Prof. Dr. Şükrü PALANDUZ

Yayın Ağı

Makaleler 129

1. 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 , cilt.42, sa.4, ss.1223-1237, 2025 (SCI-Expanded)

2. 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 , cilt.7, sa.1, ss.27-32, 2025 (Hakemli Dergi)

3. 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 , sa.1, ss.8-14, 2025 (ESCI, TRDizin) Sürdürülebilir Kalkınma

4. 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 , cilt.49, sa.5, ss.656-665, 2024 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

5. 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 , cilt.11, ss.334-339, 2024 (Hakemli Dergi)

6. 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 , sa.3, ss.235-245, 2024 (ESCI, TRDizin) Sürdürülebilir Kalkınma

7. 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 , sa.2, ss.135-140, 2024 (ESCI) Sürdürülebilir Kalkınma

8. 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 , cilt.20, sa.2, ss.135-140, 2024 (ESCI)

9. 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.37, sa.3, ss.1066-1082, 2024 (ESCI) Sürdürülebilir Kalkınma

10. 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) Sürdürülebilir Kalkınma

11. A Novel ADRA1A Missence Variant (c.939G > T) in Two Related Patients with Anejaculation: Case Report

Sharifi S., Dursun M., Palanduz S., Sahin A., Kadioglu A.

Indian Journal of Clinical Biochemistry , 2024 (ESCI)

12. **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 , cilt.48, sa.5, ss.563-569, 2023 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

13. Lactobacillus GG is associated with mucin genes expressions in type 2 diabetes mellitus: a randomized, placebo-controlled trial

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

EUROPEAN JOURNAL OF NUTRITION , cilt.62, sa.5, ss.2155-2164, 2023 (SCI-Expanded, Scopus)

14. 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, Scopus)

15. 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, Scopus) Sürdürülebilir Kalkınma

16. 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, Scopus)

17. 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)

18. 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

19. 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)

20. 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)

21. 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 , cilt.206, sa.4, ss.1050, 2021 (SCI-Expanded)

22. 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, Scopus)

23. 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)

24. 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, Scopus) Sürdürülebilir Kalkınma

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

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

UROLOGY , cilt.146, ss.113-117, 2020 (SCI-Expanded)

26. 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)

27. 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, Scopus)

28. 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)

29. 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, Scopus, TRDizin)

30. 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 , cilt.12, sa.6, ss.2152-2156, 2018 (SSCI)

31. 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)

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

Oztan G., Palanduz S., Cefle K.

NOBEL MEDICUS , cilt.14, sa.2, ss.5-16, 2018 (ESCI)

33. 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 , cilt.6, sa.2, ss.126-129, 2018 (ESCI, TRDizin)

34. 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)

35. KRONİK LENFOSİTİK LÖSEMİDE P53 YOLAĞINDAKİ GENLERİN HASTALIĞIN PROGNOZUNA OLAN ETKİSİ

ÖZTAN G., PALANDUZ Ş., ÇEFLE K.

NOBEL MEDICUS , cilt.14, sa.2, ss.5-16, 2018 (Scopus)

36. 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, Scopus)

37. 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)

38. 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)

39. 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, Scopus)

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

PALANDUZ Ş.

MARMARA PHARMACEUTICAL JOURNAL , sa.18, ss.139-146, 2014 (Hakemli Dergi)

41. 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)

42. 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 , cilt.45, sa.2, ss.92-100, 2013 (SCI-Expanded)

43. 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)

44. 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 , cilt.33, sa.8, ss.1175-1181, 2012 (SCI-Expanded)

45. 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 , cilt.413, sa.9-10, ss.950-1, 2012 (SCI-Expanded)

46. 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

47. 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)

48. 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)

49. 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 , cilt.6, sa.2, ss.57-62, 2010 (SCI-Expanded)

50. 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, Scopus)

51. 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 , cilt.15, sa.7, ss.499-504, 2009 (SCI-Expanded)

52. 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)

53. 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)

54. 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

55. 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)

56. 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, Scopus)

57. 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)

58. 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 , cilt.12, sa.3, ss.427-430, 2008 (SCI-Expanded, Scopus)

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

PALANDUZ Ş.

Turk J Pediatr , sa.50, ss.415-417, 2008 (Hakemli Dergi)

60. 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 , cilt.97, ss.188, 2008 (SCI-Expanded) Sürdürülebilir Kalkınma

61. 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)

62. 47,X,i(Xq),Y KARYOTİPİ SAPTANAN BİR KLİNEFELTER SENDROMU OLGUSU

PALANDUZ Ş.

