Prof. ERGÜN PINARBAŞI

Publication Network

Published journal articles indexed by SCI, SSCI, and AHCI

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 , 2024 (SCI-Expanded)

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 , vol.42, no.8, pp.3464-3470, 2022 (SCI-Expanded) Sustainable Development

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 , vol.754, 2020 (SCI-Expanded)

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 , vol.40, no.4, pp.495-499, 2020 (SCI-Expanded) Sustainable Development

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 , vol.21, no.10, pp.1779-1786, 2018 (SCI-Expanded)

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 , vol.19, no.2, pp.131-136, 2018 (SCI-Expanded)

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

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

GENE , vol.626, pp.9-13, 2017 (SCI-Expanded)

Association between the soluble epoxide hydrolase gene and preeclampsia

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

HYPERTENSION IN PREGNANCY , vol.36, no.4, pp.315-325, 2017 (SCI-Expanded) Sustainable Development

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 , vol.154, no.7, pp.1287-1292, 2012 (SCI-Expanded)

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 , vol.68, no.2, pp.111-116, 2012 (SCI-Expanded)

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 , vol.37, no.12, pp.1824-1827, 2011 (SCI-Expanded) Sustainable Development

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 , vol.28, no.4, pp.1373-1378, 2011 (SCI-Expanded) Sustainable Development

Microsomal epoxide hydrolase polymorphisms

PINARBAŞI H., SİLİĞ Y., PINARBAŞI E.

MOLECULAR MEDICINE REPORTS , vol.3, no.4, pp.723-727, 2010 (SCI-Expanded)

AXIN2 polymorphism and its association with astrocytoma in a Turkish population

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

MOLECULAR MEDICINE REPORTS , vol.3, no.4, pp.705-709, 2010 (SCI-Expanded)

Strong association between lung cancer and the AXIN2 polymorphism

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

MOLECULAR MEDICINE REPORTS , vol.2, no.6, pp.1029-1035, 2009 (SCI-Expanded)

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 , vol.33, no.1, pp.32-37, 2007 (SCI-Expanded) Sustainable Development

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 , vol.127, no.2, pp.213-217, 2006 (SCI-Expanded) Sustainable Development

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 , vol.31, no.3, pp.236-41, 2005 (SCI-Expanded)

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 , vol.146, no.2, pp.125-9, 2003 (SCI-Expanded) Sustainable Development

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 , vol.185, no.4, pp.1284-8, 2003 (SCI-Expanded)

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 , vol.25, no.2, pp.169-77, 2002 (SCI-Expanded)

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 , vol.35, no.3, pp.348-51, 2002 (SCI-Expanded)

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 , vol.44, no.1, pp.29-33, 2000 (SCI-Expanded) Sustainable Development

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 , vol.379, pp.591-4, 1998 (SCI-Expanded)

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

Pinarbasi E., Elliott J., Hornby D.

Journal of molecular biology , vol.257, pp.804-13, 1996 (SCI-Expanded)

Articles Published in Other Journals

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 , vol.37, 2023 (Scopus)

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 , vol.22, 2021 (ESCI) Sustainable Development

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 , vol.12, no.2, pp.25-27, 2018 (Peer-Reviewed Journal)

Refereed Congress / Symposium Publications in Proceedings

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, Turkey, 6 - 09 September 2007

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, Turkey, 6 - 09 September 2007

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, Turkey, 30 April - 02 May 2005

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