Alu-Mediated Deletion of FANCA in Turkish Families With Fanconi Anemia: Evidence of a Founder Effect von Durmaz, Ceren Damla, Gümrük, Fatma, Celkan, Tiraje, Unal, Sule, Çetinkaya, Arda

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DNA damage is increased in lymphocytes of patients with metabolic syndrome von Karaman, Ali, Aydın, Hatip, Geçkinli, Bilge, Çetinkaya, Arda, Karaman, Selin

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One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family von Bekircan-Kurt, Can Ebru, Çetinkaya, Arda, Gocmen, Rahsan, Koşukcu, Can, Soylemezoglu, Figen, Arsava, Ethem Murat, Tuncer, Asli, Erdem-Ozdamar, Sevim, Akarsu, Nurten A., Topcuoglu, Mehmet Akif

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Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling von Cetinkaya, Arda, Xiong, Jingwei Rachel, Vargel, İbrahim, Kösemehmetoğlu, Kemal, Canter, Halil İbrahim, Gerdan, Ömer Faruk, Longo, Nicola, Alzahrani, Ahmad, Camps, Mireia Perez, Taskiran, Ekim Zihni, Laupheimer, Simone, Botto, Lorenzo D., Paramalingam, Eeswari, Gormez, Zeliha, Uz, Elif, Yuksel, Bayram, Ruacan, Şevket, Sağıroğlu, Mahmut Şamil, Takahashi, Tokiharu, Reversade, Bruno, Akarsu, Nurten Ayse

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A Homozygous Deletion in GRID2 Causes a Human Phenotype With Cerebellar Ataxia and Atrophy von Utine, G. Eda, Haliloğlu, Göknur, Salancı, Bilge, Çetinkaya, Arda, Kiper, P. Özlem, Alanay, Yasemin, Aktaş, Dilek, Boduroğlu, Koray, Alikaşifoğlu, Mehmet

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The Predictive Value of the Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratio in Patients with Recurrent Idiopathic Granulomatous Mastitis von Cetinkaya, Omer Arda, Celik, Suleyman Utku, Terzioglu, Serdar Gokay, Eroglu, Aydan

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Novel FBN1 mutation in a family with inherited Marfan Syndrome: p.Cys2672Arg von Cetinkaya, Arda, Karaman, Ali, Mutlu, Mehmet Burak, Yavuz, Taner

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Comprehensive clinical, biochemical, radiological and genetic analysis of 28 Turkish cases with suspected metachromatic leukodystrophy and their relatives von Pekgül, Faruk, Eroğlu-Ertuğrul, Nesibe Gevher, Bekircan-Kurt, Can Ebru, Erdem-Ozdamar, Sevim, Çetinkaya, Arda, Tan, Ersin, Konuşkan, Bahadır, Karaağaoğlu, Ergun, Topçu, Meral, Akarsu, Nurten Ayşe, Oguz, Kader K., Anlar, Banu, Özkara, Hatice Asuman

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Genetic Variations in Attention Deficit Hyperactivity Disorder Subtypes and Treatment Resistant Cases von Unal, Dilek, Unal, Mehmet Fatih, Alikasifoglu, Mehmet, Cetinkaya, Arda

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The Effect of Leucocytosis, Gender Difference, and Ultrasound in the Diagnosis of Acute Cholecystitis in the Elderly Population von Polat, Onur, Çetinkaya, Arda, Tanrıverdi, Ayça Koca, Demirkan, Arda, Günalp, Müge

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Extended left hepatectomy for intrahepatic cholangiocarcinoma: hepatic vein reconstruction with in-situ hypothermic perfusion and extracorporeal membrane oxygenation von Balci, Deniz, Ozcelik, Menekse, Kirimker, Elvan Onur, Cetinkaya, Arda, Ustuner, Evren, Cakici, Mehmet, Inan, Bahadir, Alanoglu, Zekeriyya, Bilgic, Sadik, Akar, Ahmet Ruchan

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Venous stent placement ameliorates cutaneous microvascular function in iliocaval venous obstruction von Köksoy, Cüneyt, Akkoca, Muzaffer, Tokgöz, Serhat, Çetinkaya, Arda, Sevim, Yusuf, Demirel-Yılmaz, Emine