İSTANBUL TIP FAKÜLTESİ DERGİSİ , sa.71, ss.91-93, 2008 (Hakemli Dergi)

63. 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 , cilt.116, sa.2, ss.163-166, 2008 (SCI-Expanded)

64. 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)

65. 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 , cilt.15, sa.8, ss.889-897, 2007 (SCI-Expanded)

66. 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

67. 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)

68. 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)

69. 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)

70. 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, Scopus) Sürdürülebilir Kalkınma

71. 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

72. 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

73. 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)

74. 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)

75. 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

76. Myeloid/natural killer cell precursor acute leukemia with tetraploidy

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

CANCER GENETICS AND CYTOGENETICS , cilt.163, sa.2, ss.156-159, 2005 (SCI-Expanded)

77. Two siblings with distal pachydermodactyly

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

CLINICAL AND EXPERIMENTAL DERMATOLOGY , cilt.30, sa.6, ss.707-709, 2005 (SCI-Expanded)

78. 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)

79. 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)

80. 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)

81. 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)

82. 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 , cilt.5, sa.4, ss.661-666, 2005 (SCI-Expanded)

83. 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)

84. 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

85. 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 , cilt.14, sa.6, ss.382-386, 2005 (SCI-Expanded) Sürdürülebilir Kalkınma

86. 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 , cilt.558, ss.137-144, 2004 (SCI-Expanded, Scopus)

87. 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 , sa.4, ss.356-363, 2004 (SCI-Expanded)

88. 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)

89. 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

90. 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

91. 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 , cilt.11, sa.11, ss.858-865, 2003 (SCI-Expanded)

92. Effect of montelukast on polymorphonuclear leukocyte functions in asthmatic patients

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

INTERNATIONAL IMMUNOPHARMACOLOGY , cilt.3, sa.9, ss.1257-1260, 2003 (SCI-Expanded)

93. 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 , cilt.12, sa.3, ss.184-188, 2003 (SCI-Expanded) Sürdürülebilir Kalkınma

94. 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 , cilt.535, sa.2, ss.205-213, 2003 (SCI-Expanded, Scopus)

95. korpus kallozum agenezisi olan bir olgu bildirimi

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

Dişhekimliği Dergisi , cilt.49, ss.28-31, 2003 (Hakemli Dergi)

96. 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)

97. 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)

98. Rheological properties of blood in patients with chronic liver disease

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

CLINICAL HEMORHEOLOGY AND MICROCIRCULATION , cilt.26, sa.1, ss.9-14, 2002 (SCI-Expanded) Sürdürülebilir Kalkınma

99. 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)

100. 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

101. 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)

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

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

ENDOCRINE RESEARCH , cilt.27, sa.3, ss.377-386, 2001 (SCI-Expanded) Sürdürülebilir Kalkınma

103. 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

104. 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)

105. 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)

106. 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)

107. 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 , cilt.70, sa.1, ss.3-7, 2000 (SCI-Expanded)

108. 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 , cilt.4, sa.1, ss.55-56, 2000 (SCI-Expanded)

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

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

MEDICAL SCIENCE RESEARCH , cilt.27, sa.12, ss.825-826, 1999 (SCI-Expanded)

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

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

NEUROSCIENCE RESEARCH COMMUNICATIONS , cilt.25, sa.2, ss.111-119, 1999 (SCI-Expanded)

111. 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 , cilt.27, sa.5, ss.305-306, 1999 (SCI-Expanded)

112. 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)

113. 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)

114. 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)

115. 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)

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

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

BIOCHEMICAL ARCHIVES , cilt.15, sa.1, ss.59-67, 1999 (SCI-Expanded) Sürdürülebilir Kalkınma

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

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

JOURNAL OF PERIODONTOLOGY , cilt.70, sa.2, ss.201-204, 1999 (SCI-Expanded)

118. 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)

119. 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)

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

palandüz ş., TANYERİ H., güç ü.

Diş Hek. Der. , cilt.32, ss.76-82, 1999 (Hakemsiz Dergi)

121. 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)

122. 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 , cilt.6, sa.1, ss.9-12, 1998 (Hakemli Dergi)

123. 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 , sa.2, ss.180-182, 1998 (SCI-Expanded) Sürdürülebilir Kalkınma

124. 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 , cilt.26, sa.2, ss.105-106, 1998 (SCI-Expanded)

125. 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)

126. High plasma fibronectin levels in pulmonary embolism

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

MEDICAL SCIENCE RESEARCH , cilt.25, sa.9, ss.589-590, 1997 (SCI-Expanded)

127. 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 , cilt.25, sa.4, ss.233-234, 1997 (SCI-Expanded)

128. 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)

129. Familial Osteodisplasia (Anderson Syndrome) Bir Vaka Takdimi

PALANDUZ Ş., ÖZTÜRK O., Erdoğan G.

