Inge Buntinx
Impact in
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 8
- Genetic Syndromes and Imprinting 4
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 2
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- Prenatal Screening and Diagnostics 2
- Fetal and Pediatric Neurological Disorders 1
- Co-authors
- Joke Beuten (4 shared papers)Oebele F. Brouwer (3 shared papers)Hans Stroink (2 shared papers)Kathelijne Mangelschots (3 shared papers)J. P. Fryns (1 shared paper)Raoul C. M. Hennekam (1 shared paper)Laura Laan (1 shared paper)W.O. Renier (1 shared paper)
- Journals
- Human Genetics (2 papers)Journal of Medical Genetics (2 papers)Epilepsia (1 paper)Journal of Cardiovascular Pharmacology (1 paper)Genomics (1 paper)
- Partner nations
- BelgiumNetherlands
In The Last Decade
Inge Buntinx
12 papers receiving 364 citations
Peers
Comparison fields: 5 of 52
- Genetics 301
- Pediatrics, Perinatology and Child Health 76
- Molecular Biology 175
- Genetics 19
- Cardiology and Cardiovascular Medicine 29
Countries citing papers authored by Inge Buntinx
This map shows the geographic impact of Inge Buntinx'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 Inge Buntinx with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Inge Buntinx more than expected).
Fields of papers citing papers by Inge Buntinx
This network shows the impact of papers produced by Inge Buntinx. 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 Inge Buntinx. The network helps show where Inge Buntinx may publish in the future.
Co-authors
The 25 scholars most cited alongside Inge Buntinx, 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 | 1995 | 115 | |
| 2 | 1997 | 109 | |
| 3 | 1991 | 40 | |
| 4 | 1993 | 20 | |
| 5 | 1993 | 19 | |
| 6 | 1995 | 19 | |
| 7 | 1990 | 16 | |
| 8 | 1993 | 15 | |
| 9 | 1989 | 12 | |
| 10 | 1991 | 11 | |
| 11 | 1992 | 4 | |
| 12 | A new association of mental retardation, short stature, unusual face, radio-ulnar synostosis and retinal pigment abnormalities. | 1991 | 4 |
About Inge Buntinx
Inge Buntinx is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Cardiology and Cardiovascular Medicine and Surgery, having authored 12 papers that have together received 384 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (4 papers), Genetics and Neurodevelopmental Disorders (2 papers), Prenatal Screening and Diagnostics (2 papers), RNA modifications and cancer (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Fetal and Pediatric Neurological Disorders (1 paper), Epigenetics and DNA Methylation (1 paper) and Cardiac electrophysiology and arrhythmias (1 paper). The work is most often cited by research in Genetics (301 citations), Pediatrics, Perinatology and Child Health (76 citations), Molecular Biology (175 citations), Genetics (19 citations) and Cardiology and Cardiovascular Medicine (29 citations). Inge Buntinx has collaborated with scholars based in Belgium and Netherlands. Frequent co-authors include Joke Beuten, Oebele F. Brouwer, Hans Stroink, Kathelijne Mangelschots, J. P. Fryns, Raoul C. M. Hennekam, Laura Laan, W.O. Renier, Koos Zwinderman and J. Gert van Dijk. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Epilepsia, Journal of Cardiovascular Pharmacology and Genomics.
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.