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 CANER VİLDAN,ÇETİN GÖKHAN OZAN,HACIOĞLU SİBEL,BARIŞ MOĞUL CANSU,TEPELİ EMRE,ŞEN TÜRK NİLAY,BAĞCI GÜLSEREN,YARARBAŞ KANAY,AKGÜN ÇAĞLIYAN GÜLSÜM Cancer Biomarkers Cilt.32 Sayf.- 2021 https://doi.org/10.3233/cbm-210110
The Relationship Between Sexual Dysfunctions With Disease Prolactin and Genetic Polymorphisms in Schizophrenia and Bipolar Disorder Patients Receiving Pharmacotherapy ÖZTÜRK NEŞE,ÖZDEL OSMAN,TÜREL SAMET,TEPELİ EMRE Cureus Cilt.5 Sayf.- 2024 https://doi.org/10.7759/cureus.60654
Relationship of Plasminogen Activator Inhibitor 1 4G/5G Gene Polymorphism and Nontraumatic Lunatum Avascular Necrosis GÖNEN METİN,YÖRÜKOĞLU ALİ ÇAĞDAŞ,AYDEMİR AHMET NADİR,AKINCI GÖNEN GİZEM,TEPELİ EMRE,DEMİRKAN AHMET FAHİR American Society for Surgery of the Hand Cilt.45 Sayf.450-454 2019 https://www.jhandsurg.org/article/S0363-5023(19)31419-4/abstract
Increased expression of pentraxin 3 in placental tissues from patients with unexplained recurrent pregnancy loss ZEYBEK SELCAN,TEPELİ EMRE,ÇETİN GÖKHAN OZAN,CANER VİLDAN,ŞENOL HANDE,YILDIRIM NAZAN BAŞAK,BAĞCI GÜLSEREN Balkan Journal of Medical Genetics Cilt.22 Sayf.21-28 2019 https://content.sciendo.com/view/journals/bjmg/22/1/article-p21.xml
Mutational status of EZH2 and CD79B hot spots in mature B cell non Hodgkin s lymphomas novel CD79B variations have been revealed ÇETİN GÖKHAN OZAN,BARIŞ İKBAL CANSU,CANER VİLDAN,SARIKEPE BİLGE,ŞEN TÜRK NİLAY,TEPELİ EMRE,HACIOĞLU SİBEL,SARI HAKAN İSMAİL,BAĞCI GÜLSEREN,KESKİN ALİ European Review for Medical and Pharmacological Sciences Cilt.20 Sayf.830-836 2016
Comparison of IL 23 receptor gene polymorphisms in patients with primary sjögren syndrome ankylosing spondylitis and ankylosing spondylitis with sjögren s syndrome TEMEL ŞAHİN,Balkarlı Ayşe,ELMAS LEVENT,TEPELİ EMRE,ÇOBANKARA VELİ International Journal of Clinical and Experimental Medicine Cilt. Sayf.- 2016
Relationship between the SNAP 25 gene and the effects of methylphenidate on the anterior cingulate cortex of patients with adult attention deficit hyperactivity disorder a magnetic resonance spectroscopy study Ünal Ayşe Gonca,İnce Kenar Ayşe Nur,TEPELİ EMRE,Kıroğlu Yılmaz,Herken Hasan European Review for Medical and Pharmacological Sciences Cilt. Sayf.- 2016
MEFV gene variation R202Q is associated with metabolic syndrome Balkarlı Ayşe,Akyol Mahmut,TEPELİ EMRE,ELMAS LEVENT,ÇOBANKARA VELİ European Review for Medical and Pharmacological Sciences Cilt. Sayf.- 2016
Neonatal Bartter syndrome with cholelithiasis and hydrocephalus Rare association ÖZDEMİR ÖZMERT MUHAMMET ALİ,ÇIRALI CEREN,Yılmaz Ağladıoğlu Sabahat,EVRENGÜL HAVVA,TEPELİ EMRE,ERGİN HACER Pediatrics International Cilt.58 Sayf.912-915 2016 http://doi.wiley.com/10.1111/ped.12999
A variant allele of the Mediterranean fever gene increases the severity of gout Balkarlı Ayşe,TEPELİ EMRE,BALKARLI HÜSEYİN,KAYA ARİF,ÇOBANKARA VELİ International Journal of Rheumatic Diseases Cilt. Sayf.- 2016 http://doi.wiley.com/10.1111/1756-185X.12872
