Metrics
Publication
262
Open Access
8
UN Sustainable Development Goals
Education
2002 - 2008
2002 - 2008Doctorate
Istanbul University, Health Sciences Institute, Genetik Anabilim Dalı, Turkey
1987 - 1992
1987 - 1992Expertise In Medicine
Istanbul University, Istanbul Medical Faculty, İç Hastalıkları Anabilim Dalı, Turkey
1981 - 1987
1981 - 1987Undergraduate
Uludağ Üniversitesi, Uludağ Üniversitesi Tıp Fakültesi, Turkey
Dissertations
2008
2008Doctorate
Ailevi Akdeniz Ateşi Patogenezinde ASC Ve MEFV Genlerinin Metilasyonunun Rolü
Istanbul University, Health Sciences Institute, Genetik Anabilim Dalı
1998
1998Expertise In Medicine
İdyopatik portal hipertansiyon (87 olgunun değerlendirilmesi)
Istanbul University, Istanbul Medical Faculty, Division of Medical Sciences
Foreign Languages
B2 Upper Intermediate
B2 Upper IntermediateEnglish
Research Areas
Medicine
Internal Medicine Sciences
Internal Diseases
Medical Genetics
Health Sciences
Academic Positions
2018 - Present
2018 - PresentProfessor
Istanbul University, Istanbul Medical Faculty, Basic Medical Sciences
2016 - Present
2016 - PresentProfessor
Istanbul University, Istanbul Medical Faculty, Division of Medical Sciences
2008 - Present
2008 - PresentProfessor
Istanbul University, Istanbul Medical Faculty, Division of Medical Sciences
Managerial Experience
2015 - 2017
2015 - 2017Surgeon General
İstanbul Üniversitesi
Articles
All (133)
SCI-E, SSCI, AHCI (101)
SCI-E, SSCI, AHCI, ESCI (117)
ESCI (16)
Scopus (114)
TRDizin (22)
Other Publications (7)
2025
20251. In Silico and In Vitro Analysis of the Regulatory Role of miR-145-5p on Its Potential Target Genes in Acute Myeloid Leukemia Cell Lines
Aslan R., Kaya M., Suer İ., Çefle K., Öztürk Ş.
EXPERIMED , vol.15, no.3, pp.252-260, 2025 (Scopus, TRDizin)
2025
20252. Search for electroweak production of vector-like leptons in τ-lepton and b-jet final states in pp collisions at s = 13 TeV with the ATLAS detector
Zwalinski L., Zormpa O., Zorbas T., Zografos A., Zoch K., Zoccoli A., et al.
European Physical Journal C
, vol.85, no.11, 2025 (SCI-Expanded, Scopus)
2025
20253. A precise measurement of the jet energy scale derived from single-particle measurements and in situ techniques in proton–proton collisions at s= 13 TeV with the ATLAS detector
Zwalinski L., Zou W., Zormpa O., Zorbas T., Zoch K., Zoccoli A., et al.
European Physical Journal C
, vol.85, no.9, 2025 (SCI-Expanded, Scopus)
2025
20254. Curcumin as an Epigenetic Modulator: Suppression of Breast Cancer via the Hsa_circ_0001946/MiR-7-5p/Target Gene Axis
Abuaisha A., Kaya M., Suer İ., Emiroglu S., Bayram A., Tukenmez M., et al.
MEDICINA-LITHUANIA
, vol.61, no.9, 2025 (SCI-Expanded, Scopus)
2025
20255. Measurements of W+W− production cross-sections in pp collisions at s=13 TeV with the ATLAS detector
Aad G., Abbott B., Abeling K., Abicht N., Abidi S., Aboulhorma A., et al.
Journal of High Energy Physics
, vol.2025, no.8, 2025 (SCI-Expanded)
2025
20256. Search for long-lived charged particles using large specific ionisation loss and time of flight in 140 fb−1 of pp collisions at s = 13 TeV with the ATLAS detector
Aad G., Aakvaag E., Abbott B., Abdelhameed S., Abeling K., Abicht N., et al.
Journal of High Energy Physics
, vol.2025, no.7, 2025 (SCI-Expanded, Scopus)
2025
20257. Advances in focal segmental glomerulosclerosis research: genetic causes to non-coding RNAs.
Esmaeilzadeh Aghjeh M., Suer İ., Dirim A. B., Kaya M., Ozturk Ş.
Molecular biology reports
, vol.52, no.1, pp.384, 2025 (SCI-Expanded, Scopus)
2025
20258. Genetic insights into non-obstructive azoospermia: Implications for diagnosis and TESE outcomes
Sharifi S., DURSUN M., Sahin A., TURAN S., ALTUN A., Ozcan O., et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
, vol.42, no.4, pp.1223-1237, 2025 (SCI-Expanded)
2025
20259. Measurements of WH and ZH production with Higgs boson decays into bottom quarks and direct constraints on the charm Yukawa coupling in 13 TeV pp collisions with the ATLAS detector
Aad G., Aakvaag E., Abbott B., Abdelhameed S., Abeling K., Abicht N., et al.
Journal of High Energy Physics
, vol.2025, no.4, 2025 (SCI-Expanded, Scopus)
2025
202510. Let-7b-5p sensitizes breast cancer cells to doxorubicin through Aurora Kinase B
Kaya M., Abuaisha A., Suer İ., Emiroglu S., Önder S., Onay Ucar E., et al.
PLOS ONE
, vol.20, no.1, 2025 (SCI-Expanded, Scopus)
2025
202511. MiR-7-5p May Inhibit AML Cell Proliferation Via SKP2, KLF4, OGTTarget Genes
Mehteroglu E., SUER İ., KAYA M., ÖZTÜRK Ş., ÇEFLE K., PALANDUZ Ş.
CLINICAL AND EXPERIMENTAL HEALTH SCIENCES
, no.1, pp.8-14, 2025 (ESCI, TRDizin)
2025
202512. Elevated expression of let-7b-3p enhances aggressiveness of Larynx Squamous Cell Carcinoma Cells
Kaya M., Güzel Tanoğlu E., Suer İ., Öztürk Ş., Palanduz Ş., Çefle K., et al.
Anatolian Current Medical Journal , vol.7, no.1, pp.27-32, 2025 (Peer-Reviewed Journal)
2025
202513. Two potential regulatory axes in breast cancer patients: hsa_circ_0001546/hsa-miR-532-5p/ZFHX3 and hsa_circ_0025244/hsa-miR-210-5p/BTG2
Abanoz F., Suer İ., Kaya M., Abuaisha A., Emiroğlu S., Öztürk Ş.
CUKUROVA MEDICAL JOURNAL
, vol.50, no.3, pp.782-795, 2025 (ESCI, TRDizin)
2025
202514. Enhanced Expression of miR-638-5p May Suppress Acute Myeloid Leukemia in vitro Cell Proliferation Through PGK1 and PIM1
Ozkaynak S. O., SUER İ., KAYA M., ÖZTÜRK Ş.
KONURALP TIP DERGISI
, vol.17, no.1, pp.39-47, 2025 (ESCI)
2024
202415. Curcumin suppresses cell viability in breast cancer cell line by affecting the expression of miR-15a-5p
Suer İ., Abuaisha A., Kaya M., Abanoz F., Çefle K., Palanduz Ş., et al.
TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI
, vol.49, no.5, pp.656-665, 2024 (SCI-Expanded, Scopus)
2024
202416. Synchronized Diabetes Monitoring System: Development of Smart Mobile Apparatus for Diabetes Using Insulin
Kahraman M., Düdükçü H. V., Kurt S., Yıldız H., Aydın N., Mutlu Ü., et al.
IRBM
, vol.45, no.5, 2024 (SCI-Expanded)
2024
202417. Akut Miyeloid Lösemi’li Olgularda inv(3)/t(3;3) ile 7.Kromozomun Anomalilerinin Prognoza Etkisi
BAYRAK TOKAÇ A. G., BAĞATIR G., ERDEM S., ÇEFLE K., ÖZTÜRK Ş., YENEREL M. N., et al.
Manisa Celal Bayar Üniversitesi Eğitim Fakültesi Dergisi
, vol.11, pp.334-339, 2024 (Peer-Reviewed Journal)
2024
202418. Overexpression of CDC25A, AURKB, and TOP2A Genes Could Be an Important Clue for Luminal A Breast Cancer.
Kaya M., Abuaisha A., Süer İ., Alptekin M. S., Abanoz F., Emiroğlu S., et al.
European journal of breast health
, vol.20, no.4, pp.284-291, 2024 (ESCI)
2024
202419. EFFECT of CURCUMIN on BREAST CANCER CELLS THROUGH miR-145-5p AND ITS TARGET GENES
Abuaisha A., Kaya M., Suer İ., Emiroğlu S., Abanoz F., Palanduz Ş., et al.
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
, no.3, pp.235-245, 2024 (ESCI, TRDizin)
2024
202420. A CLASTOGENICITY STUDY WITH DISTINGUISHING FANCONI ANEMIA
Bagatir G., ÖZTÜRK Ş., BAYRAK TOKAÇ A. G., ÇEFLE K., ÜNÜVAR A., KARAKAŞ Z., et al.
NOBEL MEDICUS
, no.2, pp.135-140, 2024 (ESCI)
2024
202421. A CLASTOGENICITY STUDY WITH MITOMYCIN-C IN APLASTIC ANEMIA: DISTINGUISHING FANCONI ANEMIA APLASTİK ANEMİDE MİTOMİSİN-C İLE BİR KLASTOJENİTE ÇALIŞMASI: FANKONİ ANEMİSİNİ AYIRT ETME
Bağatir G., Karakaş Z., Öztürk Ş., Tokaç A. G., Çefle K., Ünüvar A., et al.
Nobel Medicus
, vol.20, no.2, pp.135-140, 2024 (ESCI)
2024
202422. A CLASTOGENICITY STUDY WITH MITOMYCIN-C IN APLASTIC ANEMIA: DISTINGUISHING FANCONI ANEMIA
Bağatir G., Öztürk Ş., Tokuç A. G. B., Çefle K., Ünüvar A., Karakaş Z., et al.
NOBEL MEDICUS
, vol.20, no.2, pp.135-140, 2024 (ESCI)
2024
202423. Bioinformatics analysis of the potentially functional circRNA-miRNA-mRNA network in breast cancer.
Erdogan C., Suer İ., Kaya M., Ozturk Ş., Aydin N., Kurt Z.
PloS one
, vol.19, no.4, 2024 (SCI-Expanded)
2024
202424. Turmeric Inhibits MDA-MB-231 Cancer Cell Proliferation, Altering miR-638-5p and Its Potential Targets
Kaya M., Abuaisha A., Suer İ., Emiroglu S., Abanoz F., Palanduz S., et al.
EUROPEAN JOURNAL OF BREAST HEALTH
, vol.20, no.2, pp.102-109, 2024 (ESCI, Scopus, TRDizin)
2024
202425. Expression Patterns of Eighteen Genes Involved in Crucial Cellular Processes in the TP53 Pathway in Multiple Myeloma
Öztan G., Suer İ., Aday A., Ayer M., Öztürk Ş., Çefle K., et al.
GAZI UNIVERSITY JOURNAL OF SCIENCE
, vol.37, no.3, pp.1066-1082, 2024 (ESCI)
2024
202426. CDR1as/miR-7-5p/IGF1R axis contributes to the suppression of cell viability in prostate cancer
Kaya M., Suer I., Aytatli A., Karatas O. F., Palanduz S., Cefle K., et al.
Turkish Journal of Biochemistry
, 2024 (SCI-Expanded)
2024
202427. Late diagnosis of a rare multisystemic genetic disorder: Transaldolase deficiency due to homozygous TALDO1 c.345dupA variant
Dirim A. B., Kalayci T., Safak S., Garayeva Guller N., Oto Ö. A., Artan A. S., et al.
NEPHROLOGY
, vol.29, no.1, pp.55-56, 2024 (SCI-Expanded)
2024
202428. Clastogenicity Study with Mitomycin-C in Aplastic Anemia: Distinguishing Fanconi Anemia
Bağatır G., Öztürk Ş., Tokaç Bayrak A. G., Çefle K., Ünüvar A., Karakaş Z., et al.
, vol.2, no.3, pp.35-45, 2024 (Peer-Reviewed Journal)
2023
202329. Clinical Features of the Patients with NLRP1 Gene Variants and a Systemic Autoinflammatory Phenotype
AMIKISHIYEV S., KALAYCI T., Deniz R., YALÇINKAYA Y., ARTIM ESEN B., İNANÇ M., et al.
