GÖKHAN OZAN ÇETİN, MD, PhD

1. PERSONAL DATA

Name: Gokhan Ozan CETIN

Nationality: Turkey

Contact:

Tel (Mobile): 00905058963453

E-mail: ocetin@pau.edu.tr

2. ACADEMIC/PROFESSIONAL PARTICULARS

  1. (a)  Field of Specialization:

    Major Field of Specialization, Medical Genetics

    Fine Field Specialization Ophthalmic Genetics, Cancer Genetics, Rare Diseases, Personalized Medicine

  2. (b)  Academic Qualifications

    March 2023 - Present: Consultant Physician, Professor of Medical Genetics, Medical School of Pamukkale University -Department of Medical Genetics Denizli, Turkey

    December 2017 - March 2023: Consultant Physician, Associate professor of Medical Genetics in Medical School of Pamukkale University -Department of Medical Genetics, Denizli, Turkey

    May 2011-April 2012: Visiting Scientist, Division of Human Genetics, Medical School of Washington University in St. Louis, St. Louis, Missouri, USA

    October 2007 - December 2017: Consultant Physician, Assistant professor of Medical Genetics in Medical School of Pamukkale University -Department of Medical Genetics, Denizli, Turkey

    October 2006- October 2007: Military Service; Consultant Physician and Resident in Gülhane Military Medical Academy, Department of Medical Biology, Division of Medical Genetics, Ankara, Turkey

    September 2001- June 2006: Graduate Student in Dokuz Eylül University Institution of Health Sciences, Department of Medical Biology and Genetics, Izmir, Turkey

    September 1999- September 2001: Graduate Student in Pamukkale University Institution of Health Sciences, Department of Medical Biology and Genetics, Denizli, Turkey

    August 1998- September 1999: General Practitoner and Institutional Physician in Ministry of Forestry, Konya Regional Devision, Konya, Turkey

    1992-1998: Medical School of Dokuz Eylül University, Izmir, Turkey

    PhD Thesis in Medical Biology and Genetics "The effect of STBM/VANGL expression on properties of hepatocellular cancer cells”, Supervisors: Meral SAKIZLI, PhD, Ahmet Ugur YILMAZ, MD (Published in Genet Test Mol Biomarkers. 2015 Jun;19(6):283-7. doi: 10.1089/gtmb.2015.0014.)

    (c)  Academic Honors and Awards

    Name of the Award, Awarding Institution, Year

    1. 2nd Best Oral Presentation in the 2021 Congress of Turkish Society of Neonatalogy: (DEMIR AYKUT, ERGIN HACER, ÖZDEMIR ÖZMERT MUHAMMET ALI, ÇETIN GÖKHAN OZAN, Türel Samet, ERTUGRUL SABAHATTIN, Çalkavur Sebnem, SAHIN ÖZLEM, ÇETINKAYA MERIH, UZLU SAFIYE ELIF, OKULU EMEL, NARTER FATMA, ÖNCEL MEHMET YEKTA, OYGÜR NIHAL, AYDIN MUSTAFA, SATAR MEHMET, SENOL HANDE (2021): miRNA expression profiles of new borns with severe hyperbilirubinemia.

    2. Best Oral Presentation in the 2021 Congress of Turkish Society of Pediatrics: (DEMIR AYKUT, ERGIN HACER, ÖZDEMIR ÖZMERT MUHAMMET ALI, ÇETIN GÖKHAN OZAN, Türel Samet, ERTUGRUL SABAHATTIN, Çalkavur Sebnem, SAHIN ÖZLEM, ÇETINKAYA MERIH, UZLU SAFIYE ELIF, OKULU EMEL, NARTER FATMA, ÖNCEL MEHMET YEKTA, OYGÜR NIHAL, AYDIN MUSTAFA, SATAR MEHMET, SENOL HANDE (2021): miRNA expression profiles of new borns with severe hyperbilirubinemia.

    3. Best Abstract Award, International Congress on Leukemia Lymphoma Myeloma, 2015: CANER VILDAN,SEN TÜRK NILAY,BARIS IKBAL CANSU,ÇETIN GÖKHAN OZAN,TEPELI EMRE,HACIOGLU SIBEL,SARI HAKAN ISMAIL,ZENCIR SEVIL,DOGU MEHMET HILMI,BAGCI GÜLSEREN,KESKIN ALI (2015). MYD88 expression and L265P mutation in mature B cell non Hodgkin lymphomas. 5th International Congress on Leukemia Lymphoma Myeloma, 157-157.

    4. Best Poster Award in 9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation 2010: Tepeli E, Caner V, Büyükpınarbaslı N, Çetin GO, Düzcan F, Elmas L, Bagcı G (2010). Determination of expression profiles of ERCC1 status at protein mRNA and DNA level in different stages of non small cell lung cancer.

    5. 2nd Best Oral Presentation in the 2009 National Congress of Pathology: Düzcan F, Sen S, Yörükoglu K, Caner V, Sen Türk N, Çetin GO, Kelten C, Tuna B, Sarsık B, Tepeli E, Düzcan SE (2009). Amplification and expression of Topoisomerase II and its correlation with HER2 NEU Expression in Papillary Renal Cell Carcinomas. Abstract Book of 19th National Congress of Pathology, 25, 9-9.

    6. Best Oral Presentation in Cancer Molecular Genetics in the 2006 National Congress of Prenatal Diagnosis and Medical Genetics: Çetin GO, Toylu A, Atabey N, Sercan Z, Sakızlı M (2006). The effects of VANGL1 silencing on the hepatocellular cancer cells.       

