Which prognostic marker is responsible for the clinical heterogeneity in CLL with 13q deletion?
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
Published in Molecular cytogenetics (06.01.2021)
Published in Molecular cytogenetics (06.01.2021)
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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 synthase 3 gene polymorphisms
Ilguy, Serdar, Cilingir, Oguz, Bilgec, Mustafa Deger, Ozalp, Onur, Erzurumluoglu Gokalp, Ebru, Arslan, Serap, Tekin, Neslihan, Aydemir, Ozge, Erol, Nazmiye, Colak, Ertugrul, Gursoy, Huseyin
Published in Ophthalmic genetics (01.12.2021)
Published in Ophthalmic genetics (01.12.2021)
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A novel SACS p.Pro4154GlnfsTer20 mutation in a family with autosomal recessive spastic ataxia of Charlevoix-Saguenay
Samanci, Bedia, Gokalp, Ebru Erzurumluoglu, Bilgic, Basar, Gurvit, Hakan, Artan, Sevilhan, Hanagasi, Hasmet A.
Published in Neurological sciences (01.07.2021)
Published in Neurological sciences (01.07.2021)
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Journal Article
Frequency of frontotemporal dementia-related gene variants in Turkey
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
Published in Neurobiology of aging (01.10.2021)
Published in Neurobiology of aging (01.10.2021)
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A Turkish patient with novel AHCY variants and presumed diagnosis of S‐adenosylhomocysteine hydrolase deficiency
Bas, Hasan, Cilingir, Oguz, Tekin, Neslihan, Saylisoy, Suzan, Durak Aras, Beyhan, Uzay, Elif, Erzurumluoglu Gokalp, Ebru, Artan, Sevilhan
Published in American journal of medical genetics. Part A (01.04.2020)
Published in American journal of medical genetics. Part A (01.04.2020)
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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
Isik, Sevgi, Uskudar Teke, Hava, Gunden, Gulcin, Erzurumluoglu Gokalp, Ebru, Cilingir, Oguz, Artan, Sevilhan, Durak Aras, Beyhan
Published in Cancer genetics (01.08.2021)
Published in Cancer genetics (01.08.2021)
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A novel PSEN2 p.Ser175Phe variant in a family with Alzheimer’s disease
Guven, Gamze, Samanci, Bedia, Gulec, Cagri, Hanagasi, Hasmet, Gurvit, Hakan, Gokalp, Ebru Erzurumluoglu, Tepgec, Fatih, Guler, Suleyman, Uyguner, Oya, Bilgic, Basar
Published in Neurological sciences (01.06.2021)
Published in Neurological sciences (01.06.2021)
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Journal Article
Genetic variants associated with atrial fibrillationand long-term recurrence after catheter ablation for atrialfibrillation in Turkish patients
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
Published in Anatolian journal of cardiology (01.02.2021)
Published in Anatolian journal of cardiology (01.02.2021)
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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
Şimşek, Enver, Çilingir, Oğuz, Şimşek, Tülay, Kocagil, Sinem, Erzurumluoğlu Gökalp, Ebru, Demiral, Meliha, Binay, Ciğdem
Published in Journal of clinical research in pediatric endocrinology (01.06.2024)
Published in Journal of clinical research in pediatric endocrinology (01.06.2024)
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NDE1‐related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephaly
Bas, Hasan, Saylisoy, Suzan, Cilingir, Oguz, Gokalp, Ebru Erzurumluoglu, Kocagil, Sinem, Yarar, Coskun, Aras, Beyhan Durak, Artan, Sevilhan
Published in American journal of medical genetics. Part A (01.01.2022)
Published in American journal of medical genetics. Part A (01.01.2022)
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An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3
Isik, Sevgi, Gunden, Gulcin, Gunduz, Eren, Akay, Olga Meltem, Aslan, Abdulvahap, Ozen, Hulya, Cilingir, Oguz, Erzurumluoglu Gokalp, Ebru, Kocagil, Sinem, Artan, Sevilhan, Gulbas, Zafer, Durak Aras, Beyhan
Published in Cytogenetic and genome research (01.01.2021)
Published in Cytogenetic and genome research (01.01.2021)
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A pediatric BAL case with double Ph chromosomes and trisomy 5
Gunden, Gulcin, Isik, Sevgi, Ozdemir, Canan, Cİlİngİr, Oguz, Bor, Ozcan, Gokalp, Ebru Erzurumluoglu, Kocagil, Sinem, Artan, Sevilhan, Aras, Beyhan Durak
Published in Cancer genetics (01.11.2021)
Published in Cancer genetics (01.11.2021)
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Journal Article
Extra Chromosome, Extra Love
Durak Aras,Beyhan, Işık,Sevgi, Baş,Hasan, Öcal,Ece Elif, Erzurumluoğlu Gökalp,Ebru, Çilingir,Oğuz, Artan,Sevilhan, Arslantaş,Didem
Published in Gazi tıp dergisi (01.01.2021)
Published in Gazi tıp dergisi (01.01.2021)
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NDE1-related disorders: A recurrent NDE1 pathogenic variant causing Lissencephaly 4 can also be associated with microhydranencephaly
Bas, Hasan, Saylisoy, Suzan, Cilingir, Oguz, Gokalp, Ebru Erzurumluoglu, Kocagil, Sinem, Yarar, Coskun, Aras, Beyhan Durak, Artan, Sevilhan
Published in American journal of medical genetics. Part A (01.01.2022)
Published in American journal of medical genetics. Part A (01.01.2022)
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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 synthase 3 gene polymorphisms
Ilguy, Serdar, Cilingir, Oguz, Bilgec, Mustafa Deger, Ozalp, Onur, Erzurumluoglu Gokalp, Ebru, Arslan, Serap, Tekin, Neslihan, Aydemir, Ozge, Erol, Nazmiye, Colak, Ertugrul, Gursoy, Huseyin
Published in Ophthalmic Genetics (02.11.2021)
Published in Ophthalmic Genetics (02.11.2021)
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Can prothrombotic gene variants and Apoa1 rs5069 polymorphism be the predictors of early myocardial infarctions?
BALCIOĞLU, HÜSEYİN, ÖZKAN PEHLİVANOĞLU, ELİF FATMA, BİLGE, UĞUR, MERT, KADİR UĞUR, DURAL, MUHAMMET, ERZURUMLUOĞLU GÖKALP, EBRU, ÇİLİNGİR, OĞUZ, ARTAN, SEVİLHAN
Published in Turkish journal of medical sciences (23.08.2024)
Published in Turkish journal of medical sciences (23.08.2024)
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