| Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21 NE Lamb, E Feingold, A Savage, D Avramopoulos, S Freeman, Y Gu, ... Human molecular genetics 6 (9), 1391-1399, 1997 | 278 | 1997 |
| 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 |
| Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans AR Savage, MB Petersen, D Pettay, L Taft, K Allran, SB Freeman, ... Human molecular genetics 7 (8), 1221-1227, 1998 | 120 | 1998 |
| Association between the dopamine D3 receptor gene locus (DRD3) and unipolar affective disorder DG Dikeos, GN Papadimitriou, D Avramopoulos, G Karadima, ... Psychiatric genetics 9 (4), 189-196, 1999 | 84 | 1999 |
| Association between the GABAA receptor α5 subunit gene locus (GABRA5) and bipolar affective disorder GN Papadimitriou, DG Dikeos, G Karadima, D Avramopoulos, ... American journal of medical genetics 81 (1), 73-80, 1998 | 77 | 1998 |
| Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism G Karadima, M Bugge, P Nicolaidis, D Vassilopoulos, D Avramopoulos, ... European Journal of Human Genetics 6 (5), 432-438, 1998 | 70 | 1998 |
| Apolipoprotein E polymorphism in the Greek population E Sklavounou, E Economou‐Petersen, G Karadima, M Panas, ... Clinical genetics 52 (4), 216-218, 1997 | 66 | 1997 |
| 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 |
| Huntington's disease in Greece: the experience of 14 years M Panas, G Karadima, E Vassos, N Kalfakis, A Kladi, K Christodoulou, ... Clinical genetics 80 (6), 586-590, 2011 | 51 | 2011 |
| 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 |
| Late-onset Huntington's disease: diagnostic and prognostic considerations G Koutsis, G Karadima, A Kladi, M Panas Parkinsonism & related disorders 20 (7), 726-730, 2014 | 46 | 2014 |
| Apolipoprotein E and presenilin-1 genotypes in Huntington’s disease M Panas, D Avramopoulos, G Karadima, MB Petersen, D Vassilopoulos Journal of neurology 246, 574-577, 1999 | 43 | 1999 |
| Hereditary neuropathy with liability to pressure palsies emerging during vincristine treatment N Kalfakis, M Panas, G Karadima, P Floroskufi, N Kokolakis, ... Neurology 59 (9), 1470-1471, 2002 | 39 | 2002 |
| Association between presenilin‐1 polymorphism and maternal meiosis II errors in Down syndrome MB Petersen, G Karadima, M Samaritaki, D Avramopoulos, ... American journal of medical genetics 93 (5), 366-372, 2000 | 36 | 2000 |
| Replication study of GWAS risk loci in Greek multiple sclerosis patients GM Hadjigeorgiou, PM Kountra, G Koutsis, V Tsimourtou, V Siokas, ... Neurological Sciences 40, 253-260, 2019 | 35 | 2019 |
| GABA‐A receptor β3 and α5 subunit gene cluster on chromosome 15q11–q13 and bipolar disorder: A genetic association study GN Papadimitriou, DG Dikeos, G Karadima, D Avramopoulos, ... American journal of medical genetics 105 (4), 317-320, 2001 | 32 | 2001 |
| The challenge of juvenile Huntington disease: to test or not to test G Koutsis, G Karadima, A Kladi, M Panas Neurology 80 (11), 990-996, 2013 | 30 | 2013 |
| Association between GABA-A receptor alpha 5 subunit gene locus and schizophrenia of a later age of onset G Papadimitriou, D Dikeos, E Daskalopoulou, G Karadima, ... Neuropsychobiology 43 (3), 141-144, 2001 | 29 | 2001 |
| Molecular cytogenetic characterization and origin of two de novo duplication 9p cases A Tsezou, S Kitsiou, A Galla, MB Petersen, G Karadima, M Syrrou, ... American journal of medical genetics 91 (2), 102-106, 2000 | 29 | 2000 |
