| Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study E Nelis, C Van Broeckhoven, P De Jonghe, A Löfgren, A Vandenberghe, ... European Journal of Human Genetics 4 (1), 25-33, 1996 | 530 | 1996 |
| Systematic Review and Meta-Analysis of the Association between β2-Adrenoceptor Polymorphisms and Asthma: A HuGE Review A Thakkinstian, M McEvoy, C Minelli, P Gibson, B Hancox, D Duffy, ... American journal of epidemiology 162 (3), 201-211, 2005 | 435 | 2005 |
| The involvement of ErbB4 with schizophrenia: association and expression studies G Silberberg, A Darvasi, R Pinkas‐Kramarski, R Navon American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141 …, 2006 | 294 | 2006 |
| Is the G72/G30 locus associated with schizophrenia? Single nucleotide polymorphisms, haplotypes, and gene expression analysis M Korostishevsky, M Kaganovich, A Cholostoy, M Ashkenazi, Y Ratner, ... Biological psychiatry 56 (3), 169-176, 2004 | 213 | 2004 |
| The mutations in Ashkenazi Jews with adult GM2 gangliosidosis, the adult form of Tay-Sachs disease R Navon, RL Proia Science 243 (4897), 1471-1474, 1989 | 183 | 1989 |
| Apparent deficiency of hexosaminidase A in healthy members of a family with Tay-Sachs disease. R Navon, B Padeh, A Adam American Journal of Human Genetics 25 (3), 287, 1973 | 136 | 1973 |
| Clinical and genetic variations in the syndrome of adult GM2 gangliodosis resulting from hexosaminidase a deficiency Z Argov, R Navon Annals of neurology 16 (1), 14-20, 1984 | 134 | 1984 |
| Hexosaminidase A deficiency in adults R Navon, Z Argov, A Frisch, JM Opitz, JF Reynolds American journal of medical genetics 24 (1), 179-196, 1986 | 132 | 1986 |
| Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish population M Horowitz, M Pasmanik‐Chor, Z Borochowitz, T Falik‐Zaccai, ... Human mutation 12 (4), 240-244, 1998 | 123 | 1998 |
| Deregulation of the A-to-I RNA editing mechanism in psychiatric disorders G Silberberg, D Lundin, R Navon, M Öhman Human molecular genetics 21 (2), 311-321, 2012 | 106 | 2012 |
| hKCa3/KCNN3 potassium channel gene: association of longer CAG repeats with schizophrenia in Israeli Ashkenazi Jews, expression in human tissues and localization to chromosome 1q21 V Dror, E Shamir, S Ghanshani, R Kimhi, M Swartz, Y Barak, R Weizman, ... Molecular psychiatry 4 (3), 254-260, 1999 | 99 | 1999 |
| Ganglioside GM2 N-acetyl-beta-D-galactosaminidase activity in cultured fibroblasts of late-infantile and adult GM2 gangliosidosis patients and of healthy probands with low … E Conzelmann, HJ Kytzia, R Navon, K Sandhoff American journal of human genetics 35 (5), 900, 1983 | 99 | 1983 |
| A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening BL Triggs-Raine, EH Mules, MM Kaback, JST Lim-Steele, CE Dowling, ... American journal of human genetics 51 (4), 793, 1992 | 94 | 1992 |
| MicroRNA-382 expression is elevated in the olfactory neuroepithelium of schizophrenia patients E Mor, SI Kano, C Colantuoni, A Sawa, R Navon, N Shomron Neurobiology of disease 55, 1-10, 2013 | 76 | 2013 |
| A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24‐q32 SC Blumen, S Bevan, S Abu‐Mouch, D Negus, M Kahana, R Inzelberg, ... Annals of Neurology: Official Journal of the American Neurological …, 2003 | 74 | 2003 |
| Stargazin involvement with bipolar disorder and response to lithium treatment G Silberberg, A Levit, D Collier, DS Clair, J Munro, RW Kerwin, L Tondo, ... Pharmacogenetics and genomics 18 (5), 403-412, 2008 | 72 | 2008 |
| Transmission disequilibrium and haplotype analyses of the G72/G30 locus: suggestive linkage to schizophrenia in Palestinian Arabs living in the North of Israel M Korostishevsky, I Kremer, M Kaganovich, A Cholostoy, I Murad, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141 …, 2006 | 71 | 2006 |
| Adult GM2 gangliosidosis in association with Tay‐Sachs disease: A new phenotype R Navon, Z Argov, N Brand, U Sandbank Neurology 31 (11), 1397-1397, 1981 | 70 | 1981 |
| Ashkenazi-Jewish and non-Jewish adult GM2 gangliosidosis patients share a common genetic defect. R Navon, EH Kolodny, H Mitsumoto, GH Thomas, RL Proia American journal of human genetics 46 (4), 817, 1990 | 66 | 1990 |
| Tampon wetness detection system N Navot, R Botton US Patent 5,904,671, 1999 | 58 | 1999 |
