Jury Memberships
June 2022 | Post Graduate, Post Graduate, Acıbadem Mehmet Ali Aydınlar Üniversitesi |
Published journal articles indexed by SCI, SSCI, and AHCI
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The Modulatory Action of C-Vx Substance on the Immune System in COVID-19.Tahrali I., Akdeniz N., Yilmaz V., Kucuksezer U. C., Oktelik F. B., Ozdemir Ö., Cetin-Aktas E., Ogutmen Y., Ergen A., Abaci N., et al.Emerging microbes & infections, pp.1-28, 2022 (SCI-Expanded)
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Immune modulation as a consequence of SARS-CoV-2 infectionGELMEZ M. Y., ÖKTELİK F. B., TAHRALI İ., YILMAZ V., KÜÇÜKSEZER U. C., AKDENİZ N., ÇETİN E., KÖSE M., ÇINAR Ç., OĞUZ F., et al.FRONTIERS IN IMMUNOLOGY, vol.13, 2022 (SCI-Expanded)
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Mutational landscape of SARS-CoV-2 genome in Turkey and impact of mutations on spike protein structure.Hatirnaz N., Akyoney S., Sahin I., Soykam H., Bayram A., Ozdemir Ö., Kancagi D., Sir K., Yurtsever B., Kocagoz A., et al.PloS one, vol.16, no.12, 2021 (SCI-Expanded)
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The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in Turkey.Haryanyan G., Ozdemir Ö., Tutkavul K., Dervent A., Ayta S., Ozkara C., Salman B., YÜCESAN E., Kesim Y., SÜSGÜN S., et al.Journal of human genetics, vol.66, no.12, pp.1145-1151, 2021 (SCI-Expanded)
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Peripheral blood B cell subset ratios and expression levels of B cell-associated genes are altered in benign multiple sclerosisTurkoglu R., YILMAZ V., ÖZDEMİR Ö., Akbayir E., Benbir G., Arsoy E., Sen M., ULUSOY C. A., Ozyurt S., Balic N., et al.MULTIPLE SCLEROSIS AND RELATED DISORDERS, vol.52, 2021 (SCI-Expanded)
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Clinical and genetic characterization of PYROXD1-related myopathy patients from TurkeyDaimagueler H., Akpulat U., Oezdemir Ö., YİŞ U., GÜNGÖR S., TALİM B., Diniz G., Baydan F., Thiele H., Altmueller J., et al.AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol.185, no.6, pp.1678-1690, 2021 (SCI-Expanded)
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Making sense of missense variants in TTN-related congenital myopathiesRees M., Nikoopour R., Fukuzawa A., Kho A. L., Fernandez-Garcia M. A., Wraige E., Bodi I., Deshpande C., Oezdemir Ö., Daimagueler H., et al.ACTA NEUROPATHOLOGICA, vol.141, no.3, pp.431-453, 2021 (SCI-Expanded)
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Ultra-rapid emergency genomic diagnosis of Donahue syndrome in a preterm infant within 17 hoursBamborschke D., Oezdemir Ö., Kreutzer M., Motameny S., Thiele H., Kribs A., Doetsch J., Altmueller J., Nuernberg P., Cirak S.AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol.185, no.1, pp.90-96, 2021 (SCI-Expanded)
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The genomic and clinical landscape of fetal akinesiaPergande M., Motameny S., Oezdemir Ö., Kreutzer M., Wang H., Daimagueler H., Becker K., Karakaya M., Ehrhardt H., ELÇİOĞLU H. N., et al.GENETICS IN MEDICINE, vol.22, no.3, pp.511-523, 2020 (SCI-Expanded)
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Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane TraffickingWang H., Bayram A. K., Sprute R., ÖZDEMİR Ö., Cooper E., Pergande M., Efthymiou S., Nedic I., Mazaheri N., Stumpfe K., et al.FRONTIERS IN NEUROSCIENCE, vol.13, 2019 (SCI-Expanded)