  3. (d)  Membership of Professional Bodies

    1. Founder member of Dokuz Eylul University Faculty of Medicine-Club Against Infectious Diseases and Substance Abuse in 1997 and executive committee member until August 1999.

    2. Turkish Society of Medical Doctors

    3. Turkish Society of Medical Genetics

    4. Society of Izmir Oncology Group

    5. European Society of Human Genetics              

  4. (e)  Language Proficiency

List of spoken/written languages and level of proficiency

English: Yabancı Dil Sınavı 87.50 (December 2016) (National foreign language examination over 100 coresponding to level C1) (I can give lectures in English)

3. CAREER DETAILS

(a)  Academic Positions Held

  1. March 2023 - Present: Consultant Physician, Professor of Medical Genetics, Medical School of Pamukkale University -Department of Medical Genetics Denizli, Turkey
  2. December 2017 - March 2023: Consultant Physician, Associate professor of Medical Genetics in Medical School of Pamukkale University -Department of Medical Genetics, Denizli, Turkey
  3. October 2007 - December 2017: Consultant Physician, Assistant professor of Medical Genetics in Medical School of Pamukkale University -Department of Medical Genetics, Denizli, Turkey
  4. September 2001- June 2006: Graduate Student in Dokuz Eylül University Institution of Health Sciences, Department of Medical Biology and Genetics, Izmir, Turkey
  5. September 1999- September 2001: Graduate Student in Pamukkale University Institution of Health Sciences, Department of Medical Biology and Genetics, Denizli, Turkey

 (b)  Professional/Industrial Positions Held

NA

(c) Administrative Positions Held


1. Editorial Board Member: Pamukkale Medical Journal, since 2019

2. Pamukkale University Institutional Review Board Member since 2020

3. Quality Assurance Comitee Member: Turkish Society of Medical Genetics  2021-2023

4. TEACHING

  1. (a)  Summary of Courses Taught in Medical School of Pamukkale University

    Human Chromosomes 2009-2021   

    Chromosomal Anomalies 2009-2021

    Introduction to Dysmorphology 2009-2023

    Syndromes Associated with Chromosomal Abnormalities 2009-2023

    Neurogenetics 2016-2023

    Cancer Genetics 2016-2023

    To 2nd, 4th and 5th Grade students in Medical School of Pamukkale University

  2. (b) Research Students Supervised/Trained

1)Thesis supervisor of Volkan OKUR, MD

“Association of age related macular degeneration and CFH, HIF1A, SKIV2L and MYRIP polymorphisms” (2013)

(Published in Clin Exp Ophthalmol. 2015 Jan-Feb;43(1):47-53.                  

doi: 10.1111/ceo.12376.)

Mentor of the following:

Kadri Murat ERDOĞAN

Tarkan KALKAN

Volkan OKUR

Metin ESER

Akif AYAZ

Selcan ZEYBEK

Gizem AKINCI-GÖNEN

Yasemin Anıl EYÜBOĞLU-TANRIVERDİ

Bilge SARIKEPE

Özlem ANLAŞ

Burcu ALBUZ

Menekşe ÖZTÜRK

Nesligül GÖNEN

5. RESEARCH

(a) Research Interests

List of research interests in order of priority.

Cancer Genetics

Hematological Malignancies

Ophthalmic Genetics

Rare Diseases

Clinical Genetics

(b) Publications/Citations Data

Articles in International Refereed Journals

A total of 40 papers in peer journals.

26 papers in SCI-e indexed journals, 4 in journals indexed in other international indexes, 10 in national/Turkish journals

 (c) Research Grants

1) "The effect of STBM/VANGL expression on properties of hepatocellular cancer cells”, Grant No: 04 KB SAG 094 (Dokuz Eylül University Grant-30,000 usd) (2004-2006)

2)” The role of VANGL1 heterozygous missense mutations V239I R274Q M328T in neural tube defects”  Grant No: 109S198, TÜBITAK (Research Grant from Scientific and Technical Research Council of Türkiye-7,500 usd) (2009-2010)

3) “Association of age related macular degeneration and CFH, HIF1A, SKIV2L and MYRIP polymorphisms” Grant No: 2012TPF021 (Pamukkale University Grant-7,500 usd) (2012-2013) 

4) “The efficacy of combined proteasome inhibitors in multiple myeloma” TÜBITAK Grant No: 114S905 (7,500 usd) (2015-2016)

5) “The effect of vitamine D receptor polymorphism on metabolic syndrome and liver dysfunction in childhood obesity” (Pamukkale University Grant-7,500 usd) (2015-2016) 

6) “Functional significance of tumor derived exosomes in diffuse large B-cell lymphoma” TÜBITAK Grant No:114S442 (120,000 usd) (2014-2018)

7) “Expression profiles of miR-124- 3p, miR-4447, miR-107,miR-Let-7d, miR-5692b in Attention Deficiency and Hiperactivity Disorder” miRNAlarının ekspresyon profilleri” (Pamukkale University Grant-7,500 usd) (2016-2018) 

 8) “Association of methylation status of DRD4, DAT1, VIPR2, 5-HT1B and BDNF and Attention Deficiency and Hiperactivity Disorder”, (Pamukkale University Grant-7,500 usd) (2016-2018) 

9) “Methylation patterns of exosomal and nuclear DNA in Diffuse Large B-cell Lymphoma” (Pamukkale University Grant-7,500 usd) (2016-2018) 

 

6. LIST of PUBLICATIONS (in chronological order, starting with most recent )

(a)  International Refereed Journals (Published or Accepted only!)

