Rein P. Stulp

2.4k total citations · 1 hit paper
20 papers, 1.8k citations indexed

About

Rein P. Stulp is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Oncology. According to data from OpenAlex, Rein P. Stulp has authored 20 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Pathology and Forensic Medicine and 5 papers in Oncology. Recurrent topics in Rein P. Stulp's work include Genetic factors in colorectal cancer (5 papers), Skin and Cellular Biology Research (3 papers) and Thyroid Cancer Diagnosis and Treatment (3 papers). Rein P. Stulp is often cited by papers focused on Genetic factors in colorectal cancer (5 papers), Skin and Cellular Biology Research (3 papers) and Thyroid Cancer Diagnosis and Treatment (3 papers). Rein P. Stulp collaborates with scholars based in Netherlands, Germany and Denmark. Rein P. Stulp's co-authors include Robert M.W. Hofstra, Charles H.C.M. Buys, Tineke Stelwagen, Rudy M. Landsvater, Isabella Ceccherini, Barbara Pasini, Jo W.M. Höppener, Yin Luo, Giovanni Romeo and Hans Kristian Ploos van Amstel and has published in prestigious journals such as Nature, Cell and Nature Genetics.

In The Last Decade

Rein P. Stulp

20 papers receiving 1.8k citations

Hit Papers

A mutation in the RET proto-oncogene associated with mult... 1994 2026 2004 2015 1994 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma
    1994 872 citations Robert M.W. Hofstra, Rudy M. Landsvater et al. Nature profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rein P. Stulp Netherlands 14 767 544 501 405 312 20 1.8k
Griffith Harsh United States 18 742 1.0× 254 0.5× 576 1.1× 167 0.4× 273 0.9× 36 1.8k
Elena Arighi Italy 17 1.2k 1.5× 326 0.6× 515 1.0× 326 0.8× 682 2.2× 19 1.9k
J M Alexander United States 21 1.7k 2.2× 343 0.6× 966 1.9× 338 0.8× 194 0.6× 27 2.7k
Philippe Bertolino France 25 976 1.3× 421 0.8× 313 0.6× 272 0.7× 624 2.0× 56 2.1k
Laura Papi Italy 25 1.2k 1.5× 610 1.1× 791 1.6× 706 1.7× 766 2.5× 68 3.2k
A. Bardoel Netherlands 13 461 0.6× 326 0.6× 147 0.3× 466 1.2× 154 0.5× 14 1.3k
José M. de Campos Spain 30 985 1.3× 320 0.6× 144 0.3× 150 0.4× 274 0.9× 77 2.3k
Gianluca Marucci Italy 25 643 0.8× 355 0.7× 206 0.4× 101 0.2× 263 0.8× 121 2.0k
Lorin E. Olson United States 19 833 1.1× 202 0.4× 169 0.3× 222 0.5× 172 0.6× 31 1.6k
Ludmila Matyakhina United States 19 413 0.5× 636 1.2× 458 0.9× 195 0.5× 317 1.0× 29 1.7k

Countries citing papers authored by Rein P. Stulp

Since Specialization
Citations

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

Fields of papers citing papers by Rein P. Stulp

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rein P. Stulp. 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 Rein P. Stulp. The network helps show where Rein P. Stulp may publish in the future.

