Assoc. Prof. SEZİN YAKUT UZUNER

Metrics

Publication

168

Publication (WoS)

Publication (Scopus)

Citation (WoS)

106

H-Index (WoS)

Citation (Scopus)

147

H-Index (Scopus)

Citation (Scholar)

H-Index (Scholar)

Citation (Sobiad)

H-Index (Sobiad)

Citation (Sum Other)

Project

Thesis Advisory

Open Access

UN Sustainable Development Goals

Education

2001 - 2007

Doctorate

Akdeniz University, Institute of Health Sciences , Tıbbi Biyoloji Ve Genetik, Turkey

1998 - 2001

Postgraduate

Akdeniz University, Institute of Health Sciences , Tıbbi Biyoloji Ve Genetik, Turkey

1993 - 1997

Undergraduate

Hacettepe University, Fen Fakültesi, Biyoloji, Turkey

Dissertations

2007

Doctorate

Glial Tümörlerde ARHI Tümör Süpresör Geninde LOH ve Metilasyon Profillerinin Araştırılması

Akdeniz University, Faculty of Medicine, Tıbbi Biyoloji Ve Genetik

2000

Postgraduate

Tekrarlayan düşükleri olan ve sitogenetik olarak karyotipleri normal bulunan çiftlerde kriptik translokasyonların FISH ile araştırılması

Akdeniz University, Faculty of Medicine, Tıbbi Biyoloji Ve Genetik

Foreign Languages

C1 Advanced

English

Certificates, Courses and Trainings

2015

Eğitim Program FEP,ÇEP Çalıştayı

Health&Medicine

Akdeniz Üniversitesi

2015

Soru Kalite Çalıştayı

Health&Medicine

Akdeniz Üniversitesi

2015

Eğitim Ölçme Yöntemlerinin Güncelleştirilmesi ve Geliştirilmesi Kursu

Health&Medicine

Akdeniz Üniversitesi

2014

Mikrodizin Eğitim Çalıştayı

Health&Medicine

Akdeniz Üniversitesi, Tıp Fakültesi, Tıbbi Biyoloji ve Genetik ABD

2011

II. Ulusal Fetal Prenatal ve Postmortem Tanı Kursu

Health&Medicine

Tıbbi Genetik Derneği

2009

İzole ve Akraba Populasyonunda Tıbbi Genetik ve Genomik Analiz Kursu

Health&Medicine

Bilkent Üniversitesi

2007

Eğitim Becerilerinin Geliştirilmesi ve Eğitici Eğitimi Kursu

Education Management and Planning

Akdeniz Üniversitesi, Tıp Fakültesi,

2007

Probleme Dayalı Öğrenim Kursu

Education Management and Planning

Akdeniz Üniversitesi, Tıp Fakültesi,

2007

Avrupa Sitogenetik Kursu

Health&Medicine

european cytogeneticists association

2007

XVII. Ulusal Kanser Kongresi, Temel Onkoloji Kursu

Health&Medicine

Tıbbi Onkoloji Derneği

2005

ESGM 9. Kanser Genetik Hibrid Kursu

Health&Medicine

İstanbul Üniversitesi Detae

2004

IV. Hematoloji İlk Basamak Kursu

Health&Medicine

Türk Hematoloji Derneği

2002

XXIX. Ulusal Hematoloji Kongresi, II. Hematoloji İlk Basamak Kursu

Health&Medicine

Türk Hematoloji Derneği

2002

XXIX. Ulusal Hematoloji Kongresi, VI. Mezuniyet Sonrası Eğitim Kursu

Health&Medicine

Türk Hematoloji Derneği

2000

Moleküler Biyoloji ve Genetik Tekniklerinin Yaşam Bilimlerindeki Uygulamaları

Health&Medicine

Bilkent Üniversitesi

1999

Araştırma Eğitimi Kursu

Education Management and Planning

Akdeniz Üniversitesi, Tıp Fakültesi,

Research Areas

Medicine

Health Sciences

Fundamental Medical Sciences

Research Areas Based on Academic Activities

Avesis Research Areas

WoS Research Areas

Scopus Research Areas

Academic Positions

2011 - Present

Assistant Professor

Akdeniz University, Faculty of Medicine, Tıbbi Genetik

2007 - 2011

Expert

Akdeniz University, Faculty of Medicine, Tıbbi Genetik

1999 - 2007

Research Assistant

Akdeniz University, Faculty of Medicine, Tıbbi Genetik

Managerial Experience

Supervised Theses

2017

Postgraduate

rader-Willi Sendromu Bulgularını Taşıyan Normal Karyotipe Sahip Olgularda Metilasyon ve Uniparental Dizomi (UPD) Profillerinin Araştırılması

YAKUT UZUNER S.

P.Bahşi(Student)

Articles

2025

1. A Single-Center Genotype-Phenotype Correlation Cohort Study of Hyperphenylalaninemia Patients: Genetic Analysis as a Deterministic Tool for Treatment Consistency

Peker A., YAKUT UZUNER S., ALTIOK CLARK Ö., Dal Demirelli G., Akcan Paksoy B., Soyuçen E., et al.

Molecular Syndromology , pp.1-14, 2025 (SCI-Expanded, Scopus)

2024

2. Is intermediate risk really intermediate? Comparison of karyotype and non-invasive prenatal testing results of pregnancies at intermediate risk of trisomy 21 on maternal serum screening

Alkan Bulbul G., Kirtis E., KANDEMİR H., Sanhal C. Y., YAKUT UZUNER S., Karauzum S. B., et al.

Journal of Genetic Counseling , 2024 (SCI-Expanded)

2023

3. Microwave-assisted biofabrication of silver nanoparticles using Helichrysum arenarium flower extract: characterization and biomedical applications.

Acar Ç. A., Pehlivanoğlu S., Yeşilot Ş., Yakut Uzuner S.

Biomass Conversion and Biorefinery , vol.1, pp.5-10, 2023 (SCI-Expanded)

2022

4. Investigation of the relationship between reproductive disorders and chromosomal abnormalities in a large-scale, single-center 10-year retrospective study.

Ertosun M. G., Aracı D. G., Peker A., Uzuner S., Toylu A., Özekıncı M., et al.

JOURNAL OF GYNECOLOGY OBSTETRICS AND HUMAN REPRODUCTION , vol.51, no.9, pp.102467, 2022 (SCI-Expanded, Scopus)

2022

5. Effect of Ultrasound Therapy on Expression of Vascular Endothelial Growth Factor, Vascular Endothelial Growth Factor Receptors, CD31 and Functional Recovery After Facial Nerve Injury.

HİZAY A., ÖZSOY U., Savas K., YAKUT UZUNER S., Ozbey Ö., Akkan S. S., et al.

Ultrasound in medicine & biology , vol.48, no.8, pp.1453-1467, 2022 (SCI-Expanded, Scopus)

2020

6. Erken ve geç gebelik terminasyonu olgularının değerlendirilmesi

KAYA S., Vaizoğlu F., YAKUT UZUNER S., TORU H. S., ŞİMŞEK M., Kumru S.

PERİNATOLOJİ DERGİSİ , vol.28, no.2, pp.82-88, 2020 (TRDizin)

2017

7. Associations between the clinical findings of cases having submicroscopic chromosomal imbalances at chromosomal breakpoints of apparently balanced structural rearrangements

Yakut S., Cetin Z., Clark Ö., Nur B., Mıhçı E., Karauzum S. B.

Gene Reports , vol.7, pp.50-58, 2017 (Scopus)

2016

8. A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES

Cetin Z., ALTIOK-CLARK O., Yakut S., GUZEL-NUR B., MIHÇI E., Berker-Karauzum S.

GENETIC COUNSELING , vol.27, no.1, pp.51-66, 2016 (SCI-Expanded)

2016

9. A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOMPASSING THE 11Q14.1-Q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES

Cetin Z., ALTIOK CLARK Ö., YAKUT UZUNER S., NUR B., MIHÇI E., KARAÜZÜM S.

GENETIC COUNSELING , vol.27, no.1, pp.51-66, 2016 (SCI-Expanded)

2015

10. A familial interstitial 4q35 deletion with no discernible clinical effects.

Yakut S., Clarck Ö., Sanhal C., Nur B., Mendilcioglu İ. İ., Karauzum S. B., et al.

American journal of medical genetics. Part A , no.8, pp.1836-41, 2015 (SCI-Expanded, Scopus)

2015

11. Chromosome Abnormalities Identified in 457 Spontaneous Abortions and Their Histopathological Findings

Yakut S., TORU H. S., Cetin Z., ÖZEL ERKAN D., ŞİMŞEK M., Mendilcioglu I., et al.

TURKISH JOURNAL OF PATHOLOGY , vol.31, no.2, pp.111-118, 2015 (ESCI)

2015

12. PRENATAL DIAGNOSIS OF DE NOVO PERICENTRIC INVERSION INV(2)(p11.2z13)

Yakut S., Cetin Z., SANHAL C. Y., KARAMAN B., MENDİLCİOĞLU İ. İ., KARAÜZÜM S.

