Arş. Gör. Ahmet Okay ÇAĞLAYAN

1. Childhood-Onset Neurodegeneration with Cerebellar Atrophy Syndrome: Severe Neuronal Degeneration and Cardiomyopathy with Loss of Tubulin Deglutamylase Cytosolic Carboxypeptidase 1

Samur M. B., Ercan-Sencicek A. G., GÜMÜŞ H., Ali G. G., Baykan B., Caglayan A. O., et al.

JOURNAL OF PEDIATRIC NEUROLOGY , cilt.21, sa.05, ss.371-376, 2023 (ESCI, Scopus)

2. A rare case of congenital fibrosis of extraocular muscle type IA due to KIF2IA mutation with Marcus Gunn jaw-winking phenomenon

BAYRAM A. K., PER H., Quon J., CANPOLAT M., Uelgen E., Dogan H., et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , cilt.19, sa.6, ss.743-746, 2015 (SCI-Expanded, Scopus)

3. A new syndrome of microtia with unilateral renal agenesis and short stature

Caglayan A. O., Stevens S. J. C., Albrechts J. C. M., DÜNDAR M., Engelen J.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , sa.8, ss.1837-1840, 2012 (SCI-Expanded, Scopus)

4. Magnetic Resonance Spectroscopy in Two Siblings with Chorea-Acanthocytosis

Ismailogullari S., Caglayan A. O., BADER B., DANEK A., Korkmaz S., Sharifov E., et al.

MOVEMENT DISORDERS , cilt.25, sa.16, ss.2894-2897, 2010 (SCI-Expanded, Scopus)

5. Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

Bilguvar K., Ozturk A. K., Louvi A., Kwan K. Y., Choi M., Tatli B., et al.

NATURE , cilt.467, sa.7312, ss.207-211, 2010 (SCI-Expanded, Scopus)

6. Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency

GÜMÜŞ H., Ghesquiere S., Per H., KONDOLOT M., ICHIDA K., POYRAZOĞLU G., et al.

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY , cilt.52, sa.9, ss.868-872, 2010 (SCI-Expanded, Scopus)

7. Frank-ter Haar syndrome with unusual clinical features

DÜNDAR M., SAATÇİ Ç., Taşdemir S., AKÇAKUŞ M., ÇAĞLAYAN A. O., ÖZKUL Y.

EUROPEAN JOURNAL OF MEDICAL GENETICS , cilt.52, sa.4, ss.247-249, 2009 (SCI-Expanded, Scopus)

8. Detection of p16 promotor hypermethylation in "Maras powder" and tobacco users

SAATÇİ Ç., Çağlayan A. O., ÖZKUL Y., Tahiri S., Turhan A. B., DÜNDAR M.

CANCER EPIDEMIOLOGY , cilt.33, sa.1, ss.47-50, 2009 (SCI-Expanded, Scopus)

9. Inherited diseases and syndromes leading to aortic aneurysms and dissections

ÇAĞLAYAN A. O., DÜNDAR M.

EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY , cilt.35, sa.6, ss.931-940, 2009 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

10. Lack of association between the Glu298Asp polymorphism of endothelial nitric oxide synthase and slow coronary flow in the Turkish population

Caglayan A. O., KALAY N., SAATÇİ Ç., YALCIN A., AKALIN H., DÜNDAR M.

CANADIAN JOURNAL OF CARDIOLOGY , cilt.25, sa.3, 2009 (SCI-Expanded, Scopus)

11. Lack of Association of the Glu298Asp Polymorphism of Endothelial Nitric Oxide Synthase with Coronary Slow Flow in the Turkish Population.

ÇAĞLAYAN A. O., KALAY N., SAATÇİ Ç., YALÇIN A., AKALIN H., DÜNDAR M.

