Education Information
2012 - 2017
2012 - 2017Doctorate
Eskisehir Osmangazi University, Sağlık Bilimleri Enstitüsü, Tıbbi Genetik (Dr), Turkey
2008 - 2012
2008 - 2012Postgraduate
Eskisehir Osmangazi University, Sağlık Bilimleri Enstitüsü, Tıbbi Genetik (Yl) (Tezli), Turkey
2003 - 2008
2003 - 2008Undergraduate
Eskisehir Osmangazi University, Fen-Edebiyat Fakültesi, Biyoloji Bölümü, Turkey
Dissertations
2017
2017Doctorate
Frontotemporal lobar dejenerasyon spektrumunda C9orf72 geni GGGGCC heksanükleotid tekrar artışları ile fenotipik çeşitliliğin karşılaştırılması
Eskisehir Osmangazi University, Sağlık Bilimleri Enstitüsü, Tıbbi Genetik (Dr)
2012
2012Postgraduate
Mesane kanserli olguların mesane yıkama sıvılarında moleküler markerların fısh yöntemi ile incelenmesi 
Eskisehir Osmangazi University, Sağlık Bilimleri Enstitüsü, Tıbbi Genetik (Yl) (Tezli)
Research Areas
Medical Genetics
Academic Titles / Tasks
2019 - Continues
2019 - ContinuesAssistant Professor
Eskisehir Osmangazi University, Tıp Fakültesi, Dahili Tıp Bil. Bölüm
2017 - 2019
2017 - 2019Research Assistant PhD
Eskisehir Osmangazi University, Tıp Fakültesi, Dahili Tıp Bil. Bölüm
2012 - 2017
2012 - 2017Research Assistant
Eskisehir Osmangazi University, Sağlık Bilimleri Enstitüsü
Advising Theses
2021
2021Postgraduate
Alzheimer ve Vasküler Demans Tanısında miRNA-29a ve miRNA-31'in Biyobelirteç Olarak Değerlendirilmesi
Erzurumluoğlu Gökalp E. (Advisor)
A.AKBAŞ(Student)
2021
2021Postgraduate
Parkinson hastalığında GRIN2B gen polimorfizmlerinin dürtü kontrol bozukluğu ile ilişkisi
Erzurumluoğlu Gökalp E. (Advisor)
G.MEMARI(Student)
Published journal articles indexed by SCI, SSCI, and AHCI
2022
2022Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
Dundar M., Fahrioglu U., Yildiz S. H., Bakir-Gungor B., Temel S. G., Akin H., et al.
FUNCTIONAL & INTEGRATIVE GENOMICS, vol.22, no.3, pp.291-315, 2022 (SCI-Expanded)
2022
2022NDE1-related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephaly
BAŞ H., ŞAYLISOY S., ÇİLİNGİR O., Gokalp E., KOCAGİL S., YARAR C., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol.188, no.1, pp.326-331, 2022 (SCI-Expanded)
2021
2021An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3
IŞIK S., Gunden G., GÜNDÜZ E., Akay O. M., Aslan A., ÖZEN H., et al.
CYTOGENETIC AND GENOME RESEARCH, vol.161, no.10-11, pp.479-487, 2021 (SCI-Expanded)
2021
2021The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide synthase 3 gene polymorphisms
Ilguy S., Cilingir O., Bilgec M. D., Ozalp O., Erzurumluoglu Gokalp E., Arslan S., et al.
OPHTHALMIC GENETICS, vol.42, no.6, pp.725-731, 2021 (SCI-Expanded)
2021
2021A pediatric BAL case with double Ph chromosomes and trisomy 5
Gunden G., Işık S., Özdemir C., Çilingir O., Bör Ö., Gokalp E. E., et al.
Cancer Genetics, vol.258, pp.7-9, 2021 (SCI-Expanded)
2021
2021Frequency of frontotemporal dementia-related gene variants in Turkey
Artan S., Erzurumluoğlu Gökalp E., Samancı B., Ozbabalik Adapinar D., Bas H., Tepgec F., et al.
Neurobiology of Aging, vol.106, 2021 (SCI-Expanded)
2021
2021A new four-way complex translocation variant involving the t(8;5;21;4)(q21;q13,q22,q31) and the relocalization of AML1/ETO fusion gene
Işık S., Üsküdar Teke H., Gunden G., Erzurumluoğlu Gökalp E., Çilingir O., Artan S., et al.
Cancer Genetics, vol.256, pp.1-4, 2021 (SCI-Expanded)
2021
2021A novel SACS p.Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-Saguenay
Samanci B., Gokalp E. E., BİLGİÇ B., GÜRVİT İ. H., ARTAN S., Hanagasi H. A.
Neurological Sciences, vol.42, no.7, pp.2969-2973, 2021 (SCI-Expanded)
2021
2021Association of eleven single nucleotide polymorphisms with refractive disorders from Eskisehir, Turkey
Unlu N., Gokalp E. E., Arslan S., Çilingir O., Bilgin M., Yıldırım E., et al.
International Journal of Ophthalmology, vol.14, no.6, pp.812-817, 2021 (SCI-Expanded)
2021
2021A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer’s disease
Guven G., Samanci B., Gulec C., Hanagasi H., GÜRVİT İ. H., Gokalp E. E., et al.
Neurological Sciences, vol.42, no.6, pp.2497-2504, 2021 (SCI-Expanded)
2021
2021Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients.
Ulus T., Dural M., Meşe P., Yetmiş F., Mert K. U., Görenek B., et al.
Anatolian journal of cardiology, vol.25, no.2, pp.129-138, 2021 (SCI-Expanded)
2021
2021Which prognostic marker is responsible for the clinical heterogeneity in CLL with 13q deletion?
Durak Aras B., Isik S., Uskudar Teke H., Aslan A., Yavasoglu F., Gulbas Z., et al.