ARTHRITIS & RHEUMATOLOGY
, pp.3800-3802, 2023 (SCI-Expanded)
2023
202330. Phenotypes of the Patients with More Than One Autoinflammatory Gene Variant: Classified Diseases and Mixed Autoinflammatory Disorders (MAID)
Amıkıshıyev S., Kalaycı T., Soltanova L., Yalçınkaya Y., Artim-Esen B., İnanç M., et al.
ARTHRITIS & RHEUMATOLOGY
, pp.506-508, 2023 (SCI-Expanded)
2023
202331. miR-145-5p suppresses cell proliferation by targeting IGF1R and NRAS genes in multiple myeloma cells
Kaya M., Suer İ., Ozgur E., Capik O., Karatas O. F., Ozturk Ş., et al.
TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI
, vol.48, no.5, pp.563-569, 2023 (SCI-Expanded, Scopus)
2023
202332. Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature.
Dirim A. B., Kalayci T., Safak S., Garayeva N., Gultekin B., Hurdogan O., et al.
Clinical rheumatology
, vol.42, no.2, pp.597-606, 2023 (SCI-Expanded)
2023
202333. Evaluation of TMED9, DNAJC1, LMAN2, COPE and KDELR1 Biomarkers in Patients with Monoclonal Gammopathy of Undetermined Significance and Multiple Myeloma
Sariman M., Salman Yaylaz B., Yabaci Tak A., Ayer M., Sirma Ekmekci S., Suer İ., et al.
UHOD - Uluslararasi Hematoloji-Onkoloji Dergisi
, vol.33, no.2, pp.92-102, 2023 (SCI-Expanded)
2022
202234. Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13
Kaya M., Suer İ., Kalayci T., Karaman B., Ozturk Ş., Palanduz Ş.
SCOTTISH MEDICAL JOURNAL
, vol.67, no.4, pp.173-177, 2022 (SCI-Expanded, Scopus)
2022
202235. The effect of Anzer honey on X-ray induced genotoxicity in human lymphocytes: An in vitro study
Bagatir G., Kaya M., Suer İ., Çefle K., Palanduz A., Palanduz Ş., et al.
MICROSCOPY RESEARCH AND TECHNIQUE
, vol.85, no.6, pp.2241-2250, 2022 (SCI-Expanded, Scopus)
2022
202236. OCT-1 Expression in Patients with Chronic Myeloid Leukemia: A Comparative Analysis with Respect to Response to Imatinib Treatment
Bozkurt Bulakçı B., Aday A., Gürtekin B., Yavuz A. S., Öztürk Ş., Çefle K., et al.
INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION
, vol.1, no.1, pp.1-7, 2022 (SCI-Expanded)
2022
202237. Is there a relationship between ACTN3 R577X gene polymorphism and sarcopenia?
Kahraman M., Ozulu Turkmen B., Bahat-Ozturk G., Catikkas N. M., Oren M. M., Sahin A., et al.
AGING CLINICAL AND EXPERIMENTAL RESEARCH
, vol.34, no.4, pp.757-765, 2022 (SCI-Expanded, Scopus)
2022
202238. ERAP1 Gen İfadesinin Plazma Hücre Diskrazilerinde İncelenmesi
Sariman M., KARAÇAM B., Ayer M., SIRMA EKMEKCİ S., SUER İ., ÇEFLE K., et al.
İstanbul Kanuni Sultan Süleyman Tıp Dergisi
, vol.14, no.2, pp.120-124, 2022 (Peer-Reviewed Journal)
2021
202139. Overview of clinical and genetic features of CML patients with variant Philadelphia translocations involving chromosome 7: A case series
Bayrak A. G., Daglar Aday A., Yavuz A. S., Nalcaci M., Ozbalak M. M., Cefle K., et al.
LEUKEMIA RESEARCH
, vol.111, 2021 (SCI-Expanded)
2021
202140. Clinical Characteristics and Mutation Spectrum of Neurofibromatosis Type 1 in 27 Turkish Families
Sharifi S., Kalayci T., Palanduz S., Ozturk S., Cefle K.
BALKAN MEDICAL JOURNAL
, vol.38, no.6, pp.365-373, 2021 (SCI-Expanded)
2021
202141. THE EFFECT OF SMARTPHONE APPS AND TECHNOLOGY COMPATIBILITY ON DIABETES CONTROL IN DIABETIC PATIENTS USING INSULIN
Kahraman M., Cakmak R., Satman İ., Karşıdağ K., Öztürk Ş., Ören M. M., et al.
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
, vol.84, no.4, pp.543-551, 2021 (ESCI, TRDizin)
2021
202142. Vaccine Passport Use and Travel Health Status Among Turkish Travelers at an International Airport
Kahraman M., Yuksel I., Boz E. B., Ozbek H. E., Mert E., Reyhanli A., et al.
International Journal of Travel Medicine and Global Health
, no.9, pp.161-169, 2021 (Peer-Reviewed Journal)
2021
202143. Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey
Berkay E. G., Elkanova L., Kalayci T., ULUDAĞ ALKAYA D., Altunoglu U., Cefle K., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
, vol.185, no.8, pp.2488-2495, 2021 (SCI-Expanded, Scopus)
2021
202144. A case mimicking chronic myeloid leukemia with t(8;22)(p11;q11)/BCR-FGFR1 and sequential transformation to B-acute lymphoblastic leukemia and acute myeloid leukemia
Bayrak A. G., Ucur A., Aday A., Bagatır G., Erdem S., Hancer V. S., et al.
Journal of Hematopathology
, vol.14, no.2, pp.151-156, 2021 (SCI-Expanded)
2021
202145. miR-145 suppresses epithelial-mesenchymal transition by targeting stem cells in Ewing sarcoma cells
Tanoglu E. G., Ozturk S.
BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY
, vol.122, no.1, pp.71-77, 2021 (SCI-Expanded)
2021
202146. Mir-129-2-3p Has Tumor Suppressor Role in Ewing Sarcoma Cell Lines and Cancer Tissue Samples
Tanoglu E. G., Arikan Y., Kabukcuoglu Y. S., Kabukcuoglu F., Tanoglu A., Ozturk S.
BRAZILIAN ARCHIVES OF BIOLOGY AND TECHNOLOGY
, vol.64, 2021 (SCI-Expanded)
2021
202147. Potential therapeutic road for targeting the SARS-CoV-2 at throat
Kaya M., Abuaisha A. M., Serakinci N., Ozturk S.
BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY
, vol.122, no.3, pp.206-211, 2021 (SCI-Expanded)
2021
202148. Dysregulation of MS4A3 and PRDX5 Gene Expression in Multiple Myeloma Patients
Suer İ., Aday A., Sariman M., Ayer M., Hindilerden I. Y., Ekmekci S. S., et al.
UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI
, vol.31, no.4, pp.205-213, 2021 (SCI-Expanded, Scopus)
2020
202049. RELATIONSHIP BETWEEN CHROMOSOMAL ABERRATIONS AND GENE EXPRESSIONS IN THE p53 PATHWAY IN CHRONIC LYMPHOCYTIC LEUKEMIA
ÖZTAN G., Aktan M., Palanduz Ş., İŞSEVER H., ÖZTÜRK Ş., Nikerel E., et al.
BALKAN JOURNAL OF MEDICAL GENETICS
, vol.23, no.1, pp.15-23, 2020 (SCI-Expanded)
2020
202050. De novo t(1;6)(p13p21.3) Dengeli Resiprokal Translokasyonun İnfertilite ile İlişkisi
Kaya M., Bağatır Ozan G., Çefle K., Öztürk Ş., Palanduz Ş.
Sağlık bilimlerinde değer (Online) , vol.10, no.1, pp.108-110, 2020 (Peer-Reviewed Journal)
2020
202051. Ewing Sarkoma ile Primitif Nöroektodermal Tümör HücreHatlarında Agresiflik Paterninin Karşılaştırılması
GÜZEL TANOĞLU E., ÖZTÜRK Ş.
Kocaeli Tıp Dergisi , vol.9, no.1, pp.24-31, 2020 (Peer-Reviewed Journal)
2019
201952. DNA damage effects of inhalation anesthetics in human bronchoalveolar cells
ÇUKUROVA Z., Cetingok H., Ozturk S., Gedikbasi A., HERGÜNSEL O., Ozturk D., et al.
MEDICINE
, vol.98, no.32, 2019 (SCI-Expanded, Scopus)
2019
201953. A Rare Variant Translocation (t(5922)(q13q34q11.2)) In A Case With Chronic Myeloid Leukemia
ERKAL H., ÖZTÜRK Ş., YÜCEL S., ÇEFLE K., BAGATIR G., BAYRAK A., et al.
Tıp Fakültesi Klinikleri Dergisi , 2019 (Peer-Reviewed Journal)
2019
201954. Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability.
Kaya M., Suer İ., Öztürk Ş., ÇEFLE K., Karaman B., Palanduz Ş.
F1000Research
, vol.8, pp.281, 2019 (Scopus)
2019
201955. Investigation of Gene Expressions of Myeloma Cells in the Bone Marrow of Multiple Myeloma Patients by Transcriptome Analysis
Sariman M., Abaci N., Ekmekci S., Cakiris A., Pacal F., Ustek D., et al.
Balkan medical journal
, vol.36, no.1, pp.23-31, 2019 (SCI-Expanded, Scopus, TRDizin)
2018
201856. Investigation of ErbB and Insulin Signaling Pathways in the Pathogenesis of Multiple Myeloma
Ozturk D., Coskunpinar E. M., Osmanbasoglu E., ÇETİN G., Yenerel M. N., Ayer M., et al.
HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI
, vol.56, no.2, pp.109-113, 2018 (ESCI)
2018
201857. Molecular Diagnosis Experience in Familial Mediterranean Fever: The Most Frequent Mutations in the MEFV Gene
Coskunpinar E., Ozvarnali A., Cefle K., Palanduz A., Gül A., Ozturk D., et al.
HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI
, vol.56, no.1, pp.42-49, 2018 (ESCI)
2018
201858. Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus
Kurklu E., Ozturk S., Cassidy A. J., Ak G., Koray M., Cefle K., et al.
MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL
, no.2, 2018 (SCI-Expanded)
2018
201859. Ailevi Akdeniz Ateşinde Moleküler Tanı Deneyimi: MEFV Geninde Sık Görülen Mutasyonlar
Coşkunpınar E., Özvarnalı A., Çefle K., PALANDUZ A., GÜL A., Öztürk D., et al.
HASEKİ TIP BÜLTENİ , vol.56, no.1, pp.42-49, 2018 (Scopus)
2017
201760. REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis
BAYRAM Y., WHITE J. J., Elcioglu N., CHO M. T., ZADEH N., Gedikbasi A., et al.
AMERICAN JOURNAL OF HUMAN GENETICS
, vol.101, no.1, pp.149-156, 2017 (SCI-Expanded, Scopus)
2017
201761. WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects
Yokote K., Chanprasert S., Lee L., EIRICH K., Takemoto M., Watanabe A., et al.
HUMAN MUTATION
, vol.38, no.1, pp.7-15, 2017 (SCI-Expanded)
2017
201762. Roles of Signal Transducer Pathways in Investigation of Biopsies from Patients with Bladder Tumors
Bayrak A. G., Palanduz S., Coskunpinar E., Sanli O., Armagan A., Karakus S., et al.
Asian Pacific journal of cancer prevention : APJCP
, vol.18, no.1, pp.201-205, 2017 (SCI-Expanded)
2016
201663. The frequency of C609T polymorphism in the NQO1 gene and its relation to cytogenetic abnormalities in patients with myelodysplastic syndrome.
Bagatır G., Sırma S. Ö., Palanduz S., Ozturk Ş., Cefle K., Ozbek U., et al.
Cellular and molecular biology (Noisy-le-Grand, France)
, vol.62, no.7, pp.61-5, 2016 (SCI-Expanded)
2015
201564. Yeni Nesil Dizileme Teknolojisi Ile Transkriptom Analizi
Sarıman M., Sırma Ekmekci S., Abacı N., Çakiris A., Paçal F., Emrence Z., et al.
Deneysel Tıp Dergisi , vol.5, no.10, pp.51-59, 2015 (Peer-Reviewed Journal)
2015
201565. Transcriptom Analysis Using Next Generation Sequencing
Sarıman M., EKMEKCI S. S., ABACI N., ÇAKİRİS A., PAÇAL F., EMRENCE Z., et al.
