Prof. Şükrü PALANDUZ

Publication Network

Published journal articles indexed by SCI, SSCI, and AHCI

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) Sustainable Development

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)

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)

Re: Indication for Y Chromosome Microdeletion Analysis in Infertile Men: Is a New Sperm Concentration Threshold Needed?

Ortac M., Ergul R., Gurcan M., Kalayci T., Palanduz S., Aydin R., et al.

JOURNAL OF UROLOGY, vol.206, no.4, pp.1050, 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, vol.185, no.8, pp.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, vol.14, no.2, pp.151-156, 2021 (SCI-Expanded)

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)

Indication for Y Chromosome Microdeletion Analysis in Infertile Men: Is a New Sperm Concentration Threshold Needed?

Ortac M., Ergul R., Gurcan M., Kalayci T., Palanduz Ş., Aydin R., et al.

UROLOGY, vol.146, pp.113-117, 2020 (SCI-Expanded)

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)

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)

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)

The Effect of PAI-1 Gene Variants and PAI-1 Plasma Levels on Development of Thrombophilia in Patients With Klinefelter Syndrome

Erkal B., Yıgın A. K., Palanduz S., Dasdemir S., Seven M.

AMERICAN JOURNAL OF MENS HEALTH, vol.12, no.6, pp.2152-2156, 2018 (SSCI)

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, vol.23, no.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, vol.101, no.1, pp.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, vol.38, no.1, pp.7-15, 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 S., Cefle K., Ozbek U., et al.

Cellular and molecular biology (Noisy-le-Grand, France), vol.62, pp.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, vol.148, no.4, pp.771-793, 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, vol.19, no.4, pp.299-304, 2013 (SCI-Expanded)

Investigation of mutations in the synaptonemal complex protein 3 (SYCP3) gene among azoospermic infertile male patients in the Turkish population

Gurkan H., Aydın F. F., Kadioglu A., Palanduz S.

ANDROLOGIA, vol.45, no.2, pp.92-100, 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, vol.39, no.12, pp.1016-1021, 2012 (SCI-Expanded)

Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis

Diggle C. P., Parry D. A., Logan C. V., Laissue P., Rivera C., Martin Restrepo C., et al.

HUMAN MUTATION, vol.33, no.8, pp.1175-1181, 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, vol.413, pp.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, vol.16, no.4, pp.287-291, 2012 (SCI-Expanded) Sustainable Development

Micronucleus and Sister Chromatid Exchange Analyses in Peripheral Lymphocytes of Patients with Oral Leukoplakia - A Pilot Study

PALANDUZ Ş.

ORAL DISEASES, no.16, pp.518-519, 2010 (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, vol.16, no.6, pp.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, vol.16, no.6, pp.524-525, 2010 (SCI-Expanded)

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)

TRANSPLANTASYON BEKLEYEN DİLATE KARDİYOMİYOPATİLİ HASTALARDA YÜKSEK SERUM BAKIR DÜZEYİNİN MİYOKARD İŞLEVİ ÜZERİNDEKİ MUHTEMEL KÖTÜ ETKİSİ

PALANDUZ Ş., ÇEFLE K.

NOBEL MEDICUS, no.6, pp.32-36, 2010 (SCI-Expanded)

İMATİNİBE DİRENÇLİ VEYA ENTOLERANS GÖSTEREN, KROMOZOMAL DEĞİŞİKLİKLERİ OLAN VE OLMAYAN T(9;22) POZİTİF KRONİK MYELOİD LÖSEMİLİ 21 HASTADA NİLOTİNİB’İN ETKİNLİĞİ

PALANDUZ Ş., ÇEFLE K.

NOBEL MEDICUS, no.6, pp.57-62, 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, vol.18, no.3, pp.131-134, 2009 (SCI-Expanded)

Micronuclear and sister chromatid exchange analyses in peripheral lymphocytes of patients with oral lichen planus - a pilot study

Ergun S., Warnakulasuriya S., Duman N., Saruhanoglu A., Sevinc B., Öztürk S., et al.

