Prof. Dr. ERGÜN PINARBAŞI

Yayın Ağı

Makaleler 34

1. The impact of TMPRSS11A rs353163 and rs977728 polymorphisms on COVID-19 severity: genotypic and clinical associations

ÇEKİN N., Akin S., PINARBAŞI E., DOĞAN H. O.

Molecular Biology Reports , cilt.53, sa.1, 2026 (SCI-Expanded, Scopus)

2. Hypoxia-related miRNA dysregulation in preeclampsia: The roles of miR-210 and miR-383

ÇEKİN N., Akin S., Kucukyildiz I., PINARBAŞI E.

Gene Reports , cilt.40, 2025 (ESCI)

3. Impact of IL-6 rs1800795 and rs1800796 polymorphisms on clinical outcomes of COVID-19: a study on severity of disease in Turkish population.

ÇEKİN N., Akin S., PINARBAŞI E., Doğan O. H.

Mammalian genome : official journal of the International Mammalian Genome Society , cilt.36, sa.1, ss.213-229, 2025 (SCI-Expanded)

4. Relationship between STOX1 gene variations and preeclampsia in Turkish population

Bildirici A. E., Akin S., Atron B., PINARBAŞI E., ÇEKİN N., KÜÇÜKYILDIZ İ.

Human Gene , cilt.37, 2023 (Scopus)

5. STOX1 promotor region-922 T > C polymorphism is associated with Early-Onset preeclampsia

Akin S., PINARBAŞI E., Bildirici A. E., ÇEKİN N.

JOURNAL OF OBSTETRICS AND GYNAECOLOGY , cilt.42, sa.8, ss.3464-3470, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

6. Computationally predicted SARS-COV-2 encoded microRNAs target NFKB, JAK/STAT and TGFB signaling pathways

Aydemir M. N., Aydemir H. B., KORKMAZ E. M., BUDAK M., ÇEKİN N., PINARBAŞI E.

GENE REPORTS , cilt.22, 2021 (ESCI, Scopus) Sürdürülebilir Kalkınma

7. STOX1 gene Y153H polymorphism is associated with early-onset preeclampsia in Turkish population

PINARBAŞI E., ÇEKİN N., Bildirici A. E., Akin S., YANIK A.

GENE , cilt.754, 2020 (SCI-Expanded)

8. The role of two common FOXP3 gene promoter polymorphisms in preeclampsia in a Turkish population: a case-control study

ÇEKİN N., PINARBAŞI E., Bildirici A. E., Hatice H., YANIK A., Sonmez G.

JOURNAL OF OBSTETRICS AND GYNAECOLOGY , cilt.40, sa.4, ss.495-499, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

9. No Association between Foxp3 Promoter Region Polymorphisms (rs3761548 and rs2232365) and Crimean Congo Hemorrhagic Fever Disease.

Çekin N., Pınarbaşı E., Bildirici A. E., Bakır M., Arslan S.

journal of Applied Biological Sciences , cilt.12, sa.2, ss.25-27, 2018 (Hakemli Dergi)

10. FOXP3 rs3761548 polymorphism is associated with knee osteoarthritis in a Turkish population

ÇEKİN N., PINARBAŞI E., Bildirici A. E., Donmez G., ÖZTEMÜR Z., BULUT O., et al.

INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES , cilt.21, sa.10, ss.1779-1786, 2018 (SCI-Expanded)

11. Association between Multiple Sclerosis and FOXP3 Gene Promoter Region Mutations

cekin n., PINARBAŞI E., bildirici a. e., akin s., yildiz ö. k.

cmj , cilt.40, sa.3, ss.226-232, 2018 (Hakemli Dergi)

12. Decreased FENDRR and LincRNA-p21 expression in atherosclerotic plaque.

ÇEKİN N., Ozcan A., GÖKSEL S., ARSLAN S., Pmarbasi E., BERKAN Ö.

Anatolian journal of cardiology , cilt.19, sa.2, ss.131-136, 2018 (SCI-Expanded)

13. FOXP3 Promotor Polymorphism (-3499 A/G) is not Associated with Osteoarthritis in a Turkish Population

cekin n., PINARBAŞI E., DÖNMEZ G., bildirici a. e., öztemur Z., ARSLAN S., et al.

