[2S06a] Connecting dots of CNV-linked structural and functional phenotypes from humans to mice | The 48th Annual Meeting of the Japan Neuroscience Society

The 48th Annual Meeting of the Japan Neuroscience Society

Session Details

Symposia

[2S06a]Connecting dots of CNV-linked structural and functional phenotypes from humans to mice

Fri. Jul 25, 2025 2:10 PM - 4:10 PM JST
Fri. Jul 25, 2025 5:10 AM - 7:10 AM UTC

Room 6 (301A)

Organizer: Noboru Hiroi (Department of Pharmacology, UT Health San Antonio), Carrie Bearden (Department of Psychiatry and Behavioral Sciences, UCLA)

[2S06a-1]The development of children at high neuropsychiatric genomic risk: clinical outcomes and behavioural dimensions

*Samuel John Rupert Allen Chawner¹ (1. Cardiff University)

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[2S06a-2]Developmental dysconnectivity in a genetic risk model for schizophrenia

*Carrie E Bearden¹, Filomena G Alvino², Silvia Gini², Marco Pagani^2,5, David Sastre-Yugue^2,6, Noemi Barsotti⁷, E De Guzman², Charles Schleifer¹, Alexia Stuefer^2,6, Leila Kushan¹, Caterina Montani², Alberto Galbusera², Francisco Papaleo^8,3, Michael V Lombardo⁸, Massimo Pasqualetti^2,7, Alessandro Gozzi , A Minetti⁴, Alessandro Gozzi² (1. Departments of Psychiatry and Biobehavioral Sciences and Psychology, Semel Institute for Neuroscience and Human Behavior, University of California at Los Angeles, Los Angeles, 2. Functional Neuroimaging Laboratory, Istituto Italiano di Tecnologia, Center for Neuroscience and Cognitive Systems, University of Trento, Rovereto, Italy, 3. Genetics of Cognition Laboratory, Neuroscience area, Istituto Italiano di Tecnologia, Genova, Italy, 4. Department of Biology, Unit of Cell and Developmental Biology, University of Pisa, Pisa, Italy, 5. IMT School for Advanced Studies, Lucca, Italy, 6. Center for Mind and Brain Sciences, University of Trento, Rovereto, Italy, 7. Centro per l’Integrazione della Strumentazione Scientifica dell’Università di Pisa (CISUP), Pisa, Italy, 8. Laboratory for Autism and Neurodevelopmental Disorders, Center for Neuroscience and Cognitive Systems, Istituto Italiano di Tecnologia, Rovereto, Italy)

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[2S06a-3]Cytoarchitectural alterations in a mouse model of the 22q11.2 microdeletion syndrome

*Hidenori Tabata¹, Daisuke Mori^2,5, Tohru Matsuki³, Kaichi Yoshizaki⁴, Masato Asai⁴, Atsuo Nakayama³, Norio Ozaki^5,6, Koh-ichi Nagata¹ (1. Dep Mol Neurobiol, Inst Dev Res, Aichi Develop Disability Cen (ADDC), Aichi, Japan, 2. Brain and Mind Res Cen, Nagoya University, Nagoya 466-8550, Japan, 3. Dep Cellular Pathology, Inst Dev Res, ADDC, Aichi, Japan, 4. Dep Disease Model, Inst Dev Res, ADDC, Aichi, Japan, 5. Pathophysiology of Mental Disorders, Nagoya Univ Grad Sch Med, Aichi, Japan, 6. Inst Glyco-core Res (iGCORE), Nagoya Univ, Aichi, Japan)

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[2S06a-4]Investigating abnormalities in top-down cortical processing and behavior in a model of the 22q11.2 deletion

*Renata Batista-Brito¹ (1. Albert Einstein College of Medicine)

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[2S06a-5]TBX1, a gene encoded in 22q11.2 copy number variation, contributes to structural, cellular, and behavioral deficits via neonatal and embryonic neurogenesis

*Noboru Hiroi¹, Takeshi Hiramoto¹, Shuken Boku², Akira Sumiyoshi^4,3, Risa Kato⁵, Takahira Yamauchi¹, Takeshi Takano¹, Emily T. Averyt¹, Takaki Tanifuji¹, Gina Kang¹, Marisa Esparza¹, Yukiko J Hiroi¹, Rie Ryoke³, Hiroi Nonaka³, Akihiro Machida⁵, Kensaku Nomoto⁵, Kazutaka Mogi⁵, Takefumi Kikusui⁵, Ryuta Kawashima³, Jason Pugh¹ (1. UT Health San Antonio, San Antonio, USA, 2. Kumamoto University, Kumamoto, Japan, 3. Tohoku University, Miyagi, Japan, 4. NIRS-QST, Chiba, Japan, 5. Azabu University, Kanagawa, Japan)

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