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Çağlayan, Ahmet Okay
183
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Online (183)
Mediatypes
E-Books (1)
Articles (Online) (81)
Bookchapter (Online) (3)
OpenAccess-fulltext (98)
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1
Investigation of genotype-phenotype and familial features o..:
Ozkalayci, Hande
;
Bora, Elcin
;
Cankaya, Tufan
...
Neurogenetics. 25 (2024) 3 - p. 201-213 , 2024
Link:
https://doi.org/10.1007/..
?
2
An investigation of the etiology and follow‐up findings in ..:
Yüksel Ülker, Aylin
;
Uludağ Alkaya, Dilek
;
Çağlayan, Ahmet Okay
...
American Journal of Medical Genetics Part A. 191 (2023) 6 - p. 1530-1545 , 2023
Link:
https://doi.org/10.1002/..
?
3
Genetic evaluation of 50 Turkish patients with neurofibroma..:
Kocabey, Mehmet
;
Özkalaycı, Hande
;
Çankaya, Tufan
...
International Journal of Developmental Neuroscience. 83 (2023) 5 - p. 456-465 , 2023
Link:
https://doi.org/10.1002/..
?
4
Genetic, serological and clinical evaluation of childhood m..:
Özsoy, Özlem
;
Cinleti, Tayfun
;
Günay, Çağatay
...
Acta Neurologica Belgica. 123 (2023) 6 - p. 2325-2335 , 2023
Link:
https://doi.org/10.1007/..
?
5
Evaluation of hereditary/familial breast cancer patients wi..:
Bora, Elcin
;
Caglayan, Ahmet Okay
;
Koc, Altug
...
Cancer Genetics. 262-263 (2022) - p. 118-133 , 2022
Link:
https://doi.org/10.1016/..
?
6
Further delineation of familial polycystic ovary syndrome (..:
Karakaya, Cengiz
;
Çil, Aylin Pelin
;
Bilguvar, Kaya
...
Journal of Obstetrics and Gynaecology Research. 48 (2022) 5 - p. 1202-1211 , 2022
Link:
https://doi.org/10.1111/..
?
7
Biallelic BICD2 variant is a novel candidate for Cohen-like..:
Caglayan, Ahmet Okay
;
Tuysuz, Beyhan
;
Gül, Ece
...
Journal of Human Genetics. 67 (2022) 9 - p. 553-556 , 2022
Link:
https://doi.org/10.1038/..
?
8
Unexpected finding in kidney biopsy of a child with nephrot..:
Bayram, Meral Torun
;
Yildiz, Gizem
;
Cağlayan, Ahmet Okay
...
Pediatric Nephrology. , 2022
Link:
https://doi.org/10.1007/..
?
9
Unexpected finding in kidney biopsy of a child with nephrot..:
Bayram, Meral Torun
;
Yildiz, Gizem
;
Cağlayan, Ahmet Okay
...
Pediatric Nephrology. , 2022
Link:
https://doi.org/10.1007/..
?
10
Congenital Myasthenic Syndromes in Turkey: Clinical and Mol..:
Öztürk, Selcan
;
Güleç, Ayten
;
Erdoğan, Murat
...
Pediatric Neurology. 136 (2022) - p. 43-49 , 2022
Link:
https://doi.org/10.1016/..
?
11
Analysis of genotype-phenotype correlation in Walker-Warbur..:
Bayram, Nurettin
;
Bayram, Ayşe Kaçar
;
Per, Hüseyin
...
European Journal of Ophthalmology. 32 (2021) 5 - p. NP71-NP76 , 2021
Link:
https://doi.org/10.1177/..
?
12
METAP1 mutation is a novel candidate for autosomal recessiv..:
Caglayan, Ahmet Okay
;
Aktar, Fesih
;
Bilguvar, Kaya
...
Journal of Human Genetics. 66 (2020) 2 - p. 215-218 , 2020
Link:
https://doi.org/10.1038/..
?
13
COQ4 Mutation Leads to Childhood-Onset Ataxia Improved by C..:
Caglayan, Ahmet Okay
;
Gumus, Hakan
;
Sandford, Erin
...
The Cerebellum. 18 (2019) 3 - p. 665-669 , 2019
Link:
https://doi.org/10.1007/..
?
14
Loss of Protocadherin‐12Leads to Diencephalic‐Mesencephalic..:
Guemez‐Gamboa, Alicia
;
Çağlayan, Ahmet Okay
;
Stanley, Valentina
...
Annals of Neurology. 84 (2018) 5 - p. 638-647 , 2018
Link:
https://doi.org/10.1002/..
?
15
Biallelic loss of human CTNNA2, encoding αN-catenin, leads ..:
Schaffer, Ashleigh E.
;
Breuss, Martin W.
;
Caglayan, Ahmet Okay
...
Nature Genetics. 50 (2018) 8 - p. 1093-1101 , 2018
Link:
https://doi.org/10.1038/..
1-15