ORAL DISEASES, vol.15, no.7, pp.499-504, 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, vol.13, no.5, pp.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, vol.26, no.8, pp.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, vol.134, no.12, pp.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, vol.49, no.5, pp.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, vol.31, no.9, pp.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, vol.12, no.3, pp.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, vol.97, pp.155, 2008 (SCI-Expanded)

Vitamin D receptor gene polymorphisms in childhood tuberculosis

Palanduz A., Ozbek U., Sirma S., Coskunpinar E., Telhan L., Kadioglu L. E., et al.

ACTA PAEDIATRICA, vol.97, pp.188, 2008 (SCI-Expanded) Sustainable Development

Acute megakaryoblastic leukemia mimicking small round cell tumor with novel t(1;5)(q21;p13)

Bozkurt S. U., Berrak S. G., Tugtepe H., Canpolat C., Palanduz S., Tecimer T.

APMIS, vol.116, no.2, pp.163-166, 2008 (SCI-Expanded)

Treatment of acquired severe aplastic anemia with antilymphocyte globulin, cyclosporin A, methyprednisolone, and granulocyte colony-stimulating factor.

PALANDUZ Ş.

Am J Hematol., no.82, pp.783-6, 2007 (SCI-Expanded)

A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24

Deglincerti A., De Giorgio R., Cefle K., Devoto M., Pippucci T., Castegnaro G., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS, vol.15, no.8, pp.889-897, 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, vol.22, no.3, pp.393-399, 2007 (SCI-Expanded) Sustainable Development

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)

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)

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)

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) Sustainable Development

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) Sustainable Development

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) Sustainable Development

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)

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)

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) Sustainable Development

Myeloid/natural killer cell precursor acute leukemia with tetraploidy

Dincol G., Palanduz S., Nalcaci M., Ucur A., Buyukaydin B.

CANCER GENETICS AND CYTOGENETICS, vol.163, no.2, pp.156-159, 2005 (SCI-Expanded)

Two siblings with distal pachydermodactyly

Saka B., Mezdegi A., Ozturk A., Erten N., Cefle K., Palanduz S.

CLINICAL AND EXPERIMENTAL DERMATOLOGY, vol.30, no.6, pp.707-709, 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, vol.103, no.3, pp.285-288, 2005 (SCI-Expanded)

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)

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)

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)

The effects of allergen-specific immunotherapy on polymorphonuclear leukocyte functions in patients with seasonal allergic rhinitis

GURER U., Buyukozturk S., PALANDUZ S., RAYAMAN E., Çolakoğlu B., CEVIKBAS A.

INTERNATIONAL IMMUNOPHARMACOLOGY, vol.5, no.4, pp.661-666, 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, vol.33, pp.81-8, 2005 (SCI-Expanded) Sustainable Development

Comparison of polymorphonuclear leukocyte functions in elderly patients and healthy young volunteers

Gocer P., Gurer U., Erten N., Palanduz S., Rayaman E., Akarsu B., et al.

MEDICAL PRINCIPLES AND PRACTICE, vol.14, no.6, pp.382-386, 2005 (SCI-Expanded) Sustainable Development

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)

In vitro effects of selective and non-selective nonsteroidal anti-inflammatory drugs on the frequency of sister chromatid exchanges.

PALANDUZ Ş., ÇEFLE K.

Drugs R D, no.5, pp.327-30, 2004 (SCI-Expanded)

Clastogenicity of selective serotonin-reuptake inhibitors

Bozkurt G., Abay E., Ates I., Karabogaz G., Ture M., Savran F., et al.

MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, vol.558, pp.137-144, 2004 (SCI-Expanded)

Brachydactyly type C caused by a homozygous missense mutation in the prodomain of CDMP1

Schwabe G., Turkmen S., Leschik G., Palanduz S., Stover B., Goecke T., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, no.4, pp.356-363, 2004 (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, vol.5, pp.327-30, 2004 (SCI-Expanded)

Sister chromatid exchange and mitotic index in patients with cirrhosis related to hepatitis B and C viruses and in chronic carriers.

PALANDUZ Ş.

