Prof.Dr. Şükrü ÖZTÜRK

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

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 , cilt.19, sa.4, 2024 (SCI-Expanded)

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 (Carlton, Vic.) , cilt.29, sa.1, ss.55-56, 2024 (SCI-Expanded)

miR-145-5p suppresses cell proliferation by targeting <i>IGF1R </i>and <i>NRAS </i>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 , cilt.48, ss.563-569, 2023 (SCI-Expanded)

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 , cilt.42, sa.2, ss.597-606, 2023 (SCI-Expanded)

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 , cilt.33, sa.2, ss.92-102, 2023 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.67, sa.4, ss.173-177, 2022 (SCI-Expanded)

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 , cilt.85, sa.6, ss.2241-2250, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.1, sa.1, ss.1-7, 2022 (SCI-Expanded)

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 , cilt.34, sa.4, ss.757-765, 2022 (SCI-Expanded)

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 , cilt.111, 2021 (SCI-Expanded)

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 , cilt.38, sa.6, ss.365-373, 2021 (SCI-Expanded)

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 , cilt.185, sa.8, ss.2488-2495, 2021 (SCI-Expanded)

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 , cilt.14, sa.2, ss.151-156, 2021 (SCI-Expanded)

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 , cilt.122, sa.1, ss.71-77, 2021 (SCI-Expanded)

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 , cilt.122, sa.3, ss.206-211, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.31, sa.4, ss.205-213, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.64, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.23, sa.1, ss.15-23, 2020 (SCI-Expanded)

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 , cilt.98, sa.32, 2019 (SCI-Expanded)

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 , cilt.36, sa.1, ss.23-31, 2019 (SCI-Expanded)

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 , sa.2, 2018 (SCI-Expanded)

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 , cilt.101, sa.1, ss.149-156, 2017 (SCI-Expanded)

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 , cilt.38, sa.1, ss.7-15, 2017 (SCI-Expanded)

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 , cilt.18, sa.1, ss.201-205, 2017 (SCI-Expanded)

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) , cilt.62, sa.7, ss.61-5, 2016 (SCI-Expanded)

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 , cilt.148, sa.4, ss.771-793, 2015 (SCI-Expanded)

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 , cilt.60, sa.1, ss.1-9, 2015 (SCI-Expanded)

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 , cilt.19, sa.4, ss.299-304, 2013 (SCI-Expanded)

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 , cilt.39, sa.12, ss.1016-1021, 2012 (SCI-Expanded)

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 , cilt.413, ss.950-951, 2012 (SCI-Expanded)

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 , cilt.16, sa.4, ss.287-291, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.43, sa.5, ss.1566-1569, 2011 (SCI-Expanded)

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 , cilt.16, sa.6, ss.518-519, 2010 (SCI-Expanded)

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 , cilt.16, sa.6, ss.524-525, 2010 (SCI-Expanded)

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 , cilt.128, sa.1, ss.103-111, 2010 (SCI-Expanded)

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 , cilt.6, sa.2, ss.32-36, 2010 (SCI-Expanded)

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 , cilt.18, sa.3, ss.131-134, 2009 (SCI-Expanded)

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 , cilt.13, sa.5, ss.599-602, 2009 (SCI-Expanded)

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 , cilt.26, sa.8, ss.943-949, 2009 (SCI-Expanded)

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 , cilt.134, sa.12, ss.1267-1276, 2008 (SCI-Expanded)

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 , cilt.49, sa.5, ss.742-7, 2008 (SCI-Expanded)

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 , cilt.31, sa.9, ss.1140-1145, 2008 (SCI-Expanded)

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. S., Kaya Ş., et al.

GENETIC TESTING , cilt.12, sa.3, ss.427-430, 2008 (SCI-Expanded)

Cytogenetic findings in pediatric myelodysplastic and myeloproliferative diseases

Bagatir G., Palanduz A., Ozturk S., Cefle K., Telhan L., Palanduz S.

