P.M. Steijlen
Impact in
- Dermatology top 5%
- Cancer and Skin Lesions
- Dermatologic Treatments and Research
-
- Genetic and rare skin diseases.
Papers in
- Genetics 7
- Genetic and rare skin diseases. 4
- Connective tissue disorders research 2
- Dermatological and Skeletal Disorders 2
-
- Connexins and lens biology 2
- Co-authors
- Maurice A. M. Van Steensel (7 shared papers)E. Scheffer (1 shared paper)Jo Hermans (1 shared paper)W. Bergman (1 shared paper)D. J. Ruiter (1 shared paper)Michel van Geel (3 shared papers)Huckaby Lewis (1 shared paper)Conrad P. Glade (1 shared paper)
- Journals
- Dermatology (2 papers)British Journal of Dermatology (2 papers)Histopathology (1 paper)Human Molecular Genetics (1 paper)American Journal of Medical Genetics Part A (3 papers)
- Partner nations
- NetherlandsSwitzerlandHungary
In The Last Decade
P.M. Steijlen
18 papers receiving 299 citations
Peers
Comparison fields: 5 of 58
- Dermatology 84
- Genetics 142
- Cell Biology 66
- Oncology 83
- Molecular Biology 116
Countries citing papers authored by P.M. Steijlen
This map shows the geographic impact of P.M. Steijlen'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 P.M. Steijlen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P.M. Steijlen more than expected).
Fields of papers citing papers by P.M. Steijlen
This network shows the impact of papers produced by P.M. Steijlen. 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 P.M. Steijlen. The network helps show where P.M. Steijlen may publish in the future.
Co-authors
The 25 scholars most cited alongside P.M. Steijlen, 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 | 1999 | 108 | |
| 2 | 1988 | 48 | |
| 3 | 2014 | 31 | |
| 4 | 2010 | 26 | |
| 5 | [CHILD syndrome in a mother and daughter]. | 1990 | 19 |
| 6 | Hypotrichosis, lymphedema of the legs and acral telangiectasias--new syndrome? | 2001 | 17 |
| 7 | 2005 | 16 | |
| 8 | 1995 | 11 | |
| 9 | 2009 | 10 | |
| 10 | 2009 | 8 | |
| 11 | 2009 | 5 | |
| 12 | Further delineation of the hypotrichosis-deafness syndrome. | 2006 | 5 |
| 13 | 2000 | 4 | |
| 14 | Ehlers-Danlos syndroom IV: variatie in fenotypen | 1997 | 3 |
| 15 | 2007 | 3 | |
| 16 | [Pigmented vascular phakomatosis]. | 1990 | 2 |
| 17 | Het congenitale angiodysplasiesyndroom van het type Klippel-Trenaunay; medische en psychologische aspecten | 1997 | 1 |
| 18 | [From gene to disease; cutaneous leiomyomatosis]. | 2007 | 1 |
| 19 | 2008 | 0 |
About P.M. Steijlen
P.M. Steijlen is a scholar working on Genetics, Molecular Biology, Oncology, Surgery and Dermatology, having authored 19 papers that have together received 318 indexed citations. Recurring topics across this work include Genetic and rare skin diseases. (4 papers), Vascular Malformations and Hemangiomas (3 papers), Cancer and Skin Lesions (3 papers), Bone and Dental Protein Studies (2 papers), Connective tissue disorders research (2 papers), Dermatological and Skeletal Disorders (2 papers), Diagnosis and Treatment of Venous Diseases (2 papers) and Connexins and lens biology (2 papers). The work is most often cited by research in Dermatology (84 citations), Genetics (142 citations), Cell Biology (66 citations), Oncology (83 citations) and Molecular Biology (116 citations). P.M. Steijlen has collaborated with scholars based in Netherlands, Switzerland and Hungary. Frequent co-authors include Maurice A. M. Van Steensel, E. Scheffer, Jo Hermans, W. Bergman, D. J. Ruiter, Michel van Geel, Huckaby Lewis, Conrad P. Glade, Jonathan L. Rees and Peter Itin. Their work appears in journals such as Dermatology, British Journal of Dermatology, Histopathology, Human Molecular Genetics and American Journal of Medical Genetics Part A.
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.