Journal of Turkish Medicine Association , cilt.58, ss.287-292, 1992 (Hakemli Dergi)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 66

1. Identifying genes variations in fibrosis-related pathways determine susceptibility to fibrotic pathogenesis in Peyronie’s disease

Gürcan M., Sharifi S., Palanduz Ş., Dursun M., Kadıoğlu A.

24. Ulusal Androloji Kongresi ve 1. Global Androloji Forum Kongresi, Muğla, Türkiye, 22 - 25 Mayıs 2025, ss.120, (Özet Bildiri)

2. 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, İspanya, 21 - 24 Mart 2025, ss.87, (Özet Bildiri)

3. MONOALLELIC VARIANTS IN THE LAMININ BETA-2 (LAMB2) GENE INDUCE FIBROTIC PATHOLOGY IN PEYRONIE’S DISEASE

Dursun M., Gürcan M., Sharifi S., Palanduz Ş., Kadıoğlu A.

European Society of Sexual Medicine Congress 2025, Vienna, Avusturya, 20 - 22 Şubat 2025, ss.53-54, (Özet Bildiri)

4. Monoallelic Variants in the Laminin Beta-2 (LAMB2) Gene Induce Fibrotic Pathology in Peyronie’s Disease

Gürcan M., Sharifi S., Palanduz Ş., Dursun M., Kadıoğlu A.

33. Ulusal Üroloji Kongresi, Antalya, Türkiye, 29 Ekim - 01 Kasım 2024, ss.75-76, (Tam Metin Bildiri)

5. First Report Unveiling Genetic Etiopathogenesis of Anejaculation: Involvement of Alpha-1a Adrenergic Receptor Gene in a in Familial Cases

Sharifi S., Dursun M., Palanduz Ş., Şahin A., Kadıoğlu A.

23. Ulusal Androloji Kongresi, Eskişehir, Türkiye, 17 - 19 Mayıs 2024, ss.14, (Özet Bildiri)

6. 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, Türkiye, 17 - 19 Mayıs 2024, ss.22, (Özet Bildiri)

7. 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, İsveç, 23 - 26 Mayıs 2024, (Özet Bildiri)

8. 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, Kuzey Mariana Adaları, 5 - 09 Aralık 2023, (Özet Bildiri)

9. Şiddetli Oligospermi ve Tekrarlayan Gebelik Kaybıyla İlişkili Perisentrik Inv(1)(p34.1q25)

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, Türkiye, 23 - 24 Aralık 2023, cilt.1, ss.586-591, (Tam Metin Bildiri)

10. 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, (Tam Metin Bildiri)

11. 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, (Özet Bildiri)

12. 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, (Özet Bildiri)

13. 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, cilt.1, ss.116-122, (Tam Metin Bildiri) Sürdürülebilir Kalkınma

14. 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, 18 - 19 Şubat 2022, ss.264-270, (Tam Metin Bildiri)

15. 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, (Özet Bildiri)

16. 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, Türkiye, 18 - 19 Mart 2021, (Özet Bildiri)

17. 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, Türkiye, 16 - 17 Ocak 2021, ss.123, (Özet Bildiri)

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

Tipici B., 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 Eylül 2020, (Özet Bildiri) Sürdürülebilir Kalkınma

19. 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, (Özet Bildiri) Sürdürülebilir Kalkınma

20. 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, Türkiye, 3 - 04 Ekim 2019, (Özet Bildiri)

21. 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, (Özet Bildiri)

22. 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, cilt.1, ss.141, (Özet Bildiri)

23. 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, Fransa, 4 - 07 Nisan 2019, cilt.30, (Özet Bildiri)

24. 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, (Özet Bildiri)

25. 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, (Özet Bildiri)

26. 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, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.957, (Özet Bildiri)

27. 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, Türkiye, 7 - 10 Mart 2018, cilt.1, ss.16, (Özet Bildiri)

28. 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, Türkiye, 7 - 10 Mart 2018, ss.32, (Özet Bildiri)

29. 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, (Özet Bildiri)

30. 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, (Tam Metin Bildiri)

31. İnhalasyon Anestezisi ile Oluşan Genotoksik Etkilerin Bronkoalveoler Lavaj Sıvısında "Tek Hücre Jel Elektroforezi, Komet" Yöntemi il İncelenmesi

