C. Schaap
Impact in
-
- Thyroid Cancer Diagnosis and Treatment
-
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Craniofacial Disorders and Treatments
Papers in
- Genetics 5
- Genomic variations and chromosomal abnormalities 2
- Genomics and Rare Diseases 1
- Genetics and Neurodevelopmental Disorders 1
- Genetic Syndromes and Imprinting 1
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- Thyroid Cancer Diagnosis and Treatment 3
- Co-authors
- C. T. R. M. Schrander‐Stumpel (2 shared papers)G.J.C.M. van Buggenhout (1 shared paper)Ben C.J. Hamel (1 shared paper)J P Fryns (1 shared paper)Maureen Holvoet (1 shared paper)J. P. Fryns (1 shared paper)R. H. Kuijten (2 shared papers)Rudy M. Landsvater (1 shared paper)
- Journals
- Journal of Pediatric Surgery (1 paper)The American Journal of Medicine (1 paper)European Journal of Pediatrics (1 paper)Journal of Medical Genetics (1 paper)American Journal of Medical Genetics (1 paper)
- Partner nations
- NetherlandsGermanyBelgium
In The Last Decade
C. Schaap
8 papers receiving 204 citations
Peers
Comparison fields: 5 of 44
- Endocrinology, Diabetes and Metabolism 76
- Genetics 84
- Neurology 21
- Epidemiology 42
- Urology 7
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 | 60 | |
| 2 | 2000 | 50 | |
| 3 | 1999 | 49 | |
| 4 | 1992 | 20 | |
| 5 | Opitz-C syndrome: on the nosology of mental retardation and trigonocephaly. | 1992 | 20 |
| 6 | Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes: are they related? | 1998 | 11 |
| 7 | [A Dutch family with hereditary joint symptoms; multiple epiphyseal dysplasia]. | 1993 | 3 |
| 8 | 1999 | 2 | |
| 9 | Handboek psychologische interventies bij chronisch-somatische aandoeningen. | 2004 | 1 |
| 10 | 2015 | 0 |
About C. Schaap
C. Schaap is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism, Molecular Biology, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 10 papers that have together received 216 indexed citations. Recurring topics across this work include Thyroid Cancer Diagnosis and Treatment (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Metalloenzymes and iron-sulfur proteins (1 paper), Mental Health and Psychiatry (1 paper), Genomics and Rare Diseases (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Childhood Cancer Survivors' Quality of Life (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (76 citations), Genetics (84 citations), Neurology (21 citations), Epidemiology (42 citations) and Urology (7 citations). C. Schaap has collaborated with scholars based in Netherlands, Germany and Belgium. Frequent co-authors include C. T. R. M. Schrander‐Stumpel, G.J.C.M. van Buggenhout, Ben C.J. Hamel, J P Fryns, Maureen Holvoet, J. P. Fryns, R. H. Kuijten, Rudy M. Landsvater, Erik Heineman and Gerard Freling. Their work appears in journals such as Journal of Pediatric Surgery, The American Journal of Medicine, European Journal of Pediatrics, Journal of Medical Genetics 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.