Metrics
Publication
178
Open Access
10
UN Sustainable Development Goals
Education
1999 - 2004
1999 - 2004Doctorate
Akdeniz University, Institute of Health Sciences , Tıbbi Genetik Programı, Turkey
1997 - 1999
1997 - 1999Postgraduate
Akdeniz University, Institute of Health Sciences , Tıbbi Biyoloji Programı, Turkey
1992 - 1997
1992 - 1997Undergraduate
Middle East Technical University, Faculty Of Arts And Sciences, Biyolojik Bilimler, Turkey
Research Areas
Life Sciences
Natural Sciences
Research Areas Based on Academic Activities
Avesis Research Areas
WoS Research Areas
Scopus Research Areas
Academic Positions
2007 - Present
2007 - PresentAssistant Professor
Akdeniz University, Faculty of Medicine, Temel Tıp Bilimleri
Supervised Theses
in Progress
in ProgressPostgraduate
Osteopetrozis tanılı hastalarda TCIRG1 ve SNX10 gen mutasyonlarının araştırılması
MANGUOĞLU A. E.
G.Koçak(Student)
2016
2016Postgraduate
MEME/OVER KANSER AİLELERİNDE BRCA1/BRCA2 DIŞI GENLERİN HASTALIK RİSKİNE ETKİSİNİN ARAŞTIRILMASI
MANGUOĞLU A. E.
A.MOBALLEGH(Student)
2016
2016Postgraduate
Meme/over kanseri ailelerinde BRCA1/BRCA2 dışı genlerin hastalık riskine etkisinin araştırılması
MANGUOĞLU A. E. (Advisor)
A.Moballegh(Student)
2010
2010Postgraduate
PERİYODİK ATEŞ SENDROMLARINDA TNFRSF1A GENİ VARYANTLARININ ÖNEMİNİN ARAŞTIRILMASI
MANGUOĞLU A. E.
S.AKDENİZ(Student)
Articles
All (36)
SCI-E, SSCI, AHCI (29)
SCI-E, SSCI, AHCI, ESCI (31)
ESCI (2)
Scopus (31)
TRDizin (3)
Other Publications (3)
2025
20251. Evaluation of Expression Levels of Relapse-Associated Survivin, S100A8, GPM6B, NUDT15, AURKA and CASP1 Genes at Time of Diagnosis: A Case-Control Research Study in Childhood Pre-B-Acute Lymphoblastic Leukemia
Tokta O., Berker Karauzum S., MANGUOĞLU A. E., KÜPESİZ O. A., Kupesiz F., GÜLER E., et al.
UHOD - Uluslararasi Hematoloji-Onkoloji Dergisi
, vol.35, no.1, pp.60-67, 2025 (SCI-Expanded, Scopus)
2024
20242. Turkish population-based screening for first identified changes of BRCA1 and BRCA2 genes in breast and/or ovarian cancer patients
SEMERCİ SEVİMLİ T., SEVİMLİ M., MANGUOĞLU A. E., Lüleci G.
Egyptian Journal of Medical Human Genetics
, vol.25, no.1, 2024 (ESCI)
2024
20243. Autophagy dysregulation plays a crucial role in regulatory T-cell loss and neuroinflammation in amyotrophic lateral sclerosis (ALS)
Azad A., Gökmen Ü. R., UYSAL H., KÖKSOY S., BİLGE U., MANGUOĞLU A. E.
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
, vol.25, no.3-4, pp.336-344, 2024 (SCI-Expanded)
2024
20244. From islet transplantation to beta-cell regeneration: an update on beta-cell-based therapeutic approaches in type 1 diabetes
Azad A., Altunbas H. A., MANGUOĞLU A. E.
Expert Review of Endocrinology and Metabolism
, vol.19, no.3, pp.217-227, 2024 (ESCI)
2019
20195. TCIRG1 and SNX10 gene mutations in the patients with autosomal recessive osteopetrosis
Koçak G., Güzel B., Mıhçı E., Küpesiz O. A., Yalçın K., Manguoğlu A. E.
Gene
, vol.702, pp.83-88, 2019 (SCI-Expanded)
2017
20176. Conventional cytogenetics findings t(12;21)(p13;q22) translocation and 9p21deletion in pediatric ALL patients
Manguoglu E., Berker-Karauzum S., Akkurt H., Yalcin K., Kupesiz A.
MOLECULAR CYTOGENETICS
, vol.10, 2017 (SCI-Expanded, Scopus)
2017
20177. Identification of a constitutional t(1;19)(q23;p13) translocation in an Extranodal Natural Killer T cell Lmyphoma patient
KARAÜZÜM S., ERDEM R., ALTIOK CLARK Ö., MANGUOĞLU A. E., Ulas T., AKKAYA B., et al.
MOLECULAR CYTOGENETICS
, vol.10, 2017 (SCI-Expanded, Scopus)
2016
20168. Pyridoxine-responsive seizures in infantile hypophosphatasia and a novel homozygous mutation in ALPL gene
NUR B., CELMELI G., Manguoglu E., SOYUÇEN E., Bircan I., MIHÇI E.
JCRPE Journal of Clinical Research in Pediatric Endocrinology
, vol.8, no.3, pp.360-364, 2016 (SCI-Expanded)
2016
20169. Evaluation of ETV6/RUNX1 Fusion and Additional Abnormalities Involving ETV6 and/or RUNX1 Genes Using FISH Technique in Patients with Childhood Acute Lymphoblastic Leukemia.
Aydin C., Cetin Z., Manguoğlu A. E., Tayfun F., Clark Ö., Kupesiz A., et al.
Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
, vol.32, no.2, pp.154-61, 2016 (SCI-Expanded)
2015
201510. Evaluation of TEL/AML1 fusion and additional abnormalities involving TEL and/or AML1 genes using FISH technique in patients with childhood acute lymphoblastic leukemia
Manguoglu E., Aydin C., Çetin Z., Tayfun Küpesiz F., Altıok Clark Ö., Kupesiz A., et al.
CHROMOSOME RESEARCH
, vol.23, 2015 (SCI-Expanded, Scopus)
2014
201411. 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
201312. 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)
2012
201213. Mutational analysis of ten Turkish patients with glycogen storage disease type III: identification of four novel mutations
Manguoglu E., Uygun V., Ozkaya F., Luleci G., ARTAN R., Berker S.
TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS
, vol.47, no.4, pp.278-282, 2012 (SCI-Expanded)
2012
201214. 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
201215. The value of donor lymphocyte infusions in thalassemia patients at imminent risk of graft rejection following stem cell transplantation
KARASU G. T., YESILIPEK M. A., KARAUZUM S. B., Uygun V., Manguoğlu E., Kupesiz A., et al.