ACTA PAEDIATRICA , cilt.97, ss.155, 2008 (SCI-Expanded)

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 , cilt.82, sa.9, ss.783-786, 2007 (SCI-Expanded)

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 , cilt.22, sa.3, ss.393-399, 2007 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.36, sa.3, ss.247-252, 2007 (SCI-Expanded)

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 , cilt.118, sa.1, ss.38-41, 2007 (SCI-Expanded)

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 , cilt.13, sa.1, ss.57-64, 2007 (SCI-Expanded)

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 , cilt.28, sa.3, ss.175-178, 2007 (SCI-Expanded)

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 , cilt.81, sa.11, ss.883-887, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

Werner syndrome associated with renal involvement

KOCABAY G., Ozturk S., ECDER T.

SAUDI MEDICAL JOURNAL , cilt.27, sa.11, ss.1768-1769, 2006 (SCI-Expanded)

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 , cilt.171, ss.65-7, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.60, sa.10, ss.1306-1309, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.33, 2006 (SCI-Expanded)

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 , cilt.33, 2006 (SCI-Expanded)

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 , cilt.49, sa.1, ss.63-69, 2006 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.103, ss.285-8, 2005 (SCI-Expanded)

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 , cilt.103, sa.3, ss.285-288, 2005 (SCI-Expanded)

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 , sa.2, ss.185-189, 2005 (SCI-Expanded)

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 , cilt.159, ss.148-50, 2005 (SCI-Expanded)

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 , cilt.33, ss.81-8, 2005 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.23, sa.1, ss.74-78, 2005 (SCI-Expanded)

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 , cilt.5, ss.327-30, 2004 (SCI-Expanded)

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 , cilt.50, sa.54, ss.2031-2034, 2003 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.98, sa.11, ss.2556-2560, 2003 (SCI-Expanded)

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 , cilt.50, sa.54, ss.2137-2140, 2003 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.31, sa.2, ss.76-83, 2003 (SCI-Expanded)

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 , cilt.88, sa.1, ss.1-5, 2003 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.48, ss.844-9, 2002 (SCI-Expanded)

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 , cilt.56, sa.4, ss.316-318, 2002 (SCI-Expanded)

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 , cilt.26, sa.4, ss.265-271, 2002 (SCI-Expanded)

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 , cilt.40, ss.115-20, 2002 (SCI-Expanded) Sürdürülebilir Kalkınma

A case of severe partial hypodontia associated with simple hemihypertrophy.

Erdilek D., Koray F., Ozturk S., Palanduz S.

JOURNAL OF DENTAL RESEARCH , cilt.80, sa.4, ss.1202, 2001 (SCI-Expanded)

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 , cilt.123, sa.1, ss.49-51, 2000 (SCI-Expanded) Sürdürülebilir Kalkınma

A case of turner syndrome with a rare reciprocal translocation between an autosome and the X chromosome

PALANDUZ Ş., ÖZTÜRK Ş., ÇEFLE K., KARAMAN B., ÜSTEK D., BAŞARAN S.

BALKAN JOURNAL OF MEDICAL GENETICS , cilt.3, ss.45-48, 2000 (AHCI)

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 , cilt.64, sa.1, ss.78-79, 2000 (SCI-Expanded)

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 , cilt.54, sa.4, ss.274-276, 2000 (SCI-Expanded)

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 , cilt.118, sa.1, ss.62-64, 2000 (SCI-Expanded)

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 , cilt.27, sa.5, ss.327-329, 1999 (SCI-Expanded)

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 , cilt.27, sa.5, ss.315-318, 1999 (SCI-Expanded)

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 , cilt.15, sa.1, ss.13-17, 1999 (SCI-Expanded)

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 , cilt.24, sa.2, ss.157-158, 1999 (SCI-Expanded)

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 , cilt.85, ss.159, 1999 (SCI-Expanded)

47,XYY karyotype in acute myeloid leukemia

Palanduz S., Aktan M., Ozturk S., Tutkan G., Cefle K., Pekcelen Y.