Molecular cytogenetics, vol.14, no.1, pp.2, 2021 (SCI-Expanded)
2020
2020A Turkish patient with novel AHCY variants and presumed diagnosis of S-adenosylhomocysteine hydrolase deficiency
BAŞ H., ÇİLİNGİR O., TEKİN N., ŞAYLISOY S., DURAK ARAS B., Uzay E., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol.182, no.4, pp.740-745, 2020 (SCI-Expanded)
2019
2019The association between repeat number in C9orf72 and phenotypic variability in Turkish patients with frontotemporal lobar degeneration
ERZURUMLUOĞLU GÖKALP E., ÇİLİNGİR O., Adapinar B. D. O., Bilgic B., Kocagil S., ÖZEN H., et al.
Neurobiology of Aging, vol.76, 2019 (SCI-Expanded)
2019
2019An Interstitial 6q25.1 Microdeletion Syndrome in a Patient with Dysmorphic Features, Intellectual Dysability and Stereotypical Movements.
Kocagil S., Durak Aras B., Erzurumluoğlu Gökalp E., Çilingir O., Aynacı S., Artan S.
Balkan Journal Of Medical Genetics, vol.22, no.1, pp.85, 2019 (SCI-Expanded)
2019
2019Importance of Cytocenetic Analysis in Hematological Malignancies: with Two Rare Cases Reports
Işık S., Günden G., Çilingir O., Eker İ., Üsküdar Teke H., Gündüz E., et al.
Balkan Journal Of Medical Genetics, vol.22, no.1, pp.76, 2019 (SCI-Expanded)
2019
2019The 15q11.2 BP1-BP2 Microdeletion Syndrome with Variable Expressivity.
Erzurumluoğlu Gökalp E., Çilingir O., Durak Aras B., Kocagil S., Susam E., Artan S.
Balkan Journal Of Medical Genetics, vol.22, no.1, pp.92, 2019 (SCI-Expanded)
2017
2017Association of functional RAGE gene polymorphisms with Parkinson’s disease in a Turkish cohort
ÇİLİNGİR O., ÖZKAN S., DURAK ARAS B., ERZURUMLUOĞLU E., KUTLAY Ö., EMİR B., et al.
Biomedical Research-India, vol.28, no.19, pp.8454-8460, 2017 (SCI-Expanded)
2017
2017De novo 7q31 deletion involving FOXP2 gene associated with speech disability
ERZURUMLUOĞLU GÖKALP E., Ozdemir M., Kocagil S., ÇİLİNGİR O., Tosumoglu E., DURAK ARAS B., et al.
MOLECULAR CYTOGENETICS, vol.10, 2017 (SCI-Expanded)
2013
2013Quantitation of Gene Copy Numbers of Aurora Kinases In Exfoliated Cells From Bladder Washings and Bladder Cancer Detection
ERZURUMLUOĞLU GÖKALP E., ARTAN S., Can C., Canturk M., Aras I., Ozdemir M., et al.
CHROMOSOME RESEARCH, vol.21, 2013 (SCI-Expanded)
Articles Published in Other Journals
2023
2023Analyzing The Mutations Of Notch1 And Sf3b1 Genes In Cases With CLL Detected Isolated 13q Deletion
Günden G., Işık S., Üsküdar Teke H., Çilingir O., Oğuz Davutoğlu N., Erzurumluoğlu Gökalp E., et al.
Osmangazi Tıp Dergisi, vol.45, no.2, pp.480-484, 2023 (Peer-Reviewed Journal)
2022
2022Evaluation of the Effect of Circulating IncRNAs in Colorectal Cancers: As a Potential Biomarker
ARSLAN S., DİNCER M., BAYIR D., EKER SARIBOYACI A., ERZURUMLUOĞLU GÖKALP E., KOCAGİL S., et al.
TURK ONKOLOJI DERGISI, vol.37, pp.305-313, 2022 (ESCI)
2021
2021The Importance of FISH Test Targeting EGFR, CCND1and RREB1 Genes in Differentiating MalignantMelanomas from Melanocytic Nevus
Işık S., Töre T., Canaz F., Özen H., Erzurumluoğlu Gökalp E., Çilingir O., et al.
Osmangazi Tıp Dergisi, vol.43, no.5, 2021 (Peer-Reviewed Journal)
2021
2021Extra Chromosome, Extra Love
Aras B., Işık S., Baş H., Ocal E. E., Gokalp E., Çilingir O., et al.
GAZI MEDICAL JOURNAL, vol.32, no.1, pp.83-87, 2021 (ESCI)
2020
2020Bağımlılıkta Genetiğin Katkısına Genel Bir Bakış
ERZURUMLUOĞLU GÖKALP E., ARTAN S.
Türkiye Klinikleri Farmakoloji - Özel Konular, 2020 (Non Peer-Reviewed Journal)
2020
2020Türk Popülasyonunda APOE Polimorfizmleri ve Alzheimer Hastalığı Arasındaki İlişki
ÇİLİNGİR O., ÖZBABALIK ADAPINAR B. D., DURAK ARAS B., ERZURUMLUOĞLU GÖKALP E., ÖZKAN S., ARSLAN S., et al.
OSMANGAZİ JOURNAL OF MEDICINE, 2020 (Peer-Reviewed Journal)
2018
2018Ailesel Akdeniz Ateşi Tanısı Alan Olgularda MEFV Geni Mutasyonlarının ve Allel Frekanslarının Dağılımı - Tek Merkez Deneyimi
ÇİLİNGİR O., DURAK ARAS B., ARSLAN S., KUTLAY Ö., ERZURUMLUOĞLU E., KOCAGİL S., et al.
Osmangazi Tıp Dergisi, vol.40, no.2, pp.39-46, 2018 (Peer-Reviewed Journal)
2018
2018Prenatal Sitogenetik Anomalilerde İleri Tanı Yöntemi Olarak Array CGH
ERZURUMLUOĞLU E., ARTAN S.
Türkiye Klinikleri Tıbbi Genetik Özel Dergisi, vol.3, no.1, pp.63-69, 2018 (Non Peer-Reviewed Journal)
2018
2018The Relationship between Glutathione-S-Transferases Polymorphisms and Lichen Planus Susceptibility
ÇİLİNGİR O., BULUR I., DURAK ARAS B., KUTLAY Ö., ERZURUMLUOĞLU E., HAZİYEVA K., et al.