Publications in journals indexed in Science Citation Index-expanded (Total 26)

  1. Dundar M, Fahrioglu U, Yildiz SH, Bakir-Gungor B, Temel SG, Akin H, Artan S, Cora T, Sahin FI, Dursun A, Sezer O, Gurkan H, Erdogan M, Gunduz CNS, Bisgin A, Ozdemir O, Ulgenalp A, Percin EF, Yildirim ME, Tekes S, Bagis H, Yuce H, Duman N, Bozkurt G, Yararbas K, Yildirim MS, Arman A, Mihci E, Eraslan S, Altintas ZM, Aymelek HS, Ruhi HI, Tatar A, Ergoren MC, Cetin GO, Altunoglu U, Caglayan AO, Yuksel B, Ozkul Y, Saatci C, Kenanoglu S, Karasu N, Dundar B, Ozcelik F, Demir M, Siniksaran BS, Kulak H, Kiranatlioglu K, Baysal K, Kazimli U, Akalin H, Dundar A, Boz M, Bayram A, Subasioglu A, Colak FK, Karaduman N, Gunes MC, Kandemir N, Aynekin B, Emekli R, Sahin IO, Ozdemir SY, Onal MG, Senel AS, Poyrazoglu MH, Kisaarslan ANP, Gursoy S, Baskol M, Calis M, Demir H, Zararsiz GE, Erdogan MO, Elmas M, Solak M, Ulu MS, Thahir A, Aydin Z, Atasever U, Sag SO, Aliyeva L, Alemdar A, Dogan B, Erguzeloglu CO, Kaya N, Ozkinay F, Cogulu O, Durmaz A, Onay H, Karaca E, Durmaz B, Aykut A, Cilingir O, Aras BD, Gokalp EE, Arslan S, Temena A, Haziyeva K, Kocagil S, Bas H, Susam E, Keklikci AR, Sarac E, Kocak N, Nergiz S, Terzi YK, Dincer SA, Baskin ES, Genc GC, Bahadir O, Sanri A, Yigit S, Tozkir H, Yalcintepe S, Ozkayin N, Kiraz A, Balta B, Gonen GA, Kurt EE, Ceylan GG, Ceylan AC, Erten S, Bozdogan ST, Boga I, Yilmaz M, Silan F, Kocabey M, Koc A, Cankaya T, Bora E, Bozkaya OG, Ercal D, Ergun MA, Ergun SG, Duman YS, Beyazit SB, Uzel VH, Em S, Cevik MO, Eroz R, Demirtas M, Firat CK, Kabayegit ZM, Altan M, Mardan L, Sayar C, Tumer S, Turkgenc B, Karakoyun HK, Tunc B, Kuru S, Zamani A, Geckinli BB, Ates EA, Clark OA, Toylu A, Coskun M, Nur B, Bilge I, Bayramicli OU, Emmungil H, Komesli Z, Zeybel M, Gurakan F, Tasdemir M, Kebudi R, Karabulut HG, Tuncali T, Kutlay NY, Kahraman CY, Onder NB, Beyitler I, Kavukcu S, Tulay P, Tosun O, Tuncel G, Mocan G, Kale H, Uyguner ZO, Acar A, Altinay M, Erdem L; National Genetics Consortium Study. Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium. Funct Integr Genomics. 2022 Jun;22(3):291-315. doi: 10.1007/s10142-021-00819-3.
  2. ÇETIN GÖKHAN OZAN, ÇETIN EBRU NEVIN, AKYOL TUNAHAN, ILHAN HATICE DENIZ, PEKEL GÖKHAN (2022). Genotype and phenotype characteristics of X-linked retinoschisis: the first report of a Turkish population. Ophthalmic Genetics, 1-8., Doi: 10.1080/13816810.2021.2010772
  3. ÖLMEZ TÜRKER AKGÜN, ÇETIN GÖKHAN OZAN, KARAER KADRI (2022). Early onset disease, anarthria, areflexia, and dystonia can be the distinctive features of SPG64, a very rare form of hereditary spastic paraplegias. American Journal of Medical Genetics Part A, 188(9), 2712-2717., Doi: 10.1002/ajmg.a.62878
  4. CANER VILDAN, ÇETIN GÖKHAN OZAN, HACIOGLU SIBEL, BARIS IKBAL CANSU, TEPELI EMRE, SEN TÜRK NILAY, BAGCI GÜLSEREN, YARARBAS KANAY, AKGÜN ÇAGLIYAN GÜLSÜM (2021). The miRNA content of circulating exosomes in DLBCL patients and in vitro influence of DLBCL-derived exosomes on miRNA expression of healthy B-cells from peripheral blood. Cancer Biomarkers, 32(4), Doi: 10.3233/CBM-210110
  5. ÇETIN SAHABETTIN, VARMA GÜLFIZAR, ÇETIN GÖKHAN OZAN, TÜREL SAMET, TOKER UGURLU TUGÇE, ÖZDEL OSMAN (2021). The Relationship Between Methylation of the Glucocorticoid Receptor Gene (NR3C1) and Childhood Trauma and Alexithymia. ISRAEL JOURNAL OF PSYCHIATRY AND RELATED SCIENCES, 58(3), 13-20.
  6. BARIS IKBAL CANSU, HACIOGLU SIBEL, SEN TÜRK NILAY, ÇETIN GÖKHAN OZAN, ZENCIR SEVIL, BAGCI GÜLSEREN, CANER VILDAN (2021). Expression and DNA methylation profiles of EZH2-target genes in plasma exosomes and matched primary tumor tissues of the patients with diffuselarge B-cell lymphoma. Clinical and Translational Oncology, 23(6), 1152-1166., Doi:10.1007/s12094-020-02504-6
  7. ALBUZ BURCU,ÇETIN GÖKHAN OZAN,ÖZHAN BAYRAM,SARIKEPE Bilge,ANLAS Özlem,ÖZTÜRK MENEKSE,ZEYBEK SELCAN,A. SABIR AKKOYUNLU NURAN,BAGCI GÜLSEREN,SEMERCI GÜNDÜZ CAVIDAN NUR (2020). A novel nonsense mutation in CHST3 in a Turkish patient with spondyloepiphyseal dysplasia, Omani type. Clinical Dysmorphology, 29(1),61-64., Doi: 10.1097/MCD.0000000000000295
  8. ZEYBEK SELCAN,TEPELI EMRE,ÇETIN GÖKHAN OZAN,CANER VILDAN,SENOL HANDE,YILDIRIM NAZAN BASAK,BAGCI GÜLSEREN (2019). Increased expression of pentraxin 3 in placental tissues from patients with unexplained recurrent pregnancy loss. Balkan Journal of Medical Genetics,22(1), 21-28., Doi: 10.2478/bjmg-2019-0002
  9. AYDIN SEZAI ÜSTÜN,KABUKÇU BASAY BÜRGE,ÇETIN GÖKHAN OZAN,GÜNGÖR AYSEGÜL,TEPELI EMRE (2019). Altered microRNA 5692b and microRNA let-7d expression levels in children and adolescents with attention deficit hyperactivity disorder. JOURNAL OF PSYCHIATRIC RESEARCH;115:158-164. doi: 10.1016/j.jpsychires.2019.05.021.
  10. ÇETIN GÖKHAN OZAN,BARIS IKBAL CANSU,CANER VILDAN,SARIKEPE BILGE,SEN TÜRK NILAY,TEPELI EMRE,HACIOGLU SIBEL,SARI HAKAN ISMAIL,BAGCI GÜLSEREN,KESKIN ALI (2016). Mutational status of EZH2 and CD79B hot spots in mature B cell non Hodgkin s lymphomas novel CD79B variations have been revealed. European Review for Medical and Pharmacological Sciences, 20(5), 830-836.
