Ruthie E. Amir

6.9k citations
21 papers · 5.1k indexed · 1 hit paper · h-index 14
Topics
Genetics and Neurodevelopmental Disorders (8 papers)Epigenetics and DNA Methylation (5 papers)Autism Spectrum Disorder Research (5 papers)

In The Last Decade

Ruthie E. Amir

21 papers receiving 5.0k citations

Hit Papers

Rett syndrome is caused by mutations in X-linked MECP2, e...1999202620082017199910002.0k3.0k

Peers

Ruthie E. Amir
Comparison fields: 5 of 106
  • Genetics 4.1k
  • Molecular Biology 3.0k
  • Cognitive Neuroscience 2.3k
  • Clinical Psychology 541
  • Cellular and Molecular Neuroscience 260
Replace Maria H. Chahrour with:
Maria H. Chahrour United States
Michele Zappella Italy
Sakkubai Naidu United States
N. Carolyn Schanen United States
Yong‐hui Jiang United States
Hyejung Won United States
Jane B. Lane United States
B. A. Oostra Netherlands
Sébastien Jacquemont United States
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Ruthie E. Amir relative to Maria H. Chahrour United States Maria H. Chahrour's profile →
Citations per field
00.5×2.8×
Maria H. Chahrour · 1×
Citations per year

Countries citing papers authored by Ruthie E. Amir

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Ruthie E. Amir

This figure shows the co-authorship network connecting the top 25 collaborators of Ruthie E. Amir. A scholar is included among the top collaborators of Ruthie E. Amir based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ruthie E. Amir. Ruthie E. Amir is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
#WorkIndexed citations
1 67
2 13
3
Effect of different sprint training regimes on the oxygen delivery-extraction in elite sprinters.
1
4 24
5
Acute incremental exercise to maximal performance does not cause alterations in serum oxidant levels of healthy young individuals.
3
6 74
7 35
8 11
9 13
10 54
11 45
12 8
13 87
14 66
15
[The ubiquitin-proteasome system: the relationship between protein degradation and human diseases].
8
16 132
17 148
18 28
19 369
20
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2breakdown →
3664

About Ruthie E. Amir

Ruthie E. Amir is a scholar working on Genetics, Cardiology and Cardiovascular Medicine and Rehabilitation, having authored 21 papers that have together received 5.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (8 papers), Epigenetics and DNA Methylation (5 papers) and Autism Spectrum Disorder Research (5 papers). The work is most often cited by research in Genetics (4.1k citations), Cognitive Neuroscience (2.3k citations) and Developmental Neuroscience (221 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, H.-R. Song, Xianyu Zhang, José Luiz Pinto Pereira and N. Carolyn Schanen. Their work appears in journals such as Journal of Biological Chemistry, Nature Genetics and Oncogene.

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.

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