title The Analysis of the Relationship Between A1298C and C677T Polymorphisms of the i MTHFR i Gene with Prostate Cancer in Eskisehir Population title MÜSLÜMANOĞLU MUHAMMED HAMZA,TEPELİ EMRE,ULUSAL SELMA,ULUDAĞ AHMET,Uzun Derya,ATLI ENGİN,Cantürk Kemal Murat,ÖZDEMİR MUHSİN,Turgut Mehmet Genetic Testing and Molecular Biomarkers Cilt.13 Sayf.641-645 2009 http://www.liebertonline.com/doi/abs/10.1089/gtmb.2009.0046
Detection of deletions and or amplifications of genes related with lung cancer by multiplex ligation dependent probe amplification MLPA technique TEPELİ EMRE,MÜSLÜMANOĞLU MUHAMMED HAMZA,ULUDAĞ AHMET,BÜYÜKPINARBAŞILI NUR,ÖZDEMİR MUHSİN,ÖZNUR MURAT,ASLAN HÜSEYİN,ARTAN SEVİLHAN Cancer Biology & Therapy Cilt.8 Sayf.2160-2164 2014 http://www.tandfonline.com/doi/abs/10.4161/cbt.8.22.9840
title Determination of i O i sup 6 sup Methylguanine DNA Methyltransferase Promoter Methylation in Non Small Cell Lung Cancer title Ekim Mehmet,CANER VİLDAN,BÜYÜKPINARBAŞILI NUR,TEPELİ EMRE,ELMAS LEVENT,BAĞCI GÜLSEREN Genetic Testing and Molecular Biomarkers Cilt.15 Sayf.357-360 2011 http://www.liebertonline.com/doi/abs/10.1089/gtmb.2010.0211
Expression and Amplification of Topoisomerase 2 in Type 1 and Type 2 Papillary Renal Cell Carcinomas and Its Correlation with HER2 neu Amplification DÜZCAN FÜSUN,Düzcan Süleyman Ender,ŞEN SAİT,YÖRÜKOĞLU KUTSAL,CANER VİLDAN,ŞEN TÜRK NİLAY,ÇETİN GÖKHAN OZAN,Kelten Canan,TUNA EMİNE BURÇİN,SARSIK KUMBARACI BANU,TEPELİ EMRE Pathology & Oncology Research Cilt.17 Sayf.697-703 2011 http://link.springer.com/10.1007/s12253-011-9372-0
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 Koç Esin,CANER VİLDAN,BÜYÜKPINARBAŞILI NUR,TEPELİ EMRE,ŞEN TÜRK NİLAY,ÇETİN GÖKHAN OZAN,BAĞCI GÜLSEREN Molecular Biology Reports Cilt.39 Sayf.375-380 2012 http://link.springer.com/10.1007/s11033-011-0748-8
Expression of ERCC1 and its clinicopathological correlations in non small cell lung cancer TEPELİ EMRE,CANER VİLDAN,BÜYÜKPINARBAŞILI NUR,ÇETİN GÖKHAN OZAN,DÜZCAN FÜSUN,BAĞCI GÜLSEREN Molecular Biology Reports Cilt.39 Sayf.335-341 2012 http://link.springer.com/10.1007/s11033-011-0743-0
Vitamin D receptor gene polymorphisms and haplotypes Apa I Bsm I Fok I Taq I in Turkish psoriasis patients Acikbas I, Sanlı B, Tepeli E, Ergin S, Aktan S, Bagci H. Med Sci Monit. Cilt.18 Sayf.661-666 2012
MYD88 Expression and L265P Mutation in Mature B Cell Non Hodgkin Lymphomas CANER VİLDAN,ŞEN TÜRK NİLAY,BARIŞ İKBAL CANSU,ÇETİN GÖKHAN OZAN,TEPELİ EMRE,HACIOĞLU SİBEL,SARI HAKAN İSMAİL,ZENCİR SEVİL,DOĞU MEHMET HİLMİ,BAĞCI GÜLSEREN,KESKİN ALİ Genetic Testing and Molecular Biomarkers Cilt.19 Sayf.372-378 2015 http://online.liebertpub.com/doi/10.1089/gtmb.2015.0041