Deneysel Tıp Araştırma Enstitüsü Dergisi , vol.4, no.10, pp.51-59, 2015 (Peer-Reviewed Journal)
2015
201566. Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction
BONORA E., BIANCO F., Cordeddu L., Bamshad M., Francescatto L., Dowless D., et al.
GASTROENTEROLOGY
, vol.148, no.4, pp.771-793, 2015 (SCI-Expanded, Scopus)
2015
201567. The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey
Ozantürk A., Marshall J. D., Collin G. B., Düzenli S., Marshall R. P., Candan Ş., et al.
Journal of Human Genetics
, vol.60, no.1, pp.1-9, 2015 (SCI-Expanded)
2013
201368. Genotoxicity of fixation devices analyzed by the frequencies of sister chromatid exchange
Aydil B. A., Kocak Berberoglu H., Ozturk S., Cefle K., Palanduz S., Erkal H.
ULUSAL TRAVMA VE ACIL CERRAHI DERGISI-TURKISH JOURNAL OF TRAUMA & EMERGENCY SURGERY
, vol.19, no.4, pp.299-304, 2013 (SCI-Expanded)
2012
201269. A Turkish trichothiodystrophy patient with homozygous XPD mutation and genotype-phenotype relationship
Pehlivan D., Cefle K., Raams A., Ozturk Ş., Baykal C., Kleijer W. J., et al.
JOURNAL OF DERMATOLOGY
, vol.39, no.12, pp.1016-1021, 2012 (SCI-Expanded)
2012
201270. A novel two bases deletion in the albumin gene causes analbuminaemia in a young Turkish man.
CARIDI G., DAGNINO M., Di D., AKYÜZ F., BOZTAS G., BESISIK F., et al.
Clinica chimica acta; international journal of clinical chemistry
, vol.413, no.9-10, pp.950-1, 2012 (SCI-Expanded)
2012
201271. Multidisciplinary treatment of non-syndromic oligodontia
BURAL C., OZTAS E., Ozturk S., BAYRAKTAR G.
European Journal of Dentistry
, vol.6, no.2, pp.218-226, 2012 (Scopus)
2012
201272. Investigation of Arg399Gln and Arg194Trp Polymorphisms of the XRCC1 (X-Ray Cross-Complementing Group 1) Gene and Its Correlation to Sister Chromatid Exchange Frequency in Patients with Chronic Lymphocytic Leukemia
Duman N., Aktan M., Ozturk S., Palanduz S., Cakiris A., Ustek D., et al.
GENETIC TESTING AND MOLECULAR BIOMARKERS
, vol.16, no.4, pp.287-291, 2012 (SCI-Expanded)
2011
201173. Outcome of Kidney Transplantation Following End-Stage Renal Disease Due to Reflux Nephropathy
Yazici H., Caliskan Y., Ozturk S., Ozkan O., Turkmen A., Sever M. S.
TRANSPLANTATION PROCEEDINGS
, vol.43, no.5, pp.1566-1569, 2011 (SCI-Expanded, Scopus)
2010
201074. No difference in micronuclear scores in both circulating lymphocytes and Buccal Epithelial Cells between Patients with Oral Lichen Planus and Oral Lichenoid Stomatitis
Ergun S., Kaya M., Warnakulasuriya S., Erbagci M., Oeztuerk Ş., Saruhanoglu A., et al.
ORAL DISEASES
, vol.16, no.6, pp.524-525, 2010 (SCI-Expanded)
2010
201075. Micronucleus and Sister Chromatid Exchange Analyses in Peripheral Lymphocytes of Patients with Oral Leukoplakia - A Pilot Study
Saruhanoglu A., Tanyeri H., Duman N., Sevinc B., Oeztuerk Ş., Ergun S., et al.
ORAL DISEASES
, vol.16, no.6, pp.518-519, 2010 (SCI-Expanded)
2010
201076. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations
Friedrich K., Lee L., Leistritz D. F., Nuernberg G., Saha B., Hisama F. M., et al.
HUMAN GENETICS
, vol.128, no.1, pp.103-111, 2010 (SCI-Expanded)
2010
201077. A POSSIBLE DELETERIOUS EFFECT OF INCREASED SERUM COPPER ON MYOCARDIAL FUNCTION IN PATIENTS WITH DILATED CARDIOMYOPATHY AWAITING TRANSPLANTATION
Cefle K., Ercag E., Gezertas S., Uzer A., Oeztuerk Ş., Cefle A., et al.
NOBEL MEDICUS
, vol.6, no.2, pp.32-36, 2010 (SCI-Expanded)
2010
201078. NILOTINIB EFFICACY IN 21 IMATINIB-RESISTANT OR-INTOLERANT T (9;22) POSITIVE CHRONIC MYELOID LEUKEMIA PATIENTS WITH AND WITHOUT ADDITIONAL CHROMOSOMAL CHANGES
Yavuz A. S., Elcioglu O. C., Akpinar T. S., Cosan F., Ucur A., Bayrak A., et al.
NOBEL MEDICUS
, vol.6, no.2, pp.57-62, 2010 (SCI-Expanded)
2009
200979. Cytogenetic Analysis and Examination of SOS1 Gene Mutation in a Turkish Family with Hereditary Gingival Fibromatosis
Pehlivan D., Abe S., Ozturk S., Kayhan K., Gunduz E., Cefle K., et al.
JOURNAL OF HARD TISSUE BIOLOGY
, vol.18, no.3, pp.131-134, 2009 (SCI-Expanded, Scopus)
2009
200980. Comparison of the Cytogenetic and Molecular Analyses in the Assessment of Imatinib Response in Chronic Myelocytic Leukemia
Palanduz S., Bayrak A., Sirma S., Vural B., Cefle K., Ucur A., et al.
GENETIC TESTING AND MOLECULAR BIOMARKERS
, vol.13, no.5, pp.599-602, 2009 (SCI-Expanded)
2009
200981. Left Ventricular Thickness Is Increased in Nonhypertensive Turner's Syndrome
Sozen A. B., Cefle K., Kudat H., Ozturk Ş., Oflaz H., Akkaya V., et al.
ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES
, vol.26, no.8, pp.943-949, 2009 (SCI-Expanded)
2008
200882. Investigation of Genomic Instability in Patients with Sjogren's Syndrome by Using Sister Chromatid Exchange Analysis
ERGUN S., Tanyeri H., Ozturk Ş., Duman N., Kamal S., GÜL A., et al.
ACTA STOMATOLOGICA CROATICA
, vol.42, no.4, pp.318-325, 2008 (ESCI)
2008
200883. ARTERIAL OBSTRUCTION IN A KLINEFELTER SYNDROME PATIENT WITH RARE KARYOTYPE (48, XXYY)
Pehlivan D., Cefle K., Ozturk S., Akbulut M. F., Palazduz S.
TURKISH JOURNAL OF UROLOGY
, vol.34, no.4, pp.491-494, 2008 (ESCI)
2008
200884. Loss of heterozygosity at chromosome 14q is associated with poor prognosis in head and neck squamous cell carcinomas
Pehlivan D., Gunduz E., Gunduz M., Nagatsuka H., Beder L. B., Cengiz B., et al.
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
, vol.134, no.12, pp.1267-1276, 2008 (SCI-Expanded)
2008
200885. The effects of etodolac, nimesulid and naproxen sodium on the frequency of sister chromatid exchange after enclused third molars surgery.
Koeseoglu B., Oeztuerk Ş., Kocak H., Palanduz S., Cefle K.
Yonsei medical journal
, vol.49, no.5, pp.742-7, 2008 (SCI-Expanded, Scopus)
2008
200886. Atrial and ventricular arryhthmogenic potential in Turner syndrome
Sozen A. B., Cefle K., Kudat H., Ozturk Ş., Oflaz H., Pamukcu B., et al.
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY
, vol.31, no.9, pp.1140-1145, 2008 (SCI-Expanded)
2008
200887. Effect of Cyclosporin A and Tacrolimus on sister chromatid exchange frequency in renal transplant patients
Ozturk Ş., Ayna T. K., Cefle K., Palanduz S., Ciftci H., Kaya Ş., et al.
GENETIC TESTING
, vol.12, no.3, pp.427-430, 2008 (SCI-Expanded)
2008
200888. Cytogenetic findings in pediatric myelodysplastic and myeloproliferative diseases
Bagatir G., Palanduz A., Ozturk S., Cefle K., Telhan L., Palanduz S.
ACTA PAEDIATRICA
, vol.97, pp.155, 2008 (SCI-Expanded)
2008
200889. A 47,X,i(Xq),Y KARYOTYPE DETECTED KLINEFELTER SYNDROME PATIENT
Pehlivan D., Cefle K., Ozturk Ş., Akbulut F. M., PALANDUZ Ş.
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
, vol.71, no.3, pp.91-93, 2008 (ESCI)
2007
200790. Treatment of acquired severe aplastic anemia with antilymphocyte globulin, cyclosporin A, methyprednisolone, and granulocyte colony-stimulating factor
Dinçol G., Aktan M., Diz-Küçükkaya R., Yavuz S., Nalçaci M., Öztürk Ş., et al.
American Journal of Hematology
, vol.82, no.9, pp.783-786, 2007 (SCI-Expanded)
2007
200791. The genotoxic effects in lymphocyte cultures of children treated with radiosynovectomy by using yttrium-90 citrate colloid
Turkmen C., Ozturk Ş., Unal S. N., Zulrikar B., Taser O., Sanfi Y., et al.
CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS
, vol.22, no.3, pp.393-399, 2007 (SCI-Expanded)
2007
200792. Initial maternal meiotic I error leading to the formation of a maternal i(2q) and a paternal i(2p) in a healthy male
Baumer A., Basaran S., Taralczak M., Cefle K., Ozturk S., Palanduz S., et al.
CYTOGENETIC AND GENOME RESEARCH
, vol.118, no.1, pp.38-41, 2007 (SCI-Expanded)
2007
200793. Monitoring the genotoxic effects of radiosynovectomy with Re-186 in paediatric age group undergoing therapy for haemophilic synovitis
Turkmen C., Ozturk Ş., Unal N., Zulfikar B., Taser O., Sanli Y., et al.
HAEMOPHILIA
, vol.13, no.1, pp.57-64, 2007 (SCI-Expanded)
2007
200794. Comparison of rheological parameters in patients with post hepatitic and alcoholic cirrhosis
Tamer S., Cefle K., Gokkusu C., Ademoglu E., Ozturk Ş., Vatansever S., et al.
CLINICAL HEMORHEOLOGY AND MICROCIRCULATION
, vol.36, no.3, pp.247-252, 2007 (SCI-Expanded)
2007
200795. Lens opacities in Bloom syndrome: Case report and review of the literature
Cefle K., Ozturk Ş., Gozum N., Duman N., Mantar F., Guler K., et al.
OPHTHALMIC GENETICS
, vol.28, no.3, pp.175-178, 2007 (SCI-Expanded)
2006
200696. A case of myelodysplastic syndrome with erythroid hypoplasia associated with a familial translocation t(3 ; 14)(p21.1 ; q24.1)
Dincol G., Ozturk S., Palanduz S., Tutkan G., Yildirim N., Ayer M., et al.
AMERICAN JOURNAL OF HEMATOLOGY
, vol.81, no.11, pp.883-887, 2006 (SCI-Expanded)
2006
200697. Werner syndrome associated with renal involvement
KOCABAY G., Ozturk S., ECDER T.
SAUDI MEDICAL JOURNAL
, vol.27, no.11, pp.1768-1769, 2006 (SCI-Expanded)
2006
200698. Increased sister chromatid exchange frequency in young women with breast cancer and in their first-degree relatives.
Cefle K., Ucur A., Guney N., Ozturk S., Palanduz S., Tas F., et al.
Cancer genetics and cytogenetics
, vol.171, pp.65-7, 2006 (SCI-Expanded, Scopus)
2006
200699. A case of progressive pseudorheumatoid arthropathy of 'childhood' with the diagnosis delayed to the fifth decade
Cefle A., Cefle K., Tunaci M., Ozturk S., Palanduz S.
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE
, vol.60, no.10, pp.1306-1309, 2006 (SCI-Expanded)
2006
2006100. The genotoxic effects in lymphocyte cultures of infants treated with radiosynovectomy by using Yittrium-90 citrate colloid.