PEDIATRIC BLOOD & CANCER
, vol.58, no.3, pp.453-458, 2012 (SCI-Expanded)
2011
201116. RLIP76 GENE VARIANTS ARE NOT ASSOCIATED WITH DRUG RESPONSE IN TURKISH EPILEPSY PATIENTS
MANGUOGLU E., AKDENİZ Ş., DUNDAR N. O., DUMAN Ö., Aktekin B., HASPOLAT Ş., et al.
BALKAN JOURNAL OF MEDICAL GENETICS
, vol.14, no.1, pp.25-30, 2011 (SCI-Expanded, Scopus)
2011
201117. Genomic Large Rearrangement Screening of BRCA1 and BRCA2 Genes in High-Risk Turkish Breast/Ovarian Cancer Patients by Using Multiplex Ligation-Dependent Probe Amplification Assay
Manguoglu E., Guran S., Yamac D., ŞİMŞEK M., Akdeniz S., Colak T., et al.
CANCER INVESTIGATION
, vol.29, no.1, pp.73-77, 2011 (SCI-Expanded, Scopus)
2010
201018. Germline mutations of BRCA1 and BRCA2 genes in Turkish breast, ovarian, and prostate cancer patients
Manguoglu E., Guran S., Yamac D., Colak T., ŞİMŞEK M., Baykara M., et al.
CANCER GENETICS AND CYTOGENETICS
, vol.203, no.2, pp.230-237, 2010 (SCI-Expanded)
2008
200819. Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11
Marshall C. R., Young E. J., Pani A. M., Freckmann M., Lacassie Y., Howald C., et al.
AMERICAN JOURNAL OF HUMAN GENETICS
, vol.83, no.1, pp.106-111, 2008 (SCI-Expanded, Scopus)
2007
200720. Short report. The AIDIT and IMPACT conference 2006: Outcomes and future directions
Doherty R., Lubinski J., Manguoglu E., Luleci G., Christie M., Craven P., et al.
HEREDITARY CANCER IN CLINICAL PRACTICE
, vol.5, no.1, pp.53-55, 2007 (SCI-Expanded)
2006
200621. AIDIT and IMPACT: building research collaborations in targeted prostate cancer screening.
Doherty R., Lubinski J., MANGUOĞLU AYDEMİR A. E., Lüleci G., Christie M., Craven P., et al.
Journal of BOUN
, vol.11, pp.415-418, 2006 (Peer-Reviewed Journal)
2006
200622. Donor cell-derived acute myeloblastic leukemia after allogeneic peripheral blood hematopoietic stem cell transplantation for juvenile myelomonocytic leukemia
Cetin Z., Tezcan G., Karauzum S. B., Kupesiz A., Manguoglu A. E., Yesilipek A., et al.
JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
, vol.28, no.11, pp.763-767, 2006 (SCI-Expanded)
2006
200623. IMPACT and AIDIT: Strenghening Research Ties in Eastern Europe
Morgan S., Lubinski J., MANGUOĞLU AYDEMİR A. E., Lüleci G., Doherty R., Christie M., et al.
HEREDITY CANCER IN CLINICAL PRACTICE , vol.4, no.2, pp.111-112, 2006 (Peer-Reviewed Journal)
2005
200524. Molecular diagnosis of hematological malignancies by RT-PCR
BERKER-KARAÜZÜM S., MANGUOĞLU A. E., NAL N., YAKUT S., SARGIN C. F., Alper Ö., et al.
Turkish Journal of Cancer
, vol.35, no.3, pp.113-118, 2005 (Scopus)
2005
200525. Two rare mutations in Turkey: IVSI.130(G-C) and IVSII.848(C-A)
Nal N., MANGUOGLU A. E., SARGIN C. F., KESER I., Kupesiz A., Yesilipek A., et al.
CLINICAL AND LABORATORY HAEMATOLOGY
, vol.27, no.4, pp.274-277, 2005 (SCI-Expanded, Scopus)
2005
200526. Combination of IVS2.849 A-G with IVS1.1 G-A: A mutation of beta-globin gene in a Turkish beta-thalessemia major patient
Manguoglu E., SARGIN C. F., Nal N., KESER İ., Kupesiz A., Yesilipek A., et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY
, vol.22, no.4, pp.291-295, 2005 (SCI-Expanded)
2005
200527. 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
200528. Prenatal Diagnosis of B-Thalassemia in the Antalya Province
KESER İ., MANGUOĞLU E., Kayisli O., Kurt F., MENDİLCİOĞLU İ. İ., ŞİMŞEK M., et al.
TURKISH JOURNAL OF MEDICAL SCIENCES , vol.35, pp.251-253, 2005 (Scopus)
2005
200529. A case with de novo interstitial deletion of chromosome 7q21.1-q22
Manguoglu E., Berker-Karauzum S., Baumer A., Mihci E., Tacoy S., Luleci G., et al.
GENETIC COUNSELING
, vol.16, no.2, pp.155-159, 2005 (SCI-Expanded)
2005
200530. The phenotypic effect of Hb G-Coushatta [beta 22 (B4) Glu-Ala] and association with IVS. II.1 (G-A) in a Turkish family
Sargin C., Nal N., Manguoglu A. E., Keser I., Mendilcioglu I., Yesilipek A., et al.
GENETIC COUNSELING
, vol.16, no.3, pp.307-308, 2005 (SCI-Expanded)
2004
200431. Lack of association between RNASEL Arg462Gln variant and the risk of breast cancer
Sevinc A., Yannoukakos D., Konstantopoulou I., Manguoglu E., Luleci G., Colak T., et al.
ANTICANCER RESEARCH
, vol.24, no.4, pp.2547-2549, 2004 (SCI-Expanded)
2004
200432. Consanguineous marriages in the province of Antalya, Turkey
Alper O., Eregin H., Manguoglu A. E., Bilgen T., Cetin Z., Dedeoglu N., et al.
ANNALES DE GENETIQUE
, vol.47, no.2, pp.129-138, 2004 (SCI-Expanded, Scopus)
2004
200433. Molecular analysis of beta-thalassemia and sickle cell anemia in Antalya
Keser İ., Sanlioglu A., Manguoglu E., Kayisli O., Nal N., Sargin F., et al.
ACTA HAEMATOLOGICA
, vol.111, no.4, pp.205-210, 2004 (SCI-Expanded, Scopus)
2004
200434. AZF microdeletions on the Y chromosome of infertile men from Turkey
Sargin C., Berker-Karauzum S., Manguoglu E., Erdogru T., Karaveli S., Gulkesen K. H., et al.
ANNALES DE GENETIQUE
, vol.47, no.1, pp.61-68, 2004 (SCI-Expanded, Scopus)
2003
200335. Analysis of polymorphic patterns in candidate genes in Israeli patients with prostate cancer
Figer A., Friedman T., Manguoglu A. E., Flex D., Vazina A., Novikov I., et al.
