Erik Simons

1.8k total citations
17 papers, 786 citations indexed

About

Erik Simons is a scholar working on Neurology, Neurology and Molecular Biology. According to data from OpenAlex, Erik Simons has authored 17 papers receiving a total of 786 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Neurology, 8 papers in Neurology and 4 papers in Molecular Biology. Recurrent topics in Erik Simons's work include Parkinson's Disease Mechanisms and Treatments (10 papers), Neurological diseases and metabolism (8 papers) and Immune Cell Function and Interaction (3 papers). Erik Simons is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (10 papers), Neurological diseases and metabolism (8 papers) and Immune Cell Function and Interaction (3 papers). Erik Simons collaborates with scholars based in Netherlands, Italy and Germany. Erik Simons's co-authors include Vincenzo Bonifati, Ben A. Oostra, Guido J. Breedveld, Alessio Di Fonzo, Marina van Doeselaar, Rou-Shayn Chen, Chin-Song Lu, Hsiu‐Chen Chang, Yi‐Hsin Weng and Yah‐Huei Wu‐Chou and has published in prestigious journals such as Blood, Neurology and Frontiers in Immunology.

In The Last Decade

Erik Simons

17 papers receiving 768 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Erik Simons Netherlands	13	548	256	239	194	157	17	786
Jay P. Ross Canada	15	241 0.4×	74 0.3×	226 0.9×	111 0.6×	97 0.6×	39	653
Masayoshi Tada Japan	11	209 0.4×	157 0.6×	299 1.3×	174 0.9×	86 0.5×	29	598
Francesco Limone United States	10	411 0.8×	113 0.4×	611 2.6×	88 0.5×	87 0.6×	13	886
Federica Lombardi Italy	8	166 0.3×	152 0.6×	179 0.7×	246 1.3×	65 0.4×	10	633
Atossa Shaltouki United States	9	347 0.6×	127 0.5×	568 2.4×	254 1.3×	182 1.2×	10	911
Michael J. Hipp United States	9	200 0.4×	137 0.5×	518 2.2×	69 0.4×	107 0.7×	12	775
Kristin A. Politi United States	6	188 0.3×	94 0.4×	326 1.4×	74 0.4×	108 0.7×	6	557
Jeffrey Rothstein United States	6	394 0.7×	88 0.3×	630 2.6×	159 0.8×	73 0.5×	9	987
Christelle Tesson France	10	208 0.4×	124 0.5×	196 0.8×	211 1.1×	125 0.8×	17	496
Rebecca Bounds United States	13	197 0.4×	67 0.3×	260 1.1×	129 0.7×	81 0.5×	18	665

Countries citing papers authored by Erik Simons

Since Specialization

Citations

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

Fields of papers citing papers by Erik Simons

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erik Simons

This figure shows the co-authorship network connecting the top 25 collaborators of Erik Simons. A scholar is included among the top collaborators of Erik Simons 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 Erik Simons. Erik Simons is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

IJspeert, Hanna, Jacob Rozmus, Klaus Schwarz, et al.. (2016). XLF deficiency results in reduced N-nucleotide addition during V(D)J recombination. Blood. 128(5). 650–659. 25 indexed citations

IJspeert, Hanna, Marjolein Wentink, Gertjan J. Driessen, et al.. (2015). Strategies for B-Cell Receptor Repertoire Analysis in Primary Immunodeficiencies: From Severe Combined Immunodeficiency to Common Variable Immunodeficiency. Frontiers in Immunology. 6. 157–157. 16 indexed citations

Wentink, Marjolein, Annechien J.A. Lambeck, Menno C. van Zelm, et al.. (2015). CD21 and CD19 deficiency: Two defects in the same complex leading to different disease modalities. Clinical Immunology. 161(2). 120–127. 24 indexed citations

Rolfe, E B, Simone Olgiati, Marialuisa Quadri, et al.. (2015). Novel GCH1 variant in Dopa-responsive dystonia and Parkinson's disease. Parkinsonism & Related Disorders. 21(4). 394–397. 22 indexed citations

Vliet, Martin H. van, Erik Simons, Lars Bullinger, et al.. (2013). Detection of Mutant NPM1 mRNA in Acute Myeloid Leukemia Using Custom Gene Expression Arrays. Genetic Testing and Molecular Biomarkers. 17(4). 295–300. 4 indexed citations

Zhang, Lei, Marialuisa Quadri, Leonor Correia Guedes, et al.. (2013). Comprehensive LRRK2 and GBA screening in Portuguese patients with Parkinson's disease: Identification of a new family with the LRRK2 p.Arg1441His mutation and novel missense variants. Parkinsonism & Related Disorders. 19(10). 897–900. 8 indexed citations

Yonova‐Doing, Ekaterina, Masharip Atadzhanov, Marialuisa Quadri, et al.. (2012). Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease. Parkinsonism & Related Disorders. 18(5). 567–571. 40 indexed citations

Quadri, Marialuisa, Giovanni Cossu, Valeria Saddi, et al.. (2011). Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson’s disease in Sardinia. Neurogenetics. 12(3). 203–209. 68 indexed citations

Criscuolo, Chiara, Anna De Rosa, Erik Simons, et al.. (2011). The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from Southern Italy. Movement Disorders. 26(9). 1732–1736. 23 indexed citations

10.

Fonzo, Alessio Di, S. L. M. Bakker, Erik Simons, et al.. (2010). Autosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS‐5) in a Dutch kindred. Movement Disorders. 25(11). 1715–1722. 8 indexed citations

11.

Lu, Chin-Song, Yah‐Huei Wu‐Chou, Marina van Doeselaar, et al.. (2008). The LRRK2 Arg1628Pro variant is a risk factor for Parkinson’s disease in the Chinese population. Neurogenetics. 9(4). 271–276. 50 indexed citations

12.

Hoogeveen‐Westerveld, Marianne, et al.. (2008). A reliable cell-based assay for testing unclassified TSC2 gene variants. European Journal of Human Genetics. 17(3). 301–310. 23 indexed citations

13.

Oldenburg, Reinhard, M. F. van Dooren, Erik Simons, et al.. (2008). A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus. Human Reproduction. 23(12). 2835–2841. 28 indexed citations

14.

Fonzo, Alessio Di, Marieke C. J. Dekker, P. Montagna, et al.. (2008). FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome. Neurology. 72(3). 240–245. 248 indexed citations

15.

Fonzo, Alessio Di, Yah‐Huei Wu‐Chou, Chin-Song Lu, et al.. (2006). A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson’s disease risk in Taiwan. Neurogenetics. 7(3). 133–138. 180 indexed citations

16.

Bertoli‐Avella, Aida M., Marieke Dekker, Yurii S. Aulchenko, et al.. (2005). Evidence for novel loci for late-onset Parkinson’s disease in a genetic isolate from the Netherlands. Human Genetics. 119(1-2). 51–60. 4 indexed citations

17.

Scarpella, Enrico, Erik Simons, & Annemarie H. Meijer. (2005). Multiple Regulatory Elements Contribute to the Vascular-specific Expression of the Rice HD-Zip Gene Oshox1 in Arabidopsis. Plant and Cell Physiology. 46(8). 1400–1410. 15 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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