Prof. NACİ ÇİNE

Publication Network

Articles 82

1. Clinical classification and molecular interpretation of germline pathogenic TP53 variations detected by multigene panel testing in patients with possible cancer predisposition

ÖNDER G., Unal B., ÖZDEMİR Ö., Amanvermez U., AÇIKEL ELMAS M., Gokbayrak M., et al.

Molecular Genetics and Genomics , vol.300, no.1, 2025 (SCI-Expanded, Scopus)

2. Functional Abdominal Bloating Is Associated With Gut Microbiota Dysbiosis and Altered Intestinal Barrier Function: Experimental Evidence.

Akkoyunlu D., ÇELEBİ A., Gur B., KANLI A., Ugurtas C., ÖZER T., et al.

In vivo (Athens, Greece) , vol.39, no.6, pp.3320-3332, 2025 (SCI-Expanded, Scopus)

3. Genetic Etiology of Developmental and Epileptic Encephalopathy in a Turkish Cohort: A Single-Center Study with Targeted Gene Panel and Whole Exome Sequencing

Sünnetçi Akkoyunlu D., Kara B., Özer T., Deniz A., Sakarya Güneş A., Isik E. B., et al.

Genes , vol.16, no.10, 2025 (SCI-Expanded, Scopus)

4. Innovative design and comprehensive characterization of a valine-enhanced lipid nanoparticle-coated mRNA vaccine targeting the SARS-CoV-2 S-RBD antigen.

Duran T., Cine N., Karaselek M. A., Gul N., Kuccukturk S., Hatipoglu D., et al.

Scientific reports , vol.15, no.1, pp.33898, 2025 (SCI-Expanded, Scopus)

5. Distinct Breast Tissue Microbiota Profiles in Early-Stage Breast Cancer: A Prospective Study in Turkish Women.

ÖZSARAY M. F., ŞİMŞEK T., Akkoyunlu D., ÇİNE N., CANTÜRK N. Z.

Life (Basel, Switzerland) , vol.15, no.10, 2025 (SCI-Expanded, Scopus)

6. Identification of Common miRNAs Differentially Expressed in Periodontitis and Pancreatic Cancer

Sunnetci‐Akkoyunlu D., Ugurtas C., Kulcu‐Sarikaya N., ÖZER T., ÇİNE N., Eren‐Keskin S., et al.

IN VIVO , vol.39, no.3, pp.1422-1439, 2025 (SCI-Expanded, Scopus) Sustainable Development

7. The Role of Ultrasonography in Predicting Genetic Characteristics of Endometrial Cancers

Uzel K., Bilir F., Tosun M., Topbas Selcuki N. F., Eren Keskin S., Gokbayrak M., et al.

Journal of Clinical Medicine , vol.14, no.9, 2025 (SCI-Expanded, Scopus)

8. Comparison of cytogenetic and molecular features observed in endometrial cancers: known clinic and difficulties in treatment

Uzel K., KESKİN S., Bilir F., Gokbayrak M., Demir G., ÇİNE N., et al.

CIRUGIA Y CIRUJANOS , vol.93, no.2, 2025 (SCI-Expanded, Scopus) Sustainable Development

9. Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study

Kanmaz S., Tekgul H., Kayilioglu H., Atas Y., Kart P. O., Yildiz N., et al.

SEIZURE-EUROPEAN JOURNAL OF EPILEPSY , vol.123, pp.17-25, 2024 (SCI-Expanded, Scopus)

10. Molecular and In Silico Analysis of the CHEK2 Gene in Individuals with High Risk of Cancer Predisposition from Türkiye.

Ozdemir O., Bychkovsky B. L., Unal B., Onder G., Amanvermez U., Aydin E., et al.

Cancers , vol.16, no.22, 2024 (SCI-Expanded, Scopus)

11. Bariatrik Cerrahi Sonrası Ortaya Çıkan Mide Adenokarsinomu: Obezite ve Mide Kanseri Arasındaki Genetik İlişkinin İncelenmesi

Şahin S., Eren Keskin S., Şahin E., Sünnetçi Akkoyunlu D., Doğruoğlu B., İlkay Z., et al.

Acta Medica Nicomedia , vol.7, no.3, pp.359-361, 2024 (TRDizin)

12. Cytogenetic evaluation of 661 prenatal samples

EREN KESKİN S., Dogruoglu B., Ilkay Z., SÜNNETÇİ AKKOYUNLU D., ÇİNE N., SAVLI H., et al.

CUKUROVA MEDICAL JOURNAL , vol.49, no.2, pp.248-259, 2024 (ESCI, TRDizin)

13. The effect of epetraborole on the transcriptome and proteome profiles of an Escherichia coli strain overexpressing leuS, Leucyl-tRNA Synthetase

BABAYEVA A., DİBEK E., SÜNNETÇİ AKKOYUNLU D., ÇİNE N., KASAP M., AKPINAR G., et al.

Frontiers in Life Sciences and Related Technologies (Online) , vol.5, no.1, pp.48-58, 2024 (TRDizin)

14. Differentially expressed miRNAs associated with generalized aggressive periodontitis

Guzeldemir-Akcakanat E., Sunnetci-Akkoyunlu D., Balta-Uysal V. M., Özer T., Işik E. B., Cine N.

CLINICAL ORAL INVESTIGATIONS , vol.28, no.1, 2024 (SCI-Expanded, Scopus) Sustainable Development

15. Importance of Structural Abnormalities Detected by Array-Comparative Genomic Hybridization in Recurrent Miscarriage: A retrospective Study

Akar B., Köle E., Sünnetçi Akkoyunlu D., Çakır Köle M., Çine N., Savlı H., et al.

Adnan Menderes Üniversitesi Sağlık Bilimleri Fakültesi Dergisi , vol.7, no.3, pp.631-639, 2023 (Peer-Reviewed Journal)

16. Quantification of MMP-2 and TIMP-1 expressions in breast cancer

Keskin S., SÜNNETÇİ AKKOYUNLU D., Tezcan M. Y., ŞİMŞEK T., GÜLER S. A., ÇİNE N., et al.

ISTANBUL JOURNAL OF PHARMACY , no.2, pp.211-218, 2023 (ESCI, TRDizin)

17. The role of next-generation sequencing in the examination of signaling genes in Brca1/2-negative breast cancer cases

ÇİNE N., Ugurtas C., Gokbayrak M., AYDIN D., Demir G., Kuru S., et al.

ANNALS OF HUMAN GENETICS , vol.87, no.1-2, pp.28-49, 2023 (SCI-Expanded, Scopus)

18. Copy Number Variations in a Turkish Cohort of Children with Intellectual Disability*

SÜNNETÇİ AKKOYUNLU D., KARA B., ÇİNE N., EREN KESKİN S., Dogruoglu B., Ilkay Z., et al.

Experimed , vol.13, no.3, pp.263-275, 2023 (ESCI, Scopus, TRDizin)

19. NETosis Induced by Serum of Patients with COVID-19 is Reduced with Reparixin or Antibodies Against DEK and IL-8

Kilic I. B., Yasar A., Camci I. Y., Guzel T., KARAHASAN A., YAĞCI T., et al.

TURKISH JOURNAL OF IMMUNOLOGY , vol.11, no.3, pp.127-135, 2023 (ESCI, Scopus, TRDizin)

20. Optimization of High Concentration Plasmid DNA for Use in COVID-19 mRNA Vaccine Development: Comparison of Between Alkaline Lysis Method and Commercial Kit Results

DURAN T., ÇİNE N., KOÇAK N., KURT S.

Harran Üniversitesi Veteriner Fakültesi Dergisi , vol.11, no.2, pp.154-161, 2022 (TRDizin)

21. Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study

Günay Ç., Aykol D., Özsoy Ö., Sonmezler E., Hanci Y. S., Kara B., et al.

NEUROPEDIATRICS , vol.54, no.4, pp.225-238, 2022 (SCI-Expanded, Scopus)

22. THE MUTATION PROFILES OF K-RAS/N-RAS GENES IN METASTATIC COLORECTAL CANCER PATIENTS

KESKİN S. E., Güzdolu E., SERTDEMİR N., DEMİR G., SÜNNETÇİ D., ÇABUK D., et al.

Kocaeli Üniversitesi Sağlık Bilimleri Dergisi , vol.8, no.3, pp.172-178, 2022 (TRDizin)

23. The diagnostic importance of pathogenic variants and variant coexistence determined by NGS-based liquid biopsy approach in patients with lung adenocarcinoma

Çine N., Sen E. A., Demir G., Gokbayrak M., Guzdolu E., Sertdemir N., et al.

MOLECULAR AND CELLULAR PROBES , vol.64, 2022 (SCI-Expanded, Scopus)

24. DEK level was reduced in the serum of patients with COVID-19

Camci I. Y., Kilic I. B., Cakar T., Avci A., KARAHASAN A., ÇİNE N., et al.

EUROPEAN JOURNAL OF IMMUNOLOGY , pp.183, 2021 (SCI-Expanded, Scopus)

25. Haplotype Analysis of Vitamin D Receptor (VDR) Gene in Breast Cancer Patients

Ergul E., Simsek T., Uren N., Korak T., Simsek H., Cine N., et al.

