C. Schaap
Impact in
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- Thyroid Cancer Diagnosis and Treatment
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 5
- Genomic variations and chromosomal abnormalities 2
- Dermatological and Skeletal Disorders 1
- Connective tissue disorders research 1
- Genetic and Kidney Cyst Diseases 1
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- Hedgehog Signaling Pathway Studies 2
- Co-authors
- C. T. R. M. Schrander‐Stumpel (2 shared papers)G.J.C.M. van Buggenhout (1 shared paper)Maureen Holvoet (1 shared paper)Ben C.J. Hamel (1 shared paper)J P Fryns (1 shared paper)L.W. Ernest van Heurn (1 shared paper)Erik Heineman (1 shared paper)Willem J.M. Gerver (1 shared paper)
- Journals
- The American Journal of Medicine (1 paper)Journal of Medical Genetics (1 paper)Journal of Pediatric Surgery (1 paper)European Journal of Pediatrics (1 paper)American Journal of Medical Genetics (1 paper)
- Partner nations
- NetherlandsBelgium
In The Last Decade
C. Schaap
8 papers receiving 183 citations
Peers
Comparison fields: 5 of 40
- Endocrinology, Diabetes and Metabolism 67
- Genetics 88
- Epidemiology 52
- Neurology 21
- Genetics 12
Countries citing papers authored by C. Schaap
This map shows the geographic impact of C. Schaap'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 C. Schaap with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. Schaap more than expected).
Fields of papers citing papers by C. Schaap
This network shows the impact of papers produced by C. Schaap. 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 C. Schaap. The network helps show where C. Schaap may publish in the future.
Co-authors
The 24 scholars most cited alongside C. Schaap, 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 | 1996 | 51 | |
| 2 | 2000 | 46 | |
| 3 | 1999 | 45 | |
| 4 | Opitz-C syndrome: on the nosology of mental retardation and trigonocephaly. | 1992 | 19 |
| 5 | 1992 | 14 | |
| 6 | Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes: are they related? | 1998 | 9 |
| 7 | [A Dutch family with hereditary joint symptoms; multiple epiphyseal dysplasia]. | 1993 | 3 |
| 8 | 1999 | 2 |
About C. Schaap
C. Schaap is a scholar working on Genetics, Molecular Biology, Rheumatology, Endocrinology, Diabetes and Metabolism and Surgery, having authored 8 papers that have together received 189 indexed citations. Recurring topics across this work include Hedgehog Signaling Pathway Studies (2 papers), Thyroid Cancer Diagnosis and Treatment (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Soft tissue tumor case studies (1 paper), Dermatological and Skeletal Disorders (1 paper), Connective tissue disorders research (1 paper), Genetic and Kidney Cyst Diseases (1 paper) and Cancer-related Molecular Pathways (1 paper). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (67 citations), Genetics (88 citations), Epidemiology (52 citations), Neurology (21 citations) and Genetics (12 citations). C. Schaap has collaborated with scholars based in Netherlands and Belgium. Frequent co-authors include C. T. R. M. Schrander‐Stumpel, G.J.C.M. van Buggenhout, Maureen Holvoet, Ben C.J. Hamel, J P Fryns, L.W. Ernest van Heurn, Erik Heineman, Willem J.M. Gerver, Gerard Freling and J. P. Fryns. Their work appears in journals such as The American Journal of Medicine, Journal of Medical Genetics, Journal of Pediatric Surgery, European Journal of Pediatrics and American Journal of Medical 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.