CANCER GENETICS AND CYTOGENETICS , cilt.106, sa.1, ss.76-77, 1998 (SCI-Expanded)

A Probable Case of MEN 1 Syndrome Presenting with Intractable Peptic Ulcer Disease and Episodic Confusion

PALANDUZ Ş., Taşçıoğlu C., ERTEN S. N., KARAN M. A., Cefle K., GÜLER K., et al.

Turkish Journal of Medical Sciences , cilt.28, ss.451-455, 1998 (SCI-Expanded)

An unusual translocation between 12tel and 14q11 in a large kindred.

Palanduz S., Ustek D., Karaman B., Ozturk S., Cefle K., Basaran S.

Hereditas , cilt.128, sa.3, ss.231-4, 1998 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

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 , cilt.20, sa.2, ss.102-109, 2024 (ESCI) Sürdürülebilir Kalkınma

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 , cilt.1, sa.1, ss.1, 2024 (ESCI)

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 , cilt.14, sa.2, ss.120-124, 2022 (Hakemli Dergi) Sürdürülebilir Kalkınma

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 , cilt.84, sa.4, ss.543-551, 2021 (ESCI)

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 , sa.9, ss.161-169, 2021 (Hakemli Dergi)

Ewing Sarkoma ile Primitif Nöroektodermal Tümör HücreHatlarında Agresiflik Paterninin Karşılaştırılması

GÜZEL TANOĞLU E., ÖZTÜRK Ş.

Kocaeli Tıp Dergisi , cilt.9, sa.1, ss.24-31, 2020 (Hakemli Dergi)

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 (Hakemli Dergi)

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 , cilt.8, ss.281, 2019 (Scopus)

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 , cilt.56, sa.2, ss.109-113, 2018 (ESCI)

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 , cilt.56, sa.1, ss.42-49, 2018 (Scopus)

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 , cilt.56, sa.1, ss.42-49, 2018 (ESCI)

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 , cilt.5, sa.10, ss.51-59, 2015 (Hakemli Dergi)

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 , cilt.4, sa.10, ss.51-59, 2015 (Hakemli Dergi)

Multidisciplinary treatment of non-syndromic oligodontia

BURAL C., OZTAS E., Ozturk S., BAYRAKTAR G.

European Journal of Dentistry , cilt.6, sa.2, ss.218-226, 2012 (Scopus)

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 , cilt.34, sa.4, ss.491-494, 2008 (ESCI)

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 , cilt.42, sa.4, ss.318-325, 2008 (ESCI) Sürdürülebilir Kalkınma

Investigation of Genomic Instability in Patients with Sjögren’s Syndrome by Using Sister Chromatid Exchange Analysis

ERGÜN S., TANYERİ H., ÖZTÜRK Ş., Duman N., KAMALI S., GÜL A., et al.

ACTA STOMATOLOGICA CROATICA , cilt.42, sa.4, ss.318-325, 2008 (ESCI)

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 , cilt.71, sa.3, ss.91-93, 2008 (ESCI)

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 , cilt.32, sa.2, ss.196-199, 1999 (Hakemli Dergi)

Dört Mikrosefalili Olguda Genetik, Dental, Morfolojik Özellikler ve Genel Değerlendirme

KATİPOĞLU A. B., PALANDUZ Ş., ÖZTÜRK Ş., Horasan S.

Türk Tıp Derneği Dergisi , cilt.60, ss.49-57, 1994 (Hakemli Dergi)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

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, Türkiye, 23 - 24 Aralık 2023, cilt.1, ss.586-591

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, Türkiye, 21 - 26 Kasım 2023

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, İstanbul, Türkiye, 13 - 14 Ağustos 2022, ss.514

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, Türkiye, 26 - 28 Mayıs 2022, cilt.1, ss.42-43

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, Türkiye, 18 - 20 Mart 2022, ss.116-122 Sürdürülebilir Kalkınma

Sürekli Diyabet Takibi Sistemi

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, Türkiye, 11 - 14 Mayıs 2022, ss.294-297

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, Türkiye, 11 - 13 Mayıs 2022, ss.294-297

A RARE CASE OF MUCINOUS CARCINOMA OF THE BREAST IN A 30-YEAR-OLD FEMALE

Emiroğlu S., Abuaisha A., Tükenmez M., Kaya M., Suer İ., Bayram A., et al.