Turkmen C., Ozturk S., Unal S., Zulfikar B., Taser O., Sanli Y., et al.
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING
, vol.33, 2006 (SCI-Expanded)
2006
2006101. The genotoxic effects in lymphocyte cultures of infants treated with radiosynovectomy by using Yittrium-90 citrate colloid.
Turkmen C., Ozturk S., Unal S., Zulfikar B., Taser O., Sanli Y., et al.
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING
, vol.33, 2006 (SCI-Expanded)
2006
2006102. A different approach to telomere analysis with ddPRINS in chronic lymphocytic leukemia
Palanduz S., Serakinci N., Cefle K., Aktan M., Tutkan G., Ozturk S., et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS
, vol.49, no.1, pp.63-69, 2006 (SCI-Expanded)
2005
2005103. A solitary calvarial lytic lesion with typical histopathological findings of juvenile hyaline fibromatosis - Case report
Bas N., Guzey F., Emel E., Cefle K., Turgut H., Alatas I., et al.
JOURNAL OF NEUROSURGERY
, vol.103, no.3, pp.285-288, 2005 (SCI-Expanded)
2005
2005104. A solitary calvarial lytic lesion with typical histopathological findings of juvenile hyaline fibromatosis.
BAS N., GÜZEY F., EMEL E., CEFLE K., TURGUT H. Z., ALATAS I., et al.
Journal of neurosurgery
, vol.103, pp.285-8, 2005 (SCI-Expanded)
2005
2005105. Clinical and molecular characterization of two adults with autosomal recessive Robinow syndrome
Tufan F., Cefle K., Turkmen S., Turkmen A., Zorba U., Dursun M., et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
, no.2, pp.185-189, 2005 (SCI-Expanded)
2005
2005106. Genotoxicity and sister chromatid exchange in patients with myelodysplastic disorders.
Oztürk S., PALANDUZ S., CEFLE K., TUTKAN G., UCUR A., DINCOL G., et al.
Cancer genetics and cytogenetics
, vol.159, pp.148-50, 2005 (SCI-Expanded)
2005
2005107. Maxillofacial and dental manifestations in a patient with mandibulo-acral dysplasia
Tanyeri H., Kurklu E., Ak G., Ozturk S., Koray M., Palanduz S.
CRANIO-THE JOURNAL OF CRANIOMANDIBULAR PRACTICE
, vol.23, no.1, pp.74-78, 2005 (SCI-Expanded)
2005
2005108. Alterations in rheological properties and erythrocyte membrane proteins in cats with diabetes mellitus.
KAYMAZ A., TAMER S., ALBENIZ I., CEFLE K., PALANDUZ S., Ozturk S., et al.
Clinical hemorheology and microcirculation
, vol.33, pp.81-8, 2005 (SCI-Expanded)
2004
2004109. In vitro effects of selective and non-selective nonsteroidal anti-inflammatory drugs on the frequency of sister chromatid exchanges.
Oztürk S., Köseoglu B., Koçak H., Palanduz S., Cefle K., Erkal H.
Drugs in R&D
, vol.5, pp.327-30, 2004 (SCI-Expanded)
2003
2003110. Familial visceral myopathy with pseudo-obstruction, megaduodenum, Barrett's esophagus, and cardiac abnormalities
MUNGAN Z., AKYUZ F., Bugra Z., YONAL O., OZTURK S., ACAR A., et al.
AMERICAN JOURNAL OF GASTROENTEROLOGY
, vol.98, no.11, pp.2556-2560, 2003 (SCI-Expanded)
2003
2003111. The in vitro effect of interferon-alpha 2a on CD95 expression of T cells in hepatitis B
Karan M., Ozturk S., Yenerel M. N., Erten N., Cefle K., Palanduz S., et al.
HEPATO-GASTROENTEROLOGY
, vol.50, no.54, pp.2031-2034, 2003 (SCI-Expanded)
2003
2003112. Sister chromatid exchange and mitotic index in patients with cirrhosis related to hepatitis B and C viruses and in chronic carriers
Ucur A., Palanduz S., Cefle K., Ozturk Ş., Tutkan G., Vatansever S., et al.
HEPATO-GASTROENTEROLOGY
, vol.50, no.54, pp.2137-2140, 2003 (SCI-Expanded)
2003
2003113. The diagnostic value of troponin T and myoglobin levels in acute myocardial infarction: A study in Turkish patients
Vatansever S., Akkaya V., Erk O., Ozturk S., Karan M., Salmayeni N., et al.
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH
, vol.31, no.2, pp.76-83, 2003 (SCI-Expanded)
2003
2003114. A patient with metachronous gastric, colonic, and thyroid cancers: A case report
Oncel M., Kurt N., Altuntas Y., Ozturk S., Ozdemir N., Bahadir I.
INTERNATIONAL SURGERY
, vol.88, no.1, pp.1-5, 2003 (SCI-Expanded)
2002
2002115. Molecular diagnosis of analbuminemia: a novel mutation identified in two Amerindian and two Turkish families.
GALLIANO M., CAMPAGNOLI M., ROSSI A., Wirsing v., LYON A., CEFLE K., et al.
Clinical chemistry
, vol.48, pp.844-9, 2002 (SCI-Expanded)
2002
2002116. Chronic renal failure in a patient with Sotos syndrome due to autosomal dominant polycystic kidney disease
Cefle K., Yildiz A., Palanduz S., Ozturk S., Ozbey N., Kylycaslan I., et al.
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE
, vol.56, no.4, pp.316-318, 2002 (SCI-Expanded)
2002
2002117. The effect of atorvastatin on hemorheological parameters in rabbits fed on a normal diet
Cefle K., Tamer S., Kaymaz A., Balci M., Ahmetov S., Palanduz S., et al.
CLINICAL HEMORHEOLOGY AND MICROCIRCULATION
, vol.26, no.4, pp.265-271, 2002 (SCI-Expanded)
2002
2002118. Acute wood or coal exposure with carbon monoxide intoxication induces sister chromatid exchange.
Oztürk S., VATANSEVER S., CEFLE K., PALANDUZ S., GÜLER K., ERTEN N., et al.
Journal of toxicology. Clinical toxicology
, vol.40, pp.115-20, 2002 (SCI-Expanded)
2001
2001119. A case of severe partial hypodontia associated with simple hemihypertrophy.
Erdilek D., Koray F., Ozturk S., Palanduz S.
JOURNAL OF DENTAL RESEARCH
, vol.80, no.4, pp.1202, 2001 (SCI-Expanded)
2000
2000120. Sister chromatid exchange frequency in B-cells stimulated by TPA in chronic lymphocytic leukemia
Ozturk S., Palanduz S., Aktan M., Cefle K., Serakinci N., Perkcelen Y.
CANCER GENETICS AND CYTOGENETICS
, vol.123, no.1, pp.49-51, 2000 (SCI-Expanded)
2000
2000121. Very severe aplastic anemia following resection of lymphocytic thymoma: Effectiveness of antilymphocyte globulin, cyclosporin A, and granulocyte-colony stimulating factor
Dincol G., Saka B., Aktan M., Nalcaci M., Keskin H., Palanduz S., et al.
AMERICAN JOURNAL OF HEMATOLOGY
, vol.64, no.1, pp.78-79, 2000 (SCI-Expanded)
2000
2000122. A case of Noonan syndrome with pulmonary and abdominal lymphangiectasia
Ozturk Ş., Cefle K., Palanduz S., Erten N., Karan M., Tascioglu C., et al.
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE
, vol.54, no.4, pp.274-276, 2000 (SCI-Expanded)
2000
2000123. A case of chronic lymphocytic leukemia with a constitutional pericentric inversion of chromosome 1
Palanduz S., Cefle K., Aktan M., Tutkan G., Ozturk S., Pekcelen Y.
CANCER GENETICS AND CYTOGENETICS
, vol.118, no.1, pp.62-64, 2000 (SCI-Expanded)
1999
1999124. Effect of cefodizime, ofloxacin, ciprofloxacin and interferon alpha-2a, alone and in combination, on phagocytic and candidacidal functions of leucocytes from patients with chronic renal failure
Gurer U., Palanduz S., Cevikbas A., Derici K., Johansson C., Ozturk S.
MEDICAL SCIENCE RESEARCH
, vol.27, no.5, pp.315-318, 1999 (SCI-Expanded)
1999
1999125. Rheological properties of blood in patients with ischaemic heart disease
Palanduz S., Tamer S., Vatansever S., Karan M., Cefle K., Ozturk Ş., et al.
MEDICAL SCIENCE RESEARCH
, vol.27, no.5, pp.327-329, 1999 (SCI-Expanded)
1999
1999126. Genotoxic potential of cyclosporin A in patients with renal transplantation
Palanduz S., Sever M., Ozturk S., Tascioglu C., Karan M., Sonmez G., et al.
CELL BIOLOGY AND TOXICOLOGY
, vol.15, no.1, pp.13-17, 1999 (SCI-Expanded)
1999
1999127. A case of McCune-Albright syndrome mimicking Paget's disease of bone
Palanduz S., Cefle K., Ozturk S., Tanakol R., Tascioglu C., Koldas T., et al.
BONE
, vol.24, no.2, pp.157-158, 1999 (SCI-Expanded)
1999
1999128. Two sisters with hereditary multiple exositosis
Palanduz Ş., Öztürk Ş., Palanduz A., Çefle K., Erden S., Odabaş A. R., et al.
Medical Bulletin of Istanbul Medical Faculty , vol.32, no.2, pp.196-199, 1999 (Peer-Reviewed Journal)
1999
1999129. A case of mental retardation associated with a partial tetrasomy of chromosome 15
Palanduz S., Ozturk S., Cefle K., Tutkan G., Karaman B., Ustek D., et al.
CYTOGENETICS AND CELL GENETICS
, vol.85, pp.159, 1999 (SCI-Expanded)
1998
1998130. 47,XYY karyotype in acute myeloid leukemia
Palanduz S., Aktan M., Ozturk S., Tutkan G., Cefle K., Pekcelen Y.
CANCER GENETICS AND CYTOGENETICS
, vol.106, no.1, pp.76-77, 1998 (SCI-Expanded)
1998
1998131. In vitro chromosomal radiosensitivity in common variable immune deficiency
Palanduz S., Palanduz A., Yalcin I., Somer A., Ones U., Ustek D., et al.
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY
, no.2, pp.180-182, 1998 (SCI-Expanded)
1998
1998132. An unusual translocation between 12tel and 14q11 in a large kindred.
Palanduz S., Ustek D., Karaman B., Ozturk S., Cefle K., Basaran S.
Hereditas
, vol.128, no.3, pp.231-4, 1998 (SCI-Expanded)
1994
1994133. Dört Mikrosefalili Olguda Genetik, Dental, Morfolojik Özellikler ve Genel Değerlendirme
KATİPOĞLU A. B., PALANDUZ Ş., ÖZTÜRK Ş., Horasan S.
Türk Tıp Derneği Dergisi , vol.60, pp.49-57, 1994 (Peer-Reviewed Journal)
Papers Presented at Peer-Reviewed Scientific Conferences
2025
20251. A novel compound heterozygous COL4A4 variant in a 24-year-old Alport syndrome case
Nazligul E., SUER İ., Kaya M., KALAYCI T., DİRİM A. B., ÇEFLE K., et al.
14. ULUSAL MOLEKÜLER BİYOLOJİ VE BİYOTEKNOLOJİ KONGRESİ, 1 - 02 November 2025, pp.124-130, (Full Text)
2025
20252. Norrie Disease due to a Hemizygous NDP Gene Variant: A Case Report of a 20-Year-Old Male
Aktaş Ç., SUER İ., Kaya M., KALAYCI T., ÇEFLE K., ÖZTÜRK Ş.
20. Uluslararası Hipokrat Tıp ve Sağlık Bilimleri Kongresi, 19 - 20 December 2025, (Full Text)
2025
20253. A novel compound heterozygous COL4A4 variant in a 24-year-old Alport syndrome case
Nazlıgül E., Suer İ., Kaya M., Kalaycı T., Dirim A. B., Çefle K., et al.
14. Ulusal Moleküler Biyoloji ve Biyoteknoloji Kongresi, Konya, Turkey, 1 - 02 November 2025, pp.124-130, (Full Text)
2025
20254. Identification of a novel variant in the PODXL gene in a Turkish family with focal segmental glomerulosclerosis
Esmaeilzadeh Aghjeh M., SUER İ., KALAYCI T., DİRİM A. B., Kaya M., ÖZTÜRK Ş.
