Pirim, İ., Eyerci, N. (2009) "Assesment of protein gene product pgp9 5 enzyme activity against potential Peptide substrate", The Eurasian Journal of Medicine., (0) [TR Dizin] 
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Pirim, İ., Eyerci, N. (2009) "Assesment of protein gene product pgp9 5 enzyme activity against potential Peptide substrate", The Eurasian Journal of Medicine., (0) [TR Dizin] Pirim, İ., Eyerci, N. (2009) "Assesment of protein gene product pgp9 5 enzyme activity against potential Peptide substrate", The Eurasian Journal of Medicine., (0) [TR Dizin]
Eyerci, N., Öncel, G.Z., İngeç, M., Topçu, A., Pirim, İ. (2006) "Anti HLA Antikorlarının Multipar Gebelerden Alınan SerumlardaTespiti", The Eurasian Journal of Medicine, (0) [TR Dizin]
Balkan, E., Eyerci, N., Keleş, S., Bilen, H., Akdeniz, N., Pirim, İ. (2019) "Effect of Colchicine on Th1 and Th17 Cytokines, Cytokine Receptors, and Chemokine Gene Expression Profiles in Behçet’xxs Disease", Trends Journal of Sciences Research, (0) DOI " data-bs-content-id="YazarBilgi-18977">
Balkan, E., Eyerci, N., Keleş, S., Bilen, H., Akdeniz, N., Pirim, İ. (2019) "Effect of Colchicine on Th1 and Th17 Cytokines, Cytokine Receptors, and Chemokine Gene Expression Profiles in Behçet’xxs Disease", Trends Journal of Sciences Research, (0) DOI Balkan, E., Eyerci, N., Keleş, S., Bilen, H., Akdeniz, N., Pirim, İ. (2019) "Effect of Colchicine on Th1 and Th17 Cytokines, Cytokine Receptors, and Chemokine Gene Expression Profiles in Behçet’xxs Disease", Trends Journal of Sciences Research, (0) DOI
Beysel, S., Eyerci, N., Pinarli, F.A., Apaydin, M., Kizilgul, M., Caliskan, M., Ozcelik, O., Kan, S., Çakal, E. (2018) "VDR gene FokI polymorphism as a poor prognostic factor for papillary thyroid cancer/title", Tumor Biology, 40 (11) p. 2147483647 Link DOI " data-bs-content-id="YazarBilgi-18978">
Beysel, S., Eyerci, N., Pinarli, F.A., Apaydin, M., Kizilgul, M., Caliskan, M., Ozcelik, O., Kan, S., Çakal, E. (2018) "VDR gene FokI polymorphism as a poor prognostic factor for papillary thyroid cancer/title", Tumor Biology, 40 (11) p. 2147483647 Link DOI Beysel, S., Eyerci, N., Pinarli, F.A., Apaydin, M., Kizilgul, M., Caliskan, M., Ozcelik, O., Kan, S., Çakal, E. (2018) "VDR gene FokI polymorphism as a poor prognostic factor for papillary thyroid cancer/title", Tumor Biology, 40 (11) p. 2147483647 Link DOI
Eyerci, N., Balkan, E., Akdeniz, N., Keleş, S. (2018) "Association of MICA Alleles and Human Leukocyte Antigen B in Turkish Patients Diagnosed With Behçet’xxs Disease", Archives of Rheumatology, 33 (3) pp. 352-357 [SCI Expanded] DOI " data-bs-content-id="YazarBilgi-18979">
Eyerci, N., Balkan, E., Akdeniz, N., Keleş, S. (2018) "Association of MICA Alleles and Human Leukocyte Antigen B in Turkish Patients Diagnosed With Behçet’xxs Disease", Archives of Rheumatology, 33 (3) pp. 352-357 [SCI Expanded] DOI Eyerci, N., Balkan, E., Akdeniz, N., Keleş, S. (2018) "Association of MICA Alleles and Human Leukocyte Antigen B in Turkish Patients Diagnosed With Behçet’xxs Disease", Archives of Rheumatology, 33 (3) pp. 352-357 [SCI Expanded] DOI
Gülseren, Y.D., Adiloğlu, A.K., Yücel, M., Dağ, Z., Eyerci, N., Berkem, R., Filik, L., Çaydere, M. (2019) "Comparison of non-invasive tests with invasive tests in the diagnosis of celiac disease", JOURNAL OF CLINICAL LABORATORY ANALYSIS, (0) p. 22722 [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-18980">
Gülseren, Y.D., Adiloğlu, A.K., Yücel, M., Dağ, Z., Eyerci, N., Berkem, R., Filik, L., Çaydere, M. (2019) "Comparison of non-invasive tests with invasive tests in the diagnosis of celiac disease", JOURNAL OF CLINICAL LABORATORY ANALYSIS, (0) p. 22722 [SCI Expanded] Link DOI Gülseren, Y.D., Adiloğlu, A.K., Yücel, M., Dağ, Z., Eyerci, N., Berkem, R., Filik, L., Çaydere, M. (2019) "Comparison of non-invasive tests with invasive tests in the diagnosis of celiac disease", JOURNAL OF CLINICAL LABORATORY ANALYSIS, (0) p. 22722 [SCI Expanded] Link DOI
