Ruthie E. Amir

6.9k total citations · 1 hit paper
21 papers, 5.1k citations indexed

About

Ruthie E. Amir is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Ruthie E. Amir has authored 21 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Ruthie E. Amir's work include Genetics and Neurodevelopmental Disorders (8 papers), Epigenetics and DNA Methylation (5 papers) and Autism Spectrum Disorder Research (5 papers). Ruthie E. Amir is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Epigenetics and DNA Methylation (5 papers) and Autism Spectrum Disorder Research (5 papers). Ruthie E. Amir collaborates with scholars based in Israel, United States and Portugal. Ruthie E. Amir's 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 and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Oncogene.

In The Last Decade

Ruthie E. Amir

21 papers receiving 5.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1999 3.7k citations Ruthie E. Amir, Ignatia B. Van den Veyver et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ruthie E. Amir Israel	14	4.1k	3.0k	2.3k	541	260	21	5.1k
Santhosh Girirajan United States	34	3.4k 0.8×	2.5k 0.8×	1.0k 0.5×	134 0.2×	399 1.5×	82	5.0k
Jeffrey L. Neul United States	45	6.1k 1.5×	3.2k 1.0×	4.4k 1.9×	1.6k 3.0×	612 2.4×	129	7.6k
B. A. Oostra Netherlands	35	2.1k 0.5×	1.9k 0.6×	999 0.4×	212 0.4×	422 1.6×	72	3.7k
Jacky Guy United Kingdom	27	3.9k 1.0×	4.3k 1.4×	1.9k 0.8×	188 0.3×	362 1.4×	33	5.7k
Michele Zappella Italy	30	3.5k 0.8×	1.5k 0.5×	2.5k 1.1×	833 1.5×	147 0.6×	96	4.2k
James S. Sutcliffe United States	45	6.7k 1.6×	5.1k 1.7×	3.9k 1.7×	467 0.9×	1.4k 5.3×	92	9.5k
N. Carolyn Schanen United States	27	3.1k 0.8×	2.0k 0.7×	1.9k 0.8×	474 0.9×	271 1.0×	45	3.8k
Sakkubai Naidu United States	33	1.0k 0.3×	3.2k 1.1×	645 0.3×	211 0.4×	351 1.4×	80	4.4k
Maria H. Chahrour United States	17	3.0k 0.7×	2.8k 0.9×	1.8k 0.8×	191 0.4×	632 2.4×	31	4.5k
Hyejung Won United States	21	2.1k 0.5×	2.3k 0.7×	1.4k 0.6×	125 0.2×	518 2.0×	45	4.0k

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

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20 of 20 papers shown

Eynon, Nir, Yoav Meckel, Michael Sagiv, et al.. (2010). Do PPARGC1A and PPARα polymorphisms influence sprint or endurance phenotypes?. Scandinavian Journal of Medicine and Science in Sports. 20(1). e145–50. 67 indexed citations

Amir, Offer, Moran Sagiv, Nir Eynon, et al.. (2010). The response of circulating brain natriuretic peptide to academic stress in college students. Stress. 13(1). 83–90. 13 indexed citations

Amir, Ruthie E., et al.. (2010). Effect of different sprint training regimes on the oxygen delivery-extraction in elite sprinters.. PubMed. 50(2). 121–5. 1 indexed citations

Amir, Offer, Ori Rogowski, Marina Bar‐Shai, et al.. (2009). Serum Oxidative Stress Level Correlates with Clinical Parameters in Chronic Systolic Heart Failure Patients. Clinical Cardiology. 32(4). 199–203. 24 indexed citations

Amir, Offer, et al.. (2009). Acute incremental exercise to maximal performance does not cause alterations in serum oxidant levels of healthy young individuals.. PubMed. 49(1). 105–11. 3 indexed citations

Chen, Yamin, José Alberto Duarte, José Oliveira, et al.. (2008). IL6 (-174) and TNFA (-308) promoter polymorphisms are associated with systemic creatine kinase response to eccentric exercise. European Journal of Applied Physiology. 104(3). 579–586. 74 indexed citations

Amir, Offer, et al.. (2008). Aldosterone Synthase Gene Polymorphism as a Determinant of Atrial Fibrillation in Patients With Heart Failure. The American Journal of Cardiology. 102(3). 326–329. 35 indexed citations

Amir, Offer, et al.. (2008). Relation between AT1R Gene Polymorphism and Long-Term Outcome in Patients with Heart Failure. Cardiology. 112(2). 151–157. 11 indexed citations

Amir, Ruthie E., et al.. (2008). Genotype-phenotype associations between chymase and angiotensin—converting enzyme gene polymorphisms in chronic systolic heart failure patients. Genetics in Medicine. 10(8). 593–598. 13 indexed citations

10.

Chen, Yamin, Offer Amir, Moran Sagiv, et al.. (2007). ACE ID genotype affects blood creatine kinase response to eccentric exercise. Journal of Applied Physiology. 103(6). 2057–2061. 54 indexed citations

11.

Amir, Ruthie E., et al.. (2005). Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome. Journal of Medical Genetics. 42(2). e15–e15. 45 indexed citations

12.

Amir, Ruthie E., V. Reid Sutton, & Ignatia B. Van den Veyver. (2005). Newborn Screening and Prenatal Diagnosis for Rett Syndrome: Implications for Therapy. Journal of Child Neurology. 20(9). 779–783. 8 indexed citations

13.

Amir, Ruthie E., et al.. (2003). Mechanism of processing of the NF-κB2 p100 precursor: identification of the specific polyubiquitin chain-anchoring lysine residue and analysis of the role of NEDD8-modification on the SCFβ-TrCP ubiquitin ligase. Oncogene. 23(14). 2540–2547. 87 indexed citations

14.

Amir, Ruthie E., Kazuhiro Iwaï, & Aaron Ciechanover. (2002). The NEDD8 Pathway Is Essential for SCFβ-TrCP-mediated Ubiquitination and Processing of the NF-κB Precursor p105. Journal of Biological Chemistry. 277(26). 23253–23259. 66 indexed citations

15.

Amir, Ruthie E., Aaron Ciechanover, & Shai Cohen. (2001). [The ubiquitin-proteasome system: the relationship between protein degradation and human diseases].. PubMed. 140(12). 1172–6, 1229. 8 indexed citations

16.

Buyse, I., et al.. (2000). Diagnostic Testing for Rett Syndrome by DHPLC and Direct Sequencing Analysis of the MECP2 Gene: Identification of Several Novel Mutations and Polymorphisms. The American Journal of Human Genetics. 67(6). 1428–1436. 132 indexed citations

17.

Amir, Ruthie E. & Huda Y. Zoghbi. (2000). Rett syndrome: Methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations. American Journal of Medical Genetics. 97(2). 147–152. 148 indexed citations

18.

Amir, Ruthie E., Ignatia B. Van den Veyver, Denise Malicki, et al.. (2000). Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes. Annals of Neurology. 47(5). 670–679. 28 indexed citations

19.

Wan, Mimi, Xianyu Zhang, Elisa J. F. Houwink, et al.. (1999). Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG Hotspots. The American Journal of Human Genetics. 65(6). 1520–1529. 369 indexed citations

20.

Amir, Ruthie E., et al.. (1999). Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nature Genetics. 23(2). 185–188. 3664 indexed citations breakdown →

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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