Novel mutations with clinical variability and surgical experience in van der woude syndrome
Ahmet Cevdet Ceylan, Figen Ozgur, Ibrahim Vargel
Published in Turkish Journal of Plastic Surgery (01.07.2020)
Published in Turkish Journal of Plastic Surgery (01.07.2020)
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Journal Article
Impact of Inflammation-Related Genes on COVID-19: Prospective Study at Turkish Cohort
Ceylan, Ahmet Cevdet, Çavdarlı, Büşranur, Ceylan, Gülay Güleç, Topçu, Vehap, Satılmış, S. Betül Arslan, Bektaş, Şerife Gökbulut, Kalem, Ayşe K., Kayaaslan, Bircan, Eser, Fatma, Kalkan, Emra Asfuroğlu, İnan, Osman, Hasanoğlu, İmran, Yüksel, Selcen, Ateş, İhsan, İzdeş, Seval, Güner, Rahmet, Gündüz, C. Nur Semerci
Published in The Tohoku Journal of Experimental Medicine (2023)
Published in The Tohoku Journal of Experimental Medicine (2023)
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Journal Article
Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders
Ceylan, Ahmet Cevdet, Citli, Senol, Erdem, Haktan Bagis, Sahin, Ibrahim, Acar Arslan, Elif, Erdogan, Murat
Published in Molecular cytogenetics (24.09.2018)
Published in Molecular cytogenetics (24.09.2018)
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Journal Article
Determinación de los polimorfismos rs2058265, rs6464214 y rs7456421 de la proteína cinasa 2 que interactúan con el homeodominio en pacientes con cálculos renales
Ceylan, Cavit, Gokhan-Doluoglu, Omer, TaÓtemur, Sedat, KeleÓ, Ibrahim, Ceylan, Gulay, Cevdet-Ceylan, Ahmet, Uzun, Emre, Tokat, Eda
Published in Cirugia y cirujanos (01.10.2023)
Published in Cirugia y cirujanos (01.10.2023)
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Journal Article
Validation of SMA screening kits with SMN1 gene analysis in a Turkish cohort
Gülşen, Murat, Ceylan, Ahmet Cevdet, Bahsi, Taha, Çubukçu, Hikmet Can, Dursun, Onur Burak
Published in Clinica chimica acta (01.03.2024)
Published in Clinica chimica acta (01.03.2024)
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Journal Article
High Expression of Stem Cell-Related Genes in Polyps with Villous Features and High-Grade Dysplasia Support Malignant Phenotype and Colorectal Carcinogenesis
Sahin, Ibrahim, Gündoğdu, Betül, Ceylan, Ahmet Cevdet, Erdem, Haktan Bagis, Tatar, Abdulgani
Published in Asian Pacific journal of cancer prevention : APJCP (01.08.2021)
Published in Asian Pacific journal of cancer prevention : APJCP (01.08.2021)
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Journal Article
A Mild Skeletal Dysplasia Caused by a Biallelic Missense Variant in the SLC35D1 Gene
Esen, Tuna Eren, Uzun, Özlem Ünal, Ceylan, Ahmet Cevdet
Published in Molecular syndromology (01.12.2023)
Published in Molecular syndromology (01.12.2023)
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Journal Article
c.4168GA
Yildiz, M. Irem, Alp, Anil, Ozer, Suzan, Ceylan, Ahmet Cevdet, Eroglu, Elcin Ozcelik, Demir, Basaran
Published in Noro-Psikiyatri Arsivi (01.12.2023)
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Published in Noro-Psikiyatri Arsivi (01.12.2023)
Journal Article
Coexistence of Megaconial Congenital Muscular Dystrophy and Cystinuria: Mimicking Hypotonia-Cystinuria Syndrome
Surucu Kara, Ilknur, Oncul, Ummuhan, Kose, Engin, Turan, Husnu Mutlu, Ceylan, Ahmet Cevdet, Eminoglu, Fatma Tuba
Published in Molecular syndromology (01.05.2022)
Published in Molecular syndromology (01.05.2022)
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Journal Article
A novel homozygous mutation in the USP53 gene as the cause of benign recurrent intrahepatic cholestasis in children: a case report
Ateş, Burcu Berberoğlu, Ceylan, Ahmet Cevdet, Hızal, Gülin, Duran, Fatih, Doğan, Hayriye Tatlı, Hızlı, Şamil
Published in The Turkish journal of pediatrics (01.11.2023)
Published in The Turkish journal of pediatrics (01.11.2023)
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Journal Article
SMN1 gene copy number analysis for spinal muscular atrophy (SMA) in a Turkish cohort by CODE-SEQ technology, an integrated solution for detection of SMN1 and SMN2 copy numbers and the “2+0” genotype
Ceylan, Ahmet Cevdet, Erdem, Haktan Bağış, Şahin, İbrahim, Agarwal, Meenal
Published in Neurological sciences (01.09.2020)
Published in Neurological sciences (01.09.2020)
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Journal Article
Evaluation of clinical, laboratory, and molecular genetic features of patients with biotinidase deficiency
Yılmaz, Begüm, Ceylan, Ahmet Cevdet, Gündüz, Mehmet, Ünal Uzun, Özlem, Küçükcongar Yavaş, Aynur, Bilginer Gürbüz, Berrak, Öncül, Ümmühan, Güleç Ceylan, Gülay, Kasapkara, Çiğdem Seher
Published in European journal of pediatrics (01.03.2024)
Published in European journal of pediatrics (01.03.2024)
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Journal Article
c.4168GA Variation in KMT2D Gene Detected in an Ultra-treatment-resistant Schizophrenia Patient: A Case Report and Literature Review
Alp, Anil, Eroglu, Elcin Ozcelik, Yildiz, M. Irem, Ceylan, Ahmet Cevdet, Demir, Basaran, Ozer, Suzan
Published in Noro-Psikiyatri Arsivi (01.12.2023)
Published in Noro-Psikiyatri Arsivi (01.12.2023)
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Journal Article
Autosomal recessive spinocerebellar ataxia 18 caused by homozygous exon 14 duplication in GRID2 and review of the literature
Ceylan, Ahmet Cevdet, Acar Arslan, Elif, Erdem, Haktan Bağış, Kavus, Haluk, Arslan, Mutluay, Topaloğlu, Haluk
Published in Acta neurologica Belgica (01.12.2021)
Published in Acta neurologica Belgica (01.12.2021)
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Journal Article
High diagnostic yield of targeted next‐generation sequencing panel as a first‐tier molecular test for the patients with myopathy or muscular dystrophy
Çavdarlı, Büşranur, Köken, Özlem Yayici, Satılmış, Saide Betül Arslan, Bilen, Şule, Ardıçlı, Didem, Ceylan, Ahmet Cevdet, Gündüz, Cavidan Nur Semerci, Topaloğlu, Haluk
Published in Annals of human genetics (01.05.2023)
Published in Annals of human genetics (01.05.2023)
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Journal Article