Femke Hannes
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 11
- Genomics and Rare Diseases 2
- Genetics and Neurodevelopmental Disorders 2
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- Prenatal Screening and Diagnostics 3
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- Genomics and Chromatin Dynamics 3
- DNA and Biological Computing 2
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- Chromosomal and Genetic Variations 7
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- Bacteriophages and microbial interactions 1
- Co-authors
- Joris VermeeschKoenraad DevriendtGriet Van BuggenhoutJP FrynsThomy de RavelRegina ReganAnnick VogelsHelen Stewart
- Partner nations
- BelgiumUnited KingdomUnited States
In The Last Decade
Femke Hannes
13 papers receiving 611 citations
Peers
Comparison fields: 5 of 62
- Genetics 476
- Pediatrics, Perinatology and Child Health 146
- Developmental Biology 11
- Molecular Biology 336
- Cell Biology 66
Countries citing papers authored by Femke Hannes
This map shows the geographic impact of Femke Hannes'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 Femke Hannes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Femke Hannes more than expected).
Fields of papers citing papers by Femke Hannes
This network shows the impact of papers produced by Femke Hannes. 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 Femke Hannes. The network helps show where Femke Hannes may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Femke Hannes, 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 | 2023 | 0 | |
| 2 | 2012 | 15 | |
| 3 | 2012 | 38 | |
| 4 | 2011 | 58 | |
| 5 | 2010 | 15 | |
| 6 | 2010 | 15 | |
| 7 | 2009 | 12 | |
| 8 | 2008 | 207 | |
| 9 | 2008 | 36 | |
| 10 | 2008 | 4 | |
| 11 | 2007 | 99 | |
| 12 | The t(4;8) is mediated by homologous recombination between olfactory receptor gene clusters, but other 4p16 translocations occur at random. | 2007 | 16 |
| 13 | 2006 | 28 | |
| 14 | 2005 | 91 |
About Femke Hannes
Femke Hannes is a scholar working on Genetics, Plant Science and Pediatrics, Perinatology and Child Health, having authored 14 papers that have together received 634 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (7 papers), Prenatal Screening and Diagnostics (3 papers), Genomics and Chromatin Dynamics (3 papers), Genomics and Rare Diseases (2 papers), DNA and Biological Computing (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Bacteriophages and microbial interactions (1 paper). The work is most often cited by research in Genetics (476 citations), Pediatrics, Perinatology and Child Health (146 citations) and Developmental Biology (11 citations). Femke Hannes has collaborated with scholars based in Belgium, United Kingdom and United States. Frequent co-authors include Joris Vermeesch, Koenraad Devriendt, Griet Van Buggenhout, JP Fryns, Thomy de Ravel, Regina Regan, Annick Vogels, Helen Stewart, Sarah T. South and Heather C. Mefford. Their work appears in journals such as The EMBO Journal, PLoS ONE and Human Molecular 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.