Nicolas Simonis

6.5k citations

18 papers · 1.1k indexed · h-index 14

Impact in

Molecular Biology top 10%
- RNA and protein synthesis mechanisms
- Bioinformatics and Genomic Networks
- Genomics and Phylogenetic Studies
- RNA modifications and cancer
- RNA Research and Splicing
- Microbial Metabolic Engineering and Bioproduction
- Genomics and Chromatin Dynamics
- Fungal and yeast genetics research
Genetics top 10%

Papers in ⓘ

Molecular Biology 14
- Fungal and yeast genetics research 4
- Bioinformatics and Genomic Networks 3
- Hedgehog Signaling Pathway Studies 2
- Epigenetics and DNA Methylation 2
Genetics 2
- Chronic Lymphocytic Leukemia Research 2

Co-authors: Marc Vidal (5 shared papers)Anne‐Ruxandra Carvunis (4 shared papers)Michael E. Cusick (4 shared papers)Aviv Regev (2 shared papers)Ilan Wapinski (2 shared papers)Muhammed A. Yıldırım (1 shared paper)Benoît Charloteaux (1 shared paper)Nicolas Thierry‐Mieg (1 shared paper)
Journals: Nature Methods (2 papers)Journal of Medical Genetics (2 papers)Child s Nervous System (1 paper)PLoS Genetics (1 paper)Bioinformatics (1 paper)
Partner nations: Belgium United States France

In The Last Decade

Nicolas Simonis

18 papers receiving 1.1k citations

Peers

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-authors

The 25 scholars most cited alongside Nicolas Simonis, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Nicolas Simonis Line = papers co-authored together Nicolas Simonis links everyone, so they are left out of the graph.

