Education
2001 - 2007
2001 - 2007Doctorate
Akdeniz University, Institute of Health Sciences , Tıbbi Biyoloji Ve Genetik, Turkey
1998 - 2001
1998 - 2001Postgraduate
Akdeniz University, Institute of Health Sciences , Tıbbi Biyoloji Ve Genetik, Turkey
1993 - 1997
1993 - 1997Undergraduate
Hacettepe University, Fen Fakültesi, Biyoloji, Turkey
Dissertations
2007
2007Doctorate
Glial Tümörlerde ARHI Tümör Süpresör Geninde LOH ve Metilasyon Profillerinin Araştırılması
Akdeniz University, Tıp Fakültesi, Tıbbi Biyoloji Ve Genetik
2000
2000Postgraduate
Tekrarlayan düşükleri olan ve sitogenetik olarak karyotipleri normal bulunan çiftlerde kriptik translokasyonların FISH ile araştırılması
Akdeniz University, Tıp Fakültesi, Tıbbi Biyoloji Ve Genetik
Foreign Languages
C1 Advanced
C1 AdvancedEnglish
Certificates, Courses and Trainings
2015
2015Eğitim Program FEP,ÇEP Çalıştayı
Health&Medicine
Akdeniz Üniversitesi
2015
2015Soru Kalite Çalıştayı
Health&Medicine
Akdeniz Üniversitesi
2015
2015Eğitim Ölçme Yöntemlerinin Güncelleştirilmesi ve Geliştirilmesi Kursu
Health&Medicine
Akdeniz Üniversitesi
2014
2014Mikrodizin Eğitim Çalıştayı
Health&Medicine
Akdeniz Üniversitesi, Tıp Fakültesi, Tıbbi Biyoloji ve Genetik ABD
2011
2011II. Ulusal Fetal Prenatal ve Postmortem Tanı Kursu
Health&Medicine
Tıbbi Genetik Derneği
2009
2009İzole ve Akraba Populasyonunda Tıbbi Genetik ve Genomik Analiz Kursu
Health&Medicine
Bilkent Üniversitesi
2007
2007Probleme Dayalı Öğrenim Kursu
Education Management and Planning
Akdeniz Üniversitesi, Tıp Fakültesi,
2007
2007Eğitim Becerilerinin Geliştirilmesi ve Eğitici Eğitimi Kursu
Education Management and Planning
Akdeniz Üniversitesi, Tıp Fakültesi,
2007
2007Avrupa Sitogenetik Kursu
Health&Medicine
european cytogeneticists association
2007
2007XVII. Ulusal Kanser Kongresi, Temel Onkoloji Kursu
Health&Medicine
Tıbbi Onkoloji Derneği
2005
2005ESGM 9. Kanser Genetik Hibrid Kursu
Health&Medicine
İstanbul Üniversitesi Detae
2004
2004IV. Hematoloji İlk Basamak Kursu
Health&Medicine
Türk Hematoloji Derneği
2002
2002XXIX. Ulusal Hematoloji Kongresi, VI. Mezuniyet Sonrası Eğitim Kursu
Health&Medicine
Türk Hematoloji Derneği
2002
2002XXIX. Ulusal Hematoloji Kongresi, II. Hematoloji İlk Basamak Kursu
Health&Medicine
Türk Hematoloji Derneği
2000
2000Moleküler Biyoloji ve Genetik Tekniklerinin Yaşam Bilimlerindeki Uygulamaları
Health&Medicine
Bilkent Üniversitesi
1999
1999Araştırma Eğitimi Kursu
Education Management and Planning
Akdeniz Üniversitesi, Tıp Fakültesi,
Research Areas
Medicine
Health Sciences
Fundamental Medical Sciences
Academic Positions
2011 - Continues
2011 - ContinuesAssistant Professor
Akdeniz University, Faculty of Medicine, Tıbbi Genetik
2007 - 2011
2007 - 2011Expert
Akdeniz University, Faculty of Medicine, Tıbbi Genetik
1999 - 2007
1999 - 2007Research Assistant
Akdeniz University, Faculty of Medicine, Tıbbi Genetik
Managerial Experience
Supervised Theses
2017
2017Postgraduate
rader-Willi Sendromu Bulgularını Taşıyan Normal Karyotipe Sahip Olgularda Metilasyon ve Uniparental Dizomi (UPD) Profillerinin Araştırılması
YAKUT UZUNER S.
P.Bahşi(Student)
Journal articles indexed in SCI, SSCI, and AHCI
2024
2024Is 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
2023Microwave-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
2022Investigation 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)
2022
2022Effect 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)
2016
2016A 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
2016A 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
2015A 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)
2015
2015PRENATAL 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
2015PRENATAL 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)
2014
2014Prenatal 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
2014PRENATAL 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
2013Prenatal 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
2013Prenatal 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
2013Absence 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)
2013
2013A 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)
2013
2013Exceptional 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)
2012
2012A 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)
2012
2012Aberrations 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
2012MOSAIC 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
2011DETECTING 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)
2011
2011The 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
2011Pure 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
2011INTERSTITIAL 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
2011PRENATAL 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
2011APLASIA 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
2011DE 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
2011DEL (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)
2011
2011TURNER 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
2009PRENATAL 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)
2007
2007LOH 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
2007Maternal origin and clinical findings in a case with trisomy 22
Mihci E., Tacoy S., Yakut S., Ongun H., Keser I., Kilicarslan B., et al.
TURKISH JOURNAL OF PEDIATRICS
, vol.49, no.3, pp.322-326, 2007 (SCI-Expanded)
2006
2006An 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)
2005
2005M-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)
2002
2002Telomere-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)
Articles Published in Other Journals
2020
2020Erken 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 (Peer-Reviewed Journal)
2017
2017Associations 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)
2015
2015Chromosome 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
2015Rare 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)
2005
2005Molecular 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
2005Akdeniz 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)
Papers Presented at Peer-Reviewed Scientific Conferences
2022
2022Reprodüktif 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
2022
2022Musculocontractural 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
2019Prader-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
2017
2017Ailesel 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
2016Patau 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
2016Patau 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
2016Patau 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
2015
2015Prenatal 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
2015
2015Prenatal 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
2015Prenatal 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
2015
2015Çoklu 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
2015A 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
2015
2015A 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
2015A 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
2014
2014Tekil 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
2014
2014Tekil 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
2014Tekil 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
2014
2014Dengeli 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
2014Dengeli 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
2014
2014de 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
2014Belirgin 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
2014Dengeli 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
2014
2014Diagnostic 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
2014Bilateral 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
2014Diagnostic 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
2014
2014Diagnostic 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
2014
2014Bilateral 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
2014Mesomelic 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
2014
2014Diagnostic 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
2014Diagnostic 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
2013Absence 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
2012Kompleks 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
2012
2012HTR1A 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
2012Kompleks 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
2012
2012HTR1A 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
2012
2012Prenatal 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
2012Prenatal 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
2011
2011Detecting 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