GENETIC COUNSELING , vol.26, no.2, pp.243-247, 2015 (SCI-Expanded, Scopus)

2015

13. PRENATAL DIAGNOSIS OF DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATED FROM CHROMOSOME 16 BY ARRAY-CGH

Yakut S., Cetin Z., SANHAL C. Y., KARAÜZÜM S., KARAMAN B., ŞİMŞEK M.

GENETIC COUNSELING , vol.26, no.3, pp.299-305, 2015 (SCI-Expanded)

2015

14. Rare Structural Chromosomal Abnormalities in Prenatal Diagnosis; Clinical and Cytogenetic Findings on 10125 Prenatal Cases

YAKUT UZUNER S., Cetin Z., ŞİMŞEK M., MENDİLCİOĞLU İ. İ., TORU H. S., Berker Karauzum S., et al.

TURKISH JOURNAL OF PATHOLOGY , vol.31, no.1, pp.36-44, 2015 (ESCI)

2014

15. Prenatal management, pregnancy and pediatric outcomes in fetuses with septated cystic hygroma

SANHAL C. Y., MENDİLCİOĞLU İ. İ., Ozekinci M., Yakut S., Merdun Z., ŞİMŞEK M., et al.

BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH , vol.47, no.9, pp.799-803, 2014 (SCI-Expanded)

2014

16. PRENATAL DIAGNOSIS OF ISOCHROMOSOME 21p AND ISOCHROMOSOME 21q IN A FETUS WITH DOWN SYNDROME

Yakut S., SANHAL C. Y., Manguoglu E., Cetin Z.

GENETIC COUNSELING , vol.25, no.3, pp.257-264, 2014 (SCI-Expanded)

2013

17. Prenatal diagnosis of isolated ventriculomegaly as a second trimester manifestation of de novo terminal 6q25 deletion

Cetin Z., SANHAL C. Y., GÜZEL B., Toru S., Yakut S.

Genetic Counseling , vol.24, no.4, pp.427-429, 2013 (SCI-Expanded)

2013

18. Prenatal diagnosis of isolated ventriculomegaly as a second trimester manifestation of de novo terminal 6q25 deletion.

Cetin Z., Sanhal C. Y., Nur B., Toru H. S., Yakut Uzuner S.

GENETIC COUNSELING , vol.24, pp.427-429, 2013 (SCI-Expanded)

2013

19. Absence of the SLC22A12 gene mutation in Turkish population with primary gout disease

Yakut S., Cetin Z., Arman M., Akbas H., MANGUOĞLU A. E., Luleci G.

RHEUMATOLOGY INTERNATIONAL , vol.33, no.11, pp.2921-2925, 2013 (SCI-Expanded, Scopus)

2013

20. A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement

Cetin Z., Yakut S., Clark O. A., MIHÇI E., Berker S., Luleci G.

GENE , vol.516, no.1, pp.176-180, 2013 (SCI-Expanded, Scopus)

2013

21. Exceptional complex chromosomal rearrangement and microdeletions at the 4q22.3q23 and 14q31.1q31.3 regions in a patient with azoospermia

Yakut S., Cetin Z., Clark O. A., USTA M. F., Berker S., Luleci G.

GENE , vol.512, no.1, pp.157-160, 2013 (SCI-Expanded, Scopus)

2012

22. A patient with Down syndrome with a de novo derivative chromosome 21

Cetin Z., Yakut S., MIHÇI E., MANGUOĞLU A. E., Berker S., KESER İ., et al.

GENE , vol.507, no.2, pp.159-164, 2012 (SCI-Expanded, Scopus)

2012

23. Aberrations of Chromosomes 9 and 22 in Acute Lymphoblastic Leukemia Cases Detected by ES-Fluorescence In Situ Hybridization

Cetin Z., Yakut S., Karadogan I., Kupesiz A., Timuragaoglu A., SALİM O., et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS , vol.16, no.5, pp.318-323, 2012 (SCI-Expanded)

2012

24. MOSAIC INTRACHROMOSOMAL TRIPLICATION OF (12)(p11.2p13) IN A PATIENT WITH PALLISTER-KILLIAN SYNDROME

Yakut S., MIHÇI E., Clark A. O., Cetin Z., KESER İ., Berker S., et al.

BALKAN JOURNAL OF MEDICAL GENETICS , vol.15, no.1, pp.61-64, 2012 (SCI-Expanded)

2011

25. DETECTING CHROMOSOMAL ANOMALIES THROUGH M-FISH IN ACUTE LYMPHOBLASTIC LEUKEMIA

Hazar V., Cetin Z., YAKUT UZUNER S., KARAÜZÜM S.

PEDIATRIC BLOOD & CANCER , vol.57, no.5, pp.868-869, 2011 (SCI-Expanded, Scopus)

2011

26. The prenatal diagnosis of familial satellited Yq chromosomes

Yakut S., ÖZTÜRK S., ŞİMŞEK M., MENDİLCİOĞLU İ. İ., LULECI G.

TURKISH JOURNAL OF MEDICAL SCIENCES , vol.41, no.5, pp.945-948, 2011 (SCI-Expanded)

2011

27. Pure and Complete 12p Trisomy Due To a Maternal Centric Fission of Chromosome 12

Cetin Z., MIHÇI E., Yakut S., KESER İ., Karauzum S. B., Luleci G.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.155A, no.2, pp.349-352, 2011 (SCI-Expanded)

2011

28. DEL (18p) SYNDROME WITH INCREASED NUCHAL TRANSLUCENCY REVEALED IN PRENATAL DIAGNOSIS

YAKUT S., ŞİMŞEK M., PEŞTERELİ H. E., Baumer A., LULECI G., Schinzel A.

GENETIC COUNSELING , vol.22, no.3, pp.317-319, 2011 (SCI-Expanded, Scopus)

2011

29. DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATING FROM CHROMOSOME 17 RESULTING IN A NORMAL PREGNANCY OUTCOME

Yakut S., Cetin Z., Berker-Karauzum S., MIHÇI E., MENDİLCİOĞLU İ. İ., Luleci G.

GENETIC COUNSELING , vol.22, no.1, pp.63-68, 2011 (SCI-Expanded)

2011

30. INTERSTITIAL DELETION OF 13q22-q32: A CASE WITH CHOANAL ATRESIA AND MEGA-CISTERNA MAGNA AND REVIEW OF THE LITERATURE

Cetin Z., MIHÇI E., Yakut S., KARAALİ K., Luleci G., KESER İ.

GENETIC COUNSELING , vol.22, no.3, pp.313-316, 2011 (SCI-Expanded)

2011

31. PRENATAL DIAGNOSIS OF beta-THALASSEMIA AND OTHER HEMOGLOBINOPATHIES IN SOUTHWESTERN TURKEY

Mendilcioglu I., Yakut S., KESER İ., ŞİMŞEK M., YESILIPEK A., BAGCI G., et al.

HEMOGLOBIN , vol.35, no.1, pp.47-55, 2011 (SCI-Expanded)

2011

32. APLASIA RAS HOMOLOGOUS MEMBER I GENE AND DEVELOPMENT OF GLIAL TUMORS

Yakut S., TUNCER M. R., BERKER M., GÖKSU E., GÜRER İ. E., Ozes O. N., et al.

BALKAN JOURNAL OF MEDICAL GENETICS , vol.14, no.1, pp.37-43, 2011 (SCI-Expanded)

2011

33. TURNER SYNDROME WITH ISOCHROMOSOME Xq AND FAMILIAL RECIPROCAL TRANSLOCATION t(4;16)(p15.2;p13.1)

Cetin Z., MENDİLCİOĞLU İ. İ., Yakut S., Berker-Karauzum S., KARAMAN B., Luleci G.

BALKAN JOURNAL OF MEDICAL GENETICS , vol.14, no.1, pp.57-60, 2011 (SCI-Expanded)

2009

34. PRENATAL DIAGNOSIS OF A DE NOVO SUPERNUMERARY MARKER CHROMOSOME ORIGINATING FROM CHROMOSOME 16

Yakut S., Cetin Z., ŞİMŞEK M., KARAÜZÜM S., Tukun A., Luleci G.

GENETIC COUNSELING , vol.20, no.4, pp.327-332, 2009 (SCI-Expanded, Scopus)

2007

35. LOH on 1p/19q and 10q and Ki-67 labelling index in glial tumors

GÜRER İ. E., Yakut S., Karauzum S. B., Coksu E., Gokhan G.

VIRCHOWS ARCHIV , vol.451, no.2, pp.243, 2007 (SCI-Expanded)

2007

36. Maternal origin and clinical findings in a case with trisomy 22

Mihci E., Tacoy S., Yakut S., Ongun H., Keser İ., Kilicarslan B., et al.