title i HIF1A i as a major vascular endothelial growth factor regulator do its polymorphisms have an association with age related macular degeneration title Okur Volkan,ÇETİN GÖKHAN OZAN,ÇETİN EBRU NEVİN,TEPELİ EMRE,Bulgu Yunus,YILDIRIM CEM Clinical & Experimental Ophthalmology Cilt.43 Sayf.47-53 2015 http://doi.wiley.com/10.1111/ceo.12376
Could serum pentraxin 3 levels and IgM deposition in skin biopsies predict subsequent renal involvement in children with Henoch Schönlein purpura YÜKSEL SELÇUK,Çağlar Murat,EVRENGÜL HAVVA,Becerir Tülay,TEPELİ EMRE,ERGİN AHMET,Çiçek EA,AYBEK HÜLYA,YALÇIN NAGİHAN,DEMİRKAN NEŞE Pediatric Nephrology Cilt.30 Sayf.969-974 2015 http://link.springer.com/10.1007/s00467-014-3026-x
Contribution of MLPA to routine testing to detect the prognostic chromosomal abnormalities in chronic lymphocytic leukemia Ayaz akif,TEPELİ EMRE,SARI HAKAN İSMAİL,ÇETİN GÖKHAN OZAN,Eser Metin,DOĞU MEHMET HİLMİ,BAĞCI GÜLSEREN Gene Ther Mol Biol Cilt. Sayf.1-9 2014
GADD45 Methylation Is More Common In Benign Prostatic Hyperplasia Than In Prostate Cancer Can Özge,CANER VİLDAN,ŞEN TÜRK NİLAY,TUNCAY ÖMER LEVENT,Eskiçorapcı Sadettin Yılmaz,TEPELİ EMRE,ÇETİN GÖKHAN OZAN,BARIŞ İKBAL CANSU,BAĞCI GÜLSEREN Gene Ther Mol Biol Cilt. Sayf.44-54 2014
Synaptosomal associated protein 25 Snap 25 gene Polymorphism frequency in fibromyalgia syndrome and relationship with clinical symptoms Ayşe Balkarlı,ŞENGÜL ABDULLAH CEM,TEPELİ EMRE,BALKARLI HÜSEYİN,ÇOBANKARA VELİ BMC Musculoskeletal Disorders Cilt.15 Sayf.191- 2014 http://www.biomedcentral.com/1471-2474/15/191
Possible Role of GADD45 Methylation in Diffuse Large B Cell Lymphoma Does It Affect the Progression and Tissue Involvement BARIŞ İKBAL CANSU,CANER VİLDAN,ŞEN TÜRK NİLAY,SARI HAKAN İSMAİL,HACIOĞLU SİBEL,DOĞU MEHMET HİLMİ,ÇETİN GÖKHAN OZAN,TEPELİ EMRE,Can Özge,BAĞCI GÜLSEREN,KESKİN ALİ Turkish Journal of Hematology Cilt.32 Sayf.295-303 2015 http://www.journalagent.com/tjh/pdfs/TJH_32_SUP_4_295_303.pdf
Quantitative comparison of immunohistochemical and PCR analysis of midkineexpression in breast cancer types and serum midkine level Hülya Çetin Sorkun,AKBULUT METİN,ENLİ YAŞAR,TEPELİ EMRE,ÖZKAN SEVGİ,ERDEM ERGÜN Turkish Journal Of Medical Sciences Cilt.45 Sayf.1-9 2015
Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46 XX der 6 t 6 12 p25 3 q24 31 karyotype Phenotypic overlap with Mutchinick syndrome TEPELİ EMRE Am J Med Genet A Cilt. Sayf.1724- 2010 http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.33383/abstract;jsessionid=87CAC49A5AFFCE8500CB4D6FDD60B00D.d03t04
Tekrarlayan Gebelik Kaybı Olan Hastalarda İnterlökin 1 Beta Gen Polimorfizminin Değerlendirilmesi Emre Tepeli, Ahmet Uludağ, Tayfun Şengel, Özden Kutlay, M. Hamza Müslümanoğlu. Nobel Med Cilt. Sayf.34- 2010 http://www.nobelmedicus.com/contents/201061/34-38.pdf
The mRNA expression of cytochrome P450 isoforms in human gastric tissue Canturk P, Caner V, Oruc N, Akarca US, Tepeli E, Cetin OG, Zencir S, Topcu Z. HEPATO-GASTROENTEROLOGY Cilt. Sayf.372- 2010 http://www.ncbi.nlm.nih.gov/pubmed/20583446
