Metrikler
Yayın
17
Açık Erişim
3
BM Sürdürülebilir Kalkınma Amaçları
Makaleler
Tümü (15)
SCI-E, SSCI, AHCI (14)
SCI-E, SSCI, AHCI, ESCI (14)
Scopus (13)
Diğer Yayınlar (1)
2022
20221. Management of endocrine surgical disorders during COVID-19 pandemic: expert opinion for non-surgical options
Agcaoglu O., Sezer A., MAKAY Ö., ERDOĞAN M. F., BAYRAM F., GÜLDİKEN S., et al.
Updates in Surgery
, cilt.74, sa.1, ss.325-335, 2022 (SCI-Expanded)
2019
20192. The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance
Pehlivan D., Bayram Y., Gunes N., Akdemir Z. C., Shukla A., Bierhals T., et al.
AMERICAN JOURNAL OF HUMAN GENETICS
, cilt.105, sa.1, ss.132-150, 2019 (SCI-Expanded)
2019
20193. Mitochondrial DNA deletions in patients with esophagitis, Barrett's esophagus, esophageal adenocarcinoma and squamous cell carcinoma
KELEŞ M., Sahin I., Kurt A., Bozoglu C., Simsek G., Kabalar E., et al.
AFRICAN HEALTH SCIENCES
, cilt.19, sa.1, ss.1671-1676, 2019 (SCI-Expanded)
2018
20184. Becker’xxs myotonia: novel mutations and clinical variability in patients born to consanguineous parents.
Şahin İ., Erdem H. B., TAN H., TATAR A.
Acta Neurologica Belgica , 2018 (SCI-Expanded)
2018
20185. Becker's myotonia: novel mutations and clinical variability in patients born to consanguineous parents
ŞAHİN İ., ERDEM H. B., TAN H., TATAR A.
ACTA NEUROLOGICA BELGICA
, cilt.118, sa.4, ss.567-572, 2018 (SCI-Expanded)
2018
20186. Myhre syndrome with novel findings: bilateral congenital cortical cataract, bilateral papilledema, accessory nipple, and adenoid hypertrophy
Erdem H. B., Sahin I., TATAR A.
CLINICAL DYSMORPHOLOGY
, cilt.27, sa.1, ss.12-14, 2018 (SCI-Expanded)
2017
20177. Deri Hastalıklarında Genetik Temeller ve Yaklaşımlar
ERDEM H. B., ŞAHİN İ., TATAR A.
TÜRKİYE KLİNİKLERİ DERMATOLOJİ ÖZEL DERGİSİ , cilt.10, ss.81-88, 2017 (Hakemli Dergi)
2016
20168. Mitochondrial DNA deletions in patients with chronic suppurative otitis media
TATAR A., Tasdemir S., Sahin I., BOZOĞLU C., Erdem H. B., YÖRÜK Ö., et al.
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
, cilt.273, sa.9, ss.2473-2479, 2016 (SCI-Expanded)
2016
20169. Correlation with Platelet Parameters and Genetic Markers of Thrombophilia Panel (Factor II g.20210G > A, Factor V Leiden, MTHFR (C677T, A1298C), PAI-1, beta-Fibrinogen, Factor XIIIA (V34L), Glycoprotein IIIa (L33P)) in Ischemic Strokes
Tasdemir S., Erdem H. B., Sahin I., Ozel L., Ozdemir G., Eroz R., et al.
NEUROMOLECULAR MEDICINE
, cilt.18, sa.2, ss.170-176, 2016 (SCI-Expanded)
2016
201610. A rare cause of dyspnea in emergency medicine: Keutel syndrome
BAYRAMOĞLU A., Saritemur M., Tasdemir S., OMEROGLU M., Erdem H. B., Sahin I.
AMERICAN JOURNAL OF EMERGENCY MEDICINE
, cilt.34, sa.5, 2016 (SCI-Expanded)
2016
201611. The Relationship Between Endothelial Nitric Oxide Synthase Gene (NOS3) Polymorphisms, NOS3 Expression, and Varicocele.
Kahraman Ç., Tasdemir S., Sahin I., Ozdemir E. M., Yaralı O., Ziypak T., et al.
Genetic testing and molecular biomarkers
, cilt.20, sa.4, ss.191-6, 2016 (SCI-Expanded)
2016
201612. Association Between Human Hair Loss and the Expression Levels of Nucleolin, Nucleophosmin, and UBTF Genes
Tasdemir S., Eroz R., DOĞAN H., Erdem H. B., Sahin I., Kara M., et al.
GENETIC TESTING AND MOLECULAR BIOMARKERS
, cilt.20, sa.4, ss.197-202, 2016 (SCI-Expanded)
2016
201613. Vici Syndrome in Siblings Born to Consanguineous Parents
Tasdemir S., Sahin I., ÇAYIR A., Yuce I., CEYLANER S., TATAR A.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
, cilt.170, sa.1, ss.220-225, 2016 (SCI-Expanded)
2015
201514. Waardenburg syndrome type 1 and a rare finding of anal atresia
TAŞDEMİR Ş., ERDEM H. B., ŞAHİN İ., KARA M., TATAR A.
Genetic Counseling , cilt.26, ss.467-470, 2015 (SCI-Expanded)
2014
201415. Holoprosencephaly: ZIC2 mutation in a case with panhypopituitarism
Taşdemir Ş., Şahin İ., Cayir A., Döneray H., Solomon B. D., Muenke M., et al.
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
, cilt.27, ss.777-781, 2014 (SCI-Expanded)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
2016
20161. Is there any association between nasal polyposis and ADAMTS gene expressions
ŞAHİN İ., TATAR A.
EUROPEAN HUMAN GENETICS CONFERENCE, 21 - 24 Mayıs 2016
2016
20162. Tekrarlayan Gebelik Kaybı Öyküsü Olan Hastalarda Genetik Trombofili Paneli ve Platelet Parametreleri Arasındaki İlişkinin Araştırılması
ATIŞ Ö., ERDEM H. B., ŞAHİN İ., YAZICI Z., DOĞAN H., YILMAZ M., et al.
2. HEMATOLOJİK GENETİK SEMPOZYUMU, İzmir, Türkiye, 24 - 26 Şubat 2016, (Özet Bildiri)