C. Schaap

676 total citations
8 papers, 189 citations indexed

About

C. Schaap is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, C. Schaap has authored 8 papers receiving a total of 189 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Rheumatology. Recurrent topics in C. Schaap's work include Hedgehog Signaling Pathway Studies (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Thyroid Cancer Diagnosis and Treatment (2 papers). C. Schaap is often cited by papers focused on Hedgehog Signaling Pathway Studies (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Thyroid Cancer Diagnosis and Treatment (2 papers). C. Schaap collaborates with scholars based in Netherlands and Belgium. C. Schaap's co-authors include C. T. R. M. Schrander‐Stumpel, Maureen Holvoet, J P Fryns, G.J.C.M. van Buggenhout, Ben C.J. Hamel, Gerard Freling, J. P. Fryns, Willem J.M. Gerver, L.W. Ernest van Heurn and Erik Heineman and has published in prestigious journals such as The American Journal of Medicine, Journal of Medical Genetics and Journal of Pediatric Surgery.

In The Last Decade

C. Schaap

8 papers receiving 183 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
C. Schaap Netherlands	6	88	67	61	52	44	8	189
Myriam Rosenberg‐Bourgin France	5	87 1.0×	160 2.4×	116 1.9×	70 1.3×	146 3.3×	11	406
Masashi Kitagawa Japan	8	39 0.4×	49 0.7×	104 1.7×	17 0.3×	47 1.1×	21	234
Cristina Ghervan Romania	9	132 1.5×	132 2.0×	119 2.0×	28 0.5×	55 1.3×	30	360
Jacquelyn Roberson United States	10	223 2.5×	75 1.1×	151 2.5×	43 0.8×	28 0.6×	18	341
Heiko Schweizer Germany	5	69 0.8×	53 0.8×	103 1.7×	34 0.7×	41 0.9×	5	222
Hongyi Deng China	6	201 2.3×	36 0.5×	135 2.2×	20 0.4×	19 0.4×	7	336
Amandine Septier France	8	82 0.9×	87 1.3×	114 1.9×	14 0.3×	63 1.4×	12	273
Clemens Freiberg Germany	10	124 1.4×	66 1.0×	134 2.2×	18 0.3×	65 1.5×	15	287
Hye‐Young Nam South Korea	8	81 0.9×	30 0.4×	78 1.3×	14 0.3×	82 1.9×	11	220
M.-H. Quentien France	8	73 0.8×	134 2.0×	107 1.8×	8 0.2×	25 0.6×	11	231

Countries citing papers authored by C. Schaap

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of C. Schaap

This figure shows the co-authorship network connecting the top 25 collaborators of C. Schaap. A scholar is included among the top collaborators of C. Schaap based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with C. Schaap. C. Schaap is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

1.

Buggenhout, G.J.C.M. van, et al.. (2000). Cri du chat syndrome: Changing phenotype in older patients. American Journal of Medical Genetics. 90(3). 203–215. 46 indexed citations

2.

Heurn, L.W. Ernest van, et al.. (1999). Predictive DNA testing for multiple endocrine neoplasia 2: A therapeutic challenge of prophylactic thyroidectomy in very young children. Journal of Pediatric Surgery. 34(4). 568–571. 45 indexed citations

3.

Schaap, C., et al.. (1999). Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?. Journal of Medical Genetics. 36(6). 481–484. 2 indexed citations

4.

Schaap, C., M.P.M. ten Tusscher, J. J. P. Schrander, R. H. Kuijten, & C. T. R. M. Schrander‐Stumpel. (1998). Phenotypic overlap between McKusick-Kaufman and Bardet-Biedl syndromes: are they related?. PubMed. 157(2). 170–1. 9 indexed citations

5.

Landsvater, Rudy M., C. Schaap, Geert H. Blijham, et al.. (1996). Familial medullary thyroid carcinoma: Not a distinct entity? Genotype-phenotype correlation in a large family. The American Journal of Medicine. 101(6). 635–641. 51 indexed citations

6.

Schaap, C., et al.. (1993). [A Dutch family with hereditary joint symptoms; multiple epiphyseal dysplasia].. PubMed. 137(1). 32–6. 3 indexed citations

7.

Schaap, C., Christine de Die‐Smulders, R. H. Kuijten, & J. P. Fryns. (1992). McKusick-Kaufman syndrome: The diagnostic challenge of abdominal distension in the neonatal period. European Journal of Pediatrics. 151(8). 583–585. 14 indexed citations

8.

Schaap, C., C. T. R. M. Schrander‐Stumpel, & J. P. Fryns. (1992). Opitz-C syndrome: on the nosology of mental retardation and trigonocephaly.. PubMed. 3(4). 209–15. 19 indexed citations

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.

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