International Journal of Research Studies in Medical and Health Sciences, vol.3, no.1, pp.15-22, 2018 (Peer-Reviewed Journal)
2018
2018Glutathıone S-Transferases M1/T1 and P1 Polymorphisms in Patıents with Alopecia Areata
Çilingir O., Saraçoğlu Z. N., Durak Aras B., Haziyeva K., Kutlay Ö., Erzurumluoğlu E., et al.
International Journal of Research Studies in Medical and Health Sciences V, vol.3, no.2, pp.1-8, 2018 (Peer-Reviewed Journal)
2015
2015The effects of a heterochromatin polymorphism in chromosome 6 on premature ovarian failure
KÜÇÜK H., AYDIN Y., ERZURUMLUOĞLU E., ÖZDEMİR M., HASSA H., ARTAN S.
Asian Pacific Journal of Reproduction, vol.4, no.1, pp.41-43, 2015 (Scopus)
Refereed Congress / Symposium Publications in Proceedings
2022
2022COQ8A varyantlarına bağlı otozomal-resesif serebellar ataksi tip 2: İki nadir aile
Erzurumluoğlu Gökalp E., Şahin E.
15. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 8 - 13 November 2022
2022
2022Nörogelişimsel Bozukluk ve/veya Konjenital Anomali Saptanan Olgularda Kromozomal Mikrodizin Analizleri: Tek Merkez Deneyimi
AYNACI S., ERZURUMLUOĞLU GÖKALP E., ÇARMAN K. B., ARTAN S.
15. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 09 November 2022
2022
2022Demans hastalarında plazma sTREM2 düzeyi: TREM2 varyantları ve beyin omurilik sıvısındaki amiloid ve tau düzeyleri ile ilişkisi
GÜVEN Z. G., SAMANCI B., GEZEGEN H., ULUKAN Ç., ŞAHİN E., HANAĞASI H. A., et al.
15. Ulusal Tıbbi Genetik Kongresi, 09 November 2022
2022
2022Deep Brain Stimulation for Rare Neurodegenerative Diseases: Three-Center Experience
DURMAZ ÇELİK F. N., SAMANCI B., YALÇIN ÇAKMAKLI G., AKSOY GÜNDOĞDU A., ERZURUMLUOĞLU GÖKALP E., SAMANCI M. Y., et al.
International Congress of Parkinson's Disease and Movement Disorders, Madrid, Spain, 16 September 2022, vol.37, pp.148-149
2022
2022NANCE-HORAN SYNDROME: AN ULTRA RARE PHENOTYPE DIGNOSED IN A FAMILY WITH FEMALE SIBLING AFFECTED AS SEVERE AS THE MALE
Kocagil S., Kaplan E., Erzurumluoğlu Gökalp E.
EuroDysmorpho 2022, Barcelona, Spain, 14 - 17 September 2022, pp.95-96
2022
2022Kronik Myeloid Lösemi Hastalarının Sentrozom Defekti ve Nadir Kromozom Anomalileri
Günden G., Işık S., Oğuz Davutoğlu N., Erzurumluoğlu Gökalp E.
7. Erciyes Uluslararası Tıp Tıbbi Genetik Kongresi , Kayseri, Turkey, 26 - 28 May 2022, pp.1-2
2021
2021POSSIBLE GENETIC CAUSES OF NEURODEGENERATIVE DEMENTIAS IN TURKISH POPULATION
ERZURUMLUOĞLU GÖKALP E., SAMANCI B.
1st International Balkan Congress on Neurology & Neuroscience, Turkey, 01 October 2021
2021
2021Meme Kanserindeki Kromozom 17 Anösomileri
GÜNDEN G., ERZURUMLUOĞLU GÖKALP E.
1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Turkey, 25 November 2021
2021
2021NEW TSC2 MUTATION IN A RARE CASE WITH KERATOCONUS AND TUBEROUS SCLEROSIS
ÖREN D., EROL M. A., ERZURUMLUOĞLU GÖKALP E., YILDIRIM N.
12th Eucornea Congress, France, 24 - 26 September 2021
2021
2021A NOVEL FRAMESHIFT VARIANT IN A PATIENT WITH CHD8-RELATED OVERGROWTH SYNDROME
KOCAGİL S., KEKLİKCİ A. R., KILIÇ YILDIRIM G., ÇİLİNGİR O., ERZURUMLUOĞLU GÖKALP E., DURAK ARAS B., et al.
31TH EUROPEAN MEETING ON DYSMORPHOLOGY ONLINE, Germany, 23 - 25 September 2021, vol.1, pp.34-35
2020
2020Atipik bulguları olan Smith-Magenis sendromlu bir olgu sunumu
SARAÇ E., ÖZBAKIR D. H., KOCAGİL S., ERZURUMLUOĞLU GÖKALP E., ÇİLİNGİR O., DURAK ARAS B., et al.
14. ULUSAL TIBBİ GENETİK KONGRESİ’xx’xxULUSLARAARSI KATILIMLI’xx’xx, Turkey, 20 - 22 November 2020, vol.31, pp.92
2019
2019CADASIL TANISINDA NOTCH3 GENMUTASYONLARININ YORUMLANMASI
DURMAZ ÇELİK F. N., AYKAÇ Ö., ERZURUMLUOĞLU GÖKALP E., ARTAN S., ÖZKAN S., ÖZDEMİR A. Ö.
3rd Stroke Academy of Turkey Special Issue, Turkey, 3 - 06 October 2019
2020
2020İzole Del13q Kronik Lenfositik Lösemi Olgularında NOTCH1 ve SF3B1 Genlerinin Mutasyonel Durumu
günden g., IŞIK S., ÜSKÜDAR TEKE H., ERZURUMLUOĞLU GÖKALP E., ÇİLİNGİR O., ARTAN S., et al.
14. ULUSAL TIBBİ GENETİK KONGRESİ’xx’xxULUSLARAARSI KATILIMLI’xx’xx, Turkey, 20 - 22 November 2020, vol.31, pp.28
2020
2020A Rare Form Of Constitutional Chromoanasynthesis: Ring Chromosome 18
Susam E., Erzurumluoğlu Gökalp E., Tosumoğlu E., Kocagil S., Çilingir O., Durak Aras B., et al.
