":"https:\/\/orcid.org\/0009-0005-0195-8039","authenticated-orcid":false,"given":"Shreya","family":"Tripathy","sequence":"first","affiliation":[{"name":"Department of Neurology, Boston Children\u2019s Hospital, Harvard Medical School , Boston, MA 02115 ,","place":["USA"]},{"name":"Boston University Chobanian and Avedisian School of Medicine , Boston, MA 02118 ,","place":["USA"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0009-0001-6306-8163","authenticated-orcid":false,"given":"Gillian N","family":"Miller","sequence":"additional","affiliation":[{"name":"Department of Neurology, Boston Children\u2019s Hospital, Harvard Medical School , Boston, MA 02115 ,","place":["USA"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6557-5866","authenticated-orcid":false,"given":"Alexander L","family":"Cohen","sequence":"additional","affiliation":[{"name":"Department of Neurology, Boston Children\u2019s Hospital, Harvard Medical School , Boston, MA 02115 ,","place":["USA"]},{"name":"Center for Brain Circuit Therapeutics, Brigham and Women's Hospital , Boston, MA 02115 ,","place":["USA"]},{"name":"Department of Neurology, Harvard Medical School , Boston, MA 02115 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