TURKISH JOURNAL OF PEDIATRICS , vol.49, no.3, pp.322-326, 2007 (SCI-Expanded, Scopus)

2006

37. An unusual case of chromosome 22q11 deletion syndrome with psychiatric disorder, hypoparathyroidism and precocious puberty

Karaguzel G., Akcurin S., Yakut S., Bircan I.

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM , vol.19, no.5, pp.761-764, 2006 (SCI-Expanded, Scopus)

2005

38. Molecular Diagnosis of Hematological Malignancies by RT-PCR

BERKER S., MANGUOĞLU A. E., Nal N., YAKUT S., Sargin F., Alper O., et al.

TURKISH JOURNAL OF CANCER , vol.35, no.3, pp.113-118, 2005 (Peer-Reviewed Journal)

2005

39. M-FISH applications in clinical genetics

Cetin Z., Karauzum S., Yakut S., Mihci E., Baumer A., Wey E., et al.

GENETIC COUNSELING , vol.16, no.3, pp.257-268, 2005 (SCI-Expanded)

2005

40. Akdeniz Üniversitesi, Tıp Fakültesinin prenatal tanı sitogenetik tanı sonuçları

ALPER Ö., Çalışkan M., Nal N., Yakut Uzuner S., Şimşek M., Mendilcioğlu İ., et al.

Jinekoloji ve Obstetrik , vol.19, pp.10-16, 2005 (Peer-Reviewed Journal)

2002

41. Telomere-specific fluorescence in situ hybridization analysis of couples with five or more recurrent miscarriages

Yakut S., Berker-Karauzum S., Simsek M., ZORLU G., TRAK B., LULECI G.

CLINICAL GENETICS , vol.61, no.1, pp.26-31, 2002 (SCI-Expanded)

Papers Presented at Peer-Reviewed Scientific Conferences

2022

1. Reprodüktif Hastalıklar ile Kromozomal Anormallikler Arasındaki İlişkinin İncelenmesi, Tek Merkezli ve Büyük Ölçekli 10 Yıllık Retrospektif Bir Çalışma

ERTOSUN M. G., ARACI D. G., PEKER A., YAKUT UZUNER S., TOYLU A., ÖZEKİNCİ M., et al.

15. Ulusal Tıbbi Genetik Kongresi, Muğla-Bodrum, Turkey, 9 - 13 November 2022, (Summary Text)

2022

2. Musculocontractural type of Ehler-Danlos syndrome with severeskeletal findings in the novel variant of CHST14 gene

Yılmaz Bayer Ö., Öztürk N., Yakut Uzuner S., Karamık G., Nur B., Mıhçı E.

ESHG, Vienna, Austria, 11 - 14 June 2022, (Summary Text)

2019

3. Prader-Willi Sendromu bulgularını taşıyan normal karyotipe sahip olgularda metilasyon ve uniparental dizomi profillerinin araştırılması

BAHŞİ P., YAKUT UZUNER S., NUR B.

ULUSLARARASI KATILIMLI TIBBİ BİYOLOJİ VE GENETİK KONGRESİ, 27 - 30 October 2019, (Summary Text)

2017

4. Ailesel amiloidozis polinöropatisi olduğudüşünülen olgularda TTR gen mutasyonlarınınaraştırılması

BAHŞİ P., YAKUT UZUNER S., UYSAL H., KARAÜZÜM S.

XV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Fethiye, Turkey, 26 - 29 October 2017, (Summary Text)

2016

5. Patau sendromlu bir fetus olgusu nedeniyle holoprozensefali ve siklopi anomalisine yaklaşım Poster kabul edildi

NUR B., YÜKSEL N., YAKUT UZUNER S., MENDİLCİOĞLU İ. İ.

52. Türk Pediatri Kongresi, Turkey, 15 - 19 May 2016

2016

6. Patau sendromlu bir fetus olgusu nedeniyle holoprozensefali ve siklopi anomalisine yaklaşım

NUR B., Yuksek N., YAKUT UZUNER S., MENDİLCİOĞLU İ. İ.

52. Türk Pediatri Kongresi, Antalya, Turkey, 15 - 19 May 2016, pp.93, (Full Text)

2016

7. Patau sendromlu bir fetus olgusu nedeniyle holoprozensefali ve siklopi anomalisine yaklaşım

Nur B., Yuksek N., Yakut Uzuner S., Mendilcioğlu İ. İ.

52. Türk Pediatri Kongresi, Antalya, Turkey, 15 - 19 May 2016, pp.93, (Summary Text)

2015

8. Prenatal Dönemde Tanı Almıs Bir Pallister-Killian Olgu Sunumu.

Cetin Z., Sanhal c., MENDİLCİOĞLU İ. İ., YAKUT UZUNER S.

XIV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 - 30 October 2015, pp.396, (Full Text)

2015

9. Prenatal Tanıda Belirlenmis ve array-CGH ile 16 Numaralı Kromozomdan Orijin Aldıgı Saptanmıs Olan Marker Kromozom

Cetin Z., YAKUT UZUNER S., sanhal c., KARAÜZÜM S., Karaman B., ŞİMŞEK M.

XIV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 - 30 October 2015, pp.386, (Full Text)

2015

10. Prenatal Dönemde Tanı Almıs Bir Pallister-Killian Olgu Sunumu.

Cetin Z., Sanhal c., MENDİLCİOĞLU İ. İ., YAKUT UZUNER S.

XIV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 - 30 October 2015, pp.396, (Full Text)

2015

11. Çoklu konjenital anomaliye sahip bir olguda moleküler olarak karekterize edilmiş 11q14.1-q23.3 ara delesyonu

Çetin Z., Altıok Clark Ö., Yakut Uzuner S., Nur B., Mıhçı E., Karaüzüm S.

14. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 - 30 October 2015, pp.385, (Full Text)

2015

12. A familial Interstitial 4q35 deletion with no discernible clinical effects.

Altıok Clark Ö., Yakut Uzuner S., Nur B., Mıhçı E., Karaüzüm S., Cetin Z.

10. European Cytogenetics Conference, Strasbourg, France, 4 - 07 July 2015, (Summary Text)

2015

13. A familial Interstitial 4q35 deletion with no discernible clinical effects.

ALTIOK CLARK Ö., YAKUT UZUNER S., NUR B., MIHÇI E., KARAÜZÜM S., Cetin Z.

10. European Cytogenetics Conference, Strasbourg, France, 4 - 07 July 2015, (Full Text)

2015

14. A familial interstitial 4q35 deletion with no discernible clinical effects.

ALTIOK CLARK Ö., YAKUT UZUNER S., NUR B., MIHÇI E., KARAÜZÜM S., ÇETİN Z.

10th European Cytogenetics Conference, Strasburg, France, 4 - 07 July 2015, pp.51, (Full Text)

2014

15. Tekil Gebelikte Multiple Konjenital Anomalili Fetus ve Parsiyel Mol Hidatidiform Birlikteliği: Olgu Sunumu

TORU H. S., AYIK E., SANHAL C. Y., YAKUT UZUNER S., MENDİLCİOĞLU İ. İ.

24.Ulusal Patoloji Kongresi, Trabzon, Turkey, 19 - 23 November 2014, pp.123, (Full Text)

2014

16. Tekil Gebelikte Multiple Konjenital Anomalili Fetus ve Parsiyel Mol Hidatidiform Birlikteliği: Olgu Sunumu

TORU H. S., AYIK E., SANHAL C. Y., YAKUT UZUNER S., MENDİLCİOĞLU İ. İ.

24.Ulusal Patoloji Kongresi, Trabzon, Turkey, 19 - 23 November 2014, pp.123, (Full Text)

2014

17. Tekil Gebelikte Multiple Konjenital Anomalili Fetus ve Parsiyel Mol Hidatidiform Birlikteliği: Olgu Sunumu

TORU H. S., AYIK E., SANHAL C. Y., YAKUT UZUNER S., MENDİLCİOĞLU İ. İ.

24.Ulusal Patoloji Kongresi, Trabzon, Turkey, 19 - 23 November 2014, pp.123, (Full Text)

2014

18. Dengeli olduğu düşünülen kromozom aberasyonları ve klinik bulguları bulunan olgularda kırık noktalarının Array CGH yöntemi ile incelenmesi

ÇETİN Z., YAKUT UZUNER S., ALTIOK CLARK Ö., NUR B., MIHÇI E., KARAÜZÜM S.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 26 September 2014

2014

19. Dengeli olduğu düşünülen kromozom aberasyonları ve klinik bulguları bulunan olgularda kırık noktalarının array-CGH yöntemi ile incelenmesi

Cetin Z., YAKUT UZUNER S., ALTIOK CLARK Ö., NUR B., MIHÇI E., KARAÜZÜM S.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, vol.1, no.1, pp.93, (Full Text)

2014

20. de novo Perisentrik İnversiyon inv(2)(p11.2q13)’ ye Sahip Prenatal Dönemde Belirlenmiş Bir Olgu Sunumu.

