Simon Ardui
Impact in
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- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
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- Genomics and Phylogenetic Studies
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
Papers in
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- Chromatin Remodeling and Cancer 2
- Advanced biosensing and bioanalysis techniques 1
- Single-cell and spatial transcriptomics 1
- RNA Research and Splicing 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)Valérie Race (2 shared papers)Gert Matthijs (2 shared papers)
- Journals
- Human Mutation (1 paper)Nucleic Acids Research (1 paper)Human Molecular Genetics (1 paper)Frontiers in Genetics (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Simon Ardui
6 papers receiving 628 citations
Simon Ardui's Hit Papers
Peers
Comparison fields: 5 of 84
- Genetics 165
- Molecular Biology 391
- Cancer Research 84
- Pediatrics, Perinatology and Child Health 89
- Ecology 75
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 | 493 |
| 2 | 2015 | 98 | |
| 3 | 2016 | 31 | |
| 4 | 2018 | 27 | |
| 5 | 2020 | 5 | |
| 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 655 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Chromatin Remodeling and Cancer (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Prenatal Screening and Diagnostics (2 papers), Fetal and Pediatric Neurological Disorders (2 papers), Advanced biosensing and bioanalysis techniques (1 paper), Single-cell and spatial transcriptomics (1 paper) and RNA Research and Splicing (1 paper). The work is most often cited by research in Genetics (165 citations), Molecular Biology (391 citations), Cancer Research (84 citations), Pediatrics, Perinatology and Child Health (89 citations) and Ecology (75 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, Valérie Race, Gert Matthijs, Kris Van Den Bogaert and Eric Legius. Their work appears in journals such as Human Mutation, Nucleic Acids Research, Human Molecular Genetics, Frontiers in Genetics and European Journal of Human Genetics.
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.