Eyal Reinstein

4.2k total citations · 2 hit papers
41 papers, 1.5k citations indexed

About

Eyal Reinstein is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Eyal Reinstein has authored 41 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 16 papers in Molecular Biology and 10 papers in Cell Biology. Recurrent topics in Eyal Reinstein's work include Connective tissue disorders research (10 papers), Ubiquitin and proteasome pathways (8 papers) and Cardiomyopathy and Myosin Studies (4 papers). Eyal Reinstein is often cited by papers focused on Connective tissue disorders research (10 papers), Ubiquitin and proteasome pathways (8 papers) and Cardiomyopathy and Myosin Studies (4 papers). Eyal Reinstein collaborates with scholars based in Israel, United States and Netherlands. Eyal Reinstein's co-authors include Aaron Ciechanover, Alan L. Schwartz, Christopher J. Cummings, Harry T. Orr, Yong‐hui Jiang, Yaling Sun, Huda Y. Zoghbi, Barbara Antalffy, Arthur L. Beaudet and David L. Rimoin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Neuron.

In The Last Decade

Eyal Reinstein

41 papers receiving 1.5k 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.

Mutation of the E6-AP Ubiquitin Ligase Reduces Nuclear Inclusion Frequency While Accelerating Polyglutamine-Induced Pathology in SCA1 Mice

1999 409 citations Eyal Reinstein, Aaron Ciechanover et al. profile →
Frequent aneuploidy in primary human T cells after CRISPR–Cas9 cleavage

2022 122 citations Alessio D. Nahmad, Eli Reuveni et al. Nature Biotechnology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eyal Reinstein Israel	16	1.0k	359	342	324	235	41	1.5k
Pieter Faber United States	15	1.0k 1.0×	190 0.5×	435 1.3×	227 0.7×	78 0.3×	22	1.6k
Ilse Wieland Germany	23	1.3k 1.3×	391 1.1×	192 0.6×	237 0.7×	79 0.3×	81	1.9k
Nessa Carey United Kingdom	16	1.2k 1.2×	188 0.5×	298 0.9×	194 0.6×	94 0.4×	36	1.5k
Mario Sirito United States	18	1.0k 1.0×	195 0.5×	347 1.0×	123 0.4×	68 0.3×	25	2.0k
Andrew Dearlove United Kingdom	13	846 0.8×	223 0.6×	357 1.0×	54 0.2×	210 0.9×	17	1.9k
Y. Sawamura Japan	18	528 0.5×	139 0.4×	125 0.4×	290 0.9×	191 0.8×	65	1.6k
Antoaneta Mincheva Germany	21	992 1.0×	380 1.1×	160 0.5×	192 0.6×	170 0.7×	41	1.5k
Luciana Chessa Italy	28	2.1k 2.1×	371 1.0×	319 0.9×	693 2.1×	121 0.5×	75	2.7k
Xiaobing Qian United States	19	1.0k 1.0×	456 1.3×	136 0.4×	202 0.6×	99 0.4×	47	1.5k
Irina Golovleva Sweden	25	927 0.9×	284 0.8×	76 0.2×	225 0.7×	151 0.6×	78	1.9k

Countries citing papers authored by Eyal Reinstein

Since Specialization

Citations

This map shows the geographic impact of Eyal Reinstein'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 Eyal Reinstein with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eyal Reinstein more than expected).

Fields of papers citing papers by Eyal Reinstein

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eyal Reinstein. 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 Eyal Reinstein. The network helps show where Eyal Reinstein may publish in the future.

Co-authorship network of co-authors of Eyal Reinstein

This figure shows the co-authorship network connecting the top 25 collaborators of Eyal Reinstein. A scholar is included among the top collaborators of Eyal Reinstein 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 Eyal Reinstein. Eyal Reinstein 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

Nahmad, Alessio D., Eli Reuveni, Tamar Tenne, et al.. (2022). Frequent aneuploidy in primary human T cells after CRISPR–Cas9 cleavage. Nature Biotechnology. 40(12). 1807–1813. 122 indexed citations breakdown →

Lachover‐Roth, Idit, et al.. (2022). Hyper IgE Syndrome in an Isolated Population in Israel. Frontiers in Immunology. 13. 829239–829239. 3 indexed citations

Singer, Amihood, et al.. (2021). A founder mutation in TCTN2 causes Meckel‐Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin. American Journal of Medical Genetics Part A. 185(5). 1610–1613. 1 indexed citations