14. ULUSAL TIBBİ GENETİK KONGRESİ’xx’xxULUSLARAARSI KATILIMLI’xx’xx, Ankara, Turkey, 20 - 22 November 2020, vol.31, pp.15
2020
2020Prenatal tanıda kromozomal mikroarrayin kullanımı: 423 olgu üzerinden merkezimizin deneyimi
BAŞ H., ERZURUMLUOĞLU GÖKALP E., BÜTÜN Z., SUMAN K., KHADEM ANSARİ S., ARTAN S.
14. ULUSAL TIBBİ GENETİK KONGRESİ, Turkey, 20 - 22 November 2020, vol.31, pp.12
2020
2020Genetic analysis of a large Osteogenesis Imperfecta Family
Çilingir O., Erzurumluoğlu Gökalp E.
14. ULUSLARARASI KATILIMLI ULUSAL TIBBİ GENETİK KONGRESİ, Ankara, Turkey, 20 - 22 November 2020, vol.31, pp.47
2020
2020A complex chromosomal rearrangement in a patient with developmental delay and dysmorphic features
AYNACI S., TOSUMOĞLU E., KEKLİKÇİ A. R., KOCAGİL S., ERZURUMLUOĞLU GÖKALP E., ÇİLİNGİR O., et al.
14. ULUSAL TIBBİ GENETİK KONGRESİ’xx’xxULUSLARAARSI KATILIMLI’xx’xx, Turkey, 20 - 22 November 2020, vol.31, pp.94
2020
2020Prenatal Tanıda QF-PCR’ın Kullanımı: Kendi Tanı Merkezimizdeki Nadir Vakalar Üzerinden Avantaj ve Dezavantajlarının Örneklendirilmesi
KHADEM ANSARİ S., TEMENA A., BAŞ H., DURAK ARAS B., ÇİLİNGİR O., ERZURUMLUOĞLU GÖKALP E., et al.
14. ULUSAL TIBBİ GENETİK KONGRESİ’xx’xxULUSLARAARSI KATILIMLI’xx’xx, Turkey, 20 - 22 November 2020, vol.31, pp.12
2020
2020Genetic variants associated with long term atrial tachyarrhythmia recurrence aftercatheter ablation for atrial fibrillation in Turkish patients
ULUS T., DURAL M., MEŞE P., YETMİŞ F., MERT K. U., GÖRENEK B., et al.
36. Uluslararası Katılımlı Türk Kardiyoloji Kongresi, Online, Turkey, 3 - 06 December 2020
2020
2020Saraç E., Özbakır D. H., Kocagil S., Erzurumluoğlu Gökalp E., Çilingir O., Durak Aras B., et al.
14. ULUSAL TIBBİ GENETİK KONGRESİ, 20 - 22 November 2020, pp.91
2020
2020KML olgularında Ph kromozomuna ek kromozomal anomaliler ve varyant t(922) tek merkez deneyimi
DURAK ARAS B., IŞIK S., GÜNDÜZ E., RAŞAN M. B., GÜNDEN G., ÇİLİNGİR O., et al.
46.Ulusal Hematoloji Kongresi, Turkey, 28 - 31 October 2020
2020
2020A Novel Mutation of DYSF Gene in A Patient with Limb Girdle Muscular Dystrophy Type 2b
KOCAGİL S., KAPLAN E., SUSAM E., DURAK ARAS B., ARTAN S., ERZURUMLUOĞLU GÖKALP E., et al.
European Human Genetics Virtual Conference, 06 June 2020
2019
2019Screening by Multiple ligation – dependent probe amplification assay of AZF a, b, c regions in primary infertile men with azoospermia
HAZİYEVA K., ÇİLİNGİR O., DURAK ARAS B., ÜRE İ., ERZURUMLUOĞLU GÖKALP E., TOSUMOĞLU E., et al.
ESHG 2019, 15 - 19 June 2019
2019
2019Assessment of genes known to be associated with MODY by next-generation sequencing
ÇİLİNGİR O., DURAK ARAS B., ŞİMŞEK E., ÇINAR D., TEMENA M. A., ARSLAN S., et al.
ESHG 2019, 15 - 19 June 2019, vol.27
2019
2019EVALUATING THE FREQUENCIES OF EGFR, ALK/EML4, AND ROS1 ALTERATIONS IN LUNG CANCER: A SINGLE-CENTER EXPERIENCE
DURAK ARAS B., ÇİLİNGİR O., IŞIK S., ARSLAN S., DÜNDAR E., AK G., et al.
ESHG 2019, 15 - 19 June 2019
2019
2019MACROORCHIDISM AS A UNIQUE SIGN IN 3q13.31 DELETION SYNDROME
SUSAM E., ÇİLİNGİR O., DURAK ARAS B., ERZURUMLUOĞLU GÖKALP E., KOCAGİL S., ARTAN S.
ESHG 2019, Gothenburg, Sweden, 15 - 19 June 2019, vol.27, pp.1843
2019
2019KLL’de 13q delesyon büyüklüğünün önemi
IŞIK S., GÜNDEN G., AKAY O. M., ÇİLİNGİR O., ERZURUMLUOĞLU GÖKALP E., GÜNDÜZ E., et al.
45.Ulusal Hematoloji Kongresi, Turkey, 30 October - 02 November 2019
2019
2019Evaluating the frequencies of EGFR, ALK/EML4, and ROS1 in lung cancer: Asingle-center expreince
Durak Aras B., Çilingir O., Işık S., Arslan S., Dündar E., Ak G., et al.
52nd Conference of European Society of Human Genetics, 15 - 18 June 2019
2019
2019An interstitial 6q25.1 microdeletion syndrome in a patient with dysmorphic features, intellectual dysability and stereotypical movements
KOCAGİL S., DURAK ARAS B., ERZURUMLUOĞLU GÖKALP E., ÇİLİNGİR O., AYNACI S., ARTAN S.