  11. BARIS IKBAL CANSU,CANER VILDAN,SEN TÜRK NILAY,SARI HAKAN ISMAIL,HACIOGLU SIBEL,DOGU MEHMET HILMI,ÇETIN GÖKHAN OZAN,TEPELI EMRE,CAN ÖZGE,BAGCI GÜLSEREN,KESKIN ALI (2015). Possible Role of GADD45 Methylation in Diffuse Large B Cell Lymphoma Does It Affect the Progression and Tissue Involvement. Turkish Journal of Hematology, 32(4), 295-303., Doi: 10.4274/tjh.2014.0174
  12. CANER VILDAN,SEN TÜRK NILAY,BARIS IKBAL CANSU,ÇETIN GÖKHAN OZAN,TEPELI EMRE,HACIOGLU SIBEL,SARI HAKAN ISMAIL,ZENCIR SEVIL,DOGU MEHMET HILMI,BAGCI GÜLSEREN,KESKIN ALI (2015). MYD88 Expression and L265P Mutation in Mature B Cell Non Hodgkin Lymphomas. Genetic Testing and Molecular Biomarkers, 19(7), 372-378., Doi:10.1089/gtmb.2015.0041
  13. ÇETIN GÖKHAN OZAN,TOYLU ASLI,ATABEY SAFIYE NESE,YÜCE ZEYNEP,Sakızlı Meral (2015).Downregulation of VANGL1 Inhibits Cellular Invasion Rather than Cell Motility in Hepatocellular Carcinoma Cells Without Stimulation. Genetic Testing and Molecular Biomarkers, 19(6), 283-287.,Doi: 10.1089/gtmb.2015.0014
  14. Okur Volkan,ÇETIN GÖKHAN OZAN,ÇETIN EBRU NEVIN,TEPELI EMRE,Yunus Bulgu,YILDIRIM CEM (2015). HIF1A as a major vascular endothelial growth factor regulator do its polymorphisms have an association with age related macular degeneration. Clinical & Experimental Ophthalmology, 43(1), 47-53., Doi: 10.1111/ceo.12376
  15. Bulğu Yunus,ÇETIN GÖKHAN OZAN,CANER VILDAN,ÇETIN EBRU NEVIN,YAYLALI VOLKAN,YILDIRIM CEM (2014). Vascular endothelial growth factor gene polymorphisms in age related macular degeneration in a Turkish population. International Journal of Ophthalmology,7(15), 773-777., Doi: 10.3980/j.issn.2222-3959.2014.05.06
  16. TEPELI EMRE,CANER VILDAN,BÜYÜKPINARBASILI NUR,ÇETIN GÖKHAN OZAN,DÜZCAN FÜSUN,ELMAS LEVENT,BAGCI GÜLSEREN (2012). Expression of ERCC1 and its clinicopathological correlations in non small cell lung cancer. Molecular Biology Reports, 39(1), 335-341., Doi: 10.1007/s11033-011-0743-0
  17. Koç Esin,CANER VILDAN,BÜYÜKPINARBASILI NUR,TEPELI EMRE,SEN TÜRK NILAY,ÇETIN GÖKHAN OZAN,BAGCI GÜLSEREN (2012). The determination of relationship between excision repair cross complementing group 1 ERCC1 gene T19007C and C8092A single nucleotide polymorphisms and clinicopathological parameters in non small cell lung cancer. Molecular Biology Reports, 39(1),375-380., Doi: 10.1007/s11033-011-0748-8
  18. BAGCI GÜLSEREN,ÇETIN GÖKHAN OZAN,SEMERCI CAVIDAN NUR,Toruner Gokce A,Cinbis Mine (2012). Terminal 14q deletion with unbalanced t Y 14 q12 q32 translocation. Clinical Dysmorphology, 21(1), 37-41., Doi: 10.1097/MCD.0b013e32834d6ba3
  19. SEMERCI CAVIDAN NUR,Eser Metin,TUFAN NACIYE LALE,KALKAN TARKAN,ÇETIN GÖKHAN OZAN,ÖZTÜRK Özkan,BAGCI GÜLSEREN (2012). Translocation Y 21 in an Infertile Male Patient Having 45 X Karyotype Case Report. Turkiye Klinikleri Journal of Medical Sciences, 32(6), 1732-1736., Doi: 10.5336/medsci.2011-23453 .
  20. ÖZDEMIR ÖZMERT MUHAMMET ALI,KILIÇ ILKNUR,Küçüktasçı Kazım,GÜRSES DOLUNAY,Karaca A,OTO MURAT,ÇETIN GÖKHAN OZAN,CANER VILDAN (2011). Congenital arterial thrombosis in newborn a case report SCI Expanded Kapsamına Girmektedir. Balkan Medical Journal, 28(3), 331-334., Doi: 10.5174/tutfd.2009.03229.2
  21. DÜZCAN FÜSUN,Düzcan Süleyman Ender,SEN SAIT,YÖRÜKOGLU KUTSAL,CANER VILDAN,SEN TÜRK NILAY,ÇETIN GÖKHAN OZAN,Kelten Canan,TUNA EMINE BURÇIN,SARSIK KUMBARACI BANU,TEPELI EMRE (2011). Expression and Amplification of Topoisomerase-2? in Type 1 and Type2 Papillary Renal Cell Carcinomas and Its Correlation with HER2/neu Amplification. Pathology & Oncology Research, 17(3), 697-703., Doi: 10.1007/s12253-011-9372-0
  22. Canturk Pakize,CANER VILDAN,Oruc Nevin,AKARCA ULUS SALIH,TEPELI EMRE,ÇETIN GÖKHAN OZAN,ZENCIR SEVIL,TOPÇU ZEKI (2010). The mRNA Expression of Cytochrome P450 Isoforms in Human Gastric Tissue. HEPATO-GASTROENTEROLOGY, 57(98), 372-376.
  23. SENGÜL ABDULLAH CEM,Efe Muharrem,TEPELI EMRE,ÇETIN GÖKHAN OZAN,DÜZCAN FÜSUN,HERKEN HASAN (2009). A Case of Schizophrenia Accompanying Velocardiofacial Syndrome. NOROPSIKIYATRI ARSIVI ARCHIVES OF NEUROPSYCHIATRY, 46(1), 27-29.
  24. DÜZCAN FÜSUN,AYBEK ZAFER,TEPELI EMRE,CANER VILDAN,ÇETIN GÖKHAN OZAN,AYBEK HÜLYA,BAGCI HÜSEYIN (2006). Sex chromosome aneuploidy rates in the somatic cells of infertile men. JOURNAL OF REPRODUCTIVE MEDICINE, 51(6), 489-492.
  25. DÜZCAN FÜSUN,Atmaca Münevver,ÇETIN GÖKHAN OZAN,BAGCI HÜSEYIN (2003). Cytogenetic studies in patients with reproductive failure. ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA, 82(1), 53-56.
  26. DÜZCAN FÜSUN,ZENCIR MEHMET,Özdemir Fatma,ÇETIN GÖKHAN OZAN,BAGCI HÜSEYIN,Heutink Peter,Bonifati Vincenzo,Sahiner Türker (2003). Familial influence on parkinsonism in a rural area of Turkey Kizilcaboluk Denizli a community based case control study. MOVEMENT DISORDERS, 18(7), 799-804.