A Case of Schizophrenia Accompanying Velocardiofacial Syndrome Cem ŞENGÜL, Muharrem EFE, Emre TEPELİ, Ozan ÇETİN, Füsun DÜZCAN, Hasan HERKEN Archives of Neuropsychiatry Cilt. Sayf.27- 2009 http://www.noropsikiyatriarsivi.com/PDF/2009/Mart/27-29.pdf
Angiotensin converting enzyme gene insertion deletion polymorphism frequency in normotensive children with a positive family history of essential hypertension Camci L, Kilic Z, Dinleyici EC, Muslumanoglu H, Tepeli E, Ucar B. . J Paediatr Child Health Cilt.12 Sayf.742-746 2009 http://onlinelibrary.wiley.com/doi/10.1111/j.1440-1754.2009.01605.x/abstract
Sex chromosome aneuploidy rates in the somatic cells of infertile men Duzcan F, Aybek Z, Tepeli E, Caner V, Cetin GO, Aybek H, Bagci H. JOURNAL OF REPRODUCTIVE MEDICINE Cilt.6 Sayf.489-492 2006 http://www.ncbi.nlm.nih.gov/pubmed/16846089
Femoral facial syndrome with hemifacial microsomia and hypoglossia Düzcan F, Ergin H, Perçin FE, Tepeli E, Ekula G. Clinical Dysmorphology Cilt. Sayf.43- 2004 http://www.ncbi.nlm.nih.gov/pubmed/15127766
Makaleler (Ulusal)
IL-23R gene polymorphisms in rheumatoid arthritis SOYSAL ERGÜN,ULUTAŞ FİRDEVS,TEPELİ EMRE,KAYMAZ SERDAR,ÇOBANKARA VELİ Rheumatology International Cilt.42 Sayf.555-562 2021 https://doi.org/10.1007/s00296-021-04881-9
Altered microRNA 5692b and microRNA let-7d expression levels in children and adolescents with attention deficit hyperactivity disorder AYDIN SEZAİ ÜSTÜN,KABUKÇU BAŞAY BÜRGE,ÇETİN GÖKHAN OZAN,GÜNGÖR AYŞEGÜL,TEPELİ EMRE Journal of Psychiatric Research Cilt.115 Sayf.158-164 2019 https://doi.org/10.1016/j.jpsychires.2019.05.021
Bağ Dokusu Hastalıkları TEPELİ EMRE,ÖK NUSRET türkiye klinikleri Cilt. Sayf.- 2017
Non-mosaic tetrasomy 9p in an infant with multiple congenital anomalies Düzcan Füsun,ERGİN HACER,Aytan M,TEPELİ EMRE,Özdemir Özmert,Başaran S Gynecology Obstetrics and Reproductive Medicine Cilt.13 Sayf.114-116 2018
A case with vascular anomalies: differential diagnosis and management ALBUZ BURCU,KOCAMAZ HALİL,ÖZTÜRK MENEKŞE,SARIKEPE BİLGE,TEPELİ EMRE,BAĞCI GÜLSEREN,SEMERCİ GÜNDÜZ CAVİDAN NUR erciyes medical journal Cilt. Sayf.- 2017
Investigation of polymorphisms of CHGA gene s promoter region in patients with essential hypertension Eser Metin,Şanlıalp Musa,TEPELİ EMRE,TUFAN NACİYE LALE,KAFTAN HAVANE ASUMAN,SEMERCİ CAVİDAN NUR Pamukkale Medical Journal Cilt.8 Sayf.23-30 2015 http://www.journalagent.com/z4/download_fulltext.asp?pdir=ptd&plng=eng&un=PTD-26121
Investigation of LRRK2 G2019S Mutation in the Patients with Sporadic Parkinson s Disease in Turkey Huseyin Aslan, Serhat Ozkan, Emre Tepeli, Ramazan Emre, Ozden Kutlay, Abdullah Ihsan Gurler, Ahmet Uludag, M. Hamza Muslumanoglu Konuralp Tıp Dergisi Cilt. Sayf.- 2014
The Relationship between Insulin PSTI Polymorphism and Prostate Cancer in Turkish Population Muhammed Hamza MÜSLÜMANOĞLU, Tanju BASMACI, Selma DEMİR ULUSAL, Hüseyin ASLAN, Emre TEPELİ, Muhsin ÖZDEMİR, Mehmet TURGUT Çukurova Medical Journal Cilt. Sayf.- 2013
