Defining Molecular Treatment Targets for Bladder Pain Syndrome/Interstitial Cystitis: Uncovering Adhesion Molecules von Inal-Gultekin, Guldal, Gormez, Zeliha, Mangir, Naside

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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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Coffin-Siris syndrome with café-au-lait spots, obesity and hyperinsulinism caused by a mutation in the ARID1B gene von Sonmez, Fatma Mujgan, Uctepe, Eyyup, Gunduz, Mehmet, Gormez, Zeliha, Erpolat, Seval, Oznur, Murat, Sagiroglu, Mahmut Samil, Demirci, Huseyin, Gunduz, Esra

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Myophosphorylase ( PYGM ) mutations determined by next generation sequencing in a cohort from turkey with McArdle disease von Inal-Gültekin, Güldal, Toptaş-Hekimoğlu, Bahar, Görmez, Zeliha, Gelişin, Özlem, Durmuş, Hacer, Ergüner, Bekir, Demirci, Hüseyin, Sağıroğlu, Mahmut Ş, Parman, Yeşim, Deymeer, Feza, Yılmaz-Aydoğan, Hülya, Pençe, Sadrettin, Bekircan-Kurt, Can Ebru, Tan, Ersin, Erdem-Özdamar, Sevim, Üstek, Duran, Giger, Urs, Öztürk, Oğuz, Serdaroğlu-Oflazer, Piraye

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HomSI: a homozygous stretch identifier from next-generation sequencing data von Görmez, Zeliha, Bakir-Gungor, Burcu, Sagiroglu, Mahmut Samil

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Deetect: A Deep Learning-Based Image Analysis Tool for Quantification of Adherent Cell Populations on Oxygenator Membranes after Extracorporeal Membrane Oxygenation Therapy von Hoeren, Felix, Görmez, Zeliha, Richter, Manfred, Troidl, Kerstin

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A novel truncating mutation of DOCK7 gene with an early-onset non-encephalopathic epilepsy von Turkdogan, Dilsad, Turkyilmaz, Ayberk, Gormez, Zeliha, Sager, Gunes, Ekinci, Gazanfer

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A Novel and Mosaic WDR45 Nonsense Variant Causes Beta-Propeller Protein-Associated Neurodegeneration Identified Through Whole Exome Sequencing and X chromosome Heterozygosity Analy... von Akçakaya, Nihan Hande, Salman, Barış, Görmez, Zeliha, Tarkan Argüden, Yelda, Çırakoğlu, Ayşe, Çakmur, Raif, Dönmez Çolakoğlu, Berril, Hacıhanefioğlu, Seniha, Özbek, Uğur, Yapıcı, Zuhal, Uğur İşeri, Sibel Aylin

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FMFilter: A fast model based variant filtering tool von Akgün, Mete, Faruk Gerdan, Ö., Görmez, Zeliha, Demirci, Hüseyin

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A further family of Stromme syndrome carrying CENPF mutation von Ozkinay, Ferda, Atik, Tahir, Isik, Esra, Gormez, Zeliha, Sagiroglu, Mahmut, Sahin, Ozlem Atan, Corduk, Nergul, Onay, Huseyin

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Multi objective SNP selection using pareto optimality von Gumus, Ergun, Gormez, Zeliha, Kursun, Olcay

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Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy von Sahin, Yavuz, Güngör, Olcay, Gormez, Zeliha, Demirci, Huseyin, Ergüner, Bekir, Güngör, Gülay, Dilber, Cengiz

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A clinical variant in SCN1A inherited from a mosaic father cosegregates with a novel variant to cause Dravet syndrome in a consanguineous family von Tuncer, Feyza N, Gormez, Zeliha, Calik, Mustafa, Altiokka Uzun, Gunes, Sagiroglu, Mahmut S, Yuceturk, Betul, Yuksel, Bayram, Baykan, Betul, Bebek, Nerses, Iscan, Akin, Ugur Iseri, Sibel A, Ozbek, Ugur

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

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Statistical bias and variance of gene selection and cross validation methods: A case study on hypertension prediction von Gormez, Z., Kursun, O., Sertbas, A., Aydin, N., Seker, H.

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Comparison of aggregators for multi-objective SNP selection von Gormez, Zeliha, Gumus, Ergun, Sertbas, Ahmet, Kursun, Olcay

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A novel truncating mutation of DOCK7 gene with an early-onset non-encephalopathic epilepsy von Turkdogan, Dilsad, Turkyilmaz, Ayberk, Gormez, Zeliha, Sager, Gunes, Ekinci, Gazanfer

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Coffin-Siris syndrome with café-au-lait spots, obesity and hyperinsulinism caused by a mutation in the ARID1B gene von Sonmez, Fatma Mujgan, Uctepe, Eyyup, Gunduz, Mehmet, Gormez, Zeliha, Erpolat, Seval, Oznur, Murat, Sagiroglu, Mahmut Samil, Demirci, Huseyin, Gunduz, Esra

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Evaluation of the Concatenative Turkish Text-to-Speech System von Orhan, Z., Gormez, Z.

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The role of mediastinal adipose tissue 11β-hydroxysteroid d ehydrogenase type 1 and glucocorticoid expression in the development of coronary atherosclerosis in obese patients with... von Atalar, Fatmahan, Gormez, Selcuk, Caynak, Baris, Akan, Gokce, Tanriverdi, Gamze, Bilgic-Gazioglu, Sema, Gunay, Demet, Duran, Cihan, Akpinar, Belhhan, Ozbek, Ugur, Buyukdevrim, Ahmet Sevim, Yazici, Zeliha

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