13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.85
2019
2019THE RARE ABNORMALITIES OF CHROMOSOME 1 IN MYELOIDMALIGNANCIES
Gunden G., Isik S., Cilingir O., Davutoglu N. O., Yavasoglu F., EKER İ., et al.
13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.184
2019
2019IMPORTANCE OF CYTOGENETIC ANALYSIS IN HEMATOLOGICALMALIGNANCIES: WITH TWO RARE CASES REPORTS
IŞIK S., Gunden G., Cilingir O., EKER İ., USKUDAR TEKE H., Gunduz E., et al.
13 th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.76
2019
2019The 15q11.2 BP1–BP2 Microdeletion Syndrome with Variable Expressivity
ERZURUMLUOĞLU GÖKALP E., ÇİLİNGİR O., DURAK ARAS B., KOCAGİL S., SUSAM E., ARTAN S.
13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.95
2019
2019A RARE CASE OF FRONTOTEMPORAL LOBAR DEGENERATION CAUSED BY VARIANTS OF GRN AND CHMP2B GENES
ARTAN S., ERZURUMLUOĞLU GÖKALP E., ÖZBABALIK ADAPINAR B. D., BAŞ H., ÇİLİNGİR O., DURAK ARAS B.
FENS Regional Meeting 2019, Belgrade, Serbia, 10 - 13 July 2019
2019
2019DO INTERMEDIATE REPEAT EXPANSION LENGTH IN C9ORF72 HAVE AN EFFECT ON CLINICS IN CASES WITH FRONTOTEMPORAL LOBAR DEGENERATION?
ERZURUMLUOĞLU GÖKALP E., ÖZBABALIK ADAPINAR B. D., TEPGEÇ F., ÇİLİNGİR O., BİLGİÇ B., KOCAGİL S., et al.
FENS Regional Meeting 2019, Belgrade, Serbia, 10 - 13 July 2019
2019
2019Clinical use of chromosomal microarray analysis in detection of fetal chromosomal abnormalities
ARTAN S., BAŞ H., ERZURUMLUOĞLU GÖKALP E., VELİPAŞAOĞLU M., KOCAGİL S., DURAK ARAS B., et al.
12th EuropeanCytogenomics Conference 2019, Salzburg, Austria, 6 - 09 July 2019, vol.12
2019
2019A patient with a balanced inversion of chromosome 11 and unbalanced inversion of chromosome 2
SUSAM E., ÇİLİNGİR O., BAŞ H., DURAK ARAS B., ERZURUMLUOĞLU GÖKALP E., ARTAN S.
Erciyes Meidcal Genetics Days 2019, Kayseri, Turkey, 21 - 23 February 2019, vol.41, pp.20
2019
2019THE RARE ABNORMALITIES OF CHROMOSOME 1 IN MYELOIDMALIGNANCIES
Gunden G., IŞIK S., ÇİLİNGİR O., OĞUZ DAVUTOĞLU N., YAVAŞOĞLU F., EKER İ., et al.
13th Balkan Congress of Human Genetics, 17 - 20 April 2019
2018
2018Frontotemporal Lobar Dejenerasyon Spektrumunda Aday Genlerin Değerlendirilmesi
ARTAN S., ERZURUMLUOĞLU E., ÖZBABALIK ADAPINAR B. D., TEPGEÇ F., ÇİLİNGİR O., BİLGİÇ B., et al.
54. Ulusal Nöroloji Kongresi, Turkey, 1 - 05 December 2018
2018
2018NPHP1 HOMOZİGOT GEN DELESYONU SAPTANAN JOUBERT SENDROMU TİP 4 TANILI İKİ OLGU SUNUMU
KOCAGİL S., eren m. c., ELMAS M., YARAR C., ERZURUMLUOĞLU GÖKALP E., ÇİLİNGİR O., et al.
Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 7 - 11 November 2018, pp.119
2018
2018PGRN RS5848 POLİMORFİZMİ TÜRK FTLD KOHORTU İÇİN BİR RİSK FAKTÖRÜ MÜDÜR?
ERZURUMLUOĞLU GÖKALP E., ÖZBABALIK ADAPINAR B. D., ÇİLİNGİR O., EKENEL E. Q., ARTAN S.
Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Turkey, 7 - 11 November 2018, pp.149
2019
2019CADASIL Tanısında Notch3 Gen Mutasyonlarının Yorumlanması
DURMAZ ÇELİK F. N., AYKAÇ Ö., ERZURUMLUOĞLU GÖKALP E., ARTAN S., ÖZKAN S., ÖZDEMİR A. Ö.
3. Türkiye İnme Akademisi, Muğla, Turkey, 3 - 06 October 2019, vol.25, pp.165
2018
2018CYP21A2 mutations in congenital adrenal hyperplasia due to 21 hydroxylase deficiency in Turkish population
ÇİLİNGİR O., ŞİMŞEK E., DURAK ARAS B., ERZURUMLUOĞLU E., TEMENA A., KOCAGİL S., et al.
European Human Genetics Conference 2018, Milan, Italy, 16 - 19 June 2018
2018
2018Distribution of BRAF gene mutations in the patients with malignant melanoma
ÇİLİNGİR O., DİNCER M., ARSLAN S., DURAK ARAS B., ERZURUMLUOĞLU E., KUTLAY Ö., et al.
European Human Genetics Conference 2018, Milan, Italy, 16 - 19 June 2018
2018
2018Comparison of phenotypic variability with C9orf72 gene GGGGCC hexanucleotide repeat expansion in frontotemporal lobar degeneration spectrum
ERZURUMLUOĞLU E., ÇİLİNGİR O., ÖZBABALIK ADAPINAR B. D., BİLGİÇ B., KOCAGİL S., DURAK ARAS B., et al.
European Human Genetics Conference 2018, Milan, Italy, 16 - 19 June 2018
2018
2018Assesment of candidate genes in patients with frontotemporal lobar degeneration spectrum: preliminary findings
ARTAN S., ERZURUMLUOĞLU E., ÇİLİNGİR O., ÖZBABALIK ADAPINAR B. D., TEPGEÇ F., BAŞ H., et al.
