W.P. de Groot

684 total citations
25 papers, 494 citations indexed

About

W.P. de Groot is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, W.P. de Groot has authored 25 papers receiving a total of 494 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in W.P. de Groot's work include Skin and Cellular Biology Research (4 papers), Genetic and rare skin diseases. (4 papers) and Vascular Malformations and Hemangiomas (4 papers). W.P. de Groot is often cited by papers focused on Skin and Cellular Biology Research (4 papers), Genetic and rare skin diseases. (4 papers) and Vascular Malformations and Hemangiomas (4 papers). W.P. de Groot collaborates with scholars based in Netherlands and United Kingdom. W.P. de Groot's co-authors include A. C. Jöbsis, Ruth Sanger, J.W. Delleman, M.J. Woerdeman, P Fleury, B Verbeeten, Robert R. Kierland, John M. Opitz, R. R. Race and David Wise and has published in prestigious journals such as Gastroenterology, Clinica Chimica Acta and British Journal of Dermatology.

In The Last Decade

W.P. de Groot

24 papers receiving 437 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
W.P. de Groot Netherlands 15 217 154 143 126 84 25 494
M Tolksdorf Germany 13 112 0.5× 185 1.2× 32 0.2× 183 1.5× 31 0.4× 50 505
M Chaâbouni Tunisia 12 97 0.4× 108 0.7× 21 0.1× 133 1.1× 33 0.4× 43 369
Rita A. Monahan United States 5 104 0.5× 83 0.5× 20 0.1× 92 0.7× 78 0.9× 7 472
G. Cohnen Germany 13 69 0.3× 105 0.7× 21 0.1× 35 0.3× 25 0.3× 40 462
Alfred Grassegger Austria 11 45 0.2× 184 1.2× 36 0.3× 27 0.2× 43 0.5× 19 545
Dominick Amato Canada 10 200 0.9× 144 0.9× 150 1.0× 14 0.1× 13 0.2× 26 427
John R. Luckasen United States 7 35 0.2× 127 0.8× 21 0.1× 39 0.3× 20 0.2× 9 387
Raleigh Hankins Japan 12 33 0.2× 120 0.8× 104 0.7× 27 0.2× 117 1.4× 18 538
H Høyer Denmark 9 17 0.1× 62 0.4× 63 0.4× 77 0.6× 46 0.5× 15 336
Elena Schnabel‐Besson Germany 8 63 0.3× 348 2.3× 69 0.5× 110 0.9× 14 0.2× 17 582

Countries citing papers authored by W.P. de Groot

Since Specialization
Citations

This map shows the geographic impact of W.P. de Groot'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 W.P. de Groot with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites W.P. de Groot more than expected).

Fields of papers citing papers by W.P. de Groot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by W.P. de Groot. 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 W.P. de Groot. The network helps show where W.P. de Groot may publish in the future.

Co-authorship network of co-authors of W.P. de Groot

This figure shows the co-authorship network connecting the top 25 collaborators of W.P. de Groot. A scholar is included among the top collaborators of W.P. de Groot 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 W.P. de Groot. W.P. de Groot is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Pope, F M, et al.. (1992). Clinical features of an affected father and daughter with Ehlers-Danlos syndrome type VIIB. British Journal of Dermatology. 126(1). 77–82. 12 indexed citations
2.
Fleury, P, K. P. Dingemans, W.P. de Groot, et al.. (1986). Ito's hypomelanosis (incontinentia pigmenti achromians). Clinical Neurology and Neurosurgery. 88(1). 39–44. 14 indexed citations
3.
Groot, W.P. de, et al.. (1980). Sex-linked ichthyosis and placental sulphatase C deficiency. British Journal of Dermatology. 103(1). 73–79. 14 indexed citations
4.
Leschot, N. J., et al.. (1980). Severe congenital skin defects in a newborn. European Journal of Obstetrics & Gynecology and Reproductive Biology. 10(6). 381–388. 28 indexed citations
5.
Fleury, P, et al.. (1980). Tuberous sclerosis: The incidence of sporadic cases versus familial cases. Brain and Development. 2(2). 107–117. 47 indexed citations
6.
Fleury, P, et al.. (1980). Tuberous sclerosis: The incidence of sporadic cases versus familial cases. Clinical Neurology and Neurosurgery. 82(3). 210–210. 1 indexed citations
7.
Groot, W.P. de, et al.. (1980). Familial acrogeria (Gottron). British Journal of Dermatology. 103(2). 213–223. 26 indexed citations
8.
Groot, W.P. de, et al.. (1978). X-linked icthyosis. A sulphatase deficiency.. Archives of Disease in Childhood. 53(10). 803–806. 75 indexed citations
9.
Tytgat, G. N. J., S. Surachno, W.P. de Groot, & P T Schellekens. (1977). A Case of Chronic Oropharyngo-Esophageal Candidiasis with Immunological Deficiency: Successful Treatment with Miconazole. Gastroenterology. 72(3). 536–540. 15 indexed citations
10.
Groot, W.P. de & J. Wuite. (1974). Livedo Racemosa-Like Photosensitivity Reaction during Quinidine Durettes Medication. Dermatology. 148(6). 371–376. 4 indexed citations
11.
Rietra, P. J. G. M., J. M. Tager, & W.P. de Groot. (1972). Detection of fabry hemizygotes and heterozygotes by measurement of α-galactosidase in urine. Clinica Chimica Acta. 40(1). 229–235. 15 indexed citations
12.
Groot, W.P. de, et al.. (1971). Ocular manifestations in angiokeratoma corporis diffusum (Fabry).. British Journal of Ophthalmology. 55(10). 683–692. 15 indexed citations
13.
Groot, W.P. de. (1970). FABRY'S DISEASE IN CHILDREN. British Journal of Dermatology. 82(4). 329–332. 5 indexed citations
14.
Visser, S.L. & W.P. de Groot. (1970). Electroencephalographic and Electromyographic Changes in a Case of Angiokeratoma corporis diffusum (Fabry's Disease). Stereotactic and Functional Neurosurgery. 32(1). 25–32. 8 indexed citations
15.
Groot, W.P. de. (1968). Provisional Results of Treatment of the Mélanose précancéreuse circonscrite Dubreuilh by Bucky-Rays. Dermatology. 136(5). 429–431. 13 indexed citations
16.
Ruiter, M. & W.P. de Groot. (1967). Methods of Demonstration of Lipid Deposits in Angiokeratoma Corporis Diffusum. Dermatology. 135(1). 75–83. 3 indexed citations
17.
Opitz, John M., David Wise, R. R. Race, et al.. (1965). The Genetics of Angiokeratoma Corporis Diffusum (Fabry's Disease) and Its Linkage Relations with the Xg Locus.. PubMed. 17(4). 325–42. 74 indexed citations
18.
19.
Groot, W.P. de. (1964). Angiokeratoma corporis diffusum Fabry (Thesaurismosis hereditaria Ruiter-Pompen-Wyers). Dermatology. 128(5). 321–349. 40 indexed citations
20.
Groot, W.P. de, et al.. (1963). The Value of Grenz-Ray Therapy for Acne Vulgaris. Dermatology. 126(5). 319–325. 2 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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