Prof. ŞÜKRÜ ÖZTÜRK

Publication Network

Articles 146

1. IDH1 Mutations in Acute Myeloid Leukemia: Frequency and Clinical Features in the Context of FLT3 and NPM1 Co-Mutations-A Single-Center Study from Turkey.

Catma Y., Erdem S., Aday A., Bayrak Tokaç A. G., Mastanzade M., Ozbalak M. M., et al.

Current issues in molecular biology , vol.48, no.8, 2026 (SCI-Expanded, Scopus)

2. Missing-mass search in forward-proton-tagged dilepton events with the ATLAS detector

Aad G., Aakvaag E., Abbott B., Abdelhameed S., Abeling K., Abicht N., et al.

Journal of High Energy Physics , vol.2026, no.7, 2026 (SCI-Expanded, Scopus)

3. Breaking barriers: the impact of ATLAS Virtual Visits in science communication

Zwalinski L., Zorbas T., Zografos A., Zoch K., Zoccoli A., Živković L., et al.

European Physical Journal Plus , vol.141, no.7, 2026 (SCI-Expanded, Scopus)

4. Effective field theory interpretation of ATLAS measurements involving the Higgs boson, electroweak bosons and the top quark

Aad G., Aakvaag E., Abbott B., Abdelhameed S., Abeling K., Abicht N., et al.

Journal of High Energy Physics , vol.2026, no.7, 2026 (SCI-Expanded, Scopus)

5. Mechanistic focus on miR-34a-5p/E2F1 axis in multiple myeloma cells

SUER İ., Kaya M., Karatas O. F., ÖZGÜR E., GEZER U., Cefle K., et al.

FEBS OPEN BIO , vol.16, 2026 (SCI-Expanded, Scopus)

6. Effects of medical mud-pack therapy on inflammatory gene expression and clinical outcomes in patients with knee osteoarthritis

Kahraman M., Karabulut S. S., Gumussu K., Bozdogan Polat S. H., Sahin A., Misirlioglu F. N., et al.

INTERNATIONAL JOURNAL OF BIOMETEOROLOGY , vol.70, no.8, 2026 (SCI-Expanded, Scopus)

7. Search for long-lived charginos and τ-sleptons using final states with a disappearing track in pp collisions at s=13 TeV with the ATLAS detector

Aad G., Aakvaag E., Abbott B., Abdelhameed S., Abeling K., Abicht N., et al.

Journal of High Energy Physics , vol.2026, no.7, 2026 (SCI-Expanded, Scopus)

8. Cytogenetic Diversity of Variant Philadelphia Translocations in Chronic Myeloid Leukemia

Tokac A. G., Aday A., Erdem S., Bagatir G., Don B., Ozcan O., et al.

INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY , 2026 (SCI-Expanded, Scopus)

9. Regulatory Role of miR-15a-5p and miR-16-5p in Suppressing Acute Myeloid Leukemia Cell Growth through Target Gene Interaction Name

Teomete Ş., Kaya M., Suer İ., Çefle K., Palanduz Ş., Öztürk Ş.

DUZCE MEDICAL JOURNAL , vol.28, no.1, pp.84-92, 2026 (ESCI, Scopus, TRDizin)

10. Efficacy of synchronized diabetes monitoring system in patients with type 2 diabetes: Preliminary results of a pilot, randomized clinical trial

Kahraman M., Mutlu U., Ozbek H. E., Boz E. B., Cakmak R., Kurt S., et al.

PRIMARY CARE DIABETES , vol.20, no.1, pp.36-46, 2026 (SCI-Expanded, Scopus)

11. EVALUATION OF GENETIC TESTING IN ADULT PATIENTS WITH SUSPECTED SYSTEMIC AUTOINFLAMMATORY DISORDERS

Amikishiyev S., Engin Y. A., KALAYCI T., Soltanova L., YALÇINKAYA Y., ARTIM ESEN B., et al.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , vol.89, no.1, pp.70-81, 2026 (ESCI, Scopus, TRDizin) Sustainable Development

12. Genetic Insights into Persistent Hypouricemia in Adults: Novel Findings from an Adult Nephrogenetic Clinic

Dirim A. B., Suer İ., Kalaycı T., Tahillioglu Y., Safak S., Ucar A. R., et al.

KIDNEY DISEASES , vol.12, no.1, pp.622-634, 2026 (SCI-Expanded, Scopus) Sustainable Development

13. INVESTIGATION OF CYTOGENETIC ABNORMALITIES IN NEWLY DIAGNOSED MULTIPLE MYELOMA PATIENTS BY OPTICAL GENOME MAPPING

Guney D. K., BAYRAK TOKAÇ A. G., ADAY A., ERDEM S., ÖZTÜRK Ş., BEŞIŞIK S., et al.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , vol.89, no.1, pp.82-90, 2026 (ESCI, Scopus, TRDizin)

14. Investigation of cytogenetic abnormalities in newly diagnosed multiple myeloma patients by optical genome mapping

GÜNEY D. K., BAYRAK TOKAÇ A. G., ADAY A., ERDEM S., ÖZTÜRK Ş., BEŞIŞIK S., et al.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , vol.89, no.1, pp.82-90, 2026 (ESCI, Scopus, TRDizin)

15. Phenotypes of patients with more than one autoinflammatory disease-associated gene variant: overlapping and mixed autoinflammatory disorders

Amikishiyev S., Kalaycı T., Deniz R., Soltanova L., Sen B., Yalçınkaya Y., et al.

RHEUMATOLOGY , 2025 (SCI-Expanded, Scopus)

16. Pilot evaluation of optical genome mapping in chronic lymphocytic leukemia: complementing FISH analysis

Erdem S., Bayrak Tokaç A. G., Aday A., Karaca D., Mutlu M. B., Çefle K., et al.

BMC CANCER , vol.25, no.1, 2025 (SCI-Expanded, Scopus)

17. Curcumin as an Epigenetic Modulator: Suppression of Breast Cancer via the Hsa_circ_0001946/MiR-7-5p/Target Gene Axis

Abuaisha A., Kaya M., Suer İ., Emiroglu S., Bayram A., Tukenmez M., et al.

MEDICINA-LITHUANIA , vol.61, no.9, 2025 (SCI-Expanded, Scopus) Sustainable Development

18. Advances in focal segmental glomerulosclerosis research: genetic causes to non-coding RNAs.

Esmaeilzadeh Aghjeh M., Suer İ., Dirim A. B., Kaya M., Ozturk Ş.

Molecular biology reports , vol.52, no.1, pp.384, 2025 (SCI-Expanded, Scopus)

19. Genetic insights into non-obstructive azoospermia: Implications for diagnosis and TESE outcomes

Sharifi S., DURSUN M., Sahin A., TURAN S., ALTUN A., Ozcan O., et al.

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS , vol.42, no.4, pp.1223-1237, 2025 (SCI-Expanded, Scopus)

20. MiR-7-5p May Inhibit AML Cell Proliferation Via SKP2, KLF4, OGTTarget Genes

Mehteroglu E., SUER İ., KAYA M., ÖZTÜRK Ş., ÇEFLE K., PALANDUZ Ş.

CLINICAL AND EXPERIMENTAL HEALTH SCIENCES , no.1, pp.8-14, 2025 (ESCI, TRDizin) Sustainable Development

21. Two potential regulatory axes in breast cancer patients: hsa_circ_0001546/hsa-miR-532-5p/ZFHX3 and hsa_circ_0025244/hsa-miR-210-5p/BTG2

Abanoz F., Suer İ., Kaya M., Abuaisha A., Emiroğlu S., Öztürk Ş.

CUKUROVA MEDICAL JOURNAL , vol.50, no.3, pp.782-795, 2025 (ESCI, TRDizin)

22. Let-7b-5p sensitizes breast cancer cells to doxorubicin through Aurora Kinase B

Kaya M., Abuaisha A., Suer İ., Emiroglu S., Önder S., Onay Ucar E., et al.

PLOS ONE , vol.20, no.1, 2025 (SCI-Expanded, Scopus) Sustainable Development

23. Enhanced Expression of miR-638-5p May Suppress Acute Myeloid Leukemia in vitro Cell Proliferation Through PGK1 and PIM1

Ozkaynak S. O., SUER İ., KAYA M., ÖZTÜRK Ş.

KONURALP TIP DERGISI , vol.17, no.1, pp.39-47, 2025 (ESCI, TRDizin) Sustainable Development

24. In Silico and In Vitro Analysis of the Regulatory Role of miR-145-5p on Its Potential Target Genes in Acute Myeloid Leukemia Cell Lines

Aslan R., Kaya M., Suer İ., Çefle K., Öztürk Ş.

EXPERIMED , vol.15, no.3, pp.252-260, 2025 (ESCI, Scopus, TRDizin)

25. Elevated expression of let-7b-3p enhances aggressiveness of Larynx Squamous Cell Carcinoma Cells

Kaya M., Güzel Tanoğlu E., Suer İ., Öztürk Ş., Palanduz Ş., Çefle K., et al.

Anatolian Current Medical Journal , vol.7, no.1, pp.27-32, 2025 (TRDizin)

26. Synchronized Diabetes Monitoring System: Development of Smart Mobile Apparatus for Diabetes Using Insulin

Kahraman M., Düdükçü H. V., Kurt S., Yıldız H., Aydın N., Mutlu Ü., et al.