ISRAEL MEDICAL ASSOCIATION JOURNAL
, vol.5, no.10, pp.741-745, 2003 (SCI-Expanded)
2003
200336. Germline Mutations in the BRCA1 and BRCA2 Genes in Turkish Breast/Ovarian Cancer Patients
MANGUOĞLU A. E., Lüleci G., Ozcelik T., ÇOLAK T., Schayek H., Akaydın M., et al.
HUMAN MUTATION
, vol.21, no.4, pp.444-445, 2003 (SCI-Expanded, Scopus)
Papers Presented at Peer-Reviewed Scientific Conferences
0
01. Hematopoietic Chimerism Analysis in Paediatric Allogeneic Cell Transplantation Patients
MANGUOĞLU ., BERKER S., KÜPESİZ O. A., Tezcan G., Hazar V., Yesilipek A., et al.
8th Balkan Meeting on Human Genetics, Croatia, pp.113, (Full Text)
0
02. The Importance of BRCA1/2 Germline Mutations in Turkish Breast and Prostate Cancer Patients
Luleci G., MANGUOĞLU E., Guran S., Yamac D., BAYKARA M., ÇOLAK T., et al.
, 8th Balkan Meeting on Human Genetics, Croatia, pp.116, (Full Text)
0
03. The Importance of BRCA1/2 Germline Mutations in Turkish Breast and Prostate Cancer Patients
Luleci G., MANGUOĞLU E., Guran S., Yamac D., BAYKARA M., ÇOLAK T., et al.
, 8th Balkan Meeting on Human Genetics, Croatia, pp.116, (Full Text)
2019
20194. A rare HNF1A gene mutation in a Turkish family with maturity-onset diabetes of the young (MODY)
Moballegh A., DOĞAN Ö., KARGÜN S., YILMAZ N., MANGUOĞLU AYDEMİR A. E.
Uluslararası Katılımlı Erciyet Tıp Genetik Günleri 2019, Kayseri, Turkey, 21 - 23 February 2019
2018
20185. Effects of Cetuximab and Stabilized Silver Solution on Cell Cycle in Lung Cancer Cells
Erdoğan A., ÖZKAN A., Özkan Ö., MANGUOĞLU A. E., KİRAZ N.
1st Eurasia Biochemical Approaches & Technologies (EBAT) Congress, Antalya, Turkey, 27 - 30 October 2018, pp.21, (Summary Text)
2017
20176. A novel mutation in TCIRG1 gene in a Turkish patient with malignant autosomal recessive osteopetrosis
Kocak G., Nur B., Mihci E., Akkurt H., Manguoglu E.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.246, (Summary Text)
2017
20177. Evaluation of three patients with Bannayan-Riley-Ruvalcaba Syndrome
Mihci E., Manguoglu E., Ozucetin P., Algul F., Guzel B. N.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.952, (Summary Text)
2017
20178. A novel mutation in TCIRG1 gene in a Turkish patient with malignant autosomal recessive osteopetrosis
Koçak G., Nur B., Mıhçı E., Akkurt H., Manguoğlu Aydemir A. E.
European Human Genetics Conference, Kobenhavn, Denmark, 27 - 30 May 2017, (Summary Text)
2017
20179. Evaluation of three patients with Bannayan-Riley-Ruvalcaba Syndrome
MIHÇI E., MANGUOĞLU AYDEMİR A. E., özüçetin p., algül f., NUR B.
European Human Genetics Conference, 27 - 30 May 2017, (Summary Text)
2017
201710. Evaluation of three patients with Bannayan-Riley Ruvalcaba syndrome
Mıhçı E., Manguoğlu Aydemir A. E., Algül F., Özüçetin P., Nur B.
ESHG 2017, Kobenhavn, Denmark, 27 - 30 May 2017, (Summary Text)
2016
201611. Identification of the germline mutations of P53,Chek2 and PTEN genes in non BRCA1/2 mutation carrier high risk Turkish breast cancer families
MANGUOĞLU A. E., moballegh a., Ozdogan M., ARICI C.
European Human Genetics Conference, Barselona, Spain, 21 - 24 May 2016, pp.469, (Full Text)
2015
201512. Stabilized-Silver Ion Solution Enhances Cetuximab Cytotoxicity in Lung and Epidermoid Carcinoma Cells
ERDOĞAN A., ÖZKAN A., MANGUOĞLU AYDEMİR A. E., KİRAZ N., Özkan Ö.
4th Inter. Congress of the Molecular Biology Association of Turkey, Ankara, Turkey, 27 - 29 November 2015, pp.77, (Full Text)
2015
201513. Evaluation of TEL/AML1 fusion and additional abnormalities involving TEL and/or AML1 genes using FISH technique in patients with childhood acute lymphoblastic leukemia.
MANGUOĞLU AYDEMİR A. E., Aydın Acar Ç., Cetin Z., Tayfun F., ALTIOK CLARK Ö., KÜPESİZ O. A., et al.
European Cytogenetics Conference, Strasbourg, France, 4 - 07 July 2015, (Full Text)
2015
201514. Combined effect of Cetuximab and Stabilized- Ag ion solution on epirubicin-resistant human Non-Small Cell Lung Cancer (NSCLC) comparing with parental cells
ÖZKAN A., ERDOĞAN A., MANGUOĞLU AYDEMİR A. E., KİRAZ N.
40 th FEBS Congress, Berlin, Germany, 4 - 09 July 2015, pp.248, (Full Text)
2015
201515. Evaluation of TEL/AML1 fusion and additional abnormalities involving TEL and/or AML1 genes using FISH technique in patients with childhood acute lymphoblastic leukemia.
MANGUOĞLU AYDEMİR A. E., Aydın Acar Ç., Cetin Z., Tayfun F., ALTIOK CLARK Ö., KÜPESİZ O. A., et al.
European Cytogenetics Conference, Strasbourg, France, 4 - 07 July 2015, (Full Text)
2015
201516. Evaluation of TEL/AML1 fusion and additional abnormalities involving TEL and/or AML1 genes using FISH technique in patients with childhood acute lymphoblastic leukemia.
Manguoğlu Aydemir A. E., Aydın Acar Ç., Cetin Z., Tayfun F., Altıok Clark Ö., Küpesiz O. A., et al.
European Cytogenetics Conference, Strasbourg, France, 4 - 07 July 2015, (Full Text)
2015
201517. Combined effect of Cetuximab and Stabilized-Ag ion solution on epirubicin-resistant human Non-Small Cell Lung Cancer (NSCLC) comparing with parental cells
ÖZKAN A., Erdogan A., Manguoglu E., KİRAZ N.
