Publications by authors named "Okay Caglayan"

Claim this Profile
D
Dysregulation of mTOR signalling is a converging mechanism in lissencephaly.
Ce Zhang, Dan Liang, A Gulhan Ercan-Sencicek, Aybike S Bulut, Joelly Cortes, A Okay Caglayan

Nature· February 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Peripheral Expression of Gene Is Reduced Among a Sample of Turkish Children with Autism Spectrum Disorder.
Alper Alnak, İpek Kuşcu Özücer, Ahmet Okay Çağlayan, Murat Coşkun

Psychiatry Clin Psychopharmacol· September 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Autosomal recessive spastic tetraplegia caused by AP4M1 and AP4B1 gene mutation: expansion of the facial and neuroimaging features.
Beyhan Tüysüz, Kaya Bilguvar, Naci Koçer, Cengiz Yalçınkaya, Okay Çağlayan

Am J Med Genet A· July 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Idiopathic hirsutism: local and peripheral expression of aromatase (CYP19A) and 5α-reductase genes (SRD5A1 and SRD5A2).
A Okay Caglayan, Munis Dundar, Fatih Tanriverdi, Nuran A Baysal, Kursad Unluhizarci

Fertil Steril· August 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis.
Mehmet Bakircioglu, Ofélia P Carvalho, Maryam Khurshid, James J Cox, Beyhan Tuysuz, Okay Caglayan

Am J Hum Genet· May 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex.
Nadia Bahi-Buisson, Karine Poirier, Nathalie Boddaert, Catherine Fallet-Bianco, Nicola Specchio, Okay Caglayan

Brain· November 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Expression of WT1 gene in multiple myeloma patients at diagnosis: is WT1 gene expression a useful marker in multiple myeloma?
Cetin Saatci, A Okay Caglayan, Ismail Kocyigit, Hilal Akalin, Leyla G Kaynar

Hematology· February 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The deletion polymorphism of the angiotensin-converting enzyme gene is associated with acute aortic dissection.
Nihat Kalay, Okay Caglayan, Hasan Akkaya, Ibrahim Ozdogru, Ali Dogan

Tohoku J Exp Med· September 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Megarbane syndrome.
Caglayan Ahmet Okay, Dundar Munis

Indian J Hum Genet· January 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
ICR1 epimutations in llp15 are restricted to patients with Silver-Russell syndrome features.
Thomas Eggermann, Esther Meyer, A Okay Caglayan, Munis Dundar, N Schönherr

J Pediatr Endocrinol Metab· January 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molybdenum cofactor deficiency: clinical features in a Turkish patient.
Hüseyin Per, Hakan Gümüş, Kimiyoshi Ichida, Okay Cağlayan, Sefer Kumandaş

Brain Dev· July 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prenatal diagnosis of a fetus with partial trisomy 7p.
Mahmut Tuncay Ozgun, Cem Batukan, Mustafa Basbug, Hulya Akgun, Okay Caglayan

Fetal Diagn Ther· May 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Sacrococcygeal teratoma in a fetus with prenatally diagnosed partial trisomy 10q (10q24.3-->qter) and partial monosomy 17p (p13.3-->pter).
Cem Batukan, Mahmut Tuncay Ozgun, Mustafa Basbug, Okay Caglayan, Munis Dundar

Prenat Diagn· April 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis