Rein P. Stulp

2.4k citations

20 papers · 1.8k indexed · 1 hit paper · h-index 14

Endocrinology, Diabetes and Metabolism top 2%
- Thyroid Cancer Diagnosis and Treatment 3
Neurology top 5%
- Neuroblastoma Research and Treatments 2
Cell Biology top 5%
- Skin and Cellular Biology Research 3
Genetics top 5%
- Neurogenetic and Muscular Disorders Research 2
Genetics top 10%
- Neurogenetic and Muscular Disorders Research 2
Pathology and Forensic Medicine
- Genetic factors in colorectal cancer 5
- Autoimmune Bullous Skin Diseases 2
Epidemiology
- Neuroendocrine Tumor Research Advances 2
Cancer Research
- Cancer, Hypoxia, and Metabolism 2

Co-authors: Robert M.W. Hofstra Charles H.C.M. Buys Tineke Stelwagen Rudy M. Landsvater Isabella Ceccherini Barbara Pasini Jo W.M. Höppener Yin Luo
Cited by: Endocrinology, Diabetes and Metabolism Neurology Cell Biology
Journals: Human Genetics (3 papers)Nature Genetics (1 paper)European Journal of Human Genetics (1 paper)
Partner nations: Netherlands Germany Denmark

In The Last Decade

Rein P. Stulp

20 papers receiving 1.8k citations

Hit Papers

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Peers

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

The 25 scholars most cited alongside Rein P. Stulp, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Rein P. Stulp Line = papers co-authored together Rein P. Stulp links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome Hereditary Cancer in Clinical Practice ·E. van Riel,Margreet G.E.M. Ausems,Frans B.L. Hogervorst,Irma Kluijt,Mariëlle van Gijn,J. L. Boettinger,G Madhubala,David M. Candelario,Rein P. Stulp,Yvonne J. Vos,G. Johan A. Offerhaus,Fred H. Menko,Gilles Thomas	2010	16
2	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 ·Rein P. Stulp,Johanna C. Herkert,Arend Karrenbeld,Maxwell Standen,Yvonne J. Vos,Rolf H. Sijmons	2008	21
3	First report of ade novogermline mutation in theMLH1gene World Journal of Gastroenterology ·Rein P. Stulp	2006	8
4	Clinical Vignette: Early-Onset Head and Neck Cancer: Beware of Fanconi Anaemia! Hereditary Cancer in Clinical Practice ·Rolf H. Sijmons,Rein P. Stulp	2004	1
5	Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS Neurology ·Jan H. Veldink,Leonard H. van den Berg,J. M. Cobben,Rein P. Stulp,J.M.B.V. de Jong,O.J.M. Vogels,Frank Baas,J.H.J. Wokke,Hans Scheffer	2001	80
6	SMA carrier testing – validation of hemizygous SMN exon 7 deletion test for the identification of proximal spinal muscular atrophy carriers and patients with a single allele deletion European Journal of Human Genetics ·Hans Scheffer,Frank Ndaks Ndakala,Rob G.J. Mensink,Rein P. Stulp,Gerrit van der Steege,Charles H.C.M. Buys	2000	42
7	RET andGDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems Human Mutation ·Robert M.W. Hofstra,Ying Wu,Rein P. Stulp,Peter Elfferich,B. A. Nadkarni,Nejc Krušnik,Liesbeth Siderius,Tomás Echarri,Ιωάννης Λιόντος,Vera M. R. Heydendael,H. Overhof,Dudley Hoys,Carel Meijers,C.H.C.M. Buys	2000	70
8	Implications of intragenic marker homozygosity and haplotype sharing in a rare autosomal recessive disorder: the example of the collagen type XVII (COL17A1) locus in generalised atrophic benign epidermolysis bullosa Human Genetics ·Hans Scheffer,Rein P. Stulp,Edwin Verlind,Merel van der Meulen,Leena Bruckner‐Tuderman,Tobias Gedde‐Dahl,G.J. te Meerman,Arnoud Sonnenberg,Charles H.C.M. Buys,Marcel F. Jonkman	1997	14
9	Revertant Mosaicism in Epidermolysis Bullosa Caused by Mitotic Gene Conversion Cell ·Marcel F. Jonkman,Hans Scheffer,Rein P. Stulp,Hendri H. Pas,Miranda Nijenhuis,K Heeres,Katsushi Owaribe,Leena Pulkkinen,Jouni Uitto	1997	196
10	Absence of mutations in the RET gene in acute myeloid leukemia Annals of Hematology ·L. A. Higgs,Robert M.W. Hofstra,Rein P. Stulp,Ying Wu,C.H.C.M. Buys,Roel Willemze,J. E. Landegent	1997	12