40th Congress of the Federation-of-European-Biochemical-Societies (FEBS) - The Biochemical Basis of Life, Berlin, Germany, 4 - 09 July 2015, vol.282, pp.248, (Summary Text)
2013
201318. Triple negatif bilateral meme kanserli bir olguda saptanan yeni bir BRCA1 geni mutasyonu
MANGUOĞLU AYDEMİR A. E., Özdoğan M.
XII.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, İzmir, Turkey, 27 - 30 October 2013, pp.213-214, (Full Text)
2013
201319. 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
201220. Familial Anatomic Megalencephaly and Relevant Genes
ARUN Ö., UYSAL H., MANGUOĞLU AYDEMİR A. E., GÜLKESEN K. H., Akarsu N., Kaplan B., et al.
48th National Neurology Congress, Antalya, Turkey, 16 - 22 November 2012, pp.10-20, (Full Text)
2012
201221. Familyal anatomik megaloensefali ve ilgili genler
UYSAL H., MANGUOĞLU E., GÜLKESEN K. H., Akarsu N., ARUN Ö., Kaplan B., et al.
48.Ulusal Nöroloji Kongresi, Antalya, Turkey, 16 - 22 November 2012, pp.20, (Full Text)
2012
201222. R320H MUTATION IN THE THYROID HORMONE RECEPTOR BETA TRB ASSOCIATED WITH AUTOIMMUNE THYROID DISEASE IN A TURKISH FAMILY
PARLAK M., DURMAZ E., BARAN R. T., MANGUOĞLU AYDEMİR A. E., BİRCAN İ., AKÇURİN S.
51th ANNUAL MEETING EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRYNOLOGY, 20 - 23 September 2012
2011
201123. Down sendromu olgusunda gözlenen de novo Rekombinant Kromozom 21
ÇETİN Z., YAKUT S., MIHÇI E., MANGUOĞLU A. E., BERKER-KARAÜZÜM S., KESER İ., et al.
XII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Turkey, 27 - 30 October 2011, (Full Text)
2011
201124. 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
201125. 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
201126. NCF Geninde Yeni Bir Mutasyon İle Kronik Granülamatöz Hastalığı Olan Bir Ailede Prenatal Tanı
MANGUOĞLU E., Çelmeli F., MIHÇI E., Yeğin O., BİNGÖL BOZ A., Lüleci G.
XII.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Turkey, 27 - 30 October 2011, pp.185, (Full Text)
2011
201127. 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
201128. 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
201129. 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
201130. 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
201131. 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
201132. 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
201033. Association of Several Genetic Variants with Myocardial Infarction: A Pilot Study in Mediterranean Region
MANGUOĞLU A. E., Alper O., Küçük M., Pehlivanoğlu S., DEMİR D., ERENGİN K. H., et al.
9. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 1 - 05 December 2010, pp.87, (Full Text)
2010
201034. Association of Several Genetic Variants with Myocardial Infarction: A Pilot Study in Mediterranean Region
MANGUOĞLU A. E., Alper O., Küçük M., Pehlivanoğlu S., DEMİR D., ERENGİN K. H., et al.
9. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 1 - 05 December 2010, pp.87, (Full Text)
2010
201035. Association of Several Genetic Variants with Myocardial Infarction: A Pilot Study in Mediterranean Region
MANGUOĞLU A. E., Alper O., Küçük M., Pehlivanoğlu S., DEMİR D., ERENGİN K. H., et al.
9. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 1 - 05 December 2010, pp.87, (Full Text)
2010
201036. Mutational Screening of ALG (Glycogen Debaranching Enzyme) Gene in Glycogen Storage Disease Type III
Sargın C., MANGUOĞLU ., Uygun V., ARTAN R., Luleci G., BERKER S.
60.th Annual Meeting of the American Society of Human Genetics, Wsahington Dc, United States Of America, 2 - 06 November 2010, pp.1, (Full Text)
2010
201037. Talasemi Transplantında Mikst Kimerizm Graft Reddi İçin Belirleyici mi?
Karasu G. T., Uygun V., BERKER S., Akcan M., MANGUOĞLU E., KÜPESİZ O. A., et al.
6.Ulusal Kemik İliği Transplantasyonu ve Kök Hücre Tedavileri Kongresi, Antalya, Turkey, 4 - 06 March 2010, pp.157-158, (Full Text)
2010
201038. Talasemi Transplantında Mikst Kimerizm Graft Reddi İçin Belirleyici mi?
Karasu G. T., Uygun V., BERKER S., Akcan M., MANGUOĞLU E., KÜPESİZ O. A., et al.
6.Ulusal Kemik İliği Transplantasyonu ve Kök Hücre Tedavileri Kongresi, Antalya, Turkey, 4 - 06 March 2010, pp.157-158, (Full Text)
2010
201039. The role of mixed chimerism on transplant outcome in patients with thalassaemia
Kazik M., Karasu G., Karauzum S., Uygun V., Manguoglu E., Kupesiz A., et al.
36th Annual Meeting of the European-Group-for-Blood-and-Marrow-Transplantat/9th Meeting of the EBMT Data-Management-Group/26th Meeting of the EBMT Nurses Group/2nd EBMT Qual Management Meeting, Vienna, Austria, 21 - 24 March 2010, vol.45, (Summary Text)
2009
200940. Periyodik Ateş Sendromlarında TNFRSF1A Gen Mutasyonlarının Rolü
BİNGÖL BOZ A., Akdeniz S., Dayar E., Çelmeli F., KESER İ., Lüleci G., et al.
XVII. Ulusal Allerji ve Klinik İmmünoloji Kongresi, Antalya, Turkey, 3 - 07 November 2009, pp.54, (Full Text)
2009
200941. Large Genomik Rearrangement Screening of BRCA1 and BRCA2 Genes in High Risk Turkish Breast/Ovarian Cancer Patients by Using MLPA
MANGUOĞLU E., Güran Ş., Yamaç D., ŞİMŞEK M., Akdeniz S., ÇOLAK T., et al.
Mediterranean Medical Genetics Meeting, Ankara, Turkey, 28 June - 01 July 2009, pp.37, (Full Text)
2009
200942. No Correlation Between RLIP76 Gene Polymorphisms and Drug Response in Epilepsy
MANGUOĞLU ., Akdeniz S., Dundar N. O., Aktekin B., DUMAN Ö., HASPOLAT Ş., et al.
Mediterrranean Medical Genetics Meeting, Ankara, Turkey, 28 June - 01 July 2009, pp.37-38, (Full Text)
2009
200943. Hematopoietic Chimerism Analysis in Paediatric Allogeneic Cell Transplantation Patients
MANGUOĞLU ., BERKER S., KÜPESİZ O. A., Tezcan G., Hazar V., Yesilipek A., et al.
8th Balkan Meeting on Human Genetics, Dubrovnig, Croatia, 14 - 17 May 2009, pp.113, (Full Text)
2009
200944. The Importance of BRCA1/2 Germline Mutations in Turkish Breast and Prostate Cancer Patients
Luleci G., MANGUOĞLU E., Guran S., Yamac D., BAYKARA M., ÇOLAK T., et al.
, 8th Balkan Meeting on Human Genetics, Dubrovnik, Croatia, 14 - 17 May 2009, pp.116, (Full Text)
2009
200945. Hematopoietic Chimerism Analysis in Paediatric Allogeneic Cell Transplantation Patients
MANGUOĞLU ., BERKER S., KÜPESİZ O. A., Tezcan G., Hazar V., Yesilipek A., et al.
8th Balkan Meeting on Human Genetics, Dubrovnik, Croatia, 14 - 17 May 2009, pp.113, (Full Text)
2008
200846. Meme ve Prostat Kanserli Hastalarda BRCA Genlerinin Kalıtsal Mutasyonlarının Önemi
MANGUOĞLU E., Guran S., Yamaç D., BAYKARA M., ÇOLAK T., Akaydin M., et al.
VIII.Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 06 May 2008 - 09 May 2009, pp.108, (Full Text)
2008
200847. Glukojen Depo Hastalığı Tip III'de AGL Genindeki Mutasyonların Taranması
MANGUOĞLU E., BERKER S., Uygun V., Ozkaya F., Lüleci G., ARTAN R.
VIII.Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 6 - 09 May 2008, pp.14, (Full Text)
2008
200848. Glukojen Depo Hastalığı Tip III'de AGL Genindeki Mutasyonların Taranması
MANGUOĞLU E., BERKER S., Uygun V., Ozkaya F., Lüleci G., ARTAN R.
VIII.Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 6 - 09 May 2008, pp.14, (Full Text)
2008
200849. Meme ve Prostat Kanserli Hastalarda BRCA Genlerinin Kalıtsal Mutasyonlarının Önemi
MANGUOĞLU E., Guran S., Yamaç D., BAYKARA M., ÇOLAK T., Akaydin M., et al.
VIII.Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 06 May 2008 - 09 May 2009, pp.108, (Full Text)
2008
200850. Glukojen Depo Hastalığı Tip III'de AGL Genindeki Mutasyonların Taranması
MANGUOĞLU E., BERKER S., Uygun V., Ozkaya F., Lüleci G., ARTAN R.
VIII.Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 6 - 09 May 2008, pp.14, (Full Text)
2008
200851. Meme ve Prostat Kanserli Hastalarda BRCA Genlerinin Kalıtsal Mutasyonlarının Önemi
MANGUOĞLU E., Guran S., Yamaç D., BAYKARA M., ÇOLAK T., Akaydin M., et al.
VIII.Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 06 May 2008 - 09 May 2009, pp.108, (Full Text)
2007
200752. Combination of Hb Knossos [Cod 27 (G-T)]and IVSII-745 (C-G) in a Turkish Patient with Beta-Thalassemia Major
KESER İ., MANGUOĞLU ., Kayisli O., Yesilipek A., Luleci G.
European Human Genetics Conference 2007, Nice, France, 16 - 19 June 2007, pp.18-19, (Full Text)
2007
200753. Meme, Yumurtalık ve Prostat Kanseri Hastalarındad BRCA1 ve BRCA2 Kalıtsal Mutasyon Taramaları
MANGUOĞLU E., ÇOLAK T., Yamac D., ŞİMŞEK M., Akaydin M., KÖKSAL İ. T., et al.
XVII.Ulusal Kanser Kongresi, Antalya, Turkey, 19 - 23 April 2007, pp.202, (Full Text)
2007
200754. Meme, Yumurtalık ve Prostat Kanseri Hastalarındad BRCA1 ve BRCA2 Kalıtsal Mutasyon Taramaları
MANGUOĞLU E., ÇOLAK T., Yamac D., ŞİMŞEK M., Akaydin M., KÖKSAL İ. T., et al.
XVII.Ulusal Kanser Kongresi, Antalya, Turkey, 19 - 23 April 2007, pp.202, (Full Text)
2006
200655. Obstacles Faced in Setting up Genetic Testing, Perspectives From Turkey
MANGUOĞLU .
The AIDIT and IMPACT Meeting, Stetin, Poland, 28 - 30 November 2006, pp.1
2006
200656. AIDIT and IMPACT: Strenghtening Research Ties Across Europe
Doherty R., Lubinski J., MANGUOĞLU ., Luleci G., Christie M., Bancroft E., et al.
Al II-leaCongres National de Genetica Medicala, Cluj-Napoca, Romania, 20 - 23 September 2006, pp.46-47, (Full Text)
2006
200657. Strenghtening Research Ties in Eastern Europe
Doherty R., Lubinski J., MANGUOĞLU ., Luleci G., Christie M., Bancroft E., et al.
6th Congress of Balkan Union of Oncology, Sofya, Bulgaria, 13 - 16 September 2006, pp.110
2006
200658. AIDIT and IMPACT: Strengthening research ties in Eastern Europe
Lüleci G., Doherty R., Lubinski J., MANGUOĞLU ., Christie M., Bancroft E., et al.
7th Balkan Meeting of Human Genetics, Üsküp, Macedonia, 30 August - 01 September 2006, pp.76, (Full Text)
2006
200659. AIDIT and IMPACT: Strengthening Research Ties in Eastern Europe
Doherty R., Lubinski J., Zieba K., MANGUOĞLU E., Luleci G., Christie M., et al.
Cancer 2006, Tatras, Slovakia, 20 - 24 August 2006, pp.25, (Full Text)
2006
200660. The Spectrum of Abnormal Hemoglobins in Antalya Province, Mediterranean Region of Turkey
KESER İ., MANGUOĞLU AYDEMİR A. E., Kayisli O., ŞANLIOĞLU A. D., ŞİMŞEK M., MENDİLCİOĞLU İ. İ.
31st FEBS Congress, İstanbul, Turkey, 24 - 29 June 2006, pp.354, (Full Text)
2006
200661. The effects of the OPRM1 gene polymorphisims on pain control in Turkish patients
ÖZCAN M., MANGUOĞLU ., KESER İ., AKBAŞ M., KARSLI B., Luleci G.
31st FEBS Congress, İstanbul, Turkey, 24 - 29 June 2006, pp.261, (Full Text)
2006
200662. The effects of the OPRM1 gene polymorphisims on pain control in Turkish patients
ÖZCAN M., MANGUOĞLU ., KESER İ., AKBAŞ M., KARSLI B., Luleci G.