Publications in journals indexed in Pubmed/Scopus/ESCI (not in SCI-e or SCI) (Total 4)

  1. Cetin GO, Caner V, Sen Turk N, Okur V, Can O, Eskicorapci S, Tuncay L, Elmas L, Bagci G. (2014). Correlation of O6 Methylguanine DNA methyltransferase promoter methylation and clinicopathological parameters in bladder cancer. Gene Therapy and Molecular Biology, 16, 181-189. (Yayın No: 1178115)
  2. Can O, Caner V, Sen Turk N, Tuncay OL, Eskicorapci SY, Tepeli E, Cetin O, Baris IC, Bagci G.(2014). GADD45 Methylation Is More Common In Benign Prostatic Hyperplasia Than In Prostate Cancer. Gene Therapy and Molecular Biology, 16, 44-54. (Yayın No: 1178086)
  3. Ayaz A, Tepeli E, Sarı I, Çetin O, Eser M, Dogu H, Bagcı G. (2014). Contribution of MLPA to routine testing to detect the prognostic chromosomal abnormalities in chronic lymphocytic leukemia. Gene Therapy and Molecular Biology, 16, 1-9. (Yayın No: 1178103)
  4. Özden Serap,DÜZCAN FÜSUN,Wollnik Bernd,ÇETIN GÖKHAN OZAN,Sahiner Türker,BAYRAMOGLU ISMET,Yüksel Apak Memnune,BAGCI HÜSEYIN (2002). Progressive autosomal dominant optic atrophy and sensorineural hearing loss in a Turkish family. Ophthalmic Genetics, 23(1), 29-36.