All Works

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18 of 18 papers shown

#	Work
1	Proto-genes and de novo gene birth Nature ·Anne‐Ruxandra Carvunis, Thomas Rolland, Ilan Wapinski, Michael A. Calderwood, Muhammed A. Yıldırım, Nicolas Simonis, Benoît Charloteaux, César A. Hidalgo, Justin Barbette, Balaji Santhanam, Gloria A. Brar, Jonathan S. Weissman, Aviv Regev, Nicolas Thierry‐Mieg, Michael E. Cusick, Marc Vidal	2012	444
2	Literature-curated protein interaction datasets Nature Methods ·Michael E. Cusick, Haiyuan Yu, Alex Smolyar, K. Venkatesan, Anne‐Ruxandra Carvunis, Nicolas Simonis, Jean‐François Rual, Heather Borick, Pascal Falter‐Braun, Matija Dreze, Jean Vandenhaute, Mary Galli, Junshi Yazaki, David E. Hill, Joseph R. Ecker, Frederick P. Roth, Marc Vidal	2008	212
3	tRNA Methyltransferase Homolog Gene TRMT10A Mutation in Young Onset Diabetes and Primary Microcephaly in Humans PLoS Genetics ·Mariana Igoillo‐Esteve, Anne Genin, Nelle Lambert, Julie Désir, Isabelle Pirson, Baroj Abdulkarim, Nicolas Simonis, Anaïs Drielsma, Lorella Marselli, Piero Marchetti, Pierre Vanderhaeghen, Décio L. Eizirik, Wim Wuyts, Cécile Julier, Ali Chakera, Sian Ellard, Andrew T. Hattersley, Marc Abramowicz, Miriam Cnop	2013	95
4	FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly Journal of Medical Genetics ·Nicolas Simonis, Isabelle Migeotte, Nelle Lambert, Camille Perazzolo, Deepthi C. de Silva, Boyan Dimitrov, Claudine Heinrichs, Sandra Janssens, Bronwyn Kerr, Geert Mortier, Guy Van Vliet, Philippe Lepage, Georges Casimir, Marc Abramowicz, Guillaume Smits, Catheline Vilain	2013	61
5	Two novel CCDC88C mutations confirm the role of DAPLE in autosomal recessive congenital hydrocephalus Journal of Medical Genetics ·Anaïs Drielsma, Chaim Jalas, Nicolas Simonis, Julie Désir, Natalia Simanovsky, Isabelle Pirson, Orly Elpeleg, Marc Abramowicz, Simon Edvardson	2012	51
6	PP2A regulatory subunit Bα controls endothelial contractility and vessel lumen integrity via regulation of HDAC7 The EMBO Journal ·Maud Martin, Ilse Geudens, Jonathan Bruyr, Michael Potente, Anouk Bleuart, Marielle Lebrun, Nicolas Simonis, Christophe Deroanne, Jean‐Claude Twizere, Philippe Soubeyran, Paul Peixoto, Denis Mottet, Veerle Janssens, Wolf‐Karsten Hofmann, Filip Claes, Peter Carmeliet, Richard Kettmann, Holger Gerhardt, Samuel Dequiedt	2013	41
7	Protein interactions of the transcription factor Hoxa1 BMC Developmental Biology ·Barbara Lambert, Julie Vandeputte, Sophie Remacle, Isabelle Bergiers, Nicolas Simonis, Jean‐Claude Twizere, Marc Vidal, René Rezsöhazy	2012	41
8	MME mutation in dominant spinocerebellar ataxia with neuropathy (SCA43) Neurology Genetics ·Chantal Depondt, Simona Donatello, Myriam Rai, François‐Charles Wang, Mario Manto, Nicolas Simonis, Massimo Pandolfo	2016	40
9	Transcriptional regulation of protein complexes in yeast Genome biology ·Nicolas Simonis, Jacques van Helden, G. N. Cohen, Shoshana J. Wodak	2004	30
10	Autosomal recessive cerebellar ataxia of adult onset due to STUB1 Mutations Neurology ·Chantal Depondt, Simona Donatello, Nicolas Simonis, Myriam Rai, Roxane Van Heurck, Marc Abramowicz, Marc D’Hooghe, Massimo Pandolfo	2014	28
11	Revisiting the Saccharomyces cerevisiae predicted ORFeome Genome Research ·Qianru Li, Anne‐Ruxandra Carvunis, Haiyuan Yu, Jing‐Dong J. Han, Quan Zhong, Nicolas Simonis, Stanley Tam, Tong Hao, Niels Klitgord, Denis Dupuy, Danny Mou, Ilan Wapinski, Aviv Regev, David E. Hill, Michael E. Cusick, Marc Vidal	2008	23
12	Combining pattern discovery and discriminant analysis to predict gene co-regulation Bioinformatics ·Nicolas Simonis, Shoshana J. Wodak, (unknown), Jacques van Helden	2004	22
13	Modularity of the Transcriptional Response of Protein Complexes in Yeast Journal of Molecular Biology ·Nicolas Simonis, Didier Gonze, Chris Orsi, Jacques van Helden, Shoshana J. Wodak	2006	21
14	Systematic interactome mapping of acute lymphoblastic leukemia cancer gene products reveals EXT-1 tumor suppressor as a Notch1 and FBWX7 common interactor BMC Cancer ·Sarah Daakour, Leon Hajingabo, Despoina Kerselidou, Aurelie Devresse, Richard Kettmann, Nicolas Simonis, Samuel Dequiedt, Jean‐Claude Twizere	2016	14
15	Predicting interactome network perturbations in human cancer: application to gene fusions in acute lymphoblastic leukemia Molecular Biology of the Cell ·Leon Hajingabo, Sarah Daakour, Maud Martin, Reinhard Grausenburger, Renate Panzer‐Grümayer, Samuel Dequiedt, Nicolas Simonis, Jean‐Claude Twizere	2014	9
16	Addendum: Literature-curated protein interaction datasets Nature Methods ·Michael E. Cusick, Haiyuan Yu, Alex Smolyar, K. Venkatesan, Anne‐Ruxandra Carvunis, Nicolas Simonis, Jean‐François Rual, Heather Borick, Pascal Falter‐Braun, Matija Dreze, Jean Vandenhaute, Mary Galli, Junshi Yazaki, David E. Hill, Joseph R. Ecker, Frederick P. Roth, Marc Vidal	2009	7
17	An unusual presentation of de novo RAC3 variation in prenatal diagnosis Child s Nervous System ·Colombine Meunier, Marie Cassart, Karole Kostyla, Nicolas Simonis, Olivier Monestier, Aude Tessier	2024	3
18	Loss-of-function of the tRNA methyltransferase homolog gene TRMT10A causes young onset diabetes and primary microcephaly in humans Mariana Igoillo‐Esteve, Anne Genin, Nelle Lambert, Isabelle Pirson, Baroj Abdulkarim, Nicolas Simonis, Anaïs Drielsma, Lorella Marselli, Piero Marchetti, Pierre Vanderhaeghen, Décio L. Eizirik, Wim Wuyts, Cécile Julier, Ali Chakera, Sian Ellard, Andrew T. Hattersley, Marc Abramowicz, Miriam Cnop	2013	1

About Nicolas Simonis

Nicolas Simonis is a scholar working on Molecular Biology, Genetics, Hematology, Immunology and Allergy and Cellular and Molecular Neuroscience, having authored 18 papers that have together received 1.1k indexed citations. Recurring topics across this work include Fungal and yeast genetics research (4 papers), Bioinformatics and Genomic Networks (3 papers), Hedgehog Signaling Pathway Studies (2 papers), Chronic Lymphocytic Leukemia Research (2 papers), Acute Lymphoblastic Leukemia research (2 papers), Epigenetics and DNA Methylation (2 papers), Genetic Neurodegenerative Diseases (2 papers) and Chronic Myeloid Leukemia Treatments (2 papers). The work is most often cited by research in Molecular Biology (952 citations), Genetics (203 citations), Cancer Research (96 citations), Cell Biology (94 citations) and Cellular and Molecular Neuroscience (90 citations). Nicolas Simonis has collaborated with scholars based in Belgium, United States and France. Frequent co-authors include Marc Vidal, Anne‐Ruxandra Carvunis, Michael E. Cusick, Aviv Regev, Ilan Wapinski, Muhammed A. Yıldırım, Benoît Charloteaux, Nicolas Thierry‐Mieg, Thomas Rolland and Michael A. Calderwood. Their work appears in journals such as Nature Methods, Journal of Medical Genetics, Child s Nervous System, PLoS Genetics and Bioinformatics.

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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