Sağlıklı Çocuk Sahibi Olabilme Metodları Emre TEPELİ Turkiye Klinikleri J Hem Onc-Special Topics Cilt. Sayf.44- 2010
Üç Adet Hemifasiyal Mikrosomia Hastası Ve Literatürün Gözden Geçirilmesi Anatol J Clin Investig Ahmet ULUDAĞ, Emre TEPELİ, Altuğ KOÇ, Salih KOZAN, Deniz TORUN, Şefik GÜRAN, Muhterem BAHÇE Anatol J Clin Investig Cilt. Sayf.252- 2009
Non mosaic Tetrasomy 9p in an infant with multiple congenital anomalies Gynecology Obstetrics Reproductive Medicine GORM Dergisi Füsun Düzcan, Hacer Ergin, Melike Aytan, Emre Tepeli, Özmert Özdemir, Seher Başaran Obstetrics-Reproductive Medicine (GORM) Dergisi Cilt. Sayf.114- 2007
Eskişehir İlinde İdiyopatik Tekrarlayan Gebelik Kayıpları İle Metilentetrahidrofolat Reduktaz MTHFR C677T Ve A1298C Polimorfizmleri Arasındaki İlişki Osmangazi Tıp Dergisi Emre Tepeli, M. Hamza Müslümanoğlu, Ahmet Uludağ, Engin Atlı, Derya Uzun, Sevilhan Artan Osmangazi Tıp Dergisi Cilt. Sayf.1- 2007
Kliniğimizde 7 Yıllık Amniosentez Sonuçları Perinatoloji Dergisi Kamil Turgay .Şener, Beyhan Durak, H. Mete Tanır, Emre Tepeli, Mehmet Kaya, Sevilhan Artan Perinatoloji Dergisi Cilt. Sayf.4- 2006
Albinoid Fundus Bulunan Cerebro Oculo Facio Skeletal COFS Pena Shokeir Tip II Sendromlu Bir Olgu Türkiye Klinikleri J Pediatr Semerci N.C., Cinbiş M., Tatlıpınar S., Kılıç İ., Yağcı B., Tepeli E., Düzcan F. Türkiye Klinikleri J Pediatr Cilt. Sayf.92- 2005
Ailesel ve de nova Translokasyonların Klinik Tanı ve Fenotipik Bulgular ile Uyumu PAÜTF Dergisi Düzcan F., Atmaca M., Çetin G.O., Tepeli E., Gümüş D., Bağcı H. PAÜTF Dergisi Cilt. Sayf.39- 2002
Family history clinical features and molecular characterization of a patient with autosomal recessive non syndromic hearing loss Duzcan F, Wollnik B, Tepeli E, Ardic FN, Uyguner O, Bagci H. Kulak Burun Bogaz Ihtis Derg. Cilt. Sayf.85- 2003 http://www.ncbi.nlm.nih.gov/pubmed/14699249
Bildiriler (Uluslararası)
Correlation of plasma exosome concentrations with stage in patients with Diffuse large B-cellLymphoma CANER VİLDAN,BARIŞ İKBAL CANSU,ÇETİN GÖKHAN OZAN,TEPELİ EMRE,ŞEN TÜRK NİLAY,HACIOĞLU SİBEL,ZENCİR SEVİL,ÇAĞLAYAN G,BAĞCI GÜLSEREN 6th International Congress on Leukemia Lymphoma Myeloma Cilt. Sayf.- 13.05.2017
Correlation of plasma exosome concentrations with stage in patients with diffuse large b cell lymphoma. CANER VİLDAN,BARIŞ İKBAL CANSU,ÇETİN GÖKHAN OZAN,TEPELİ EMRE,ŞEN TÜRK NİLAY,HACIOĞLU SİBEL,ZENCİR SEVİL,ÇAĞLAYAN GÜLSÜM,BAĞCI GÜLSEREN 6th Internatioanl Congress On Leukemia Lymphoma Myeloma Cilt. Sayf.- 10.05.2017
MOLECULAR CYTOGENETIC PROFILE OF COMPLEX/VARIANT TRANSLOCATIONS IN CHRONIC MYELOIDLEUKEMIA CANER VİLDAN,ÇETİN GÖKHAN OZAN,TEPELİ EMRE,SARIKEPE BİLGE,anlas özlem,bağlar menekşe,ALBUZ BURCU,atmaca münevver,HACIOĞLU SİBEL 6th International Congress onLeukemia – Lymphoma – Myeloma Cilt. Sayf.- 10.05.2017