4th International Congress on Medical Sciences and Multidisciplinary Approaches, 26 Mart - 28 Ağustos 2022, ss.302-308 Sürdürülebilir Kalkınma

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 Mart 2022

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, Türkiye, 18 - 19 Mart 2022, ss.505-510 Sürdürülebilir Kalkınma

Miyeloid maligniteli hastalarda TET2 gen varyasyonları

Aday A., Sırma Ekmekci S., Bayrak A. G., Çefle K., Öztürk Ş., Nalçacı M., et al.

XVII. Tıbbi Biyoloji ve Genetik Kongresi, 28 - 31 Ekim 2021, cilt.52, ss.242-243

CUMHURİYET VE TIP

ÖZTÜRK Ş.

8. ULUSAL İSTAHED AİLE HEKİMLİĞİ KONGRESİ, Antalya, Türkiye, 27 Ekim 2021

Investigation Of Some Candidate Genes Determined From Multiple Myeloma Whole Genome Transcriptome Data

Sarıman M., Karaçam B., Ayer M., Sırma Ekmekci S., Suer İ., Çefle K., et al.

8th Multidisciplinary Cancer Research Congress, İstanbul, Türkiye, 16 - 17 Ocak 2021, ss.123-124

CEBPA c.584589dup p.His195Pro196dup variant in myeloid malignancies

Suer İ., Sırma Ekmekci S., Aday A., Bayrak A. G., Çefle K., Öztürk Ş., et al.

The Virtual Conference on Current Challenges in Hematology (C-HEM2021), 18 - 19 Mart 2021

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), İstanbul, Türkiye, 20 - 23 Kasım 2020, ss.37

Overexpression of FUS and PRDX5 Genes In Multiple Myeloma Patients

Suer İ., Aday A., Sariman M., Ayer M., Yönal Hindilerden İ., Sırma Ekmekci S., et al.

14. Ulusal Tıbbi Genetik Kongresi (Uluslararası katılımlı), İstanbul, Türkiye, 20 - 23 Kasım 2020, ss.23 Sürdürülebilir Kalkınma

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), İstanbul, Türkiye, 20 Kasım - 22 Aralık 2020, ss.89

Relationship between sarcopenia and ACTN3 R577X gene in older adults

Kahraman M., Bahat-Öztürk G., Şahin A., Aday A., Diler A. S., Öztürk Ş., et al.

16th International E-Congress of the European Geriatric Medicine Society, 7 - 09 Ekim 2020, cilt.11, ss.1-309

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, Türkiye, 20 - 22 Şubat 2020, cilt.2584, ss.37 Sürdürülebilir Kalkınma

Seyahate çıkan vatandaşlarımızın seyahat sağlığı ve aşılar konusunda bilgi düzeyleri

Kahraman M., Öztürk Ş.

Geleneksel İç Hastalıkları Günleri - İnteraktif Güncelleştirme, Sakarya, Türkiye, 12 - 15 Mart 2020, ss.93 Sürdürülebilir Kalkınma

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, Türkiye, 18 - 22 Eylül 2019, cilt.1, ss.96

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, Türkiye, 5 - 07 Eylül 2019, ss.141

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 Nisan 2019

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, Türkiye, 17 - 20 Nisan 2019, cilt.BJMG, sa.39, ss.76

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 Nisan 2019

İnsülin kullanan DM hastalarında teknolojik cihazlar kullanımı ve teknolojiye uyumun diyabet kontrolü üzerine etkisi

Kahraman M., Öztürk Ş., Karşıdağ K., Karan M. A., Satman İ.