2011Detecting 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
2011Down 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
2011
2011Down 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
2011Down 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
2011Prenatal 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
2011ürk 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
2011
2011ürk 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
2011Abnormal 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
2011Abnormal 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
2011
2011A 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
2011
2011A 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
2011
2011A 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
2010Two 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
2010Two 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
2010Two 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
2010Results 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
2009Rare 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
2008
2008Low 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
2008
2008Low 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
2008Low 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
2008
2008Prenatal 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
2008
2008ARHI 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
2007
2007Rearrangement 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
2007Rearrangement 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
2007LOH 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
2007
2007LOH 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
2007
2007Amplification 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
2007Amplification 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
2007Screening 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
2007
2007Pediatrik 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
2007
2007ARHI 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
2007
2007Rearrangements 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
2006
2006KML 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
2006
2006ALL 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
2006ALL 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
2006Evaluation 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
2006Evaluation 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
2006
2006Evaluation 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
2006
2006Evaluation 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
2005Cytogenetic 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
2005Hematopoietic 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
2005Hematopoietic 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
2005
2005Cytogenetic 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
2005Hematopoietic 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
2005
2005Characterization 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
2005New 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
2005
2005New 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
2005
2005Hematopoietic 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
2005
2005Hematopoietic 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
2005Hematopoietic 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
2005Determination 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
2004Pediatric 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
2004JMML 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
2004
2004JMML 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
2004
2004Pediatric 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
2004Pediatric 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
2004
2004JMML 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
2004Evaluation 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
2004Williams 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
2004
2004Tandem 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
2003
2003Determination 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
2003
2003Cytogenetic, 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
2003Determination 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
2003Determination 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
2003
2003Cytogenetic, 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
2003
2003Follow-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
2003Cytogenetic, 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
2003Monozomi 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
2003Monozomi 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
2002Kemik 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
2002Hematolojik 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
2002
2002Hematolojik 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
2002
2002Hematolojik 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
2002Hematolojik 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
2002Tekrarlayan 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
2002Hematolojik 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
2002Detection 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
2001Ribozomal 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
2001
2001Detection 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
2001
2001De 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
2001De 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
2000Prenatal 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
