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R. Navon

European Journal of Human Genetics, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Biological Psychiatry, Science, American journal of medical genetics, Human Mutation, Annals of Neurology, American Journal of Human Genetics, Human Molecular Genetics Show more
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Role
Title
Level Year L/R
🐜 Estimation of the Mutation Frequencies in Charcot-Marie-Tooth Disease Type 1 and Hereditary Neuropathy with Liability to Pressure Palsies: A European Collaborative Study
54 auth. E. Nelis, C. Broeckhoven, P. Jonghe, A. Löfgren, A. Vandenberghe, P. Latour, É. Guern, A. Brice, M. Mostacciuolo, F. Schiavon, F. Palau, S. Bort, M. Upadhyaya, M. Rocchi, N. Archidiacono, ... P. Mandich, E. Bellone, K. Silander, M. Savontaus, R. Navon, H. Goldberg-Stern, X. Estivill, V. Volpini, W. Friedl, K. Zerres, J. Tyson, S. Malcolm, B. Holmberg, G. Holmgren, E. Mariman, A. Gabreëls-Festen, C. Yapijakis, D. Vassilopoulos, C. Clark, N. Haites, P. Hilbert, L. Maldergem, B. Rautenstrauss, H. Grehl, R. Mountford, K. Mann, T. Bettecken, J. Burgunder, C. Hanemann, H. Müller, J. Hertz, D. Schorderet, T. Küntzer, C. Wolf, E. Kunert, F. Muntoni, P. Emmerick-Bock, U. Orth, A. Gal 		8 1996
8
🐜
🐜 HUMAN GENOME EPIDEMIOLOGY (HuGE) REVIEW Systematic Review and Meta-Analysis of the Association between b 2 -Adrenoceptor Polymorphisms and Asthma: A HuGE Review
15 auth. A. Thakkinstian, M. McEvoy, C. Minelli, P. Gibson, B. Hancox, D. Duffy, J. Thompson, I. Hall, J. Kaufman, T. Leung, ... P. Helms, H. Hakonarson, Eva Halpi, R. Navon, J. Attia 		8 2005
8
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🐢 The involvement of ErbB4 with schizophrenia: Association and expression studies
G. Silberberg, A. Darvasi, R. Pinkas-Kramarski, R. Navon 		8 2006
8
🐢
🐢 Is the G72/G30 locus associated with schizophrenia? single nucleotide polymorphisms, haplotypes, and gene expression analysis
12 auth. M. Korostishevsky, M. Kaganovich, Alina Cholostoy, M. Ashkenazi, Y. Ratner, Dvir Dahary, ... Jeanne Bernstein, Ullrike Bening-Abu-Shach, E. Ben‐Asher, D. Lancet, M. Ritsner, R. Navon 		7 2004
7
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🦁 The mutations in Ashkenazi Jews with adult GM2 gangliosidosis, the adult form of Tay-Sachs disease.
R. Navon, R. Proia 		7 1989
7
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🦁 Hexosaminidase A deficiency in adults.
R. Navon, Z. Argov, A. Frisch, J. M. Opitz, J. Reynolds 		6 1986
6
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🐜 Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish population
22 auth. M. Horowitz, M. Pasmanik-Chor, Z. Borochowitz, T. Falik-Zaccai, Keren Heldmann, R. Carmi, R. Parvari, Hannah Beit‐Or, B. Goldman, L. Peleg, ... E. Levy-Lahad, P. Renbaum, Searl Legum, R. Shomrat, H. Yeger, Dalit Benbenisti, R. Navon, V. Dror, M. Shohat, N. Magal, N. Navot, N. Eyal 		6 1998
6
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🐢 Clinical and genetic variations in the syndrome of adult GM2 gangliodosis resulting from hexosaminidase a deficiency
Z. Argov, R. Navon 		6 1984
6
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🦁 Apparent deficiency of hexosaminidase A in healthy members of a family with Tay-Sachs disease.
R. Navon, B. Padeh, A. Adam 		6 1973
6
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🐬 Deregulation of the A-to-I RNA editing mechanism in psychiatric disorders.
G. Silberberg, D. Lundin, R. Navon, Marie Öhman 		6 2012
6
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