Investigation of Genetic Changes in Three Families with Bipolar Disease.

Autor: Çolak-Geniş E; Department of Medical Genetics, Manisa Celal Bayar University Faculty of Medicine, Manisa, Turkey., Özdemir Erdoğan M; Department of Medical Genetics, Afyonkarahisar University of Health Sciences, Afyonkarahisar, Turkey., Çam FS; Department of Medical Genetics, Manisa Celal Bayar University Faculty of Medicine, Manisa, Turkey., Aydemir Ö; Department of Psychiatry, Manisa Celal Bayar University Faculty of Medicine, Manisa, Turkey., Akin F; Department of Psychiatry, Manisa Celal Bayar University Faculty of Medicine, Manisa, Turkey., Gerik-Celebi HB; Department of Medical Genetics, Balikesir Atatürk City Hospital, Balikesir, Turkey., Solak M; Department of Medical Genetics, Afyonkarahisar University of Health Sciences, Afyonkarahisar, Turkey.

Publikováno v: Molecular syndromology [Mol Syndromol] 2024 Dec; Vol. 15 (6), pp. 464-473. Date of Electronic Publication: 2024 Jun 14.

Rare heterozygous genetic variants of NRXN and NLGN gene families involved in synaptic function and their association with neurodevelopmental disorders.

Autor: Gerik-Celebi HB; Department of Medical Genetics, Balıkesir Ataturk City Hospital, Balıkesir, Turkey., Bolat H; Department of Medical Genetics, Balıkesir University Faculty of Medicine, Balıkesir, Turkey., Unsel-Bolat G; Department of Child and Adolescent Psychiatry, Balıkesir University Faculty of Medicine, Balıkesir, Turkey.

Publikováno v: Developmental neurobiology [Dev Neurobiol] 2024 Jul; Vol. 84 (3), pp. 158-168. Date of Electronic Publication: 2024 May 13.

Association of ABCA13 Gene Variants with Autism Spectrum Disorder and Other Neuropsychiatric Disorders.

Autor: Gerik-Celebi HB; Department of Medical Genetics, Balıkesir Ataturk City Hospital, Balıkesir, Turkey., Unsel-Bolat G; Department of Child and Adolescent Psychiatry, Balıkesir University Faculty of Medicine, Balıkesir, Turkey., Bolat H; Department of Medical Genetics, Balıkesir University Faculty of Medicine, Balıkesir, Turkey.

Publikováno v: Molecular syndromology [Mol Syndromol] 2024 Feb; Vol. 15 (1), pp. 22-29. Date of Electronic Publication: 2023 Oct 16.

Coinheritance of novel mutations in NAGLU causing mucopolysaccharidosis type IIIB and in DDHD2 causing spastic paraplegia54 in a Turkish family.

Autor: Gun Bilgic D; Department of Medical Genetics, Manisa Celal Bayar University Medical Faculty, Manisa, Turkey. Electronic address: dilek.bilgic@cbu.edu.tr., Gerik Celebi HB; Department of Medical Genetics, Balıkesir City Hospital, Balıkesir, Turkey., Aydin Gumus A; Department of Medical Genetics, Manisa Celal Bayar University Medical Faculty, Manisa, Turkey., Bilgic A; Department of Orthopaedics and Traumatology, Manisa City Hospital, Manisa, Turkey., Yazici H; Department of Pediatric Metabolic Disease, Faculty of Medicine, Ege University, Bornova, Izmir, Turkey., Ceylaner S; INTERGEN Genetics and Rare Diseases Diagnosis Research & Application Center, Ankara, Turkey., Yilmaz C; Department of Pediatric Neurology, Manisa Celal Bayar University Medical Faculty, Manisa, Turkey., Polat M; Department of Pediatric Neurology, Manisa Celal Bayar University Medical Faculty, Manisa, Turkey., Akbal Sahin M; INTERGEN Genetics and Rare Diseases Diagnosis Research & Application Center, Ankara, Turkey., Dereli F; INTERGEN Genetics and Rare Diseases Diagnosis Research & Application Center, Ankara, Turkey., Cam FS; Department of Medical Genetics, Manisa Celal Bayar University Medical Faculty, Manisa, Turkey.

Publikováno v: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia [J Clin Neurosci] 2020 Dec; Vol. 82 (Pt B), pp. 214-218. Date of Electronic Publication: 2020 Nov 24.