CLINICAL LABORATORY , no.6, pp.1421-1427, 2021 (SCI-Expanded, Scopus) Sustainable Development

26. Identification of Key Genes in Papillary Thyroid Cancer by Transcriptome Analysis

SÜNNETÇİ AKKOYUNLU D., Isik E. B., Tarkun I., ÇİNE N., CANTÜRK N. Z., Devrim Uzkul N., et al.

UHOD-ULUSLARARASI HEMATOLOJI-ONKOLOJI DERGISI , vol.30, no.1, pp.11-22, 2020 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

27. TP53, EGFR and PIK3CA gene variations observed as prominent biomarkers in breast and lung cancer by plasma cell-free DNA genomic testing

SAVLI H., Sertdemir N., AYDIN D., Dursun B., KURTAŞ Ö., Reka S., et al.

JOURNAL OF BIOTECHNOLOGY , vol.300, pp.87-93, 2019 (SCI-Expanded, Scopus) Sustainable Development

28. Molecular signatures of chronic periodontitis in gingiva: A genomic and proteomic analysis

Guzeldemir-Akcakanat E., Alkan B., Sunnetci-Akkoyunlu D., Gürel B., Balta V. M., Kan B., et al.

JOURNAL OF PERIODONTOLOGY , vol.90, no.6, pp.663-673, 2019 (SCI-Expanded, Scopus)

29. HOXA-10 gene expression in ectopic and eutopic endometrium tissues: Does it differ between fertile and infertile women with endometriosis?

Özcan C., Özdamar Ö., Gökbayrak M., Doğer E., Çakıroğlu Y., Çine N.

European journal of obstetrics, gynecology, and reproductive biology , vol.233, pp.43-48, 2019 (SCI-Expanded, Scopus) Sustainable Development

30. Genomic copy number alteration of glycolytic pathway in endometrial cancer

Yilmaz M., Akkoyunlu D., Keskin S., DOĞER E., ÇİNE N., SAVLI H.

EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY , vol.40, no.4, pp.640-646, 2019 (SCI-Expanded, Scopus) Sustainable Development

31. Exenatide upregulates gene expression of glucagon-like peptide-1 receptor and nerve growth factor in streptozotocin/nicotinamide-induced diabetic mice

Gumuslu E., Çine N., Ertan M., Mutlu O., Celıkyurt I. K., Ulak G.

FUNDAMENTAL & CLINICAL PHARMACOLOGY , vol.32, pp.174-180, 2018 (SCI-Expanded) Sustainable Development

32. Exenatide Alters Gene Expression of Neural Cell Adhesion Molecule (NCAM), In-tercellular Cell Adhesion Molecule (ICAM), and Vascular Cell Adhesion Molecule (VCAM) in the Hippocampus of Type 2 Diabetic Model Mice

Gumuslu E., ÇİNE N., Gokbayrak M. E., MUTLU O., Celikyurt I. K., ULAK G.

MEDICAL SCIENCE MONITOR , vol.22, pp.2664-2669, 2016 (SCI-Expanded, Scopus) Sustainable Development

33. Deregulated Levels of the NF-kappa B1, NF-kappa B2, and Rel Genes in Ukrainian Patients with Leukemia and Lymphoma in the Post-Chernobyl Period

SAVLI H., Akkoyunlu R. U., ÇİNE N., Gluzman D. F., Zavelevich M. P., Sklyarenko L. M., et al.

TURKISH JOURNAL OF HEMATOLOGY , vol.33, no.1, pp.8-14, 2016 (SCI-Expanded, Scopus, TRDizin) Sustainable Development

34. Gene-Expression Profiles in Generalized Aggressive Periodontitis: A Gene Network-Based Microarray Analysis

Guzeldemir-Akcakanat E., Sunnetci-Akkoyunlu D., Orucguney B., ÇİNE N., Kan B., Yilmaz E. B., et al.

JOURNAL OF PERIODONTOLOGY , vol.87, no.1, pp.58-65, 2016 (SCI-Expanded, Scopus)

35. Genetic evidence for PLASMINOGEN as a shared genetic risk factor of coronary artery disease and periodontitis.

Schaefer A. S., Bochenek G., Jochens A., Ellinghaus D., Dommisch H., Guezeldemir-Akcakanat E., et al.

Circulation. Cardiovascular genetics , vol.8, no.1, pp.159-67, 2015 (SCI-Expanded, Scopus)

36. Investigation of the diagnostic value of chromosome analysis and bacterial artificial chromosome-based array comparative genomic hybridization in prenatal diagnosis

SAVLI H., EREN KESKİN S., ÇİNE N.

TURKISH JOURNAL OF MEDICAL SCIENCES , vol.45, no.6, pp.1263-1267, 2015 (SCI-Expanded, Scopus, TRDizin)

37. A CGH array study in nonsyndromic (primary) autism patients: deletions on 16p13.11, 16p11.2, 1q21.1, 2q21.1q21.2, and 8p23.1

Gümüşlü K., Savli H., Sünnetçi D., Çine N., Kara B., Eren K., et al.

TURKISH JOURNAL OF MEDICAL SCIENCES , vol.45, no.2, pp.313-319, 2015 (SCI-Expanded, Scopus, TRDizin)

38. The effect of first chromosome long arm duplication on survival of endometrial carcinoma.

Sever E., Doğer E., Çakıroğlu Y., Sünnetçi D., Çine N., Savlı H., et al.

Turkish journal of obstetrics and gynecology , vol.11, pp.207-210, 2014 (ESCI, Scopus, TRDizin)

39. **Identification of ApoA1, HPX and POTEE genes by omic analysis in breast cancer**

ÇİNE N., Baykal A. T., Sunnetci D., Canturk Z., Serhatli M., SAVLI H.

ONCOLOGY REPORTS , no.3, pp.1078-1086, 2014 (SCI-Expanded, Scopus)

40. The Antidepressant Agomelatine Improves Memory Deterioration and Upregulates CREB and BDNF Gene Expression Levels in Unpredictable Chronic Mild Stress (UCMS)-Exposed Mice.

GUMUSLU E., MUTLU O., SUNNETCI D., ULAK G., Celikyurt I., CINE N., et al.

Drug target insights , vol.8, pp.11-21, 2014 (Scopus)

41. The Antidepressant Agomelatine Improves Memory Deterioration and Upregulates CREB and BDNF Gene Expression Levels in Unpredictable Chronic Mild Stress UCMS Exposed Mice

GÜMÜŞLÜ K. E., MUTLU O., SÜNNETÇİ AKKOYUNLU D., ULAK G., KOMSUOĞLU ÇELİKYURT F. İ., ÇİNE N., et al.

Drug Target Insights , 2014 (Scopus)

42. The effect of first chromosome long arm duplication on survival of endometrial carcinoma

sever e., DOĞER E., SÜNNETÇİ AKKOYUNLU D., ÇİNE N., SAVLI H., YÜCESOY İ.

J Turk Soc Obstet Gynecol , 2014 (Peer-Reviewed Journal)

43. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.

Eyüpoğlu F., Sünnetçi D., Cine N., Savli H., Okten A., Açikgöz E., et al.

Genetic counseling (Geneva, Switzerland) , vol.25, pp.305-13, 2014 (SCI-Expanded, Scopus)

44. Expression analysis and clinical correlation of aquaporin 1 and 4 genes in human hippocampal sclerosis.

Bebek N., Özdemir Ö., Sayitoglu M., Hatırnaz O., Baykan B., Gürses C., et al.

Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia , vol.20, pp.1564-70, 2013 (SCI-Expanded, Scopus)

45. Unique variant of Adams-Oliver syndrome with dilated cardiomyopathy and heart block.

Atasoy H., Tug E., Yavuz T., Cine N.

Pediatrics international : official journal of the Japan Pediatric Society , vol.55, pp.508-12, 2013 (SCI-Expanded, Scopus)

46. The effects of tianeptine, olanzapine and fluoxetine on the cognitive behaviors of unpredictable chronic mild stress-exposed mice

Gumuslu E., MUTLU O., Sunnetci D., ULAK G., Celikyurt I., ÇİNE N., et al.

Drug Research , vol.63, no.10, pp.532-539, 2013 (SCI-Expanded, Scopus)

47. High Throughput FISH Analysis: A New, Sensitive Option For Evaluation of Hematological Malignancies.

Savlı H., Uzülmez N., Ilkay Z., Yavuz D., Sünnetçi D., Hacıhanifioğlu A., et al.

Turkish journal of haematology : official journal of Turkish Society of Haematology , vol.30, pp.122-8, 2013 (SCI-Expanded, Scopus, TRDizin)

48. Validation of reported genetic risk factors for periodontitis in a large-scale replication study.

Schaefer A. S., Bochenek G., Manke T., Nothnagel M., Graetz C., Thien A., et al.

Journal of clinical periodontology , vol.40, no.6, pp.563-72, 2013 (SCI-Expanded, Scopus)

49. Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy

Moller R. S., Weber Y. G., Klitten L. L., Trucks H., Muhle H., Kunz W. S., et al.

EPILEPSIA , vol.54, no.2, pp.256-264, 2013 (SCI-Expanded, Scopus)

50. Association of MDR1 Gene Polymorphism in Patients With Temporal Lobe Epilepsy

ÇİNE N., Sargin G., BEBEK N., Gurses C., Baykan B., Ozbek U., et al.

JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH , vol.30, no.1, pp.4-11, 2013 (SCI-Expanded, Scopus, TRDizin)

51. Effects of curcumin on global gene expression profiles in the highly invasive human breast carcinoma cell line MDA-MB 231: A gene network-based microarray analysis

ÇİNE N., Limtrakul P., Sunnetci D., Nagy B., SAVLI H.

EXPERIMENTAL AND THERAPEUTIC MEDICINE , vol.5, no.1, pp.23-27, 2013 (SCI-Expanded, Scopus) Sustainable Development

52. Prenatal diagnosis of 4p and 4q subtelomeric microdeletion in de novo ring chromosome 4.

Akbas H., Cine N., Erdemoglu M., Atay A., Simsek S., Turkyilmaz A., et al.

Case reports in obstetrics and gynecology , vol.2013, pp.248050, 2013 (Scopus)

53. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32

Steffens M., Leu C., Ruppert A., Zara F., Striano P., Robbiano A., et al.

HUMAN MOLECULAR GENETICS , vol.21, no.24, pp.5359-5372, 2012 (SCI-Expanded, Scopus)

54. Microarray-based gene expression analysis of an animal model for closed head injury

ÇOLAK T., Cine N., BAMAÇ B., Kurtas O., OZBEK A., BICER U., et al.

INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED , vol.43, no.8, pp.1264-1270, 2012 (SCI-Expanded, Scopus) Sustainable Development

55. Evaluation of glutathione S-transferase P1 polymorphisms (Ile105Val and Ala114Val) in patients with small cell lung cancer.

Vural B., Yakar F., Derin D., Saip P., Yakar A., Demirkan A., et al.

Genetic testing and molecular biomarkers , vol.16, pp.701-6, 2012 (SCI-Expanded, Scopus) Sustainable Development

56. A case of del(13)(q14.2)(q31.3) associated with hypothyroidism, hypertriglyceridemia, hypercholesterolemia and total ophthalmoplegia

Malbora B., Meral C., Malbora N., Sunnetci D., ÇİNE N., SAVLI H.

GENE , vol.498, no.2, pp.296-299, 2012 (SCI-Expanded, Scopus)

57. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

Leu C., de Kovel C. G. F., Zara F., Striano P., Pezzella M., Robbiano A., et al.

EPILEPSIA , vol.53, no.2, pp.308-318, 2012 (SCI-Expanded, Scopus)

58. Gene expression profiling of B-CLL in Ukrainian patients in post-Chernobyl period.

Savli H., Sunnetci D., Cine N., Gluzman D., Zavelevich M., Sklyarenko L., et al.

Experimental oncology , vol.34, pp.57-63, 2012 (SCI-Expanded, Scopus)

59. Microsurgical anatomy of membranous layers of the pituitary gland and the expression of extracellular matrix collagenous proteins

CEYLAN S., ANIK İ., Koc K., Kokturk S., Ceylan S., ÇİNE N., et al.

ACTA NEUROCHIRURGICA , vol.153, no.12, pp.2435-2443, 2011 (SCI-Expanded, Scopus)

60. Sequence variations of NKX2-5 and HAND1 genes in patients with atrial isomerism.

Hatemi A., Güleç C., Cine N., Vural B., Hatırnaz O., Sayitoğlu M., et al.

Anadolu kardiyoloji dergisi : AKD = the Anatolian journal of cardiology , vol.11, pp.319-28, 2011 (SCI-Expanded, Scopus, TRDizin)

61. A Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome.

Tug E., Cine N., Aydin H.

Genetic counseling (Geneva, Switzerland) , vol.22, pp.11-9, 2011 (SCI-Expanded, Scopus)

62. ITF2357 Interferes with Apoptosis and Inflammatory Pathways in the HL-60 Model: A Gene Expression Study

Galimberti S., Canestraro M., SAVLI H., Palumbo G. A., Tibullo D., Nagy B., et al.

ANTICANCER RESEARCH , vol.30, no.11, pp.4525-4535, 2010 (SCI-Expanded, Scopus)

63. Unbalanced 3;22 Translocation With 22q11 and 3p Deletion Syndrome

DÜNDAR M., Kiraz A., Tasdemir S., Akalin H., Kurtoglu S., Hafo F., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A , no.11, pp.2791-2795, 2010 (SCI-Expanded, Scopus)

64. Synergistic antiproliferative effect of arsenic trioxide combined with bortezomib in HL60 cell line and primary blasts from patients affected by myeloproliferative disorders

Canestraro M., Galimberti S., SAVLI H., Palumbo G. A., Tibullo D., Nagy B., et al.

CANCER GENETICS AND CYTOGENETICS , vol.199, no.2, pp.110-120, 2010 (SCI-Expanded, Scopus)

65. Two four-marker haplotypes on 7q36.1 region indicate that the potassium channel gene HERG1 (KCNH2, Kv11.1) is related to schizophrenia: a case control study

ATALAR F., Acuner T. T., ÇİNE N., Oncu F., Yesilbursa D., Ozbek U., et al.

BEHAVIORAL AND BRAIN FUNCTIONS , vol.6, 2010 (SCI-Expanded, Scopus)

66. GENE NETWORK AND CANONICAL PATHWAY ANALYSIS IN HEMATOPOLETIC AND SOFT TISSUE ORIGINATED MALIGNANCIES

Savli H., Cine N., Sunnetci D., Uzulmez N., Nagy B., Galimberti S., et al.

IUBMB LIFE , vol.61, no.3, pp.308, 2009 (SCI-Expanded, Scopus)

67. I405V and TaqIB polymorphisms of the cholesteryl ester transfer protein and their relation to serum lipid and lipoprotein levels in a Turkish population

Dogru-Abbasoglu S., Panldar-Karpuzoglu H., Depboylu B., ÇİNE N., Uysal M., Aykac-Toker G.

CELL BIOCHEMISTRY AND FUNCTION , vol.27, no.2, pp.76-80, 2009 (SCI-Expanded, Scopus)

68. BDNF Gene Polymorphism in Patients With Temporal Lobe Epilepsy

Sargin G., Gurses C., ÇİNE N., BEBEK N., Baykan B., Ozbek U., et al.

JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH , vol.25, no.4, pp.220-225, 2008 (SCI-Expanded, Scopus, TRDizin)

69. Association of MDR1 (C3435T) polymorphism and resistance to carbamazepine in epileptic patients from turkey

Ozgon G. O., Bebek N., Gul G., Cine N.

EUROPEAN NEUROLOGY , vol.59, pp.67-70, 2008 (SCI-Expanded, Scopus)

70. Genetic polymorphisms and endothelial dysfunction in patients with essential hypertension: A cross-sectional case-control study

Demirel S., AKKAYA V. A., Cine N., Oflaz H., Yekeler E., ÖZTÜRK Ş., et al.

Netherlands Heart Journal , vol.13, no.4, pp.126-131, 2005 (SCI-Expanded, Scopus)

71. Autosomal recessive idiopathic epilepsy in an inbred family from Turkey: Identification of a putative locus on chromosome 9q32-33

Baykan B., Madia F., Bebek N., Gianotti S., Guney A., Cine N., et al.

EPILEPSIA , vol.45, no.5, pp.479-487, 2004 (SCI-Expanded)

72. Endothelial dysfunction in patients with asthma: The role of polymorphisms of ACE and endothelial NOS genes

Yildiz P., Oflaz H., Cine N., Genchallac H., Erginel-Unaltuna N., Yildiz A., et al.

JOURNAL OF ASTHMA , vol.41, no.2, pp.159-166, 2004 (SCI-Expanded, Scopus)

73. Gene polymorphisms of endothelial nitric oxide synthase enzyme associated with pulmonary hypertension in patients with COPD

Yildiz P., Oflaz H., Cine N., Erginel-Unaltuna N., Erzengin F., Yilmaz V.

RESPIRATORY MEDICINE , vol.97, no.12, pp.1282-1288, 2003 (SCI-Expanded, Scopus)

74. Angiotensin converting enzyme gene polymorphism and development of post-transplant erythrocytosis

Yildiz A., Yazici H., Cine N., Kazancioglu R., Akkaya V., Sever M., et al.

JOURNAL OF NEPHROLOGY , vol.16, no.3, pp.399-403, 2003 (SCI-Expanded, Scopus)

75. Leptin receptor variant in women with polycystic ovary syndrome

Erel C., Cine N., Elter K., Kaleli S., Senturk L., Baysal B.

FERTILITY AND STERILITY , vol.78, no.6, pp.1334-1335, 2002 (SCI-Expanded, Scopus) Sustainable Development

76. The effect of angiotensin converting enzyme gene polymorphism on chronic allograft dysfunction in living donor renal transplant recipients

Yildiz A., Yazici H., Cine N., Akkaya V., Kayacan S., Sever M., et al.

CLINICAL TRANSPLANTATION , vol.16, no.3, pp.173-179, 2002 (SCI-Expanded, Scopus)

77. Association of a polymorphism of the ecNOS gene with myocardial infarction in a subgroup of Turkish MI patients

Cine N., Hatemi A., Erginel-Unaltuna N.

