Jan E. Dumon
Impact in
- Sensory Systems top 1%
- Hearing, Cochlea, Tinnitus, Genetics
-
- Neuroscience of respiration and sleep
Papers in
- Genetics 14
- Genomic variations and chromosomal abnormalities 8
- Connective tissue disorders research 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genetics and Neurodevelopmental Disorders 3
- Genetic Syndromes and Imprinting 2
- Co-authors
- Patrick J. Willems (10 shared papers)Thomas B. Friedman (1 shared paper)Guy Van Camp (2 shared papers)Linda J. Hood (1 shared paper)Bronya J.B. Keats (1 shared paper)Rachel Fisher (1 shared paper)Robert J. Morell (1 shared paper)Harry Ostrer (1 shared paper)
- Journals
- Journal of Medical Genetics (2 papers)Human Genetics (2 papers)New England Journal of Medicine (2 papers)Clinical Genetics (2 papers)Human Molecular Genetics (1 paper)
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Jan E. Dumon
31 papers receiving 902 citations
Peers
Comparison fields: 5 of 76
- Sensory Systems 389
- Endocrine and Autonomic Systems 125
- Neurology 143
- Otorhinolaryngology 46
- Genetics 240
Countries citing papers authored by Jan E. Dumon
This map shows the geographic impact of Jan E. Dumon'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 Jan E. Dumon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jan E. Dumon more than expected).
Fields of papers citing papers by Jan E. Dumon
This network shows the impact of papers produced by Jan E. Dumon. 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 Jan E. Dumon. The network helps show where Jan E. Dumon may publish in the future.
Co-authors
The 25 scholars most cited alongside Jan E. Dumon, 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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1998 | 432 | |
| 2 | 1991 | 115 | |
| 3 | 1990 | 48 | |
| 4 | 1992 | 46 | |
| 5 | 1991 | 34 | |
| 6 | 1973 | 32 | |
| 7 | 2000 | 32 | |
| 8 | 1983 | 27 | |
| 9 | 1992 | 23 | |
| 10 | 1993 | 23 | |
| 11 | 1991 | 21 | |
| 12 | 1970 | 17 | |
| 13 | 1992 | 17 | |
| 14 | 1995 | 15 | |
| 15 | 1996 | 12 | |
| 16 | 1991 | 11 | |
| 17 | 1993 | 7 | |
| 18 | 1990 | 5 | |
| 19 | 1992 | 4 | |
| 20 | A new association of mental retardation, short stature, unusual face, radio-ulnar synostosis and retinal pigment abnormalities. | 1991 | 4 |
About Jan E. Dumon
Jan E. Dumon is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Genetics, having authored 31 papers that have together received 944 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (8 papers), Connective tissue disorders research (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Congenital Anomalies and Fetal Surgery (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genetic Syndromes and Imprinting (2 papers) and Lysosomal Storage Disorders Research (2 papers). The work is most often cited by research in Sensory Systems (389 citations), Endocrine and Autonomic Systems (125 citations), Neurology (143 citations), Otorhinolaryngology (46 citations) and Genetics (240 citations). Jan E. Dumon has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include Patrick J. Willems, Thomas B. Friedman, Guy Van Camp, Linda J. Hood, Bronya J.B. Keats, Rachel Fisher, Robert J. Morell, Harry Ostrer, Karen H. Friderici and Charles I. Berlín. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, New England Journal of Medicine, Clinical Genetics 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.