Hepsen, S., Cakal, E., Karakose, M., Eyerci, N., Saat, H., Oztekin, S., Pinarli, F. (2019) "Melanocortin 3 receptor gene polymorphism is associated with polycystic ovary syndrome in Turkish population", Gynecological Endocrinology, (0) pp. 1-6 [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-18981">
Hepsen, S., Cakal, E., Karakose, M., Eyerci, N., Saat, H., Oztekin, S., Pinarli, F. (2019) "Melanocortin 3 receptor gene polymorphism is associated with polycystic ovary syndrome in Turkish population", Gynecological Endocrinology, (0) pp. 1-6 [SCI Expanded] Link DOI Hepsen, S., Cakal, E., Karakose, M., Eyerci, N., Saat, H., Oztekin, S., Pinarli, F. (2019) "Melanocortin 3 receptor gene polymorphism is associated with polycystic ovary syndrome in Turkish population", Gynecological Endocrinology, (0) pp. 1-6 [SCI Expanded] Link DOI
Ustun, N., Eyerci, N., Karadag, N., Yesilyurt, A., Zenciroglu, A., Okumus, N. (2019) "Association of vitamin D receptor gene FokI and TaqI polymorphisms and risk of RDS", The Journal of Maternal-Fetal Neonatal Medicine, (0) pp. 1-7 [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-18982">
Ustun, N., Eyerci, N., Karadag, N., Yesilyurt, A., Zenciroglu, A., Okumus, N. (2019) "Association of vitamin D receptor gene FokI and TaqI polymorphisms and risk of RDS", The Journal of Maternal-Fetal Neonatal Medicine, (0) pp. 1-7 [SCI Expanded] Link DOI Ustun, N., Eyerci, N., Karadag, N., Yesilyurt, A., Zenciroglu, A., Okumus, N. (2019) "Association of vitamin D receptor gene FokI and TaqI polymorphisms and risk of RDS", The Journal of Maternal-Fetal Neonatal Medicine, (0) pp. 1-7 [SCI Expanded] Link DOI
Çaylı, S., Ocaklı, S., Şenel, U., Eyerci, N., Delibaşı, T. (2016) "Role of p97 Valosin containing protein VCP and Jab1 CSN5 in testicular ischaemia reperfusion injury", Journal of Molecular Histology, 47 (1) pp. 91-100 [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-18983">
Çaylı, S., Ocaklı, S., Şenel, U., Eyerci, N., Delibaşı, T. (2016) "Role of p97 Valosin containing protein VCP and Jab1 CSN5 in testicular ischaemia reperfusion injury", Journal of Molecular Histology, 47 (1) pp. 91-100 [SCI Expanded] Link DOI Çaylı, S., Ocaklı, S., Şenel, U., Eyerci, N., Delibaşı, T. (2016) "Role of p97 Valosin containing protein VCP and Jab1 CSN5 in testicular ischaemia reperfusion injury", Journal of Molecular Histology, 47 (1) pp. 91-100 [SCI Expanded] Link DOI
Balkan, E., Eyerci, N., Uzkeser, H., Karatay, S., Topçu, A., Yıldırım, K., Pirim, İ. (2012) "HLA B27 Subtype Distribution Among Patients with Ankylosing Spondylitis in Eastern Turkey", Genetic Testing and Molecular Biomarkers, 16 (5) pp. 456-458 [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-18984">
Balkan, E., Eyerci, N., Uzkeser, H., Karatay, S., Topçu, A., Yıldırım, K., Pirim, İ. (2012) "HLA B27 Subtype Distribution Among Patients with Ankylosing Spondylitis in Eastern Turkey", Genetic Testing and Molecular Biomarkers, 16 (5) pp. 456-458 [SCI Expanded] Link DOI Balkan, E., Eyerci, N., Uzkeser, H., Karatay, S., Topçu, A., Yıldırım, K., Pirim, İ. (2012) "HLA B27 Subtype Distribution Among Patients with Ankylosing Spondylitis in Eastern Turkey", Genetic Testing and Molecular Biomarkers, 16 (5) pp. 456-458 [SCI Expanded] Link DOI
Balkan, E., Eyerci, N., Keleş, S., Ateş, O., Doğan, H., Pirim, İ., Kara, A. (2017) "Evaluation of HLA-B51 Subtypes in Behçet’s Patients with Uveitis", Kafkas Tıp Bilimleri Dergisi, 7 (3) pp. 193-196 [TR Dizin] DOI " data-bs-content-id="YazarBilgi-18985">