Publications in other peer-review journals (Total 10)

  1. SEKER ÜN EMINE, ÇETIN GÖKHAN OZAN, ÇETIN EBRU NEVIN (2022). Dominant Optik Atrofi./ Dominant optic atrophy. Güncel Retina Dergisi, 6(2), 88-91., Doi: 10.37783/CRJ-0300
  2. ÇETIN GÖKHAN OZAN, ÇETIN EBRU NEVIN (2021). Herediter Retina Hastalıklarında Genetik Geçiş ve Mutasyonlar./ Genetics of hereditary retinal diseases. Güncel Retina Dergisi (Current Retina Journal), Doi: 10.37783/CRJ-0245 (Kontrol No: 7514105)
  3. GÖK SONER,CAN GÖK Berfin,ÇETIN GÖKHAN OZAN (2021). Klinigimizde invazif prenatal tanı yöntemi olarak amniyosentez uygulanan olguların retrospektif degerlendirilmesi. / Retrospective evaluation of patients that underwent amniosynthesis. Pamukkale Tıp Dergisi, 14(1), 215-221., Doi: 10.31362/patd.795264 
  4. ANLAS ÖZLEM, ÇETIN GÖKHAN OZAN, YARARBAS KANAY, DÜZCAN FÜSUN, SEMERCI GÜNDÜZ CAVIDAN NUR, AYAZ AKIF, BAGCI GÜLSEREN (2020). A case of recombinant chromosome 4:further delineation of the clinical features. Pamukkale Tip Dergisi, 13(1), 229-234., Doi:10.31362/patd.644602 (Kontrol No: 6028137)
  5. GÜRSES DOLUNAY,KAYAKIRAN EDA DIDEM,ALBUZ BURCU,ÇETIN GÖKHAN OZAN (2020). Williams-Beuren Sendromlu Çocukların Klinik ve Ekokardiyografk Degerlendirilmesi./Clinical and ecocardiographical features of children with Williams-Beuren Syndrome Turkish J Pediatr Dis, 14, 124-128., Doi: 10.12956/tjpd.2018.400
  6. ÇETIN EBRU NEVIN,ÇETIN GÖKHAN OZAN (2017). Yas Tip (Neovasküler) Yasa Baglı Makula Dejenerasyonunda Risk Faktörleri ve Genetik./ Risk factors and genetics in wet type (neovascular) age related macular degeneration. Güncel Retina, 1(3), 167-172.
  7. ÇETIN GÖKHAN OZAN,SARIKEPE BILGE,AKINCI GÖNEN GIZEM (2016). Psikiyatrik Arastırmalarda Kullanılan Güncel Moleküler Genetik Yöntemler. /Current molecular genetic methods in psyciahtric research. Türkiye Klinikleri Psikiyatri Özel Dergisi, 9(1), 1-4.
  8. Bagcı G, Tepeli E, Düzcan F, Çetin GO, Alatas E. (2010). Familial Translocation 2 18 Ascertained Through Recurrent Spontaneous Abortions. Gynecol Obstet Reprod Med, 16, 190-193.

  9. Düzcan F, Atmaca M, Çetin GO, Tepeli E, Gümüs D, Bagcı H. (2002). Ailesel ve de novo translokasyonların klinik tanı ve fenotipik bulgular ile uyumu. / Correlation of familial and de novo translocations with clinical diagnosis and phenotype. Pamukkale Üniversitesi Tıp Fakültesi Dergisi, 8, 39-43.

    10.  

  10. Düzcan F, Kılıç I, Zencir M, Çetin GO (2001). 1997 1999 yılları arasında Pamukkale Üniversitesi Egitim Uygulama ve Arastırma Hastanesi nde dogan bebeklerde konjenital malformasyon sıklıgı. /Frequency of congenital anomalies in infants between 1997-1999 in Pamukkale University Hospital.  Çocuk Saglıgı ve Hastalıkları Dergisi, 44, 240-246.

 (b)  Conference Papers

Poster or oral presentations in international congresses (Total 34)

