Publications & Works

Publication Network
Articles 70
All (70)
SCI-E, SSCI, AHCI (28)
SCI-E, SSCI, AHCI, ESCI (34)
ESCI (6)
Scopus (29)
TRDizin (26)
Other Publications (18)

1. Investigation of extracellular matrix genes associated with Alzheimer's disease in the hippocampus of experimental diabetic model rats

Ozpak L., PAZARBAŞI A., ÖCAL I., YILMAZ M., BİNOKAY H.
INTERNATIONAL JOURNAL OF DIABETES IN DEVELOPING COUNTRIES , vol.42, no.1, pp.82-90, 2022 (SCI-Expanded, Scopus) Sustainable Development identifier identifier

2. Induction of Tumor-Selective Cytotoxicity by Myrtus communis L. Extract and its Bioactive Metabolite 1, 8-cineole

KAŞIKÇI Y., PAZARBAŞI A., KARAÇAY S., KAYA D. A., GÜLBOL DURAN G., YILMAZ M. B.
Medicinal Aromatic Plants , vol.10, no.1, pp.1-6, 2021 (Peer-Reviewed Journal)

3. Vitamin D receptor and collagen type1α1 gene polymorphisms in patients with postmenauposal osteoporosis

KOCATÜRK SEL S., PAZARBAŞI A., YILMAZ M. B., BAŞARAN S., SARPEL T., ÖZPAK L., et al.
Cukurova Medical Journal , 2019 (TRDizin)

4. Postmenopozal osteoporoz hastalarında vitamin D reseptör ve kollajen tip1α1 gen polimorfizimleri

KOCATÜRK SEL S., PAZARBAŞI A., YILMAZ M. B., BAŞARAN S., SARPEL T., ÖZPAK L., et al.
Cukurova Medical Journal , vol.44, no.3, pp.936-946, 2019 (TRDizin)

5. Vitamin D receptor and collagen type1 alpha 1 gene polymorphisms in patients with postmenauposal osteoporosis

KOCATÜRK SEL S., PAZARBAŞI A., YILMAZ M. B., BAŞARAN S., SARPEL T., ÖZPAK L., et al.
CUKUROVA MEDICAL JOURNAL , vol.44, no.3, pp.936-946, 2019 (ESCI, TRDizin) Sustainable Development identifier

6. ”Chromosomal alterations in patients with breast cancer”,

DEMİRHAN O., TANRIVERDİ N., PAZARBAŞI A., süleymanova D.
European Journal Of Human Genetics , vol.26, pp.536, 2018 (SCI-Expanded, Scopus) Sustainable Development

7. ”Analysis of maternal polymorphism of CBS gene and risk of Down syndrome offspring”,

PAZARBAŞI A., ÖZPAK L., DEMİRHAN O.
European Journal Of Human Genetics , vol.26, pp.827, 2018 (SCI-Expanded, Scopus)

8. Maternal polymorphisms of MTHFR gene and risk of Down syndrome offspring in Turkish population

Keser N., PAZARBAŞI A., ÖZPAK L.
CUKUROVA MEDICAL JOURNAL , vol.43, no.1, pp.73-80, 2018 (ESCI, TRDizin) identifier

9. Cancerous cell lines alter their genomic organization and karyotype with increased passage number: a cytogenetic study

YILMAZ M. B., Tunç E., ILGAZ N. S., ÖKSÜZ H., öztecik E., ÖZPAK L., et al.
CUKUROVA MEDICAL JOURNAL , vol.43, no.4, pp.923-930, 2018 (ESCI, TRDizin) Sustainable Development identifier

10. Frequencies and distributions of sex chromosome abnormalities in females with the Turner phenotype: a long-term retrospective study in the southern region of Turkey

TANRıVERDI N., Demirhan O., SÜLEYMANOVA D., PAZARBAŞı A.
Turkish journal of medical sciences , vol.47, pp.1447-1455, 2017 (SCI-Expanded, Scopus, TRDizin) identifier identifier identifier

11. Maternal Polymorphisms of MTHFR Gene and Risk of Down Syndrome Offspring in Turkish Population

Keser N., PAZARBAŞI A., ÖZPAK L.
CUKUROVA MEDICAL JOURNAL , no.43, pp.73-79, 2017 (SCI-Expanded, TRDizin)

12. Frequencies and distributions of sex chromosome abnormalities in females with Turner phenotype in south region of Turkey.

TANRIVERDİ N., DEMİRHAN O., süleymanova D., PAZARBAŞI A.
Turkish Journal Of Medical Sciences , vol.47, no.5, pp.1445-1457, 2017 (SCI-Expanded, Scopus, TRDizin)

13. Evaluation of single nucleotide polymorphisms of angiotensin II type 2 receptor (AGTR2) gene and interleukin 4 (IL-4) gene for their contribution to the risk of preeclampsia in Turkish population

ÖZPAK L., PAZARBAŞI A., Keser N., Yilmaz M. B., LÜLEYAP H. Ü., Ozgunen F. T.
CUKUROVA MEDICAL JOURNAL , vol.42, no.3, pp.477-483, 2017 (ESCI, TRDizin) identifier

14. Alzheimer Hastalığının Genetiği ve Epigenetiği

ÖZPAK L., PAZARBAŞI A., Keser N.
Arşiv Kaynak Tarama Dergisi , vol.26, no.1, pp.35, 2017 (TRDizin)

15. The analysis of the phenylalanine hydroxylase gene mutations by sequencing and ARMS techniques in Turkish patients

Luleyap U., PAZARCI P., CÖMERTPAY G., Onenli H. N., PAZARBAŞI A., ALPTEKİN D., et al.
CUKUROVA MEDICAL JOURNAL , vol.41, no.4, pp.702-708, 2016 (ESCI, TRDizin) identifier

16. Postmenopozal Osteoporoz ile Östrojen Reseptör Alfa Geni (ER945) XbaI ve PvuII Polimorfizmlerinin İlişkisi

bulca s., kasap h., SARPEL T., KOCATÜRK SEL S., BAŞARAN S., YILMAZ M. B., et al.
CUKUROVA MEDICAL JOURNAL , vol.39, no.1, 2014 (TRDizin)

17. The effect of conception time and maternal age upon fetal sex ratio in Çukurova population, Adana-Turkey

Tunç E., DEMİRHAN O., PAZARBAŞI A., Tastemir D., Guzel A. I., KASAP M., et al.
CUKUROVA MEDICAL JOURNAL , vol.39, no.2, pp.248-255, 2014 (TRDizin) Sustainable Development

18. Methylenetetrahydrofolate Reductase Activity and Folate Metabolism

Keser N., PAZARBAŞI A., Özpak L.
Çukurova Üniversitesi Tıp Fakültesi Arşiv Kaynak Tarama Dergisi , vol.23, no.2, pp.237-256, 2014 (Peer-Reviewed Journal)

19. Association of Estrogen Receptor Alpha Gene XbaI and PvuII Polymorphisms with Postmenopausal Osteoporosis

Bulca S., KASAP H., SARPEL T., Kocaturk-Sel S., BAŞARAN S., Yilmaz B., et al.
CUKUROVA MEDICAL JOURNAL , vol.39, no.1, pp.105-116, 2014 (TRDizin)

20. Postmenopozal Osteoporoz ile Östrojen Reseptör Alfa Geni ER XbaI ve PvuII Polimorfizmlerinin İlişkisi

Bulca S., KASAP H., SARPEL T., KOCATÜRK SEL S., BAŞARAN S., YILMAZ M. B., et al.
CUKUROVA MEDICAL JOURNAL , vol.39, no.1, pp.105-116, 2014 (TRDizin)

21. Genetic polymorphisms of estrogen receptor alpha and catechol-O-methyltransferase genes in Turkish patients with familial prostate carcinoma

PAZARBAŞI A., Yılmaz M., Alptekin D., Luleyap U., Tansug Z., Ozpak L., et al.
Indian Journal of Human Genetics , vol.19, no.4, pp.408-411, 2013 (Peer-Reviewed Journal)

22. Gelişmekte olan fare fetüs beyninde Aromataz, Östrojen Reseptör Alfa ve Progesteron reseptörünün birbirleriyle olan ilişkileri

YILMAZ M. B., Erkoç M. A., Kocatürk Sel S., Tunç E., Özpak L., PAZARBAŞI A., et al.
CUKUROVA MEDICAL JOURNAL , vol.38, no.2, pp.174-180, 2013 (TRDizin)

23. Association between pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections disease and tumor necrosis factor-? gene-308 g/a, -850 c/t polymorphisms in 4-12-year-old children in Adana/Turkey

