IDH-mutant glioma specific association of rs55705857 located at 8q24.21 involves MYC deregulation
Oktay, Yavuz, Ülgen, Ege, Can, Özge, Akyerli, Cemaliye B., Yüksel, Şirin, Erdemgil, Yiğit, Durası, İ. Melis, Henegariu, Octavian Ioan, Nanni, E. Paolo, Selevsek, Nathalie, Grossmann, Jonas, Erson-Omay, E. Zeynep, Bai, Hanwen, Gupta, Manu, Lee, William, Turcan, Şevin, Özpınar, Aysel, Huse, Jason T., Sav, M. Aydın, Flanagan, Adrienne, Günel, Murat, Sezerman, O. Uğur, Yakıcıer, M. Cengiz, Pamir, M. Necmettin, Özduman, Koray
Published in Scientific reports (10.06.2016)
Published in Scientific reports (10.06.2016)
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Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas
Akyerli, Cemaliye B, Yüksel, Şirin, Can, Özge, Erson-Omay, E Zeynep, Oktay, Yavuz, Coşgun, Erdal, Ülgen, Ege, Erdemgil, Yiğit, Sav, Aydın, von Deimling, Andreas, Günel, Murat, Yakıcıer, M Cengiz, Pamir, M Necmettin, Özduman, Koray
Published in Journal of neurosurgery (01.04.2018)
Published in Journal of neurosurgery (01.04.2018)
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Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma
Ülgen, Ege, Can, Özge, Bilguvar, Kaya, Akyerli Boylu, Cemaliye, Kılıçturgay Yüksel, Şirin, Erşen Danyeli, Ayça, Sezerman, O Uğur, Yakıcıer, M Cengiz, Pamir, M Necmettin, Özduman, Koray
Published in BMC medical genomics (23.02.2021)
Published in BMC medical genomics (23.02.2021)
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Mutations and Copy Number Alterations in IDH Wild-Type Glioblastomas Are Shaped by Different Oncogenic Mechanisms
Ülgen, Ege, Karacan, Sıla, Gerlevik, Umut, Can, Özge, Bilguvar, Kaya, Oktay, Yavuz, B Akyerli, Cemaliye, K Yüksel, Şirin, E Danyeli, Ayça, Tihan, Tarık, Sezerman, O Uğur, Yakıcıer, M Cengiz, Pamir, M Necmettin, Özduman, Koray
Published in Biomedicines (07.12.2020)
Published in Biomedicines (07.12.2020)
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Next-Generation Sequencing Identifies BRCA1 and/or BRCA2 Mutations in Women at High Hereditary Risk for Breast Cancer with Shorter Telomere Length
Peker Eyüboğlu, İrem, Yenmiş, Güven, Bingöl, Elif Naz, Yüksel, Şirin, Tokat, Fatma, Özbek, Pemra, Güllü Amuran, Gökçe, Yakıcıer, Cengiz, Akkiprik, Mustafa
Published in Omics (Larchmont, N.Y.) (01.01.2020)
Published in Omics (Larchmont, N.Y.) (01.01.2020)
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Is 1p36 deletion associated with anterior body wall defects?