9th International Congress on Biomedicine, Iran, 10 - 19 November 2025, (Summary Text)
2025
20255. Multipl Miyelom'da Genetik Karmaşa: Optik Genom Haritalamanın Yeri
BAYRAK TOKAÇ A. G., ERDEM S., ADAY A., MUTLU M. B., GÜNEY D. K., MASTANZADE M., et al.
12. Hematolojik Onkoloji Kongresi, KKTC, Turkey, 02 October 2025, pp.134-137, (Summary Text)
2025
20256. Kronik Lenfositik Lösemide Optik Genom Haritalamanın FISH Analizine Tamamlayıcı Rolü: Tek Merkez Pilot Çalışma
ERDEM S., BAYRAK TOKAÇ A. G., ADAY A., KARACA D., MUTLU M. B., ÇEFLE K., et al.
51. ULUSAL HEMATOLOJİ KONGRESİ, Antalya, Turkey, 28 October - 02 November 2025, pp.121-122, (Summary Text)
2025
20257. STUB1 expression as a diagnostic biomarker and its association with drug resistance in multiple myeloma
Punar Ş., Sarıman M., Ayer M., Suer İ., Çefle K., Öztürk Ş., et al.
European Society of Human Genetics Conference (ESHG), Milan, Italy, 24 - 27 May 2025, pp.1-2, (Summary Text)
2025
20258. 47,XXX (Triple X sendromu) olgusunda tekrarlayan gebelik kaybı
Engüleç İ., Kuntsal E., Kaya M., SUER İ., ÖZTÜRK Ş., ÇEFLE K.
Başakşehir Çam ve Sakura Şehir Hastanesi 3. Kadın Doğum Günleri Kongresi, İstanbul, Turkey, 10 - 13 April 2025, pp.116-120, (Full Text)
2025
20259. STUB1 expression as a diagnostic biomarker and its association with drug resistance in multiple myeloma.
Punar Ş., Sariman M., AYER M., SUER İ., ÇEFLE K., ÖZTÜRK Ş., et al.
European Society of Human Genetics Conference (ESHG), Milan, Italy, 24 May 2025, (Summary Text)
2025
202510. Assessment of the clinical diagnostic potential of NGS-based panel tests in100 cases with renal disease pre-diagnoses
SUER İ., KALAYCI T., DİRİM A. B., Şafak S., SIRMA EKMEKCİ S., Kaya M., et al.
European Society of Human Genetics Conference (ESHG), Milan, Italy, 24 May 2025, (Summary Text)
2025
202511. Genetic insights into non-obstructive azoospermia: Identifying novel variants and enhancing clinical outcomes
Sharifi S., Dursun M., Şahin A., Altun A., Turan S., Özcan Ö., et al.
40th Annual EAU Congress, Madrid, Spain, 21 - 24 March 2025, pp.87, (Summary Text)
2024
202412. Akut miyeloid lösemi hücrelerinde EIF4E, PIM1 ve IGF1R ekspresyonunun miRNA aracılı baskılanması
Kaya M., Suer İ., Çefle K., Öztürk Ş.
26. Ulusal İç Hastalıkları Kongresi, Girne, Cyprus (Kktc), 2 - 06 October 2024, pp.105-106, (Summary Text)
2024
202413. Association of MiR-145-5p with CDK6, IRS1, and UHRF1 as Potential Target Oncogenes in Breast Cancer
Engüleç İ., Abuaisha A., Kaya M., Suer İ., Öztürk Ş.
3rd International Congress of Medical and Health Sciences Research, Ankara, Turkey, 13 - 14 December 2024, pp.291-303, (Full Text)
2024
202414. Association of MiR-145-5p with CDK6, IRS1, and UHRF1 as Potential Target Oncogenes in Breast Cancer
Engüleç İ., Abuaisha A., Kaya M., Suer İ., Öztürk Ş.
3rd International Congress of Medical and Health Sciences Research, Ankara, Turkey, 13 - 14 December 2024, vol.1, pp.291-303, (Full Text)
2024
202415. Optical Genome Mapping in Newly Diagnosed Chronic Lymphocytic Leukemia
ERDEM S., BAYRAK TOKAÇ A. G., ADAY A., KARACA D., ÖZTÜRK Ş., ÇEFLE K., et al.
66th ASH Annual Meeting and Exposition, San Diego, CA, United States Of America, 7 - 10 December 2024, pp.6758, (Summary Text)
2024
202416. DE NOVO 46,XX,t(5;7)(p15.2;q11.2) VE 46,XX,t(1;9)(q23;q21) DENGELİ RESIPROKAL TRANSLOKASYONLARI VE HABITUEL ABORTUS İLİŞKİSİ
Alptekin M. S., Kaya M., SUER İ., ÇEFLE K., ÖZTÜRK Ş.
17th International Medical and Health Sciences Research Congress, 19 - 20 October 2024, (Full Text)
2024
202417. inv(5)(q15q33) in both parents associated with recurrent pregnancy loss
Kuntsal E., SUER İ., Kaya M., KALAYCI T., ÖZTÜRK Ş., ÇEFLE K.
10th Congress of South East European Society of Perinatal Medicine (SEESPM), İstanbul, Turkey, 23 - 26 October 2024, vol.1, pp.77-79, (Summary Text)
2024
202418. De Novo 46,XX,t(5;7)(p15.2;q11.2) ve 46,XX,t(1;9)(q23;q21) Dengeli Resiprokal Translokasyonları ve Habituel Abortus İlişkisi
Alptekin M. S., Kaya M., Suer İ., Çefle K., Öztürk Ş.
17. Uluslararası Tıp ve Sağlık Bilimleri Araştırmaları Kongresi, Ankara, Turkey, 19 - 20 October 2024, pp.172-176, (Full Text)
2024
202419. Akut miyeloid lösemi hücrelerinde EIF4E, PIM1 ve IGF1R ekspresyonunun miRNA aracılı baskılanması
Kaya M., SUER İ., ÇEFLE K., ÖZTÜRK Ş.
26. Ulusal İç Hastalıkları Kongresi, Cyprus (Kktc), 2 - 06 October 2024, (Summary Text)
2024
202420. A Novel FBN1 Variant in A Large Marfan Family with High Penetrance of Aortic Features
ERBİLGİN Y., ÇEFLE K., ÖZTÜRK Ş., EKIJI L., KADIOĞLU P., Kocaağa S., et al.
Avrupa İnsan Genetiği Kongresi 2024, Berlin, Germany, 01 June 2024, (Summary Text)
2024
202421. Integrated Multi-Omics Approach for Investigating Molecular Insights into Non-Obstructive Azoospermia and Association with Potential Cancer Susceptibility
Sharifi S., Dursun M., Şahin A., Özcan Ö., Turan S., Kadıoğlu A., et al.
23. Ulusal Androloji Kongresi, Eskişehir, Turkey, 17 - 19 May 2024, pp.22, (Summary Text)
2024
202422. GENETIC VARIANTS OF UNCERTAIN SIGNIFICANCE IN DLC1 AND PRLR GENES IN A PURE MUCINOUS BREAST CARCINOMA PATIENT
Abuaisha A., SUER İ., Kaya M., EMİROĞLU S., TÜKENMEZ M., ÖZTÜRK Ş.
TASHKENT INTERNATIONAL CONGRESS ON MODERN SCIENCES-III, Taşkent, Uzbekistan, 22 - 23 April 2024, (Summary Text)
2023
202323. Curcumin inhibits breast cancer cell proliferation by regulating ciRS-7/miR-7-5p/CKS2 axis
Abuaisha A., Kaya M., SUER İ., EMİROĞLU S., Abanoz F., TÜKENMEZ M., et al.
San Antonio Breast Cancer Symposium, San-Antonio, Northern Mariana Islands, 5 - 09 December 2023, (Summary Text)
2024
202424. Retrospective evaluation of etiology, clinical and laboratory findings in patients diagnosed with secondary and genetic FSGS
Yilmaz A., SULEYMANOVA V., DİRİM A. B., KALAYCI T., ARTAN A. S., OTO Ö. A., et al.
61st Congress of European-Renal-Association (ERA), Stockholm, Sweden, 23 - 26 May 2024, (Summary Text)
2023
202325.
Kuntsal E., Suer İ., Kaya M., Bayrak Tokaç A. G., Palanduz Ş., Öztürk Ş., et al.
14th International Medical and Health Sciences Research Congress (UTSAK), Ankara, Turkey, 23 - 24 December 2023, vol.1, pp.586-591, (Full Text)
2023
202326. Şiddetli Oligospermi ve Tekrarlayan Gebelik Kaybıyla İlişkili Perisentrik Inv(1)(p34.1q25)
Kuntsal E., SUER İ., Kaya M., Bayrak A. G., PALANDUZ Ş., ÖZTÜRK Ş., et al.
14th International Medical and Health Sciences Research Congress (UTSAK), Ankara, Turkey, 23 - 24 December 2023, vol.1, pp.586-591, (Full Text)
2023
202327. Wilson Hastalığında Aile İçi Genetik Taramanın Kliniğe Önemli Katkıları
Şahin A., ÇİFCİBAŞI ÖRMECİ A., SUER İ., DEMİR K., KALAYCI T., ÇEFLE K., et al.
40. Ulusal Gastroenteroloji Haftası ve 11. Gastroenteroloji Cerrahisi Kongresi, Antalya, Turkey, 21 - 26 November 2023, (Summary Text)
2022
202228. Herediter Periyodik Ateş Sendromu Düşünülen Hastalarda Ateş Paneli ile Yapılan Genetik İncelemelerin Sonuçları
AMİKİSHİYEV S., KALAYCI T., BEKTAŞ M., ÇETİN Ç., AGHAMURADOV S., YALÇIN DULUNDU B. Ç., et al.
XXII. ULUSAL ROMATOLOJİ KONGRESİ, Antalya, Turkey, 26 - 30 October 2022, pp.128-129, (Summary Text)
2022
202229. BLOOD SERUM AND PLASMA WITH STRIKING GREEN COLOR IN BREAST CANCER PATIENTS
Abuaisha A., EMİROĞLU S., Kaya M., SUER İ., CABIOĞLU N., ÖZTÜRK Ş.
International Congress on Innovative Approaches in Medical and Health Sciences, Turkey, 13 - 14 August 2022, pp.514, (Summary Text)
2022
202230. The Phenotypic Effect of X;Autosome Balanced Chromosomal Translocations: A Case with Premature Ovarian Failure and Familial t(X;9)(q22;q34)
Abuaisha A., Kaya M., SUER İ., ÇEFLE K., PALANDUZ Ş., ÖZTÜRK Ş.
7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, İstanbul, Turkey, 26 - 28 May 2022, vol.1, pp.42-43, (Summary Text)
2022
202231. miR-16-5p/CCNE1 Relation in AML Cells
Teomete Ş., Kaya M., SUER İ., ÇEFLE K., PALANDUZ Ş., ÖZTÜRK Ş.
VIII. INSAC International Congress on Health Sciences (ICHES-2022), Konya, Turkey, 18 - 20 March 2022, vol.1, pp.116-122, (Full Text)
2022
202232. Senkronize Diyabet Takip Sistemi
KAHRAMAN M., MUTLU Ü., ÇAKMAK R., ERTÜRK M. A., YILDIZ H., KARAN M. A., et al.
58. Ulusal Diyabet Metabolizma ve Beslenme Hastalıkları Kongresi, Antalya, Turkey, 11 May 2022, (Full Text)
2022
202233. Senkronize Diyabet Takip Sistemi
KAHRAMAN M., MUTLU Ü., ÇAKMAK R., ERTÜRK M. A., YILDIZ H., KARAN M. A., et al.
58. Ulusal Diyabet Metabolizma ve Beslenme Hastalıkları Kongresi, Antalya, Turkey, 11 May 2022, (Full Text)
2022
202234. Senkronize Diyabet Takip Sistemi
KAHRAMAN M., MUTLU Ü., ÇAKMAK R., ERTÜRK M. A., YILDIZ H., KARAN M. A., et al.
58. Ulusal Diyabet Metabolizma ve Beslenme Hastalıkları Kongresi, Antalya, Turkey, 11 May 2022, (Full Text)
2022
202235. Senkronize Diyabet Takip Sistemi
KAHRAMAN M., MUTLU Ü., ÇAKMAK R., ERTÜRK M. A., YILDIZ H., KARAN M. A., et al.