Luleyap U., Onatoglu D., Yılmaz M., Alptekin D., Tahiroglu A., Çetiner S., et al.
Indian Journal of Human Genetics , vol.19, no.2, pp.196-201, 2013 (Peer-Reviewed Journal)

24. Gelişmekte Olan Fare Fetüs Beyninde Aromataz, Östrojen Reseptör Alfa ve Progesteron Reseptörünün Birbirleriyle Olan İlişkileri

YILMAZ M. B., PAZARBAŞI A., LÜLEYAP H. Ü., ALPTEKİN D., OZPAK L., PAZARBAŞI A., et al.
CUKUROVA MEDICAL JOURNAL , vol.38, no.2, pp.175-180, 2013 (TRDizin)

25. Atipik Yüz Görünümü ve Zeka Geriliği Olan Bir Olguda Homolog Olmayan İki Kromozomun Her İki Eşleri Arasındaki Translokasyonun [t(16;19)(q24;q12)x2] Varlığı

Tanriverdi N., PAZARBAŞI A., Suleymanova-Karahan D., Güney İ., Tastemir D., Tunç E., et al.
CUKUROVA MEDICAL JOURNAL , vol.38, no.3, pp.540-545, 2013 (TRDizin)

26. Gelişmekte Olan Fare Fetüs Beyninde Aromataz, Östrojen Reseptör Alfa ve Progesteron Reseptörünün Birbirleriyle Olan İlişkileri

YILMAZ M. B., PAZARBAŞI A., LÜLEYAP H. Ü., ALPTEKİN D., OZPAK L., PAZARBAŞI A., et al.
CUKUROVA MEDICAL JOURNAL , vol.38, no.2, pp.175-180, 2013 (TRDizin)

27. 10. Kromozomdaki Perisentrik İnversiyonun Agresif Davranış ve Hiperaktivite Üzerine Etkisi

Tanriverdi N., PAZARBAŞI A., Suleymanova-Karahan D., Avcı A., Tahiroglu A. Y., Tunc E., et al.
CUKUROVA MEDICAL JOURNAL , vol.38, no.1, pp.108-113, 2013 (TRDizin)

28. INHERITANCE OF A CHROMOSOME 3 AND 21 TRANSLOCATION IN THE FETUSES, WITH ONE ALSO HAVING TRISOMY 21, IN THREE PREGNANCIES IN ONE FAMILY

PAZARBAŞI A., DEMİRHAN O., ALPTEKİN D., ÖZGÜNEN F. T., ÖZPAK L., YILMAZ M., et al.
BALKAN JOURNAL OF MEDICAL GENETICS , vol.16, no.2, pp.91-96, 2013 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

29. Association between pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections disease and tumor necrosis factor gene 308 g a 850 c t polymorphisms in 4 12 year old children in Adana Turkey

Lüleyap H. Ü., Dilge O., Yılmaz M. B., Alptekin D., Tahiroğlu A., Çetiner S., et al.
INDIAN JOURNAL OF HUMAN GENETICS , vol.19, no.2, pp.196, 2013 (SCI-Expanded) Creative Commons License identifier

30. Prenatal (Doğum Öncesi) Tanı

Özalp Yüreğir Ö., BÜYÜKKURT S., KOÇ A. F., PAZARBAŞI A.
Çukurova Üniversitesi Tıp Fakültesi Arşiv Kaynak Tarama Dergisi , vol.21, no.1, pp.80-94, 2012 (Peer-Reviewed Journal)

31. RAPID DETECTION OF FETAL ANEUPLOIDIES BY QUANTITATIVE FLUORESCENT-POLYMERASE CHAIN REACTION FOR PRENATAL DIAGNOSIS IN THE TURKISH POPULATION

GÜZEL A. İ., YILMAZ M., DEMİRHAN O., PAZARBAŞI A., KOCATURK-SEL S., ERKOC M. A., et al.
BALKAN JOURNAL OF MEDICAL GENETICS , vol.15, no.1, pp.11-17, 2012 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

32. Studies on angiotensin-converting enzyme insertion/deletion polymorphism and genotype distributions in Turkish preeclampsia patients.

Bereketoglu C., Kasap M., Pazarbaşı A.
Journal of pregnancy , vol.2012, pp.108206, 2012 (Scopus) Creative Commons License identifier identifier

33. Association between Obsessive Compulsive Disorder and Tumor Necrosis Factor Gene 308 G A and 850 C T Polymorphisms in Turkish Children

Lüleyap H. Ü., Onatoğlu D., Tahiroğlu A., Alptekin D., Yılmaz M., Çetiner S., et al.
Balkan Journal of Medical Genetics , vol.15, no.2, pp.61-66, 2012 (SCI-Expanded, Scopus) Creative Commons License

34. ASSOCIATION BETWEEN OBSESSIVE COMPULSIVE DISORDER AND TUMOR NECROSIS FACTOR-alpha GENE-308 (G > A) AND-850 (C > T) POLYMORPHISMS IN TURKISH CHILDREN

Lüleyap H. Ü., Onatoglu D., Tahiroglu A. Y., Alptekin D., Yılmaz M., Çetiner S., et al.
BALKAN JOURNAL OF MEDICAL GENETICS , vol.15, no.2, pp.61-66, 2012 (SCI-Expanded, Scopus) Creative Commons License Sustainable Development identifier identifier identifier

35. The Reliability of Maternal Serum Triple Test in Prenatal Diagnosis of Fetal Chromosomal Abnormalities of Pregnant Turkish Women

DEMİRHAN O., PAZARBAŞI A., GÜZEL A. İ., Tastemir D., Yilmaz B., KASAP M., et al.
GENETIC TESTING AND MOLECULAR BIOMARKERS , vol.15, no.10, pp.701-707, 2011 (SCI-Expanded, Scopus) Sustainable Development identifier identifier identifier

36. Amniyosentez ile Tanı Konulan 4707 Olgunun Sitogenetik Bulgularının Değerlendirilmesi.

Pazarbaşi A., DEMİRHAN O., Taştemir D., ark. v.
Ç.Ü. Tıp Fakültesi Dergisi , vol.36, no.1, pp.8-14, 2011 (Peer-Reviewed Journal)

37. Erkek İnfertilitesinin Sitogenetiği

Özpak L., PAZARBAŞI A.
Çukurova Üniversitesi Tıp Fakültesi Arşiv Kaynak Tarama Dergisi , vol.20, no.4, pp.230-245, 2011 (Peer-Reviewed Journal)

38. Kanser Yolakları

PAZARBAŞI A., Kasap M., Kasap H.
Çukurova Üniversitesi Tıp Fakültesi Arşiv Kaynak Tarama Dergisi , vol.20, no.4, pp.187-229, 2011 (Peer-Reviewed Journal) Sustainable Development

39. Cancer Pathways

PAZARBAŞI A., Kasap M., KASAP H.
Çukurova Üniversitesi Tıp Fakültesi Arşiv Kaynak Tarama Dergisi , vol.20, no.4, 2011 (Peer-Reviewed Journal) Sustainable Development

40. Amniyosentez ile Tanı Konulan 4707 Olgunun Sitogenetik Bulgularının Değerlendirilmesi

PAZARBAŞI A., DEMIRHAN O., Tastemir D., Tunc E., Ozgunen F. T., Alptekin D., et al.
CUKUROVA MEDICAL JOURNAL , vol.36, pp.8-14, 2011 (ESCI, TRDizin)

41. Association of serum sex steroid levels and bone mineral density with CYP17 and CYP19 gene polymorphisms in postmenopausal women in Turkey

YILMAZ M., PAZARBAŞI A., GÜZEL A. B., Kocaturk-Sel S., KASAP H., Kasap M., et al.
GENETICS AND MOLECULAR RESEARCH , vol.10, no.3, pp.1999-2008, 2011 (SCI-Expanded, Scopus) Sustainable Development identifier identifier identifier

42. Investigation of p53 Tumor Suppressor Gene Mutations in Patients with a Lung Mass Using Sequence Analysis

LÜLEYAP H. Ü., İzmirli M., Onatoğlu D., Koç S., TOPÇUOĞLU M. Ş., ALPTEKİN D., et al.
TURKIYE KLINIKLERI TIP BILIMLERI DERGISI , vol.30, no.5, pp.1447-1453, 2010 (SCI-Expanded, Scopus) Creative Commons License Sustainable Development identifier identifier

43. Detection of Parental Origin and Cell Stage Errors of a Double Nondisjunction in a Fetus by QF-PCR

Guzel A. I., DEMİRHAN O., PAZARBAŞI A., Ozgunen F. T., Kocaturk-Sel S., Tastemir D.
GENETIC TESTING AND MOLECULAR BIOMARKERS , vol.13, no.1, pp.73-77, 2009 (SCI-Expanded, Scopus) identifier identifier identifier