Cetin Z., YAKUT S., SANHAL C. Y., Karaman B., Mendilcioglu İ.

11. Ulusal Tıbbi genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.114, (Full Text)

2014

21. Belirgin Bir Fenotipe Neden Olmayan 4q35.1-4q35.2 Delesyonuna Sahip Bir Aile Sunumu.

Altıok Clark Ö., Yakut S., Sanhal C. Y., Nur B., Mendilcioğlu İ. İ., Cetin Z.

11. Ulusal Tıbbi genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.33, (Summary Text)

2014

22. Dengeli Olduğu Düşünülen Kromozom Aberasyonları ve Klinik Bulguları Bulunan Olgularda Kırık Noktalarının Array-CGH Yöntemi ile İncelenmesi.

Cetin Z., Yakut S., Altıok Clark Ö., Nur B., Mıhçı E., Berker S.

11. Ulusal Tıbbi genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.93, (Summary Text)

2014

23. Diagnostic pitfall for placenta placental mesenchymal dysplasia

TORU H. S., ÇOBANKENT AYTEKİN E., SANHAL C. Y., YAKUT UZUNER S., ÇETİN Z., MENDİLCİOĞLU İ. İ., et al.

26th European Congress of Pathology, 30 August - 03 September 2014

2014

24. Bilateral renal agenesis associated with left lung agenesis, cleft-lib, hydrocephalus and placental malformation: Is it a spectrum of the so-called Potter's Syndrome

TORU H. S., SANHAL C. Y., YILMAZ G. T., YAKUT UZUNER S., ÇETİN Z.

26th European Congress of Pathology, Londra, United Kingdom, 30 August - 03 September 2014, vol.465, pp.202, (Full Text)

2014

25. Diagnostic pitfall for placenta: placental mesenchymal dysplasia

TORU H. S., ÇOBANKENT AYTEKİN E., SANHAL C. Y., YAKUT S., Cetin Z., MENDİLCİOĞLU İ. İ., et al.

26th European Congress of Pathology, Londra, United Kingdom, 1 - 30 August 2014, pp.200, (Full Text)

2014

26. Diagnostic pitfall for placenta: placental mesenchymal dysplasia

TORU H. S., ÇOBANKENT AYTEKİN E., SANHAL C. Y., YAKUT S., Cetin Z., MENDİLCİOĞLU İ. İ., et al.

x, Londra, United Kingdom, 1 - 30 August 2014, pp.200, (Full Text)

2014

27. Bilateral renal agenesis associated with left lung agenesis, cleft-lip, hydrocephalus and placental malformation: Is it on a spectrum of the so-called Potter’s Syndrome?

TORU H. S., SANHAL C. Y., TAŞOVA YILMAZ G., YAKUT S., Cetin Z.

Virchows Archiv, Londra, United Kingdom, 1 - 05 August 2014, pp.202, (Full Text)

2014

28. Mesomelic dysplasia mimicking Robert’s Syndrome.

TORU H. S., NUR B., SANHAL C. Y., AYIK E., YAKUT S., Cetin Z., et al.

Virchows Archiv, Londra, United Kingdom, 1 - 05 August 2014, pp.202, (Full Text)

2014

29. Diagnostic pitfall for placenta: placental mesenchymal dysplasia

TORU H. S., ÇOBANKENT AYTEKİN E., SANHAL C. Y., YAKUT S., Cetin Z., MENDİLCİOĞLU İ. İ., et al.

x, Londra, United Kingdom, 1 - 30 August 2014, pp.200, (Full Text)

2014

30. Diagnostic pitfall for placenta: placental mesenchymal dysplasia

TORU H. S., ÇOBANKENT AYTEKİN E., SANHAL C. Y., YAKUT S., Cetin Z., MENDİLCİOĞLU İ. İ., et al.

Virchows Archiv, Londra, United Kingdom, 1 - 05 August 2014, pp.200, (Full Text)

2013

31. Absence of the SLC22A12 gene mutation in Turkish population with primary gout disease.

YAKUT UZUNER S., Cetin Z., Arman M., AKBAŞ S. H., MANGUOĞLU A. E., Lüleci G., et al.

5th European Molecular Biology Organization (EMBO)Meeting, Amsterdam, Netherlands, 21 - 24 September 2013, pp.134, (Full Text)

2012

32. Kompleks Kromozom Aberasyonu ile 4q22.3q23 ve 14q31.1q31.3 Bölgelerinde Mikrodelesyona Sahip Azoospermi’li Olgu Sunumu.

Cetin Z., Yakut S., Altıok Clark Ö., Usta M. F., Berker S., Lüleci G.

10. Ulusal Tıbbi genetik Kongresi, Bursa, Turkey, 19 - 23 December 2012, pp.87, (Summary Text)

2012

33. HTR1A ve RNF180 Genlerini İçeren 5q12.1-5q12.3 Bölgesinin Mikrodelesyonuna Sahip Bir Olgu Sunumu.

Cetin Z., YAKUT S., ALTIOK CLARK Ö., MIHÇI E., BERKER S., Luleci G.

10. Ulusal Tıbbi genetik Kongresi, Bursa, Turkey, 19 - 23 December 2012, pp.54, (Full Text)

2012

34. Kompleks Kromozom Aberasyonu ile 4q22.3q23 ve 14q31.1q31.3 Bölgelerinde Mikrodelesyona Sahip Azospermi’li Olgu Sunumu

Cetin Z., YAKUT UZUNER S., ALTIOK CLARK Ö., USTA M. F., KARAÜZÜM S., Lüleci G.

10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 19 - 22 December 2012, pp.87, (Full Text)

2012

35. HTR1A ve RNF180 Genlerini İçeren 5q12.1 -5q12.3 Bölgesinin Mikrodelesyonuna Sahip Bir Olgu Sunumu

Cetin Z., Yakut Uzuner S., Altıok Clark Ö., Mıhçı E., Karaüzüm S., Lüleci G.

10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 19 - 23 December 2012, pp.54, (Summary Text)

2012

36. Prenatal management pregnancy and pediatric outcome in fetuses with septated cystic hygroma.

MENDİLCİOĞLU İ. İ., SANHAL C. Y., YAKUT UZUNER S., ŞİMŞEK M., ÖZEKİNCİ M., sarıtaş z., et al.

22nd World Congress on Ultrasound in Obstetrics and Gynecology, Copenhagen, Denmark, 9 - 12 September 2012, vol.40, no.1, pp.190, (Full Text)

2012

37. Prenatal management pregnancy and pediatric outcome in fetuses with septated cystic hygroma.

MENDİLCİOĞLU İ. İ., SANHAL C. Y., YAKUT UZUNER S., ŞİMŞEK M., ÖZEKİNCİ M., sarıtaş z., et al.

22nd World Congress on Ultrasound in Obstetrics and Gynecology, Copenhagen, Denmark, 9 - 12 September 2012, vol.40, no.1, pp.190, (Full Text)

2011

38. Detecting Chromosomal Anomalies Through M-FISH in Acute Lymphoblastic Leukemia.

Hazar V., Çetin Z., YAKUT S., BERKER S.

43 rd Congress of Tha International Society of Pediatric Oncology (SIOP) 2011, Auckland, New Zealand, 28 - 30 November 2011, pp.868-869, (Full Text)

2011

39. Detecting Chromosomal Anomalies Through M-FISH in Acute Lymphoblastic Leukemia.

Hazar V., Çetin Z., YAKUT S., BERKER S.

43 rd Congress of Tha International Society of Pediatric Oncology (SIOP) 2011, Auckland, New Zealand, 28 - 30 November 2011, pp.868-869, (Full Text)

2011

40. Down Sendromu Olgusunda Gözlenen de novo Rekombinant Kromozom 21

Cetin Z., YAKUT S., MANGUOĞLU A. E., MIHÇI E., BERKER S., KESER İ., et al.

XII.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Turkey, 27 - 30 October 2011, pp.158-159, (Full Text)

2011

41. Down Sendromu Olgusunda Gözlenen de novo Rekombinant Kromozom 21

Cetin Z., YAKUT S., MANGUOĞLU A. E., MIHÇI E., BERKER S., KESER İ., et al.

XII.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Turkey, 27 - 30 October 2011, pp.158-159, (Full Text)

2011

42. Down Sendromu Olgusunda Gözlenen de novo Rekombinant Kromozom 21

Cetin Z., YAKUT S., MANGUOĞLU A. E., MIHÇI E., BERKER S., KESER İ., et al.

XII.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Turkey, 27 - 30 October 2011, pp.158-159, (Full Text)

2011

43. Prenatal Tanıda Nadir Görülen Kromozomal Abnormaliteler; 10125 Prenatal Olgunun Sitogenetik ve Klinik Bulguları.

Lüleci G., YAKUT S., Cetin Z., ŞİMŞEK M., MENDİLCİOĞLU İ. İ., Toru S., et al.

