J. M. J. C. Scheres
- Genetics top 10%
- Genomic variations and chromosomal abnormalities 12
- Genetics and Neurodevelopmental Disorders 3
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- Prenatal Screening and Diagnostics 7
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- Congenital limb and hand anomalies 4
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- Chromosomal and Genetic Variations 11
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- Genomics and Chromatin Dynamics 7
- DNA and Nucleic Acid Chemistry 4
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- Neurobiology and Insect Physiology Research 2
- Co-authors
- T. W. J. HustinxG. OttThomas HaafMichael SchmidA.M.Th. BeenakkersGerard MerkxB. G. A. ter HaarDominique Smeets
- Partner nations
- NetherlandsGermanyCuracao
In The Last Decade
J. M. J. C. Scheres
28 papers receiving 433 citations
Peers
Comparison fields: 5 of 47
- Genetics 305
- Pediatrics, Perinatology and Child Health 122
- Developmental Biology 12
- Plant Science 147
- Reproductive Medicine 28
Countries citing papers authored by J. M. J. C. Scheres
This map shows the geographic impact of J. M. J. C. Scheres'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 J. M. J. C. Scheres with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J. M. J. C. Scheres more than expected).
Fields of papers citing papers by J. M. J. C. Scheres
This network shows the impact of papers produced by J. M. J. C. Scheres. 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 J. M. J. C. Scheres. The network helps show where J. M. J. C. Scheres may publish in the future.
Co-authorship network
The 25 scholars most cited alongside J. M. J. C. Scheres, 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 | 2003 | 10 | |
| 2 | 1998 | 11 | |
| 3 | 1997 | 4 | |
| 4 | 1986 | 18 | |
| 5 | 1986 | 7 | |
| 6 | 1985 | 9 | |
| 7 | 1982 | 15 | |
| 8 | 1980 | 2 | |
| 9 | 1979 | 21 | |
| 10 | 1978 | 28 | |
| 11 | 1978 | 1 | |
| 12 | 1977 | 2 | |
| 13 | 1977 | 5 | |
| 14 | 1976 | 27 | |
| 15 | 1976 | 1 | |
| 16 | 1976 | 9 | |
| 17 | 1975 | 16 | |
| 18 | Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution. | 1974 | 6 |
| 19 | 1974 | 33 | |
| 20 | 1972 | 22 |
About J. M. J. C. Scheres
J. M. J. C. Scheres is a scholar working on Developmental Biology, Genetics and Pediatrics, Perinatology and Child Health, having authored 28 papers that have together received 457 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Chromosomal and Genetic Variations (11 papers), Prenatal Screening and Diagnostics (7 papers), Genomics and Chromatin Dynamics (7 papers), Congenital limb and hand anomalies (4 papers), DNA and Nucleic Acid Chemistry (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Neurobiology and Insect Physiology Research (2 papers). The work is most often cited by research in Genetics (305 citations), Pediatrics, Perinatology and Child Health (122 citations) and Developmental Biology (12 citations). J. M. J. C. Scheres has collaborated with scholars based in Netherlands, Germany and Curacao. Frequent co-authors include T. W. J. Hustinx, G. Ott, Thomas Haaf, Michael Schmid, A.M.Th. Beenakkers, T. W. J. Hustinx, Gerard Merkx, B. G. A. ter Haar, Dominique Smeets and G. A. M. de Vaan.
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.