Mutational status of EZH2 and CD79B hot spots in mature B cell non Hodgkin s lymphomas novel CD79B variations have been revealed ÇETİN GÖKHAN OZAN,CANER VİLDAN,SARIKEPE BİLGE,ŞEN TÜRK NİLAY,TEPELİ EMRE,HACIOĞLU SİBEL,SARI HAKAN İSMAİL,BAĞCI GÜLSEREN,KESKİN ALİ Europan Human Genetics Conference Cilt. Sayf.-
An ultracentrifugation based protocol for exosome isolation in diffuse large B cell lymphoma CANER VİLDAN,ZENCİR SEVİL,HACIOĞLU SİBEL,BAĞCI GÜLSEREN,SARI HAKAN İSMAİL,BARIŞ İKBAL CANSU,TEPELİ EMRE,ŞEN TÜRK NİLAY,ÇETİN GÖKHAN OZAN ISEV Cilt. Sayf.-
Molecular cytogenetics findings of clinically suspected acute myeloid leukemia and or myelodysplastic syndrome AML MDS patients SARIKEPE BİLGE,ZEYBEK SELCAN,gönen gizem,Tanrıverdi Eyüpoğlu Yasemin,BOZ ÖZLEM,CEYLAN EMİNE İPEK,TEPELİ EMRE,ÇETİN GÖKHAN OZAN,SARI HAKAN İSMAİL,DÜZCAN FÜSUN,CANER VİLDAN Europan Human Genetics Conference, Barcelona, Cilt. Sayf.-
A patient with 7p and 17p terminal deletions and 17q terminal duplication ZEYBEK SELCAN,TEPELİ EMRE,ÇETİN GÖKHAN OZAN,CANER VİLDAN,CEYLAN EMİNE İPEK,gönen gizem,SEMERCİ CAVİDAN NUR,BAĞCI GÜLSEREN,DÜZCAN FÜSUN Europan Human Genetics Conference Cilt. Sayf.-
A partial deletion Xp duplication Xq case due to maternal pericentric inversion X confirmed by microarray BOZ ÖZLEM,SARIKEPE BİLGE,Gönen Gizem,TEPELİ EMRE,SEMERCİ CAVİDAN NUR,DÜZCAN FÜSUN,Kırbıyık Özgür,Özyılmaz Berk,BAĞCI GÜLSEREN Europan Human Genetics Conference Cilt. Sayf.-
RENAL INVOLVEMENT IN CHILDREN WITH HENOCH SCHONLEIN PURPURA HIGH LEVEL OF SERUM PENTRAXIN 3 AND IgM IN LESIONAL SKIN Yuksel S, Caglar M, Becerir T, Tepeli E, Demirkan NC, Yalcin N, Ergin A 50th European-Renal-Association - European-Dialysis-and-Transplant-Association Congress Location: Istanbul, TURKEY Cilt. Sayf.-
The 82delT Mutation in the Gene Encoding SLURP 1 in a Turkish Male with Mal de Meleda Şeyma Yılmaz, Emre Tepeli, C. Nur Semerci, Seniz Ergin, Akif Ayaz, Annual Meeting of the American Academy of Dermatology in Miami Beach, Florida, 01-05 March 2013 Cilt. Sayf.-
Developmental delay mental reterdation and facial dysmorphism due to subtelomeric deletion of 7q G. Ozan Cetin, Volkan Okur, Tarkan Kalkan, Akgun Olmez, Emre Tepeli, Fusun Duzcan 8. European Cytogenetics Conference, Porto, Portugal, 02-05 July 2011 Cilt. Sayf.-
Expression and Amplification of Topoisomerase 2 in Type 1 and Type 2 Papillary Renal Cell Carcinomas and Its Correlation with HER2 neu Amplification Duzcan F., Duzcan S.E., Sen S., Yorukoglu K., Caner V., Sen Turk N., Cetin G.O., Kelten C., Tuna B., Sarsik B., Tepeli E. 8th European Cytogenetics Conference, Porto, Portugal Cilt. Sayf.-
Prenatally diagnosed two distinct cell lines of 18p terminal deletion monosomy X possibly due to chimerism Düzcan F, Çetin GO, Tepeli E, Ayaz A. Eur J Hum Genet, Europen Human Genetics Conference 2010, June 12-15, 2010 Cilt. Sayf.-