  1. BARIS IKBAL CANSU,HACIOGLU SIBEL,SEN TÜRK NILAY,ÇETIN GÖKHAN OZAN,ZENCIR SEVIL,BAGCI GÜLSEREN,CANER VILDAN (2019). Exosomal DNA From Plasma of Patients With DLBCL: Comparison DNA Methylation Patterns Of EZH2-Target Genes Of Exosomes And Matching Primary Tumor Tissue. 7th International Congress on Leukemia Lymphoma Myeloma
  2. BARIS IKBAL CANSU,HACIOGLU SIBEL,SEN TÜRK NILAY,ÇETIN GÖKHAN OZAN,ZENCIR SEVIL,BAGCI GÜLSEREN,CANER VILDAN (2019). The Presence of EZH2 and EZH2-targeted Genes in Exosomes of Diffuse Large B-cell Lymphoma Patients. 13th Balkan Congress of Human Genetics
  3. KIRKGÖZ TARIK,ÖZHAN BAYRAM,ÇETIN GÖKHAN OZAN,KAYGUSUZ SARE BETÜL,DEMIRCIOGLU SERAP,BEREKET ABDULLAH,GÜRAN TÜLAY (2018). Isolated Congenital Central Hypothyroidism due to a Novel Mutation in TSH Beta Subunit Gene. HORMONE RESEARCH IN PAEDIATRICS-57th Annual Meeting of the European Society for Paediatric Endocrinology, 90(null), 597-597.
  4. CANER VILDAN,SEN TÜRK NILAY,ÇETIN GÖKHAN OZAN,ALBUZ BURCU,AY YILMAZ (2018). Coexistence of multiple subclones in ETV6/RUNX1 at diagnosis of B-cell lymphoblastic leukemia.European Human Genetics Conference 2018
  5. ZEYBEK SELCAN,Farre Genis,ÖZTÜRK MENEKSE,ALBUZ BURCU,Beltran Sergi,Bowcock Anne,ÇETIN GÖKHAN OZAN (2018). Further delineation of ACPHD syndrome and a novel mutation in DNAJC3. European Human Genetics Conference 2018
  6. ÖZTÜRK MENEKSE,ZEYBEK SELCAN,DURSUN BELDA,ALBUZ BURCU,BOZ ÖZLEM,GÜRKAN HAKAN,ÇETIN GÖKHAN OZAN (2018). A novel nonsense mutation in the EYA1 gene found in a patient with BOR syndrome. European Human Genetics Conference 2018
  7. ALBUZ BURCU,ÇETIN GÖKHAN OZAN,ÖZTÜRK MENEKSE,CANER VILDAN,SEMERCI GÜNDÜZ CAVIDAN NUR,BAGCI GÜLSEREN (2018). Fetus with partial trisomy 4 and t(216) due to maternal complex rearrangement involving three chromosomes: a case report. European Human Genetics Conference 2018
  8. BOZ ÖZLEM,SARIKEPE BILGE,ZEYBEK SELCAN,ÖZTÜRK MENEKSE,BAGCI GÜLSEREN,ÇETIN GÖKHAN OZAN (2018). The co-existence of Nablus Mask-Like Syndrome and Klinefelter Syndrome. European Human Genetics Conference 2018
  9. ALTIOK CLARK ÖZDEN,ÇETIN GÖKHAN OZAN,NUR BANU,TOYLU ASLI,KARAÜZÜM SIBEL,MIHÇI ERCAN (2017). A de novo ins(2113) and two interstitial deletions in 13q in a boy with multple congenital anomalies. 11th European Cytogenetic Conference, 10(null), 32-33.
  10. CANER VILDAN,BARIS IKBAL CANSU,ÇETIN GÖKHAN OZAN,TEPELI EMRE,SEN TÜRK NILAY,HACIOGLU SIBEL,ZENCIR SEVIL,ÇAGLAYAN G,BAGCI GÜLSEREN (2017). Correlation of plasma exosome concentrations with stage in patients with Diffuse large B-cellLymphoma. 6th International Congress on Leukemia Lymphoma Myeloma

     

