| The distinct genetic pattern of ALS in Turkey and novel mutations A Özoğuz, Ö Uyan, G Birdal, C Iskender, E Kartal, S Lahut, Ö Ömür, ... Neurobiology of aging 36 (4), 1764. e9-1764. e18, 2015 | 109 | 2015 |
| Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia ZS Agim, M Esendal, L Briollais, O Uyan, M Meschian, LAM Martinez, ... PloS one 8 (1), e53042, 2013 | 57 | 2013 |
| ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population S Lahut, Ö Ömür, Ö Uyan, ZS Ağım, A Özoğuz, Y Parman, F Deymeer, ... Public Library of Science 7 (8), e42956, 2012 | 56 | 2012 |
| A novel dysferlin mutant pseudoexon bypassed with antisense oligonucleotides JA Dominov, Ö Uyan, PC Sapp, D McKenna‐Yasek, BRR Nallamilli, ... Annals of clinical and translational neurology 1 (9), 703-720, 2014 | 34 | 2014 |
| Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor Ö Uyan, Ö Ömür, ZS Ağım, A Özoğuz, H Li, Y Parman, F Deymeer, ... PLoS One 8 (8), e72381, 2013 | 34 | 2013 |
| Inner nuclear protein Matrin-3 coordinates cell differentiation by stabilizing chromatin architecture HJ Cha, Ö Uyan, Y Kai, T Liu, Q Zhu, Z Tothova, GA Botten, J Xu, ... Nature communications 12 (1), 6241, 2021 | 32 | 2021 |
| Correction of pseudoexon splicing caused by a novel intronic dysferlin mutation JA Dominov, Ö Uyan, D McKenna‐Yasek, BRR Nallamilli, V Kergourlay, ... Annals of Clinical and Translational Neurology 6 (4), 642-654, 2019 | 24 | 2019 |
| Mutation in protein disulfide isomerase A3 causes neurodevelopmental defects by disturbing endoplasmic reticulum proteostasis D Bilches Medinas, S Malik, E Yıldız‐Bölükbaşı, J Borgonovo, ... The EMBO Journal 41 (2), e105531, 2022 | 21 | 2022 |
| Imaging net retrograde axonal transport in vivo: a physiological biomarker PTJ Lee, Z Kennedy, Y Wang, Y Lu, C Cefaliello, Ö Uyan, CQ Song, ... Annals of neurology 91 (5), 716-729, 2022 | 6 | 2022 |
| Inner Nuclear Protein Matrin-3 Coordinates Hematopoietic Cell Transcription and Differentiation By Stabilizing Chromatin Architecture HJ Cha, Ö Uyan, J Dekker, SH Orkin Blood 138, 285, 2021 | | 2021 |
| Reply to comment on: A novel dysferlin mutant pseudoexon bypassed with antisense oligonucleotides JA Dominov, Ö Uyan, PC Sapp, D McKenna-Yasek, BRR Nallamilli, ... Annals of Clinical and Translational Neurology 2 (7), 785, 2015 | | 2015 |
| Madras Pattern Motor Neuron Disease Caused By A Novel Mutation In The UBQLN2 Gene (P2. 068) H Durmus, A Ozoguz, O Uyan, F Deymeer, P Serdaroglu, N Basak, ... Neurology 82 (10_supplement), P2. 068, 2014 | | 2014 |
| The genetics of sporadic als: The first Turkish gwas and novel snp and cnv association Ö Uyan Fen Bilimleri Enstitüsü, 2012 | | 2012 |
| Gene-‐gene Interactions and Haplotype Analyses of fALS Genes in the Development of sALS Ö Uyan, M Meschian, A Martinez, Y Ding, H Özçelik, AN Başak | | |
Zeynep Sena Agim, PhDPostdoctoral fellow @ UMass Medical School在 umassmed.edu 的电子邮件经过验证
Zeynep Sena Agim, PhDPostdoctoral fellow @ UMass Medical School在 umassmed.edu 的电子邮件经过验证