11	No mutations found byRET mutation scanning in sporadic and hereditary neuroblastoma Human Genetics ·Robert M.W. Hofstra,Rein P. Stulp,Kimball Robert Murphy-Stewart,A Klepke,Ngan Ching Cheng,S. Dufour,Jorge Ramos Avalos,Rogier Versteeg,Claus Thustrup Hansen,Niels Tommerup,Niels Clausen	1996	23
12	No mutations found by RET mutation scanning in sporadic and hereditary neuroblastoma Human Genetics ·Robert M.W. Hofstra,N C Cheng,Claus Thustrup Hansen,Rein P. Stulp,Tineke Stelwagen,Niels Clausen,Niels Tommerup,Hubert Caron,A. Westerveld,Rogier Versteeg,Samuel Gilliéron	1996	3
13	A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome) Nature Genetics ·Robert M.W. Hofstra,B. A. Nadkarni,Gita Tan-Sindhunata,Ying Wu,Christoph D. Kacir,Rein P. Stulp,Conny M.A. van Ravenswaaij‐Arts,Daniëlle Majoor‐Krakauer,Misha Angrist,Aravinda Chakravarti,Carel Meijers,Charles H.C.M. Buys	1996	231
14	RET Mutation Screening in Familial Cutaneous Lichen Amyloidosis and in Skin Amyloidosis Associated With Multiple Endocrine Neoplasia Journal of Investigative Dermatology ·Robert M.W. Hofstra,Rolf H. Sijmons,Kimball Robert Murphy-Stewart,Rein P. Stulp,C.H.C.M. Buys,Boris G. Kousseff,Hécate Torres Angenot,Peter M. Steijlen,Pieter C. van Voorst Vader	1996	39
15	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 ·Robert M.W. Hofstra,Tineke Stelwagen,Rein P. Stulp,Diederick De Jong,Miriam Hulsbeek,Erik-Jan Kamsteeg,Anke van den Berg,Rudy M. Landsvater,A Vermey,W. M. Molenaar,C.J.M. Lips,Samuel Gilliéron	1996	66
16	Hereditary myokymia and paroxysmal ataxia linked to chromosome 12 is responsive to acetazolamide. Journal of Neurology Neurosurgery & Psychiatry ·Lorena Patricia Peña,E. R. Brunt,Hans Scheffer,M. Litt,Rein P. Stulp,D.L. Browne,Tiemen W. van Weerden	1995	54
17	RET mutations in MEN 2 associated diseases The American Journal of Human Genetics ·Robert M.W. Hofstra,Tineke Stelwagen,Rein P. Stulp	1994	8
18	A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinomabreakdown → Nature ·Robert M.W. Hofstra,Rudy M. Landsvater,Isabella Ceccherini,Rein P. Stulp,Tineke Stelwagen,Yin Luo,Barbara Pasini,Jo W.M. Höppener,Hans Kristian Ploos van Amstel,Giovanni Romeo,Josefine Apell,Charles H.C.M. Buys	1994	872
19	A Mutation in the RET Protooncogene Associated with Multiple Endocrine Neoplasia Type 2B and Sporadic Medullary Thyroid Carcinoma The Endocrinologist ·T G Matthews,Rudy M. Landsvater,Isabella Ceccherini,Rein P. Stulp,Tineke Stelwagen,Yi Luo,Barbara Pasini,Manuel Escudero,Stefan Westius,Percival M. Dubasi,庞加光,Evelyn K. Stein	1994	49
20	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 ·Peter Reuvekamp,Rein P. Stulp,H. Schraffordt Koops,J. Wolter Oosterhuis,Hans Scheffer,Samuel Gilliéron	1992	2

About Rein P. Stulp

Rein P. Stulp is a scholar working on Pathology and Forensic Medicine, Genetics and Cancer Research, having authored 20 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (5 papers), Skin and Cellular Biology Research (3 papers), Thyroid Cancer Diagnosis and Treatment (3 papers), Neuroendocrine Tumor Research Advances (2 papers), Cancer, Hypoxia, and Metabolism (2 papers), Autoimmune Bullous Skin Diseases (2 papers), Neuroblastoma Research and Treatments (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (501 citations), Neurology (235 citations) and Cell Biology (242 citations). Rein P. Stulp has collaborated with scholars based in Netherlands, Germany and Denmark. Frequent 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. Their work appears in journals such as Human Genetics, Nature Genetics, European Journal of Human Genetics, Journal of Investigative Dermatology and Neurology.

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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