CLINICAL GENETICS , vol.61, no.1, pp.66-70, 2002 (SCI-Expanded, Scopus)

78. Comparison of the effects of enalapril and losartan on posttransplantation erythrocytosis in renal transplant recipients - Prospective randomized study

Yildiz A., Cine N., Akkaya V., Sahin S., Ismailoglu V., Turk S., et al.

TRANSPLANTATION , vol.72, no.3, pp.542-545, 2001 (SCI-Expanded, Scopus)

79. HLA-DQ alleles in patients with celiac disease in Turkey

Tuysuz B., Dursun A., Kutlu T., Sokucu S., Cine N., Suoglu O., et al.

TISSUE ANTIGENS , vol.57, no.6, pp.540-542, 2001 (SCI-Expanded, Scopus)

80. No association between deletion-type angiotensin-converting enzyme gene polymorphism and left-ventricular hypertrophy in hemodialysis patients

Yildiz A., Akkaya V., Hatemi A., Cine N., Tukek T., Gorcin B., et al.

NEPHRON , vol.84, no.2, pp.130-135, 2000 (SCI-Expanded, Scopus)

81. Role of the mutations Trp(8)double right arrow Arg and Ile(15)double right arrow Thr of the human luteinizing hormone beta-subunit in women with polycystic ovary syndrome

Elter K., Erel C., Cine N., Ozbek U., Hacihanefioglu B., Ertungealp E.

FERTILITY AND STERILITY , vol.71, no.3, pp.425-430, 1999 (SCI-Expanded, Scopus) Sustainable Development

82. Allele and genotype frequencies of the angiotensin - converting - enzyme (ACE) gene insertion - deletion polymorphism in the Turkish population

HATEMİ A. C., ÇİNE N., ÖZÇELİK H. T.

Turkish Journal of Medical Sciences , vol.27, no.3, pp.205-208, 1997 (TRDizin)

Papers Presented at Peer-Reviewed Scientific Conferences 112

1. Whole Exome Analysis in Seronegative Autoimmune Encephalitis: Insights from a Single-Center Study

CIRDI G., ÖZER T., GÖK A., SAKARYA GÜNEŞ A., TEKİN ORGUN L., SÜNNETÇİ AKKOYUNLU D., et al.

European Paediatric Neurology Society (EPNS) Congress, 8-12 Temmuz 2025, Münih, Almanya, Munich, Germany, 08 July 2025, (Full Text)

2. Seronegatif otoimmün ensefalitte tüm ekzom analizi: Tek merkez deneyimi

Cırdı G., Özer T., Gök A., Sakarya Güneş A., Tekin Orgun L., Sünnetçi Akkoyunlu D., et al.

26. Ulusal Çocuk Nörolojisi Kongresi, Antalya, Turkey, 30 April 2025, (Summary Text)

3. Prospective Evaluation Of The Relationship Between Intestinal Microbiata In Cases Diagnosed With Breast Cancer

ÖZSARAY M. F., ŞİMŞEK T., GÜLER S. A., ÇİNE N., SÜNNETÇİ AKKOYUNLU D., CANTÜRK N. Z.

Breastanbul 2024 The Conference, İstanbul, Turkey, 10 - 12 October 2024, vol.15, pp.68, (Summary Text)

4. Evaluation of the affected pathway and accompanying epilepsy type in central nervous system cell trafficking disorders - Single centre experience

Cirdi G., Akkoyunlu D. S., ÖZER T., Deniz A., SAKARYA GÜNEŞ A., TEKİN ORGUN L., et al.

15th European Epilepsy Congress, Rome, Italy, 7 - 11 September 2024, vol.65, pp.480-481, (Summary Text)

5. Otizm Spektrum Bozukluğu Olan Çocuklarda ve Sağlıklı Çocuklarda Nöroenflamatuvar Gen Ekspresyon Düzeylerinin Karşılaştırılması

KARA B., GÜLEN ŞİŞMANLAR Ş., YAVUZ S., AKPINAR Ş., SAKARYA GÜNEŞ A., DENİZ A., et al.

25. Ulusal Çocuk Nörolojisi Kongresi, Ankara, Turkey, 22 - 26 May 2024, (Summary Text)

6. Merkezi Sinir Sistemi Hücre Trafik Bozukluklarında Etkilenen Yolak ve Eşlik Eden Epilepsi Tipinin Değerlendirilmesi- Kocaeli Üniversitesi Deneyimi

CIRDI G., SÜNNETÇİ AKKOYUNLU D., ÖZER T., DENİZ A., SAKARYA GÜNEŞ A., OLGUN L., et al.

25. Ulusal Çocuk Nörolojisi Kongresi, Ankara, Turkey, 22 - 26 May 2024, (Summary Text)

7. A Different Perspective On Obesity Treatment: Gene Therapy

ŞAHİN S., EREN KESKİN S., SÜNNETÇİ AKKOYUNLU D., DOĞRUOĞLU B., İLKAY Z., VAROL E., et al.

12th Congress Of The International Federation For The Society Of Obesity And Metabolic Disorders European Chapter IFSO-EC 2024, Viyena, Austria, 2 - 04 May 2024, (Summary Text)

8. Guion- Almeida Tipi Mandibulofasiyal Disostozisin Genetik Araşatırması: Bir Olgu Sunumu

Yılmaz E. B., SÜNNETÇİ AKKOYUNLU D., Devrim N. N., İskenderoğlu E. T., ÇİNE N., CANTÜRK N. Z., et al.

International Gevher Nesibe Health Sciences Conference-XI, Ankara, Turkey, 10 - 11 October 2023, (Summary Text) Sustainable Development

9. Obezite Tedavisinde Farklı Bir Bakış: Gen Terapisi

ŞAHİN S., EREN KESKİN S., SÜNNETÇİ AKKOYUNLU D., DOĞRUUĞLU B., İLKAY Z., VAROL E., et al.

8.Uluslararası Morbid Obezite Ve Metabolik Hastalıklar Cerrahisi Kongresi, Antalya, Turkey, 5 - 08 October 2023, (Summary Text)

10. SARS-CoV-2 (COVID-19) Spike Reseptör Bağlanma Domain (S-RBD) Antijenine Yönelik Özgün Bir mRNA Aşısının Moleküler Modellemesi ve Geliştirilmesi

DURAN T., ÇİNE N., KOÇAK N., HATİPOĞLU D., ATEŞ M. B., ÇALIŞKAN Ü.

8. Klinik İmmunoloji Kongresi, Antalya, Turkey, 26 October 2022, (Summary Text)

11. The role of next-generation sequencing in the examination of breast cancer genetics in BRCA1/2-negative cases

CANTÜRK N. Z., ÇİNE N., UĞURTAŞ C., Gokbayrak M., Aydın D., Demir G., et al.

BREASTANBUL THE CONFERENCE 2022, İstanbul, Turkey, 13 - 15 October 2022, vol.13, pp.51, (Full Text)

12. The role of next-generation sequencing in the examination of breast cancer genetics in BRCA1/2-negative cases

CANTÜRK N. Z., ÇİNE N., ugurtas c., Gokbayrak M., Aydin D., Demir G., et al.

Breastanbul 2022, İstanbul, Turkey, 13 October 2022, (Summary Text)

13. INVESTIGATION OF THE EFFECT OF CHLORAMPHENICOL AND IPTG ON Escherichia coli TRANSCRIPTOME IN THE PRESENCE OF RECOMBINANT PLASMID

Babayeva A., Sünnetçi Akkoyunlu D., Dibek E., Çine N., Çöl B.

KARABAKH III. INTERNATIONAL CONGRESS OF APPLIED SCIENCES, Susa, Azerbaijan, 7 - 10 October 2022, pp.63-73, (Full Text)

14. Developmental Epileptic Encephalopathies in A National Cohort Study (Turkish EPISTEP -1): A Step-based Approachment for Etiologic Diagnosis

Kanmaz S., Ataş Y., Kayılıoğlu H., Ölçülü C. B., Özkan Kart P., Yıldız N., et al.

17th International Child Neurology Congress, Antalya, Turkey, 3 - 07 October 2022, pp.739, (Summary Text)

15. An Enrichment-based Approach to Understanding the Genetic Pathogenesis of Neurodevelopmental Disorders

Aykol D., Sönmezler E., Hancı Y. S., Tosun A. F., Ayanoğlu M., Gazeteci Tekin H., et al.

17th International Child Neurology Congress, Antalya, Turkey, 3 - 07 October 2022, pp.385, (Summary Text)

16. BRCA MUTASYONLU HASTALARIN KLİNİKOPATOLOJİK ÖZELLİKLERİ

Şahin E., Çabuk D., Gökbayrak M., Çine N., Özden E., Seyyar M., et al.

8. TÜRK TIBBİ ONKOLOJİ KONGRESİ, Antalya, Turkey, 3 - 07 November 2021, no.187, pp.112, (Full Text) Sustainable Development

17. Glial beyin tümörleri ile ilgili merkez genleri tanımlamak için gen ifadesi profil verilerinin analizi

Sünnetçi Akkoyunlu D., Külcü Sarıkaya N., Çine N., Eren Keskin S., Savlı H.

XVII. Tıbbi Biyoloji ve Genetik Kongresi, İstanbul, Turkey, 28 - 31 October 2021, pp.337, (Summary Text)

18. Erken-Başlangıçlı Epileptik Ensefalopati Tanılı 153 Olguda Gen paneli Analizleri

Sünnetçi Akkoyunlu D., Kara B., Çine N., Dursun B., Işık E. B., Eren Keskin S., et al.

17. Ulusal Uludağ Pediatri Kış Kongresi, Bursa, Turkey, 13 - 14 March 2021, pp.115, (Summary Text)

19. Solid Tümörlerde BRAF varyasyonlarının Yeni Nesil Dizileme ve Real Time-PCR Metodları ile Saptanması

Eren Keskin S., Sertdemir N., Demir G., Güzdolu E., Gül C., Sünnetçi Akkoyunlu D., et al.

9. Ulusal Moleküler Biyoloji ve Biyoteknoloji Kongresi, İstanbul, Turkey, 19 - 20 December 2020, pp.46-47, (Summary Text)

20. Hipomiyelinizan Lökodistrofi-14 İlişkili Biallelik UFM1 Delesyon Olgularının Klinik Bulgularında Nörotransmitter Bozuklukları Etken Olabilir mi?

Sünnetçi Akkoyunlu D., Kara B., Cerrah Güneş M., Çine N., Eren Keskin S., Savlı H.

14. uluslararası katılımlı ulusal tıbbi genetik kongresi, İstanbul, Turkey, 20 - 22 November 2020, pp.1-2, (Summary Text)

21. İntestinal Mikrobiyota Analizinin Yaygın Fonksiyonel Gastrointestinal Bozuklukların Tedavisindeki Etkisi

Sünnetçi Akkoyunlu D., Çelebi A., Dursun B., Külcü Sarıkaya N., Çine N., Hülagü S., et al.

6.Ulusal Bağısak Mikrobiyotası ve Probiyotik Kongresi, Antalya, Turkey, 28 October - 31 December 2019, (Summary Text)

22. Erken başlangıçlı epileptik ensefalopati tanılı hastalarda tanımlanan yeni ve de novo mutasyonlar

Sünnetçi Akkoyunlu D., Kara B., Çine N., Işık E. B., Dursun B., Külcü Sarıkaya N., et al.

16. Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 October - 30 December 2019, (Summary Text)

23. Meme kanserinde MMP2 ve TIMP1 Gen ifadesi Düzeylerinin Belirlenmesi

EREN KESKİN S., SÜNNETÇİ AKKOYUNLU D., SAVLI H., ÇİNE N., CANTÜRK N. Z., ŞİMŞEK T., et al.

16. Tıbbi Biyoloji ve Genetik Kongresi, Turkey, 27 October - 30 December 2019, (Summary Text) Sustainable Development

24. Olgu sunumu: Pallister-Killian Sendromunun Prenatal Tanısı

EREN KESKİN S., DOĞRUOĞLU B., İLKAY Z., SÜNNETÇİ AKKOYUNLU D., ÇİNE N., SAVLI H.

4. ÇOCUK GENETİK KONGRESİ, Ankara, Turkey, 25 September - 27 December 2019, (Summary Text)

25. Mozaik 22q11.2 mikrodelesyon sendromu

CERRAH GÜNEŞ M., EREN KESKİN S., ARSLAN O., BABAOĞLU A., SÜNNETÇİ AKKOYUNLU D., ÇİNE N., et al.

4. ÇOCUK GENETİK KONGRESİ, Turkey, 25 September - 27 December 2019, (Summary Text)

26. Detection of MEFV gene mutation frequency patients Familial Mediterrenean Fever (FMF) in Kocaeli region

İLKAY Z., ÇİNE N., AYDIN D., DAL B., SERTDEMİR N., SÜNNETÇİ AKKOYUNLU D., et al.

9. Ulusal Tıbbi Genetik Kongresi, Turkey, 1 - 05 December 2019, (Summary Text)

27. An investigation of Transcriptome Analyzes Related to endometrium cancer pathogenesis

İskenderoğlu E. T., SÜNNETÇİ AKKOYUNLU D., Devrim N. N., Yılmaz E. B., ÇİNE N., DOĞER E., et al.

Tıbbi Biyoloji ve Genetik Kongresi, 27 - 30 October 2019, (Summary Text) Sustainable Development

28. An investigation of non-functioning pituitary adenoma pathogenesis by transcriptome analysis

Devrim N. N., SÜNNETÇİ AKKOYUNLU D., Yılmaz E. B., İskenderoğlu E. T., ÇİNE N., ÇABUK B., et al.

Tıbbi Biyoloji ve Genetik Kongresi, 27 - 30 October 2019, (Summary Text)

29. Diskinetik serebral hareket bozukluğu ve bazal ganglion atrofisi olan 2 hastada biallelik 3 bç’xxlik UFM1 delesyonu: sık görülen bir varyant ve nadir görülen bir hipomyelinizan lökodistrofi, HLD14.

SÜNNETÇİ AKKOYUNLU D., KARA B., DURSUN B., CERRAH GÜNEŞ M., ÇİNE N., EREN KESKİN S., et al.

4.ÇOCUK GENETİK KONGRESİ, Turkey, 25 - 27 September 2019, (Summary Text)

30. Alternative approaches to conventional antiepileptic drugs in early infantile epileptic encephalopathies:Galactose and inositol therapies for SLC35A2 and PLCB1 gene mutations

KARA B., SÜNNETÇİ AKKOYUNLU D., KAVRAK M., seven karaman d., SAKARYA GÜNEŞ A., GÜNGÖR M., et al.

13th European Paediatric Meurology Society (EPNS) Congress, 17 - 21 September 2019, (Summary Text)

31. Diagnostic rate of targeted gene panel analysis of patients with early-infantile epileptic encephalopathy

KARA B., SÜNNETÇİ AKKOYUNLU D., SAKARYA GÜNEŞ A., GÜNGÖR M., ÇİNE N.

13th European Paediatric Neurology Society (EPNS) Congress, Greece, 17 - 21 September 2019, (Summary Text)

32. SLC35A2-CDG (CDG-2M) TANISI ALAN OLGUDA İZLEM VE GALAKTOZ DESTEĞİNİN YERİ

KAVRAK M., SÜNNETÇİ AKKOYUNLU D., SAKARYA GÜNEŞ A., GÜNGÖR M., ÇİNE N., KARA B.

21. ULUSLARARASI KATILIMLI ULUSAL ÇOCUK NÖROLOJİSİ KONGRESİ, Muğla, Turkey, 1 - 05 May 2019, (Summary Text)

33. ERKEN-BAŞLANGIÇLI EPİLEPTİK ENSEFALOPATİ TANILI 67 OLGUDAHEDEF GEN PANELİ ANALİZLERİ

Sünnetçi Akkoyunlu D., Kara B., Çine N., Yılmaz E. B., Dursun B., Külcü Sarıkaya N., et al.

13. ULUSAL TIBBİ GENETİK KONGRESİ, Antalya, Turkey, 7 - 11 November 2018, (Summary Text)

34. Importance of detection of ALK gene rearrengement with FISH method in non-small cell lung carcinoma patients

Seymen P., Gumuslu E., ÇİNE N.

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.962, (Summary Text)

35. NGS based ctDNA-liquide biopsy analysis in Turkish Cancer patients

ÇİNE N., sertdemir n., yavuz d., gökbayrak m., güzdolu e., demir g., et al.

5th Central-Eastern European Congresson Cell-Free Nucleic Acids, 21 - 22 June 2018, (Full Text) Sustainable Development

36. Identification of molecular signatures in gingiva of the patients with chronic periodontitis by genomic and proteomic analysis

GÜZELDEMİR AKÇAKANAT E., ORUÇGÜNEY B., SÜNNETÇİ AKKOYUNLU D., aydoğdu b., KAN B., akgün e., et al.

Europerio 9, 20 - 23 June 2018, (Summary Text)

37. Identiﬁcation of molecular signatures in gingiva ofthe patients with chronic periodontitis by genomic and proteomic analysis

GÜZELDEMİR AKÇAKANAT E., B O., SÜNNETÇİ AKKOYUNLU D., AKGÜN E., YILMAZ E. B. S., Baaykal A., et al.

Europerio9, 20 - 23 June 2018, pp.95, (Summary Text)

38. MULTİPL MYELOMDA GÖZLENEN KROMOZOM ANOMALİLERİNİN TESPİTİNDE KONVANSİYONEL SİTOGENETİK VE FLORESAN IN SITU HIBRIDIZASYON (FISH) YÖNTEMİNİN BİRLİKTE KULLANIMININ TANISAL DEĞERİNİN BELİRLENMESİ

DEMİR G., EREN KESKİN S., ÇİNE N., SAVLI H., REKA S., DOĞRUOĞLU B., et al.

15. ULUSAL TIBBİ BİYOLOJİ VE GENETİK KONGRESİ, Turkey, 26 - 29 October 2017, (Summary Text)

39. HLA-B27 ALLEL SIKLIĞININ ANKİLOZAN SPONDİLİT HASTALARINDA KLİNİK ÖNEMİNİN ARAŞTIRILMASI

AKICIOĞLU S., EREN KESKİN S., CEFLE A., GÜZDOLU E., SERTDEMİR N., ERTAN M., et al.

