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Unmasking genetic etiologies in neurodevelopmental disorders characterized by Cerebral Palsy: insights from integrative genomic approaches.

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Title: Unmasking genetic etiologies in neurodevelopmental disorders characterized by Cerebral Palsy: insights from integrative genomic approaches.
Authors: Yigit A; Genome Studies, Graduate School of Health Sciences, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.; Izmir International Biomedicine and Genome Institute, Dokuz Eylul University, Izmir, Türkiye.; Rare and Undiagnosed Disease Platform, IBG - Izmir Biomedicine and Genome Center, Izmir, Türkiye.; Rare Diseases and Orphan Drugs Application and Research Center (ACURARE), Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye., Akgun-Dogan O; Rare Diseases and Orphan Drugs Application and Research Center (ACURARE), Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.; Department of Medical Genetics, School of Medicine, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.; Department of Child Health and Diseases, School of Medicine, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.; Department of Translational Medicine, Graduate School of Health Sciences, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye., Ozkeserli Z; Department of Medical Biotechnology, Graduate School of Health Sciences, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye., Bayram Akcapınar G; Department of Medical Biotechnology, Graduate School of Health Sciences, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye., Ayta S; Spastic Children's Foundation of Turkey, Istanbul, Türkiye., Gencpinar P; Department of Pediatric Neurology, School of Medicine, Katip Celebi University, Izmir, Türkiye., Maras Genc H; Pediatric Neurology, Umraniye Training and Research Hospital, University of Health Sciences, İstanbul, Türkiye., Kutlubay B; Pediatric Neurology, Umraniye Training and Research Hospital, University of Health Sciences, İstanbul, Türkiye., Kara B; Department of Pediatric Neurology, School of Medicine, Kocaeli University, Kocaeli, Türkiye., Sozen HG; Department of Pediatric Neurology, School of Medicine, Bahcesehir University, Istanbul, Türkiye., Agaoglu NB; Department of Medical Genetics, Division of Cancer Genetics, Umraniye Training and Research Hospital, Istanbul, Türkiye.; Department of Neurology, Krankenhaus Nordwest, Frankfurt, Germany., Ozdemir O; Rare Diseases and Orphan Drugs Application and Research Center (ACURARE), Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.; Department of Medical Biology, School of Medicine, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye., Bilguvar K; Rare Diseases and Orphan Drugs Application and Research Center (ACURARE), Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.; Department of Medical Genetics, School of Medicine, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.; Department of Translational Medicine, Graduate School of Health Sciences, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.; Departments of Neurosurgery and Genetics, Yale Center for Genome Analysis, Yale School of Medicine, New Haven, CT, United States., Ozbek U; Genome Studies, Graduate School of Health Sciences, Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.; Rare and Undiagnosed Disease Platform, IBG - Izmir Biomedicine and Genome Center, Izmir, Türkiye.; Rare Diseases and Orphan Drugs Application and Research Center (ACURARE), Acibadem Mehmet Ali Aydinlar University, Istanbul, Türkiye.
Source: Frontiers in neurology [Front Neurol] 2026 Feb 23; Vol. 17, pp. 1742186. Date of Electronic Publication: 2026 Feb 23 (Print Publication: 2026).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101546899 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2295 (Print) Linking ISSN: 16642295 NLM ISO Abbreviation: Front Neurol Subsets: PubMed not MEDLINE
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  Data: Unmasking genetic etiologies in neurodevelopmental disorders characterized by Cerebral Palsy: insights from integrative genomic approaches.
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