Can prothrombotic gene variants and Apoa1 rs5069 polymorphism be the predictors of early myocardial infarctions? by BALCIOĞLU, HÜSEYİN, ÖZKAN PEHLİVANOĞLU, ELİF FATMA, BİLGE, UĞUR, MERT, KADİR UĞUR, DURAL, MUHAMMET, ERZURUMLUOĞLU GÖKALP, EBRU, ÇİLİNGİR, OĞUZ, ARTAN, SEVİLHAN

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The Impact of Cytogenetic Aberrations in the Clonal Evolution of Chronic Myeloid Leukemia: A Single-Center Experience Among 450 Turkish Patients (Cohort Study) by Işık, Sevgi, Günden, Gülçin, Üsküdar Teke, Hava, Akay, Olga Meltem, Oğuz Davutoğlu, Nur, Aslan, Vahap, Karagülle, Mustafa, Özen, Hülya, Çilingir, Oğuz, Artan, Sevilhan, Durak Aras, Beyhan

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Association of eleven single nucleotide polymorphisms with refractive disorders from Eskisehir, Turkey by Unlu, Nadir, Arslan, Serap, Cilingir, Oguz, Bilgin, Muzaffer, Yildirim, Engin, Gursoy, Huseyin

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Which prognostic marker is responsible for the clinical heterogeneity in CLL with 13q deletion? by Durak Aras, Beyhan, Isik, Sevgi, Uskudar Teke, Hava, Aslan, Abdulvahap, Yavasoglu, Filiz, Gulbas, Zafer, Demirkan, Fatih, Ozen, Hulya, Cilingir, Oguz, Inci, Nur Sena, Gunden, Gulcin, Bulduk, Tuba, Erzurumluoglu Gokalp, Ebru, Kocagil, Sinem, Artan, Sevilhan, Akay, Olga Meltem

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The impact of klotho gene polymorphisms on urinary tract stone disease by Gürel, Abdullah, Üre, İyimser, Temel, Halide Edip, Çilingir, Oğuz, Uslu, Sema, Celayir, Mehmet Fatih, Aslan, Serap, Başeskioğlu, Ali Barbaros

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Patient with Mal de Meleda in whom a Novel Gene Mutation was Identified by Gurel, Gulhan, Cilingir, Oguz, Kutluay, Ozden, Arslan, Serap, Sahin, Sevinc, Colgecen, Emine

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Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients by Ulus, Taner, Dural, Muhammet, Meşe, Pelin, Yetmiş, Furkan, Mert, Kadir Uğur, Görenek, Bülent, Çilingir, Oğuz, Erzurumluoglu Gökalp, Ebru, Arslan, Serap, Artan, Sevilhan, Aykaç, Özlem, Çolak, Ertuğrul, Yorgun, Hikmet, Canpolat, Uğur, Aytemir, Kudret

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Correlation of HER2/TOP2A Gene Aberrations with RASSF1A/APC Gene Methylation Status in High-Risk Breast Cancer by NURSAL, Ayşe Feyda

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Evaluation of the Effect of Circulating IncRNAs in Colorectal Cancers: As a Potential Biomarker by arslan, serap

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Prevalence of Nonclassic Congenital Adrenal Hyperplasia in Turkish Children Presenting with Premature Pubarche, Hirsutism, or Oligomenorrhoea by Kutlay, Ozden, Yuksel, Zafer, Cilingir, Oguz, Simsek, Enver, Binay, Cigdem, Artan, Sevilhan

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Early-onset Chronic Keratitis as the First Presenting Component of Autoimmune Polyendocrinopathy Syndrome Type 1 (APS-1): A Case Report and Review of the Literature by Şimşek, Enver, Simsek, Tulay, Cilingir, Oguz

