| Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ... Nature genetics 46 (9), 989-993, 2014 | 1993 | 2014 |
| Cognitive impairment in different MS subtypes and clinically isolated syndromes C Potagas, E Giogkaraki, G Koutsis, D Mandellos, E Tsirempolou, ... Journal of the neurological sciences 267 (1-2), 100-106, 2008 | 328 | 2008 |
| DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases C Bettencourt, D Hensman‐Moss, M Flower, S Wiethoff, A Brice, C Goizet, ... Annals of neurology 79 (6), 983-990, 2016 | 231 | 2016 |
| The neuropsychiatry of multiple sclerosis: focus on disorders of mood, affect and behaviour T Paparrigopoulos, P Ferentinos, A Kouzoupis, G Koutsis, ... International review of psychiatry 22 (1), 14-21, 2010 | 215 | 2010 |
| AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders V Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ... Nature communications 10 (1), 3094, 2019 | 187 | 2019 |
| A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies M Coutelier, G Coarelli, ML Monin, J Konop, CS Davoine, C Tesson, ... Brain 140 (6), 1579-1594, 2017 | 118 | 2017 |
| NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases MA Nalls, J Bras, DG Hernandez, MF Keller, E Majounie, AE Renton, ... Neurobiology of aging 36 (3), 1605. e7-1605. e12, 2015 | 111 | 2015 |
| Efficacy of exome-targeted capture sequencing to detect mutations in known cerebellar ataxia genes M Coutelier, MB Hammer, G Stevanin, ML Monin, CS Davoine, F Mochel, ... JAMA neurology 75 (5), 591-599, 2018 | 106 | 2018 |
| The emerging role of microRNA in stroke G Koutsis, G Siasos, K Spengos Current Topics in Medicinal Chemistry 13 (13), 1573-1588, 2013 | 100 | 2013 |
| Kennedy’s disease (spinal and bulbar muscular atrophy): a clinically oriented review of a rare disease M Breza, G Koutsis Journal of neurology 266 (3), 565-573, 2019 | 78 | 2019 |
| Clinical and subclinical autonomic dysfunction in chronic inflammatory demyelinating polyradiculoneuropathy E Stamboulis, N Katsaros, G Koutsis, H Iakovidou, A Giannakopoulou, ... Muscle & Nerve: Official Journal of the American Association of …, 2006 | 71 | 2006 |
| High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients KY Mok, G Koutsis, LV Schottlaender, J Polke, M Panas, H Houlden Neurobiology of aging 33 (8), 1851. e1-1851. e5, 2012 | 68 | 2012 |
| PDXK mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation V Chelban, MP Wilson, J Warman Chardon, J Vandrovcova, MN Zanetti, ... Annals of Neurology 86 (2), 225-240, 2019 | 67 | 2019 |
| Progression characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS): a 4-year cohort study K Reetz, I Dogan, RD Hilgers, P Giunti, MH Parkinson, C Mariotti, ... The Lancet Neurology 20 (5), 362-372, 2021 | 62 | 2021 |
| Bi-allelic JAM2 variants lead to early-onset recessive primary familial brain calcification LV Schottlaender, R Abeti, Z Jaunmuktane, C Macmillan, V Chelban, ... The American Journal of Human Genetics 106 (3), 412-421, 2020 | 54 | 2020 |
| Hereditary spastic paraplegia in Greece: characterisation of a previously unexplored population using next-generation sequencing DS Lynch, G Koutsis, A Tucci, M Panas, M Baklou, M Breza, G Karadima, ... European journal of human genetics 24 (6), 857-863, 2016 | 54 | 2016 |
| APOE ε4 is associated with impaired verbal learning in patients with MS G Koutsis, M Panas, E Giogkaraki, C Potagas, G Karadima, C Sfagos, ... Neurology 68 (8), 546-549, 2007 | 53 | 2007 |
| Relationship of CSF neurotransmitter metabolite levels to disease severity and disability in multiple sclerosis M Markianos, G Koutsis, ME Evangelopoulos, D Mandellos, G Karahalios, ... Journal of neurochemistry 108 (1), 158-164, 2009 | 52 | 2009 |
| Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination S Efthymiou, V Salpietro, N Malintan, M Poncelet, Y Kriouile, S Fortuna, ... Brain 142 (10), 2948-2964, 2019 | 49 | 2019 |
| C9ORF72 hexanucleotide repeat expansions are a frequent cause of Huntington disease phenocopies in the Greek population G Koutsis, G Karadima, C Kartanou, A Kladi, M Panas Neurobiology of aging 36 (1), 547. e13-547. e16, 2015 | 47 | 2015 |
Georgia KaradimaAssistant Professor of Biology &Neurogenetics, Medical School, National and Kapodistrian University of AthensVerifierad e-postadress på med.uoa.gr