European Human Genetics Conference 2018, Milan, Italy, 16 - 19 June 2018
2018
2018SEVERE PELIZAEUS - MERZBACHER DISEASE ON A CASE WITH DEVELOPMENTAL DELAY AND ABNORMAL MYELINATION
BAŞ H., YARAR C., ERZURUMLUOĞLU E., DURAK ARAS B., KOCAGİL S., ARTAN S.
Erciyes Medical Genetics Days 2018, Turkey, 7 - 10 March 2018
2018
2018Parsiyel Trizomi 15 tanımlanan 2 kardeş olgu
KOCAGİL S., TEKİN A. N., ERZURUMLUOĞLU E., ÇAKIL SAĞLIK A., Tosumoğlu E., ARTAN S.
Ulusal Neonatoloji Kongresi (UNEKO-26), Girne, Cyprus (Kktc), 14 - 18 April 2018, pp.221
2017
2017De novo 7q31 deletion involving FOXP2 gene associated with speech disability
ERZURUMLUOĞLU E., ÖZDEMİR M., KOCAGİL S., ÇİLİNGİR O., TOSUMOĞLU E., DURAK ARAS B., et al.
11th European Cytogenetic Conference 2017, 1 - 04 July 2017, vol.10
2017
2017A New Mutation Associated With Bannayan Riley Ruvalcaba Syndrome
ÇİLİNGİR O., ÖZDEMİR M., YARAR C., ERZURUMLUOĞLU E., DURAK ARAS B., KOCAGİL S., et al.
Erciyes Tıp Genetik Günleri, Turkey, 11 - 13 May 2017, vol.39
2017
2017S-adenosylhomocysteine hydrolase deficiency: a Turkish girl with novel mutations in the AHYC gene. European Human Genetics Conference
ÇİLİNGİR O., TEKİN A. N., DURMUŞ AYDOĞDU S., ÖZDEMİR M., DURAK ARAS B., UZAY E., et al.
European Human Genetics Conference, 27 - 31 May 2017
2017
2017The frequencies of CFTR M470V, intron 8 poly-T and pathogenic mutations in cystic fibrosis patients
ARTAN S., ÇİLİNGİR O., DURMUŞ AYDOĞDU S., ERZURUMLUOĞLU E., KOCAGİL S., DURAK ARAS B., et al.
European Human Genetics Conference, 27 - 30 May 2017
2017
2017The frequencies of CFTR M470V, intron 8 poly-T and pathogenic mutations in cystic fibrosis patients
ARTAN S., ÇİLİNGİR O., DURMUŞ AYDOĞDU S., ERZURUMLUOĞLU E., KOCAGİL S., DURAK ARAS B., et al.
European Human Genetic Conference 2017, 27 - 30 May 2017
2016
2016Association of GSTM1 GSTT1 and GSTP1 gene polymorphisms of Lichen Planus in Turkish population
ARTAN S., BULUR I., ASLAN H., DURAK ARAS B., ÖZDEMİR M., KUTLAY Ö., et al.
ESHG-2016, 21 - 24 June 2016
2016
2016A novel mutation in SLC16A2 gene in a Turkish boy with Allan-Herndon-Dudley Syndrome
TAŞDELEN E., BAŞ V., ASLAN H., ÇİLİNGİR O., ERZURUMLUOĞLU E., ÖZDEMİR M., et al.
ESHG-2016, 21 - 24 June 2016
2016
2016Association of functional RAGE gene polymorphisms in the pathogenesis of inflammatory with Parkinson s disease in Turkish population
ASLAN H., ÇİLİNGİR O., ÖZDEMİR M., DURAK ARAS B., KUTLAY Ö., ERZURUMLUOĞLU E., et al.
ESHG 2016, 21 - 24 June 2016
2016
2016Mesane Kanserli OlgularınMesane Yıkama Sıvılarında AURKA ve AURKB Gen Değişikliklerinin FISH Yöntemi ile İncelenmesi
ERZURUMLUOĞLU E., ARTAN S., CAN Y. S. C., cantürk k. m., aras i., ÖZDEMİR M., et al.
2. Ege Hematoloji Onkoloji Kongresi, Turkey, 18 - 20 March 2016
2016
2016PATERNALLY INHERITED PROXIMAL 22Q11.2 DELETION IN TWOSIBLINGS
ÖZDEMİR M., KÜÇÜK H., TEKİN A. N., ERZURUMLUOĞLU E., ASLAN H., DURAK ARAS B., et al.
Medical Genetics and Clinical Applications (with International Participation), Turkey, 11 - 13 February 2016
2016
2016A Clinical Report of an Infant with Russel Silver Sendrom
ÖZDEMİR M., ÖNÜR H., TEKİN A. N., ERZURUMLUOĞLU E., ASLAN H., DURAK ARAS B., et al.
Gevher Nesibe Tıp Günleri 2016 Tıbbi Genetik ve Klinik Uygulamaları Kongresi, Turkey, 11 - 13 February 2016
2015
2015Prenatal diagnosis of 16p duplication presenting with ultrasound abnormalities
ÇİLİNGİR O., ERZURUMLUOĞLU E., KUÇÜK H., VELİPAŞAOĞLU M., ASLAN H., ÖZDEMİR M., et al.
10th European Cytogenetic Conference, 4 - 07 July 2015
2015
2015Copy number variants in prematüre ovarian failure
KÜÇÜK H., ARTAN S., AYDIN Y., ERZURUMLUOĞLU E., ASLAN H., HASSA H.
10th European Cytogenetic Conference, 4 - 07 July 2015
2015
2015An assessment of three cases with distal 15q duplication
ÖZDEMİR M., GÜMÜŞ E., TEKİN A. N., ONUR KUCUK H., ERZURUMLUOĞLU E., ASLAN H., et al.
10th European Cytogenetic Conference, 4 - 07 July 2015
2014
2014Miller-Dieker Sendromlu Bir Olgu Sunumu
GÜMÜŞ E., AYNACI S., ERZURUMLUOĞLU E., ASLAN H., ÇİLİNGİR O., ARTAN S.