15. ULUSAL TIBBİ BİYOLOJİ VE GENETİK KONGRESİ, Turkey, 26 - 29 October 2017, (Summary Text)

40. Effect of the nanoparticle mediated gene silencing therapy in prostate cancer: Importance of the KLK14 gene in prostate cancer development

ÇİNE N., SÜNNETÇİ AKKOYUNLU D., EREN KESKİN S., İskenderoğlu E. T., Devrim N. N., Yılmaz E. B., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS, Copenhagen, 27 - 30 May 2017, vol.26, pp.974, (Summary Text) Sustainable Development

41. Importance of structural abnormalities detected by array comparative genomic hybridızation in recurrent miscarriage: a retrospective study

ÇALIŞKAN E., BENDER R. A., AKAR B., KABEGENOVA M., ASLAN U., ÇİNE N., et al.

25th European Congress of Obstetrics and Gynaecology 15th Congress of Turkish Society of Obstetrics and Gynaecology, Antalya, Turkey, 17 - 21 May 2017, (Summary Text)

42. Importance Of Structural Abnormalities Detected By Array Comparative Genomic Hybridization In Recurrent Miscarriage: A Retrospective Study

ÇALIŞKAN E., BENDER R. A., AKAR B., KOBEGONOVA M., ASLAN U., ÇİNE N., et al.

25th European Congress of Obstetrics and Gynaecology15th Congress of Turkish Society of Obstetrics and Gynaecology, 17 - 21 May 2017, (Summary Text)

43. Gene Expression Profiles in Chronic Periodontitis: Gene Network-Based Microarray Analysis

GÜZELDEMİR AKÇAKANAT E., SÜNNETÇİ AKKOYUNLU D., ORUÇGÜNEY B., ÇİNE N., KAN B., Yılmaz E. B., et al.

IADR, 22 - 25 March 2017, (Summary Text)

44. Gold nanoparticle-siRNA mediated NF-кB silencing in prostate cancer

SÜNNETÇİ AKKOYUNLU D., EREN KESKİN S., ÇİNE N., İSKENDEROĞLU E. T., YILMAZ E. B., DEVRİM N., et al.

6. Multidisipliner Kanser Araştırma Kongresi, Turkey, 27 October - 30 December 2016, (Summary Text) Sustainable Development

45. MDS Olgularında Konvansiyonel Sitogenetik ve FISH Yöntemlerinin Birlikte Kullanımının Prognostik Önemi

EREN KESKİN S., DOĞRUOĞLU B., İLKAY Z., SEYMEN P., REKA S., DEMİR G., et al.

42. Ulusal Hematoloji Kongresi, Turkey, 18 October - 22 December 2016, (Summary Text)

46. Multipl Myelom Olgularında P53 Delesyonun FISH Yöntemi İle Tespitinin Prognostik Değeri

EREN KESKİN S., SAVLI H., ÇİNE N., DOĞRUOĞLU B., İLKAY Z., DEMİR G., et al.

42. Ulusal Hematoloji Kongresi, Turkey, 18 October - 22 December 2016, (Summary Text)

47. MULTİPL MYELOM OLGULARINDA P53 DELESYONUN FISH YÖNTEMİ İLE TESPİTİNİN PROGNOSTİK DEĞERİ

EREN KESKİN S., SAVLI H., ÇİNE N., DOĞRUOĞLU B., İLKAY Z., DEMİR G., et al.

42. Ulusal Hematoloji Kongresi, Antalya, Turkey, 19 - 22 October 2016, pp.160, (Summary Text)

48. MDS OLGULARINDA KONVANSİYONEL SİTOGENETİK VE FISH YÖNTEMLERİNİN BİRLİKTE KULLANIMININ PROGNOSTİK ÖNEMİ

EREN KESKİN S., DOĞRUOĞLU B., İLKAY Z., SEYMEN P., REKA S., DEMİR G., et al.

42. Ulusal Hematoloji Kongresi, Antalya, Turkey, 19 - 22 October 2016, pp.68, (Summary Text)

49. Agresif Periodontitiste Gen Ekspresyonu ve Aktivitesinin Genomik ve Proteomik Yöntemlerle Değerlendirilmesi

GÜZELDEMİR AKÇAKANAT E., BAYKAL A. T., SÜNNETÇİ AKKOYUNLU D., ORUÇGÜNEY B., AKGÜN E., ÇİNE N., et al.

Türk Periodontoloji Derneği 46. Bilimsel Kongresi, Turkey, 5 - 06 May 2016, (Summary Text)

50. Gene Expression Profiles in Chronic and Aggressive Periodontitis

SÜNNETÇİ AKKOYUNLU D., GÜZELDEMİR AKÇAKANAT E., ORUÇGÜNEY B., ÇİNE N., KAN B., YILMAZ E. B., et al.

XIV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Turkey, 27 October - 30 December 2015, (Summary Text)

51. Gene expression profiles in chronic and aggressive periodontits

SÜNNETÇİ AKKOYUNLU D., GÜZELDEMİR AKÇAKANAT E., ORUÇGÜNEY B., ÇİNE N., KAN B., yılmaz e. b., et al.

XIV. ulusal Tıbbi Biyoloji ve Genetik Kongresi, Turkey, 27 - 30 October 2015

52. Kronik ve Agresif Periodontitiste Gen Ekspresyon Profilleri

SÜNNETÇİ AKKOYUNLU D., GÜZELDEMİR AKÇAKANAT E., ORUÇGÜNEY B., ÇİNE N., KAN B., YILMAZ E. B., et al.

XIV. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Turkey, 27 - 30 October 2015, (Summary Text)

53. Gene expression profiles in patients with aggressive periodontitis: a gene network-based microarray analysis

GÜZELDEMİR AKÇAKANAT E., SÜNNETÇİ AKKOYUNLU D., ORUÇGÜNEY B., ÇİNE N., KAN B., SAVLI H., et al.

2015 IADR/AADR/CADR, 11 - 14 March 2015, (Summary Text)

54. Gene expression profiles in patients with aggressive periodontitis a gene netwoek based microarray analysis

GÜZELDEMİR AKÇAKANAT E., SÜNNETÇİ AKKOYUNLU D., ORUÇGÜNEY B., ÇİNE N., KAN B., SAVLI H., et al.

IADR/AADR/CADR General Session and Exhibtion 2015, 10 - 14 March 2015, vol.94, pp.3145, (Summary Text)

55. Copy number variation profiling of patients with Intellectual Disability

SÜNNETÇİ AKKOYUNLU D., ÇİNE N., KARA B., GÜMÜŞLÜ K. E., AKKOYUNLU R. U., EREN KESKİN S., et al.

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

56. Ankara’da Satışı Yapılan Bazı Bebek Ek Gıda Numunelerinde Genetiği Değiştirilmiş Gıda Varlığı.

YAVUZ C. I., ÇİNE N., Vaizoglu S. A., GÜLER Ç.

17. Ulusal Halk Sağlığı Kongresi 20-24 Ekim 2014, Edirne, Turkey, 24 October 2014, (Summary Text)

57. Phenotype-Genotype Correlation of a patient with 2q22.3 duplication distrupting ZEB2 gene associatiated with Mowat Wilson syndrome

SÜNNETÇİ AKKOYUNLU D., ÇİNE N., GÜMÜŞLÜ K. E., KARA B., EREN KESKİN S., DOĞRUOĞLU B., et al.

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

58. Mosaic Trisomy 9: A case study

GÜMÜŞLÜ K. E., EREN KESKİN S., DOĞRUOĞLU B., İLKAY Z., ÇİNE N., SÜNNETÇİ AKKOYUNLU D., et al.

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

59. 46,XX,t(2222) karyotipli olgu sunumu

EREN KESKİN S., DOĞRUOĞLU B., İLKAY Z., GÜMÜŞLÜ K. E., SÜNNETÇİ AKKOYUNLU D., ÇİNE N., et al.

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

60. Olgu sunumu: 46,XY, t(36)(p13q27) karyotipli fetüsün prenatal tanısı

EREN KESKİN S., DOĞRUOĞLU B., İLKAY Z., BURHANOĞLU T., GÜMÜŞLÜ K. E., SÜNNETÇİ AKKOYUNLU D., et al.

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

61. BAC tabanlı array CGH teknolojisinin ve kromozom analizinin prenatal tanıda kullanım etkinliğinin araştırılması

EREN KESKİN S., SÜNNETÇİ AKKOYUNLU D., DOĞRUOĞLU B., İLKAY Z., GÜMÜŞLÜ K. E., ÇİNE N., et al.

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

62. Renal parankimal tümörlere genomik yaklaşımlar

GÜMÜŞLÜ K. E., YILDIZ D. K., ÇİNE N., SAVLI H.

23.Ulusal Patoloji Kongresi, Turkey, 6 - 10 November 2013, (Summary Text)

63. Yeni nesil DNA dizi analizi metodu ile taranan FMF olgularında MEFV gen mutasyonlarının sıklığı

AYDIN D., SERTDEMİR N., NİGİZ B., SÜNNETÇİ AKKOYUNLU D., EREN KESKİN S., ÇİNE N., et al.