58. Ulusal Diyabet Metabolizma ve Beslenme Hastalıkları Kongresi, Antalya, Turkey, 11 May 2022, (Full Text)
2022
202236.
Kahraman M., Mutlu Ü., Çakmak R., Ertürk M. A., Yıldız H., Düdükçü H. V., et al.
58. Ulusal Diyabet Metabolizma ve Beslenme Hastalıkları Kongresi, Antalya, Turkey, 11 - 14 May 2022, pp.294-297, (Summary Text)
2022
202237. Senkronize Diyabet Takibi Sistemi
Kahraman M., Mutlu Ü., Çakmak R., Ertürk M. A., Yıldız H., Düdükçü H. V., et al.
58. ULUSAL DİYABET Metabolizma ve Beslenme Hastalıkları KONGRESİ, Antalya, Turkey, 11 - 13 May 2022, pp.294-297, (Full Text)
2022
202238. A RARE CASE OF MUCINOUS CARCINOMA OF THE BREAST IN A 30-YEAR-OLD FEMALE
EMİROĞLU S., Abuaisha A., TÜKENMEZ M., Kaya M., SUER İ., BAYRAM A., et al.
4th International Congress on Medical Sciences and Multidisciplinary Approaches, İstanbul, Turkey, 26 March - 28 August 2022, vol.1, pp.302-308, (Full Text)
2022
202239. Hl60 ve Nb4 Hücrelerı̇nde Mı̇r-638-5p/pgk1 Gen Etkı̇leşı̇mı̇
Özbakış S., SUER İ., KAYA M., ÖZTÜRK Ş.
9th International Medicine and Health Sciences Researches Congress, 18 - 19 March 2022, (Full Text)
2022
202240. Hl60 ve NB4 Hücrelerinde miR-638-5P/PGK1 Gen Etkileşimi
Özbakış S., SUER İ., Kaya M., ÖZTÜRK Ş.
9th International Medicine and Health Sciences Researches Congress, Ankara, Turkey, 18 - 19 March 2022, pp.505-510, (Full Text)
2021
202141. TET2 gene variations in patients with myeloid malignancies
Aday A., Sırma Ekmekci S., Bayrak A. G., Çefle K., Öztürk Ş., Nalçacı M., et al.
XVII. Tıbbi Biyoloji ve Genetik Kongresi, 28 - 31 October 2021, vol.52, pp.242-243, (Summary Text)
2021
202142. CUMHURİYET VE TIP
ÖZTÜRK Ş.
8. ULUSAL İSTAHED AİLE HEKİMLİĞİ KONGRESİ, Antalya, Turkey, 27 October 2021, (Full Text)
2021
202143. Investigation Of Some Candidate Genes Determined From Multiple Myeloma Whole Genome Transcriptome Data
Sariman M., KARAÇAM B., Ayer M., SIRMA EKMEKCİ S., SUER İ., ÇEFLE K., et al.
EACR 2021 Virtual Congress-Innovative Cancer Science: Better Outcomes through Research, 9 - 12 June 2021, pp.1, (Summary Text)
2021
202144. CEBPA c.584_589dup p.His195Pro196dup variant in myeloid malignancies
SUER İ., SIRMA EKMEKCİ S., Aday A., Bayrak A. G., ÇEFLE K., ÖZTÜRK Ş., et al.
The Virtual Conference on Current Challenges in Hematology (C-HEM2021), İstanbul, Turkey, 18 - 19 March 2021, (Summary Text)
2021
202145. Investigation Of Possibly Related Genes Determined From Bioinformatic Analysis Of Multiple Myeloma Whole Genome Transcriptome Data
Sariman M., KARAÇAM B., AYER M., SIRMA EKMEKCİ S., SUER İ., ÇEFLE K., et al.
8th Multidisciplinary Cancer Research Congress, İstanbul, Turkey, 16 - 17 January 2021, pp.123, (Summary Text)
2020
202046. Relationship between sarcopenia and ACTN3 R577X gene in older adults
KAHRAMAN M., BAHAT-ÖZTÜRK G., KARAN M. A., ÖZTÜRK Ş., ÖZULU TÜRKMEN B., DİLER A. S.
16th International E-Congress of the European Geriatric Medicine Society, Lisbon, Portugal, 7 - 09 October 2020, (Summary Text)
2020
202047. Overexpression of FUS and PRDX5 Genes In Multiple Myeloma Patients
SUER İ., Aday A., Sariman M., Ayer M., Hindilerden I. Y., SIRMA EKMEKCİ S., et al.
14. Ulusal Tıbbi Genetik Kongresi (Uluslararası katılımlı), Turkey, 20 - 23 November 2020, pp.23, (Summary Text)
2020
202048. Steroide duyarlı kronik anemisi ve osteosklerozu olan erişkin olguda moleküler tanının klinik izleme etkisi
Sharifi S., Kalaycı T., Kaya M., SUER İ., ÖZTÜRK Ş., ÇEFLE K., et al.
14. Ulusal Tıbbi Genetik Kongresi (Uluslararası katılımlı), Turkey, 20 - 23 November 2020, pp.37, (Summary Text)
2020
202049. 46,XX,t(8;9)(q12;q12) translokasyon taşıyıcısı tekrarlayan gebelik kayıp öykülü olgu sunumu
SUER İ., Kaya M., Sharifi S., Kalaycı T., ÖZTÜRK Ş., ÇEFLE K., et al.
14. Ulusal Tıbbi Genetik Kongresi (Uluslararası katılımlı), Turkey, 20 - 22 November 2020, pp.89, (Summary Text)
2020
202050. Abstracts of the 16th International E-Congress of the European Geriatric Medicine Society
KAHRAMAN M., KARAN M. A., BAHAT-ÖZTÜRK G., ÖZULU TÜRKMEN B., ÖZTÜRK Ş., DİLER A. S.
16th International E-Congress of the European Geriatric Medicine Society, Portugal, 07 October 2020, (Full Text)
2020
202051. Investigation of miR-145 target genes in multiple myeloma cell lines
Kaya M., SUER İ., KARATAŞ Ö. F., ÖZGÜR E., GEZER U., ÇEFLE K., et al.
V. International Participated Erciyes Medical Genetics Days Congress, Nevşehir, Turkey, 20 - 22 February 2020, vol.2584, pp.37, (Summary Text)
2020
202052. Seyahate çıkan vatandaşlarımızın seyahat sağlığı ve aşılar konusunda bilgi düzeyleri
Kahraman M., Öztürk Ş.
Geleneksel İç Hastalıkları Günleri - İnteraktif Güncelleştirme, Sakarya, Turkey, 12 - 15 March 2020, pp.93, (Summary Text)
0
053. A Case of Severe Partial Hypodontia Associated with Simple Hemihypertrophy
ERDİLEK A. D., KORAY F., ÖZTÜRK Ş., PALANDUZ Ş.
35th Annual Meeting of the IADR/CED, France, pp.9, (Summary Text)
0
054. Pseudo-anadontia with Multiple Impactions- A Case Report
ERDİLEK A. D., KAYNAR A., KORAY F., YILDIRIM M., ÖZTÜRK Ş.
13th International Conference on Oral and Maxillofacial Surgery, Japan, pp.252, (Summary Text)
2019
201955. Evaluation of Spermatogenesis Process in Cases with Azospermic and Oligospermic Normal Karyotype and Azospermic Klinefelter Syndrome
ÖZTAN G., PALANDUZ Ş., ÇEFLE K., ÖZTÜRK Ş.
Cell Death Symposium, Turkey, 3 - 04 October 2019, (Summary Text)
2019
201956. Investigation of TMD-ERAP1 Candidate Gene Expressions Obtained from Multiple Myeloma Transcriptome Data by RT-PCR
Sariman M., KARAÇAM B., Ayer M., SIRMA EKMEKCİ S., SUER İ., ÇEFLE K., et al.
1.International Multidisciplinary Cancer Research Congress, Diyarbakır, Turkey, 18 - 22 September 2019, vol.1, pp.96, (Summary Text)
2019
201957. Investigation of miR-34a target genes in multiple myeloma cell lines
SUER İ., Kaya M., KARATAŞ Ö. F., ÖZGÜR E., GEZER U., ÇEFLE K., et al.
VII. International Congress of Molecular Medicine, İstanbul, Turkey, 5 - 07 September 2019, vol.1, pp.141, (Summary Text)
2019
201958. Spectrum of Skeletal Abnormalities and Pathogenic RUNX2 Variants in 50 CleidocranialPatients from Turkey
Berkay E. G., Elkanova L., Kalaycı T., Karaman V., GÜNEŞ N., Toksoy G., et al.
13th Balkan Congress of Human Genetics, 17 - 20 April 2019, (Summary Text)
2019
201959. S-29 - Spectrum of Skeletal Abnormalities and Pathogenic RUNX2 Variants in 50 CleidocranialPatients from Turkey
BERKAY E. G., ELKANOVA L., KALAYCI T., KARAMAN V., GÜNEŞ N., TOKSOY G., et al.
13TH BALKAN CONGRESS OF HUMAN GENETICS, 17 - 20 April 2019, (Summary Text)
2019
201960. A Case of a Variant Philadelphia Translocation Involving Chromosomes (7;9;22)(q22;q34;q11) in Chronic Myeloid Leukemia
BAYRAK A. G., ADAY A., UÇUR A., ÖZBALAK M. M., NALÇACI M., ÇEFLE K., et al.
13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.BJMG, no.39, pp.76, (Summary Text)
2019
201961. İnsülin kullanan DM hastalarında teknolojik cihazlar kullanımı ve teknolojiye uyumun diyabet kontrolü üzerine etkisi
KAHRAMAN M., ÖZTÜRK Ş., KARŞIDAĞ K., KARAN M. A., SATMAN İ.
Geleneksel İç Hastalıkları Günleri - İnteraktif Güncelleştirme, Sakarya, Turkey, 14 - 17 March 2019, vol.2019, pp.76-77, (Summary Text)
2018
201862. KML Hastalarında Moleküler Monitorizasyon-Klinik Seyir İlişkisinin ve SLC22A1 MRNA Ekspresyonunun Araştırılması
Bulakçı B., Dağlar Aday A., YAVUZ A. S., Gürtekin B., ÇEFLE K., ÖZTÜRK Ş., et al.
44. Ulusal Hematoloji Kongresi, Turkey, 21 October - 03 November 2018, (Summary Text)
2018
201863. Larenks Kanseri Primer Hücre Kültüründe Oluşturulan Küre (Sphere)’lerde Oct4 ve Klf4 Ekspresyon Analizi
SUER İ., KARATAŞ Ö. F., Kaya M., ÖZTÜRK Ş.
7. Kök Hücre Sempozyumu, İstanbul, Turkey, 11 May 2018, vol.1, pp.7-10, (Full Text)
2018
201864. Ailesel beyaz süngersi nevuslu olgularda oral mukozal infeksiyonlara yatkınlığın incelenmesi.
KÜRKLÜ E., AK G., TOPÇUOĞLU N., ÖZTÜRK Ş., BEKA H., AĞAÇFİDAN A., et al.
33. ANKEM Kongresi, Antalya, Turkey, 2 - 06 May 2018, (Summary Text)
2018
201865. Akut Myeloid Lösemi ve 3q Kromozomal Yeniden Düzenlenmeleri
Bagatir G., Kaya M., Dön B., SUER İ., NALÇACI M., YENEREL M. N., et al.
3. Ulusal Uygulamalı Biyolojik Bilimler Kongresi (UBBK), Eskişehir, Turkey, 3 - 05 May 2018, vol.1, pp.35, (Summary Text)
2018
201866. idic(Y)(q11.2) ABNORMALITY IN CASES WITH MIXT GONADAL DYSGENESIS AND INFERTILITY
Kaya M., SUER İ., KALAYCI T., KARAMAN B., Dön B., Bagatir G., et al.
Erciyes Medical Genetics Days, Kayseri, Turkey, 7 - 10 March 2018, vol.1, pp.16, (Summary Text)
2018
201867. A Novel Insertional Translocation in a Patient with Infertility and Undiagnosed Mild Intellectual Disability
SUER İ., Kaya M., Bagatir G., KARAMAN B., ÇEFLE K., ÖZTÜRK Ş., et al.
Erciyes Medical Genetics Days, Kayseri, Turkey, 7 - 10 March 2018, pp.32, (Summary Text)
2017
201768. RNA sequencing and in silico analysis of Myeloma cells in multiple myeloma patients
Sarıman M., SIRMA EKMEKCİ S., ABACI N., ÇAKİRİS A., PAÇAL F., ÜSTEK D., et al.