44. PARENTAL ORIGIN AND CELL STAGE ERRORS IN X-CHROMOSOME POLYSOMY 49,XXXXY

GÜZEL A. B., DEMİRHAN O., PAZARBAŞI A., YÜKSEL B.
BALKAN JOURNAL OF MEDICAL GENETICS , vol.12, no.1, pp.45-50, 2009 (SCI-Expanded, Scopus) Creative Commons License identifier identifier

45. THE CLINICAL EFFECTS OF ISOCHROMOSOME Xq IN KLINEFELTER SYNDROME: REPORT OF A CASE AND REVIEW OF LITERATURE

DEMİRHAN O., PAZARBAŞI A., TANRIVERDİ N., ARIDOGAN A., KARAHAN D.
GENETIC COUNSELING , vol.20, no.3, pp.235-242, 2009 (SCI-Expanded, Scopus) identifier identifier identifier

46. THE EFFECT OF A DE NOVO PERICENTRIC INVERSION (10)(p11.1;q22.1) ON AGGRESSIVE BEHAVIOR AND HYPERACTIVITY

Demirhan O., PAZARBAŞI A., TUNC E., KARAHAN D., TANRIVERDI N., AVCI A., et al.
GENETIC COUNSELING , vol.20, no.1, pp.69-71, 2009 (SCI-Expanded, Scopus) identifier identifier identifier

47. Suppression of the Tumorigenicity of B-16V Melanoma Cells via Lysozyme Gene

GÜZEL A. B., KASAP H., Tuncer I., Ozgunen K., SERTDEMİR Y., KASAP M., et al.
CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS , vol.23, no.5, pp.603-608, 2008 (SCI-Expanded, Scopus) identifier identifier identifier

48. Correlation of clinical phenotype with a pericentric inversion of chromosome 9 and genetic counseling

DEMİRHAN O., PAZARBAŞI A., Suleymanova-Karahan D., Tanriverdi N., KILINÇ Y.
SAUDI MEDICAL JOURNAL , vol.29, no.7, pp.946-951, 2008 (SCI-Expanded, Scopus) identifier identifier identifier

49. PRENATAL DIAGNOSIS OF TRANSLOCATION 13;13 PATAU SYNDROME: CLINICAL FEATURES OF TWO CASES

PAZARBAŞI A., DEMİRHAN O., SLEYMANOVA-KARAHAN D., TASTEMIR D., TUNC E., GUEMUERDUELUE D.
BALKAN JOURNAL OF MEDICAL GENETICS , vol.11, no.1, pp.69-73, 2008 (SCI-Expanded, Scopus) Creative Commons License identifier identifier identifier

50. INHERITANCE OF A TRANSLOCATION BETWEEN CHROMOSOMES 12 AND 16 IN A FAMILY WITH RECURRENT MISCARRIAGES AND A NEWBORN WITH DOWN SYNDROME CARRYING THE SAME TRANSLOCATION

PAZARBAŞI A., DEMİRHAN O., TURGUT M. M., GUZEL I., TASTEMIR D.
GENETIC COUNSELING , vol.19, no.3, pp.301-308, 2008 (SCI-Expanded, Scopus) identifier identifier identifier

51. Polymorphisms in the tumor necrosis factor-alpha gene in Turkish women with pre-eclampsia and eclampsia

Pazarbasi A., Kasap M., Guzel A. I., Kasap H., Onbasioglu M., Ozbakir B., et al.
ACTA MEDICA OKAYAMA , vol.61, no.3, pp.153-160, 2007 (SCI-Expanded, Scopus) Sustainable Development identifier identifier identifier

52. Screening of codon 236, 238, 244, 248 and 259 mutations of p53 gene in ovarianandendometrialcarcinomasby RFLP analysis

PAZARBASI A., KASAP M., VARDAR M. A., ALPTEKIN D., GUZEL A. I., LÜLEYAP H. Ü., et al.
ÇÜ Sağlık Bilimleri Enstitüsü Dergisi , vol.23, pp.1-8, 2007 (Peer-Reviewed Journal)

53. Screening of Codon 236, 238, 244, 248 and 259 Mutations of p53 Gene In Ovarian and Endometrial Carcinomas by RFLP Analysis

PAZARBAŞI A., Kasap M., VARDAR M. A., Alptekin D., Guzel A. I., Lüleyap H. U., et al.
Çukurova Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi , vol.23, pp.1-8, 2007 (Peer-Reviewed Journal)

54. Chromosomal abnormalities in endometrial and ovarian carcinomas

PAZARBAŞI A., KASAP M., DEMİRHAN O., VARDAR M. A., Suleymanova-Karahan D., DORAN F.
BALKAN JOURNAL OF MEDICAL GENETICS , vol.10, no.2, pp.61-69, 2007 (SCI-Expanded, Scopus) Creative Commons License Sustainable Development identifier identifier

55. The importance of arginine mutation for the evolutionary structure and function of phenylalanine hydroxylase gene

Luleyap H. U., Alptekin D., Pazarbasi A., Kasap M., Kasap H., Demirhindi H., et al.
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS , vol.601, pp.39-45, 2006 (SCI-Expanded, Scopus) identifier identifier identifier

56. The sister-chromatid exchange and acetylcholine esterase enzyme levels among patients with insecticide intoxication in the Cukurova Region, Turkey

Alptekin D., Luleyap H., Yilmaz L., Demirhindi H., Gokel Y., Pazarbasi A., et al.
ACTA MEDICA OKAYAMA , vol.60, no.2, pp.121-126, 2006 (SCI-Expanded, Scopus) Sustainable Development identifier identifier identifier

57. Use of enzyme-linked immunosorbent assay for detection of natural leishmania infections in phlebotomine sand flies from southeastern Turkey

Pazarbasi A., Alptekin D., Luleyap H., Kasap M., Kasap H.
JOURNAL OF MEDICAL ENTOMOLOGY , vol.43, no.2, pp.248-251, 2006 (SCI-Expanded, Scopus) identifier identifier identifier

58. Kanser genetiği

PAZARBAŞI A., Kasap M.
Çukurova Üniversitesi Tıp Fakültesi Arşiv Kaynak Tarama Dergisi , vol.12, no.4, pp.328-339, 2003 (Peer-Reviewed Journal) Sustainable Development

59. Hücre Yaşlanması

PAZARBAŞI A., Kasap M.
Çukurova Üniversitesi Tıp Fakültesi Arşiv Kaynak Tarama Dergisi , vol.12, no.4, pp.441-456, 2003 (Peer-Reviewed Journal)

60. İnsektisit uygulaması yapan işçilerde kardeş kromatid değişimi ve kolinesteraz seviyesinin incelenmesi.

ALPTEKİN D., LÜLEYAP H. Ü., PAZARBAŞI A., KASAP H., KASAP M.
Ç.Ü. Tıp Fak. Derg. , vol.2, no.24, pp.49-56, 1999 (Peer-Reviewed Journal)

61. İnsektisit uygulaması yapan işçilerde kardeş kromatid değişimi ve kolinesteraz seviyesinin incelenmesi.

ALPTEKİN D., LÜLEYAP H. Ü., PAZARBAŞI A., KASAP H., KASAP M.
Ç.Ü. Tıp Fak. Derg. , vol.2, no.24, pp.49-56, 1999 (Peer-Reviewed Journal)

62. İnsektisit Uygulaması yapan işçilerde kardeş kromatid değişimi ve kolinesteraz seviyesinin incelenmesi

Alptekin D., Lüleyap H. Ü., PAZARBAŞI A., KASAP H., Kasap M.
CUKUROVA MEDICAL JOURNAL , vol.24, no.2, pp.49-56, 1999 (TRDizin)

63. Çukurova?da sivrisinek Mücadelesinde Kullanılan Bendiocarb?ın Memelilere (sıçanlara) Dermal Etkisi

PAZARBAŞI A., Kasap M., Kasap H.
Turkish Journal of Zoology , vol.23, no.1, pp.303-308, 1999 (Scopus, TRDizin)

64. Çeşitli örnekleme yöntemleri ile Tarsus (Çukurova) yöresinde Mayıs-Ekim aylarında gece toplanan sivrisineklerin yoğunluk ve aktivitelerinin karşılaştırılması

KASAP M., KASAP H., ALPTEKİN D., DEMIRHAN O., LÜLEYAP H. Ü., PAZARBAŞI A.
Türk Zooloji Dergisi, 20, 191-196. , vol.20, pp.191-196, 1996 (Peer-Reviewed Journal)

65. Çeşitli örnekleme yöntemleri ile Tarsus (Çukurova) yöresinde Mayıs-Ekim aylarında gece toplanan sivrisineklerin yoğunluk ve aktivitelerinin karşılaştırılması

