Tayfun Ozcelik
Affiliations: | 2007-2011 | Molecular Biology and Genetics | Bilkent University, Long Beach, Ankara, Turkey |
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"Tayfun Ozcelik"Children
Sign in to add trainee| Gokce Toruner | grad student | Rutgers New Jersey Medical School | |
| Gokce Toruner | grad student | Rutgers New Jersey Medical School | |
| Suleyman Gulsuner | grad student | 2007-2011 | Bilkent University |
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Publications
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| Akar OS, Gunes S, Abur U, et al. (2020) Multiscale analysis of SRY-positive 46,XX testicular disorder of sex development: Presentation of nine cases. Andrologia. e13739 |
| Demirayak P, Onat OE, Gevrekci AÖ, et al. (2018) Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation. Diagnostic and Interventional Radiology (Ankara, Turkey). 24: 392-401 |
| Urgen BM, Topac Y, Ustun FS, et al. (2018) Homozygous LAMC3 mutation links to structural and functional changes in visual attention networks. Neuroimage |
| Demirayak P, Sen M, Ustun S, et al. (2018) Morphometric and Microstructural Alterations Differ with Age of Onset in Patients with Essential Tremor Journal of Neurological Disorders. 6 |
| Özçelik T, Onat OE. (2016) Genomic landscape of the Greater Middle East. Nature Genetics. 48: 978-9 |
| Kanaan SB, Onat OE, Balandraud N, et al. (2016) Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis. Plos One. 11: e0158550 |
| Doldur-Balli F, Ozel MN, Gulsuner S, et al. (2015) Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ). Bmc Neuroscience. 16: 96 |
| Unal Gulsuner H, Gulsuner S, Mercan FN, et al. (2015) Reply to Tzoulis et al.: Genetic and clinical heterogeneity of essential tremor. Proceedings of the National Academy of Sciences of the United States of America. 112: E2269 |
| Doldur-Balli F, Ozel MN, Gulsuner S, et al. (2015) Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ) Bmc Neuroscience. 16 |
| Unal Gulsuner H, Gulsuner S, Mercan FN, et al. (2014) Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease. Proceedings of the National Academy of Sciences of the United States of America. 111: 18285-90 |