XV.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Fethiye- Muğla, Turkey, 26 - 29 October 2017, pp.108, (Summary Text)
2017
201769. Multiple Myeloma hastalarının Myeloma hücrelerinde RNA dizileme ve in-silico analizler.
Sarıman M., Sırma Ekmekci S., Abacı N., Çakiris A., Perçin Paçal F., Üstek D., et al.
XV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Fethiye, Muğla, Turkey, 26 October 2017, (Unpublished)
2017
201770. Multiple Myeloma hastalarının Myeloma hücrelerinde RNA dizileme ve insilico analizler.
Sarıman M., Sırma Ekmekci S., Abacı N., Çakiris A., Paçal F., Üstek D., et al.
XV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi , Muğla, Turkey, 26 - 29 October 2017, pp.108-109, (Summary Text)
2016
201671. Investigation of gene expression of myeloma cells in bone marrow of multiple myeloma patients by transcriptome analysis
Sarıman M., SIRMA EKMEKCİ S., ABACI N., ÇAKİRİS A., PAÇAL F., ÜSTEK D., et al.
ESHG 2016, Barcelona, Spain, 21 - 24 May 2016, pp.153, (Full Text)
2014
201472.
Çukurova Z., Gedikbaşı A., Öztürk Ş., Çetingök H., Öztürk D., Eren G., et al.
11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.107-108, (Summary Text)
2014
201473. mos 46,XX/47,XXX/48,XXXX Karyotipli Cinsel Kimlik Bozukluğu Tanılı Olgu
Kaya M., Gedikbaşı A., Öztürk Ş., Çefle K., Palanduz Ş.
11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.100, (Summary Text)
2014
201474. 47,XXY,inv(12)(q15q24) Karyotip Özelliği Gösteren Klinefelter Sendromlu Bir Olgu
Kaya M., Gedikbaşı A., Bağatır G., Öztürk Ş., Çefle K., Palanduz Ş.
11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.101, (Summary Text)
2014
201475. 46,XY,t(11;22)(q23;q11) Dengeli Translokasyonunu Taşıyan İnfertil Bir Olgu
Kaya M., Bağatır G., Gedikbaşı A., Öztürk Ş., Çefle K., Palanduz Ş.
11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.100-101, (Summary Text)
2014
201476. Kleidokranial Displazi: Olgu Sunumu
Gedikbaşı A., Çefle K., Kaya M., Öztürk Ş., Palanduz Ş.
11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.67-68, (Summary Text)
2014
201477. Büyük Yq Delesyonlu [46,X,del(Yq)] İnfertil Olguda Sadece AZFc Delesyonu
Kaya M., Öztan G., Gedikbaşı A., Bağatır G., Coşkunpınar E., Öztürk Ş., et al.
11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.108, (Summary Text)
2014
201478. Habituel Abortus Nedeniyle Başvuran 46,XX,inv(12)(p11.2q14) Karyotip Özelliği Saptanan Olgu
Kaya M., Dön B., Gedikbaşı A., Öztürk Ş., Çefle K., Palanduz Ş.
11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.102, (Summary Text)
2014
201479. 46,XY,t(4;6)(p15.3;q23) Kriptik Dengeli Resiprokal Translokasyonunu Taşıyan İnfertil Olgu
Kaya M., Bağatır G., Gedikbaşı A., Öztürk Ş., Çefle K., Palanduz Ş.
11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.100, (Summary Text)
2014
201480. Habituel Abortus Nedeniyle Başvuran ve 46,XX,t(1;6)(p35;p21) Dengeli Resiprokal Translokasyonu Saptanan Olgu
Kaya M., Bağatır G., Gedikbaşı A., Dön B., Öztürk Ş., Çefle K., et al.
11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.101, (Summary Text)
2014
201481. Erkek İnfertilitesinde AZF
COŞKUNPINAR E., ÖZTÜRK D., ÖZTAN G., KADIOĞLU A., ÖZTÜRK Ş., ÇEFLE K., et al.
11. Ulusal Tıbbi Genetik Kongresi, Turkey, 24 - 27 September 2014, (Summary Text)
2014
201482. Erkek İnfertiliteside AZF
Çoşkunpınar E. M., Öztürk D., Öztan G., Kadıoğlu A., Öztürk Ş., Cefle K., et al.
11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.5, (Summary Text)
2014
201483. Midkine as an Indicator of Inflammation in Renal Transplantation.
Ozturk S., Kaya B., Celik K., Ozkan O., Doventas Y., Gursu M., et al.
World Transplant Congress, San-Francisco, Costa Rica, 26 - 31 July 2014, vol.14, pp.495, (Summary Text)
2013
201384. Adherence and effectiveness of omalizumab treatment in severe allergic asthma patients
Ozseker Z. F., Bulut I., Erdenen F., Erdogdu D., Asli G., Ersoy R., et al.
World Allergy and Asthma Congress of the European-Academy-of-Allergy-and-Clinical-Immunology and World-Allergy-Organization, Milan, Italy, 22 - 26 June 2013, vol.68, pp.363-364, (Summary Text)
2012
201285. Sistemik Lupus Eritematozus ve Romatoid Artritin Eşlik Ettiği Klinefelter Sendromu Olgusu
Gedikbaşı A., ÇEFLE K., Bayrak A., Tutkan G., Uçur A., Kamalı S., et al.
10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 19 - 23 December 2012, pp.314, (Full Text)
2010
201086. ‘‘No Difference in Micronuclear Scores in both Circulating Lymphocytes and Buccal Epithelial Cells between Patients with Oral Lichen Planus and Oral Lichenoid Stomatitis’
ERGUN S., SARUHANOĞLU A., ÇEFLE K., Warnakulasuriya S., ÖZTÜRK Ş., PALANDUZ Ş.
10th Biennal Congress European Association of Oral Medicine (EAOM), Londra, United Kingdom, 23 - 25 September 2010, pp.524-525, (Full Text)
2010
201087. ‘‘Micronucleus and Sister Chromatid Exchange Analyses in Peripheral Lymphocytes of Patients with Oral Leukoplakia – A Pilot Study’’
SARUHANOĞLU A., Tanyeri H., ERGUN S., ÇEFLE K., ÖZTÜRK Ş., PALANDUZ Ş.
10th Biennal Congress European Association of Oral Medicine (EAOM), Londra, United Kingdom, 23 - 25 September 2010, pp.518-519, (Full Text)
2009
200988. Variant philadelphia translocations in patients with chronic myeloid leukemia
Satkın B. N., PALANDUZ Ş., KARAMAN B., ÖZTÜRK Ş., ÇEFLE K., Bagatır G., et al.
European Cytogenetic Conference (7th), Stockholm, Sweden, 4 - 07 July 2009, pp.161-162, (Full Text)
2009
200989. Translocation (1;14) in hairy cell leukemia variant
Bayrak A., Ucur A., Satkin B., Palanduz S., Karan M., Ozturk S., et al.
7th European Cytogenetics Conference, Stockholm, Sweden, 4 - 07 July 2009, vol.17, pp.162, (Summary Text)
2009
200990. The evaluation of the genomic instability by micronucleus and sister chromatid exchange in myelodysplastic syndrome
Nazligul E., Palanduz P., Ozturk O., Bayrak A., Ucur A., Bagatir G., et al.
7th European Cytogenetics Conference, Stockholm, Sweden, 4 - 07 July 2009, vol.17, pp.137-138, (Summary Text)
2008
200891. Determination of genomic instability of patients with oral lichen planus’’
ERGUN S., SARUHANOĞLU A., TANYERİ H., ÇEFLE K., DUMAN N., ÖZEL YILDIZ S., et al.
9th Biennal Congress European Association of Oral Medicine (EAOM),, Salzburg, Austria, 18 - 20 September 2008, pp.35, (Full Text)
2007
200792. ‘‘Ligneous Periodontitis with Conjunctival Involvement: A Case Report’’
kürklü e., ERGUN S., TANYERİ H., ÇEFLE K., Mete Ö., ÖZTÜRK Ş., et al.
1st International Congress of Oral and Maxillofacial Surgery Society, Antalya, Turkey, 16 - 20 May 2007, pp.42, (Full Text)
2007
200793. Pericentric inversion of chromosome 8 and paracentric inversion of the long of arm of chromosome 11 in the male partner of a couple presenting with recurrent miscarriage
Kivanc C., Haluk E., Birsen K., Sukru O., Seher B., Sukru P.
6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.85-86, (Summary Text)
2007
200794. The use of FISH/M-FISH in patients with hematological malignancies for further characterization chromosomal abnormalities detected on conventional cytogenetic analysis
Ali U., Aysegul B., Nedime S., Gulcin B., Sukru P., Sukru O., et al.
6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.201-202, (Summary Text)
2007
200795. Constitutional chromosome abnormalities
Sukru P., Gulcin B., Kivanc C., Sukru O., Ali U., Aysegul B., et al.
6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.211, (Summary Text)
2007
200796. Two cases with euchromatic variation in 5P and 9Q
Sukru O., Aysegul B., Kivanc C., Nigun D., Davut P., Birsen K., et al.
6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.78, (Summary Text)
2007
200797. Loss of the Y chromosome in Leukemia: a report of 9 patients
Bagatir P. S., Sukru O., Kivanc C., Ali U., Aysegul B., Meliha N., et al.
6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.210-211, (Summary Text)
2007
200798. The association of Down Syndrome and acute myeloid leukemia: accompanying Trisomy 8
Ayse P., Gulcin B., Sukru P., Sukru O., Kivanc C., Ali U., et al.
6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.210, (Summary Text)
2007
200799. Variant Philadelphia translocations in patients with Chronic Myeloid Leukemia
Aysegul B., Ali U., Sukru P., Sukru O., Kivanc C., Gulcin B., et al.
6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.202, (Summary Text)
2007
2007100. t(5;22)(q13;q12) variant translocation in a case of chronic myeloid leukemia refractory to treatment
Haluk E., Sukru O., Serap Y., Kivanc C., Gulcin B., Ali U., et al.
6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.223, (Summary Text)
2007
2007101. Spontaneous micronucleus frequency in the bone marrow cells of patients with leukemia
Basak S., Sukru O., Sukru P., Gulcin B., Ali U., Aysegul B., et al.
6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.199, (Summary Text)
2006
2006102. Cardiac Investigation (Echocardiography, Heart Rate Variability and QT dispertion parameters ) in Turner Syndrome.
Sözen A. B., Çefle K., Kudat H., Öztürk Ş.
Abstracts of the Second Annual Congress on Update in Cardiology and Cardiovascular Surgery., Muğla, Turkey, 20 - 24 September 2006, vol.29, pp.143, (Summary Text)
2006
2006103. Cardiac İnvestigation ( Echocardiography, Heart Rate Variability and QT dispertion patameters ) in Turner Syndrome. Clinical Cardiology.
Sözen A. B., Çefle K., Kudat H., Öztürk Ş.
Abstracts of the Secont Annual Congress on Update in Cardiology and Cardiovascular Surgery, Muğla, Turkey, 20 - 24 September 2006, vol.29, pp.50, (Summary Text)
2008
2008104. . Is there any relation between the NQO1 C609T polymorphism and cytogenetics abnormalities in MDS?
Bağatır G., Sırma Ekmekci S., Palandüz Ş., Özbek U., Nalçacı M., Öztürk Ş., et al.
7th Balkan Meeting on Human Genetics konferansı, Skopje, Macedonia, 20 September 2008, vol.9, no.3, pp.75, (Summary Text)
2006
2006105. ‘Investigation of genomic instability of patients with Sjögren’s syndrome by using sister chromatide Exchange analysis’
ergun s., TANYERİ H., ÖZTÜRK Ş.
analysis’ Biennial Congress of the European Association of Oral Medicine, Croatia, 1 - 04 September 2006, pp.1, (Full Text)
2006
2006106. ‘Investigation of Genomic Instability of Patients with Sjögren’s Syndrome by Using Sister Chromatide Exchange Analysis’
ERGUN S., TANYERİ H., ÇEFLE K., DUMAN N., PALANDUZ S., Özel S., et al.
8th Biennal Congress European Association of Oral Medicine (EAOM, Zagreb, Croatia, 31 August - 02 September 2006, pp.24, (Full Text)
0
0107. Investigation of Human papilloma virus and Candida albicans in a family with white sponge nevus
KÜRKLÜ E., AK G., TOPCUOĞLU E. N., ÖZTÜRK Ş., Beka H., AĞAÇFİDAN A., et al.
