Nicolas Simonis

6.5k total citations
18 papers, 1.1k citations indexed

About

Nicolas Simonis is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Nicolas Simonis has authored 18 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 2 papers in Genetics. Recurrent topics in Nicolas Simonis's work include Fungal and yeast genetics research (4 papers), Bioinformatics and Genomic Networks (3 papers) and Chronic Lymphocytic Leukemia Research (2 papers). Nicolas Simonis is often cited by papers focused on Fungal and yeast genetics research (4 papers), Bioinformatics and Genomic Networks (3 papers) and Chronic Lymphocytic Leukemia Research (2 papers). Nicolas Simonis collaborates with scholars based in Belgium, United States and France. Nicolas Simonis's co-authors include Marc Vidal, Anne‐Ruxandra Carvunis, Michael E. Cusick, Ilan Wapinski, Aviv Regev, Thomas Rolland, Michael A. Calderwood, Jonathan S. Weissman, Benoît Charloteaux and César A. Hidalgo and has published in prestigious journals such as Nature, The EMBO Journal and Bioinformatics.

In The Last Decade

Nicolas Simonis

18 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nicolas Simonis Belgium	14	952	203	120	96	94	18	1.1k
Hatice Özel Abaan United States	10	803 0.8×	247 1.2×	101 0.8×	185 1.9×	28 0.3×	14	1.1k
Vincent E. Sollars United States	13	467 0.5×	149 0.7×	73 0.6×	55 0.6×	74 0.8×	24	724
Damian Smedley United Kingdom	5	1.1k 1.1×	318 1.6×	137 1.1×	133 1.4×	29 0.3×	8	1.4k
Andreas Kähäri United Kingdom	6	832 0.9×	393 1.9×	216 1.8×	181 1.9×	44 0.5×	6	1.3k
Orit Shmueli Israel	10	997 1.0×	346 1.7×	169 1.4×	212 2.2×	112 1.2×	15	1.4k
Syed Haider United Kingdom	3	795 0.8×	373 1.8×	162 1.4×	260 2.7×	45 0.5×	3	1.3k
Andrey Alexeyenko Sweden	20	912 1.0×	154 0.8×	116 1.0×	180 1.9×	114 1.2×	42	1.4k
Bernd Klaus Germany	12	735 0.8×	109 0.5×	66 0.6×	143 1.5×	63 0.7×	21	1.1k
Anastasia Samsonova Russia	17	847 0.9×	108 0.5×	153 1.3×	207 2.2×	56 0.6×	48	1.1k
Fabrice Lopez France	18	1.1k 1.1×	158 0.8×	214 1.8×	141 1.5×	40 0.4×	24	1.3k

Countries citing papers authored by Nicolas Simonis

Since Specialization

Citations

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

Fields of papers citing papers by Nicolas Simonis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicolas Simonis

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

All Works

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18 of 18 papers shown

Cassart, Marie, et al.. (2024). An unusual presentation of de novo RAC3 variation in prenatal diagnosis. Child s Nervous System. 40(5). 1597–1602. 3 indexed citations

Daakour, Sarah, et al.. (2016). Systematic interactome mapping of acute lymphoblastic leukemia cancer gene products reveals EXT-1 tumor suppressor as a Notch1 and FBWX7 common interactor. BMC Cancer. 16(1). 335–335. 14 indexed citations

Depondt, Chantal, Simona Donatello, Myriam Rai, et al.. (2016). MME mutation in dominant spinocerebellar ataxia with neuropathy (SCA43). Neurology Genetics. 2(5). e94–e94. 40 indexed citations

Daakour, Sarah, Maud Martin, Reinhard Grausenburger, et al.. (2014). Predicting interactome network perturbations in human cancer: application to gene fusions in acute lymphoblastic leukemia. Molecular Biology of the Cell. 25(24). 3973–3985. 9 indexed citations

Depondt, Chantal, Simona Donatello, Nicolas Simonis, et al.. (2014). Autosomal recessive cerebellar ataxia of adult onset due to STUB1 Mutations. Neurology. 82(19). 1749–1750. 28 indexed citations

Igoillo‐Esteve, Mariana, Nelle Lambert, Julie Désir, et al.. (2013). tRNA Methyltransferase Homolog Gene TRMT10A Mutation in Young Onset Diabetes and Primary Microcephaly in Humans. PLoS Genetics. 9(10). e1003888–e1003888. 95 indexed citations

Martin, Maud, Ilse Geudens, Michael Potente, et al.. (2013). PP2A regulatory subunit Bα controls endothelial contractility and vessel lumen integrity via regulation of HDAC7. The EMBO Journal. 32(18). 2491–2503. 41 indexed citations

Simonis, Nicolas, Isabelle Migeotte, Nelle Lambert, et al.. (2013). FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly. Journal of Medical Genetics. 50(9). 585–592. 61 indexed citations

Igoillo‐Esteve, Mariana, Nelle Lambert, Isabelle Pirson, et al.. (2013). Loss-of-function of the tRNA methyltransferase homolog gene TRMT10A causes young onset diabetes and primary microcephaly in humans. 1 indexed citations

10.

Carvunis, Anne‐Ruxandra, Thomas Rolland, Ilan Wapinski, et al.. (2012). Proto-genes and de novo gene birth. Nature. 487(7407). 370–374. 444 indexed citations

11.

Remacle, Sophie, et al.. (2012). Protein interactions of the transcription factor Hoxa1. BMC Developmental Biology. 12(1). 29–29. 41 indexed citations

12.

Jalas, Chaim, Nicolas Simonis, Julie Désir, et al.. (2012). Two novel CCDC88C mutations confirm the role of DAPLE in autosomal recessive congenital hydrocephalus. Journal of Medical Genetics. 49(11). 708–712. 51 indexed citations

13.

Cusick, Michael E., Haiyuan Yu, Alex Smolyar, et al.. (2009). Addendum: Literature-curated protein interaction datasets. Nature Methods. 6(12). 934–935. 7 indexed citations

14.

Li, Qianru, Anne‐Ruxandra Carvunis, Haiyuan Yu, et al.. (2008). Revisiting the Saccharomyces cerevisiae predicted ORFeome. Genome Research. 18(8). 1294–1303. 23 indexed citations

15.

Cusick, Michael E., Haiyuan Yu, Alex Smolyar, et al.. (2008). Literature-curated protein interaction datasets. Nature Methods. 6(1). 39–46. 212 indexed citations

16.

Simonis, Nicolas, Didier Gonze, Chris Orsi, Jacques van Helden, & Shoshana J. Wodak. (2006). Modularity of the Transcriptional Response of Protein Complexes in Yeast. Journal of Molecular Biology. 363(2). 589–610. 21 indexed citations

17.

Simonis, Nicolas, Jacques van Helden, G. N. Cohen, & Shoshana J. Wodak. (2004). Transcriptional regulation of protein complexes in yeast. Genome biology. 5(5). R33–R33. 30 indexed citations

18.

Simonis, Nicolas, et al.. (2004). Combining pattern discovery and discriminant analysis to predict gene co-regulation. Bioinformatics. 20(15). 2370–2379. 22 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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