IRBM , vol.45, no.5, 2024 (SCI-Expanded, Scopus) Sustainable Development

27. Curcumin suppresses cell viability in breast cancer cell line by affecting the expression of miR-15a-5p

Suer İ., Abuaisha A., Kaya M., Abanoz F., Çefle K., Palanduz Ş., et al.

TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI , vol.49, no.5, pp.656-665, 2024 (SCI-Expanded, Scopus) Sustainable Development

28. Akut Miyeloid Lösemi’li Olgularda inv(3)/t(3;3) ile 7.Kromozomun Anomalilerinin Prognoza Etkisi

BAYRAK TOKAÇ A. G., BAĞATIR G., ERDEM S., ÇEFLE K., ÖZTÜRK Ş., YENEREL M. N., et al.

Manisa Celal Bayar Üniversitesi Eğitim Fakültesi Dergisi , vol.11, pp.334-339, 2024 (TRDizin)

29. Overexpression of CDC25A, AURKB, and TOP2A Genes Could Be an Important Clue for Luminal A Breast Cancer.

Kaya M., Abuaisha A., Süer İ., Alptekin M. S., Abanoz F., Emiroğlu S., et al.

European journal of breast health , vol.20, no.4, pp.284-291, 2024 (ESCI, Scopus, TRDizin) Sustainable Development

30. EFFECT of CURCUMIN on BREAST CANCER CELLS THROUGH miR-145-5p AND ITS TARGET GENES

Abuaisha A., Kaya M., Suer İ., Emiroğlu S., Abanoz F., Palanduz Ş., et al.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , no.3, pp.235-245, 2024 (ESCI, TRDizin) Sustainable Development

31. A CLASTOGENICITY STUDY WITH MITOMYCIN-C IN APLASTIC ANEMIA: DISTINGUISHING FANCONI ANEMIA APLASTİK ANEMİDE MİTOMİSİN-C İLE BİR KLASTOJENİTE ÇALIŞMASI: FANKONİ ANEMİSİNİ AYIRT ETME

Bağatir G., Karakaş Z., Öztürk Ş., Tokaç A. G., Çefle K., Ünüvar A., et al.

Nobel Medicus , vol.20, no.2, pp.135-140, 2024 (ESCI, Scopus)

32. A CLASTOGENICITY STUDY WITH DISTINGUISHING FANCONI ANEMIA

Bagatir G., ÖZTÜRK Ş., BAYRAK TOKAÇ A. G., ÇEFLE K., ÜNÜVAR A., KARAKAŞ Z., et al.

NOBEL MEDICUS , no.2, pp.135-140, 2024 (ESCI, Scopus) Sustainable Development

33. A CLASTOGENICITY STUDY WITH MITOMYCIN-C IN APLASTIC ANEMIA: DISTINGUISHING FANCONI ANEMIA

Bağatir G., Öztürk Ş., Tokuç A. G. B., Çefle K., Ünüvar A., Karakaş Z., et al.

NOBEL MEDICUS , vol.20, no.2, pp.135-140, 2024 (ESCI, Scopus)

34. Bioinformatics analysis of the potentially functional circRNA-miRNA-mRNA network in breast cancer.

Erdogan C., Suer İ., Kaya M., Ozturk Ş., Aydin N., Kurt Z.

PloS one , vol.19, no.4, 2024 (SCI-Expanded, Scopus) Sustainable Development

35. Turmeric Inhibits MDA-MB-231 Cancer Cell Proliferation, Altering miR-638-5p and Its Potential Targets

Kaya M., Abuaisha A., Suer İ., Emiroglu S., Abanoz F., Palanduz S., et al.

EUROPEAN JOURNAL OF BREAST HEALTH , vol.20, no.2, pp.102-109, 2024 (ESCI, Scopus, TRDizin) Sustainable Development

36. Expression Patterns of Eighteen Genes Involved in Crucial Cellular Processes in the TP53 Pathway in Multiple Myeloma

Öztan G., Suer İ., Aday A., Ayer M., Öztürk Ş., Çefle K., et al.

GAZI UNIVERSITY JOURNAL OF SCIENCE , vol.37, no.3, pp.1066-1082, 2024 (ESCI, Scopus, TRDizin) Sustainable Development

37. Clastogenicity Study with Mitomycin-C in Aplastic Anemia: Distinguishing Fanconi Anemia

Bağatır G., Öztürk Ş., Tokaç Bayrak A. G., Çefle K., Ünüvar A., Karakaş Z., et al.

, vol.2, no.3, pp.35-45, 2024 (Peer-Reviewed Journal)

38. 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, Scopus) Sustainable Development

39. **Late diagnosis of a rare multisystemic genetic disorder: Transaldolase deficiency due to homozygous TALDO1 c.345dupA variant**

Dirim A. B., Kalayci T., Safak S., Garayeva Guller N., Oto Ö. A., Artan A. S., et al.

NEPHROLOGY , vol.29, no.1, pp.55-56, 2024 (SCI-Expanded, Scopus) Sustainable Development

40. **miR-145-5p suppresses cell proliferation by targeting IGF1R and NRAS genes in multiple myeloma cells**

Kaya M., Suer İ., Ozgur E., Capik O., Karatas O. F., Ozturk Ş., et al.

TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI , vol.48, no.5, pp.563-569, 2023 (SCI-Expanded, Scopus) Sustainable Development

41. Phenotypes of the Patients with More Than One Autoinflammatory Gene Variant: Classified Diseases and Mixed Autoinflammatory Disorders (MAID)

Amıkıshıyev S., Kalaycı T., Soltanova L., Yalçınkaya Y., Artim-Esen B., İnanç M., et al.

ARTHRITIS & RHEUMATOLOGY , pp.506-508, 2023 (SCI-Expanded, Scopus)

42. **Clinical Features of the Patients with NLRP1 Gene Variants and a Systemic Autoinflammatory Phenotype**

AMIKISHIYEV S., KALAYCI T., Deniz R., YALÇINKAYA Y., ARTIM ESEN B., İNANÇ M., et al.

ARTHRITIS & RHEUMATOLOGY , pp.3800-3802, 2023 (SCI-Expanded, Scopus)

43. Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature.

Dirim A. B., Kalayci T., Safak S., Garayeva N., Gultekin B., Hurdogan Ö., et al.

Clinical rheumatology , vol.42, no.2, pp.597-606, 2023 (SCI-Expanded, Scopus)

44. Evaluation of TMED9, DNAJC1, LMAN2, COPE and KDELR1 Biomarkers in Patients with Monoclonal Gammopathy of Undetermined Significance and Multiple Myeloma

Sariman M., Salman Yaylaz B., Yabaci Tak A., Ayer M., Sirma Ekmekci S., Suer İ., et al.

UHOD - Uluslararasi Hematoloji-Onkoloji Dergisi , vol.33, no.2, pp.92-102, 2023 (SCI-Expanded, Scopus) Sustainable Development

45. Cytogenetic and molecular characterization of a patient having infertility and mild intellectual disability with a very rare unstable ring chromosome 13

Kaya M., Suer İ., Kalayci T., Karaman B., Ozturk Ş., Palanduz Ş.

SCOTTISH MEDICAL JOURNAL , vol.67, no.4, pp.173-177, 2022 (SCI-Expanded, Scopus)

46. The effect of Anzer honey on X-ray induced genotoxicity in human lymphocytes: An in vitro study

Bagatir G., Kaya M., Suer İ., Çefle K., Palanduz A., Palanduz Ş., et al.

MICROSCOPY RESEARCH AND TECHNIQUE , vol.85, no.6, pp.2241-2250, 2022 (SCI-Expanded, Scopus) Sustainable Development

47. 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, Scopus)

48. Is there a relationship between ACTN3 R577X gene polymorphism and sarcopenia?

Kahraman M., Ozulu Turkmen B., Bahat-Ozturk G., Catikkas N. M., Oren M. M., Sahin A., et al.

AGING CLINICAL AND EXPERIMENTAL RESEARCH , vol.34, no.4, pp.757-765, 2022 (SCI-Expanded, Scopus)

49. ERAP1 Gen İfadesinin Plazma Hücre Diskrazilerinde İncelenmesi

Sariman M., KARAÇAM B., Ayer M., SIRMA EKMEKCİ S., SUER İ., ÇEFLE K., et al.

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

50. Overview of clinical and genetic features of CML patients with variant Philadelphia translocations involving chromosome 7: A case series

Bayrak A. G., Daglar Aday A., Yavuz A. S., Nalcaci M., Ozbalak M. M., Cefle K., et al.

LEUKEMIA RESEARCH , vol.111, 2021 (SCI-Expanded, Scopus)

51. 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, Scopus, TRDizin)

52. Vaccine Passport Use and Travel Health Status Among Turkish Travelers at an International Airport

Kahraman M., Yuksel I., Boz E. B., Ozbek H. E., Mert E., Reyhanli A., et al.

International Journal of Travel Medicine and Global Health , no.9, pp.161-169, 2021 (Peer-Reviewed Journal)

53. THE EFFECT OF SMARTPHONE APPS AND TECHNOLOGY COMPATIBILITY ON DIABETES CONTROL IN DIABETIC PATIENTS USING INSULIN

Kahraman M., Cakmak R., Satman İ., Karşıdağ K., Öztürk Ş., Ören M. M., et al.

JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI , vol.84, no.4, pp.543-551, 2021 (ESCI, TRDizin)

54. Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey

Berkay E. G., Elkanova L., Kalayci T., ULUDAĞ ALKAYA D., Altunoglu U., Cefle K., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.185, no.8, pp.2488-2495, 2021 (SCI-Expanded, Scopus)

55. 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)

56. miR-145 suppresses epithelial-mesenchymal transition by targeting stem cells in Ewing sarcoma cells

Tanoglu E. G., Ozturk S.

BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY , vol.122, no.1, pp.71-77, 2021 (SCI-Expanded, Scopus)

57. Dysregulation of MS4A3 and PRDX5 Gene Expression in Multiple Myeloma Patients

Suer İ., Aday A., Sariman M., Ayer M., Hindilerden I. Y., Ekmekci S. S., et al.

UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI , vol.31, no.4, pp.205-213, 2021 (SCI-Expanded, Scopus) Sustainable Development

58. Potential therapeutic road for targeting the SARS-CoV-2 at throat

Kaya M., Abuaisha A. M., Serakinci N., Ozturk S.

BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY , vol.122, no.3, pp.206-211, 2021 (SCI-Expanded, Scopus) Sustainable Development

59. Mir-129-2-3p Has Tumor Suppressor Role in Ewing Sarcoma Cell Lines and Cancer Tissue Samples

Tanoglu E. G., Arikan Y., Kabukcuoglu Y. S., Kabukcuoglu F., Tanoglu A., Ozturk S.

BRAZILIAN ARCHIVES OF BIOLOGY AND TECHNOLOGY , vol.64, 2021 (SCI-Expanded, Scopus) Sustainable Development

60. 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, Scopus)

61. De novo t(1;6)(p13p21.3) Dengeli Resiprokal Translokasyonun İnfertilite ile İlişkisi

Kaya M., Bağatır Ozan G., Çefle K., Öztürk Ş., Palanduz Ş.

Sağlık bilimlerinde değer (Online) , vol.10, no.1, pp.108-110, 2020 (Peer-Reviewed Journal)

62. Ewing Sarkoma ile Primitif Nöroektodermal Tümör HücreHatlarında Agresiflik Paterninin Karşılaştırılması

GÜZEL TANOĞLU E., ÖZTÜRK Ş.

Kocaeli Tıp Dergisi , vol.9, no.1, pp.24-31, 2020 (TRDizin)

63. DNA damage effects of inhalation anesthetics in human bronchoalveolar cells

ÇUKUROVA Z., Cetingok H., Ozturk S., Gedikbasi A., HERGÜNSEL O., Ozturk D., et al.

MEDICINE , vol.98, no.32, 2019 (SCI-Expanded, Scopus)

64. 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 (TRDizin)

65. Case Report: a novel chromosomal insertion, 46, XY, inv ins(18;2)(q11.2;q13q22), in a patient with infertility and mild intellectual disability.

Kaya M., Suer İ., Öztürk Ş., ÇEFLE K., Karaman B., Palanduz Ş.

F1000Research , vol.8, pp.281, 2019 (Scopus)

66. Investigation of Gene Expressions of Myeloma Cells in the Bone Marrow of Multiple Myeloma Patients by Transcriptome Analysis

Sariman M., Abaci N., Ekmekci S., Cakiris A., Pacal F., Ustek D., et al.

Balkan medical journal , vol.36, no.1, pp.23-31, 2019 (SCI-Expanded, Scopus, TRDizin)

67. 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, Scopus, TRDizin)

68. Ailevi Akdeniz Ateşinde Moleküler Tanı Deneyimi: MEFV Geninde Sık Görülen Mutasyonlar

Coşkunpınar E., Özvarnalı A., Çefle K., PALANDUZ A., GÜL A., Öztürk D., et al.

HASEKİ TIP BÜLTENİ , vol.56, no.1, pp.42-49, 2018 (Scopus, TRDizin)

69. Molecular Diagnosis Experience in Familial Mediterranean Fever: The Most Frequent Mutations in the MEFV Gene

Coskunpinar E., Ozvarnali A., Cefle K., Palanduz A., Gül A., Ozturk D., et al.

HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI , vol.56, no.1, pp.42-49, 2018 (ESCI, Scopus, TRDizin)

70. Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus

Kurklu E., Ozturk S., Cassidy A. J., Ak G., Koray M., Cefle K., et al.

MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL , no.2, 2018 (SCI-Expanded, Scopus)

71. REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis

BAYRAM Y., WHITE J. J., Elcioglu N., CHO M. T., ZADEH N., Gedikbasi A., et al.

AMERICAN JOURNAL OF HUMAN GENETICS , vol.101, no.1, pp.149-156, 2017 (SCI-Expanded, Scopus)

72. Roles of Signal Transducer Pathways in Investigation of Biopsies from Patients with Bladder Tumors

Bayrak A. G., Palanduz S., Coskunpinar E., Sanli O., Armagan A., Karakus S., et al.

Asian Pacific journal of cancer prevention : APJCP , vol.18, no.1, pp.201-205, 2017 (SCI-Expanded, Scopus)

73. 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, Scopus)

74. The frequency of C609T polymorphism in the NQO1 gene and its relation to cytogenetic abnormalities in patients with myelodysplastic syndrome.

Bagatır G., Sırma S. Ö., Palanduz S., Ozturk Ş., Cefle K., Ozbek U., et al.

Cellular and molecular biology (Noisy-le-Grand, France) , vol.62, no.7, pp.61-5, 2016 (SCI-Expanded, Scopus)

75. Yeni Nesil Dizileme Teknolojisi Ile Transkriptom Analizi

Sarıman M., Sırma Ekmekci S., Abacı N., Çakiris A., Paçal F., Emrence Z., et al.

Deneysel Tıp Dergisi , vol.5, no.10, pp.51-59, 2015 (Peer-Reviewed Journal)

76. Transcriptom Analysis Using Next Generation Sequencing

Sarıman M., EKMEKCI S. S., ABACI N., ÇAKİRİS A., PAÇAL F., EMRENCE Z., et al.

Deneysel Tıp Araştırma Enstitüsü Dergisi , vol.4, no.10, pp.51-59, 2015 (Peer-Reviewed Journal)

77. Mutations in RAD21 Disrupt Regulation of APOB in Patients With Chronic Intestinal Pseudo-Obstruction

BONORA E., BIANCO F., Cordeddu L., Bamshad M., Francescatto L., Dowless D., et al.

GASTROENTEROLOGY , vol.148, no.4, pp.771-793, 2015 (SCI-Expanded, Scopus)

78. The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

Ozantürk A., Marshall J. D., Collin G. B., Düzenli S., Marshall R. P., Candan Ş., et al.

Journal of Human Genetics , vol.60, no.1, pp.1-9, 2015 (SCI-Expanded, Scopus)

79. Yeni Nesil Dizileme Teknolojisi İle Transkriptom Analizi

sarıman m., SIRMA EKMEKCİ S., ABACI N., ÇAKİRİS A., paçal f., EMRENCE Z., et al.

iDeneysel Tıp Araştırma Enstitüsü Dergisi , vol.5, no.10, pp.51-59, 2015 (Peer-Reviewed Journal)

80. 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, Scopus, TRDizin)

81. 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, Scopus)

82. A novel two bases deletion in the albumin gene causes analbuminaemia in a young Turkish man.

CARIDI G., DAGNINO M., Di D., AKYÜZ F., BOZTAS G., BESISIK F., et al.

Clinica chimica acta; international journal of clinical chemistry , vol.413, no.9-10, pp.950-1, 2012 (SCI-Expanded, Scopus)

83. 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, Scopus) Sustainable Development

84. Multidisciplinary treatment of non-syndromic oligodontia

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

European Journal of Dentistry , vol.6, no.2, pp.218-226, 2012 (Scopus)

85. Outcome of Kidney Transplantation Following End-Stage Renal Disease Due to Reflux Nephropathy

Yazici H., Caliskan Y., Ozturk S., Ozkan O., Turkmen A., Sever M. S.

TRANSPLANTATION PROCEEDINGS , vol.43, no.5, pp.1566-1569, 2011 (SCI-Expanded, Scopus)

86. 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, Scopus)

87. 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, Scopus)

88. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

Friedrich K., Lee L., Leistritz D. F., Nuernberg G., Saha B., Hisama F. M., et al.

HUMAN GENETICS , vol.128, no.1, pp.103-111, 2010 (SCI-Expanded, Scopus)

89. 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, Scopus)

90. A POSSIBLE DELETERIOUS EFFECT OF INCREASED SERUM COPPER ON MYOCARDIAL FUNCTION IN PATIENTS WITH DILATED CARDIOMYOPATHY AWAITING TRANSPLANTATION

Cefle K., Ercag E., Gezertas S., Uzer A., Oeztuerk Ş., Cefle A., et al.

NOBEL MEDICUS , vol.6, no.2, pp.32-36, 2010 (SCI-Expanded, Scopus)

91. Cytogenetic Analysis and Examination of SOS1 Gene Mutation in a Turkish Family with Hereditary Gingival Fibromatosis

Pehlivan D., Abe S., Ozturk S., Kayhan K., Gunduz E., Cefle K., et al.