Cumhuriyet Medical Journal , cilt.39, sa.4, ss.659-664, 2017 (Hakemli Dergi)

14. MEFV mutations and their relation to major clinical symptoms of Familial Mediterranean Fever

ÇEKİN N., Akyurek M. E., PINARBAŞI E., Ozen F.

GENE , cilt.626, ss.9-13, 2017 (SCI-Expanded)

15. Association between the soluble epoxide hydrolase gene and preeclampsia

Sari I., PINARBAŞI H., PINARBAŞI E., YILDIZ Ç.

HYPERTENSION IN PREGNANCY , cilt.36, sa.4, ss.315-325, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

16. Intracranial arachnoid cyst family with autosomal recessive trait mapped to chromosome 6q22.31-23.2

BAYRAKLI F., Okten A. I., Kartal U., Menekse G., Guzel A., ÖZTOPRAK İ., et al.

ACTA NEUROCHIRURGICA , cilt.154, sa.7, ss.1287-1292, 2012 (SCI-Expanded)

17. A Novel Locus for Restless Legs Syndrome on Chromosome 13q

BALABAN H., BAYRAKLI F., Kartal U., PINARBAŞI E., Topaktas S., KARS H. Z.

EUROPEAN NEUROLOGY , cilt.68, sa.2, ss.111-116, 2012 (SCI-Expanded)

18. AXIN2 polymorphism and its association with prostate cancer in a Turkish population

PINARBAŞI E., GÜNEŞ E. G., Pinarbasi H., DÖNMEZ G., SİLİĞ Y.

MEDICAL ONCOLOGY , cilt.28, sa.4, ss.1373-1378, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma

19. Fibroblast growth factor receptor 4 Gly388Arg polymorphism is not associated with pre-eclampsia in Turkish women

GÜNEŞ E. G., PINARBAŞI E.

JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH , cilt.37, sa.12, ss.1824-1827, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma

20. Microsomal epoxide hydrolase polymorphisms

PINARBAŞI H., SİLİĞ Y., PINARBAŞI E.

MOLECULAR MEDICINE REPORTS , cilt.3, sa.4, ss.723-727, 2010 (SCI-Expanded)

21. AXIN2 polymorphism and its association with astrocytoma in a Turkish population

GÜNEŞ E. G., PINARBAŞI E., PINARBAŞI H.

MOLECULAR MEDICINE REPORTS , cilt.3, sa.4, ss.705-709, 2010 (SCI-Expanded)

22. Strong association between lung cancer and the AXIN2 polymorphism

GÜNEŞ E. G., PINARBAŞI E., PINARBAŞI H., SİLİĞ Y.

MOLECULAR MEDICINE REPORTS , cilt.2, sa.6, ss.1029-1035, 2009 (SCI-Expanded)

23. Association of microsomal epoxide hydrolase gene polymorphism and pre-eclampsia in Turkish women

Pinarbasi E., Percin F. E., Yilmaz M., Akgun E., Cetin M., Cetin A.

JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH , cilt.33, sa.1, ss.32-37, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma

24. Sivas populasyonunda CYP11B2 geninin promoter bölgesindeki 344T C polimorfizminin araştırılması

AKGÜN E., YILMAZ M., DÖNMEZ G., YILMAZ A., GÜNEŞ E. G., PINARBAŞI E.

Cumhuriyet Üniversitesi Tıp fakültesi Dergisi , cilt.29, sa.1, ss.13-18, 2007 (Hakemli Dergi)

25. Lack of association between the CYP11B2 gene polymorphism and preeclampsia, eclampsia, and the HELLP syndrome in Turkish women

Percin F. E., Cetin M., Pinarbasi E., Akgun E., Gurlek F., Cetin A.

EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY , cilt.127, sa.2, ss.213-217, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

26. Q fever şüphesi olan hasta kan ve serum örneklerinde nested PCR yöntemiyle Coxiella burnetti nin saptanması

AKGÜN E., YILMAZ M., PINARBAŞI E.

