Metrikler
Yayın
17
Açık Erişim
3
BM Sürdürülebilir Kalkınma Amaçları
Makaleler
Tümü (17)
SCI-E, SSCI, AHCI (16)
SCI-E, SSCI, AHCI, ESCI (17)
ESCI (1)
Scopus (16)
2023
20231. 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)
2015
20152. 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)
2012
20123. 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)
2010
20104. 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)
2010
20105. 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)
2010
20106. 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)
2009
20097. 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)
2009
20098. 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)
2009
20099. 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)
2009
200910. 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)
2009
200911. 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)
2008
200812. 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)
2008
200813. 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)
2008
200814. 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)
2008
200815. Megarbane Syndrome; Second Report.
ÇAĞLAYAN A. O., DÜNDAR M.
Indian Journal of Human Genetic , cilt.14, ss.27-29, 2008 (SCI-Expanded)
2008
200816. 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)
2007
200717. 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)
Desteklenen Projeler
2005 - 2006
2005 - 2006MULTİPL MYELOMALI HASTALARDA WT1 GENİNİN EKSPRESYONUNUN VE DE 13Q NUN ARAŞTIRILMASI
Yükseköğretim Kurumları Destekli Proje , BAP Araştırma Projesi
SAATÇİ Ç. (Yürütücü), ÇAĞLAYAN A. O., DÜNDAR M., ESER B., ÖZKUL Y., ÇETİN M.
2005 - 2005
2005 - 2005İDİOPATİK HİRŞUTİZMLİ VAKALARDA CYP19 GENİ VE SRD5A2 GENİ POLİFORFİZMLERİNİN VE BUNLARIN LOKAL OLARAK ANDROJENE DUYARLI DOKUDAKİ EKSPRESYONLARININ ARAŞTIRILMASI.
Yükseköğretim Kurumları Destekli Proje , BAP Doktora
ÇAĞLAYAN A. O. (Yürütücü), BORLU M., ÜNLÜHİZARCI K., DÜNDAR M.