JOURNAL OF HARD TISSUE BIOLOGY , vol.18, no.3, pp.131-134, 2009 (SCI-Expanded, Scopus)

92. 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, Scopus)

93. 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, Scopus)

94. 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, Scopus)

95. ARTERIAL OBSTRUCTION IN A KLINEFELTER SYNDROME PATIENT WITH RARE KARYOTYPE (48, XXYY)

Pehlivan D., Cefle K., Ozturk S., Akbulut M. F., Palazduz S.

TURKISH JOURNAL OF UROLOGY , vol.34, no.4, pp.491-494, 2008 (ESCI, Scopus, TRDizin)

96. 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, Scopus) Sustainable Development

97. The effects of etodolac, nimesulid and naproxen sodium on the frequency of sister chromatid exchange after enclused third molars surgery.

Koeseoglu B., Oeztuerk Ş., Kocak H., Palanduz S., Cefle K.

Yonsei medical journal , vol.49, no.5, pp.742-7, 2008 (SCI-Expanded, Scopus)

98. 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, Scopus)

99. Effect of Cyclosporin A and Tacrolimus on sister chromatid exchange frequency in renal transplant patients

Ozturk Ş., Ayna T. K., Cefle K., Palanduz S., Ciftci H., Kaya Ş., et al.

GENETIC TESTING , vol.12, no.3, pp.427-430, 2008 (SCI-Expanded, Scopus)

100. 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, Scopus)

101. 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, TRDizin)

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

Dinçol G., Aktan M., Diz-Küçükkaya R., Yavuz S., Nalçaci M., Öztürk Ş., et al.

American Journal of Hematology , vol.82, no.9, pp.783-786, 2007 (SCI-Expanded, Scopus)

103. 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, Scopus) Sustainable Development

104. 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, Scopus)

105. 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, Scopus)

106. Monitoring the genotoxic effects of radiosynovectomy with Re-186 in paediatric age group undergoing therapy for haemophilic synovitis

Turkmen C., Ozturk Ş., Unal N., Zulfikar B., Taser O., Sanli Y., et al.

HAEMOPHILIA , vol.13, no.1, pp.57-64, 2007 (SCI-Expanded, Scopus)

107. 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, Scopus)

108. Werner syndrome associated with renal involvement

KOCABAY G., Ozturk S., ECDER T.

SAUDI MEDICAL JOURNAL , vol.27, no.11, pp.1768-1769, 2006 (SCI-Expanded, Scopus)

109. 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, Scopus) Sustainable Development

110. Increased sister chromatid exchange frequency in young women with breast cancer and in their first-degree relatives.

Cefle K., Ucur A., Guney N., Ozturk S., Palanduz S., Tas F., et al.

Cancer genetics and cytogenetics , vol.171, pp.65-7, 2006 (SCI-Expanded, Scopus) Sustainable Development

111. 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, Scopus) Sustainable Development

112. 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, Scopus)

113. 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, Scopus)

114. 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, Scopus) Sustainable Development

115. 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, Scopus)

116. 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, Scopus)

117. 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, Scopus)

118. 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, Scopus)

119. 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, Scopus)

120. 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, Scopus) Sustainable Development

121. 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, Scopus)

122. Familial visceral myopathy with pseudo-obstruction, megaduodenum, Barrett's esophagus, and cardiac abnormalities

MUNGAN Z., AKYUZ F., Bugra Z., YONAL O., OZTURK S., ACAR A., et al.

AMERICAN JOURNAL OF GASTROENTEROLOGY , vol.98, no.11, pp.2556-2560, 2003 (SCI-Expanded, Scopus)

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

Ucur A., Palanduz S., Cefle K., Ozturk Ş., Tutkan G., Vatansever S., et al.

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

124. 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, Scopus) Sustainable Development

125. The diagnostic value of troponin T and myoglobin levels in acute myocardial infarction: A study in Turkish patients

Vatansever S., Akkaya V., Erk O., Ozturk S., Karan M., Salmayeni N., et al.

JOURNAL OF INTERNATIONAL MEDICAL RESEARCH , vol.31, no.2, pp.76-83, 2003 (SCI-Expanded, Scopus)

126. A patient with metachronous gastric, colonic, and thyroid cancers: A case report

Oncel M., Kurt N., Altuntas Y., Ozturk S., Ozdemir N., Bahadir I.

INTERNATIONAL SURGERY , vol.88, no.1, pp.1-5, 2003 (SCI-Expanded, Scopus) Sustainable Development

127. 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, Scopus)

128. 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, Scopus)

129. 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, Scopus)

130. 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, Scopus) Sustainable Development

131. 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, Scopus)

132. 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, Scopus) Sustainable Development

133. 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, Scopus)

134. A case of Noonan syndrome with pulmonary and abdominal lymphangiectasia

Ozturk Ş., Cefle K., Palanduz S., Erten N., Karan M., Tascioglu C., et al.

INTERNATIONAL JOURNAL OF CLINICAL PRACTICE , vol.54, no.4, pp.274-276, 2000 (SCI-Expanded, Scopus)

135. 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, Scopus)

136. 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, Scopus)

137. 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)

138. 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, Scopus)

139. 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, Scopus)

140. Two sisters with hereditary multiple exositosis

Palanduz Ş., Öztürk Ş., Palanduz A., Çefle K., Erden S., Odabaş A. R., et al.

Medical Bulletin of Istanbul Medical Faculty , vol.32, no.2, pp.196-199, 1999 (Peer-Reviewed Journal)

141. 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)

142. 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, Scopus)

143. Hallerman-streiff sendromlu bir olgu

Palanduz Ş., Çefle K., Öztürk Ş., Kudat H.

İstanbul Üniversitesi İstanbul Tıp Fakültesi Mecmuası , vol.61, no.3, pp.399-403, 1998 (TRDizin)

144. In vitro chromosomal radiosensitivity in common variable immune deficiency

Palanduz S., Palanduz A., Yalcin I., Somer A., Ones U., Ustek D., et al.

CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY , no.2, pp.180-182, 1998 (SCI-Expanded) Sustainable Development

145. 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, Scopus)

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

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

Türk Tıp Derneği Dergisi , vol.60, pp.49-57, 1994 (Peer-Reviewed Journal)

Papers Presented at Peer-Reviewed Scientific Conferences 127

1. Exploring Ferroptosis-Related Gene Variants in Focal Segmental Glomerulosclerosis

Aday A., Kaya M., Suer İ., Kalaycı T., Dirim A. B., Esmaeilzadeh Aghjeh M., et al.

XI. Multidisciplinary Cancer Research Congress, İstanbul, Turkey, 2 - 05 July 2026, pp.44, (Summary Text)

2. Renal bir tübülopatiden HELIX sendromuna: Tüm ekzom dizileme ile yeni bir CLDN10 varyantının tanımlanması

Çefle K., Kalaycı T., Suer İ., Dirim A. B., Aday A., Kaya M., et al.

İstanbul Tıp Fakültesi Geleneksel İç Hastalıkları Günleri İnteraktif Güncelleştirme 2026, Sakarya, Turkey, 2 - 05 April 2026, pp.9, (Summary Text)

3. Norrie Disease due to a Hemizygous NDP Gene Variant: A Case Report of a 20-Year-Old Male

Aktaş Ç., Suer İ., Kaya M., Kalaycı T., Dirim A. B., Çefle K., et al.

20th International Hippocrates Congress on Medical and Health Sciences, İstanbul, Turkey, 19 - 20 December 2025, pp.186-191, (Full Text)

4. A novel compound heterozygous COL4A4 variant in a 24-year-old Alport syndrome case

Nazligul E., SUER İ., Kaya M., KALAYCI T., DİRİM A. B., ÇEFLE K., et al.

14. ULUSAL MOLEKÜLER BİYOLOJİ VE BİYOTEKNOLOJİ KONGRESİ, 1 - 02 November 2025, pp.124-130, (Full Text)

5. Norrie Disease due to a Hemizygous NDP Gene Variant: A Case Report of a 20-Year-Old Male

Aktaş Ç., SUER İ., Kaya M., KALAYCI T., ÇEFLE K., ÖZTÜRK Ş.

20. Uluslararası Hipokrat Tıp ve Sağlık Bilimleri Kongresi, 19 - 20 December 2025, (Full Text)

6. A novel compound heterozygous COL4A4 variant in a 24-year-old Alport syndrome case

Nazlıgül E., Suer İ., Kaya M., Kalaycı T., Dirim A. B., Çefle K., et al.

14. Ulusal Moleküler Biyoloji ve Biyoteknoloji Kongresi, Konya, Turkey, 1 - 02 November 2025, pp.124-130, (Full Text)

7. Identification of a Novel Variant in the PODXL Gene in a Turkish Family With Focal Segmental Glomerulosclerosis

Aghjeh M. E., Suer İ., Kalaycı T., Dirim A. B., Kaya M., Öztürk Ş.

9th International Congress on Biomedicine, Tehran, Iran, 10 - 19 November 2025, pp.572-573, (Summary Text)

8. Identification of a novel variant in the PODXL gene in a Turkish family with focal segmental glomerulosclerosis

Esmaeilzadeh Aghjeh M., SUER İ., KALAYCI T., DİRİM A. B., Kaya M., ÖZTÜRK Ş.