CANADIAN JOURNAL OF CARDIOLOGY , cilt.25, ss.69-72, 2009 (SCI-Expanded, Scopus)

12. Down syndrome like appearance with a novel de novo translocation t(6;21)(q21;q13)

DÜNDAR M., ÇAĞLAYAN A. O., SAATÇİ Ç., ARSLAN K., ÖZKUL Y.

INDIAN JOURNAL OF MEDICAL RESEARCH , cilt.128, sa.5, ss.666-668, 2008 (SCI-Expanded, Scopus)

13. Apolipoprotein E3/E3 Genotype Decreases the Risk of Pituitary Dysfunction after Traumatic Brain Injury due to Various Causes: Preliminary Data

TANRIVERDİ F., TAHERİ S., ULUTABANCA H., Caglayan A. O., ÖZKUL Y., DÜNDAR M., et al.

JOURNAL OF NEUROTRAUMA , cilt.25, sa.9, ss.1071-1077, 2008 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

14. Holt-Oram syndrome in two generations with translocation t(9;15)(p12;q11.2)

Çağlayan A., Köklü E., Saatci C., GÜNEŞ T., ÖZKUL Y., NARİN N., et al.

ANNALS OF SAUDI MEDICINE , cilt.28, sa.3, ss.209-212, 2008 (SCI-Expanded, Scopus)

15. Megarbane Syndrome; Second Report.

ÇAĞLAYAN A. O., DÜNDAR M.

Indian Journal of Human Genetic , cilt.14, ss.27-29, 2008 (SCI-Expanded)

16. The effect of maras powder on DNA methylation and micronucleus formation in human buccal tissue

SAATÇİ Ç., ÖZKUL Y., Tahiri S., Çağlayan A. O., Turhan A. B., DÜNDAR M.

JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES , cilt.71, sa.6, ss.396-404, 2008 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

17. How the I1307K adenomatous polyposis coli gene variant contributes in the assessment of risk of colorectal cancer, but not stomach cancer, in a Turkish population

Dundar M., Caglayan A. O., Saatci C., Karaca H., Baskol M., Tahiri S., et al.

CANCER GENETICS AND CYTOGENETICS , cilt.177, sa.2, ss.95-97, 2007 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

Arş. Gör. Ahmet Okay ÇAĞLAYAN

Yayınlar & Eserler

1. Childhood-Onset Neurodegeneration with Cerebellar Atrophy Syndrome: Severe Neuronal Degeneration and Cardiomyopathy with Loss of Tubulin Deglutamylase Cytosolic Carboxypeptidase 1

2. A rare case of congenital fibrosis of extraocular muscle type IA due to KIF2IA mutation with Marcus Gunn jaw-winking phenomenon

3. A new syndrome of microtia with unilateral renal agenesis and short stature

4. Magnetic Resonance Spectroscopy in Two Siblings with Chorea-Acanthocytosis

5. Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

6. Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency

7. Frank-ter Haar syndrome with unusual clinical features

8. Detection of p16 promotor hypermethylation in "Maras powder" and tobacco users

9. Inherited diseases and syndromes leading to aortic aneurysms and dissections

10. Lack of association between the Glu298Asp polymorphism of endothelial nitric oxide synthase and slow coronary flow in the Turkish population

11. Lack of Association of the Glu298Asp Polymorphism of Endothelial Nitric Oxide Synthase with Coronary Slow Flow in the Turkish Population.

12. Down syndrome like appearance with a novel de novo translocation t(6;21)(q21;q13)

13. Apolipoprotein E3/E3 Genotype Decreases the Risk of Pituitary Dysfunction after Traumatic Brain Injury due to Various Causes: Preliminary Data

14. Holt-Oram syndrome in two generations with translocation t(9;15)(p12;q11.2)

15. Megarbane Syndrome; Second Report.

16. The effect of maras powder on DNA methylation and micronucleus formation in human buccal tissue

17. How the I1307K adenomatous polyposis coli gene variant contributes in the assessment of risk of colorectal cancer, but not stomach cancer, in a Turkish population

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Yayın (Scopus)

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