Ruti Parvari
Impact in
- Reproductive Medicine top 2%
- Sperm and Testicular Function
- Rheumatology top 2%
- Glycogen Storage Diseases and Myoclonus
Papers in
-
- Congenital heart defects research 9
- RNA modifications and cancer 6
- Genetics 23
- Genetics and Neurodevelopmental Disorders 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
- Co-authors
- Shimon Moses (15 shared papers)Eli Hershkovitz (26 shared papers)Val C. Sheffield (11 shared papers)Moshe Phillip (4 shared papers)Jonathan Eli Arbelle (3 shared papers)Yael Segev (3 shared papers)Esther Manor (7 shared papers)Vered Chalifa‐Caspi (5 shared papers)
- Journals
- European Journal of Human Genetics (6 papers)The American Journal of Human Genetics (5 papers)Journal of Inherited Metabolic Disease (4 papers)International Journal of Molecular Sciences (4 papers)Proceedings of the National Academy of Sciences (3 papers)
- Partner nations
- IsraelUnited StatesHungary
In The Last Decade
Ruti Parvari
87 papers receiving 2.6k citations
Peers
Comparison fields: 5 of 117
- Reproductive Medicine 306
- Rheumatology 458
- Genetics 831
- Nephrology 189
- Cellular and Molecular Neuroscience 332
Countries citing papers authored by Ruti Parvari
This map shows the geographic impact of Ruti Parvari'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 Ruti Parvari with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ruti Parvari more than expected).
Fields of papers citing papers by Ruti Parvari
This network shows the impact of papers produced by Ruti Parvari. 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 Ruti Parvari. The network helps show where Ruti Parvari may publish in the future.
Co-authors
The 25 scholars most cited alongside Ruti Parvari, 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 88 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 205 | |
| 2 | 1998 | 164 | |
| 3 | 1993 | 134 | |
| 4 | 1988 | 129 | |
| 5 | 2002 | 109 | |
| 6 | 2000 | 101 | |
| 7 | 2017 | 98 | |
| 8 | 1998 | 91 | |
| 9 | 2010 | 89 | |
| 10 | 2011 | 88 | |
| 11 | 2010 | 84 | |
| 12 | 2002 | 70 | |
| 13 | 1999 | 68 | |
| 14 | 1983 | 61 | |
| 15 | 2015 | 58 | |
| 16 | 1997 | 52 | |
| 17 | 1990 | 49 | |
| 18 | 1998 | 45 | |
| 19 | 1982 | 45 | |
| 20 | 2001 | 44 |
About Ruti Parvari
Ruti Parvari is a scholar working on Molecular Biology, Genetics, Rheumatology, Cardiology and Cardiovascular Medicine and Physiology, having authored 88 papers that have together received 2.7k indexed citations. Recurring topics across this work include Cardiomyopathy and Myosin Studies (11 papers), Glycogen Storage Diseases and Myoclonus (11 papers), Congenital heart defects research (9 papers), Carbohydrate Chemistry and Synthesis (8 papers), Genetics and Neurodevelopmental Disorders (8 papers), Lysosomal Storage Disorders Research (7 papers), RNA modifications and cancer (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). The work is most often cited by research in Reproductive Medicine (306 citations), Rheumatology (458 citations), Genetics (831 citations), Nephrology (189 citations) and Cellular and Molecular Neuroscience (332 citations). Ruti Parvari has collaborated with scholars based in Israel, United States and Hungary. Frequent co-authors include Shimon Moses, Eli Hershkovitz, Val C. Sheffield, Moshe Phillip, Jonathan Eli Arbelle, Yael Segev, Esther Manor, Vered Chalifa‐Caspi, Rivka Carmi and Aviva Levitas. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Journal of Inherited Metabolic Disease, International Journal of Molecular Sciences and Proceedings of the National Academy of Sciences.
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.