Geleneksel İç Hastalıkları Günleri - İnteraktif Güncelleştirme, Sakarya, Türkiye, 14 - 17 Mart 2019, ss.76-77 Sürdürülebilir Kalkınma

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, Türkiye, 21 Ekim - 03 Kasım 2018

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, Türkiye, 11 Mayıs 2018, ss.7-10 Sürdürülebilir Kalkınma

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, Türkiye, 2 - 06 Mayıs 2018

Akut Myeloid Lösemi ve 3q Kromozomal Yeniden Düzenlenmeleri

Bağatır Ozan G., Kaya M., Dön B., Suer İ., Nalçacı M., Yenerel M. N., et al.

3.Ulusal Uygulamalı Biyolojik Bilimler Kongresi (UBBK), Eskişehir, Türkiye, 3 - 05 Mayıs 2018, ss.35

idic(Y)(q11.2) ABNORMALITY IN CASES WITH MIXT GONADAL DYSGENESIS AND INFERTILITY

Kaya M., Suer İ., Kalaycı T., Karaman B., Dön B., Bağatır Ozan G., et al.

Erciyes Medical Genetics Days, Kayseri, Türkiye, 7 - 10 Mart 2018, ss.16

A Novel Insertional Translocation in a Patient with Infertility and Undiagnosed Mild Intellectual Disability

Suer İ., Kaya M., Bagatır Ozan G., Karaman B., Çefle K., Öztürk Ş., et al.

Erciyes Medical Genetics Days, Kayseri, Türkiye, 7 - 10 Mart 2018, ss.32

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, Türkiye, 26 - 29 Ekim 2017, ss.108

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, Türkiye, 26 Ekim 2017

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, Türkiye, 26 - 29 Ekim 2017, ss.108-109

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, İspanya, 21 - 24 Mayıs 2016, ss.153

Erkek İnnfertiliteside AZF

ÇOŞKUNPINAR E. M., ÖZTÜRK D., ÖZTAN G., KADIOĞLU A., ÖZTÜRK Ş., CEFLE K., et al.

. 11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014

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, Kostarika, 26 - 31 Temmuz 2014, cilt.14, ss.495

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, İtalya, 22 - 26 Haziran 2013, cilt.68, ss.363-364

‘‘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, Birleşik Krallık, 23 - 25 Eylül 2010, ss.524-525

‘‘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, Birleşik Krallık, 23 - 25 Eylül 2010, ss.518-519

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, İsveç, 4 - 07 Temmuz 2009, ss.161-162

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, İsveç, 4 - 07 Temmuz 2009, cilt.17, ss.162

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, Avusturya, 18 - 20 Eylül 2008, ss.35

‘‘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, Türkiye, 16 - 20 Mayıs 2007, ss.42

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, Türkiye, 7 - 10 Temmuz 2007, ss.202

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, Türkiye, 7 - 10 Temmuz 2007, ss.210

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, Türkiye, 7 - 10 Temmuz 2007, ss.223

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, Türkiye, 7 - 10 Temmuz 2007, ss.201-202

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, Türkiye, 7 - 10 Temmuz 2007, ss.199

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, Türkiye, 7 - 10 Temmuz 2007, ss.78

Constitutional chromosome abnormalities

Sukru P., Gulcin B., Kivanc C., Sukru O., Ali U., Aysegul B., et al.

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, ss.211

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, Türkiye, 7 - 10 Temmuz 2007, ss.85-86

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, Türkiye, 7 - 10 Temmuz 2007, ss.210-211

. 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, Makedonya, 20 Eylül 2008, cilt.9, sa.3, ss.75

‘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, Hırvatistan, 1 - 04 Eylül 2006, ss.1

‘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, Hırvatistan, 31 Ağustos - 02 Eylül 2006, ss.24

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, Hırvatistan, ss.30

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), Almanya, ss.29