Kasap H., Kasap M., Alptekin D., Demirhan O., Lüleyap H. Ü., PAZARBAŞI A.
Turkish Journal of Zoology , vol.20, pp.191-196, 1996 (Scopus, TRDizin)

66. Değişik in vitro ortamların Plasmodium berghei?nin in vivo gelişimine etkisi

Alptekin D., Kasap M., Allahverdiyev A., Kasap H., Çeber K., PAZARBAŞI A.
CUKUROVA MEDICAL JOURNAL , vol.21, no.1, pp.27-33, 1996 (TRDizin)

67. Çukurova Bölgesinden elde edilen çeşitli Plasmodium vivax suşlarının in vitro şartlarda gelişimi

PAZARBAŞI A., Çeber K., Kasap M., Allahverdiyev A., Kasap H.
Türkiye Parazitoloji Dergisi , vol.19, no.4, pp.449-459, 1995 (TRDizin)

68. Entomological studies on Anopheles sacharovi in Çukurova, Turkey.

Özcel M., Kasap H., Alkan M. Z., Kasap M., Alptekin D., Daldal N., et al.
TÜRKİYE PARAZİTOLOJİ DERGİSİ , vol.18, no.3, pp.317-327, 1994 (Peer-Reviewed Journal)

69. Entomological studies on Anopheles sacharovi in Çukurova, Tukey

Özcel M., KASAP H., ALKAN M., KASAP M., ALPTEKİN D., DALDAL N., et al.
Acta Parasitologica Turcica , vol.3, no.18, pp.317-323, 1994 (Peer-Reviewed Journal)

70. RESIDUAL EFFICACY OF PIRIMIPHOS METHYL (ACTELLIC(TM)) ON ANOPHELES-SACHAROVI IN CUKUROVA, TURKEY

Kasap H., Kasap M., Akbaba M., ALPTEKIN D., Demirhan O., Lüleyap U., et al.
JOURNAL OF THE AMERICAN MOSQUITO CONTROL ASSOCIATION , vol.8, no.1, pp.47-51, 1992 (SCI-Expanded, Scopus) identifier
Papers Presented at Peer-Reviewed Scientific Conferences 101

1. New player in lipopolysaccharide-induced neuroinflammation: programmed cell death ligand 1 (PDL-1)

Pazarbaşı A., Ay G., Uslu İ. N.
European Human Genetics Conference, Berlin, Germany, 1 - 04 June 2024, (Summary Text)

2. 6 GHz Radiofrequency Electromagnetic Field (RF-EMF) Can Decrease Cell Viability of N9 Microglia Cells in Time-Dependent Manner

PAZARBAŞI A., AKSOY G., EMRE M., Karamazı Y.
European Human Genetics Conference on June 10-13, 2023. Glasgow, Scotland, United Kingdom., Glasgow, England, 10 - 13 June 2023, (Summary Text)

3. Detection of chromosomal anomalies from South of Turkey: QF PCR versus cytogenetic. , June 16-19, 2018. Milan, Italy.

Kocaturk-Sel S S., Pazarbaşi A., DEMİRHAN O., ark. v.
European Human Genetics Conference, Italy, pp.32, (Full Text)

4. Results of karyotype analysis of 7975 pregnancies prenataly identified with amniocentesis in Turkey

Pazarbaşi A., DEMİRHAN O., ark. v.
European Human Genetics Conference,, Italy, pp.54, (Full Text)

5. Results of karyotype analysis of 8475 pregnancies in prenataly identified cases with amniocentesis from south of Turkey

PAZARBAŞI A., ALPTEKİN D., ILGAZ N. S., USLU İ. N., CÖMERTPAY G., AY G., et al.
16. Tıbbi Biyoloji ve Genetik Kongresi (Uluslararası Katılımlı), Muğla Bodrum, Turkey, 27 - 30 October 2019, pp.146, (Summary Text)

6. Result of karyotype analysis of 8475 pregnancies in prenataly identified cases with amniosentesis from south of Turkey.

PAZARBAŞI A., ALPTEKİN D., ILGAZ N. S., USLU İ. N., CÖMERTPAY G., AY G., et al.
16. Tıbbi Biyoloji ve Genetik Kongresi (Uluslararası Katılımlı), Turkey, 27 - 30 October 2019, (Summary Text)

7. Results of karyotype analysis of 8361 pregnancies in prenataly identified cases with amniocentesis from south of Turkey

PAZARBAŞI A., ALPTEKİN D., USLU İ. N., ILGAZ N. S., ÖZPAK L., CÖMERTPAY G., et al.
52nd European Human Genetics Conference, Gothenburg, Sweden, 15 - 18 June 2019, vol.7, pp.1175, (Summary Text)

8. Detection of chromosomal anomalies from South of Turkey: QF PCR versus cytogenetic

KOCATÜRK SEL S., PAZARBAŞI A., YILMAZ M. B., LÜLEYAP H. Ü., DEMİRHAN O., ALPTEKİN D., et al.
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.885, (Summary Text)

9. Results of karyotype analysis of 7975 pregnancies prenataly identified with amniocentesis in Turkey

PAZARBAŞI A., DEMİRHAN O., LÜLEYAP H. Ü., KOCATÜRK SEL S., ALPTEKİN D., YILMAZ M. B., et al.
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.883-884, (Summary Text)

10. Detection of chromosomal anomalies from South of Turkey: QF PCR versus cytogenetic

KOCATURK-SEL S., PAZARBAŞI A., YILMAZ B., LULEYAP U., DEMİRHAN O., ALPTEKİN D., et al.
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.885, (Summary Text) identifier

11. Results of karyotype analysis of 7975 pregnancies prenataly identified with amniocentesis in Turkey

PAZARBAŞI A., DEMİRHAN O., LÜLEYAP H. Ü., KOCATURK-SEL S., ALPTEKİN D., YILMAZ M., et al.
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.883-884, (Summary Text) identifier

12. Results of karyotype analysis of 8361 pregnancies in prenataly identified cases with amniocentesis from south of Turkey.

PAZARBAŞI A., ALPTEKİN D., USLU İ. N., ILGAZ N. S., ÖZPAK L., CÖMERTPAY G., et al.
European Human Genetics Conference, Gothenburg, Sweden, 15 - 18 June 2019, (Summary Text)

13. Determining The Mediators of GnRH Release Upon ProlactinInduction in GT1-7 Cells

EVRAN OLGUN M., KOCATÜRK SEL S., PAZARBAŞI A., YILMAZ M. B., LÜLEYAP H. Ü.
4th INTERNATIONAL CONGRESS ONAPPLIED BIOLOGICAL SCIENCES, 3 - 05 May 2019, (Summary Text)

14. Investigation the expression of ADAMTS9 gene in liver of high-fat diet and Streptozotocin-induced diabetic rats

ÖZPAK L., PAZARBAŞI A., YILMAZ M. B., ÖCAL I.
Innovation in Medicine Meeting 4, Sanko University, Gaziantep, Turkey, 11 - 13 October 2018, pp.48, (Summary Text) Sustainable Development

15. Chromosomal Abnormalities identified at prenatal diagnosis

PAZARBAŞI A., DEMİRHAN O., LÜLEYAP H. Ü., ÖZPAK L., ILGAZ N. S., USLU İ. N., et al.
Innovation in Medicine Meeting 4, Gaziantep, Turkey, 11 - 13 October 2018, pp.60-69, (Full Text)

16. "Chromosomal Abnormalities identified at prenatal diagnosis", Gaziantep, Türkıye, 11-13 Ekim 2018, no.S19, pp.60-69.

