Simon Ardui
Impact in
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- Cancer Genomics and Diagnostics
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- Genomics and Phylogenetic Studies
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- Epigenetics and DNA Methylation
Papers in
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- Chromatin Remodeling and Cancer 2
- Genomics and Phylogenetic Studies 1
- Mitochondrial Function and Pathology 1
- Genetics 4
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Joris Vermeesch (6 shared papers)Matthew S. Hestand (2 shared papers)Adam Ameur (1 shared paper)Hilde Van Esch (3 shared papers)Koenraad Devriendt (3 shared papers)Thomy de Ravel (2 shared papers)Gert Matthijs (2 shared papers)Valérie Race (2 shared papers)
- Journals
- Nucleic Acids Research (1 paper)Frontiers in Genetics (1 paper)Human Molecular Genetics (1 paper)European Journal of Human Genetics (1 paper)Human Mutation (1 paper)
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Simon Ardui
6 papers receiving 643 citations
Simon Ardui's Hit Papers
Peers
Comparison fields: 5 of 84
- Cancer Research 75
- Molecular Biology 361
- Genetics 140
- Pediatrics, Perinatology and Child Health 81
- Ecology 72
Countries citing papers authored by Simon Ardui
This map shows the geographic impact of Simon Ardui'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 Simon Ardui with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simon Ardui more than expected).
Fields of papers citing papers by Simon Ardui
This network shows the impact of papers produced by Simon Ardui. 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 Simon Ardui. The network helps show where Simon Ardui may publish in the future.
Co-authors
The 24 scholars most cited alongside Simon Ardui, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Single molecule real-time (SMRT) sequencing comes of age: applications and utilities for medical diagnostics Hit paper breakdown → | 2018 | 502 |
| 2 | 2015 | 101 | |
| 3 | 2016 | 31 | |
| 4 | 2018 | 28 | |
| 5 | 2020 | 6 | |
| 6 | 2013 | 1 |
About Simon Ardui
Simon Ardui is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cellular and Molecular Neuroscience and Cognitive Neuroscience, having authored 6 papers that have together received 669 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Fetal and Pediatric Neurological Disorders (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Prenatal Screening and Diagnostics (2 papers), Chromatin Remodeling and Cancer (2 papers), Autism Spectrum Disorder Research (1 paper), Genomics and Phylogenetic Studies (1 paper) and Mitochondrial Function and Pathology (1 paper). The work is most often cited by research in Cancer Research (75 citations), Molecular Biology (361 citations), Genetics (140 citations), Pediatrics, Perinatology and Child Health (81 citations) and Ecology (72 citations). Simon Ardui has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Joris Vermeesch, Matthew S. Hestand, Adam Ameur, Hilde Van Esch, Koenraad Devriendt, Thomy de Ravel, Gert Matthijs, Valérie Race, Paul Brady and Eric Legius. Their work appears in journals such as Nucleic Acids Research, Frontiers in Genetics, Human Molecular Genetics, European Journal of Human Genetics and Human Mutation.
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.