HEPATO-GASTROENTEROLOGY, no.50, pp.2137-40, 2003 (SCI-Expanded) Sustainable Development

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) Sustainable Development

Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes

Turkmen S., Gillessen-Kaesbach G., Meinecke P., Albrecht B., Neumann L., Hesse V., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS, vol.11, no.11, pp.858-865, 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 S., Tutkan G., Vatansever S., et al.

HEPATO-GASTROENTEROLOGY, vol.50, no.54, pp.2137-2140, 2003 (SCI-Expanded) Sustainable Development

Effect of montelukast on polymorphonuclear leukocyte functions in asthmatic patients

GURER U., Buyukozturk S., PALANDUZ S., GURBUZ B., CEVIKBAS A.

INTERNATIONAL IMMUNOPHARMACOLOGY, vol.3, no.9, pp.1257-1260, 2003 (SCI-Expanded)

A study of serological markers of hepatitis B and C viruses in Istanbul, Turkey

Erden S., Buyukozturk S., Calangu S., Yilmaz G., Palanduz S., Badur S.

MEDICAL PRINCIPLES AND PRACTICE, vol.12, no.3, pp.184-188, 2003 (SCI-Expanded) Sustainable Development

Sister chromatid exchanges in lymphocytes of nuclear medicine physicians

Bozkurt G., Yuksel M., Karabogaz G., Sut N., Savran F., Palanduz S., et al.

MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, vol.535, no.2, pp.205-213, 2003 (SCI-Expanded)

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)

The role of HLA antigens in chronic hepatitis B virus infection.

PALANDUZ Ş.

J Pak Med Assoc, no.52, pp.253-6, 2002 (SCI-Expanded) Sustainable Development

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)

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) Sustainable Development

Rheological properties of blood in patients with chronic liver disease

Tamer S., Cefle K., Palanduz S., Vatansever S.

CLINICAL HEMORHEOLOGY AND MICROCIRCULATION, vol.26, no.1, pp.9-14, 2002 (SCI-Expanded) Sustainable Development

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)

Clinical images in oral medicine and maxillofacial radiology. Turner syndrome

YALÇIN S., AYBAR B., PALANDUZ Ş., HAZNEDAROĞLU F., EMES Y., Terezhalmy G., et al.

QUINTESSENCE INTERNATIONAL, vol.32, no.9, pp.748-9, 2001 (SCI-Expanded)

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)

Plasma antioxidants and type 2 diabetes mellitus.

PALANDUZ Ş.

Res Commun Mol Pathol Pharmacol, no.109, pp.309-18, 2001 (SCI-Expanded) Sustainable Development

Oxidant and antioxidant systems in NIDDM patients: Influence of vitamin E supplementation

Gokkusu C., Palanduz S., Ademoglu E., Tamer S.

ENDOCRINE RESEARCH, vol.27, no.3, pp.377-386, 2001 (SCI-Expanded) Sustainable Development

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) Sustainable Development

A case of Noonan syndrome with pulmonary and abdominal lymphangiectasia

Ozturk S., 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)

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)

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, vol.3, pp.45-48, 2000 (AHCI)

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)

Brucellosis in a mother and her young infant: Probable transmission by breast milk

Palanduz A., PALANDUZ Ş., Güler K., Güler N.

International Journal of Infectious Diseases, vol.4, no.1, pp.55-56, 2000 (SCI-Expanded)

Vitamin E and ATPases: Protection of ATPase activities by vitamin E supplementation in various tissues of hypercholesterolemic rats

Ademoglu E., Gokkusu C., Palanduz S.

INTERNATIONAL JOURNAL FOR VITAMIN AND NUTRITION RESEARCH, vol.70, no.1, pp.3-7, 2000 (SCI-Expanded)

A case of mental retardation associated with a partial tetrasomy of chromosome 15

PALANDUZ Ş., ÇEFLE K.

CYTOGENETICS AND CELL GENETICS, no.85, 1999 (SCI-Expanded)

Effect of chronic smoking on the rheological behaviour and lipid composition of erythrocytes

Gokkusu C., Tamer S., Ademoglu E., Palanduz S.