Pazarbaşı A., DEMİRHAN O., ark. v.
Innovation in Medicine Meeting 4,, Gaziantep, Turkey, 11 - 13 October 2018, vol.519, pp.60-69, (Full Text)

17. Kisspeptin Induce Aromatase Expression via Kisspeptin Receptor (GPR54) in MCF 7 Breast Cancer Cell Line

YILMAZ B., Oksuz H., DEMİRHAN O., Luleyap U., PAZARBAŞI A., Sel S. K., et al.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.968, (Summary Text) Sustainable Development identifier

18. Analysis of maternal polymorphism of CBS gene and risk of Down syndrome offspring

PAZARBAŞI A., ÖZPAK L., KESER N., LULEYAP U., DEMİRHAN O., BUYUKKURT S.
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 27 - 30 May 2017, vol.26, pp.827, (Summary Text) identifier

19. Bisphenol a triggers ER stress mediated autophagy in SH-SY5Y cell line.

LÜLEYAP H. Ü., YOLDAŞ A., CÖMERTPAY G., AY G., EVYAPAN G., PAZARBAŞI A., et al.
European Human Genetics Conference, Milan, Italy, 16 - 19 June 2018, vol.9028, (Summary Text)

20. Low Dose Dexmethasone Decrease the Level of ATG5 in SH SY5Y cell line

ALPTEKİN D., LÜLEYAP H. Ü., YOLDAŞ A., CÖMERTPAY G., PAZARCI P., AY G., et al.
European Human Genetics Conference 2018, Milano, Italy, 16 - 19 June 2018, (Full Text)

21. Low Dose Dexmethasone Decrease the Level of ATG5 in SH SY5Y cell line

ALPTEKİN D., LÜLEYAP H. Ü., YOLDAŞ A., CÖMERTPAY G., PAZARCI P., AY G., et al.
European Human Genetics Conference 2018, Milano, Italy, 16 - 19 June 2018, (Full Text)

22. Low Dose Dexmethasone Decrease the Level of ATG5 in SH SY5Y cell line

ALPTEKİN D., LÜLEYAP H. Ü., YOLDAŞ A., CÖMERTPAY G., PAZARCI P., AY G., et al.
European Human Genetics Conference 2018, Milano, Italy, 16 - 19 June 2018, vol.27, pp.279, (Full Text)

23. Determining The Mediators of GnRH Release Upon Prolactin Induction in GT1-7 Cells

KOCATÜRK SEL S., PAZARBAŞI A., Öksüz H., Öztecik E., EVRAN M., Akbal E., et al.
4th INTERNATIONAL CONGRESS ON APPLIED BIOLOGICAL SCIENCES, Eskişehir, Turkey, 3 - 05 May 2018, pp.96, (Summary Text)

24. Investigation of expression levels of Alzheimer related-genes in HFD and STZ induced the type 2 diabetic rats.

ÖZPAK L., PAZARBAŞI A., ÖCAL I., YILMAZ M. B., Ilgaz N. S., Öksüz H.
International Congress of Health and Environment, Adana, Turkey, 23 - 25 October 2017, (Summary Text) Sustainable Development

25. Pulslu Elektromanyetik Alanın Deneysel Diyabetli Sıçanların Karaciğer Apoptotik Genlerinin Ekspresyonları Üzerine Etkisi

Öksüz H., ÖZPAK L., PAZARBAŞI A., Ilgaz N. S., KOCATÜRK SEL S., ÖCAL I., et al.
2nd International Mediterranean Science and Engineering Congress, Adana, Turkey, 25 - 27 October 2017, (Full Text) Sustainable Development

26. Hippocampal ADAMTS4, TIMP3, RELN, BCAN genesexpression levels in a intracerebroventricular streptozotocine induced rat model of Alzheimer’s disease

ÖZPAK L., PAZARBAŞI A., Yegani A. A., AKSU F., YILMAZ M. B., ÖCAL I.
2nd International Mediterranean Science and Engineering Congress, 25 - 27 October 2017, (Summary Text)

27. Amniyosentez iile prenatal tanı konulan 7821 olguda kromozom analizi sonuçları

PAZARBAŞI A., DEMİRHAN O., LÜLEYAP H. Ü., ÖZPAK L., ILGAZ N. S., USLU İ. N., et al.
15.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 26 - 29 October 2017, (Summary Text)

28. HippocampalADAMTS4, TIMP3, RELN, BCAN genes expression levels in a intracerebroventricular streptozotocine induced rat model of Alzheimer’xxs disease

ÖZPAK L., PAZARBAŞI A., Alizadeh Yegani A., AKSU F., YILMAZ M. B., ÖCAL I.
2nd International Mediterranean Science and Engineering Congress, Adana, Turkey, 25 - 27 October 2017, pp.6, (Summary Text)

29. Amniyosentez ile prenatal tanı konulan 7821 olguda kromozom analizi sonuçları

Pazarbaşı A., DEMİRHAN O., ark. v.
15.Ulusal Tıbbi Biyoloji ve Genetik Kongresi (Uluslararası Katılımlı), 26-29 Ekim 2017, Ölüdeniz/Fethiye, Kongre Kitabı: PS120, s14, Antalya, Turkey, 26 - 29 October 2017, pp.120-146, (Full Text)

30. The Transforming Growth Factor- ß1 (TGF-ß1) Gene Polymorphism (TGF- ß1 T29C) and risk of Preeclampsia in Turkish pregnant woman

PAZARBAŞI A., ÖZPAK L., Keser N., ÖZGÜNEN F. T.
International Congress of Health and Environment, Adana, Turkey, 23 - 25 October 2017, pp.143, (Summary Text) Sustainable Development

31. Sistatiyon beta sentaz geni 844ins68 polimorfizminin Down sendromlu bebek doğurma riski ile ilişkisinin değerlendirilmesi

PAZARBAŞI A., ÖZPAK L., Keser N., ÖZGÜNEN F. T.
6.Ulusal Moleküler Biyoloji ve Biyoteknoloji Kongresi, Adana, Turkey, 5 - 07 October 2017, (Summary Text)

32. Kisspeptin Induce Aromatase Expression via Kisspeptin Receptor (GPR54) in MCF 7 Breast Cancer Cell Line

YILMAZ M. B., Öksüz H., DEMİRHAN O., LÜLEYAP H. Ü., PAZARBAŞI A., KOCATÜRK SEL S., et al.
European Human Genetics Conference-ESHG 2017, Kopenhag, Denmark, 27 - 30 May 2017, (Summary Text) Sustainable Development

33. Kisspeptin induce aromatase expression via kisspeptin receptor (GPR54) in MCF 7 breast cancer cell line

YILMAZ M. B., öksüz h., DEMİRHAN O., LÜLEYAP H. Ü., PAZARBAŞI A., KOCATÜRK SEL S.
Eurpean Human Genetics Conference 2017, Kopenhag, Danımarka, 27 - 30 May 2017, (Full Text) Sustainable Development

34. Chromosomal alteraĕons in paĕents with breast cancer

DEMİRHAN O., TANRIVERDİ N., PAZARBAŞI A.
Eurpean Human Genetics Conference, Kopenhag, DANIMARKA, 27 - 30 May 2017, (Full Text) Sustainable Development

35. Analysis of maternal polymorphism of CBS gene and risk of Down syndrome offspring

PAZARBAŞI A., ÖZPAK L., Keser N., LÜLEYAP H. Ü., DEMİRHAN O., BÜYÜKKURT S.
Eurpean Human Genetics Conference 2017, Kopenhag, Denmark, 27 - 30 May 2017, pp.21, (Full Text)

36. Analysis of maternal polymorphism of CBS gene and risk of Down syndrome offspring, 2017, Kopenhag, DANIMARKA, 27-30 Mayıs 2017, pp.21-21.

Pazarbaşı A., Özpak L., DEMİRHAN O., ark. v.
Eurpean Human Genetics Conference, Kpenhag, Denmark, 27 May 2017 - 30 June 2015, pp.21-22, (Full Text)

37. Effect of sodium butyrate on some alternative splicing genes and bace1 isoforms in SH-SY5Y

LÜLEYAP H. Ü., AY G., CÖMERTPAY G., ALPTEKİN D., PAZARBAŞI A.
European Human Genetics Conference, Kopenhag, Denmark, 27 - 30 May 2017, vol.P09, (Full Text)

38. Analysis of maternal polymorphism of CBS gene and risk of Down syndrome offspring

PAZARBAŞI A., ÖZPAK L., Keser N., LÜLEYAP H. Ü., DEMİRHAN O., BÜYÜKKURT S.
Eurpean Human Genetics Conference 2017, Kopenhag, Denmark, 27 - 30 May 2017, pp.21, (Full Text)

39. "Analysis of maternal polymorphism of CBS gene and risk of Down syndrome offspring

Pazarbaşı A., DEMİRHAN O., ark. v.
Eurpean Human Genetics Conference, Kpenhag, Denmark, 27 May 2017 - 30 May 2015, pp.21, (Full Text)

40. Rapid aneuplody testing in postnatal samples from Cukurova region

KOCATÜRK SEL S., YILMAZ M. B., LÜLEYAP H. Ü., PAZARBAŞI A., ALPTEKİN D., DEMİRHAN O., et al.
Innovation in Medicine Meeting 3, Gaziantep, Turkey, 11 - 13 May 2017, (Summary Text)

41. Results of Karyotype Analysis of 7766 Pregnancies Prenataly Identified with Amniocentesis in Turkey

PAZARBAŞI A., DEMİRHAN O., LÜLEYAP H. Ü., ÖZPAK L., Ilgaz N. S., USLU İ. N., et al.
Innovation in Medicine Meetings 3, Gaziantep, Turkey, 11 - 13 May 2017, (Summary Text)

42. Rapid aneuploıdy testing in postnatal venous blood samles from Çukuova region

KOCATÜRK SEL S., YILMAZ M. B., LÜLEYAP H. Ü., PAZARBAŞI A., DEMİRHAN O., ALPTEKİN D., et al.
SANKO üniversity Innovation in Medicine, 11 - 13 May 2017, (Summary Text)

43. . Frequencies and distributions of sex chromosome abnormalities in females with Turner phenotype in south region of Turkey.