Cumhuriyet Üniversitesi Tıp fakültesi Dergisi , cilt.28, sa.2, ss.50-54, 2006 (Hakemli Dergi)

27. No association of polymorphisms in the glutathione S-transferase genes with pre-eclampsia, eclampsia and HELLP syndrome in a Turkish population.

Cetin M., Pinarbasi E., Percin F., Akgun E., Percin S., Pinarbasi H., et al.

The journal of obstetrics and gynaecology research , cilt.31, sa.3, ss.236-41, 2005 (SCI-Expanded)

28. Strong association between the GSTM1-null genotype and lung cancer in a Turkish population.

Pinarbasi H., Silig Y., Cetinkaya O., Seyfikli Z., Pinarbasi E.

Cancer genetics and cytogenetics , cilt.146, sa.2, ss.125-9, 2003 (SCI-Expanded) Sürdürülebilir Kalkınma

29. The small subunit of M. AquI is responsible for sequence-specific DNA recognition and binding in the absence of the catalytic domain.

Pinarbasi H., Pinarbasi E., Hornby D.

Journal of bacteriology , cilt.185, sa.4, ss.1284-8, 2003 (SCI-Expanded)

30. Molecular characterization of a full genome Turkish hepatitis C virus 1b isolate (HCV-TR1): a predominant viral form in Turkey.

Yildiz E., Oztan A., Sar F., Pinarbasi E., Cetin-Atalay R., Akkiz H., et al.

Virus genes , cilt.25, sa.2, ss.169-77, 2002 (SCI-Expanded)

31. Recombinant alpha and beta subunits of M.AquI constitute an active DNA methyltransferase.

Pinarbasi H., Pinarbasi E., Hornby D.

Journal of biochemistry and molecular biology , cilt.35, sa.3, ss.348-51, 2002 (SCI-Expanded)

32. A highly sensitive and specific enzyme-linked immunosorbent assay of antibodies to hepatitis C virus.

Eroglu C., Yildiz E., Ozturk M., Pinarbasi E.

Acta virologica , cilt.44, sa.1, ss.29-33, 2000 (SCI-Expanded) Sürdürülebilir Kalkınma

33. Substitution of the conserved phenylalanine in the S-adenosyl-L-methionine binding site of M.MspI with tyrosine modifies the kinetic properties of the enzyme.

Pinarbasi E., Kan M., Duran C., Ford G., Hornby D.

Biological chemistry , cilt.379, ss.591-4, 1998 (SCI-Expanded)

34. Activation of a yeast pseudo DNA methyltransferase by deletion of a single amino acid.

Pinarbasi E., Elliott J., Hornby D.

Journal of molecular biology , cilt.257, ss.804-13, 1996 (SCI-Expanded)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 11

9. Türk Populasyonunda primer hipertansiyonu olan örneklerde Cyp11b2 Geninin promoter bölgesindeki 344T C polimorfizminin araştırılması

AKGÜN E., YILMAZ M., DÖNMEZ G., GÜNEŞ E. G., ÇOLAK A., PINARBAŞI E.

10. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Türkiye, 6 - 09 Eylül 2007, (Özet Bildiri)

10. Q fever hastalarında Kırım Kongo virüsü ve Coxiella burnetii ko enfeksiyonu

YILMAZ M., AKGÜN E., DÖNMEZ G., GÜNEŞ E. G., BAKIR M., PINARBAŞI E.

10. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Türkiye, 6 - 09 Eylül 2007

11. Pre eklampsi eklampsi ve HELLP sendromu riski İnsan mikrozomal epoksid hidrolaz geni EPHX ekzon 4 polimorfizminin araştırılması

YILMAZ M., ÇETİN M., PERÇİN F. E., AKGÜN E., DÖNMEZ G., PINARBAŞI E.

Fetal Tıp Prenatal Tanı 2005, Türkiye, 30 Nisan - 02 Mayıs 2005, (Özet Bildiri)

Metrikler

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Yayın (WoS)

Yayın (Scopus)

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298

H-İndeks (WoS)

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325

H-İndeks (Scopus)

Atıf (Scholar)

246

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BM Sürdürülebilir Kalkınma Amaçları

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