Balkan, E., Eyerci, N., Keleş, S., Ateş, O., Doğan, H., Pirim, İ., Kara, A. (2017) "Evaluation of HLA-B51 Subtypes in Behçet’s Patients with Uveitis", Kafkas Tıp Bilimleri Dergisi, 7 (3) pp. 193-196 [TR Dizin] DOI Balkan, E., Eyerci, N., Keleş, S., Ateş, O., Doğan, H., Pirim, İ., Kara, A. (2017) "Evaluation of HLA-B51 Subtypes in Behçet’s Patients with Uveitis", Kafkas Tıp Bilimleri Dergisi, 7 (3) pp. 193-196 [TR Dizin] DOI
Aliağaoğlu, C., Pirim, İ., Ulusoy, M., Eyerci, N., Aktaş, A. (2005) "Association between alopecia areata and HLA Class I and II in Turkey", J.Dermatol., (0) [SCI Expanded]
Gürlertop, H.Y., Gündoğdu, F., Pirim, İ., İslamoğlu, Y., Eyerci, N., Sevimli, S., Erdem, F., Şenocak, H. (2007) "Association between factor V Leiden mutation and coronary artery disease in the northeast region of Turkey", BLOOD COAGULATION FIBRINOLYSIS, (0) [SCI Expanded] DOI " data-bs-content-id="YazarBilgi-18987">
Gürlertop, H.Y., Gündoğdu, F., Pirim, İ., İslamoğlu, Y., Eyerci, N., Sevimli, S., Erdem, F., Şenocak, H. (2007) "Association between factor V Leiden mutation and coronary artery disease in the northeast region of Turkey", BLOOD COAGULATION FIBRINOLYSIS, (0) [SCI Expanded] DOI Gürlertop, H.Y., Gündoğdu, F., Pirim, İ., İslamoğlu, Y., Eyerci, N., Sevimli, S., Erdem, F., Şenocak, H. (2007) "Association between factor V Leiden mutation and coronary artery disease in the northeast region of Turkey", BLOOD COAGULATION FIBRINOLYSIS, (0) [SCI Expanded] DOI
Şimşek, E., Yeşilyurt, A., Ferda, P., Eyerci, N., Ulus, A.T. (2014) "Combined genetic mutations have remarkable effect on deep venous thrombosis and or pulmonary embolism occurence", Gene, 536 (1) pp. 171-176 [SCI Expanded] Link DOI " data-bs-content-id="YazarBilgi-18988">
Şimşek, E., Yeşilyurt, A., Ferda, P., Eyerci, N., Ulus, A.T. (2014) "Combined genetic mutations have remarkable effect on deep venous thrombosis and or pulmonary embolism occurence", Gene, 536 (1) pp. 171-176 [SCI Expanded] Link DOI Şimşek, E., Yeşilyurt, A., Ferda, P., Eyerci, N., Ulus, A.T. (2014) "Combined genetic mutations have remarkable effect on deep venous thrombosis and or pulmonary embolism occurence", Gene, 536 (1) pp. 171-176 [SCI Expanded] Link DOI
Balkan, E., Bilen, H., Akdeniz, N., Keleş, S., Kara, A., Eyerci, N., Doğan, H. (2017) "BEHÇET HASTALARINDA IFNgamag, IFNgama R,CRP, ISP70 mRNA EKSPRESYONSEViYESiNiN BELiRLENMESi", V.DOD DERMOTOLOJI GÜNDEMİ , Aydın, Türkiye, (Eylül 2017)
Duzkale, N., Eyerci, N., Öksüzoğlu, Ö.B.Ç., Kandemir, O. (2019) "Multigen Panel ile saptanan Varyantların Kalıtsal Kanserler ile İlişkisi", 13.Uluslararası katılımlı Tıbbi Genetik Kongresi , Antalya, (Ocak 2019)
Beysel, S., Bozkurt, N.Ç., Alp, Y., Eyerci, N., Pınarlı, F., Yeşilyurt, A., Çalışkan, M., Özçelik, Ö., Hepsen, S., Delibaşı, T. (2016) "FTO gene variants are associated with polyciystic ovary sydrome in women in Turkey", ENDO 2016 , Boston, Amerika Birleşik Devletleri, (Nisan 2016)
Neslihan, T., Eyerci, N., Acar, U. (2018) "Importance of Rare Compound Heterozygous c.12580t C Variant in the USH2A Gene", 13. Ulusal Tıbbi Genetik Kongresi , Antalya, Türkiye, (Kasım 2018)
Shen, J., Cohen, M., Giersch, A., Goldenberg, P., Kenna, M., Marcie, S., Sweetser, D., Brien, A.O., Pandya, A., Duzkale, H., Eyerci, N., Cao, Y., Choy, R., Li, Y., Yilai, S., Liu, X.Z., Tekin, M., Yan, D., Azaiez, H., Smith, R., Girotto, G., Morgan, A., Gasparani, P., Morton, C. (2018) "Hear-‘n-SEQ: an international collaboration todiscover unknown genetic etiologies of hearingloss in kids", 41st Annual MidWinter Meeting , Sa Diego, Amerika Birleşik Devletleri, (Şubat 2018)
Hüsnü, E., Arıcı, N., Eyerci, N., Yeşilyurt, A. (2015) "Tıpta Bir Veri Madenciliği Uygulaması Türk Popülasyonunda Organ Nakilleri için CPRA Hesaplama", XVII. AKADEMİK BİLİŞİM KONFERANSI , Türkiye, (Şubat 2015)