11. Ulusal Tıbbi Genetik Kongresi, Turkey, 24 - 27 September 2014
2014
2014Xq21 32 23 Duplikasyonu Saptanan Olgu Sunumu
KÜÇÜK H., ASLAN H., ÇARMAN K. B., ERZURUMLUOĞLU E., DÜZKALE N., ÖZDEMİR M., et al.
11. Ulusal Tıbbi Genetik Kongresi, Turkey, 24 - 27 September 2014
2014
2014Kromozom Mikrodizin Analizlerinin Kötü Obstetrik Öykü ve Anormal Fetal USG Bulgusu Olan Öploid Abortuslardaki Önemi Olgu Sunumu
ERZURUMLUOĞLU E., KÜÇÜK H., ASLAN H., VELİPAŞAOĞLU M., DEMİREL A., TOSUMOĞLU E., et al.
11. Ulusal Tıbbi Genetik Kongresi, Turkey, 24 - 27 September 2014
2014
2014A rare case with De Novo Isochromosome 18p Syndrome
ARTAN S., ERZURUMLUOĞLU E., ÇARMAN K. B., GÜMÜŞ E., ÖZDEMİR M., DURAK ARAS B., et al.
European Human Genetics Conference 2014, Milan, Italy, 31 May - 03 June 2014, vol.22, pp.448
2014
2014Molecular cytogenetic diagnosis of melanocytic lesions
DURAK ARAS B., IŞIK S., CANAZ F., ÖZDEMİR M., ÇİLİNGİR O., ASLAN H., et al.
EUROPEAN JOURNAL OF HUMAN GENETİCS, Milan, Italy, 31 May - 03 June 2014, vol.22, pp.470
2013
2013Quantitation of Gene Copy Numbers of Aurora Kinases In Exfoliated Cells From Bladder Washings and Bladder Cancer Detection
ERZURUMLUOĞLU E., ARTAN S., CAN Y. S. C., ARAS İ., ÖZDEMİR M., DURAK ARAS B.
9th European Cytogenetics Conference, 29 June - 02 July 2013, vol.21, pp.1-168
2011
2011A rare case of inv(21)(p12q22.1) in a man and holoprocencephaly in the fetus
ÖZDEMİR M., EMRE R., DURAK ARAS B., ÇİLİNGİR O., KÜÇÜK H., ERZURUMLUOĞLU E., et al.
8th EUROPEAN CYTOGENETICS CONFERENCE, 2 - 05 July 2011
2010
2010A Clinical Report Of A Prenatally Diagnosed inv Dup (15) Syndrome
DURAK ARAS B., ÖZDEMİR M., TANIR H. M., dikoğlu e., YÜKSEL Z., ERZURUMLUOĞLU E., et al.
9 th National Medical Genetics Congress of turkısh Medical Genetics Society with İnternational Participation, Turkey, 1 - 05 December 2010, vol.78, pp.104-110
Books & Book Chapters
2021
2021Genetics of frontotemporal dementia
ERZURUMLUOĞLU GÖKALP E., ÖZBABALIK ADAPINAR B. D., ARTAN S.
in: Factors Affecting Neurological Aging , Colin Martin, Victor Preedy, Rajkumar Rajendram, Editor, Academic Press , pp.3-16, 2021
2019
2019Future Treatment of Alzheimer Disease
Keskin A. O., Durmaz Çelik F. N., Uncu G., Erzurumluoğlu Gökalp E., Yıldırım Z., Tuncer E. N., et al.
in: Geriatric Medicine and Gerontology, Dr. Edward T. Zawada Jr., Editor, IntechOpen, London, pp.1-27, 2019
Supported Projects
2022 - Continues
2022 - ContinuesAlzheimer ve Vasküler Demans Tanısında miRNA-29a ve miRNA-31'in Biyobelirteç Olarak Değerlendirilmesi
Project Supported by Higher Education Institutions
ERZURUMLUOĞLU GÖKALP E. (Executive), AKBAŞ A.
2022 - Continues
2022 - ContinuesGlokom ve Alzheimer hastalığında Aquaporin 4 AQP4 ve ilişkili miRNA ekspresyonlarının farklı biyolojik sıvılarda karekterizasyonu
Project Supported by Higher Education Institutions
YILDIRIM N. (Executive), ARTAN S., ULUPINAR E., DURMAZ ÇELİK F. N., ERZURUMLUOĞLU GÖKALP E.
2021 - Continues
2021 - ContinuesAnevrizmal Subaraknoid Kanamada miRNA Profillerinin Belirlenmesi ve Hastalık Prognozuna Etkisi
Project Supported by Higher Education Institutions
ÖZKARA E. (Executive), ÖZDEMİR A. Ö., ARTAN S., ARSLANTAŞ A., ÖZBEK Z., ÇİLİNGİR O., et al.
2021 - Continues
2021 - ContinuesSirküle miRNAların Ekspresyon Profilinin Anevrizma Prognozundaki Rolünün Değerlendirilmesi
Project Supported by Higher Education Institutions
ARTAN S. (Executive), BAŞ G., ERZURUMLUOĞLU GÖKALP E., ÖZKARA E., ÖZDEMİR A. Ö., AYKAÇ Ö., et al.
2022 - 2023
2022 - 2023Parkinson Hastalığında GRIN2B Gen Polimorfizmlerinin Dürtü Kontrol Bozukluğu ile İlişkisi
Project Supported by Higher Education Institutions
ERZURUMLUOĞLU GÖKALP E. (Executive), MEMARI G.
2021 - 2023
2021 - 2023İdiyopatik Parkinson olgularında C9orf72 geni G4C2 tekrar sayılarının değerlendirilmesi
Project Supported by Higher Education Institutions
DURMAZ ÇELİK F. N. (Executive), KOCAGİL S., DURAK ARAS B., ERZURUMLUOĞLU GÖKALP E., ÖZKAN S.
2021 - 2022
2021 - 2022KLL Olgularında NOTCH1 Gen Amplifıkasyonunun Araştırılması
Project Supported by Higher Education Institutions
Işık S. (Executive), Durak Aras B., Gündüz E., Erzurumluoğlu Gökalp E., Artan S., Oğuz Davutoğlu N., et al.