31st FEBS Congress, İstanbul, Turkey, 24 - 29 June 2006, pp.261, (Full Text)
2006
200663. The Spectrum of Abnormal Hemoglobins in Antalya Province, Mediterranean Region of Turkey
KESER İ., MANGUOĞLU AYDEMİR A. E., Kayisli O., ŞANLIOĞLU A. D., ŞİMŞEK M., MENDİLCİOĞLU İ. İ.
31st FEBS Congress, İstanbul, Turkey, 24 - 29 June 2006, pp.354, (Full Text)
2006
200664. The Effects Of The Oprm1 Gene Polymorphisims On Pain Control In Turkish Patients
ÖZCAN M., MANGUOĞLU A. E., KESER İ., AKBAŞ M., KARSLI B.
31st FEBS Congress, İstanbul, Turkey, 24 - 29 June 2006, pp.100, (Full Text)
2006
200665. Strenghtening Research Ties in Eastern Europe
MANGUOĞLU E., Doherty R., Lubinski J., Lüleci G., Christie M., Bancroft E., et al.
19.Ulusal Üroloji kongresi, Antalya, Turkey, 10 - 15 June 2006, pp.14
2006
200666. The effects of the OPRM1 gene polymorphisms on pain control in Turkish patients.
Caliskan M. O., Manguoglu E., Keser I., Akbas M., KARSLI B., Akbas H., et al.
31st Congress of the Federation-of-European-Biochemical-Societies (FEBS), İstanbul, Turkey, 24 - 29 June 2006, vol.273, pp.261, (Summary Text)
2006
200667. AIDIT ve IMPACT - Doğu Avrupa'da Araştırma Bağlarının Güçlendirilmesi
Doherty R., Lubinski J., MANGUOĞLU E., Lüleci G., Christie M., Bancroft E., et al.
VII.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Kayseri, Turkey, 17 - 20 May 2006, pp.158-159
2006
200668. Antalya'da Beta-Talasemi ve Orak Hücre Anemide Yapılan Moleküler Genetik Çalışmalar
KESER İ., MANGUOĞLU A. E., ŞANLIOĞLU A. D., Kayisli O., Sargin F., Nal N., et al.
Huisman Memorial Symposium II, Adana, Turkey, 7 - 08 May 2006, pp.14-15, (Full Text)
2006
200669. Donor cell-derived acute myeloblastic leukemia after allogeneic peripheral blood hematopoietic stem cell transplantation for juvenille myelomonocytic leukemia
BERKER S., Cetin Z., MANGUOĞLU E., Tezcan G., KÜPESİZ O. A., Yesilipek A., et al.
European Human Genetics Conference 2006, Amsterdam, Netherlands, 6 - 09 May 2006, pp.213-214, (Full Text)
2006
200670. Donor cell-derived acute myeloblastic leukemia after allogeneic peripheral blood hematopoetic stem cell transplantation for juvenile myelomonocytic leukemia
Çetin Z., Tezcan G., Berker Karaüzüm S., KÜPESİZ O. A., Manguoğlu A. E., Yesilipek A., et al.
European Journal of Human Genetics, Amsterdam, Netherlands, 6 - 09 May 2006, pp.213, (Summary Text)
2006
200671. Donor cell-derived acute myeloblastic leukemia after allogeneic peripheral blood hematopoietic stem cell transplantation for juvenille myelomonocytic leukemia
BERKER S., Cetin Z., MANGUOĞLU E., Tezcan G., KÜPESİZ O. A., Yesilipek A., et al.
European Human Genetics Conference 2006, Amsterdam, Netherlands, 6 - 09 May 2006, pp.213-214, (Full Text)
2006
200672. AIDIT-Expanding familial prostate cancer research in Eastern Europe
Doherty R., Lubinski J., MANGUOĞLU E., Lüleci G., Christie M., Bancroft E., et al.
European Human Genetics Conference 2006, Amsterdam, Netherlands, 6 - 09 May 2006, pp.227
2006
200673. Meme/Over Kanserleri Hastalarında BRCA1 ve BRCA2 Mutasyon Taramaları
MANGUOĞLU E., Yamac D., ÇOLAK T., Akaydın M., ŞİMŞEK M., Zorlu G., et al.
Multidisipliner Kanser Araştırma Sempozyumu, Bursa, Turkey, 12 - 15 April 2006, pp.154, (Full Text)
2005
200574. 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
200575. 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
200576. 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
200577. BRCA1/BRCA2
PEŞTERELİ H. E., MANGUOĞLU ., ÇOLAK T., Lüleci G., KARAVELİ F. Ş., Akaydın M.
VIII. Ulusal Meme Hastalıkları Kongresi, İstanbul, Turkey, 21 - 24 September 2005, pp.298, (Full Text)
2005
200578. X Kromozom İnaktivasyonu ve Meme Kanseri
MANGUOĞLU E., Sevinc A., Yannoukakos D., Yazıcı H., Bağışlar G., Özkaynak E., et al.
VIII. Ulusal Meme Hastalıkları Kongresi, İstanbul, Turkey, 21 - 24 September 2005, pp.260
2005
200579. Meme ve/veya Over Kanserli Hastalarda BRCA1 ve BRCA2 Gen Mutasyonlarının Taranması
Lüleci G., MANGUOĞLU E., ÇOLAK T., Akaydin M., ŞİMŞEK M., Zorlu G., et al.
VIII. Ulusal Meme Hastalıkları Kongresi, İstanbul, Turkey, 21 - 24 September 2005, pp.293, (Full Text)
2005
200580. 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
200581. 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
200582. 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
200583. Hb Knossos [Cod27 (G-T)] in a Turkish Patient with Beta-Thalassemia Major
Öztürk Z., MANGUOĞLU ., Kayisli O., KESER İ., KÜPESİZ O. A., Lüleci G.
Advances in Molecular Medicine, İstanbul, Turkey, 16 - 19 April 2005, pp.394-395, (Full Text)
2004
200484. JMML Gelişiminde Rol Oynaması Olsaı Yeni Bir Aday Gen: Grb10
Çetin Z., Berker Karaüzüm S., Yakut S., Manguoğlu A. E., Tezcan G., KÜPESİZ O. A., et al.
Türk Hematoloji Derneği XXXI. Ulusal Kongresi, Antalya, Turkey, 23 September - 28 April 2004, pp.106-107, (Full Text)
2004
200485. 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
200486. 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
200487. 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
200488. 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
200489. 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
200490. 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
200491. A New allelic variant K695M in the MEFV gene in a Turkish family suffering from FMF
KESER İ., MANGUOĞLU E., Özgüven e., Lüleci G.
European Human Genetics Conference 2004, Münih, Germany, 12 - 15 June 2004, pp.221, (Full Text)
2004
200492. X Chromosome Inactivaiton and Breast Cancer
Sevinç A., Yannoukakos D., Yazıcı H., Bağışlar G., Özkaynak E., Konstantopoulou I., et al.