TANRIVERDİ N., DEMİRHAN O., süleymanova D., PAZARBAŞI A.
SANKO ün. Innovation in medicine, 11 - 13 May 2017, (Summary Text)

44. Detection of the maternal 833T>C and 844ins68 polymorphisms of Cystathionine beta synthase gene and risk of Down sydrome offspring

PAZARBAŞI A., KOCATÜRK SEL S., ÖZPAK L., Keser N., LÜLEYAP H. Ü., BÜYÜKKURT S.
Innovation in Medicine Summit-3, Gaziantep, Turkey, 11 - 13 May 2017, pp.69, (Full Text)

45. Turner fenotipine sahip kadınlardaki cinsiyet kromozomu anomalilerinin sıklık ve dağılımları uzun süreli retrospektif çalışma

TANRIVERDİ N., DEMİRHAN O., süleymanova D., PAZARBAŞI A.
Innovation in Medicine Meetings 3, Turkey, 11 - 13 May 2017, pp.70, (Summary Text) Sustainable Development

46. Results of Karyotype Analysis of 7766 Pregnancies Prenataly Identified with Amniocentesis in Turkey. Innovation in Medicine Meetings 3, May 11-13, 2017. Innovation summit book 2017; pp: 68. The University of Sanko, GAZİANTEP/TURKEY.

Pazarbaşı A., DEMİRHAN O., ark. v.
Innovation in Medicine Meetings 3, Gaziantep, Turkey, 11 - 13 May 2017, pp.68, (Full Text)

47. Results of Karyotype Analysis of 7766 Pregnancies Prenataly Identified with Amniocentesis in Turkey. Innovation in Medicine Meetings 3

PAZARBAŞI A., DEMİRHAN O., LÜLEYAP H. Ü., KOCATÜRK SEL S., ÖZPAK L., ILGAZ N. S., et al.
Th Innovation in Medicine Meetings 3, Turkey, 11 - 13 May 2017, pp.68, (Summary Text)

48. Leptinin pubertal KİSS1 KİSS1R TAC2 ve TACR3 genlerinin ekspresyonlarına etkisinin gt 1 7hipotalamik hücre hattında değerlendirilmesi

ILGAZ N. S., cömertpay g., ÖZPAK L., akbal E., öksüz h., yılmaz m., et al.
1. Uluslararası Akdeniz Bilim ve Mühendislik Kongresi, 26 - 28 October 2016, (Full Text)

49. İnsan meme kanseri mcf7 hücre hattında kisspeptinin aromataz ekpresyonu üzerine etkisinin incelenmesi

öksüz h., barç e. d., öztecik e., KOTAN GEDİK L. D., TOPALOĞLU A. K., PAZARBAŞI A., et al.
1. Uluslararası Akdeniz Bilim ve Mühendislik Kongresi, 26 - 28 October 2016, (Full Text) Sustainable Development

50. Leptinin pubertal Kiss1 Kiss1R TacR ve TacR3 genlerinin ekspresyonlarına etkisinin GT 1 7 hipotalamik hücre hattında değerlendirilmesi

ILGAZ N. S., Cömertpay G., AKBAL E., ÖKSÜZ H., ÖZPAK L., TOPALOĞLU A. K., et al.
1st International Mediterranean Science and Engineering Congress. October 26-28, 2016. Adana, Turkey, Adana, Turkey, 26 - 28 October 2016, (Summary Text)

51. İnsan meme kanseri hücre hattında kisspeptinin aromataz ekpresyonu üzerine etkisinin incelenmesi

Öksüz H., ÖZTECİK E., Barç E. D., KOTAN GEDİK L. D., Cömertpay G., ILGAZ N. S., et al.
1st International Mediterranean Science and Engineering Congress. October 26-28, 2016. Adana, Turkey, Adana, Turkey, 26 - 28 October 2016, (Summary Text) Sustainable Development

52. Investigation of Methylenetetrahydrofolate reductase (MTHFR) gene A1298C Polymorphism and Distribution of Genotypes in Preeclampsia and Normal Pregnancies

ÖZPAK L., PAZARBAŞI A., Keser N., ILGAZ N. S., Özgünen F. T.
European Human Genetics Conference 2016, Barselona, Spain, 21 - 24 May 2016, pp.597, (Full Text)

53. Analysis of maternal polymorphisms of MTHFR gene and risk of Down syndrome offspring

Keser N., PAZARBAŞI A., ÖZPAK L., LÜLEYAP H. Ü., Pazarbaşı H. İ., Özgünen F. T.
European Human Genetics Conference 2016, Barselona, Spain, 21 - 24 May 2016, pp.581, (Full Text)

54. Analysis of maternal polymorphisms of RFC1 gene and risk of Down syndrome offspring

PAZARBAŞI A., ÖZPAK L., Keser N., KOCATÜRK SEL S., Cömertpay G., Özgünen F. T.
European Human Genetics Conference 2016, Barselona, Spain, 21 - 24 May 2016, pp.581, (Full Text)

55. Association of infertility and methylenetetrahydrofolate reductase genotypes in turkish couples

GÜVENMEZ H., PAZARBAŞI A., YILMAZ M. B., ÜRÜNSAK İ. F., LÜLEYAP H. Ü.
Sanko University Innovation in Medicine Summit, 5 - 07 May 2016

56. Plasminogen activator inhibitor 1 PAI 1 4G 5G protrombin factor II G20210A and factor V G1691A factor V leiden genotypes in turkish couples with uneplained infertility problems

GÜVENMEZ H., PAZARBAŞI A., ÜRÜNSAK İ. F., YILMAZ M. B., ÖZPAK L.
Sanko Üniversity Innovation in Medicine Summit, 5 - 07 May 2016

57. Evaluation of cytogenetic results of chromosomal abnormalities identified at prenatal diagnosis of 7300 pregnancies in Turkey

PAZARBAŞI A., DEMİRHAN O., LÜLEYAP H. Ü., ÖZPAK L., ILGAZ N. S., USLU İ. N.
Sanko Üniversity Innovation in Medicine Summit-2, Gaziantep, Turkey, 5 - 07 May 2016, (Full Text)

58. Plasminogen activator Inhibitor 1 PAI 1 4G 5G Protrombin Factor II G20210A and Factor V G1691A Factor V Leiden genotypes in Turkish couples with unexplained Infertility problems

Pazarbaşı H. İ., GÜVENMEZ H., PAZARBAŞI A., ÜRÜNSAK İ. F., YILMAZ M. B., Keser N., et al.
INNOVATION IN MEDICINE SUMMIT-2, Gaziantep, Turkey, 5 - 07 May 2016, (Summary Text)

59. Amniyosentez ile prenatal tanı konulan 7222 olgunun sitogenetik bulgularının değerlendirilmesi.

pazarbaşı a., DEMİRHAN O., ark. v.
14.Ulusal Tıbbi Biyoloji ve Genetik Kongresi (Uluslararası Katılımlı), 27-30 Ekim 2015, Ölüdeniz/Fethiye PS1013., Antalya, Turkey, 27 - 30 October 2015, pp.1013, (Full Text)

60. MetylenTetrahydrofolate Reductase MTHFR C677T Polymorphism and Risk of Preeclamlampsia in Turkish Pregnant Women

PAZARBAŞI A., ÖZPAK L., Keser N., Pazarbaşı H. İ., Özgünen F. T., LÜLEYAP H. Ü.
Pregnancy Summit 2014, October 6-8 th, London, UK., 6 - 08 October 2014, (Summary Text) Sustainable Development

61. Chromosomal Abnormalities Identified at Prenatal Diagnosis of 7050 Pregnancies in Turkey Pregnancy Summit 2014 October 6 8 th London UK

PAZARBAŞI A., LÜLEYAP H. Ü., ALPTEKİN D., ÖZPAK L., ILGAZ N. S., USLU İ. N., et al.
Pregnancy Summit, 6 - 08 October 2014, (Summary Text)

62. Metylentetrahydrofolate Reductase (MTHFR) C677T Polymorphism and risk of Preeclampsia in Turkish Pregnant Women

PAZARBAŞI A., ÖZPAK L., Keser N., Pazarbaşı H. İ., ÖZGÜNEN F. T., LÜLEYAP H. Ü.
Pregnancy Summit 2014, Londra, United Kingdom, 6 - 08 October 2014, pp.50, (Full Text) Sustainable Development