MEDICAL SCIENCE RESEARCH, vol.27, no.12, pp.825-826, 1999 (SCI-Expanded)

Acute hyperglycemia augments blood-brain barrier damage in experimental status epilepticus

Kaya M., Kucuk M., Kalayci R., Palanduz S.

NEUROSCIENCE RESEARCH COMMUNICATIONS, vol.25, no.2, pp.111-119, 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, vol.27, no.5, pp.315-318, 1999 (SCI-Expanded)

Skin test reactivity to common aeroallergens in patients treated with ACE inhibitors

Buyukozturk S., Erden S., Palanduz S., Kardes B., Colaoglu B., Dal M., et al.

MEDICAL SCIENCE RESEARCH, vol.27, no.5, pp.305-306, 1999 (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, vol.27, no.5, pp.327-329, 1999 (SCI-Expanded)

Gingival fibromatosis combined with cherubism and psychomotor retardation: A rare syndrome

Yalcin S., Yalcin F., Soydinc M., Palanduz S., Gunhan O.

JOURNAL OF PERIODONTOLOGY, vol.70, no.2, pp.201-204, 1999 (SCI-Expanded)

Gingival fibromatosis combined with cherubism and psychomotor retardation: a rare syndrome.

PALANDUZ Ş.

JOURNAL OF PERIODONTOLOGY, no.70, pp.201-4, 1999 (SCI-Expanded)

Lipid composition and hemorheology in non-insulin dependent diabetes mellitus patients

Tamer S., Palanduz S., Ademoglu E., Gokkusu C., KAYESERILIOGLU A.

BIOCHEMICAL ARCHIVES, vol.15, no.1, pp.59-67, 1999 (SCI-Expanded) Sustainable Development

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)

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)

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)

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)

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, vol.28, pp.451-455, 1998 (SCI-Expanded)

Case report: a surgical and prosthetic approach to combination syndrome presenting in a patient with craniofacial dysostosis (Crouzon syndrome).

PALANDUZ Ş.

Eur J Prosthodont Restor Dent, no.6, pp.9-12, 1998 (SCI-Expanded)

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, vol.86, no.2, pp.180-182, 1998 (SCI-Expanded) Sustainable Development

Total antioxidant status, lipid parameters, lipid peroxidation and glutathione levels in patients with acute myocardial infarction

Guler K., Palanduz S., Ademoglu E., Salmayenli N., Gokkusu C., Vatansever S.

MEDICAL SCIENCE RESEARCH, vol.26, no.2, pp.105-106, 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, vol.128, no.3, pp.231-4, 1998 (SCI-Expanded)

High plasma fibronectin levels in pulmonary embolism

Guler K., Salmayenli N., Vatansever S., Tascioglu C., Erk O., Palanduz S., et al.

MEDICAL SCIENCE RESEARCH, vol.25, no.9, pp.589-590, 1997 (SCI-Expanded)

Low circulating levels of fibronectin in patients with sepsis: Its prognostic value

Guler K., Salmayenli N., Tascioglu C., Palanduz S., Karan M., Sivas A.

MEDICAL SCIENCE RESEARCH, vol.25, no.4, pp.233-234, 1997 (SCI-Expanded)

Articles Published in Other Journals

ERAP1 Gen İfadesinin Plazma Hücre Diskrazilerinde İncelenmesi

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

İstanbul Kanuni Sultan Süleyman Tıp Dergisi, vol.14, no.2, pp.120-124, 2022 (Peer-Reviewed Journal) Sustainable Development

A Rare Variant Translocation (t(5;9;22)(q13;q34;q11.2)) In A Case With Chronic Myeloid Leukemia

ERKAL M. H., ÖZTÜRK Ş., YÜCEL S., ÇEFLE K., Bagatır G., Bayrak A. G., et al.

Tıp Fakültesi Klinikleri Dergisi, vol.2, no.2, pp.35-38, 2019 (Peer-Reviewed Journal)

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)

THE PROGNOSTIC EFFECT OF GENES IN THE P53 PATHWAY IN CHRONIC LYMPHOCYTIC LEUKEMIA

Oztan G., Palanduz S., Cefle K.