  11. CANER VILDAN,ÇETIN GÖKHAN OZAN,TEPELI EMRE,SARIKEPE BILGE,anlas özlem,bağlar menekse,ALBUZ BURCU,atmaca münevver,HACIOGLU SIBEL (2017). MOLECULAR CYTOGENETIC PROFILE OF COMPLEX/VARIANT TRANSLOCATIONS IN CHRONIC MYELOIDLEUKEMIA. 6th International Congress onLeukemia – Lymphoma – Myeloma
  12. SARIKEPE BILGE,ZEYBEK SELCAN,AKINCI GÖNEN GIZEM,EYÜBOGLU TANRIVERDI YASEMIN,BOZ ÖZLEM,CEYLAN EMINE IPEK,TEPELI EMRE,ÇETIN GÖKHAN OZAN,SARI HAKAN ISMAIL,DÜZCAN FÜSUN,CANER VILDAN (2016). Molecular cytogenetics findings of clinically suspected acute myeloid leukemia and or myelodysplastic syndrome AML MDS patients. ESHG 2016
  13. ÇETIN GÖKHAN OZAN,BARIS IKBAL CANSU,CANER VILDAN,SARIKEPE BILGE,SEN TÜRK NILAY,TEPELI EMRE,HACIOGLU SIBEL,SARI HAKAN ISMAIL,BAGCI GÜLSEREN,KESKIN ALI (2016). Mutational status of EZH2 and CD79B hot spots in mature B cell non Hodgkin s ymphomas novel CD79B variations have been revealed. ESHG 2016
  14. ZEYBEK SELCAN,ÇETIN GÖKHAN OZAN,CANER VILDAN,ÖZTÜRK MENEKSE,SEMERCI CAVIDAN NUR,BAGCI GÜLSEREN,ERGIN HACER (2016). The clinical characterization of a patient with 4p15 deletion. ESHG 2016
  15. CANER VILDAN,ZENCIR SEVIL,HACIOGLU SIBEL,BAGCI GÜLSEREN,SARI HAKAN ISMAIL,BARIS IKBAL CANSU,TEPELI EMRE,SEN TÜRK NILAY,ÇETIN GÖKHAN OZAN (2016). An ultracentrifugation based protocol for exosome isolation in diffuse B cell lymphoma. ISEV 2016
  16. CANER VILDAN,SEN TÜRK NILAY,BARIS IKBAL CANSU,ÇETIN GÖKHAN OZAN,TEPELI EMRE,HACIOGLU SIBEL,SARI HAKAN ISMAIL,ZENCIR SEVIL,DOGU MEHMET HILMI,BAGCI GÜLSEREN,KESKIN ALI (2015). MYD88 expression and L265P mutation in mature B cell non Hodgkin lymphomas. 5th International Congress on Leukemia Lymphoma Myeloma, 157-157.
  17. Okur V, Cetin O, Cetin E, Tepeli E, Bulgu Y, Yildirim C (2014). HIF1A as a major vascular endothelial growth factor regulator do its polymorphisms have an association with age related macular degeneration. 14th EURETINA Congress
  18. Cetin O, Caner V, Sen Turk N, Okur V, Can O, Eskicorapci S, Tuncay L, Elmas L, Bagci G (2014). Correlation of O6 Methylguanine DNA methyltransferase promoter methylation and clinicopathological parameters in bladder cancer. European Human Genetics Conference, 22(Supplement 1), 495-495.
  19. Bulgu Y, Çetin G, Caner V, Çetin E, Avunduk A, Yaylalı V, Yıldırım C (2013). Vascular endothelial growth factor polymorphisms in age related macular degeneration. 13th EURETINA Congress
  20. Zeybek S, Çetin O, Fenkçi V, Düzcan F, Atmaca M, Semerci N, Bagcı G (2013). Significance of Parental Karyotyping case report. 9th European Cytogenetics Conference, 21(Supplement 1),139-139.
  21. Can Ö, Caner V, Sen Türk N, Tuncay L, Eskiçorapçı SY, Tepeli E, Çetin GO, Barıs C, Bagcı G (2013). Determination of GADD45 methylation level in prostate cancer with high resolutionmelting analysis and evaluation of the possible correlation with apoptosis. European HumanGenetics Conference, 21(Supplement 2), 316-316.
  22. Baris C, Caner V, Sen Türk N, Sari HI, Kabukçu S, Çetin GO, Tepeli E, Can Ö, Bagci G (2013). Promoter Methylation of GADD45 In Diffuse Large B Cell Lymphoma. 4th International Congress on Leukemia, Lymphoma, Myeloma
  23. Duzcan F, Duzcan SE, Sen S, Yorukoglu K, Caner V, Sen Turk N, Cetin GO, Kelten C, Tuna B, Sarsik B, Tepeli E (2011). Expression and Amplification of Topoisomerase 2 in Type 1 and Type 2 Papillary Renal Cell Carcinomas and Its Correlation with HER2 neu Amplification. 8th European Cytogenetics Conference, 19(Supplement), 173-173.
  24. Cetin GO, Okur V, Kalkan T, Olmez A, Tepeli E, Duzcan F (2011). Developmental delay mental reterdation and facial dysmorphism due to subtelomeric deletion of 7q. 8th European Cytogenetics Conference, 19(Supplement), 95-95.
  25. Çetin O, Okur V, Erdogan M, Kalkan T, Duzcan F (2010). A case with Turner like phenotype carrying iso Y monosomy X mosaicism. European Human Genetics Conference 2010,18(Supplement 1), 118-118.
  26. Eser M, Satıroglu Tufan L, Kalkan T, Çetin G, Öztürk Ö, Bagcı G, Semerci C (2010). Y 21 translocation in infertile male patient with 45 X karyotype. European Human Genetics Conference 2010, 18(Supplement 1), 145-145.
  27. Düzcan F, Çetin O, Tepeli E, Ayaz A. (2010). Prenatally diagnosed two distinct cell lines of 18p terminal deletion monosomy X possibly due to chimerism. European Human Genetics Conference 2010, 18(Supplement 1), 144-144.
  28. Bagci G, Cetin G, Semerci C, Toruner G, Cinbis M (2009). A case of terminal 14q deletion with de novo unbalanced t Y 14 q q32 translocation. 7th European Cytogenetics Conference,17(Supplement ), 66-66.
  29. Cetin G, Erdogan K, Ozdemir O, Kalkan T, Kaleli B, Kilic I, Duzcan F (2009). Prenatally diagnosed de novo inverted duplication of 8p11 2 p23 region with deletion of 8pter in a dysmorphic case. 7th European Cytogenetics Conference, 17(Supplement), 63-64.
  30. Duzcan F, Cetin G, Kalkan T, Erdogan K, Semiz S. (2009). De novo partial trisomy of the subtelomeric region of 1q on 1pter causing dysmorphic features. 7th European Cytogenetics Conference, 17(Supplement), 61-62.
  31. Canturk P, Caner V, Oruc N, Akarca US, Tepeli E, Cetin GO, Zincir S, Topcu Z. (2009). The mRNA Expression Patterns of Cytochrome P450 Isoforms in Relation to Pathological Status of Human Gastric Tissue. 4th EORTC Pathobiology Group Annual Meeting & 1st International Multidisiplinary Cancer Research Congress
  32. Cetin GO, Duzcan F, Tepeli E, Kirac S. (2008). Osteoporosis pseudoglioma syndrome in two sisters. European Human Genetics Conference, 40th Annual Meeting of the ESHG, 16(Supplement 2), 113-113.
  33. Cetin GO, Toylu A, Atabey N, Sercan Z, Sakizli M. (2008). VANGL1 effects cell invasion rather than cell motility. European Human Genetics Conference, 40th Annual Meeting of the ESHG, 16(Supplement 2), 237-237.
  34. Duzcan F, Zencir M, Sahiner T, Akalin O, Celiker A, Cetin GO. (2000). High prevalence of Parkinson s Disease in Kızılcabölük Denizli Turkey familial influence and Na sulphate compound as possible risk factors. European Human Genetics Conference, 32nd Annual Meeting of the ESHG, 172-173.

7. References

Names and Contact Information of at Least 3 References

Nese Atabey- Professor of Medical Biology, Medical School of Izmir Tinaztepe University, Department of Medical Biology, and Izmir Biogenome Center, Izmir, Türkiye nese.atabey@tinaztepe.edu.tr

Uğur Özbek- Professor of Medical Genetics,  Medical School of Acibadem Mehmet Ali Aydınlar University, Department of Medical Genetics, İstanbul, Türkiye ugur.ozbek@acibadem.edu.tr

Anne M. Bowcock, Professor of Dermatology, Oncological Sciences, and Genetics and Genomic Sciences at the Icahn School of Medicine at Mount Sinai, New York, NY, USA anne.bowcock@mssm.edu

 

Updated Date:12/14/2023 10:45:16 AM

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