Sharony, Reuven, et al.. (2017). Prenatal course of metaphyseal anadysplasia associated with homozygous mutation in MMP9 identified by exome sequencing. Clinical Genetics. 92(6). 645–648. 7 indexed citations

Reinstein, Eyal, Valerie Drasinover, Rachel Lotan, et al.. (2017). Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type. Clinical Genetics. 93(1). 160–163. 8 indexed citations

Reinstein, Eyal, et al.. (2016). Terminal microdeletions of 13q34 chromosome region in patients with intellectual disability: Delineation of an emerging new microdeletion syndrome. Molecular Genetics and Metabolism. 118(1). 60–63. 13 indexed citations

Reinstein, Eyal, Shay Tzur, Rony Cohen, Concetta Bormans, & Doron M. Behar. (2016). Intellectual disability and non-compaction cardiomyopathy with a de novo NONO mutation identified by exome sequencing. European Journal of Human Genetics. 24(11). 1635–1638. 21 indexed citations

Reinstein, Eyal, Ana Gutiérrez‐Fernández, Shay Tzur, et al.. (2016). Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C. European Journal of Human Genetics. 24(12). 1792–1796. 33 indexed citations

Reinstein, Eyal. (2015). Challenges of using next generation sequencing in newborn screening. Genetics Research. 97. e21–e21. 15 indexed citations

10.

Wilcox, William R., et al.. (2013). More than meets the eye: The evolving phenotype of Weill–Marchesani syndrome—diagnostic confusion with geleophysic dysplasia. American Journal of Medical Genetics Part A. 161(12). 3126–3129. 12 indexed citations

11.

Reinstein, Eyal, Ericka Okenfuss, Yael Wilnai, et al.. (2013). Axial spondylometaphyseal dysplasia with retinitis pigmentosa—a clinical report and diagnostic clues. Journal of Applied Genetics. 54(2). 231–234. 1 indexed citations

12.

Reinstein, Eyal, Mitchel Pariani, Serguei Bannykh, David L. Rimoin, & Wouter I. Schievink. (2012). Connective tissue spectrum abnormalities associated with spontaneous cerebrospinal fluid leaks: a prospective study. European Journal of Human Genetics. 21(4). 386–390. 57 indexed citations

13.

Reinstein, Eyal, Bernard S. Chang, Stephen P. Robertson, David L. Rimoin, & Tami Katzir. (2012). Filamin A mutation associated with normal reading skills and dyslexia in a family with periventricular heterotopia. American Journal of Medical Genetics Part A. 158A(8). 1897–1901. 10 indexed citations

14.

Reinstein, Eyal, et al.. (2012). Visceroptosis of the bowel in the hypermobility type of Ehlers–Danlos syndrome: Presentation of a rare manifestation and review of the literature. European Journal of Medical Genetics. 55(10). 548–551. 29 indexed citations

15.

Klaassens, Merel, Eyal Reinstein, Yvonne Hilhorst‐Hofstee, et al.. (2011). Ehlers–Danlos arthrochalasia type (VIIA–B) – expanding the phenotype: from prenatal life through adulthood. Clinical Genetics. 82(2). 121–130. 26 indexed citations

16.

Reinstein, Eyal, et al.. (2011). Ehlers-Danlos type VIII, periodontitis-type: Further delineation of the syndrome in a four-generation pedigree. American Journal of Medical Genetics Part A. 155(4). 742–747. 12 indexed citations

17.

Reinstein, Eyal, Yoseph A. Mekori, & Adam Mor. (2008). Autoimmunity and mast cell-related diseases. Expert Review of Clinical Immunology. 4(2). 267–274. 1 indexed citations

18.

Reinstein, Eyal & Yehuda Shoenfeld. (2007). Antiphospholipid Syndrome and Cancer. Clinical Reviews in Allergy & Immunology. 32(2). 184–187. 22 indexed citations

19.

Reinstein, Eyal. (2004). Immunologic aspects of protein degradation by the ubiquitin-proteasome system.. PubMed. 6(7). 420–4. 22 indexed citations

20.

Floyd, Z. Elizabeth, Julie S. Trausch‐Azar, Eyal Reinstein, Aaron Ciechanover, & Alan L. Schwartz. (2001). The Nuclear Ubiquitin-Proteasome System Degrades MyoD. Journal of Biological Chemistry. 276(25). 22468–22475. 65 indexed citations

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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