Ahmet Okay Çağlayan (Ahmet Okay Caglayan)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 9

Top Topics

Autism Spectrum Disorder

Genome Wide Identification

Myasthenia Gravis

Top Venues

Psychiatry and clinical psychopharmacology

Journal of neurogenetics

Journal of medical genetics

The journal of obstetrics and gynaecology research

This page only lists publications with an associated author ORCID identifier.

Publications

Hilal Akköprü, Alper Alnak, Zeynep Nur Karadogan, Ahmet Okay Çağlayan, Mustafa Ozcetin, Murat Coskun
Peripheral Expression of ADORA2A Is Increased and Is Correlated with Autism Spectrum Disorder Severity in a Sample of Turkish Children. Psychiatry and clinical psychopharmacology 33 (1) (2023)
Özlem Özsoy, Tayfun Çinleti, Çağatay Günay, Gamze Sarikaya Uzan, Özlem Giray Bozkaya, Ahmet Okay Çağlayan, A Semra Hiz, Uluç Yaş
Genetic, serological and clinical evaluation of childhood myasthenia syndromes- single center subgroup analysis experience in Turkey. Acta neurologica Belgica (2023)
Hilal Akköprü, Alper Alnak, Zeynep Nur Karadogan, Ahmet Okay Çağlayan, Mustafa Ozcetin, Murat Coskun
Peripheral Expression of ADORA2A Is Increased and Is Correlated with Autism Spectrum Disorder Severity in a Sample of Turkish Children. Psychiatry and clinical psychopharmacology 33 (1) (2023)
Ahmet Okay Çağlayan, Beyhan Tuysuz, Ece Gül, Dilek Uludag Alkaya, Cengiz Yalcinkaya, Joseph G Gleeson, Kaya Bilguvar, Murat Günel
Biallelic BICD2 variant is a novel candidate for Cohen-like syndrome. Journal of human genetics 67 (9) (2022)
Cengiz Karakaya, Aylin Pelin Çil, Kaya Bilguvar, Tunahan Çakir, Mete Hakan Karalok, Recep Onur Karabacak, Ahmet Okay Çağlayan
Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified. The journal of obstetrics and gynaecology research 48 (5) (2022)
Alper Alnak, İpek Kuşcu Özücer, Ahmet Okay Çağlayan, Murat Coskun
Peripheral Expression of MACROD2 Gene Is Reduced Among a Sample of Turkish Children with Autism Spectrum Disorder. Psychiatry and clinical psychopharmacology 31 (3) (2021)
Lucia Laugwitz, Annette Seibt, Diran Herebian, Susana Peralta, Imke Kienzle, Rebecca Buchert, Ruth Falb, Darja Gauck, Amelie Müller, Mona Grimmel, Stefanie Beck-Woedel, Jan Kern, Karim Daliri, Pegah Katibeh, Katharina Danhauser, Steffen Leiz, Viola Alesi, Fabian Baertling, Gessica Vasco, Robert Steinfeld, Matias Wagner, Ahmet Okay Çağlayan, Hakan Gumus, Margit Burmeister, Ertan Mayatepek, Diego Martinelli, Parag Mohan Tamhankar, Vasundhara Tamhankar, Pascal Joset, Katharina Steindl, Anita Rauch, Penelope E Bonnen, Tawfiq Froukh, Samuel Groeschel, Ingeborg Krägeloh-Mann, Tobias B Haack, Felix Distelmaier
Human COQ4 deficiency: delineating the clinical, metabolic and neuroimaging phenotypes. Journal of medical genetics (2021)
Alper Alnak, İpek Kuşcu Özücer, Ahmet Okay Çağlayan, Murat Coskun
Peripheral Expression of MACROD2 Gene Is Reduced Among a Sample of Turkish Children with Autism Spectrum Disorder. Psychiatry and clinical psychopharmacology 31 (3) (2021)
Ahmet Okay Çağlayan, Kourosh Yaghouti, Tanyel Kockaya, Demet Kemer, Tufan Cankaya, Najim Ameziane, Ozgur Cogulu, Mahmut Coker, Cengiz Yalcinkaya
Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy. Journal of neurogenetics 35 (1) (2020)