| TREM2 Variants in Alzheimer's Disease R Guerreiro, A Wojtas, J Bras, M Carrasquillo, E Rogaeva, E Majounie, ... New England Journal of Medicine 368 (2), 117-27, 2013 | 3216 | 2013 |
| TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis G Kleinberger, Y Yamanishi, M Suárez-Calvet, E Czirr, E Lohmann, ... Science translational medicine 6 (243), 243ra86-243ra86, 2014 | 787 | 2014 |
| EFNS‐ENS Guidelines on the diagnosis and management of disorders associated with dementia S Sorbi, J Hort, T Erkinjuntti, T Fladby, G Gainotti, H Gurvit, B Nacmias, ... European Journal of Neurology 19 (9), 1159-1179, 2012 | 409 | 2012 |
| Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia–like syndrome without bone involvement RJ Guerreiro, E Lohmann, JM Brás, JR Gibbs, JD Rohrer, N Gurunlian, ... JAMA neurology 70 (1), 78-84, 2013 | 406 | 2013 |
| Comparative analysis of event-related potentials during Go/NoGo and CPT: decomposition of electrophysiological markers of response inhibition and sustained attention E Kirmizi-Alsan, Z Bayraktaroglu, H Gurvit, YH Keskin, M Emre, ... Brain research 1104 (1), 114-128, 2006 | 310 | 2006 |
| The interleukin 1 alpha, interleukin 1 beta, interleukin 6 and alpha-2-macroglobulin serum levels in patients with early or late onset Alzheimer's disease, mild cognitive … E Dursun, D Gezen-Ak, H Hanağası, B Bilgiç, E Lohmann, S Ertan, ... Journal of neuroimmunology 283, 50-57, 2015 | 278 | 2015 |
| The prevalence of dementia in an urban Turkish population H Gurvit, M Emre, S Tinaz, B Bilgic, H Hanagasi, H Sahin, E Gurol, ... American Journal of Alzheimer's Disease & Other Dementias® 23 (1), 67-76, 2008 | 249 | 2008 |
| Neuropsychological patterns and language deficits in 20 consecutive cases of autopsy-confirmed Alzheimer's disease BH Price, H Gurvit, S Weintraub, C Geula, E Leimkuhler, M Mesulam Archives of neurology 50 (9), 931-937, 1993 | 245 | 1993 |
| Association between vitamin D receptor gene polymorphism and Alzheimer's disease D Gezen-Ak, E Dursun, T Ertan, H Hanagasi, H Gürvit, M Emre, E Eker, ... The Tohoku journal of experimental medicine 212 (3), 275-282, 2007 | 236 | 2007 |
| BDNF, TNFα, HSP90, CFH, and IL-10 serum levels in patients with early or late onset Alzheimer's disease or mild cognitive impairment D Gezen-Ak, E Dursun, H Hanağası, B Bilgiç, E Lohman, ÖS Araz, ... Journal of Alzheimer's Disease 37 (1), 185-195, 2013 | 217 | 2013 |
| Cognitive impairment in amyotrophic lateral sclerosis: evidence from neuropsychological investigation and event-related potentials HA Hanagasi, IH Gurvit, N Ermutlu, G Kaptanoglu, S Karamursel, ... Cognitive Brain Research 14 (2), 234-244, 2002 | 202 | 2002 |
| Seven-year follow-up of neurologic involvement in Behçet syndrome G Akman-Demir, B Baykan-Kurt, P Serdaroǧlu, H Gürvit, S Yurdakul, ... Archives of neurology 53 (7), 691-694, 1996 | 151 | 1996 |
| Neuropsychological function in obsessive-compulsive disorder R Tükel, H Gürvit, BA Ertekin, S Oflaz, E Ertekin, B Baran, ŞA Kalem, ... Comprehensive psychiatry 53 (2), 167-175, 2012 | 148 | 2012 |
| Neuropsychological follow-up of 12 patients with neuro-Behçet disease Ö Öktem-Tanör, B Baykan-Kurt, IH Gürvit, G Akman-Demir, P Serdaroğlu Journal of neurology 246, 113-119, 1999 | 148 | 1999 |
| The effects of rasagiline on cognitive deficits in Parkinson's disease patients without dementia: a randomized, double‐blind, placebo‐controlled, multicenter study HA Hanagasi, H Gurvit, P Unsalan, H Horozoglu, N Tuncer, A Feyzioglu, ... Movement Disorders 26 (10), 1851-1858, 2011 | 146 | 2011 |
| Pain is common in Parkinson's disease HA Hanagasi, S Akat, H Gurvit, J Yazici, M Emre Clinical neurology and neurosurgery 113 (1), 11-13, 2011 | 132 | 2011 |
| A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family R Guerreiro, B Bilgic, G Guven, J Brás, J Rohrer, E Lohmann, H Hanagasi, ... Neurobiology of aging 34 (12), 2890. e1-2890. e5, 2013 | 131 | 2013 |
| Vitamin D receptor gene haplotype is associated with late-onset Alzheimer's disease D Gezen-Ak, E Dursun, B Bilgic, H Hanagasi, T Ertan, H Gürvit, M Emre, ... The Tohoku journal of experimental medicine 228 (3), 189-196, 2012 | 124 | 2012 |
| Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease RJ Guerreiro, E Lohmann, E Kinsella, JM Brás, N Luu, N Gurunlian, ... Neurobiology of aging 33 (5), 1008. e17-1008. e23, 2012 | 119 | 2012 |
| 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 |