European Human Genetics Conference 2004, Münih, Germany, 12 - 15 June 2004, pp.197, (Full Text)
2004
200493. Germline Mutations of BRCA1 ve BRCA2 Genes in High Risk Breast And/Or Ovarian Cancer Turkish Patients
MANGUOĞLU ., Lüleci G., ÇOLAK T., Akaydın M., ŞİMŞEK M., Zorlu G., et al.
Familial Cancer, Madrid, Spain, 6 - 07 May 2004, pp.43, (Full Text)
2004
200494. X Kromozom Etkinsizleştirilmesinin Meme Kanseri ile ilişkisi
Sevinç A., Yannoukakos D., Yazıcı H., Bağışlar G., Özkaynak E., Konstantopoulou I., et al.
VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Turkey, 21 - 24 April 2004, pp.63-64, (Full Text)
2004
200495. RNASEL G1385A Mutasyonunun meme kanseri ile ilişkisi
Sevinç A., Yannoukakos D., Konstantopoulou I., MANGUOĞLU ., Lüleci G., ÇOLAK T., et al.
VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Turkey, 21 - 24 April 2004, pp.62
2004
200496. Ailesel Akdeniz Ateşi Olan Bir Ailede MEFV Geninde Tanımlanan Yeni Bir Allelik Varyant: K695M
KESER İ., MANGUOĞLU E., Özgüven e., Lüleci G.
VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Turkey, 21 - 24 April 2004, pp.90, (Full Text)
2004
200497. Türkiye'de tanımlanan iki nadir mutasyon: IVS1.130 G-C ve IVS2.848 C-A
Nal N., MANGUOĞLU A. E., Sargın C., KESER İ., KÜPESİZ O. A., Yesilipek A., et al.
VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Turkey, 21 - 24 April 2004, pp.107-108, (Full Text)
2004
200498. Meme ve/veya over kanserli 75 hastanın BRCA1 ve BRCA2 genlerinde mutasyon analizi
MANGUOĞLU A. E., Lüleci G., ÇOLAK T., Akaydin M., ŞİMŞEK M., Zorlu G., et al.
VI. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Turkey, 21 - 24 April 2004, pp.64, (Full Text)
2003
200399. 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
2003100. 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
2003101. 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
2003102. 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
2003103. A rare mutation (codon 22 A>C) in beta-thalassemia and its prenatal diagnosis
Nal N., Sargin F., MANGUOĞLU E., KESER İ., Yesilipek A., MENDİLCİOĞLU İ. İ., et al.
European Human Genetics Conference 2003, Birmingham, United Kingdom, 3 - 06 May 2003, pp.241, (Full Text)
2003
2003104. 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
2003105. 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)
2002
2002106. "Erişkin dönemde hematolojik malignansi gözlenen olgularda sitogenetik, FISH ve RT-PCR sonuçlarımız
BERKER S., MANGUOĞLU A. E., Bilgen T., Nal N., Ugur A., Karadoğan İ., et al.
Türk Hematoloji Derneği 29.Ulusal Kongresi, Antalya, Turkey, 25 - 28 October 2002, pp.121, (Full Text)
2002
2002107. Çocukluk çağı hematolojik malignansilerinde kromozomal düzensizliklerin sitogenetik, FISH ve RT-PCR ile gösterilmesi
MANGUOĞLU A. E., BERKER S., Cetin Z., Nal N., KÜPESİZ O. A., Hazar V., et al.
Türk Hematoloji Derneği 29.Ulusal Kongresi, Antalya, Turkey, 25 - 28 October 2002, pp.107, (Full Text)
2002
2002108. "Erişkin dönemde hematolojik malignansi gözlenen olgularda sitogenetik, FISH ve RT-PCR sonuçlarımız
BERKER S., MANGUOĞLU A. E., Bilgen T., Nal N., Ugur A., Karadoğan İ., et al.
Türk Hematoloji Derneği 29.Ulusal Kongresi, Antalya, Turkey, 25 - 28 October 2002, pp.121, (Full Text)
2002
2002109. Çocukluk çağı hematolojik malignansilerinde kromozomal düzensizliklerin sitogenetik, FISH ve RT-PCR ile gösterilmesi
MANGUOĞLU A. E., BERKER S., Cetin Z., Nal N., KÜPESİZ O. A., Hazar V., et al.
Türk Hematoloji Derneği 29.Ulusal Kongresi, Antalya, Turkey, 25 - 28 October 2002, pp.107, (Full Text)
2002
2002110. 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
2002111. 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
2002112. Antalya'da Beta-Talasemi ve Orak Hücreli Anemide Yapılan Moleküler Genetik Çalışmalar
KESER İ., ŞANLIOĞLU A. D., Kayisli O., MANGUOĞLU A. E., Sargin F., Nal N., et al.
V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.70, (Full Text)
2002
2002113. 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
2002114. Türk meme/over kanseri hastalarında BRCA1 ve BRCA2 genlerinde kalıtsal mutasyonlar
MANGUOĞLU AYDEMİR A. E., Lüleci G., Ozcelik T., ÇOLAK T., Schayek H., Akaydın M., et al.
V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.64
2002
2002115. 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
2002116. Beta Talasemide Nadir Bir Mutasyon ve Prenatal Tanısı Kodon 22 (A-C)
Sargın C., Nal N., MANGUOĞLU AYDEMİR A. E., KESER İ., Yesilipek A., MENDİLCİOĞLU İ. İ., et al.
V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.193, (Full Text)
2002
2002117. 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
2002118. Beta Talasemide Nadir Bir Mutasyon ve Prenatal Tanısı Kodon 22 (A-C)
Sargın C., Nal N., MANGUOĞLU AYDEMİR A. E., KESER İ., Yesilipek A., MENDİLCİOĞLU İ. İ., et al.
V.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Konya, Turkey, 9 - 12 October 2002, pp.193, (Full Text)
2002
2002119. Germline mutations in the BRCA1 and BRCA2 genes in Turkish breast/ovarian cancer patients
MANGUOĞLU AYDEMİR A. E., Lüleci G., Ozcelik T., ÇOLAK T., Schayek H., Akaydın M., et al.
18th UICC International Cancer Congress, Oslo, Norway, 30 June - 05 July 2002, pp.387, (Full Text)
2002
2002120. A Rare Mutation of Beta-Globin Gene (IVS 2-849 A>G) at Exon2-Intron2 Splice Site in a Turkish Patient with Beta-Thalassemia Major
Sargın C., MANGUOĞLU E., Nal N., KESER İ., Yesilipek A., Lüleci G.
European Human Genetics Conference 2002, Strazburg, France, 25 - 29 May 2002, pp.204, (Full Text)
2001
2001121. Antalya'da Beta-Talasemi ve Orak Hücre Anemisinin Moleküler Genetik Analiz Sonuçları
KESER İ., Kayisli O., ŞANLIOĞLU A. D., MANGUOĞLU E., ŞİMŞEK M., Luleci G., et al.