9th International Congress on Biomedicine, Iran, 10 - 19 November 2025, (Summary Text)

9. Multipl Miyelom'da Genetik Karmaşa: Optik Genom Haritalamanın Yeri

BAYRAK TOKAÇ A. G., ERDEM S., ADAY A., MUTLU M. B., GÜNEY D. K., MASTANZADE M., et al.

12. Hematolojik Onkoloji Kongresi, KKTC, Turkey, 02 October 2025, pp.134-137, (Summary Text)

10. Kronik Lenfositik Lösemide Optik Genom Haritalamanın FISH Analizine Tamamlayıcı Rolü: Tek Merkez Pilot Çalışma

ERDEM S., BAYRAK TOKAÇ A. G., ADAY A., KARACA D., MUTLU M. B., ÇEFLE K., et al.

51. ULUSAL HEMATOLOJİ KONGRESİ, Antalya, Turkey, 28 October - 02 November 2025, pp.121-122, (Summary Text)

11. Genetic insights into persistent hypouricemia in adults: novel findings from a nephrogenetic clinic

Dirim A. B., Şafak S., Tahıllıoğlu Y., Mirioğlu Ş., Artan A. S., Oto Ö. A., et al.

62nd ERA Congress, Vienna, Austria, 4 - 07 June 2025, vol.40, pp.1886-1887, (Summary Text)

12. STUB1 expression as a diagnostic biomarker and its association with drug resistance in multiple myeloma

Punar Ş., Sarıman M., Ayer M., Suer İ., Çefle K., Öztürk Ş., et al.

European Society of Human Genetics Conference (ESHG), Milan, Italy, 24 - 27 May 2025, pp.1-2, (Summary Text)

13. 47,XXX (Triple X sendromu) olgusunda tekrarlayan gebelik kaybı

Engüleç İ., Kuntsal E., Kaya M., SUER İ., ÖZTÜRK Ş., ÇEFLE K.

Başakşehir Çam ve Sakura Şehir Hastanesi 3. Kadın Doğum Günleri Kongresi, İstanbul, Turkey, 10 - 13 April 2025, pp.116-120, (Full Text)

14. STUB1 expression as a diagnostic biomarker and its association with drug resistance in multiple myeloma.

Punar Ş., Sariman M., AYER M., SUER İ., ÇEFLE K., ÖZTÜRK Ş., et al.

European Society of Human Genetics Conference (ESHG), Milan, Italy, 24 May 2025, (Summary Text)

15. Assessment of the clinical diagnostic potential of NGS-based panel tests in100 cases with renal disease pre-diagnoses

SUER İ., KALAYCI T., DİRİM A. B., Şafak S., SIRMA EKMEKCİ S., Kaya M., et al.

European Society of Human Genetics Conference (ESHG), Milan, Italy, 24 May 2025, (Summary Text)

16. Genetic insights into non-obstructive azoospermia: Identifying novel variants and enhancing clinical outcomes

Sharifi S., Dursun M., Şahin A., Altun A., Turan S., Özcan Ö., et al.

40th Annual EAU Congress, Madrid, Spain, 21 - 24 March 2025, pp.87, (Summary Text)

17. Association of MiR-145-5p with CDK6, IRS1, and UHRF1 as Potential Target Oncogenes in Breast Cancer

Engüleç İ., Abuaisha A., Kaya M., Suer İ., Öztürk Ş.

3rd International Congress of Medical and Health Sciences Research, Ankara, Turkey, 13 - 14 December 2024, vol.1, pp.291-303, (Full Text)

18. Association of MiR-145-5p with CDK6, IRS1, and UHRF1 as Potential Target Oncogenes in Breast Cancer

Engüleç İ., Abuaisha A., Kaya M., Suer İ., Öztürk Ş.

3rd International Congress of Medical and Health Sciences Research, Ankara, Turkey, 13 - 14 December 2024, pp.291-303, (Full Text)

19. Optical Genome Mapping in Newly Diagnosed Chronic Lymphocytic Leukemia

ERDEM S., BAYRAK TOKAÇ A. G., ADAY A., KARACA D., ÖZTÜRK Ş., ÇEFLE K., et al.

66th ASH Annual Meeting and Exposition, San Diego, CA, United States Of America, 7 - 10 December 2024, pp.6758, (Summary Text)

20. A Novel FBN1 Variant in A Large Marfan Family with High Penetrance of Aortic Features

ERBİLGİN Y., ÇEFLE K., ÖZTÜRK Ş., Soltanova L., KADIOĞLU P., Kocaaga S., et al.

57th Conference of the European-Society-of-Human-Genetics (ESHG), Berlin, Germany, 1 - 04 June 2024, vol.32, pp.990, (Summary Text)

21. DE NOVO 46,XX,t(5;7)(p15.2;q11.2) VE 46,XX,t(1;9)(q23;q21) DENGELİ RESIPROKAL TRANSLOKASYONLARI VE HABITUEL ABORTUS İLİŞKİSİ

Alptekin M. S., Kaya M., SUER İ., ÇEFLE K., ÖZTÜRK Ş.

17th International Medical and Health Sciences Research Congress, 19 - 20 October 2024, (Full Text)

22. inv(5)(q15q33) in both parents associated with recurrent pregnancy loss

Kuntsal E., SUER İ., Kaya M., KALAYCI T., ÖZTÜRK Ş., ÇEFLE K.

10th Congress of South East European Society of Perinatal Medicine (SEESPM), İstanbul, Turkey, 23 - 26 October 2024, vol.1, pp.77-79, (Summary Text)

23. De Novo 46,XX,t(5;7)(p15.2;q11.2) ve 46,XX,t(1;9)(q23;q21) Dengeli Resiprokal Translokasyonları ve Habituel Abortus İlişkisi

Alptekin M. S., Kaya M., Suer İ., Çefle K., Öztürk Ş.

17. Uluslararası Tıp ve Sağlık Bilimleri Araştırmaları Kongresi, Ankara, Turkey, 19 - 20 October 2024, pp.172-176, (Full Text)

24. Akut miyeloid lösemi hücrelerinde EIF4E, PIM1 ve IGF1R ekspresyonunun miRNA aracılı baskılanması

Kaya M., SUER İ., ÇEFLE K., ÖZTÜRK Ş.

26. Ulusal İç Hastalıkları Kongresi, Cyprus (Kktc), 2 - 06 October 2024, (Summary Text)

25. A Novel FBN1 Variant in A Large Marfan Family with High Penetrance of Aortic Features

ERBİLGİN Y., ÇEFLE K., ÖZTÜRK Ş., EKIJI L., KADIOĞLU P., Kocaağa S., et al.

Avrupa İnsan Genetiği Kongresi 2024, Berlin, Germany, 01 June 2024, (Summary Text)

26. Integrated Multi-Omics Approach for Investigating Molecular Insights into Non-Obstructive Azoospermia and Association with Potential Cancer Susceptibility

Sharifi S., Dursun M., Şahin A., Özcan Ö., Turan S., Kadıoğlu A., et al.

23. Ulusal Androloji Kongresi, Eskişehir, Turkey, 17 - 19 May 2024, pp.22, (Summary Text)

27. GENETIC VARIANTS OF UNCERTAIN SIGNIFICANCE IN DLC1 AND PRLR GENES IN A PURE MUCINOUS BREAST CARCINOMA PATIENT

Abuaisha A., SUER İ., Kaya M., EMİROĞLU S., TÜKENMEZ M., ÖZTÜRK Ş.

TASHKENT INTERNATIONAL CONGRESS ON MODERN SCIENCES-III, Taşkent, Uzbekistan, 22 - 23 April 2024, (Summary Text)

28. Curcumin inhibits breast cancer cell proliferation by regulating ciRS-7/miR-7-5p/CKS2 axis

Abuaisha A., Kaya M., SUER İ., EMİROĞLU S., Abanoz F., TÜKENMEZ M., et al.

San Antonio Breast Cancer Symposium, San-Antonio, Northern Mariana Islands, 5 - 09 December 2023, (Summary Text)

29. Retrospective evaluation of etiology, clinical and laboratory findings in patients diagnosed with secondary and genetic FSGS

Yilmaz A., SULEYMANOVA V., DİRİM A. B., KALAYCI T., ARTAN A. S., OTO Ö. A., et al.

61st Congress of European-Renal-Association (ERA), Stockholm, Sweden, 23 - 26 May 2024, (Summary Text)

30.

Kuntsal E., Suer İ., Kaya M., Bayrak Tokaç A. G., Palanduz Ş., Öztürk Ş., et al.

14th International Medical and Health Sciences Research Congress (UTSAK), Ankara, Turkey, 23 - 24 December 2023, vol.1, pp.586-591, (Full Text)

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

Kuntsal E., SUER İ., Kaya M., Bayrak A. G., PALANDUZ Ş., ÖZTÜRK Ş., et al.

14th International Medical and Health Sciences Research Congress (UTSAK), Ankara, Turkey, 23 - 24 December 2023, vol.1, pp.586-591, (Full Text)

32. Wilson Hastalığında Aile İçi Genetik Taramanın Kliniğe Önemli Katkıları

Şahin A., ÇİFCİBAŞI ÖRMECİ A., SUER İ., DEMİR K., KALAYCI T., ÇEFLE K., et al.