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Identification of epilepsy related pathways using genome-wide DNA methylation measures: A trio-based approachÖZDEMİR Ö., Egemen E., UĞUR İŞERİ S. A., SEZERMAN O. U., BEBEK N., BAYKAL B., ÖZBEK U.PLOS ONE, vol.14, no.2, 2019 (SCI-Expanded)
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Investigation of SLC2A1 gene variants in genetic generalized epilepsy patients with eyelid myocloniaAltiokka-Uzun G., ÖZDEMİR Ö., Ugur-Iseri S., BEBEK N., Gurses C., ÖZBEK U., BAYKAL B.EPILEPTIC DISORDERS, vol.20, no.5, pp.396-400, 2018 (SCI-Expanded)
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SYNE1 related cerebellar ataxia presents with variable phenotypes in a consanguineous family from TurkeyYÜCESAN E., UĞUR İŞERİ S. A., BİLGİÇ B., Gormez Z., GÜNGÖR B., Sarac A., ÖZDEMİR Ö., Sagiroglu M., GÜRVİT İ. H., HANAĞASI H. A., et al.NEUROLOGICAL SCIENCES, vol.38, no.12, pp.2203-2207, 2017 (SCI-Expanded)
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Expression changes of genes associated with apoptosis and survival processes in Parkinson's diseaseYalcinkaya N., Haytural H., BİLGİÇ B., ÖZDEMİR Ö., Hanagasi H., KÜÇÜKALİ C. İ., Ozbek Z., Akcan U., Idrisoglu H. A., GÜRVİT İ. H., et al.NEUROSCIENCE LETTERS, vol.615, pp.72-77, 2016 (SCI-Expanded)
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Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutationKesim Y. F., Uzun G. A., YÜCESAN E., TUNCER KILINÇ F. N., ÖZDEMİR Ö., BEBEK N., ÖZBEK U., UĞUR İŞERİ S. A., BAYKAL B.EPILEPSY RESEARCH, vol.120, pp.73-78, 2016 (SCI-Expanded)
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Investigation of the possible association of NEDD4-2 (NEDD4L) gene with idiopathic photosensitive epilepsyVanli-Yavuz E. N., ÖZDEMİR Ö., Demirkan A., Catal S., BEBEK N., ÖZBEK U., BAYKAL B.ACTA NEUROLOGICA BELGICA, vol.115, no.3, pp.241-245, 2015 (SCI-Expanded)
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A homozygous splice-site mutation in CARS2 is associated with progressive myoclonic epilepsyHallmann K., Zsurka G., Moskau-Hartmann S., Kirschner J., Korinthenberg R., Ruppert A., Ozdemir Ö., Weber Y., Becker F., Lerche H., et al.NEUROLOGY, vol.83, no.23, pp.2183-2187, 2014 (SCI-Expanded)
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Bromodomain-containing protein 2 gene in photosensitive epilepsy.Yavuz E. N., Ozdemir Ö., Catal S., Bebek N., Ozbek U., Baykan B.Seizure, vol.21, no.8, pp.646-8, 2012 (SCI-Expanded)
Refereed Congress / Symposium Publications in Proceedings
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KALITSAL KANSERLERDE KLİNİK ÖNEMİ BİLİNMEYEN GENOMİK VARYANTLARIN FONKSİYONEL KARAKTERİZASYONU VE SINIFLANDIRILMASIÜstün Yılmaz S., Özdemir Ö., AĞAOĞLU N. B., HATIRNAZ NG Ö., MÜFTÜOĞLU M., ÖZBEK U.8.TÜRK TIBBİ ONKOLOJİ KONGRESİ, Antalya, Turkey, 3 - 07 November 2021
Scientific Refereeing
May 2022 | MEDENİYET MEDİCAL JOURNAL, National Scientific Refreed Journal |
May 2022 | Research Project of the Presidency of Turkey Health Institutes (TÜSEB), Mugla Sitki Kocman University, Turkey |
May 2022 | Research Project of the Presidency of Turkey Health Institutes (TÜSEB), Istanbul Medeniyet University, Turkey |
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Congress and Symposium Activities
2022 | Basic Oncology Congress, Invited Speaker, İstanbul, Turkey |