NOBEL MEDICUS, vol.14, no.2, pp.5-16, 2018 (ESCI)

Could the ENPP1 p.D85H Mutation be Associated with Hypophosphatemic Rickets?

Coskunpinar E., Tekin S., Palanduz S., Avci H., Cefle K., Tiryakioglu N. O., et al.

BEZMIALEM SCIENCE, vol.6, no.2, pp.126-129, 2018 (ESCI)

Bazı Antibiyotiklerin Hemodiyaliz Hastalarının Polimorf Nüveli Lökosit Fonksiyonları ve Oksidatif Stres Üzerine Etkilerinin İn Vitro Araştırılması

PALANDUZ Ş.

MARMARA PHARMACEUTICAL JOURNAL, no.18, pp.139-146, 2014 (Peer-Reviewed Journal)

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, vol.42, no.4, pp.318-325, 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, vol.42, no.4, pp.318-325, 2008 (ESCI) Sustainable Development

Adult height in Turkish patients with Turner syndrome without growth hormone treatment

PALANDUZ Ş.

Turk J Pediatr, no.50, pp.415-417, 2008 (Peer-Reviewed Journal)

47,X,i(Xq),Y KARYOTİPİ SAPTANAN BİR KLİNEFELTER SENDROMU OLGUSU

PALANDUZ Ş.

İSTANBUL TIP FAKÜLTESİ DERGİSİ, no.71, pp.91-93, 2008 (Peer-Reviewed Journal)

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)

korpus kallozum agenezisi olan bir olgu bildirimi

KATİBOĞLU A. B., PALANDUZ Ş., TANYERİ H., TANYEL R. C., Hatırnaz Şener H.

Dişhekimliği Dergisi, vol.49, pp.28-31, 2003 (Peer-Reviewed Journal)

Böbrek Transplantasyonu Yapılmış Hastalarda Siklosporin –A Kullanımına Bağlı Periodontal ve Sitogenetik Bulgular

palandüz ş., TANYERİ H., güç ü.

Diş Hek. Der., vol.32, pp.76-82, 1999 (Non Peer-Reviewed Journal)

Case Report: Surgical and prosthetic approach to Combination Syndrome presenting in a patient with Craniofacial Dysostosis (Crouzon Syndrome).

BAYRAKTAR B. G., PALANDUZ Ş.

Eur J Prosthodont Restor Dent, vol.6, no.1, pp.9-12, 1998 (Peer-Reviewed Journal)

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)

Familial Osteodisplasia (Anderson Syndrome) Bir Vaka Takdimi

PALANDUZ Ş., ÖZTÜRK O., Erdoğan G.

Journal of Turkish Medicine Association, vol.58, pp.287-292, 1992 (Peer-Reviewed Journal)

Refereed Congress / Symposium Publications in Proceedings

The Phenotypic Effect of X;Autosome Balanced Chromosomal Translocations: A Case with Premature Ovarian Failure and Familial t(X;9)(q22;q34)

Abuaısha A., Kaya M., Suer İ., Çefle K., Palanduz Ş., Öztürk Ş.

7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Turkey, 26 - 28 May 2022, pp.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, Turkey, 18 - 20 March 2022, pp.116-122 Sustainable Development

RELATIONSHIP BETWEEN MIR-7-5P AND SKP2 GENE IN HL60 AND NB4 CELLS

Mehteroğlu E., Suer İ., Kaya M., Palanduz Ş.

INTERNATIONAL CONGRESS OF MULTIDISCIPLINARY STUDIES IN HEALTH SCIENCES, Erzurum, Turkey, 18 - 19 February 2022, pp.264-270

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

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 March 2021

Effects of Lactobacillus GG supplementation in type 2 diabetes: Are mucin genes expressions important?

Tipici B. E., Coskunpinar E., Altunkanat D., Cagatay P., Omer B., Palanduz S., et al.