XII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Turkey, 27 - 30 October 2011, pp.165-166, (Full Text)

2011

44. ürk Popülasyonunda SLC22A12 Gen Mutasyonlarının Gut Hastalığı Üzerindeki Etkisi

YAKUT S., Cetin Z., ARMAN M. İ., AKBAŞ S. H., MANGUOĞLU A. E., Lüleci G.

XII.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Turkey, 27 - 30 October 2011, pp.209-210, (Full Text)

2011

45. ürk Popülasyonunda SLC22A12 Gen Mutasyonlarının Gut Hastalığı Üzerindeki Etkisi

YAKUT S., Cetin Z., ARMAN M. İ., AKBAŞ S. H., MANGUOĞLU A. E., Lüleci G.

XII.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Turkey, 27 - 30 October 2011, pp.209-210, (Full Text)

2011

46. Abnormal Signal Patterns Involved in t(12;21) TEL-AML1 in Childhood Acute Lymphoblastic Leukemia Patients.

ALTIOK CLARK Ö., Ozkaya C., YAKUT S., Cetin Z., KÜPESİZ O. A., Tezcan G., et al.

12th International Congress of Human Genetics/61st Annual Meeting of The American Society of Human Genetics, Montreal, Canada, 12 October 2011, pp.651, (Full Text)

2011

47. Abnormal Signal Patterns Involved in t(12;21) TEL-AML1 in Childhood Acute Lymphoblastic Leukemia Patients.

Altıok Clark Ö., Ozkaya C., Yakut S., Cetin Z., Küpesiz O. A., Tezcan G., et al.

12th International Congress of Human Genetics/61st Annual Meeting of The American Society of Human Genetics, Montreal, Canada, 12 October 2011, pp.651, (Summary Text)

2011

48. A Down Syndrome Patient with a de novo Recombinant Chromosome

Luleci G., Cetin Z., YAKUT S., MIHÇI E., MANGUOĞLU E., BERKER S., et al.

International Congress of Human Genetics and the American Society of Human Genetics 61th Annual Meeting, Montreal, Canada, 11 - 15 October 2011, pp.273, (Full Text)

2011

49. A Down Syndrome Patient with a de novo Recombinant Chromosome

Luleci G., Cetin Z., YAKUT S., MIHÇI E., MANGUOĞLU E., BERKER S., et al.

International Congress of Human Genetics and the American Society of Human Genetics 61th Annual Meeting, Montreal, Canada, 11 - 15 October 2011, pp.273, (Full Text)

2011

50. A Down Syndrome Patient with a de novo Recombinant Chromosome

Luleci G., Cetin Z., YAKUT S., MIHÇI E., MANGUOĞLU E., BERKER S., et al.

International Congress of Human Genetics and the American Society of Human Genetics 61th Annual Meeting, Montreal, Canada, 11 - 15 October 2011, pp.273, (Full Text)

2010

51. Two Cases with Rare Chromosomal Abnormality of Chromosome 12p Presenting Pallister-Killian Syndrome Phenotype.

YAKUT S., Lüleci G., MIHÇI E., Cetin Z., KESER İ., BERKER S.

IX. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 1 - 05 December 2010, pp.21, (Full Text)

2010

52. Two cases with rare chromosomal abnormality of chromosome 12p presenting Pallister-Killian syndrome phenotype.

Lüleci G., MIHÇI E., Cetin Z., YAKUT S., KESER İ., BERKER S.

The American Society of Human Genetics Annual Meeting, Washington, United States Of America, 2 - 06 October 2010, (Full Text)

2010

53. Two cases with rare chromosomal abnormality of chromosome 12p presenting Pallister-Killian syndrome phenotype.

Lüleci G., MIHÇI E., Cetin Z., YAKUT S., KESER İ., BERKER S.

The American Society of Human Genetics Annual Meeting, Washington, United States Of America, 2 - 06 October 2010, pp.382, (Full Text)

2010

54. Results of prenatal cytogenetic screening at the prenatal laboratory of the Akdeniz University 1993-2009.

YAKUT S., MENDİLCİOĞLU İ. İ., ŞİMŞEK M., Çalışkan M., BERKER S., KESER İ., et al.

Prenatal Diagnosis and Therapy, Amsterdam, Netherlands, 11 - 14 July 2010, pp.94, (Full Text)

2009

55. Rare chromosomal abnormalities and the results of prenatal cytogenetic Diagnosis.

YAKUT S., MENDİLCİOĞLU İ. İ., ŞİMŞEK M., BERKER S., KESER İ., Luleci G.

Mediterranean Medical Genetics Meeting, Ankara, Turkey, 28 June - 01 July 2009, pp.58, (Full Text)

2008

56. Low Expression of ARHI Contributes to Glial Tumor Development.

YAKUT S., TUNCER M. R., Berker M., GÖKSU E. T., Luleci G., BERKER S.

European Human Genetics Conference, Barselona, Spain, 21 May - 03 June 2008, pp.218, (Full Text)

2008

57. Low Expression of ARHI Contributes to Glial Tumor Development.

YAKUT S., TUNCER M. R., Berker M., GÖKSU E. T., Luleci G., BERKER S.

European Human Genetics Conference, Barselona, Spain, 21 May - 03 June 2008, pp.218, (Full Text)

2008

58. Low Expression of ARHI Contributes to Glial Tumor Development.

YAKUT S., TUNCER M. R., Berker M., GÖKSU E. T., Luleci G., BERKER S.

European Human Genetics Conference, Barselona, Spain, 21 May - 03 June 2008, pp.218, (Full Text)

2008

59. Prenatal dönemde tanımlanan markır kromozom.

YAKUT S., Cetin Z., ŞİMŞEK M., Bagci G., BERKER S., Tukun A., et al.

VIII. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 6 - 09 May 2008, pp.211, (Full Text)

2008

60. ARHI Tümör Süpresör Geninin Glial Beyin Tümörlerindeki Rolü.

YAKUT S., TUNCER M. R., Berker M., GÜRER İ. E., BERKER S., Luleci G.

II. Multidisipliner Kanser Sempozyumu,, Bursa, Turkey, 24 - 27 February 2008, pp.140, (Full Text)

2007

61. Rearrangement of chromosome 6 in hematological malignancies.

BERKER S., YAKUT S., Cetin Z., Karadoğan İ., ÜNDAR L., Hazar V., et al.

Chromosome Research, İstanbul, Turkey, 1 - 04 October 2007, pp.214-215, (Full Text)

2007

62. Rearrangement of chromosome 6 in hematological malignancies.

BERKER S., YAKUT S., Cetin Z., Karadoğan İ., ÜNDAR L., Hazar V., et al.

Chromosome Research, İstanbul, Turkey, 1 - 04 October 2007, pp.214-215, (Full Text)

2007

63. LOH on 1p/19q and 10q and Ki-67 labelling index in glial tumors.

GÜRER İ. E., YAKUT UZUNER S., KARAÜZÜM S., GÖKSU E. T., OCAK G. A.

21st European Congress of Pathology, İstanbul, Turkey, 8 - 13 September 2007, pp.243, (Full Text)

2007

64. LOH on 1p/19q and 10q and Ki-67 labelling index in glial tumors.

GÜRER İ. E., YAKUT S., BERKER S., GÖKSU E. T., Gokhan G.

Virchows Archiv, İstanbul, Turkey, 1 - 05 August 2007, pp.243, (Full Text)

2007

65. Amplification of ABL1 gene without BCR/ABL1 fusion in two children with acute lymphoblastic leukemia.

BERKER S., Cetin Z., YAKUT S., Tezcan G., Tulumen T., Hazar V., et al.

European Human Genetics Conference, Nice, France, 16 - 19 June 2007, pp.144

2007

66. Amplification of ABL1 gene without BCR/ABL1 fusion in two children with acute lymphoblastic leukemia.

BERKER S., Cetin Z., YAKUT S., Tezcan G., Tulumen T., Hazar V., et al.

European Human Genetics Conference, Nice, France, 16 - 19 June 2007, pp.144, (Full Text)

2007

67. Screening of 22q11.2 Microdeletion and Microduplications in 110 Patients With Clinical Findings of Digeorge/Velocardiofacial Syndrome.

Lüleci G., Cetin Z., MIHÇI E., YAKUT S., KARDELEN F., Tacoy S., et al.

European Human Genetics Conference, Nice, France, 16 - 19 June 2007, pp.97, (Full Text)

2007

68. Pediatrik akut lenfoblastik lösemide ABL1 gen amplifikasyonunun FISH yöntemi ile gösterilmesi.

BERKER S., Cetin Z., YAKUT S., Tezcan G., Tulumen T., Hazar V., et al.

17. Ulusal Kanser Kongresi, Antalya, Turkey, 19 - 23 April 2007, pp.163, (Full Text)

2007

69. ARHI Tümör Süpresör Geninin Glial Beyin Tümörlerindeki Rolü.

YAKUT S., TUNCER M. R., Berker M., GÜRER İ. E., BERKER S., Lüleci G.

