Ruthie E. Amir
Impact in
- Genetics top 0.2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 1%
- Autism Spectrum Disorder Research
Papers in
- Genetics 10
- Genetics and Neurodevelopmental Disorders 8
- Genetics and Physical Performance 2
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- Epigenetics and DNA Methylation 5
- Ubiquitin and proteasome pathways 3
- Co-authors
- Huda Y. Zoghbi (6 shared papers)Uta Francke (2 shared papers)Mimi Wan (2 shared papers)Ignatia B. Van den Veyver (4 shared papers)Aaron Ciechanover (3 shared papers)Michael Sagiv (8 shared papers)Elisa J. F. Houwink (1 shared paper)Ivan F. M. Lo (1 shared paper)
- Journals
- The American Journal of Human Genetics (2 papers)Annals of Neurology (2 papers)Journal of Child Neurology (1 paper)Stress (1 paper)Cardiology (1 paper)
- Partner nations
- IsraelUnited StatesPortugal
In The Last Decade
Ruthie E. Amir
21 papers receiving 5.1k citations
Ruthie E. Amir's Hit Papers
Peers
Comparison fields: 5 of 103
- Genetics 4.0k
- Cognitive Neuroscience 1.9k
- Developmental Neuroscience 213
- Molecular Biology 2.8k
- Clinical Psychology 359
Countries citing papers authored by Ruthie E. Amir
This map shows the geographic impact of Ruthie E. Amir'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 Ruthie E. Amir with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ruthie E. Amir more than expected).
Fields of papers citing papers by Ruthie E. Amir
This network shows the impact of papers produced by Ruthie E. Amir. 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 Ruthie E. Amir. The network helps show where Ruthie E. Amir may publish in the future.
Co-authors
The 25 scholars most cited alongside Ruthie E. Amir, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 Hit paper breakdown → | 1999 | 3697 |
| 2 | 1999 | 370 | |
| 3 | 2000 | 266 | |
| 4 | 2000 | 148 | |
| 5 | 2000 | 132 | |
| 6 | 2003 | 87 | |
| 7 | 2008 | 75 | |
| 8 | 2010 | 67 | |
| 9 | 2002 | 66 | |
| 10 | 2007 | 54 | |
| 11 | 2005 | 45 | |
| 12 | 2008 | 35 | |
| 13 | 2000 | 28 | |
| 14 | 2009 | 24 | |
| 15 | 2010 | 13 | |
| 16 | 2008 | 13 | |
| 17 | 2008 | 11 | |
| 18 | 2005 | 8 | |
| 19 | [The ubiquitin-proteasome system: the relationship between protein degradation and human diseases]. | 2001 | 8 |
| 20 | Acute incremental exercise to maximal performance does not cause alterations in serum oxidant levels of healthy young individuals. | 2009 | 3 |
About Ruthie E. Amir
Ruthie E. Amir is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Cardiology and Cardiovascular Medicine and Rehabilitation, having authored 21 papers that have together received 5.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Autism Spectrum Disorder Research (5 papers), Epigenetics and DNA Methylation (5 papers), Ubiquitin and proteasome pathways (3 papers), NF-κB Signaling Pathways (2 papers), Cardiovascular Effects of Exercise (2 papers), Muscle metabolism and nutrition (2 papers) and Genetics and Physical Performance (2 papers). The work is most often cited by research in Genetics (4.0k citations), Cognitive Neuroscience (1.9k citations), Developmental Neuroscience (213 citations), Molecular Biology (2.8k citations) and Clinical Psychology (359 citations). Ruthie E. Amir has collaborated with scholars based in Israel, United States and Portugal. Frequent co-authors include Huda Y. Zoghbi, Uta Francke, Mimi Wan, Ignatia B. Van den Veyver, Aaron Ciechanover, Michael Sagiv, Elisa J. F. Houwink, Ivan F. M. Lo, Sarojini Budden and Xianyu Zhang. Their work appears in journals such as The American Journal of Human Genetics, Annals of Neurology, Journal of Child Neurology, Stress and Cardiology.
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.