40. Ulusal Gastroenteroloji Haftası ve 11. Gastroenteroloji Cerrahisi Kongresi, Antalya, Turkey, 21 - 26 November 2023, (Summary Text)

33. Herediter Periyodik Ateş Sendromu Düşünülen Hastalarda Ateş Paneli ile Yapılan Genetik İncelemelerin Sonuçları

AMİKİSHİYEV S., KALAYCI T., BEKTAŞ M., ÇETİN Ç., AGHAMURADOV S., YALÇIN DULUNDU B. Ç., et al.

XXII. ULUSAL ROMATOLOJİ KONGRESİ, Antalya, Turkey, 26 - 30 October 2022, pp.128-129, (Summary Text)

34. BLOOD SERUM AND PLASMA WITH STRIKING GREEN COLOR IN BREAST CANCER PATIENTS

Abuaisha A., EMİROĞLU S., Kaya M., SUER İ., CABIOĞLU N., ÖZTÜRK Ş.

International Congress on Innovative Approaches in Medical and Health Sciences, Turkey, 13 - 14 August 2022, pp.514, (Summary Text)

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

Abuaisha A., Kaya M., SUER İ., ÇEFLE K., PALANDUZ Ş., ÖZTÜRK Ş.

7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, İstanbul, Turkey, 26 - 28 May 2022, vol.1, pp.42-43, (Summary Text)

36. miR-16-5p/CCNE1 Relation in AML Cells

Teomete Ş., Kaya M., SUER İ., ÇEFLE K., PALANDUZ Ş., ÖZTÜRK Ş.

VIII. INSAC International Congress on Health Sciences (ICHES-2022), Konya, Turkey, 18 - 20 March 2022, vol.1, pp.116-122, (Full Text) Sustainable Development

37. Senkronize Diyabet Takip Sistemi

KAHRAMAN M., MUTLU Ü., ÇAKMAK R., ERTÜRK M. A., YILDIZ H., KARAN M. A., et al.

58. Ulusal Diyabet Metabolizma ve Beslenme Hastalıkları Kongresi, Antalya, Turkey, 11 May 2022, (Full Text) Sustainable Development

38. Senkronize Diyabet Takip Sistemi

KAHRAMAN M., MUTLU Ü., ÇAKMAK R., ERTÜRK M. A., YILDIZ H., KARAN M. A., et al.

58. Ulusal Diyabet Metabolizma ve Beslenme Hastalıkları Kongresi, Antalya, Turkey, 11 May 2022, (Full Text) Sustainable Development

39. Senkronize Diyabet Takip Sistemi

KAHRAMAN M., MUTLU Ü., ÇAKMAK R., ERTÜRK M. A., YILDIZ H., KARAN M. A., et al.

58. Ulusal Diyabet Metabolizma ve Beslenme Hastalıkları Kongresi, Antalya, Turkey, 11 May 2022, (Full Text) Sustainable Development

40. Senkronize Diyabet Takip Sistemi

KAHRAMAN M., MUTLU Ü., ÇAKMAK R., ERTÜRK M. A., YILDIZ H., KARAN M. A., et al.

58. Ulusal Diyabet Metabolizma ve Beslenme Hastalıkları Kongresi, Antalya, Turkey, 11 May 2022, (Full Text) Sustainable Development

41.

Kahraman M., Mutlu Ü., Çakmak R., Ertürk M. A., Yıldız H., Düdükçü H. V., et al.

58. Ulusal Diyabet Metabolizma ve Beslenme Hastalıkları Kongresi, Antalya, Turkey, 11 - 14 May 2022, pp.294-297, (Summary Text)

42. Senkronize Diyabet Takibi Sistemi

Kahraman M., Mutlu Ü., Çakmak R., Ertürk M. A., Yıldız H., Düdükçü H. V., et al.

58. ULUSAL DİYABET Metabolizma ve Beslenme Hastalıkları KONGRESİ, Antalya, Turkey, 11 - 13 May 2022, pp.294-297, (Full Text)

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

EMİROĞLU S., Abuaisha A., TÜKENMEZ M., Kaya M., SUER İ., BAYRAM A., et al.

4th International Congress on Medical Sciences and Multidisciplinary Approaches, İstanbul, Turkey, 26 March - 28 August 2022, vol.1, pp.302-308, (Full Text) Sustainable Development

44. A Rare Case Of Mucınous Carcınoma Of The Breast In A 30-Year-Old Female

EMİROĞLU S., ABUAISHA A. M., TÜKENMEZ M., KAYA M., SÜER İ., BAYRAM A., et al.

4. ULUSLARARASI TIP BİLİMLERİ VE MULTİDİSİPLİNER YAKLAŞIMLAR KONGRESİ, 26 - 28 March 2022, (Full Text)

45. Hl60 ve Nb4 Hücrelerı̇nde Mı̇r-638-5p/pgk1 Gen Etkı̇leşı̇mı̇

Özbakış S., SUER İ., KAYA M., ÖZTÜRK Ş.

9th International Medicine and Health Sciences Researches Congress, 18 - 19 March 2022, (Full Text)

46. Hl60 ve NB4 Hücrelerinde miR-638-5P/PGK1 Gen Etkileşimi

Özbakış S., SUER İ., Kaya M., ÖZTÜRK Ş.

9th International Medicine and Health Sciences Researches Congress, Ankara, Turkey, 18 - 19 March 2022, pp.505-510, (Full Text) Sustainable Development

47. TET2 gene variations in patients with myeloid malignancies

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

XVII. Tıbbi Biyoloji ve Genetik Kongresi, 28 - 31 October 2021, vol.52, pp.242-243, (Summary Text)

48. CUMHURİYET VE TIP

ÖZTÜRK Ş.

8. ULUSAL İSTAHED AİLE HEKİMLİĞİ KONGRESİ, Antalya, Turkey, 27 October 2021, (Full Text)

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

Sariman M., KARAÇAM B., Ayer M., SIRMA EKMEKCİ S., SUER İ., ÇEFLE K., et al.

EACR 2021 Virtual Congress-Innovative Cancer Science: Better Outcomes through Research, 9 - 12 June 2021, pp.1, (Summary Text)

50. CEBPA c.584_589dup p.His195Pro196dup variant in myeloid malignancies

SUER İ., SIRMA EKMEKCİ S., Aday A., Bayrak A. G., ÇEFLE K., ÖZTÜRK Ş., et al.

The Virtual Conference on Current Challenges in Hematology (C-HEM2021), İstanbul, Turkey, 18 - 19 March 2021, (Summary Text)

51. Investigation Of Possibly Related Genes Determined From Bioinformatic Analysis Of Multiple Myeloma Whole Genome Transcriptome Data

Sariman M., KARAÇAM B., AYER M., SIRMA EKMEKCİ S., SUER İ., ÇEFLE K., et al.

8th Multidisciplinary Cancer Research Congress, İstanbul, Turkey, 16 - 17 January 2021, pp.123, (Summary Text)

52. Relationship between sarcopenia and ACTN3 R577X gene in older adults

KAHRAMAN M., BAHAT-ÖZTÜRK G., KARAN M. A., ÖZTÜRK Ş., ÖZULU TÜRKMEN B., DİLER A. S.

16th International E-Congress of the European Geriatric Medicine Society, Lisbon, Portugal, 7 - 09 October 2020, (Summary Text)

53. Relationship between sarcopenia and ACTN3 R577X gene in older adults

Kahraman M., Özulu Türkmen B., Bahat-Öztürk G., Şahin A., Aday A., Diler A. S., et al.

16th International E-Congress of the European Geriatric Medicine Society, Lisbon, Portugal, 7 - 09 October 2020, pp.461, (Summary Text)

54. Overexpression of FUS and PRDX5 Genes In Multiple Myeloma Patients

SUER İ., Aday A., Sariman M., Ayer M., Hindilerden I. Y., SIRMA EKMEKCİ S., et al.

14. Ulusal Tıbbi Genetik Kongresi (Uluslararası katılımlı), Turkey, 20 - 23 November 2020, pp.23, (Summary Text) Sustainable Development

55. Steroide duyarlı kronik anemisi ve osteosklerozu olan erişkin olguda moleküler tanının klinik izleme etkisi

Sharifi S., Kalaycı T., Kaya M., SUER İ., ÖZTÜRK Ş., ÇEFLE K., et al.

14. Ulusal Tıbbi Genetik Kongresi (Uluslararası katılımlı), Turkey, 20 - 23 November 2020, pp.37, (Summary Text)

56. 46,XX,t(8;9)(q12;q12) translokasyon taşıyıcısı tekrarlayan gebelik kayıp öykülü olgu sunumu

SUER İ., Kaya M., Sharifi S., Kalaycı T., ÖZTÜRK Ş., ÇEFLE K., et al.

14. Ulusal Tıbbi Genetik Kongresi (Uluslararası katılımlı), Turkey, 20 - 22 November 2020, pp.89, (Summary Text)

57. Abstracts of the 16th International E-Congress of the European Geriatric Medicine Society

KAHRAMAN M., KARAN M. A., BAHAT-ÖZTÜRK G., ÖZULU TÜRKMEN B., ÖZTÜRK Ş., DİLER A. S.

16th International E-Congress of the European Geriatric Medicine Society, Portugal, 07 October 2020, (Full Text)

58. Investigation of miR-145 target genes in multiple myeloma cell lines

Kaya M., SUER İ., KARATAŞ Ö. F., ÖZGÜR E., GEZER U., ÇEFLE K., et al.