56th Annual Meeting of the European-Association-for-the-Study-of-Diabetes (EASD), ELECTR NETWORK, 21 - 25 September 2020, vol.63 Sustainable Development

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.Uluslararası Katılımlı Erciyes Tıp Genetik Günleri Kongresi, Nevşehir, Turkey, 20 - 22 February 2020, vol.2584, pp.37 Sustainable Development

Investigation of TMD-ERAP1 Candidate Gene Expressions Obtained from Multiple Myeloma Transcriptome Data by RT-PCR

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

1.International Multidisciplinary Cancer Research Congress, Diyarbakır, Turkey, 18 - 22 September 2019, pp.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, Turkey, 5 - 07 September 2019, pp.141

INCIDENCE AND RELATED FACTORS FOR INPATIENT FALLS IN THE DEPARTMENT OF INTERNAL MEDICINE

Yilmaz O., Guder N., Kucukdagli P., Kilic C., Bahat G., Sacar D. E., et al.

World Congress on Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (WCO-IOF-ESCEO), Paris, France, 4 - 07 April 2019, vol.30

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

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

The effect of PAI-1 Gene Variants on Development of Thrombophilia in Patients with Klinefelter Syndrome

Erkal B., Dasdemir S., Yigin A. K., Palanduz S., Seven M.

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.957

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, Turkey, 3 - 05 May 2018, pp.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, Turkey, 7 - 10 March 2018, pp.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, Turkey, 7 - 10 March 2018, pp.32

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

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

Erkek İnnfertiliteside AZF

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

. 11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014

Investigation of MTA induced genotoxicity by sister chromatid exchange: a pilot study.

DİNÇOL M. E., BAYRAK A. G., UÇUR A., ERDİN H. H., YILMAZ B., DAĞLAROĞLU R., et al.

16. BIENNAL CONGRESS OF THE EUROPEAN SOCIETY OF ENDODONTOLOGY, Lizbon, Portugal, 12 - 14 September 2013, pp.41

Investigation of MTA induced genotoxicity by sister chromatid exchange

DİNÇOL M. E., BAYRAK A. G., UÇUR A., Gürbüz Erdin H. H., YILMAZ B., DAĞLAROĞLU R., et al.

16th Biennial Congress of the European Society of Endodontics, Lizbon, Portugal, 12 - 14 September 2013, pp.41

‘‘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

‘‘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

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

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

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

‘‘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

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

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 ÇİFTÇİ H., DİLER A. S., ÖZTÜRK Ş., ÖNAL A. E., Kaya S., KILIÇASLAN AYNA T., et al.

18. European Immunogenetics and Histocompatibility Conference, 8 - 11 May 2004

The Effects of Montelukast on Polymorphonuclear Leukocyte Functions in Asthmatic Patients

BÜYÜKÖZTÜRK S., Gürer U., GELİNCİK A., ÇOLAKOĞLU B., DAL B. M., Akkor A., et al.

XXII. Congress of The European Academy of Allergology and Clinical Immunology, Paris, France, 7 - 11 June 2003, pp.127

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

THE IN VITRO EFFECTS OF SELECTIVE AND NON-SELECTIVE NON-STEROIDAL ANTI-INFLAMMATORY DRUGS ON THE FREQUENCY OF SISTER CHROMATID EXCHANGES

AYDİL B. A., KOÇAK BERBEROĞLU H., PALANDUZ Ş., ÇEFLE K.

10TH INTERNATIONAL CONGRESS OF HUMAN GENETICS, Viyana, Austria, 15 - 19 May 2001, pp.161

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

Books & Book Chapters

Bölüm 8: Hematolojik Malign Hastalıklarda Moleküler Analizler

Dağlar Aday A., Palanduz Ş.

in: Klinisyenler İçin Genetik Testler, Prof. Dr. Şükrü Öztürk,Prof.Dr. Kıvanç Çefle, Editor, EMA Tıp Kitabevi Yayıncılık Tic. Ltd. Şti., İstanbul, pp.127-140, 2022

Other Publications

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

Publications & Works

Published journal articles indexed by SCI, SSCI, and AHCI

Articles Published in Other Journals

Refereed Congress / Symposium Publications in Proceedings