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Çağlayan, Ahmet Okay
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1

Investigation of genotype-phenotype and familial features o..:

Ozkalayci, Hande ; Bora, Elcin ; Cankaya, Tufan...
Neurogenetics.  , 2024
Link: https://doi.org/10.1007/..
 
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2

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/..
 
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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/..
 
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4

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/..
 
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5

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/..
 
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6

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/..
 
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7

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/..
 
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8

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/..
 
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9

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/..
 
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10

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/..
 
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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/..
 
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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/..
 
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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/..
 
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14

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/..
 
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15

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/..
 
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