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Dermal fibroblast transcriptome indicates contribution of WNT signaling pathways in the pathogenesis of Apert syndrome von Çetinkaya, Arda, Taşkıran, Ekim, Soyer, Tutku, Şimşek-Kiper, Pelin Özlem, Utine, Gülen Eda, Tunçbilek, Gökhan, Boduroğlu, Koray, Alikaşifoğlu, Mehmet

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Etiological yield of SNP microarrays in idiopathic intellectual disability von Utine, G. Eda, Haliloğlu, Göknur, Volkan-Salancı, Bilge, Çetinkaya, Arda, Kiper, Pelin Ö, Alanay, Yasemin, Aktaş, Dilek, Anlar, Banu, Topçu, Meral, Boduroğlu, Koray, Alikaşifoğlu, Mehmet

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Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria von Guleray Lafci, Naz, van Goor, Mark, Cetinkaya, Semra, van der Wijst, Jenny, Acun, Melisa, Kurt Colak, Fatma, Cetinkaya, Arda, Hoenderop, Joost

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A combination treatment of transanal total mesorectal excision and Turnbull–Cutait abdominoperineal pull-through procedure for a low rectal cancer von Celik, Suleyman Utku, Cetinkaya, Omer Arda, Akin, Furkan Atakan, Fiúza, Stéfano do Amaral, Gecim, Ibrahim Ethem

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Defining mitochondrial protein functions through deep multiomic profiling von Rensvold, Jarred W., Shishkova, Evgenia, Sverchkov, Yuriy, Miller, Ian J., Cetinkaya, Arda, Pyle, Angela, Manicki, Mateusz, Brademan, Dain R., Alanay, Yasemin, Raiman, Julian, Jochem, Adam, Hutchins, Paul D., Peters, Sean R., Linke, Vanessa, Overmyer, Katherine A., Salome, Austin Z., Hebert, Alexander S., Vincent, Catherine E., Kwiecien, Nicholas W., Rush, Matthew J. P., Westphall, Michael S., Craven, Mark, Akarsu, Nurten A., Taylor, Robert W., Coon, Joshua J., Pagliarini, David J.

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HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemia von O'Donohue, Marie-Françoise, Da Costa, Lydie, Lezzerini, Marco, Unal, Sule, Joret, Clément, Bartels, Marije, Brilstra, Eva, Scheijde-Vermeulen, Marijn, Wacheul, Ludivine, De Keersmaecker, Kim, Vereecke, Stijn, Labarque, Veerle, Saby, Manon, Lefevre, Sophie D., Platon, Jessica, Montel-Lehry, Nathalie, Laugero, Nathalie, Lacazette, Eric, van Gassen, Koen, Houtkooper, Riekelt H., Simsek-Kiper, Pelin Ozlem, Leblanc, Thierry, Yarali, Nese, Cetinkaya, Arda, Akarsu, Nurten A., Gleizes, Pierre-Emmanuel, Lafontaine, Denis L.J., MacInnes, Alyson W.

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Re: The Predictive Value of the Neutrophil-to-Lymphocyte and Platelet-to-Lymphocyte Ratio in Patients with Recurrent Idiopathic Granulomatous Mastitis von Çetinkaya, Ömer Arda, Çelik, Süleyman Utku, Terzioğlu, Serdar Gökay, Eroğlu, Aydan

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HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemia von O'Donohue, Marie-Françoise, Da Costa, Lydie M, Lezzerini, Marco, Unal, Sule, Joret, Clément, Bartels, Marije, Brilstra, Eva, Scheijde-Vermeulen, Marijn, Wacheul, Ludivine, De Keersmaecker, Kim, Vereecke, Stijn, Labarque, Veerle, Saby, Manon Juliette, LeFevre, Sophie D, Platon, Jessica, Montel-Lehry, Nathalie, Laugero, Nathalie, Lacazette, Eric, van Gassen, Koen, Houtkooper, Riekelt H, Simsek-Kiper, Pelin Ozlem, Leblanc, Thierry M, Yarali, Nese, Cetinkaya, Arda, Akarsu, Nurten A, Gleizes, Pierre-Emmanuel, Lafontaine, Denis L J, MacInnes, Alyson W

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