Hilde Peeters
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
- Genetics 51
- Genomic variations and chromosomal abnormalities 27
- Genetics and Neurodevelopmental Disorders 15
- Genomics and Rare Diseases 10
- Craniofacial Disorders and Treatments 9
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- Congenital heart defects research 11
- Co-authors
- Koenraad Devriendt (36 shared papers)V. Blaton (24 shared papers)Cathérine Derom (4 shared papers)Robert Vlietinck (3 shared papers)F. Soetewey (9 shared papers)Dries Vandamme (12 shared papers)Sofie Van Gestel (1 shared paper)R. Derom (1 shared paper)
- Journals
- European Journal of Medical Genetics (7 papers)European Journal of Human Genetics (6 papers)Clinical Genetics (5 papers)Scientific Reports (3 papers)Clinica Chimica Acta (3 papers)
- Partner nations
- BelgiumUnited StatesUnited Kingdom
In The Last Decade
Hilde Peeters
142 papers receiving 2.5k citations
Peers
Comparison fields: 5 of 153
- Genetics 753
- Pediatrics, Perinatology and Child Health 439
- Molecular Biology 1.0k
- Hematology 144
- Cognitive Neuroscience 209
Countries citing papers authored by Hilde Peeters
This map shows the geographic impact of Hilde Peeters'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 Hilde Peeters with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hilde Peeters more than expected).
Fields of papers citing papers by Hilde Peeters
This network shows the impact of papers produced by Hilde Peeters. 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 Hilde Peeters. The network helps show where Hilde Peeters may publish in the future.
Co-authors
The 25 scholars most cited alongside Hilde Peeters, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 154 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 183 | |
| 2 | 2006 | 120 | |
| 3 | 2015 | 98 | |
| 4 | 2003 | 98 | |
| 5 | 2015 | 73 | |
| 6 | 2010 | 70 | |
| 7 | 1996 | 59 | |
| 8 | 2010 | 57 | |
| 9 | Elevated levels of inflammatory cytokines in bone marrow of patients with rheumatoid arthritis and anemia of chronic disease. | 1997 | 57 |
| 10 | 1971 | 55 | |
| 11 | 2021 | 54 | |
| 12 | 2016 | 54 | |
| 13 | 2018 | 47 | |
| 14 | 2013 | 44 | |
| 15 | 1979 | 42 | |
| 16 | 2020 | 40 | |
| 17 | 2016 | 39 | |
| 18 | 2001 | 38 | |
| 19 | 1970 | 38 | |
| 20 | 1978 | 38 |
About Hilde Peeters
Hilde Peeters is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Cognitive Neuroscience, having authored 154 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (27 papers), Prenatal Screening and Diagnostics (20 papers), Genetics and Neurodevelopmental Disorders (15 papers), Autism Spectrum Disorder Research (13 papers), Congenital heart defects research (11 papers), Genomics and Rare Diseases (10 papers), Craniofacial Disorders and Treatments (9 papers) and Fetal and Pediatric Neurological Disorders (6 papers). The work is most often cited by research in Genetics (753 citations), Pediatrics, Perinatology and Child Health (439 citations), Molecular Biology (1.0k citations), Hematology (144 citations) and Cognitive Neuroscience (209 citations). Hilde Peeters has collaborated with scholars based in Belgium, United States and United Kingdom. Frequent co-authors include Koenraad Devriendt, V. Blaton, Cathérine Derom, Robert Vlietinck, F. Soetewey, Dries Vandamme, Sofie Van Gestel, R. Derom, Joris Vermeesch and Nathalie Brison. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Clinical Genetics, Scientific Reports and Clinica Chimica Acta.
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.