Publications & Works

Publication Network
Articles 9
All (9)
SCI-E, SSCI, AHCI (6)
SCI-E, SSCI, AHCI, ESCI (7)
ESCI (1)
Scopus (8)
TRDizin (3)

1. Association between ACE (rs4343 and rs1799752), AGTR1 (rs5186), and PAI-1 (rs2227631) polymorphisms in the host and the severity of Covid-19 infection

POLAT S., Şimşek Z. Ö.
Nucleosides, Nucleotides and Nucleic Acids , vol.44, no.1, pp.57-78, 2025 (SCI-Expanded, Scopus) identifier identifier

2. Host Genetic Polymorphisms and Disease Severity in Pregnant Women with COVID-19 in Türkiye

POLAT S., Kiremitli S., Kiremitli T., Kirkinci A., Kurnuç F. Z., ARSLAN Y. K.
Journal of Clinical Obstetrics and Gynecology , vol.34, no.1, pp.1-9, 2024 (ESCI, Scopus, TRDizin) Creative Commons License identifier identifier

3. Unexpectedly high mutation rate of cyp11b1 compared to cyp21a2 in randomly-selected turkish women: a large screening study

POLAT S., Karaburgu S., ÜNLÜHİZARCI K., DÜNDAR M., ÖZKUL Y., ARSLAN Y. K., et al.
Journal of Endocrinological Investigation , vol.46, no.11, pp.2367-2377, 2023 (SCI-Expanded, Scopus) identifier identifier identifier

4. 17-Hydroxyprogesterone Response to Standard Dose Synacthen Stimulation Test in CYP21A2 Heterozygous Carriers and Non-carriers in Symptomatic and Asymptomatic Groups: Meta-analyses

POLAT S., Arslan Y. K.
JCRPE Journal of Clinical Research in Pediatric Endocrinology , vol.14, no.1, pp.56-68, 2022 (SCI-Expanded, Scopus, TRDizin) Creative Commons License Sustainable Development identifier identifier identifier identifier

5. Lomber Disk Hernisi Tanısı Alan Türk Hastalarda Genetik Polimorfizim

POLAT S., ÖZÖNER B., ARSLAN Y. K., EKİNCİ B.
Erzincan Üniversitesi Fen Bilimleri Enstitüsü Dergisi , vol.14, no.2, pp.472-491, 2021 (TRDizin) identifier

6. The role of androgen receptor CAG repeat polymorphism in androgen excess disorder and idiopathic hirsutism

POLAT S., Karaburgu S., ÜNLÜHİZARCI K., DÜNDAR M., ÖZKUL Y., ARSLAN Y. K., et al.
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.43, no.9, pp.1271-1281, 2020 (SCI-Expanded, Scopus) Sustainable Development identifier identifier identifier

7. Comprehensive genotyping of Turkish women with hirsutism

POLAT S., Karaburgu S., ÜNLÜHİZARCI K., DÜNDAR M., ÖZKUL Y., ARSLAN Y. K., et al.
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION , vol.42, no.9, pp.1077-1087, 2019 (SCI-Expanded, Scopus) Sustainable Development identifier identifier identifier

8. Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations

Menabo S., Polat S., Baldazzi L., Kulle A. E., Holterhus P., Groetzinger J., et al.
EUROPEAN JOURNAL OF HUMAN GENETICS , vol.22, no.5, pp.610-616, 2014 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier identifier

9. 17 Alpha Hydroxylase Deficiency A Rare Case of PrimaryAmenorrhea and Hypertension

ŞİMSEK Y., POLAT S., DİRİ H., TANRIVERDİ F., ÖZDAMAR KARACA Z. C., ÜNLÜHİZARCI K., et al.
Turkish Journal of Endocrinology and Metabolism , 2014 (Scopus) Creative Commons License
Papers Presented at Peer-Reviewed Scientific Conferences 4

1. Gene variants of Congenital Adrenal Hyperplasia in Anatolian population

DÜNDAR M., POLAT S., SAATÇİ Ç., ÖZKUL Y.
European Biotechnology Congress, 26 - 28 April 2018, (Summary Text)

2. NCAH prevalance with novel CYP21A2 and CYP11B1 mutations in hirsut turkish women

POLAT S., karaburgu s., ÜNLÜHİZARCI K., DÜNDAR M., ÖZKUL Y., ÖZDAMAR KARACA Z. C., et al.
19th European Congress of Endocrinology, 20 - 23 May 2017, (Summary Text) Sustainable Development

3. Ankilozon Spondilit Hastalarında MDR 1 Gen Polimorfizim ve Ekspresyonunun Tedavisinde Kullanılan İlaçlara Göre Değişimi

ÇOLAK F., POLAT S., KORKMAZ K., KIRNAP M., SAATÇİ Ç., DÜNDAR M., et al.
XII. Ulusal Tıbbi Genetik Kongresi, Turkey, 5 - 09 October 2016, pp.275, (Summary Text)

4. A Nonvirilized form of Classic 3b HydroxysteroidDehydrogenase Deficiency Due to a HomozygousS218P Mutation in the HSD3B2 Gene in a Girl withClassic Phenylketonuria

ALİKAŞİFOĞLU A., BÜYÜKYILMAZ G., GONCA N., OZON A., KANDEMİR N., DÜNDAR M., et al.
European Society for Paediatric Endocrinology Congress, 10 - 12 September 2016, pp.281, (Summary Text)
Other Publications 1

1. Testicular Adrenal Rest Tumor in Two Brothers with a Novel Mutation in the 3 Beta-Hydroxysteroid Dehydrogenase-2 Gene.

POLAT S.
Other, pp.85-90, 2016
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Publication

14

Publication (WoS)

7

Publication (Scopus)

8

Citation (WoS)

24

H-Index (WoS)

2

Citation (Scopus)

25

H-Index (Scopus)

2

Project

1

Open Access

4
UN Sustainable Development Goals