1999A 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
1999
1999A 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
Funded Projects
2022 - 2024
2022 - 2024Prader-Willi Benzeri Sendrom fenotipi gösteren olgularda 6q161-q21 bölgesinin aCGH yöntemi ile incelenmesi
Project Supported by Higher Education Institutions
YAKUT UZUNER S. (Executive), NUR B., BAHŞİ P.
2019 - 2020
2019 - 2020Bilimsel Araştırmalarda Tıbbi Biyoloji ve Genetik Anabilim Dalının Yeri ve Önemi
Project Supported by Higher Education Institutions
KESER İ. (Executive), ŞANLIOĞLU A. D., Tokta Ö., Billor M., ALPER Ö., KARAÜZÜM S., et al.
2018 - 2020
2018 - 2020Fasiyal sinir hasarı sonrası rejenerasyon süresince ultrason terapinin VEGF ve VEGF reseptörlerinin ekspresyonu üzerine etkisi
Project Supported by Higher Education Institutions
HİZAY A. (Executive), ÖZSOY U., YAKUT UZUNER S., ÖZBEY ÜNLÜ Ö., BAHŞİ P.
2017 - 2019
2017 - 2019Prader-Willi Sendromu Bulgularını Taşıyan Normal Karyotipe Sahip Olgularda Metilasyon ve Uniparental Dizomi (UPD) Profillerinin Araştırılması
Project Supported by Higher Education Institutions
YAKUT UZUNER S. (Executive), MIHÇI E., ALTIOK CLARK Ö., NUR B., BAHŞİ P.
2016 - 2019
2016 - 2019Sezin 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
KARAÜZÜM S. (Executive), NUR B., ALTIOK CLARK Ö., YAKUT UZUNER S., MIHÇI E., OYGÜR N.
Memberships and Roles in Scientific Organizations
2000 - Continues
2000 - Continues
Türk Kanser Araştırma ve Savaş Kurumu
Member
2000 - Continues
2000 - ContinuesTıbbi Genetik Derneği
Member
Awards
September 2014
September 2014Poster 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
March 2010Poster Birincilik Ödülü / Retrospektif Down Sendromu(DS) Araştırması
Tıpta Görüntüleme Teknikleri, II. Ulusal Tıp Öğrenci Kongresi
September 2004
September 2004Genç 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
01 May 2018 - 01 May 20181 st International Health Science and Life Congress
Invited Speaker
Burdur-Turkey
01 May 2018 - 01 May 2018
01 May 2018 - 01 May 20181st International Health Science and Life Congress
Attendee
Burdur-Turkey
01 April 2018 - 01 April 2018
01 April 2018 - 01 April 2018Hücreden Hasta Yatağına: DNA SEmpozyumu
Invited Speaker
Antalya-Turkey
01 April 2018 - 01 April 2018
01 April 2018 - 01 April 2018Hücreden Hasta Yatağına:DNA Sempozyumu
Attendee
Antalya-Turkey
01 October 2017 - 01 October 2017
01 October 2017 - 01 October 20173. Ulusal Çocuk Genetik Sempozyumu
Session Moderator
Antalya-Turkey
01 October 2017 - 01 October 2017
01 October 2017 - 01 October 20173. Ulusal Çocuk Genetik Sempozyumu
Attendee
Antalya-Turkey
01 June 2017 - 01 June 2017
01 June 2017 - 01 June 2017Tıbbi Genetikte Algoritmalar Sempozyumu
Attendee
Ankara-Turkey
01 May 2017 - 01 May 2017
01 May 2017 - 01 May 2017Erciyes Tıp Genetik Günleri Kongresi
Attendee
Kayseri-Turkey
01 October 2016 - 01 October 2016
01 October 2016 - 01 October 2016XII. Ulusal Tıbbi Genetik Kongresi (ULUSLARARASI KATILIMLI)
Attendee
İzmir-Turkey
01 September 2013 - 01 September 2013
01 September 2013 - 01 September 2013European Molecular Biology Organisation (EMBO) meeting
Attendee
Amsterdam-Netherlands
01 October 2012 - 01 October 2012
01 October 2012 - 01 October 2012XXIX. Ulusal Hematoloji Kongresi
Attendee
Antalya-Turkey
01 October 2011 - 01 October 2011
01 October 2011 - 01 October 2011XII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi
Attendee
Antalya-Turkey
01 July 2010 - 01 July 2010
01 July 2010 - 01 July 201015th International Conference on Prenatal Diagnosis and Therapy
Attendee
Amsterdam-Turkey
01 July 2009 - 01 July 2009
01 July 2009 - 01 July 2009Mediterranean Medical Genetics Meeting
Attendee
Ankara-Turkey
01 May 2008 - 01 May 2008
01 May 2008 - 01 May 2008European Journal of Human Genetics
Attendee
Barselona-Spain
01 May 2008 - 01 May 2008
01 May 2008 - 01 May 2008VIII. Ulusal Tıbbi Genetik Kongresi
Attendee
Çanakkale-Turkey
01 February 2008 - 01 February 2008
01 February 2008 - 01 February 2008
II.Multidisipliner Kanser Sempozyumu
Attendee
Bursa-Turkey
01 April 2007 - 01 April 2007
01 April 2007 - 01 April 2007
XVII. Ulusal Kanser Kongresi
Attendee
Antalya-Turkey
01 May 2006 - 01 May 2006
01 May 2006 - 01 May 2006VII. Ulusal Tıbbi Genetik ve Prenatal Tanı Kongresi
Attendee
Kayseri-Turkey
01 May 2006 - 01 May 2006
01 May 2006 - 01 May 2006European Journal of Human Genetics
Attendee
Amsterdam-Netherlands
01 May 2005 - 01 May 2005
01 May 2005 - 01 May 2005European Journal of Human Genetics
Attendee
Prag-Czech Republic
01 September 2004 - 01 September 2004
01 September 2004 - 01 September 2004XXXI. Ulusal Hematoloji Kongresi
Attendee
Antalya-Turkey
01 April 2004 - 01 April 2004
01 April 2004 - 01 April 2004VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi
Attendee
Antalya-Turkey
01 May 2003 - 01 May 2003
01 May 2003 - 01 May 2003European Journal of Human Genetics
Attendee
Birmingham-United Kingdom
01 April 2003 - 01 April 2003
01 April 2003 - 01 April 2003Fetal Tıp;Prenatal Tanı Kongresi
Attendee
Antalya-Turkey
01 May 2002 - 01 May 2002
01 May 2002 - 01 May 2002European Journal of Human Genetics
Attendee
Strasbourg-France
01 June 2001 - 01 June 2001
01 June 2001 - 01 June 2001European Cytogenetics Conference
Attendee
Paris -France
01 May 2000 - 01 May 2000
01 May 2000 - 01 May 2000IV.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi
Attendee
İzmir-Turkey
01 May 1999 - 01 May 1999
01 May 1999 - 01 May 1999European Journal of Human Genetics
Attendee
Cenevre-Switzerland
Scholarships
2009 - Continues
2009 - ContinuesMediterranean Medical Genetics Meeting 2009 Fellowship
Other International Organizations
2008 - Continues
2008 - Continues