17. Ulusal Kanser Kongresi, Antalya, Turkey, 19 - 23 April 2007, pp.204, (Full Text)

2007

70. Rearrangements of chromosome 6 in hematological malignancies

Berker-Karauzum S. Y., Yakut S., Cetin Z., Karadogan I., Undar L., Hazar V., et al.

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, vol.15, pp.214-215, (Summary Text)

2006

71. KML Ve ALL Tanılı Olgularda t(9;22) Translokasyonuna Spesifik ES-FISH Probu İle Atipik Sinyallerin Gösterilmesi.

BERKER S., Cetin Z., YAKUT S., Dirice E., Temizkan K., Tezcan G., et al.

VII. Ulusal Tıbbi Genetik Ve Prenatal Tanı Kongresi, Kayseri, Turkey, 17 - 20 May 2006, pp.87, (Full Text)

2006

72. ALL Ve AML Hastalarında FISH Yöntemi İle 11q23 Bölgesindeki Yeniden Düzenlenmelerin Belirlenmesi.

YAKUT S., BERKER S., Cetin Z., Tezcan G., KÜPESİZ O. A., Hazar V., et al.

VII. Ulusal Tıbbi Genetik Ve Prenatal Tanı Kongresi, Kayseri, Turkey, 17 - 20 May 2006, pp.180, (Full Text)

2006

73. ALL Ve AML Hastalarında FISH Yöntemi İle 11q23 Bölgesindeki Yeniden Düzenlenmelerin Belirlenmesi.

YAKUT S., BERKER S., Cetin Z., Tezcan G., KÜPESİZ O. A., Hazar V., et al.

VII. Ulusal Tıbbi Genetik Ve Prenatal Tanı Kongresi, Kayseri, Turkey, 17 - 20 May 2006, pp.180, (Full Text)

2006

74. Evaluation of 13q14 deletions by interphase FISH in Multiple Myeloma and Chronic Lymphocytic Leukemia Patients.

Cetin Z., BERKER S., YAKUT S., ÜNDAR L., Karadoğan İ., Timuragaoglu A., et al.

European Human Genetics Conference, Amsterdam, Netherlands, 6 May - 09 June 2006, pp.223, (Full Text)

2006

75. Evaluation of 11q23 rearrangements in Turkish ALL and AML patients by FISH.

YAKUT S., BERKER S., Cetin Z., Tezcan G., KÜPESİZ O. A., Hazar V., et al.

European Human Genetics Conference, Amsterdam, Netherlands, 6 May - 09 June 2006, pp.221, (Full Text)

2006

76. Evaluation of 11q23 rearrangements in Turkish ALL and AML patients by FISH.

YAKUT S., BERKER S., Cetin Z., Tezcan G., KÜPESİZ O. A., Hazar V., et al.

European Human Genetics Conference, Amsterdam, Netherlands, 6 May - 09 June 2006, pp.221, (Full Text)

2006

77. Evaluation of 13q14 deletions by interphase FISH in Multiple Myeloma and Chronic Lymphocytic Leukemia Patients.

Cetin Z., BERKER S., YAKUT S., ÜNDAR L., Karadoğan İ., Timuragaoglu A., et al.

European Human Genetics Conference, Amsterdam, Netherlands, 6 May - 09 June 2006, pp.223, (Full Text)

2005

78. Cytogenetic findings in 133 Turkish patients with myelodysplastic syndrome.

BERKER S., Cetin Z., YAKUT S., Karadoğan İ., Temizkan K., ÜNDAR L., et al.

XXXth World of Congress of International Society of Hematology, İstanbul, Turkey, 28 September - 01 October 2005, pp.231, (Full Text)

2005

79. Hematopoietic Chimerism Analysis After Allogeneic Stem Cell Transplantation in Pediatric Cases

MANGUOĞLU ., BERKER S., KÜPESİZ O. A., Cetin Z., Tezcan G., YAKUT S., et al.

XXXth World Congress of the International Society of Hematology, İstanbul, Turkey, 28 September - 02 October 2005, pp.180-181, (Full Text)

2005

80. Hematopoietic Chimerism Analysis After Allogeneic Stem Cell Transplantation in Pediatric Cases

MANGUOĞLU ., BERKER S., KÜPESİZ O. A., Cetin Z., Tezcan G., YAKUT S., et al.

XXXth World Congress of the International Society of Hematology, İstanbul, Turkey, 28 September - 02 October 2005, pp.180-181, (Full Text)

2005

81. Cytogenetic findings in 133 Turkish patients with myelodysplastic syndrome.

BERKER S., Cetin Z., YAKUT S., Karadoğan İ., Temizkan K., ÜNDAR L., et al.

XXXth World of Congress of International Society of Hematology, İstanbul, Turkey, 28 September - 01 October 2005, pp.231, (Full Text)

2005

82. Hematopoietic Chimerism Analysis After Allogeneic Stem Cell Transplantation in Pediatric Cases

MANGUOĞLU ., BERKER S., KÜPESİZ O. A., Cetin Z., Tezcan G., YAKUT S., et al.

XXXth World Congress of the International Society of Hematology, İstanbul, Turkey, 28 September - 02 October 2005, pp.180-181, (Full Text)

2005

83. Characterization of an unbalanced whole arm translocation leading to monosomy 18p revealed in prenatal diagnosis.

YAKUT S., ŞİMŞEK M., Baumer A., Bagci G., Lüleci G., Schinzel A.

European Human Genetics Conference, Prag, Czech Republic, 7 - 10 May 2005, pp.17, (Full Text)

2005

84. New Complex Variants of the simple translocations in leukaemia cases.

Cetin Z., YAKUT S., BERKER S., Ugur A., Temizkan K., Karadoğan İ., et al.

European Human Genetics Conference, Prag, Czech Republic, 7 - 10 May 2005, pp.190, (Full Text)

2005

85. New Complex Variants of the simple translocations in leukaemia cases.

Cetin Z., YAKUT S., BERKER S., Ugur A., Temizkan K., Karadoğan İ., et al.

European Human Genetics Conference, Prag, Czech Republic, 7 - 10 May 2005, pp.190, (Full Text)

2005

86. Hematopoietic chimerism analysis after allogeneic peripheral stem cell transplantation in pediatric cases by using STR polymorphisms

MANGUOĞLU E., BERKER S., KÜPESİZ O. A., Cetin Z., Tezcan G., YAKUT S., et al.

European Human Genetics Conference 2005, Prag, Czech Republic, 7 - 10 May 2005, pp.225, (Full Text)

2005

87. Hematopoietic chimerism analysis after allogeneic peripheral stem cell transplantation in pediatric cases by using STR polymorphisms

MANGUOĞLU E., BERKER S., KÜPESİZ O. A., Cetin Z., Tezcan G., YAKUT S., et al.

European Human Genetics Conference 2005, Prag, Czech Republic, 7 - 10 May 2005, pp.225, (Full Text)

2005

88. Hematopoietic chimerism analysis after allogeneic peripheral stem cell transplantation in pediatric cases by using STR polymorphisms

MANGUOĞLU E., BERKER S., KÜPESİZ O. A., Cetin Z., Tezcan G., YAKUT S., et al.

European Human Genetics Conference 2005, Prag, Czech Republic, 7 - 10 May 2005, pp.225, (Full Text)

2005

89. Determination of typical and atypical signals of chromosomes 9 and 22 in CML and ALL cases using by Bcr/Abl ES Dual color probe.

BERKER S., YAKUT S., Cetin Z., Dirice E., Karadoğan İ., KÜPESİZ O. A., et al.

European Human Genetics Conference, Prag, Czech Republic, 7 - 10 May 2005, pp.190, (Full Text)

2004

90. Pediatric ALL'li Olgularda t(12;21) Translokasyonun Önem

MANGUOĞLU A. E., BERKER S., YAKUT S., Nal N., Alper O., KÜPESİZ O. A., et al.

Türk Hematoloji Derneği XXXI.Ulusal Kongresi, Antalya, Turkey, 23 - 28 September 2004, pp.107, (Full Text)

2004

91. JMML Gelişiminde Rol Oynaması Olası Yeni Bir Aday gen: GRB10

Cetin Z., BERKER S., YAKUT S., MANGUOĞLU A. E., Tezcan G., KÜPESİZ O. A., et al.

Türk Hematoloji Derneği XXXI.Ulusal Kongresi, Antalya, Turkey, 23 - 28 September 2004, pp.106-107, (Full Text)

2004

92. JMML Gelişiminde Rol Oynaması Olası Yeni Bir Aday gen: GRB10

Cetin Z., BERKER S., YAKUT S., MANGUOĞLU A. E., Tezcan G., KÜPESİZ O. A., et al.