V. International Participated Erciyes Medical Genetics Days Congress, Nevşehir, Turkey, 20 - 22 February 2020, vol.2584, pp.37, (Summary Text) Sustainable Development

59. Seyahate çıkan vatandaşlarımızın seyahat sağlığı ve aşılar konusunda bilgi düzeyleri

Kahraman M., Öztürk Ş.

Geleneksel İç Hastalıkları Günleri - İnteraktif Güncelleştirme, Sakarya, Turkey, 12 - 15 March 2020, pp.93, (Summary Text) Sustainable Development

60. Pseudo-anadontia with Multiple Impactions- A Case Report

ERDİLEK A. D., KAYNAR A., KORAY F., YILDIRIM M., ÖZTÜRK Ş.

13th International Conference on Oral and Maxillofacial Surgery, Japan, pp.252, (Summary Text)

61. A Case of Severe Partial Hypodontia Associated with Simple Hemihypertrophy

ERDİLEK A. D., KORAY F., ÖZTÜRK Ş., PALANDUZ Ş.

35th Annual Meeting of the IADR/CED, France, pp.9, (Summary Text)

62. Evaluation of Spermatogenesis Process in Cases with Azospermic and Oligospermic Normal Karyotype and Azospermic Klinefelter Syndrome

ÖZTAN G., PALANDUZ Ş., ÇEFLE K., ÖZTÜRK Ş.

Cell Death Symposium, Turkey, 3 - 04 October 2019, (Summary Text)

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

Sariman M., KARAÇAM B., Ayer M., SIRMA EKMEKCİ S., SUER İ., ÇEFLE K., et al.

1.International Multidisciplinary Cancer Research Congress, Diyarbakır, Turkey, 18 - 22 September 2019, vol.1, pp.96, (Summary Text)

64. Investigation of miR-34a target genes in multiple myeloma cell lines

SUER İ., Kaya M., KARATAŞ Ö. F., ÖZGÜR E., GEZER U., ÇEFLE K., et al.

VII. International Congress of Molecular Medicine, İstanbul, Turkey, 5 - 07 September 2019, vol.1, pp.141, (Summary Text)

65. Spectrum of Skeletal Abnormalities and Pathogenic RUNX2 Variants in 50 CleidocranialPatients from Turkey

Berkay E. G., Elkanova L., Kalaycı T., Karaman V., GÜNEŞ N., Toksoy G., et al.

13th Balkan Congress of Human Genetics, 17 - 20 April 2019, (Summary Text)

66. S-29 - Spectrum of Skeletal Abnormalities and Pathogenic RUNX2 Variants in 50 CleidocranialPatients from Turkey

BERKAY E. G., ELKANOVA L., KALAYCI T., KARAMAN V., GÜNEŞ N., TOKSOY G., et al.

13TH BALKAN CONGRESS OF HUMAN GENETICS, 17 - 20 April 2019, (Summary Text)

67. A Case of a Variant Philadelphia Translocation Involving Chromosomes (7;9;22)(q22;q34;q11) in Chronic Myeloid Leukemia

BAYRAK A. G., ADAY A., UÇUR A., ÖZBALAK M. M., NALÇACI M., ÇEFLE K., et al.

13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.BJMG, no.39, pp.76, (Summary Text)

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

KAHRAMAN M., ÖZTÜRK Ş., KARŞIDAĞ K., KARAN M. A., SATMAN İ.

Geleneksel İç Hastalıkları Günleri - İnteraktif Güncelleştirme, Sakarya, Turkey, 14 - 17 March 2019, vol.2019, pp.76-77, (Summary Text) Sustainable Development

69. KML Hastalarında Moleküler Monitorizasyon-Klinik Seyir İlişkisinin ve SLC22A1 MRNA Ekspresyonunun Araştırılması

Bulakçı B., Dağlar Aday A., YAVUZ A. S., Gürtekin B., ÇEFLE K., ÖZTÜRK Ş., et al.

44. Ulusal Hematoloji Kongresi, Turkey, 21 October - 03 November 2018, (Summary Text)

70. Larenks Kanseri Primer Hücre Kültüründe Oluşturulan Küre (Sphere)’lerde Oct4 ve Klf4 Ekspresyon Analizi

SUER İ., KARATAŞ Ö. F., Kaya M., ÖZTÜRK Ş.

7. Kök Hücre Sempozyumu, İstanbul, Turkey, 11 May 2018, vol.1, pp.7-10, (Full Text) Sustainable Development

71. Ailesel beyaz süngersi nevuslu olgularda oral mukozal infeksiyonlara yatkınlığın incelenmesi.

KÜRKLÜ E., AK G., TOPÇUOĞLU N., ÖZTÜRK Ş., BEKA H., AĞAÇFİDAN A., et al.

33. ANKEM Kongresi, Antalya, Turkey, 2 - 06 May 2018, (Summary Text)

72. Akut Myeloid Lösemi ve 3q Kromozomal Yeniden Düzenlenmeleri

Bagatir G., Kaya M., Dön B., SUER İ., NALÇACI M., YENEREL M. N., et al.

3. Ulusal Uygulamalı Biyolojik Bilimler Kongresi (UBBK), Eskişehir, Turkey, 3 - 05 May 2018, vol.1, pp.35, (Summary Text)

73. Response to Therapy in a Case of CML with Complex Variant Ph Translocation

Aday A., Bayrak Tokaç A. G., Uçur A., Özcan Ö., Bağatır G., Erdem S., et al.

Erciyes Tıp Genetik Günleri , Kayseri, Turkey, 7 - 10 March 2018, pp.53, (Summary Text)

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

Kaya M., SUER İ., KALAYCI T., KARAMAN B., Dön B., Bagatir G., et al.

Erciyes Medical Genetics Days, Kayseri, Turkey, 7 - 10 March 2018, vol.1, pp.16, (Summary Text)

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

SUER İ., Kaya M., Bagatir G., KARAMAN B., ÇEFLE K., ÖZTÜRK Ş., et al.

Erciyes Medical Genetics Days, Kayseri, Turkey, 7 - 10 March 2018, pp.32, (Summary Text)

76. A Case Mımıckıng Chronıc Myeloprolıferatıve Leukemıa Wıth T(8;22)(P11;Q11)/Bcr-Fgfr1 And Sequentıal Transformatıon To B-All And Aml

Bayrak Tokaç A. G., Uçur A., Aday A., Bağatır G., Erdem S., Hançer V. S., et al.

Erciyes Tıp Genetik Günleri , Kayseri, Turkey, 8 - 10 March 2018, pp.53, (Summary Text)

77. RNA sequencing and in silico analysis of Myeloma cells in multiple myeloma patients

Sarıman M., SIRMA EKMEKCİ S., ABACI N., ÇAKİRİS A., PAÇAL F., ÜSTEK D., et al.

XV.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Fethiye- Muğla, Turkey, 26 - 29 October 2017, pp.108, (Summary Text)

78. Multiple Myeloma hastalarının Myeloma hücrelerinde RNA dizileme ve insilico analizler.

Sarıman M., Sırma Ekmekci S., Abacı N., Çakiris A., Paçal F., Üstek D., et al.

XV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi , Muğla, Turkey, 26 - 29 October 2017, pp.108-109, (Summary Text)

79. Multiple Myeloma hastalarının Myeloma hücrelerinde RNA dizileme ve in-silico analizler.

Sarıman M., Sırma Ekmekci S., Abacı N., Çakiris A., Perçin Paçal F., Üstek D., et al.

XV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Fethiye, Muğla, Turkey, 26 October 2017, (Unpublished)

80. Investigation of gene expression of myeloma cells in bone marrow ofmultiple myeloma patiens by transcriptome analysis

sarıman m., SIRMA EKMEKCİ S., ABACI N., ÇAKİRİS A., EMRENCE Z., perçin paçal f., et al.

The European Society of Human Genetics 2015, Barcelona, Spain, 21 - 24 May 2016, (Full Text)

81. Investigation of gene expression of myeloma cells in bone marrow of multiple myeloma patients by transcriptome analysis

Sarıman M., SIRMA EKMEKCİ S., ABACI N., ÇAKİRİS A., PAÇAL F., ÜSTEK D., et al.

ESHG 2016, Barcelona, Spain, 21 - 24 May 2016, pp.153, (Full Text)

82. 47,XXY,inv(12)(q15q24) Karyotip Özelliği Gösteren Klinefelter Sendromlu Bir Olgu

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

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.101, (Summary Text)

83. Habituel Abortus Nedeniyle Başvuran 46,XX,inv(12)(p11.2q14) Karyotip Özelliği Saptanan Olgu

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

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.102, (Summary Text)

84. Büyük Yq Delesyonlu [46,X,del(Yq)] İnfertil Olguda Sadece AZFc Delesyonu

Kaya M., Öztan G., Gedikbaşı A., Bağatır G., Coşkunpınar E., Öztürk Ş., et al.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.108, (Summary Text)

85. mos 46,XX/47,XXX/48,XXXX Karyotipli Cinsel Kimlik Bozukluğu Tanılı Olgu

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

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.100, (Summary Text)

86. 46,XY,t(4;6)(p15.3;q23) Kriptik Dengeli Resiprokal Translokasyonunu Taşıyan İnfertil Olgu

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

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.100, (Summary Text)

87. Habituel Abortus Nedeniyle Başvuran ve 46,XX,t(1;6)(p35;p21) Dengeli Resiprokal Translokasyonu Saptanan Olgu

Kaya M., Bağatır G., Gedikbaşı A., Dön B., Öztürk Ş., Çefle K., et al.

