Yayınlar & Eserler

Yayın Ağı
Makaleler 15
Tümü (15)
SCI-E, SSCI, AHCI (14)
SCI-E, SSCI, AHCI, ESCI (14)
Scopus (13)
Diğer Yayınlar (1)

1. 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) Creative Commons License Sürdürülebilir Kalkınma identifier identifier identifier

2. 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) Creative Commons License identifier identifier identifier

3. 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) Sürdürülebilir Kalkınma identifier identifier identifier

4. 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)

5. 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) identifier identifier identifier

6. 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) identifier identifier identifier

7. 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)

8. 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) identifier identifier identifier

9. 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) identifier identifier identifier

10. 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) identifier identifier identifier

11. 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) Creative Commons License identifier identifier identifier

12. 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) Sürdürülebilir Kalkınma identifier identifier identifier

13. 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) identifier identifier identifier

14. 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)

15. 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) Creative Commons License identifier identifier identifier
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 2

1. Is there any association between nasal polyposis and ADAMTS gene expressions

ŞAHİN İ., TATAR A.
EUROPEAN HUMAN GENETICS CONFERENCE, 21 - 24 Mayıs 2016

2. 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)
Metrikler

Yayın

17

Yayın (WoS)

14

Yayın (Scopus)

13

Atıf (WoS)

118

H-İndeks (WoS)

6

Atıf (Scopus)

83

H-İndeks (Scopus)

5

Atıf (Scholar)

11

H-İndeks (Scholar)

1

Açık Erişim

3
BM Sürdürülebilir Kalkınma Amaçları