Türk Hematoloji Derneği XXXI.Ulusal Kongresi, Antalya, Turkey, 23 - 28 September 2004, pp.106-107, (Full Text)

2004

93. Pediatric ALL'li Olgularda t(12;21) Translokasyonun Önem

MANGUOĞLU A. E., BERKER S., YAKUT S., Nal N., Alper O., KÜPESİZ O. A., et al.

Türk Hematoloji Derneği XXXI.Ulusal Kongresi, Antalya, Turkey, 23 - 28 September 2004, pp.107, (Full Text)

2004

94. Pediatric ALL'li Olgularda t(12;21) Translokasyonun Önem

MANGUOĞLU A. E., BERKER S., YAKUT S., Nal N., Alper O., KÜPESİZ O. A., et al.

Türk Hematoloji Derneği XXXI.Ulusal Kongresi, Antalya, Turkey, 23 - 28 September 2004, pp.107, (Full Text)

2004

95. JMML Gelişiminde Rol Oynaması Olası Yeni Bir Aday gen: GRB10

Cetin Z., BERKER S., YAKUT S., MANGUOĞLU A. E., Tezcan G., KÜPESİZ O. A., et al.

Türk Hematoloji Derneği XXXI.Ulusal Kongresi, Antalya, Turkey, 23 - 28 September 2004, pp.106-107, (Full Text)

2004

96. Evaluation of clinical findings in our patients with Williams syndrome.

MIHÇI E., Tacoy S., Cetin Z., YAKUT S., KARDELEN F., BERKER S., et al.

European Human Genetics Conference, Munich, Germany, 12 - 15 June 2004, pp.288, (Full Text)

2004

97. Williams Sendromlu Dört Olgunun Klinik Bulgularının Değerlendirilmesi.

Tacoy S., MIHÇI E., Cetin Z., YAKUT S., KARDELEN F., BERKER S., et al.

VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi., Antalya, Turkey, 21 - 24 April 2004, pp.69, (Full Text)

2004

98. Tandem Duplikasyon ve Parsiyel Trizomilerde Parental Orijinin Belirlenmesi.

YAKUT S., BERKER S., Cetin Z., MIHÇI E., Baumer A., Wey E., et al.

VI. Ulusal Tıbbi Genetik Ve Prenatal Tanı Kongresi, Antalya, Turkey, 21 - 24 April 2004, pp.70, (Full Text)

2003

99. Determination of chromosome aberrations by cytogenetic, fluorescence in situ hybridisation, and molecular (RT-PCR) analysis in childhood haematological malignancies

MANGUOĞLU E., BERKER S., YAKUT S., Cetin Z., Nal N., KÜPESİZ O. A., et al.

European Human Genetics Conference 2003, Birmingham, United Kingdom, 3 - 06 May 2003, pp.80, (Full Text)

2003

100. Cytogenetic, fluorescence in situ hybridisaiton (FISH), and molecular (RT-PCR) analysis results of adult haematological malignancy patients

BERKER S., MANGUOĞLU E., YAKUT S., Bilgen T., Nal N., Ugur A., et al.

European Human Genetics Conference 2003, Birmingham, United Kingdom, 3 - 06 May 2003, pp.83, (Full Text)

2003

101. Determination of chromosome aberrations by cytogenetic, fluorescence in situ hybridisation, and molecular (RT-PCR) analysis in childhood haematological malignancies

MANGUOĞLU E., BERKER S., YAKUT S., Cetin Z., Nal N., KÜPESİZ O. A., et al.

European Human Genetics Conference 2003, Birmingham, United Kingdom, 3 - 06 May 2003, pp.80, (Full Text)

2003

102. Determination of chromosome aberrations by cytogenetic, fluorescence in situ hybridisation, and molecular (RT-PCR) analysis in childhood haematological malignancies

MANGUOĞLU E., BERKER S., YAKUT S., Cetin Z., Nal N., KÜPESİZ O. A., et al.

European Human Genetics Conference 2003, Birmingham, United Kingdom, 3 - 06 May 2003, pp.80, (Full Text)

2003

103. Cytogenetic, fluorescence in situ hybridisaiton (FISH), and molecular (RT-PCR) analysis results of adult haematological malignancy patients

BERKER S., MANGUOĞLU E., YAKUT S., Bilgen T., Nal N., Ugur A., et al.

European Human Genetics Conference 2003, Birmingham, United Kingdom, 3 - 06 May 2003, pp.83, (Full Text)

2003

104. Follow-up Bone Marrow Transplantation Success by FISH.

YAKUT S., BERKER S., KÜPESİZ O. A., Hazar V., Yesilipek A., Lüleci G.

European Human Genetics Conference, Birmingham, United Kingdom, 3 - 06 May 2003, pp.88, (Full Text)

2003

105. Cytogenetic, fluorescence in situ hybridisaiton (FISH), and molecular (RT-PCR) analysis results of adult haematological malignancy patients

BERKER S., MANGUOĞLU E., YAKUT S., Bilgen T., Nal N., Ugur A., et al.

European Human Genetics Conference 2003, Birmingham, United Kingdom, 3 - 06 May 2003, pp.83, (Full Text)

2003

106. Monozomi 18p’ye Yol Açan Dengesiz Translokasyonun Prenatal Tanısı ve Parental Orijininin Belirlenmesi.

YAKUT S., Çalışkan M., ŞİMŞEK M., Bagci G., Lüleci G., Trak B.

Fetal Tıp;Prenatal Tanı Kongresi, Antalya, Turkey, 17 - 19 April 2003, pp.80, (Full Text)

2003

107. Monozomi 18p’ ye Yol Açan Dengesiz Translokasyonun Prenatal Tanısı ve Parental Orijininin Belirlenmesi.

YAKUT UZUNER S., ÖZCAN M., ŞİMŞEK M.

Fetal Tıp; Prenatal Tanı Kongresi, Antalya, Turkey, 17 - 19 April 2003, pp.100, (Full Text)

2002

108. Kemik İliği Transplantasyon Başarısının Floresan In Situ Hibridizasyon (FISH) Tekniği İle Takibi.

YAKUT S., BERKER S., KÜPESİZ O. A., Hazar V., Yesilipek A., Lüleci G.

Türk Hematoloji Derneği 29.Ulusal Kongresi, Antalya, Turkey, 25 - 28 October 2002, pp.145, (Full Text)

2002

109. Hematolojik Malignansilerde t(9;22) Translokasyonunun RT-PCR ile Gösterilmesi

BERKER S., MANGUOĞLU A. E., Nal N., YAKUT S., Alper O., KÜPESİZ O. A., et al.

V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.195, (Full Text)

2002

110. Hematolojik Malignansilerde t(9;22) Translokasyonunun RT-PCR ile Gösterilmesi.

BERKER S., MANGUOĞLU AYDEMİR A. E., Nal N., YAKUT S., ALPER Ö., KÜPESİZ O. A., et al.

V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.195, (Full Text)

2002

111. Hematolojik Malignansilerde t(9;22) Translokasyonunun RT-PCR ile Gösterilmesi

BERKER S., MANGUOĞLU A. E., Nal N., YAKUT S., Alper O., KÜPESİZ O. A., et al.

V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.195, (Full Text)

2002

112. Hematolojik Malignansilerde t(9;22) Translokasyonunun RT-PCR ile Gösterilmesi

BERKER S., MANGUOĞLU A. E., Nal N., YAKUT S., Alper O., KÜPESİZ O. A., et al.

V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.195, (Full Text)

2002

113. Tekrarlayan Düşükleri Olan Çiftlerde Kriptik Translokasyonların Telomerik FISH ile Araştırılması.

YAKUT S., Karauzum S. B., ŞİMŞEK M., Zorlu G., Trak B., Lüleci G.

V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.124, (Full Text)

2002

114. Hematolojik Malignansilerde t(9;22) Translokasyonunun RT-PCR ile Gösterilmesi

BERKER S., MANGUOĞLU A. E., Nal N., YAKUT S., Alper O., KÜPESİZ O. A., et al.

V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.195, (Full Text)

2002

115. Detection of RPS4X gene expression using RT-PCR.

YAKUT S., BERKER S., Sargin F., Taksın O., Tacoy S., Lüleci G.

European Human Genetics Conference, Strasbourg,, France, 25 - 29 May 2002, pp.170, (Full Text)

2001

116. Ribozomal Protein S4 X’in Gen Ekspresyonunun RT-PCR İle Gösterilmesi.

YAKUT S., Sargin F., TAŞKIN Ö., Tacoy S., Lüleci G.

7.Ulusal Tıbbi Biyoloji Kongresi, Eskişehir, Turkey, 18 - 21 September 2001, pp.99, (Full Text)

2001

117. Detection of subtelomeric chromosomal rearrangements in couples who had recurrent miscarriages.

YAKUT S., BERKER S., ŞİMŞEK M., Lüleci G.

Third European Cytogenetics Conference, Paris, France, 7 - 10 July 2001, pp.44, (Full Text)

2001

118. De novo duplication of Xq in a girl with some clinical features.

BERKER S., YAKUT S., Cetin Z., MIHÇI E., Lüleci G.