III.Ulusal Pediatrik Hematoloji Kongresi, Ankara, Turkey, 17 - 20 October 2001, pp.97, (Full Text)
2001
2001122. İnfertil Erkeklerde Y Kromozomu Üzerinde Bulunan AZF Bölgesindeki Mikrodelesyonların PCR ile Saptanması
Sargın C., BERKER S., MANGUOĞLU E., Luleci G., KARAVELİ F. Ş., GÜLKESEN K. H., et al.
7.Ulusal Tıbbi Biyoloji Kongresi, Eskişehir, Turkey, 18 - 21 September 2001, pp.100, (Full Text)
2001
2001123. İnfertil Erkeklerde Y Kromozomu Üzerinde Bulunan AZF Bölgesindeki Mikrodelesyonların PCR ile Saptanması
Sargın C., BERKER S., MANGUOĞLU E., Luleci G., KARAVELİ F. Ş., GÜLKESEN K. H., et al.
7.Ulusal Tıbbi Biyoloji Kongresi, Eskişehir, Turkey, 18 - 21 September 2001, pp.100, (Full Text)
2001
2001124. İnfertil Erkeklerde Y Kromozomu Üzerinde Bulunan AZF Bölgesindeki Mikrodelesyonların PCR ile Saptanması
Sargın C., BERKER S., MANGUOĞLU E., Luleci G., KARAVELİ F. Ş., GÜLKESEN K. H., et al.
7.Ulusal Tıbbi Biyoloji Kongresi, Eskişehir, Turkey, 18 - 21 September 2001, pp.100, (Full Text)
2001
2001125. Determination of microdeletions in AZF regions on Y chromosome by PCR in infertile man
Sargin F., BERKER S., MANGUOĞLU E., Lüleci G., KARAVELİ F. Ş., GÜLKESEN K. H., et al.
10th International Congress of Human Genetics, Viyana, Austria, 15 - 19 May 2001, pp.203, (Full Text)
2001
2001126. Determination of microdeletions in AZF regions on Y chromosome by PCR in infertile man
Sargin F., BERKER S., MANGUOĞLU E., Lüleci G., KARAVELİ F. Ş., GÜLKESEN K. H., et al.
10th International Congress of Human Genetics, Viyana, Austria, 15 - 19 May 2001, pp.203, (Full Text)
2001
2001127. Determination of microdeletions in AZF regions on Y chromosome by PCR in infertile man
Sargin F., BERKER S., MANGUOĞLU E., Lüleci G., KARAVELİ F. Ş., GÜLKESEN K. H., et al.
10th International Congress of Human Genetics, Viyana, Austria, 15 - 19 May 2001, pp.203, (Full Text)
2000
2000128. Hematolojik Malignansilerde Sitogenetik Çalışmalar
BERKER S., MANGUOĞLU A. E., Lüleci G., Kurtoğlu E., Timurağaoğlu A., Hazar V., et al.
IV.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, İzmir, Turkey, 3 - 06 May 2000, pp.221, (Full Text)
2000
2000129. Hematolojik Malignansilerde Sitogenetik Çalışmalar
BERKER S., MANGUOĞLU A. E., Lüleci G., Kurtoğlu E., Timurağaoğlu A., Hazar V., et al.
IV.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, İzmir, Turkey, 3 - 06 May 2000, pp.221, (Full Text)
2000
2000130. Hematolojik Malignansilerde Sitogenetik Çalışmalar
BERKER S., MANGUOĞLU A. E., Lüleci G., Kurtoğlu E., Timurağaoğlu A., Hazar V., et al.
IV.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, İzmir, Turkey, 3 - 06 May 2000, pp.221, (Full Text)
2000
2000131. Maternal 7q11.23 delesyonu ile Williams Sendromu düşünülen olgu
BERKER S., MANGUOĞLU A. E., MIHÇI E., Taçoy Ş., Lüleci G.
IV.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, İzmir, Turkey, 3 - 06 May 2000, pp.186, (Full Text)
2000
2000132. Maternal 7q11.23 delesyonu ile Williams Sendromu düşünülen olgu
BERKER S., MANGUOĞLU A. E., MIHÇI E., Taçoy Ş., Lüleci G.
IV.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, İzmir, Turkey, 3 - 06 May 2000, pp.186, (Full Text)
2000
2000133. Antalya çevresinde beta-talasemi ve orak hücre anemisinin RDBH yöntemi ile taranması
KESER İ., Kayisli O., Canatan D., Yesilipek A., MANGUOĞLU A. E., ŞANLIOĞLU A. D., et al.
IV.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, İzmir, Turkey, 3 - 06 May 2000, pp.233, (Full Text)
1999
1999134. A case with de novo interstitial deletion of chromosome 7(q11.2q22)
MANGUOĞLU A. E., BERKER S., Lüleci G., Bağcı G., Acar U.
31st Annual Meeting of the European Society of Human Genetics, Cenevre, Switzerland, 29 May - 01 June 1999, pp.75, (Full Text)
206
206135. Molecular Analysis of MEFV Gene in Turkish FMF Patients in Antalya Province
MANGUOĞLU E., ÇOBAN E., Özgüven e., Lüleci G., KESER İ.
Human Genome Meeting, Helsinki, Finland, 31 May 0206 - 03 June 2006, pp.118, (Full Text)
201
201136. R320H mutation in the thyroid hormone receptor beta TRB associated with autoimmune thyroid disease in a Turkish family
Parlak M., Durmaz E., Baran R., MANGUOĞLU E., BİRCAN İ., AKÇURİN S.
51st Annual Meeting of the European Society for Paediatric Endocrinology, Leipzig, Germany, 20 September 0201 - 23 September 2012, vol.78, pp.243, (Full Text)
Other Publications
Funded Projects
2019 - 2020
2019 - 2020Bilimsel 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 - 2019
2018 - 2019Evaluation of ETV6/RUNX1 Fusion and Additional Abnormalities Involving ETV6 and/or RUNX1 Genes Using FISH Technique in Patients with Childhood Acute Lymphoblastic Leukemia
Project Supported by Higher Education Institutions , BAP Other
KARAÜZÜM S. (Executive), MANGUOĞLU A. E., ALTIOK CLARK Ö., AKKAYA B., KÜPESİZ O. A.
2007 - 2008
2007 - 2008
Meme/over Kanserlerinde Kalıtsal Yatkınlıkta BRCA1/BRCA2 Genlerinde Büyük Boyutlu Genomik Yeniden Düzenlenmelerin Rolünün Araştrılması
TUBITAK Project
MANGUOĞLU A. E. (Executive)