13. Ulusal Tıbbi biyoloji ve Genetik Kongresi, Turkey, 27 - 30 October 2013, (Summary Text)

64. Primer amenoreli bir olguda A-CGH ve konvansiyonel sitogenetik yöntemlerin karşılaştırılması

DOĞRUOĞLU B., ÇİNE N., EREN KESKİN S., SÜNNETÇİ AKKOYUNLU D., GÜMÜŞLÜ K. E., AYDIN D., et al.

13. Ulusal Tıbbi biyoloji ve Genetik Kongresi, Turkey, 27 - 30 October 2013, (Summary Text)

65. HPX, POTEE, SLC4A1 ve APOA1, meme kanserinde yeni belirteç adayları: Bir proteomik konfirmasyonlu mikroarray çalışması

SÜNNETÇİ AKKOYUNLU D., ÇİNE N., BAYKAL A. T., ACIOĞLU Ç., EREN KESKİN S., SAVLI H.

13. Ulusal Tıbbi biyoloji ve Genetik Kongresi, Turkey, 27 - 30 October 2013, (Summary Text) Sustainable Development

66. Olgu sunumu: 9p tetrazomisi

EREN KESKİN S., ÇİNE N., DOĞRUOĞLU B., SÜNNETÇİ AKKOYUNLU D., AKKOYUNLU R. U., AYDIN D.

13. Ulusal Tıbbi biyoloji ve Genetik Kongresi, Turkey, 27 - 30 October 2013, (Summary Text)

67. Konuşma bozuklukları ve genetik

ÇİNE N., GÜMÜŞLÜ K. E.

7. Ulusal dil ve konuşma bozuklukları kongresi, Turkey, 5 - 07 May 2013, (Summary Text)

68. İnversiyon 9’un Klinik Önemi

EREN KESKİN S., DOĞRUOĞLU B., AKKOYUNLU R. U., GÜMÜŞLÜ K. E., ÇİNE N., SÜNNETÇİ AKKOYUNLU D., et al.

10. Ulusal Tıbbi Genetik Kongresi, Turkey, 19 - 23 December 2012, (Summary Text)

69. 46,XX,ins(31)(q22,q25qter) karyotipli ikiz: Olgu Sunumu

AKKOYUNLU R. U., GÜMÜŞLÜ K. E., EREN KESKİN S., DOĞRUOĞLU B., SÜNNETÇİ AKKOYUNLU D., ÇİNE N., et al.

10. Ulusal Tıbbi Genetik Kongresi, Turkey, 19 - 23 December 2012, (Summary Text)

70. Mental retardasyonun molekuler tanisinda array cgh’in yeri

SÜNNETÇİ AKKOYUNLU D., ÇİNE N., KARA B., GÜMÜŞLÜ K. E., AKKOYUNLU R. U., EREN KESKİN S., et al.

10. Ulusal Tibbi Genetik Kongresi, Turkey, 19 - 23 December 2012, (Summary Text)

71. 8q11.1-q11.23 delesyonlu dismorfik olgunun fenotip ve moleküler karyotip özelliklerinin değerlendirilmesi

GÜMÜŞLÜ K. E., ÇİNE N., SÜNNETÇİ AKKOYUNLU D., AKKOYUNLU R. U., EREN KESKİN S., SAVLI H.

10. Ulusal Tibbi Genetik Kongresi, Turkey, 19 - 23 December 2012, (Summary Text)

72. Tianeptin ve olanzepinin öngörülemeyen kronik hafif stres uygulanan farelerde öğrenme ve bellek üzerine etkilerinin gen düzeyinde araştırılması

GÜMÜŞLÜ K. E., SÜNNETÇİ AKKOYUNLU D., MUTLU O., ENGÜZEL B., SAVLI H., ÇİNE N.

10. Ulusal Tıbbi Genetik Kongresi, Turkey, 19 - 23 December 2012, (Summary Text)

73. Meme Kanserinde Tüm Genom Ekspresyon, Standart Altyol ve Gen Ağı Analizleri

CANTÜRK N. Z., SÜNNETÇİ AKKOYUNLU D., ÇİNE N., ERÇİN C., ŞİMŞEK T., SAVLI H.

6. Cerrahi Araştırma Kongresi, Ankara, Turkey, 8 - 10 December 2011, (Summary Text) Sustainable Development

74. Tianeptin ve olanzepinin öngörülemeyen kronik hafif stres uygulanan farelerde öğrenme ve bellek üzerine etkileri.

MUTLU O., SÜNNETÇİ AKKOYUNLU D., GÜMÜŞLÜ K. E., KOMSUOĞLU ÇELİKYURT F. İ., ÇİNE N., SAVLI H., et al.

21.Ulusal Farmakoloji Kongresi, 19 October 2011, (Summary Text)

75. Tianeptin ve olanzapinin öngörülemeyen kronik hafif stres uygulanan farelerde öğrenme ve bellek üzerine etkileri

MUTLU O., SÜNNETÇİ AKKOYUNLU D., GÜMÜŞLÜ K. E., KOMSUOĞLU ÇELİKYURT F. İ., ÇİNE N., SAVLI H., et al.

21. Ulusal Farmakoloji Kongresi, Eskişehir, Turkey, 19 - 22 October 2011

76. Comparative genomic hybridization array study in non-syndromic (primary) autism patients

Gumuslu E., ÇİNE N., KARA B., SAVLI H.

24th Congress Meeting of European-College-of-Neuropsychopharmacology, Paris, France, 3 - 07 September 2011, vol.21, (Summary Text)

77. HTFA (High Throughput FISH Analysis): A new sensitive approach to screen hematological malignancies

UZULMEZ N., ÇİNE N., SÜNNETÇİ AKKOYUNLU D., GÜMÜŞLÜ K. E., ENGÜZEL B., EREN KESKİN S., et al.

European Human Genetics Conference 2011, 28 - 31 May 2011, (Summary Text)

78. Detection of genetic abnormalities by array comparative genomic hybridization for fetal tissues

EREN KESKİN S., ÇİNE N., SÜNNETÇİ AKKOYUNLU D., ÜZÜLMEZ N., GÜMÜŞLÜ K. E., ENGÜZEL B., et al.

European Human Genetics Conference 2011, 28 - 31 May 2011, (Summary Text)

79. Diagnostic value of a CGH method for recurrent mlscarriage and implantation failures

AKKOYUNLU R. U., ENGÜZEL B., ÇİNE N., SÜNNETÇİ AKKOYUNLU D., ÜZÜLMEZ N., EREN KESKİN S., et al.

European Human Genetics Conference 2011, Amsterdam, Netherlands, 28 - 31 May 2011, (Summary Text)

80. Behavioral abnormalities and epilepsy: Four cases with microduplication and microdeletion syndromes

KARA B., GÜMÜŞLÜ K. E., ÇİNE N., SAVLI H.

European Pediatric Neurology Society Congress (9th EPNS Congress ), 11 - 14 May 2011, (Summary Text)

81. Mutations frequency of the thrombosis risk factor genes in habituel abortus patients in the region of Kocaeli

AYDIN D., ÇİNE N., İLKAY Z., DAL B., SERTDEMİR N., GÜMÜŞLÜ K. E., et al.

9. Ulusal Tıbbi Genetik Kongresi, Turkey, 1 - 05 December 2010, (Summary Text)

82. Application of array CGH method in two 18Q21.31.Q23 deletion patients

GÜMÜŞLÜ K. E., ÇİNE N., KARA B., SÜNNETÇİ AKKOYUNLU D., ÜZÜLMEZ N., ENGÜZEL B., et al.

Tıbbi Genetik Deneği 9. Ulusal Tıbbi Genetik Kongresi, Turkey, 1 - 09 December 2010, (Summary Text)

83. A Turkish Patient With Large 17p11 2 Deletion Presenting With Smith Magenis Syndrome

TUĞ E., ÇİNE N., AYDIN H.

Ulusal 9. Tıbbi Genetik Kongresi, Turkey, 1 - 05 December 2010

84. Detection of genetic abnormalities by array comparative genomic hybridization for prenatal diagnosis

EREN KESKİN S., ÇİNE N., GÜMÜŞLÜ K. E., AKKOYUNLU R. U., İLKAY Z., DAL B., et al.

9 th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, 1 - 05 December 2010, vol.78, pp.14, (Summary Text)

85. Comparison of a CGH and conventional cytogenetics in a primary amenorrhea case

ENGÜZEL B., ÇİNE N., EREN KESKİN S., SÜNNETÇİ AKKOYUNLU D., GÜMÜŞLÜ K. E., İLKAY Z., et al.

Tıbbi Genetik Deneği 9. Ulusal Tıbbi Genetik Kongresi, Turkey, 1 - 05 December 2010, (Summary Text)

86. Value of array CGH in the evaluation of microdeletion syndromes

ÇİNE N., AKKOYUNLU R. U., GÜMÜŞLÜ K. E., SÜNNETÇİ AKKOYUNLU D., ÜZÜLMEZ N., ENGÜZEL B., et al.

Tıbbi Genetik Deneği 9. Ulusal Tıbbi Genetik Kongresi, Turkey, 1 - 05 December 2010, (Summary Text)

87. Split hand food malformation associated with sensorineural hearig loss: a case study

TUĞ E., ÇİNE N., AYDIN H., GÜMÜŞLÜ K. E.