Co-authorship network of co-authors of Rein P. Stulp

This figure shows the co-authorship network connecting the top 25 collaborators of Rein P. Stulp. A scholar is included among the top collaborators of Rein P. Stulp 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 Rein P. Stulp. Rein P. Stulp 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.
Riel, E. van, Margreet G.E.M. Ausems, Frans B.L. Hogervorst, et al.. (2010). A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome. Hereditary Cancer in Clinical Practice. 8(1). 7–7. 16 indexed citations
2.
Stulp, Rein P., et al.. (2008). Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum. Hereditary Cancer in Clinical Practice. 6(1). 15–15. 21 indexed citations
3.
Stulp, Rein P.. (2006). First report of ade novogermline mutation in theMLH1gene. World Journal of Gastroenterology. 12(5). 809–809. 8 indexed citations
4.
Sijmons, Rolf H. & Rein P. Stulp. (2004). Clinical Vignette: Early-Onset Head and Neck Cancer: Beware of Fanconi Anaemia!. Hereditary Cancer in Clinical Practice. 2(3). 147–8. 1 indexed citations
5.
Veldink, Jan H., Leonard H. van den Berg, J. M. Cobben, et al.. (2001). Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS. Neurology. 56(6). 749–752. 80 indexed citations
6.
7.
Hofstra, Robert M.W., Ying Wu, Rein P. Stulp, et al.. (2000). RET andGDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems. Human Mutation. 15(5). 418–429. 70 indexed citations
8.
9.
Jonkman, Marcel F., Hans Scheffer, Rein P. Stulp, et al.. (1997). Revertant Mosaicism in Epidermolysis Bullosa Caused by Mitotic Gene Conversion. Cell. 88(4). 543–551. 196 indexed citations
10.
Hofstra, Robert M.W., Rein P. Stulp, Ying Wu, et al.. (1997). Absence of mutations in the RET gene in acute myeloid leukemia. Annals of Hematology. 75(3). 87–90. 12 indexed citations
11.
Hofstra, Robert M.W., Rein P. Stulp, Ngan Ching Cheng, et al.. (1996). No mutations found byRET mutation scanning in sporadic and hereditary neuroblastoma. Human Genetics. 97(3). 362–364. 23 indexed citations
12.
Hofstra, Robert M.W., N C Cheng, Claus Thustrup Hansen, et al.. (1996). No mutations found by RET mutation scanning in sporadic and hereditary neuroblastoma. Human Genetics. 97(3). 362–364. 3 indexed citations
13.
Hofstra, Robert M.W., Gita Tan-Sindhunata, Ying Wu, et al.. (1996). A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome). Nature Genetics. 12(4). 445–447. 231 indexed citations
14.
Hofstra, Robert M.W., Rolf H. Sijmons, Rein P. Stulp, et al.. (1996). RET Mutation Screening in Familial Cutaneous Lichen Amyloidosis and in Skin Amyloidosis Associated With Multiple Endocrine Neoplasia. Journal of Investigative Dermatology. 107(2). 215–218. 39 indexed citations
15.
Hofstra, Robert M.W., Tineke Stelwagen, Rein P. Stulp, et al.. (1996). Extensive mutation scanning of RET in sporadic medullary thyroid carcinoma and of RET and VHL in sporadic pheochromocytoma reveals involvement of these genes in only a minority of cases.. The Journal of Clinical Endocrinology & Metabolism. 81(8). 2881–2884. 66 indexed citations
16.
Brunt, E. R., Hans Scheffer, M. Litt, et al.. (1995). Hereditary myokymia and paroxysmal ataxia linked to chromosome 12 is responsive to acetazolamide.. Journal of Neurology Neurosurgery & Psychiatry. 59(4). 400–405. 54 indexed citations
17.
Hofstra, Robert M.W., Tineke Stelwagen, & Rein P. Stulp. (1994). RET mutations in MEN 2 associated diseases. The American Journal of Human Genetics. 55. 8 indexed citations
18.
Hofstra, Robert M.W., Rudy M. Landsvater, Isabella Ceccherini, et al.. (1994). A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma. Nature. 367(6461). 375–376. 872 indexed citations breakdown →
19.
Landsvater, Rudy M., Isabella Ceccherini, Rein P. Stulp, et al.. (1994). A Mutation in the RET Protooncogene Associated with Multiple Endocrine Neoplasia Type 2B and Sporadic Medullary Thyroid Carcinoma. The Endocrinologist. 4(3). 225–225. 49 indexed citations
20.
Stulp, Rein P., et al.. (1992). Analysis of a metastasizing testicular mixed gonadal stromal tumor with osteosarcoma components suggests that a malignant tumor with the histology of osteosarcoma may develop without primary involvement of RB1 and TP53.. PubMed. 52(23). 6705–7. 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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