The mRNA Expression Patterns of Cytochrome P450 Isoforms in Relation to Pathological Status of Human Gastric Tissue Canturk, P., V. Caner, N. Oruc, U.S. Akarca, E. Tepeli, G.O. Cetin, S. Zincir ve Z. Topcu 4th EORTC Pathobiology Group Annual Meeting & 1st International Multidisiplinary Cancer Research Congress Cilt. Sayf.-
A 22q11 2 microduplicationsyndrome family concurrent additional duplication pattern in LZTR 1 gene region may be the cause of clinical variability D. Torun, S. Kozan, E. Tepeli, A. Uludag, A. Yesilyurt, M. Bahce, S. Güran 7. European Cytogenetics Conference , Stockholm, Sweden Cilt. Sayf.-
MEFV Mutations in Turkish Patients Suffering From Familial Mediterranean Fever . Cilingir, M. Ozdemir, M.H. Muslumanoglu, E. Tepeli, G. Bademci, C. Korkmaz, O. Kutlay, S. Demir, H. Aslan, B. Durak, S. Artan European Human Genetics Conference, May 31-June 3, 2008 Cilt. Sayf.-
Studying Amplification Status of HER2 NEU and EGFR Oncogenes in Non Small Cell Lung Cancer by Real Time PCR Technique M.H. Muslumanoglu, D. Uzun, O. Cilingir, M. Ozdemir, N. Buyukpinarbasili, E. Tepeli, S. Artan European Human Genetics Conference, May 31-June 3, 2008, P04.172, European Cilt. Sayf.-
Copy Number Alterations of HER2 and EGFR Genes in Non Small Cell Lung Cancer NSCLC M. Ozdemir, P. Uludag, A. Uludag, B. Durak, N. Buyukpinarbasili, E. Tepeli, S. Artan European Human Genetics Conference, May 31-June 3, 2008 Cilt. Sayf.-
Osteoporosis Pseudoglioma syndrome in two sisters G.O. Cetin, F. Duzcan, E. Tepeli, F. S. Kirac. European Human Genetics Conference, May 31-June 3, 2008 Cilt. Sayf.-
Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex Ligation Dependent amplification MLPA technique Muslumanoglu H, Yurdakul H, Durak B, Sener T, Tepeli E, Demir S, Artan S. Chromosome Research Cilt. Sayf.-
Comparison of FISH and MLPA techniques in detection of chromosomal rearrangements Artan S., Muslumanoglu MH., Ozdemir M., Durak B., Cilingir O., Bademci G., Tepeli E., Kalkan R., Oznur M., Tekin N. Chromosome Research Cilt. Sayf.-
Methylation profiles of p16 RASSF1C and hMLH1 promoter CpG islands in brain tumors Durmaz R, Uludag A, Artan S, Tepeli E, Arslantas A, Karakas Z, Cilingir O. Neuro-Oncology Cilt. Sayf.-
Vitamin D receptor gene polymorphisims in Turkish psoriasis patients Açıkbaş İ, Erdoğan BŞ, Ergin Ş, Aktan Ş, Tepeli E, Bağcı H. European Human Genetics Conference 2005 Cilt. Sayf.-
A case of prenatal diagnosis of 3p deletion O. Cilingir, E. Tepeli, D. Ustuner, M. Ozdemir, M. H. Muslumanoglu, B. Durak, T. Sezer and S. Artan, 5th European Cytogenetics Conference ( 5th ECC), Madrid, Spain, Cilt. Sayf.-
Non mosaic tetrasomy 9p in an infant with multiple congenital anomalies F.Duzcan, H. Ergin, M. Aytan, E. Tepeli, Ö. Özdemir, S. Basaran Fourth Europen Cytogenetics Conference, Bologna, Italy Cilt. Sayf.-
Bildiriler (Ulusal)
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