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.101, (Summary Text)

88.

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

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.107-108, (Summary Text)

89. 46,XY,t(11;22)(q23;q11) Dengeli Translokasyonunu Taşıyan İnfertil Bir Olgu

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

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.100-101, (Summary Text)

90. Kleidokranial Displazi: Olgu Sunumu

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

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.67-68, (Summary Text)

91. Erkek İnfertilitesinde AZF

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

11. Ulusal Tıbbi Genetik Kongresi, Turkey, 24 - 27 September 2014, (Summary Text)

92. Erkek İnfertiliteside AZF

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

11. Ulusal Tıbbi Genetik Kongresi, İstanbul, Turkey, 24 - 27 September 2014, pp.5, (Summary Text)

93. Midkine as an Indicator of Inflammation in Renal Transplantation.

Ozturk S., Kaya B., Celik K., Ozkan O., Doventas Y., Gursu M., et al.

World Transplant Congress, San-Francisco, Costa Rica, 26 - 31 July 2014, vol.14, pp.495, (Summary Text)

94. Adherence and effectiveness of omalizumab treatment in severe allergic asthma patients

Ozseker Z. F., Bulut I., Erdenen F., Erdogdu D., Asli G., Ersoy R., et al.

World Allergy and Asthma Congress of the European-Academy-of-Allergy-and-Clinical-Immunology and World-Allergy-Organization, Milan, Italy, 22 - 26 June 2013, vol.68, pp.363-364, (Summary Text)

95. Sistemik Lupus Eritematozus ve Romatoid Artritin Eşlik Ettiği Klinefelter Sendromu Olgusu

Gedikbaşı A., ÇEFLE K., Bayrak A. G., Tutkan G., Uçur A., Kamalı S., et al.

10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 19 - 23 December 2012, pp.314, (Full Text)

96. ‘‘Micronucleus and Sister Chromatid Exchange Analyses in Peripheral Lymphocytes of Patients with Oral Leukoplakia – A Pilot Study’’

SARUHANOĞLU A., Tanyeri H., ERGUN S., ÇEFLE K., ÖZTÜRK Ş., PALANDUZ Ş.

10th Biennal Congress European Association of Oral Medicine (EAOM), Londra, United Kingdom, 23 - 25 September 2010, pp.518-519, (Full Text)

97. ‘‘No Difference in Micronuclear Scores in both Circulating Lymphocytes and Buccal Epithelial Cells between Patients with Oral Lichen Planus and Oral Lichenoid Stomatitis’

ERGUN S., SARUHANOĞLU A., ÇEFLE K., Warnakulasuriya S., ÖZTÜRK Ş., PALANDUZ Ş.

10th Biennal Congress European Association of Oral Medicine (EAOM), Londra, United Kingdom, 23 - 25 September 2010, pp.524-525, (Full Text)

98. Variant philadelphia translocations in patients with chronic myeloid leukemia

Satkın B. N., PALANDUZ Ş., KARAMAN B., ÖZTÜRK Ş., ÇEFLE K., Bagatır G., et al.

European Cytogenetic Conference (7th), Stockholm, Sweden, 4 - 07 July 2009, pp.161-162, (Full Text)

99. The evaluation of the genomic instability by micronucleus and sister chromatid exchange in myelodysplastic syndrome

Nazligul E., Palanduz P., Ozturk O., Bayrak A., Ucur A., Bagatir G., et al.

7th European Cytogenetics Conference, Stockholm, Sweden, 4 - 07 July 2009, vol.17, pp.137-138, (Summary Text)

100. Translocation (1;14) in hairy cell leukemia variant

Bayrak A., Ucur A., Satkin B., Palanduz S., Karan M., Ozturk S., et al.

7th European Cytogenetics Conference, Stockholm, Sweden, 4 - 07 July 2009, vol.17, pp.162, (Summary Text)

101. Determination of genomic instability of patients with oral lichen planus’’

ERGUN S., SARUHANOĞLU A., TANYERİ H., ÇEFLE K., DUMAN N., ÖZEL YILDIZ S., et al.

9th Biennal Congress European Association of Oral Medicine (EAOM),, Salzburg, Austria, 18 - 20 September 2008, pp.35, (Full Text)

102. ‘‘Ligneous Periodontitis with Conjunctival Involvement: A Case Report’’

kürklü e., ERGUN S., TANYERİ H., ÇEFLE K., Mete Ö., ÖZTÜRK Ş., et al.

1st International Congress of Oral and Maxillofacial Surgery Society, Antalya, Turkey, 16 - 20 May 2007, pp.42, (Full Text)

103. Spontaneous micronucleus frequency in the bone marrow cells of patients with leukemia

Basak S., Sukru O., Sukru P., Gulcin B., Ali U., Aysegul B., et al.

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.199, (Summary Text)

104. The use of FISH/M-FISH in patients with hematological malignancies for further characterization chromosomal abnormalities detected on conventional cytogenetic analysis

Ali U., Aysegul B., Nedime S., Gulcin B., Sukru P., Sukru O., et al.

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.201-202, (Summary Text)

105. The association of Down Syndrome and acute myeloid leukemia: accompanying Trisomy 8

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

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.210, (Summary Text)

106. Two cases with euchromatic variation in 5P and 9Q

Sukru O., Aysegul B., Kivanc C., Nigun D., Davut P., Birsen K., et al.

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.78, (Summary Text)

107. Constitutional chromosome abnormalities

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

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.211, (Summary Text)

108. t(5;22)(q13;q12) variant translocation in a case of chronic myeloid leukemia refractory to treatment

Haluk E., Sukru O., Serap Y., Kivanc C., Gulcin B., Ali U., et al.

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.223, (Summary Text)

109. Pericentric inversion of chromosome 8 and paracentric inversion of the long of arm of chromosome 11 in the male partner of a couple presenting with recurrent miscarriage

Kivanc C., Haluk E., Birsen K., Sukru O., Seher B., Sukru P.

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.85-86, (Summary Text)

110. Loss of the Y chromosome in Leukemia: a report of 9 patients

Bagatir P. S., Sukru O., Kivanc C., Ali U., Aysegul B., Meliha N., et al.

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.210-211, (Summary Text)

111. Variant Philadelphia translocations in patients with Chronic Myeloid Leukemia

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

6th European Cytogenetics Conference, İstanbul, Turkey, 7 - 10 July 2007, pp.202, (Summary Text)

112. Cardiac Investigation (Echocardiography, Heart Rate Variability and QT dispertion parameters ) in Turner Syndrome.

Sözen A. B., Çefle K., Kudat H., Öztürk Ş.

Abstracts of the Second Annual Congress on Update in Cardiology and Cardiovascular Surgery., Muğla, Turkey, 20 - 24 September 2006, vol.29, pp.143, (Summary Text)

113. . Is there any relation between the NQO1 C609T polymorphism and cytogenetics abnormalities in MDS?

Bağatır G., Sırma Ekmekci S., Palandüz Ş., Özbek U., Nalçacı M., Öztürk Ş., et al.

7th Balkan Meeting on Human Genetics konferansı, Skopje, Macedonia, 20 September 2008, vol.9, no.3, pp.75, (Summary Text)

114. Cardiac İnvestigation ( Echocardiography, Heart Rate Variability and QT dispertion patameters ) in Turner Syndrome. Clinical Cardiology.

Sözen A. B., Çefle K., Kudat H., Öztürk Ş.

Abstracts of the Secont Annual Congress on Update in Cardiology and Cardiovascular Surgery, Muğla, Turkey, 20 - 24 September 2006, vol.29, pp.50, (Summary Text)

115. ‘Investigation of genomic instability of patients with Sjögren’s syndrome by using sister chromatide Exchange analysis’

ergun s., TANYERİ H., ÖZTÜRK Ş.

analysis’ Biennial Congress of the European Association of Oral Medicine, Croatia, 1 - 04 September 2006, pp.1, (Full Text)

116. ‘Investigation of Genomic Instability of Patients with Sjögren’s Syndrome by Using Sister Chromatide Exchange Analysis’

ERGUN S., TANYERİ H., ÇEFLE K., DUMAN N., PALANDUZ S., Özel S., et al.

8th Biennal Congress European Association of Oral Medicine (EAOM, Zagreb, Croatia, 31 August - 02 September 2006, pp.24, (Full Text)

117. Investigation of Human papilloma virus and Candida albicans in a family with white sponge nevus

KÜRKLÜ E., AK G., TOPCUOĞLU E. N., ÖZTÜRK Ş., Beka H., AĞAÇFİDAN A., et al.

8th Biennial Congress of the European Association of Oral Medicine, Croatia, pp.30, (Full Text)

118. A Novel Mutation in Keratin 13 Gene in a Turkish Family with White Sponge Nevus

KÜRKLÜ E., CASSIDY A., ÖZTÜRK Ş., KORAY M., AK G., ÇEFLE K., et al.

7th Biennial Congress of the European Association of Oral Medicine & 26th Annual Scientific Meeting of the Academy of Oral Pathology and Oral Medicine (AKOPOM), Germany, pp.29, (Full Text)