63. The Presence Of One Trisomic Diallelic Marker Of A Fetus For D21s1411 With Normal Karyotype

ALPTEKİN D., PAZARBAŞI A., LÜLEYAP H. Ü., ERKOC M. A., YILMAZ M. B., CÖMERTPAY G., et al.
European Human Genetics Conference 2013, Paris, France, 8 - 11 June 2013, vol.21, pp.57, (Full Text)

64. Chromosomal Abnormalities Identified At Prenatal Diagnosis

PAZARBAŞI A., TUNÇ E., ALPTEKİN D., LÜLEYAP H. Ü., DEMİRHAN O., TANRIVERDI N., et al.
European Human Genetics Conference 2013, Paris, France, 8 - 11 June 2013, vol.21, pp.78, (Full Text)

65. Rapid Detection Of Fetal Aneuploidies By Quantitative Fluorence Pcr (Qf-Pcr) In Prenatal Dioagnosis

TUFAN T., PAZARBAŞI A., Erkoç M. A., CÖMERTPAY G., KOCATÜRK SEL S., OZGUNEN F. T., et al.
European Human Genetics Conference 2013, Paris, France, 8 - 11 June 2013, vol.21, pp.18, (Full Text)

66. Chromosomal Abnormalities Identified At Prenatal Diagnosis. 8-11 Haziran 2013, vol.21, pp.78-78.

Pazarbaşı A., DEMİRHAN O., all. e.
European Human Genetics Conference, Paris, France, 8 - 11 June 2013, pp.78, (Full Text)

67. A Mosaic Klinefelter Syndrome Variant Identified With Amniocentesis

LÜLEYAP H. Ü., PAZARBAŞI A., OZGUNEN F. T., BOZDOĞAN S., BÜYÜKKURT S., ALPTEKİN D.
European Human Genetics Conference 2013, Paris, France, 8 - 11 June 2013, vol.21, pp.88, (Full Text)

68. Amniyosentez ile tanı prenatal tanı konulan 5671 olguda sitogenetik bulgular

PAZARBAŞI A., ALPTEKİN D., TUNÇ E., TANRIVERDİ N., DEMİRHAN O., Özgünen F. T., et al.
10. Ulusal Tıbbi Genetik Kongresi, Turkey, 19 - 23 December 2012

69. ?Amniyosentez ile Prenatal Tanı Konulan 5671 Olguda Sitogenetik Bulgular?

pazarbaşı a., DEMİRHAN O., ark. v.
10. Ulusal Tıbbi Genetik Kongresi, 19-23 Aralık 2012, Bursa, Turkey, 19 - 23 December 2012, pp.23, (Full Text)

70. Amniyosentez Ile Prenatal Tanı Konulan 5671 Olguda Sitogennetik Bulgular

PAZARBAŞI A., ALPTEKİN D., TUNÇ E., TANRIVERDİ N., DEMİRHAN O., ÖZGÜNEN F. T., et al.
10. Ulusal Tıbbi Genetik Kongresi, Bursa, Turkey, 19 - 23 September 2012, vol.PB0177, pp.63, (Full Text)

71. . Pazarbasi, O Demirhan, M. Kasap, D. Alptekin, U. Luleyap, B. Yilmaz, A. I. Guzel, S. K. Sel, E. Tunc, L. Özpak, F. T. Özgunen, H. Kasap The reliability of maternal serum triple screening for the prenatal diagnosis of fetal chromosomal abnormalities in Turkish women

PAZARBAŞI A., DEMİRHAN O., kasap m., ALPTEKİN D., LÜLEYAP H. Ü., GÜZEL A. İ., et al.
European Meeting on Psychosocial Aspects of Genetics and the German Society of Human Genetics, 23 - 26 June 2012, pp.5-65, (Summary Text) Sustainable Development

72. "The Reliability Of Maternal Serum Triple Screening For The Parental Diagnosis Of Fetal Chromosomal Abnormalities In Turkish Women"

PAZARBAŞI A., DEMİRHAN O., KASAP M., ALPTEKİN D., LÜLEYAP H. Ü., GUZEL A. I., et al.
European Human Genetics Conference, Nürnberg, Germany, 23 - 26 June 2012, vol.05, pp.65, (Full Text)

73. The reliability of maternal serum triple screening for the prenatal diagnosis of fetal chromosomal abnormalities in Turkish women. European Meeting on Psychosocial Aspects of Genetics and the German Society of Human Genetics June 23 - 26, 2012, NCC Ost, Nürnberg, Germany, P05.65.

Pazarbaşı A., DEMİRHAN O., all. e.
European Meeting on Psychosocial Aspects of Genetics and the German Society of Human Genetics, Nünberg, Germany, 23 - 26 June 2012, pp.5-65, (Full Text) Sustainable Development

74. CYP17 ve CYP19 genlerindeki polimorfizmler ile Türk postmenapozal kadınlardaki serum seks steroid seviyeleri ve kemik mineral yoğunluğu arasındaki ilişki.

pazarbaşı a., DEMİRHAN O., ark. v.
XII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi. 27-30 Ekim 2011, Antalya, Antalya, Turkey, 27 - 30 October 2011, pp.10, (Full Text)

75. "Catechol-O-Methyltransferase (Comt) Geni Genetik Polimorfizminin Türk Toplumunda Ailesel Prostat Kanseri Gelişimi Riski Ile Ilişkisi"

ALPTEKİN D., PAZARBAŞI A., TANSUG Z., IZMIRLI M., YILMAZ M. B., ÖZPAK L., et al.
XII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Antalya, Turkey, 27 - 30 October 2011, vol.pb, pp.68, (Full Text) Sustainable Development

76. Bir ailede 3 ve 21. Kromozomlar arasındaki translokasyonun kalıtımı ve Down sendromu riski,

pazarbaşı a., DEMİRHAN O., ark. v.
XII. Ulusal Tıbbi Biyoloji ve Genetik Kongresi. 27-30 Ekim 2011, Antalya., Antalya, Turkey, 27 - 30 October 2011, pp.39, (Full Text)

77. "Genetic Polymorphisms In The Estrogen Receptor Alpha Gene In Turkish Patients With Familial Prostate Carcinoma"

PAZARBAŞI A., ALPTEKİN D., LÜLEYAP H. Ü., TANSUG Z., IZMIRLI M., YILMAZ M. B., et al.
IV. International Congress of Molecular Medicine, İstanbul, Turkey, 27 - 30 June 2011, vol.231, pp.97-98, (Full Text)

78. 42. AI Guzel, O Demirhan, A Pazarbasi, B Yuksel. Detection of parental origin and cell stage errors of a chromosome X polysomy 49,XXXXY and new clinical findings.

GÜZEL A. İ., DEMİRHAN O., PAZARBAŞI A.
European Human Genetics Conference, 23 - 26 May 2009, vol.3, (Summary Text)

79. The clinical effects of isochromosome Xq in Klinefelter Syndrome: Report of a case and review of literature.

Pazarbaşı A., DEMİRHAN O., all. e.
European Human Genetics Conference; May 23-26, 2009, Vienna, Austria, P03.038., Viyana, Austria, 23 - 26 May 2009, pp.3-38, (Full Text)

80. Perisentrik İnversiyon (10)(p11.1;q22.1)?un Agresif Davranış ve Hiperaktivite Üzerine Etkisi

PAZARBAŞI A., DEMİRHAN O., TANRIVERDİ N., AVCI A., YOLGA TAHİROĞLU A.
19. Ulusal Ulusal Çocuk ve Ergen Ruh Sağlığı ve Hastalıkları Kongresi, Hatay, Turkey, 14 - 16 April 2009, pp.134, (Full Text)

81. "Reserch On P53 Tumor Supressor Gene Mutation On Patient With Lung Mass By Sequencing Analysis"

LÜLEYAP H. Ü., ALPTEKİN D., PAZARBAŞI A., ONATOGLU D., TOPÇUOĞLU M. Ş., GUZEL A. I., et al.
XX International Congress of Genetics, Berlin, Germany, 12 - 17 July 2008, vol.170, pp.101, (Full Text)

82. "A Modified Arms Tecnique For Detection Of P281l Mutations In Phenilalanine Hydroxylase Gene In Turkish Phenylketonuria Patients"

LÜLEYAP H. Ü., PAZARBAŞI A., ONATOGLU D., ALPTEKİN D., GUZEL A. I., ÖNENLİ MUNGAN H., et al.
XX International Congress of Genetics, Berlin, Germany, 12 - 17 July 2008, vol.439, pp.158, (Full Text)

83. "A Modified Arms Tecnique For Detection Of P281l Mutations In Phenilalanine Hydroxylase Gene In Turkish Phenylketonuria Patients"

