Is there a genetic predisposition for Turkish patients with sarcoidosis in the 329-bp region containing the BTNL2 rs2076530 polymorphism? von Ozdemir, Muhsin, Saydam, Faruk, Kurt, Emel, Değirmenci, Irfan, Tuncel, Tunç, Cilingir, Oğuz, Güneş, Hasan Veysi, Artan, Sevilhan

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Genetic Investigations in Turkish Idiopathic Pancreatitis Patients Show Unique Characteristics von Baş, Hasan, Dişibeyaz, Selçuk, Öztaş, Erkin, Aydemir, Yusuf, Temel, Tuncer, Çilingir, Oğuz, Durak Aras, Beyhan, Artan, Sevilhan

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Genetic Polymorphism on Chromosome 4q25 (rs17570669) May Predict Recurrence After Successful Electrical Cardioversion in Patients with Persistent Atrial Fibrillation von Ulus, Taner, Aliyev, İlkin, Arslan, Serap, Çilingir, Oğuz, Çolak, Ertuğrul

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Screening of Mutations in Maturity-onset Diabetes of the Young-related Genes and RFX6 in Children with Autoantibody-negative Type 1 Diabetes Mellitus von Şimşek, Enver, Çilingir, Oğuz, Şimşek, Tülay, Kocagil, Sinem, Erzurumluoğlu Gökalp, Ebru, Demiral, Meliha, Binay, Ciğdem

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A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome von Aung, Tin, Ozaki, Mineo, Li, Zheng, Uebe, Steffen, Harder, Jeffrey M, Chan, Anita S Y, Lee, Mei Chin, Burdon, Kathryn P, Pakravan, Mohammad, Wang, Ya Xing, Williams, Susan, Huang, Lulin, Foo, Jia Nee, Kumar, Rajesh S, Ueno, Morio, Manabe, Shin-ichi, Hayashi, Ken, Ideta, Ryuichi, Mori, Yosai, Miyata, Kazunori, Sugiyama, Kazuhisa, Higashide, Tomomi, Chihara, Etsuo, Inoue, Kenji, Yoshida, Akitoshi, Yanagi, Masahide, Aihara, Makoto, Ohashi, Tsutomu, Sakurai, Toshiya, Sugimoto, Takako, Chuman, Hideki, Yamashiro, Kenji, Gotoh, Norimoto, Osman, Essam A, Al-Obeidan, Saleh A, Al-Jasim, Leyla, Shahwan, Sami Al, Leo, Paul, Yetkin, Yaz, Oğuz, Çilingir, Kanavi, Mozhgan Rezaei, Yazdani, Shahin, Akopov, Evgeny L, Howell, Gareth R, Goh, Yufen, Meah, Wee Yang, Peh, Su Qin, Lukasik, Urszula, Krumbiegel, Mandy, Vithana, Eranga N, Wong, Tien Yin, Liu, Yutao, Challa, Pratap, Hewitt, Alex W, Mitchell, Paul, Ziskind, Ari, Venkatesh, Rangaraj, Vijayan, Saravanan, Zhao, Peiquan, Guadarrama-Vallejo, Dalia, Perera, Shamira A, Husain, Rahat, Ho, Su-Ling, Welge-Luessen, Ulrich-Christoph, Schloetzer-Schrehardt, Ursula, Herms, Stefan, Nöthen, Markus M, Weisschuh, Nicole, Ghosh, Arkasubhra, Teo, Yik Ying, Brown, Matthew A, Lischinsky, Ignacio, Crowston, Jonathan G, Sang, Jinghong, Zhang, Nihong, You, Qisheng, Founti, Panayiota, Lambropoulos, Alexandros, Anastasopoulos, Eleftherios, Rhee, Douglas J, May-Bolchakova, Inna, Heegaard, Steffen, Alward, Wallace L M, Jonas, Jost B, Xu, Liang, Chowbay, Balram, Schaeffeler, Elke, Lerner, Fabian, Yang, Zhenglin, Frezzotti, Paolo, Kinoshita, Shigeru, Inatani, Masaru, Tashiro, Kei, Reis, André, Edward, Deepak P, Pasquale, Louis R, Wiggs, Janey L, Yoshimura, Nagahisa, Ritch, Robert, Khor, Chiea-Chuen

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Three Single Nucleotide Polymorphisms of LOXL1 ' in a Turkish Population with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma von Yaz, Yetkin, Yıldırım, Nilgün, Aydın Yaz, Yasemin, Çilingir, Oğuz, Yüksel, Zafer, Mutlu, Fezan

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HB UBE-2 variant hemoglobin case detected during HBA1C measurement von Kocatürk,Evin, Küskü Kiraz,Zeynep, Demir,Şükrü Saygın, Çilingir,Oğuz, Üsküdar Teke,Hava, Alataş,İbrahim Özkan

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Performance of MLPA as a screening method for aneuploidy in uncultured amniocytes von Yurdakul, Huseyin, Durak, Beyhan, Muslumanoglu, Muhammed Hamza, Ozdemir, Muhsin, Cilingir, Oguz, Sener, Turgay, Artan, Sevilhan

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IL-15 Gene Polymorphism in Celiac Disease Patients and Their Siblings von Kara, Yalçın, Eren, Makbule, Arslan, Serap, Çilingir, Oğuz

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Is Recurrent Abortion an Indication for Subtelomeric Region Analysis? von DURAK, Beyhan, YEŞİL, Mesut, ÖZDEMİR, Muhsin, ÇİLİNGİR, Oğuz, ŞENER, Turgay, BADEMCİ, Güney, MÜSLÜMANOĞLU, M. Hamza, ARTAN, Sevilhan

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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) von 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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The Most Predictive Red Flags for Suspecting Cardiac Amyloidosis in Patients with Heart Failure with Preserved Ejection Fraction von Yalvaç, Halit Emre, Murat, Selda, Ak Sivrikoz, İlknur, Üsküdar Teke, Hava, Çilingir, Oğuz, Çolak, Ertuğrul, Çavuşoğlu, Yüksel

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Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye von 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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Can prothrombotic gene variants and Apoa1 rs5069 polymorphism be the predictors of early myocardial infarctions? von 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 klotho gene polymorphisms on urinary tract stone disease von Gürel, Abdullah, Üre, İyimser, Temel, Halide Edip, Çilingir, Oğuz, Uslu, Sema, Celayir, Mehmet Fatih, Aslan, Serap, Başeskioğlu, Ali Barbaros

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Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients von 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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Association of eleven single nucleotide polymorphisms with refractive disorders from Eskisehir, Turkey von 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? von 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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Extra Chromosome, Extra Love von Durak Aras,Beyhan, Işık,Sevgi, Baş,Hasan, Öcal,Ece Elif, Erzurumluoğlu Gökalp,Ebru, Çilingir,Oğuz, Artan,Sevilhan, Arslantaş,Didem

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Apolipoprotein E allelic variants and cerebral palsy von Gümüş, Evren, Aras, Beyhan Durak, Çilingir, Oğuz, Yarar, Coşkun, Çarman, Kürşat Bora, Laçiner-Gürlevik, Sibel, Koçak, Ozan, Artan, Sevilhan

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