8th Biennial Congress of the European Association of Oral Medicine, Croatia, pp.30, (Full Text)
0
0108. A Novel Mutation in Keratin 13 Gene in a Turkish Family with White Sponge Nevus
KÜRKLÜ E., CASSIDY A., ÖZTÜRK Ş., KORAY M., AK G., ÇEFLE K., et al.
7th Biennial Congress of the European Association of Oral Medicine & 26th Annual Scientific Meeting of the Academy of Oral Pathology and Oral Medicine (AKOPOM), Germany, pp.29, (Full Text)
2004
2004109. Effects of cyclosporin A and tacrolimus on sister chromatid exchange frequency in renal transplant patients
ŞENTÜRK ÇİFTÇİ H., DİLER A. S., Öztürk Ş., ÖNAL A. E., Aygün Kaya S., Kılıçarslan Ayna T., et al.
18. European Immunogenetics and Histocompatibility Conference, Sofya, Bulgaria, 8 - 11 May 2004, pp.20, (Full Text)
2004
2004110. Çiftçi HŞ. Diler AS. Öztürk Ş. Önal EA. Kaya S. Ayna T. Cefle K. Karahan G. Palandüz Ş. Gürtekin M. Çarin M. Effects of cyclosporin A and tacrolimus on sister chromatid exchange frequency in renal transplant patients. 18. European Immunogenetics and Histocompatibility Conference 08-11 May 2004, Sofia; Bulgaria NPG Volume 5. suplement 1. May 2004.
Şentürk Çiftçi H., Diler A. S., Öztürk Ş., Önal A. E., Kaya S., Kılıçaslan Ayna T., et al.
18. European Immunogenetics and Histocompatibility Conference, Sofija, Bulgaria, 8 - 11 May 2004, (Summary Text)
2004
2004111. Effects of cyclosporin A and tacrolimus on sister chromatid exchange frequency in rental transplant patients
Hayriye S., Sarper D., Sukru O., Emel O., Selvi K., Tulay A., et al.
18th European Histocompatibility Conference, Sofija, Bulgaria, 8 - 11 May 2004, (Summary Text)
0
0112. Phenitoin Induced Gingival Enlargement and Cytogenetic Diagnose in Epileptic Patients
AK G., GÖKYİĞİT A. Z., TANYERİ H., KÜRKLÜ E., ÖZTÜRK Ş., ÖZDEMİR Ö., et al.
Association of Oral Medicine 6th Biennial Congress, Portugal, pp.64, (Full Text)
0
0113. Mandibulo-Acral Dysplasia in A 31 Year-Old Man
TANYERİ H., KÜRKLÜ E., AK G., ÖZTÜRK Ş., KORAY M.
European Association of Oral Medicine 6th Biennial Congress, Portugal, pp.67, (Summary Text)
2002
2002114. GÖMÜK 20 YAŞ AMELİYATLARINDAN SONRA KULLANILAN ETODOLAC(ETOL), NİMESULİD (MESULİD), NAPROKSEN SODYUM (APRANAX)'IN KARDEŞ KROMATİD DEĞİŞİKLİK(KKD) SIKLIĞI ÜZERİNE ETKİSİ
AYDİL B. A., KOÇAK BERBEROĞLU H., GÜRKAN KÖSEOĞLU B., KOÇAK BERBEROĞLU H., ÇEFLE K., ÖZTÜRK Ş., et al.
7. ANKEM KLİNİKLER VE TIP BİLİMLERİ KONGRESİ, Antalya, Turkey, 26 - 30 May 2002, pp.76, (Full Text)
1998
1998115. Hallerman-Streff sendromlu bir olgu
PALANDUZ Ş., ÖZTÜRK Ş., ÇEFLE K., KATİPOĞLU A. B., KIR MERCÜL N., AKKAYA V. A.
3.Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Muğla, Turkey, 26 - 30 April 1998, pp.97, (Full Text)
1996
1996116. In vitro chromosomal radiosensitivity in common variable immune deficiency
Palanduz Ş., Palanduz A., Yalçın I., Öneş Ü., Üstek D., Öztürk Ş., et al.
2nd Balkan Meeting on Human Genetics, İstanbul, Turkey, 3 - 06 September 1996, pp.36, (Summary Text)
1996
1996117. Renal Transplantasyon Yapılan Hastalarda Siklosporin A Kullanımına Bağlı Sitogenetik, Enzimatik, İmmunolojik Ve Periodontal Bulgular
Palandüz Ş., TANYERİ H., IŞIK A. G., Sönmez G., Üstek D., Kaya S., et al.
Türk Diş Hekimleri Birliği 3. Uluslararası Dİş Hekimliği Kongresi, Ankara, Turkey, 18 - 22 June 1996, pp.242, (Full Text)
Books
2025
20251. Medical Genetics in the Centennial of Türkiye Republic
Öztürk Ş. (Editor)
Istanbul University Press, İstanbul, 2025
2024
20242. Çocuk ve Yetişkinde Genetik testler
Öztürk Ş.
in: Tıbbi, Dini ve Etik Boyutlarıyla Genetik, Maide Barış,Orhan Önder, Editor, Hisar Yayınları, İstanbul, pp.83-96, 2024
2023
20233. Klinisyenler İçin Genetik Testler
Öztürk Ş. (Editor)
EMA Tıp Kitabevi Yayıncılık Tic. Ltd. Şti., İstanbul, 2023
2023
20234. Genetic testing
Öztürk Ş.
in: Genetics for clinicians, Şükrü Öztürk, Editor, EMA tıp Kitabevi, İstanbul, pp.1-494, 2023
2023
20235. Hangi Test Ne Zaman İstenmeli?
Öztürk Ş.
in: KLİNİSYENLER İÇİN GENETİK TESTLER , ŞÜKRÜ ÖZTÜRK, Editor, EMA Tıp Kitabevi, İstanbul, pp.1-494, 2023
2023
20236. Sitogenetik Yöntemlerle Tanı Konan Tek Gen Hastalıkları
Bayrak A. G., Öztürk Ş.
in: Klinisyenler İçin Genetik Testler, Prof.Dr.Şükrü Öztürk,Prof.Dr.Kıvanç Çefle, Editor, EMA Tıp Kitabevi Yayıncılık Tic. Ltd. Şti., İstanbul, pp.115-126, 2023
2023
20237. ORGAN NAKLİNDE GENETİK GEÇİŞKENLİK MÜZAKERE
ÖZTÜRK Ş.
in: ORGAN NAKLİYLE İLGİLİ HUKUKİ, RTİK VE FIHKİ YAKLAŞIMLAR, HALİL KILIÇ, HATİCE NUR BÖLÜKBAŞI, BİLAL ESEN, Editor, DİYANET İŞLERİ BAŞKANLIĞI, Ankara, pp.107-109, 2023
2023
20238. FİZYOLOJİK VE PATOLOJİK DURUMLARDA EPİGENETİK DEĞİŞİKLİKLER
Öztürk Ş.
in: MOLEKÜLER BİYOLOJİ VE GENETİK, PROF DR MUSTAFA SOLAK, Editor, Tüba Basın Yayın, Ankara, pp.427-452, 2023
2022
20229. Hematolojik Malignitelerde Konvansiyonel Sitogenetik
Bayrak A. G., Öztürk Ş.
in: Klinisyenler İçin Genetik Testler, Prof.Dr.Şükrü Öztürk,Prof.Dr.Kıvanç Çefle, Editor, EMA Tıp Kitabevi Yayıncılık Tic. Ltd. Şti.,, İstanbul, pp.59-96, 2022
2019
201910. Erkek İnfertilitesi: Kromozomal Nedenler
ÖZTÜRK Ş.
in: İnfertilite ve Genetik Yönü, Kıvanç Çefle, Şükrü Öztürk, Editor, Türkiye Klinikleri (Ortadoğu Reklam Tanıtım Yayıncılık Turizm Eğitim İnşaat Sanayi ve Ticaret A.Ş.), Ankara, pp.12-19, 2019
Other Publications
2019
20191. Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability
Kaya M., Suer İ., Öztürk Ş., Çefle K., Karaman B., Palanduz Ş.
Other, pp.1-12, 2019
2012
20122. AML’ DE APAF-1 PROMOTÖR METİLASYONU, KARDEŞ KROMATİD DEĞİŞİMİ, K ROMOZOMAL ANOMALİLER İLE KLİNİK VE LABORATUVAR PARAMETRELERİ ARASINDAKİ İLİŞKİ
Özgen Ö., Bağatır G., Bayrak A., Uçur A., Öztürk Ş., Palanduz Ş., et al.
Other, pp.1-93, 2012
Funded Projects
2024 - 2025
2024 - 2025
Meme Kanserinde hsa_circ_0001546 ve hsa_circ_0025244’ün Ekspresyon Analizi ve circRNA/miRNA/Gen Aksislerinin in silico Yöntemler ile Araştırılması
Project Supported by Higher Education Institutions , BAP MSc
ÖZTÜRK Ş. (Executive), SUER İ., ABANOZ F.
2023 - 2025
2023 - 2025Akut Miyeloid Lösemi ve Miyelodisplastik Sendromlu Hastalarda TET2 Gen Varyantlarının Araştırılması
Project Supported by Higher Education Institutions , BAP Research Project
ADAY A. (Executive), BAYRAK A. G., PALANDUZ Ş., ERDEM S., ÇEFLE K., ÖZTÜRK Ş., et al.
2023 - 2024
2023 - 2024
Kurkuminin CDR1as/miR-7-5p/Hedef Genleri Aracılığıyla Meme Kanseri Hücrelerine Etkisinin Araştırılması
Project Supported by Higher Education Institutions , BAP PhD
ÖZTÜRK Ş. (Executive), KAYA M., ABUAISHA A. M. H.
2021 - 2023
2021 - 2023miR-34a-5p ile Olası Hedef Genlerinin HL-60 ve NB4 Hücre Hatlarında Fonksiyonel Olarak Araştırılması
Project Supported by Higher Education Institutions , BAP MSc
ÖZTÜRK Ş. (Executive), DÖNMEZ Ç.
2020 - 2023
2020 - 2023Let-7b-5p ve Let-7b-3p miRNA'larının HL-60ve NB4 Akut Myeloid Lösemi Hücre Hatlarında Fonksiyonel Etkilerinin ve Hedef Genlerinin Araştırılması
Project Supported by Higher Education Institutions , BAP MSc
ÖZTÜRK Ş. (Executive), KAYA M., KAŞITOĞLU T. N.
2020 - 2023
2020 - 2023Akut Myeloid Lösemi Hücre Hatlarında miR-15a-5p ve miR-16-5p'nin Fonksiyonel Etkilerinin ve miRNA Hedef Gen İlişkisinin İncelenmesi
Project Supported by Higher Education Institutions , BAP MSc
ÖZTÜRK Ş. (Executive), TEOMETE Ş., KAYA M.
2018 - 2020
2018 - 2020Multiple Myeloma’da miR-145 ve Hedef Genlerinin Fonksiyonel Olarak Araştırılması
Project Supported by Higher Education Institutions , BAP Research Project
Çefle K. (Executive), Suer İ., Öztürk Ş., Kaya M., Karataş Ö. F.
2015 - 2017
2015 - 2017Multiple Myeloma'da Tüm Genom Transkriptom Datasında Saptanan Füzyonlarda Belirlenen Bazı Genlerin Ekspresyon Analizi
Project Supported by Higher Education Institutions , BAP MSc
ÖZTÜRK Ş. (Executive)
2010 - 2014
2010 - 2014MULTİPLE MYELOMA, SMOLDERİNG MULTİPLE MYELOMA ve ÖNEMİ BİLİNMEYEN MONOKLONAL GAMMOPATİLİ (ÖBMG) OLGULARIN KEMİK İLİĞİ HÜCRELERİNDE KARŞILAŞTIRMALI GEN EKSPRESYON PROFİLİ ÇALIŞMASI
Project Supported by Higher Education Institutions , BAP Research Project
ÖZTÜRK Ş. (Executive)
2009 - 2011
2009 - 2011Kistik fibrozisli olgularda radyasyona bağlı genotoksik hasarın sitogenetik belirteçlerle araştırılması
Project Supported by Higher Education Institutions , BAP Other
ÖZTÜRK Ş. (Executive)
Awards