Ruth Navon
Impact in
- Physiology top 2%
- Lysosomal Storage Disorders Research
- Biological Psychiatry top 5%
Papers in
- Physiology 45
- Lysosomal Storage Disorders Research 40
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- Glycosylation and Glycoproteins Research 8
- Studies on Chitinases and Chitosanases 6
- Co-authors
- Richard L. Proia (6 shared papers)Gilad Silberberg (6 shared papers)B Padeh (7 shared papers)Zohar Argov (3 shared papers)Ariel Darvasi (3 shared papers)Ronit Pinkas‐Kramarski (1 shared paper)A. Adam (4 shared papers)Amos Frisch (4 shared papers)
- Journals
- Human Mutation (6 papers)Annals of Neurology (4 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (4 papers)Prenatal Diagnosis (2 papers)Human Genetics (2 papers)
- Partner nations
- IsraelUnited StatesGermany
In The Last Decade
Ruth Navon
79 papers receiving 2.4k citations
Peers
Comparison fields: 5 of 101
- Physiology 1.0k
- Biological Psychiatry 72
- Cellular and Molecular Neuroscience 358
- Biochemistry 131
- Cell Biology 251
Countries citing papers authored by Ruth Navon
This map shows the geographic impact of Ruth Navon's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ruth Navon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ruth Navon more than expected).
Fields of papers citing papers by Ruth Navon
This network shows the impact of papers produced by Ruth Navon. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ruth Navon. The network helps show where Ruth Navon may publish in the future.
Co-authors
The 25 scholars most cited alongside Ruth Navon, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 80 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 318 | |
| 2 | 2006 | 198 | |
| 3 | 2004 | 150 | |
| 4 | 1989 | 125 | |
| 5 | Apparent deficiency of hexosaminidase A in healthy members of a family with Tay-Sachs disease. | 1973 | 81 |
| 6 | 1986 | 79 | |
| 7 | 1984 | 76 | |
| 8 | 2011 | 74 | |
| 9 | 1999 | 65 | |
| 10 | 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 hexosaminidase level. | 1983 | 65 |
| 11 | A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening. | 1992 | 64 |
| 12 | 1978 | 60 | |
| 13 | 2005 | 45 | |
| 14 | 2013 | 45 | |
| 15 | Ashkenazi-Jewish and non-Jewish adult GM2 gangliosidosis patients share a common genetic defect. | 1990 | 44 |
| 16 | 1974 | 40 | |
| 17 | 1981 | 38 | |
| 18 | 1983 | 37 | |
| 19 | 1996 | 35 | |
| 20 | 2008 | 32 |
About Ruth Navon
Ruth Navon is a scholar working on Physiology, Molecular Biology, Epidemiology, Genetics and Organic Chemistry, having authored 80 papers that have together received 2.5k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (40 papers), Trypanosoma species research and implications (21 papers), Glycosylation and Glycoproteins Research (8 papers), Neurogenetic and Muscular Disorders Research (8 papers), Carbohydrate Chemistry and Synthesis (7 papers), Hereditary Neurological Disorders (6 papers), Studies on Chitinases and Chitosanases (6 papers) and Mosquito-borne diseases and control (5 papers). The work is most often cited by research in Physiology (1.0k citations), Biological Psychiatry (72 citations), Cellular and Molecular Neuroscience (358 citations), Biochemistry (131 citations) and Cell Biology (251 citations). Ruth Navon has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Richard L. Proia, Gilad Silberberg, B Padeh, Zohar Argov, Ariel Darvasi, Ronit Pinkas‐Kramarski, A. Adam, Amos Frisch, Ammarin Thakkinstian and John Attia. Their work appears in journals such as Human Mutation, Annals of Neurology, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Prenatal Diagnosis and Human Genetics.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.