Çöllü, Medis, Yüksel, Şirin, Şirin, Başak Kumbasar, Abbasoğlu, Latif, Alanay, Yasemin
Published in American journal of medical genetics. Part A (01.07.2016)
Published in American journal of medical genetics. Part A (01.07.2016)
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Journal Article
Angiogenesis, Invasion, and Metastasis Characteristics of Hepatocellular Carcinoma
Yüksel, Şirin, Boylu Akyerli, Cemaliye, Cengiz Yakıcıer, M
Published in Journal of gastrointestinal cancer (01.09.2017)
Published in Journal of gastrointestinal cancer (01.09.2017)
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Journal Article
Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene
Bayrakli, Fatih, Poyrazoglu, Hatice Gamze, Yuksel, Sirin, Yakicier, Cengiz, Erguner, Bekir, Sagiroglu, Mahmut Samil, Yuceturk, Betul, Ozer, Bugra, Doganay, Selim, Tanrikulu, Bahattin, Seker, Askin, Akbulut, Fatih, Ozen, Ali, Per, Huseyin, Kumandas, Sefer, Altuner Torun, Yasemin, Bayri, Yasar, Sakar, Mustafa, Dagcinar, Adnan, Ziyal, Ibrahim
Published in Journal of human genetics (01.12.2015)
Published in Journal of human genetics (01.12.2015)
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Novel mutation of aspartoacylase gene in a Turkish patient with Canavan disease
Unalp, Aycan, Altiok, Ender, Uran, Nedret, Oztürk, Aysel, Yüksel, Sirin
Published in Journal of tropical pediatrics (1980) (01.06.2008)
Published in Journal of tropical pediatrics (1980) (01.06.2008)
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Mutations in influenza A virus (H5N1) and possible limited spread, Turkey, 2006
Altiok, Ender, Taylan, Fulya, Yenen, Osman S, Demirkeser, Gülşah, Bozaci, Mürvet, Onel, Derya, Akcadag, Birsen, Iyisan, A Selma, Ciblak, Meral, Bozkaya, Emel, Yuksel, Sirin, Badur, Selim
Published in Emerging infectious diseases (01.03.2008)
Published in Emerging infectious diseases (01.03.2008)
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Evaluation of AlphaFold structure-based protein stability prediction on missense variations in cancer
Keskin Karakoyun, Hilal, Yüksel, Şirin K, Amanoglu, Ilayda, Naserikhojasteh, Lara, Yeşilyurt, Ahmet, Yakıcıer, Cengiz, Timuçin, Emel, Akyerli, Cemaliye B
Published in Frontiers in genetics (21.02.2023)
Published in Frontiers in genetics (21.02.2023)
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Journal Article
Neural tube defect family with recessive trait linked to chromosome 9q21.12-21.31
Bayri, Yasar, Soylemez, Burcak, Seker, Askin, Yuksel, Sirin, Tanrikulu, Bahattin, Unver, Olcay, Canbolat, Cagrı, Sakar, Mustafa, Kardag, Ozen, Yakicier, Cengiz, Dagcinar, Adnan, Ziyal, Ibrahim, Bayrakli, Fatih
Published in Child's nervous system (01.08.2015)
Published in Child's nervous system (01.08.2015)
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Toward In Vitro Epigenetic Drug Design for Thyroid Cancer: The Promise of PF-03814735, an Aurora Kinase Inhibitor
Dalva-Aydemir, Sevim, Akyerli, Cemaliye Boylu, Yüksel, Şirin Kılıçturgay, Keskin, Hilal, Yakıcıer, Mustafa Cengiz
Published in Omics (Larchmont, N.Y.) (01.10.2019)
Published in Omics (Larchmont, N.Y.) (01.10.2019)
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Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype
Bayrakli, Fatih, Guclu, Bulent, Yakicier, Cengiz, Balaban, Hatice, Kartal, Ugur, Erguner, Bekir, Sagiroglu, Mahmut Samil, Yuksel, Sirin, Ozturk, Ahmet Rasit, Kazanci, Burak, Ozum, Unal, Kars, Hamit Zafer
Published in BMC genetics (28.09.2013)
Published in BMC genetics (28.09.2013)
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Mutation in MEOX1gene causes a recessive Klippel-Feil syndrome subtype
Bayrakli, Fatih, Guclu, Bulent, Yakicier, Cengiz, Balaban, Hatice, Kartal, Ugur, Erguner, Bekir, Sagiroglu, Mahmut Samil, Yuksel, Sirin, Ozturk, Ahmet Rasit, Kazanci, Burak, Ozum, Unal, Kars, Hamit Zafer
Published in BMC genetics (28.09.2013)
Published in BMC genetics (28.09.2013)
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Yeni Nesil Dizileme Teknolojileri İle Kanserde Mitokondriyal DNA Analizi
KILIÇTURGAY YÜKSEL, Şirin, BOYLU AKYERLİ, Cemaliye
Published in Harran Üniversitesi Tıp Fakültesi Dergisi (28.04.2021)
Published in Harran Üniversitesi Tıp Fakültesi Dergisi (28.04.2021)
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Lack of hotspot mutations other than TP53 R249S in aflatoxin B1 associated hepatocellular carcinoma: Aflatoksin B1 kaynaklı hepatosellüler karsinomlarda özgün TP53 R249S dışındaki mutasyonların eksikliği
Akyerli, Cemaliye B., Yüksel, Şirin K., Yakıcıer, M. Cengiz
Published in Turkish Journal of Biochemistry (02.10.2020)
Published in Turkish Journal of Biochemistry (02.10.2020)
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