Evidence map›Paper›PMID 24751729›Full record

ArticleThe Journal of investigative dermatology2014

Next-generation sequencing of nevus spilus-type congenital melanocytic nevus: exquisite genotype-phenotype correlation in mosaic RASopathies.

Veronica A Kinsler, Sven Krengel, Jean-Baptiste Riviere, Regula Waelchli, Carolina Chapusot, Lara Al-Olabi, Laurence Faivre, Holger A Haenssle, Lisa Weibel, Géraldine Jeudy and 1 more

Abstract readCase ReportsLetter
In one paragraph

Article in The Journal of investigative dermatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Long-term follow-up of congenital melanocytic nevi in a pediatric population: a retrospective study.Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo · 2025
    Article
  5. Nevus Spilus: A Review of Laser-Based Therapeutic Approaches.Acta informatica medica : AIM : journal of the Society for Medical Informatics of Bosnia & Herzegovina : casopis Drustva za medicinsku informatiku BiH · 2025
    Article
  6. Article
  7. Acne Syndromes and Mosaicism.Biomedicines · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Melanoma in congenital melanocytic naevi.The British journal of dermatology · 2017
    Review
  12. Article
  13. Article
  14. [Nevus spilus: An example of mosaic RASopathy].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2015
    Article
  15. Article
  16. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Veronica A KinslerClinical and Molecular Genetics Unit, UCL Institute of Child Health, London, UK; Paediatric Dermatology, Great Ormond St Hospital for Children, London, UK. Electronic address: v.kinsler@ucl.ac.uk.
Sven KrengelDepartment of Dermatology, University of Lübeck, Lübeck, Germany.
Jean-Baptiste RiviereDepartment of Molecular Genetics, Dijon University Hospital, Dijon, France.
Regula WaelchliPaediatric Dermatology, Great Ormond St Hospital for Children, London, UK.
Carolina ChapusotDepartment of Clinical Genetics, Dijon University Hospital, Dijon, France.
Lara Al-OlabiClinical and Molecular Genetics Unit, UCL Institute of Child Health, London, UK.
Laurence FaivreDepartment of Dermatology, Dijon University Hospital, Dijon, France.
Holger A HaenssleDepartment of Dermatology, University Medical Centre, Goettingen, Germany.
Lisa WeibelDepartment of Dermatology, University Children's Hospital, Zurich, Switzerland.
Géraldine JeudyDepartment of Dermatology, Dijon University Hospital, Dijon, France.
Pierre VabresDepartment of Dermatology, Dijon University Hospital, Dijon, France. Electronic address: pierre.vabres@chu-dijon.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

GenotypePhenotypeSequence Analysis, DNAAdolescentBase SequenceChildChild, PreschoolFemaleGenetic Predisposition to DiseaseGTP PhosphohydrolasesHumansInfantMaleMembrane ProteinsMiddle AgedMolecular Sequence DataGTP PhosphohydrolasesMembrane ProteinsNRAS protein, human

Identifiers

PMID24751729
PMCPMC4165863

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.