2019 - 2020
2019 - 2020Primer Kardiyomiyopatilerde mtDNA Varyantlarının Değerlendirilmesi
Project Supported by Higher Education Institutions
ERZURUMLUOĞLU GÖKALP E. (Executive), DURAK ARAS B.
2019 - 2020
2019 - 2020Primer Kardiyomiyopatilerde mtDNA Varyantlarının Değerlendirilimesi
Project Supported by Higher Education Institutions
Durak Aras B., Erzurumluoğlu Gökalp E. (Executive), Çilingir O., Artan S., Köşger P., Kıztanır H., et al.
2018 - 2019
2018 - 2019İntrakraniyal Sakküler Anevrizmalarda Aday Genlerin Değerlendirilmesi
Project Supported by Higher Education Institutions
Arslantaş A., Artan S., Durak Aras B., Özbek Z., Özkara E., Kocagil S., et al.
2015 - 2018
2015 - 2018Assesment of candidate genes in patients with Frontotemporal Lobar Degeneration Spectrum
TUBITAK Project
Artan S. (Executive), Yenilmez Ç., Çilingir O., Özbabalık Adapınar D.
2015 - 2016
2015 - 2016SPORADİK PARKİNSON HASTALIĞINDA RAGE GEN POLİMORFİZMLERİNİN ARAŞTIRILMASI
Project Supported by Higher Education Institutions
ERZURUMLUOĞLU GÖKALP E., ARTAN S., ÇİLİNGİR O. (Executive), ÖZDEMİR M.
2015 - 2016
2015 - 2016LİKEN PLANUS HASTALIĞINDA GSTM1 GSTT1 VE GSTP1 GEN POLİMORFİZMLERİNİN ARAŞTIRILMASI
Project Supported by Higher Education Institutions
ERZURUMLUOĞLU GÖKALP E., ÇİLİNGİR O. (Executive)
Activities in Scientific Journals
2022 - Continues
2022 - ContinuesOsmangazi Tıp Dergisi
Committee Member
Scientific Refereeing
December 2022
December 2022Osmangazi Tıp Dergisi
National Scientific Refreed Journal
December 2022
December 2022THE EUROPEAN RESEARCH JOURNAL
National Scientific Refreed Journal
October 2022
October 2022BALKAN MEDICAL JOURNAL
SCI Journal
August 2022
August 2022Project Supported by Higher Education Institutions
BAP Research Project, Trakya University, Turkey
July 2022
July 2022Osmangazi Tıp Dergisi
National Scientific Refreed Journal
June 2022
June 2022JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
Journal Indexed in ESCI
February 2022
February 2022Osmangazi Tıp Dergisi
National Scientific Refreed Journal
February 2022
February 2022JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
Journal Indexed in ESCI
December 2021
December 2021Journal Of Cancer Research And Therapeutics
Journal Indexed in SCI-E
November 2021
November 2021İstanbul Tıp Fakültesi Dergisi
National Scientific Refreed Journal
April 2021
April 2021International Journal Of Clinical Practice
SCI Journal
January 2021
January 2021MOLECULAR GENETICS & GENOMIC MEDICINE
Journal Indexed in SCI-E
January 2021
January 2021TUBITAK Project
2209-A - Üniversite Öğrencileri Araştırma Projeleri Destekleme Programı, 2209-A - Üniversite Öğrencileri Araştırma Projeleri Destekleme Programı, Turkey
Tasks In Event Organizations
Mayıs 2022
Mayıs 20227. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi
Scientific Congress
Durak Aras B., Erzurumluoğlu Gökalp E., Artan S., Kocagil S., Çilingir O.
Turkey
Congress and Symposium Activities
29 September 2022 - 02 October 2022
29 September 2022 - 02 October 202212. Ulusal Alzheimer Kongresi
Invited Speaker
Eskişehir-Turkey
17 June 2022 - 18 June 2022
17 June 2022 - 18 June 2022VI. Nadir Görülen Hastalıklar Sempozyumu ve Nörogenetik Kursu
Invited Speaker
İstanbul-Turkey
26 May 2022 - 28 May 2022
26 May 2022 - 28 May 20227. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi
Invited Speaker
Kayseri-Turkey
12 February 2022 - 12 February 2022
12 February 2022 - 12 February 20221. Nörodejeneratif Hastalıklar Sempozyumu
Invited Speaker
Eskişehir-Turkey
27 November 2021 - 01 December 2021
27 November 2021 - 01 December 202157. Ulusal Nöroloji Kongresi
Invited Speaker
Antalya-Turkey
21 September 2021 - 25 September 2021
21 September 2021 - 25 September 202111. Ulusal Alzheimer Kongresi’
Invited Speaker
İstanbul-Turkey
05 November 2020 - 08 November 2020
05 November 2020 - 08 November 202010. Ulusal Alzheimer Sanal Kongresi
Invited Speaker
Eskişehir-Turkey
17 April 2019 - 20 April 2019
17 April 2019 - 20 April 2019
13. Balkan Congress of Human Genetics
Invited Speaker
Edirne-Turkey
Citations
Total Citations (WOS): 27
h-index (WOS): 3
Jury Memberships
December-2022
December 2022PhD Thesis Monitoring Committee Member
PhD Thesis Monitoring Committee Member - Eskişehir Osmangazi Üniversitesi
December-2022
December 2022PhD Thesis Monitoring Committee Member
PhD Thesis Monitoring Committee Member - Eskişehir Osmangazi Üniversitesi
November-2022
November 2022PhD Thesis Monitoring Committee Member
PhD Thesis Monitoring Committee Member - Eskişehir Osmangazi Üniversitesi
June-2022
June 2022PhD Thesis Monitoring Committee Member
PhD Thesis Monitoring Committee Member - Eskişehir Osmangazi Üniversitesi
December-2021
December 2021PhD Thesis Monitoring Committee Member
PhD Thesis Monitoring Committee Member - Eskişehir Osmangazi Üniversitesi
December-2021
December 2021