Third European Cytogenetics Conference, Paris, France, 7 - 10 July 2001, pp.181, (Full Text)

2001

119. De novo duplication of Xq in a girl with some clinical features.

BERKER S., YAKUT S., Cetin Z., MIHÇI E., Lüleci G.

Third European Cytogenetics Conference, Paris, France, 7 - 10 July 2001, pp.181, (Full Text)

2000

120. Prenatal Sitogenetik Çalışmalar.

YAKUT S., Nal N., MENDİLCİOĞLU İ. İ., Zorlu G., Lüleci G.

IV.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, İzmir, Turkey, 3 - 06 May 2000, pp.217, (Full Text)

1999

121. A family with sex chromosome aberrations together with a balanced translocation t(4;16).

YAKUT S., BERKER S., Karaman B., Lüleci G., Bagci G.

31st Annual Meeting European Society of Human Genetics, Geneva, Switzerland, 29 May - 01 June 1999, pp.78, (Full Text)

1999

122. A family with sex chromosome aberrations together with a balanced translocation t(4;16).

YAKUT S., BERKER S., Karaman B., Lüleci G., Bagci G.

31st Annual Meeting European Society of Human Genetics, Geneva, Switzerland, 29 May - 01 June 1999, pp.78, (Full Text)

Funded Projects

2023 - Present

KÜÇÜK HÜCRELİ DIŞI AKCİĞER KARSİNOMLARINDA MAKROFAJ AKTİVASYONUNDA ETKİLİ FOLLISTATIN-LIKE PROTEIN 1, HIGH MOBILITY GROUP BOX1, OSTEOPONTIN PROTEİNLERİ ARASINDAKİ İLİŞKİNİN DEĞERLENDİRİLMESİ

SADULLAHOĞLU C., KARAÜZÜM S., ÇAVUŞOĞLU YALÇIN N., YAKUT UZUNER S., ÖZBUDAK İ. H., KARAMAN MERCAN T.(Executive)

2022 - 2024

Prader-Willi Benzeri Sendrom fenotipi gösteren olgularda 6q161-q21 bölgesinin aCGH yöntemi ile incelenmesi

Project Supported by Higher Education Institutions , BAP Research Project

YAKUT UZUNER S. (Executive), NUR B., BAHŞİ P.

2019 - 2020

Bilimsel Araştırmalarda Tıbbi Biyoloji ve Genetik Anabilim Dalının Yeri ve Önemi

Project Supported by Higher Education Institutions , BAP Infrastructure

KESER İ. (Executive), ŞANLIOĞLU A. D., Tokta Ö., Billor M., ALPER Ö., KARAÜZÜM S., et al.

2018 - 2020

Fasiyal sinir hasarı sonrası rejenerasyon süresince ultrason terapinin VEGF ve VEGF reseptörlerinin ekspresyonu üzerine etkisi

Project Supported by Higher Education Institutions , BAP Research Project

HİZAY A. (Executive), ÖZSOY U., YAKUT UZUNER S., ÖZBEY ÜNLÜ Ö., BAHŞİ P.

2017 - 2019

Prader-Willi Sendromu Bulgularını Taşıyan Normal Karyotipe Sahip Olgularda Metilasyon ve Uniparental Dizomi (UPD) Profillerinin Araştırılması

Project Supported by Higher Education Institutions , BAP MSc

YAKUT UZUNER S. (Executive), MIHÇI E., ALTIOK CLARK Ö., NUR B., BAHŞİ P.

2016 - 2019

Sezin Yakut ,Ozden Altiok Clarck ,Cem Sanhal ,Banu Guzel Nur ,Inanc Mendilcioglu, Sibel Berker Karauzum ,Zafer Cetin. Familial Interstitial 4q35 Deletion with No Discernible Clinical Effects ,Am J Med Genet Part A 167A: 1836-1841, 2015(3 yayın)

Project Supported by Higher Education Institutions , BAP Other

KARAÜZÜM S. (Executive), NUR B., ALTIOK CLARK Ö., YAKUT UZUNER S., MIHÇI E., OYGÜR N.

Memberships and Roles in Scientific Organizations

2000 - Present

Türk Kanser Araştırma ve Savaş Kurumu

Member

2000 - Present

Tıbbi Genetik Derneği

Member

Awards

September 2014

Poster Üçüncülük Ödülü / Dengeli Olduğu Düşünülen Kromozom Aberasyonları ve Klinik Bulguları Bulunan Olgularda Kırık Noktalarının Array-CGH Yöntemi ile İncelenmesi.

11. Ulusal Tıbbi genetik Kongresi.

March 2010

Poster Birincilik Ödülü / Retrospektif Down Sendromu(DS) Araştırması

Tıpta Görüntüleme Teknikleri, II. Ulusal Tıp Öğrenci Kongresi

September 2004

Genç Katılımcı Ödülü / Hematolojik Malignansilerde İlk Kez Tanımlanan Kompleks Varyant Translokasyonlar.

Türk Hematoloji Derneği XXXI. Ulusal Kongresi

Congress and Symposium Activities

01 May 2018 - 01 May 2018

1st International Health Science and Life Congress

Attendee

Burdur-Turkey

01 May 2018 - 01 May 2018

1 st International Health Science and Life Congress

Invited Speaker

Burdur-Turkey

01 April 2018 - 01 April 2018

Hücreden Hasta Yatağına:DNA Sempozyumu

Attendee

Antalya-Turkey

01 April 2018 - 01 April 2018

Hücreden Hasta Yatağına: DNA SEmpozyumu

Invited Speaker

Antalya-Turkey

01 October 2017 - 01 October 2017

3. Ulusal Çocuk Genetik Sempozyumu

Attendee

Antalya-Turkey

01 October 2017 - 01 October 2017

3. Ulusal Çocuk Genetik Sempozyumu

Session Moderator

Antalya-Turkey

01 June 2017 - 01 June 2017

Tıbbi Genetikte Algoritmalar Sempozyumu

Attendee

Ankara-Turkey

01 May 2017 - 01 May 2017

Erciyes Tıp Genetik Günleri Kongresi

Attendee

Kayseri-Turkey

01 October 2016 - 01 October 2016

XII. Ulusal Tıbbi Genetik Kongresi (ULUSLARARASI KATILIMLI)

Attendee

İzmir-Turkey

01 September 2013 - 01 September 2013

European Molecular Biology Organisation (EMBO) meeting

Attendee

Amsterdam-Netherlands

01 October 2012 - 01 October 2012

XXIX. Ulusal Hematoloji Kongresi

Attendee

Antalya-Turkey

01 October 2011 - 01 October 2011

XII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi

Attendee

Antalya-Turkey

01 July 2010 - 01 July 2010

15th International Conference on Prenatal Diagnosis and Therapy

Attendee

Amsterdam-Turkey

01 July 2009 - 01 July 2009

Mediterranean Medical Genetics Meeting

Attendee

Ankara-Turkey

01 May 2008 - 01 May 2008

VIII. Ulusal Tıbbi Genetik Kongresi

Attendee

Çanakkale-Turkey

01 May 2008 - 01 May 2008

European Journal of Human Genetics

Attendee

Barselona-Spain

01 February 2008 - 01 February 2008

II.Multidisipliner Kanser Sempozyumu

Attendee

Bursa-Turkey

01 April 2007 - 01 April 2007

XVII. Ulusal Kanser Kongresi

Attendee

Antalya-Turkey

01 May 2006 - 01 May 2006

VII. Ulusal Tıbbi Genetik ve Prenatal Tanı Kongresi

Attendee

Kayseri-Turkey

01 May 2006 - 01 May 2006

European Journal of Human Genetics

Attendee

Amsterdam-Netherlands

01 May 2005 - 01 May 2005

European Journal of Human Genetics

Attendee

Prag-Czech Republic

01 September 2004 - 01 September 2004

XXXI. Ulusal Hematoloji Kongresi

Attendee

Antalya-Turkey

01 April 2004 - 01 April 2004

VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi

Attendee

Antalya-Turkey

01 May 2003 - 01 May 2003

European Journal of Human Genetics

Attendee

Birmingham-United Kingdom

01 April 2003 - 01 April 2003

Fetal Tıp;Prenatal Tanı Kongresi

Attendee

Antalya-Turkey

01 May 2002 - 01 May 2002

European Journal of Human Genetics

Attendee

Strasbourg-France

01 June 2001 - 01 June 2001

European Cytogenetics Conference

Attendee

Paris -France

01 May 2000 - 01 May 2000

IV.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi

Attendee

İzmir-Turkey

01 May 1999 - 01 May 1999

European Journal of Human Genetics

Attendee

Cenevre-Switzerland

Scholarships

2009 - Present

Mediterranean Medical Genetics Meeting 2009 Fellowship

Other International Organizations

2008 - Present