Çukurova Z., Gedikbaşı A., Öztürk Ş., Çetingök H., Öztürk D., Eren G., et al.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.107-108, (Özet Bildiri)

32. 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, Türkiye, 24 - 27 Eylül 2014, ss.100-101, (Özet Bildiri)

33. 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, Türkiye, 24 - 27 Eylül 2014, ss.100, (Özet Bildiri)

34. 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, Türkiye, 24 - 27 Eylül 2014, ss.101, (Özet Bildiri)

35. 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, Türkiye, 24 - 27 Eylül 2014, ss.108, (Özet Bildiri)

36. Kleidokranial Displazi: Olgu Sunumu

Gedikbaşı A., Çefle K., Kaya M., Öztürk Ş., Palanduz Ş.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.67-68, (Özet Bildiri)

37. 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, Türkiye, 24 - 27 Eylül 2014, ss.101, (Özet Bildiri)

38. 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, Türkiye, 24 - 27 Eylül 2014, ss.100, (Özet Bildiri)

39. 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, Türkiye, 24 - 27 Eylül 2014, ss.102, (Özet Bildiri)

40. Erkek İnfertiliteside AZF

Çoşkunpınar E. M., Öztürk D., Öztan G., Kadıoğlu A., Öztürk Ş., Cefle K., et al.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Türkiye, 24 - 27 Eylül 2014, ss.5, (Özet Bildiri)

41. Erkek İnfertilitesinde AZF

COŞKUNPINAR E., ÖZTÜRK D., ÖZTAN G., KADIOĞLU A., ÖZTÜRK Ş., ÇEFLE K., et al.

11. Ulusal Tıbbi Genetik Kongresi, Türkiye, 24 - 27 Eylül 2014, (Özet Bildiri)

42. 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, Portekiz, 12 - 14 Eylül 2013, ss.41, (Tam Metin Bildiri)

43. 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, Portekiz, 12 - 14 Eylül 2013, ss.41, (Tam Metin Bildiri)

44. ‘‘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, (Tam Metin Bildiri)

45. ‘‘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, (Tam Metin Bildiri)

46. 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, (Tam Metin Bildiri)

47. 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, (Özet Bildiri)

48. 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, (Tam Metin Bildiri)

49. ‘‘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, (Tam Metin Bildiri)

50. 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, (Özet Bildiri)

51. 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, (Özet Bildiri)

52. 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, (Özet Bildiri)

53. 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, (Özet Bildiri)

54. Investigation of genomic instability in patients with lymphoma by sister chromatid exchange analysis

Duman O. S., Basak S., Davut P., Sertan E., Mesut B., Oktay P., et al.

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, ss.209, (Özet Bildiri)

55. 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, (Özet Bildiri)

56. 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, (Özet Bildiri)

57. 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, (Özet Bildiri)

58. T(5;22)(P11,Q11) variant translocation in a case of chronic myeloid leukemia refractory to treatment

Erkal O. S., Serap Y., Kivanc C., Gulcin B., Ali U., Nilgun D., et al.

6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, ss.209-210, (Özet Bildiri)

59. 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, (Tam Metin Bildiri)

60. 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, Bulgaristan, 8 - 11 Mayıs 2004, (Özet Bildiri)

61. 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, Bulgaristan, 8 - 11 Mayıs 2004, (Özet Bildiri)

62. 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, Fransa, 7 - 11 Haziran 2003, ss.127, (Tam Metin Bildiri)

63. 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, Türkiye, 26 - 30 Mayıs 2002, ss.76, (Tam Metin Bildiri)

64. 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, Avusturya, 15 - 19 Mayıs 2001, ss.161, (Tam Metin Bildiri)

65. 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, Türkiye, 26 - 30 Nisan 1998, ss.97, (Tam Metin Bildiri)

66. 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, Türkiye, 3 - 06 Eylül 1996, ss.36, (Özet Bildiri)

Kitaplar 1

1. Bölüm 8: Hematolojik Malign Hastalıklarda Moleküler Analizler

Dağlar Aday A., Palanduz Ş.

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

Diğer Yayınlar 1

1. 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.

Diğer, ss.1-12, 2019

Metrikler

Yayın

197

Yayın (WoS)

131

Yayın (Scopus)

109

Atıf (WoS)

1090

H-İndeks (WoS)

Atıf (Scopus)

1337

H-İndeks (Scopus)

Atıf (Scholar)

H-İndeks (Scholar)

Atıf (TrDizin)

H-İndeks (TrDizin)

Atıf (Diğer Toplam)

Proje

Tez Danışmanlığı

Açık Erişim

BM Sürdürülebilir Kalkınma Amaçları

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