Tıbbi Genetik Deneği 9. Ulusal Tıbbi Genetik Kongresi, Turkey, 1 - 05 December 2010, (Summary Text)

88. Fast screening of chromosomal aneuploidies for invitro fertilization improvemenf on preimplantation genetic diagnosis samples

SAVLI H., SÜNNETÇİ AKKOYUNLU D., ÇALIŞKAN E., GÜMÜŞLÜ K. E., EREN KESKİN S., AKKOYUNLU R. U., et al.

Tıbbi Genetik Deneği 9. Ulusal Tıbbi Genetik Kongres, Turkey, 1 - 05 December 2010, (Summary Text)

89. Detectıon of genetıc abnormalities by array comperative genomic hybridization for prenatal diagnosis

EREN KESKİN S., ÇİNE N., GÜMÜŞLÜ K. E., AKKOYUNLU R. U., İLKAY Z., DAL B., et al.

9th National Medical Genetics Congress of Turkish Medical Genetics, Turkey, 1 - 05 December 2010, vol.78, pp.14, (Summary Text)

90. Diagnostic use of targeted array CGH platforms: 2009-2010 Kocaeli University experience

SAVLI H., SÜNNETÇİ AKKOYUNLU D., ÜZÜLMEZ N., GÜMÜŞLÜ K. E., YAVUZ D., EREN KESKİN S., et al.

Tıbbi Genetik Deneği 9. Ulusal Tıbbi Genetik Kongresi, Turkey, 1 - 05 December 2010, (Summary Text)

91. Complex Hemihyperplasia with Associated Cutis Marmorata: A case study.

TUĞ E., ÇİNE N., Temizkan C., Aydın H., Gümüşlü E.

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, 01 October 2010, (Full Text)

92. Split Hand/Foot Malformation Associated with Sensorineural Hearing Loss: A case study.

TUĞ E., ÇİNE N., Aydın H., Gümüşlü E.

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, 01 October 2010, (Full Text)

93. EXPRESSION AND IMMUNOHISTOCHEMICAL ANALYSIS OF AQUAPORINE GENES IN MESIAL TEMPORAL SCLEROSIS EXPRESSION AND IMMUNOHISTOCHEMICAL ANALYSIS OF AQUAPORINE GENES IN MESIAL TEMPORAL SCLEROSIS

BEBEK N., ÖZDEMİR Ö., SAYİTOĞLU M., BAYKAL B., Ozbek U., Karasu A., et al.

63rd Annual Meeting of the American-Epilepsy-Society, Massachusetts, United States Of America, 4 - 08 December 2009, vol.50, pp.302, (Summary Text)

94. Angelman sendromlarında microarray tabanlı karşılaştırmalı genomic hibridizasyon (array CGH) teknolojisi ile genomic analizler

SAVLI H., ÇİNE N., KARA B., SÜNNETÇİ AKKOYUNLU D., GÜMÜŞLÜ K. E., ÜZÜLMEZ N., et al.

XI Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Turkey, 28 - 31 October 2009, pp.70, (Summary Text)

95. Epilepsy DNA Bank Project in Istanbul University

Özdemir Ö., YÜCESAN E., KOCASOY ORHAN E., BEBEK N., ÇİNE N., Baykan B., et al.

Idiopathic Generalized Epilepsies (IGE): Developmental Aspects Bridging Basic Science and Clinical Research, Turkey, 3 - 06 October 2007

96. Determinationof E352K mutation in the GABA receptor alpha-subunit causing juvenile myoclonic epilepsy

YÜCESAN E., Maljevic S., BEBEK N., Baykan B., Uğurel E., Ozyer İ., et al.

Idiopathic Generalized Epilepsies (IGE): Developmental Aspects Bridging Basic Science and Clinical Research, Turkey, 3 - 06 October 2007

97. Endothelial dysfunction, inflammation, ACE and e-NOS gene polymorphism in haemodialysis patients

Yazici H., Cine N., Ozturk S., Pusuroglu H., Genchallac H., Erginel-Unaltuna N., et al.

43rd ERA-EDTA Congress, Glasgow, United Kingdom, 15 - 18 July 2006, vol.21, pp.431, (Summary Text)

98. Brain derived neurotrophic factor (BDNF) and multidrug resistance (MDR) gene polymorphisms in patients with mesial temporal sclerosis (MTS)

Purcu G., Gurses C., Bebek N., Cine N., Baykal B., Ozbek U., et al.

26th International Epilepsy Congress, Paris, France, 28 August - 01 September 2005, vol.46, pp.258, (Summary Text)

99. Genetic predisposition to endothelial dysfunction in chronic heart failure: A controlled study

Demirel S., Akkaya V., Erk O., Cine N., Oflaz H., Genchellac H., et al.

14th European Meeting on Hypertension, Paris, France, 13 - 17 June 2004, vol.22, (Summary Text)

100. Endothelial function: How is it affected in healthy humans without obvious cardiac risk factors?

Erk O., Demirel S., Akkaya V., Cine N., Oflaz H., Genchellac H., et al.

14th European Meeting on Hypertension, Paris, France, 13 - 17 June 2004, vol.22, (Summary Text)

101. Genetic predisposition to endothelial dysfunction in essential hypertension: A controlled study

Akkaya V., Erk O., Demirel S., Cine N., Oflaz H., Genchellac H., et al.

14th European Meeting on Hypertension, Paris, France, 13 - 17 June 2004, vol.22, (Summary Text)

102. Genetic predisposition to endothelial dysfunction in chronic heart failure: A controlled study

Demirel S., Erk O., Akkaya V., Cine N., Oflaz H., Genchellac H.

20th ISH Meeting, Sao-Paulo, Brazil, 15 - 19 February 2004, vol.22, (Summary Text)

103. Endothelial dysfunction: What does affect it in healthy humans without obvious cardiac risk factors

Demirel S., Erk O., Akkaya V., Cine N., Oflaz H., Genchellac H.

20th ISH Meeting, Sao-Paulo, Brazil, 15 - 19 February 2004, vol.22, (Summary Text)

104. Genetic predisposition to endothelial dysfunction in essential hypertension: A controlled study

Demirel S., Erk O., Akkaya V., Cine N., Oflaz H., Genchellac H.

20th ISH Meeting, Sao-Paulo, Brazil, 15 - 19 February 2004, vol.22, (Summary Text)

105. Evaluation of gabra1 gene in idiopathic epilepsies

Cine N., Bebek N., Gurses C., Baykan B., Gokyigit A., Dervent A., et al.

6th European Congress on Epileptology, Vienna, Austria, 30 May - 03 June 2004, vol.45, pp.118-119, (Summary Text)

106. Predictive C3435T polymorphism in the MDR1 for carbamazepine plasma levels

Oner G., Bebek N., Cine N., Eskazan E., Yeni N., Baykan B., et al.

6th European Congress on Epileptology, Vienna, Austria, 30 May - 03 June 2004, vol.45, pp.121, (Summary Text)

107. Autosomal recessive idiopathic epilepsy: linkage to chromosome 9q32-33

Baykan B., Madia F., Bebek N., Gianotti S., Guney A., Cine N., et al.

6th European Congress on Epileptology, Vienna, Austria, 30 May - 03 June 2004, vol.45, pp.123, (Summary Text)

108. The association of endothelial dysfunction with endothelial nitric oxide synthase gene polymorphism in essential hypertension and heart failure: A controlled study

Demirel S., Genchellac H., Cine N., Oflaz H., Ala M., Vatansever S., et al.

13th European Meeting on Hypertension, Milan, Italy, 13 - 17 June 2003, vol.21, (Summary Text)

109. Effect of methylenetetrahydrofolate reductase gene polymorphism on methotrexate toxicity after bone marrow transplantation

BEŞIŞIK S., Gurses N., Caliskan Y., Tarakci F., ÇİNE N., Aydin M., et al.

29th Annual Meeting of the European-Group-for-Blood-and-Marrow-Transplantation/19th Meeting of the EBMT-Nurses-Group/2nd Meeting of the EBMT-Data-Management-Group, İstanbul, Turkey, 23 - 26 March 2003, (Summary Text)

110. The association of endothelial dysfunction with endothelial constitutive nitric oxide synthase gene polymorphism in different patient populations

DEMİREL A. Ş., Genchallac H., Oflaz H., TÜKEK T., Akkaya V., ÇİNE N., et al.

19th Meeting of the International-Society-for-Hypertension/12th European-Society-of-Hypertension Meeting, PRAGUE, Czech Republic, 23 - 27 June 2002, (Summary Text)

111. The association of endothelial constitutive nitric oxide synthase gene polymorphism (ecNOS) in the Turkish population

Demirel S., Cine N., Oflaz H., Tukek T., Akkaya V., Demirkan A., et al.

19th Meeting of the International-Society-for-Hypertension/12th European-Society-of-Hypertension Meeting, PRAGUE, Czech Republic, 23 - 27 June 2002, vol.20, (Summary Text)

112. Leptin receptor variant in women with PCOS

EREL C. T., ÇİNE N., ELTER K., KALELİ S., ŞENTÜRK M. L., TASAN E.

56th Annual Meeting of the ASRM, 21 - 26 October 2000

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