LÜLEYAP H. Ü., PAZARBAŞI A., ONATOGLU D., ALPTEKİN D., GUZEL A. I., ÖNENLİ MUNGAN H., et al.
XX International Congress of Genetics, Berlin, Germany, 12 - 17 July 2008, vol.439, pp.158, (Full Text)

84. "A New Method For The Detection Of Ivs 10 11g-A Mutation In Phenylalanine Hydroxilase Gene With Arms Technique In Turkish Phenylketonuria Patients"

LÜLEYAP H. Ü., ONATOGLU D., PAZARBAŞI A., GUZEL A. I., OZER G., ÖNENLİ MUNGAN H., et al.
XX International Congress of Genetics,, Berlin, Germany, 12 - 17 July 2008, vol.625, pp.196, (Full Text)

85. "A New Method For The Detection Of Ivs 10 11g-A Mutation In Phenylalanine Hydroxilase Gene With Arms Technique In Turkish Phenylketonuria Patients"

LÜLEYAP H. Ü., ONATOGLU D., PAZARBAŞI A., GUZEL A. I., OZER G., ÖNENLİ MUNGAN H., et al.
XX International Congress of Genetics,, Berlin, Germany, 12 - 17 July 2008, vol.625, pp.196, (Full Text)

86. . Inheritance of a Translocation between Chromosomes 12 and 16 in a Family with Recurrent Miscarriages and a Newborn with Down Syndrome Carrying the Same Translocation

Pazarbaşı A., DEMİRHAN O., all. e.
XX. International Congress of Genetics, Berlin-Germany, July12-17, 2008, P362/29/A., Berlin, Germany, 12 - 17 June 2008, pp.369-22, (Full Text)

87. Guzel AI, Demirhan O, Pazarbaşı A, Ozgunen FT, Kocaturk-Sel S, Taştemir D. Detection of Parental Origin and Cell Stage Errors of Double Non-disjunction in a Fetus bu QF-PCR Using SRT Markers

GÜZEL A. İ., DEMİRHAN O., PAZARBAŞI A., Özgünen F., KOCATÜRK SEL S., TAŞTEMİR KORKMAZ D.
XX. Interna. Cong. Genet, Berlin-Germany, 12 - 17 June 2008, vol.17, (Summary Text)

88. VIII. Ulusal Tıbbi Genetik Kongresi

pazarbaşı a., DEMİRHAN O., ark. v.
VIII. Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 6 - 09 May 2008, pp.150, (Full Text)

89. Robertsonian tipi 2 Patau sendromu olgusunun patolojik sonuçlarının değerlendirilmesi.

Pazarbaşı A., DEMİRHAN O., ark. v.
X.Ulusal Tıbbi Biyoloji ve Genetik Kongresi, 6-9 Eylül 2007, Belek-Antalya, P-117., Antalya, Turkey, 6 - 09 September 2007, pp.117, (Full Text)

90. Kasap M, Demirhan O, Pazarbaşı A, Süleymanova-Karahan D, Tunç E, Taştemir D. Frequencies of chromosomal abnormalities at amniocentesis: over 4 years of cytogenetic analyses.

kasap m., DEMİRHAN O., PAZARBAŞI A., süleymanova D., Tunç E., TAŞTEMİR KORKMAZ D.
The American Society of Human Genetics, 55th Annual Meeting, 25 - 29 October 2005, vol.2256, (Summary Text)

91. ., "Akciğer Kanserli Hastalarda P53 Tümör Süpressör Gen Mutasyonlarının Dizi Analizi Ile Araştırılması",

ALPTEKİN D., LÜLEYAP H. Ü., TOPÇUOĞLU M. Ş., WOLFRAM H., GUZEL A. I., PAZARBAŞI A., et al.
8. Ulusal Tıbbi Biyoloji Kongresi, Adana, Turkey, 14 - 17 October 2003, vol.PS82, pp.174, (Full Text) Sustainable Development

92. "İnsektisit Ve Tıbbi Ilaç Zehirlenmesi Ile Gelen Hastalarda Kardeş Kromatid Değişimi Ve Kolinesteraz Enzimi Seviyesinin Araştırılması"

ALPTEKİN D., YILMAZ L., DOKUR M., PAZARBAŞI A., LÜLEYAP H. Ü., DİLMEÇ F., et al.
IV. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, İzmir, Turkey, 03 May 2001 - 06 May 2000, vol.SG29, pp.211, (Full Text)

93. "İnsektisit Ve Tıbbi Ilaç Zehirlenmesi Ile Gelen Hastalarda Kardeş Kromatid Değişimi Ve Kolinesteraz Enzimi Seviyesinin Araştırılması"

ALPTEKİN D., YILMAZ L., DOKUR M., PAZARBAŞI A., LÜLEYAP H. Ü., DİLMEÇ F., et al.
IV. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, İzmir, Turkey, 03 May 2001 - 06 May 2000, vol.SG29, pp.211, (Full Text)

94. "İnsektisit Uygulaması Yapan Işçilerde Görülen Kardeş Kromatit Değişimi Ve Kolinesteraz Seviyelerinin Incelenmesi",

ALPTEKİN D., LÜLEYAP H. Ü., PAZARBAŞI A., KASAP H., KASAP M.
5. Ulusal Tıbbi Biyoloji Kongresi ,, İzmir, Turkey, 21 - 24 September 1998, vol.PB5, pp.51, (Full Text)

95. "Population Density And Nocturnal Activity Of Anopheles Sacharovi And Anopheles Hyrcanus Collected By Different Sampling Methods"

KASAP H., KASAP M., ALPTEKİN D., DEMİRHAN O., LÜLEYAP H. Ü., PAZARBAŞI A.
8th International Congress of Parasitology, İzmir, Turkey, 10 - 14 October 1994, vol.2, pp.414, (Full Text)

96. Farklı Plasmodium vivax suşlarının in vitro gelişiminde değişik konak eritrositlerin etkisi

PAZARBAŞI A., ALPTEKİN D., KASAP M., KASAP H.
5. Ulusal Tıbbi Biyoloji Kongresi, İzmir, Turkey, 21 September 1998 - 24 August 1994, pp.35, (Summary Text)

97. "Culicinae Erginlerinin Mayıs-Ekim Aylarında Tarsus Yöresinde Gece Aktiviteleri Ve Populasyon Yoğunluğu",

KASAP H., KASAP M., ALPTEKİN D., DEMİRHAN O., LÜLEYAP H. Ü., PAZARBAŞI A.
XII. Ulusal Biyoloji Kongresi,, Edirne, Turkey, 6 - 08 July 1994, pp.26, (Full Text)

98. "Entomological Studies On Anopheles Sacharovi In Çukurova, Turkey"

Özcel M., KASAP H., ALKAN M., KASAP M., AK M., ALPTEKİN D., et al.
XIIIth International Congress for Tropical Medicine and Malaria, Pattaya, Thailand, 29 - 04 November 1992, vol.2, pp.15, (Full Text)

99. The History Of Use Of Adulticides In Malaria Control In Turkey With Reference To The Detection Of Resistance To Carbamates And Some Organophosphorus Insecticides And The Management Of Malaria Incidence To Acceptable Low Levels"

KASAP H., KASAP M., AKBABA M., ALPTEKİN D., DEMİRHAN O., LÜLEYAP H. Ü., et al.
Iranian Congress of Malaria, Zahedan, Iran, 22 - 26 February 1992, vol.24, pp.42-43, (Full Text) Sustainable Development

100. "Residual Efficacy Of Primiphos Methyl (Actellic) On Anopheles Sacharovi In Çukurova, Turkey"

KASAP H., KASAP M., AKBABA M., ALPTEKİN D., DEMİRHAN O., LÜLEYAP H. Ü., et al.
VII. International Congress of Parasitology,, Paris, France, 8 - 12 November 1990, vol.8, pp.1198, (Full Text)

101. Residual efficacy of primiphos methyl Actellic on Anopheles sacharovi in Çukurova Turkey Bull Soc Franc Parasitol Tome 8 1990 Supplt No 2 Abstracts S 10 D 13 p 1198 Paris France

KASAP H., KASAP M., AKBABA M., ALPTEKİN D., DEMİRHAN O., LÜLEYAP H. Ü., et al.
VII. International Congress of Parasitology, Paris, France, 20 - 24 August 1990, (Summary Text)
Books 2

1. Tıbbi Biyoloji ve Genetik

Kasap H., Kasap M., Demirhan O., Alptekin D., Luleyap H. U., Pazarbaşı A., et al.
Nobel Kitabevi, Adana, 2009

2. Tıbbi Biyoloji ve Genetik

KASAP H., KASAP M., DEMİRHAN O., ALPTEKİN D., LÜLEYAP H. Ü., PAZARBAŞI A., et al.
Nobel, Adana, 2009
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7

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7

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9
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