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Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye by Lee, Mei Chin, Zenkel, Matthias, Peh, Esther, Ozaki, Mineo, Topouzis, Fotis, Nakano, Satoko, Chan, Anita, Chen, Shuwen, Orr, Andrew, Nakano, Masakazu, Kobakhidze, Nino, Zarnowski, Tomasz, Popa-Cherecheanu, Alina, Mizoguchi, Takanori, Manabe, Shin-ichi, Hayashi, Ken, Kazama, Shigeyasu, Inoue, Kenji, Mori, Yosai, Miyata, Kazunori, Sugiyama, Kazuhisa, Higashide, Tomomi, Chihara, Etsuo, Ideta, Ryuichi, Ishiko, Satoshi, Kiuchi, Yoshiaki, Ohashi, Tsutomu, Sugimoto, Takako, Chuman, Hideki, Aihara, Makoto, Mori, Kazuhiko, Ikeda, Yoko, Rafuse, Paul, Shuba, Lesya, Saunders, Joseph, Nicolela, Marcelo, Chichua, George, Tabagari, Sergo, Founti, Panayiota, Sim, Kar Seng, Soo, Hui Meng, Chen, Xiao Yin, Chatzikyriakidou, Anthi, Keskini, Christina, Pappas, Theofanis, Anastasopoulos, Eleftherios, Lambropoulos, Alexandros, Panagiotou, Evangelia S, Mikropoulos, Dimitrios G, Kosior-Jarecka, Ewa, Lukasik, Urszula, Husain, Rahat, Perera, Shamira A, Álvarez, Lydia, García, Montserrat, González-Iglesias, Héctor, Fernández-Vega Cueto, Andrés, Fernández-Vega Cueto, Luis, Martinón-Torres, Federico, Salas, Antonio, Oguz, Çilingir, Tamcelik, Nevbahar, Atalay, Eray, Batu, Bilge, Irkec, Murat, Aktas, Dilek, Kasim, Burcu, Astakhov, Yury S, Astakhov, Sergei Y, Akopov, Eugeny L, Giessl, Andreas, Mardin, Christian, Hellerbrand, Claus, Cooke Bailey, Jessica N, Igo, Robert P, Haines, Jonathan L, Edward, Deepak P, Davila, Sonia, Tan, Patrick, Kang, Jae H, Pasquale, Louis R, Kruse, Friedrich E, Reis, André, Carmichael, Trevor R, Hauser, Michael, Ramsay, Michele, Mossböck, Georg, Tashiro, Kei, Konstas, Anastasios G. P, Coca-Prados, Miguel, Foo, Jia Nee, Kinoshita, Shigeru, Sotozono, Chie, Kubota, Toshiaki, Dubina, Michael, Ritch, Robert, Schlötzer-Schrehardt, Ursula, Ho, Ying Swan, Aung, Tin, Tam, Wai Leong

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Conventional and molecular cytogenetic analyses in Turkish patients with multiple myeloma by Durak, Beyhan Aras, Akay, Olga Meltem, Sungar, Gülçin, Bademci, Güney, Aslan, Vahap, Caferler, Jülide, Ozdemir, Muhsin, Cilingir, Oğuz, Artan, Sevilhan, Gülbaş, Zafer

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NDE1‐related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephaly by Bas, Hasan, Saylisoy, Suzan, Cilingir, Oguz, Gokalp, Ebru Erzurumluoglu, Kocagil, Sinem, Yarar, Coskun, Aras, Beyhan Durak, Artan, Sevilhan

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The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide synt... by Ilguy, Serdar, Cilingir, Oguz, Bilgec, Mustafa Deger, Ozalp, Onur, Erzurumluoglu Gokalp, Ebru, Arslan, Serap, Tekin, Neslihan, Aydemir, Ozge, Erol, Nazmiye, Colak, Ertugrul, Gursoy, Huseyin

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The association between repeat number in C9orf72 and phenotypic variability in Turkish patients with frontotemporal lobar degeneration by Erzurumluoglu, Ebru, Cilingir, Oguz, Ozbabalik Adapinar, Belgin Demet, Bilgic, Basar, Kocagil, Sinem, Ozen, Hulya, Durak Aras, Beyhan, Yenilmez, Cinar, Artan, Sevilhan

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Frequency of frontotemporal dementia-related gene variants in Turkey by Artan, Sevilhan, Erzurumluoglu Gokalp, Ebru, Samanci, Bedia, Ozbabalik Adapinar, Demet, Bas, Hasan, Tepgec, Fatih, Qomi Ekenel, Emilia, Cilingir, Oguz, Bilgic, Basar, Gurvit, Hakan, Hanagasi, Hasmet Ayhan, Kocagil, Sinem, Durak Aras, Beyhan, Uyguner, Oya, Emre, Murat

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A Turkish patient with novel AHCY variants and presumed diagnosis of S‐adenosylhomocysteine hydrolase deficiency by Bas, Hasan, Cilingir, Oguz, Tekin, Neslihan, Saylisoy, Suzan, Durak Aras, Beyhan, Uzay, Elif, Erzurumluoglu Gokalp, Ebru, Artan, Sevilhan

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Conventional and molecular cytogenetic analyses in Turkish patients with multiple myeloma / Multipl Miyelom Tanili Turk Hastalarda Konvansiyonel ve Molekuler Sitogenetik Analizler by Aras, Beyhan Durak, Akay, Olga Meltem, Sungar, Gulcin, Bademci, Guney, Aslan, Vahap, Caferler, Julide, Ozdemir, Muhsin, Cilingir, Oguz, Artan, Sevilhan, Gulbas, Zafer

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A new four-way complex translocation variant involving the t(8;5;21;4)(q21;q13;q22;q31) and the relocalization of AML1/ETO fusion gene by Isik, Sevgi, Uskudar Teke, Hava, Gunden, Gulcin, Erzurumluoglu Gokalp, Ebru, Cilingir, Oguz, Artan, Sevilhan, Durak Aras, Beyhan

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