Evidence map›Paper›PMID 31382694›Full record

ArticleCancers2019

Families with BAP1-Tumor Predisposition Syndrome in The Netherlands: Path to Identification and a Proposal for Genetic Screening Guidelines.

Cindy Chau, Remco van Doorn, Natasha M van Poppelen, Nienke van der Stoep, Arjen R Mensenkamp, Rolf H Sijmons, Barbara W van Paassen, Ans M W van den Ouweland, Nicole C Naus, Annemieke H van der Hout and 10 more

Abstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
–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

36 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Hereditary Renal Cancer Syndromes.Medical sciences (Basel, Switzerland) · 2024
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Medical and Surgical Care of Patients With Mesothelioma and Their Relatives Carrying Germline BAP1 Mutations.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2022
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Cindy ChauDepartment of Ophthalmology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID 0000-0003-0660-6268
Remco van DoornDepartment of Dermatology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Natasha M van PoppelenDepartment of Clinical Genetics, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
Nienke van der StoepDepartment of Clinical Genetics, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Arjen R MensenkampDepartment of Clinical Genetics, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.ORCID 0000-0003-3805-877X
Rolf H SijmonsDepartment of Genetics, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
Barbara W van PaassenDepartment of Clinical Genetics, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
Ans M W van den OuwelandDepartment of Clinical Genetics, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
Nicole C NausDepartment of Ophthalmology, Erasmus Medical Center, 3015 GD Rotterdam, The Netherlands.
Annemieke H van der HoutDepartment of Genetics, University Medical Center Groningen, 9713 GZ Groningen, The Netherlands.
Thomas P PotjerDepartment of Clinical Genetics, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Fonnet E BleekerDepartment of Clinical Genetics, Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands.
Marijke R WeversDepartment of Clinical Genetics, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Liselotte P van HestDepartment of Clinical Genetics, Amsterdam University Medical Centers, 1081 HV Amsterdam, The Netherlands.
Marjolijn C J JongmansDepartment of Clinical Genetics, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Marina MarinkovicDepartment of Ophthalmology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Jaco C BleekerDepartment of Ophthalmology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Martine J JagerDepartment of Ophthalmology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID 0000-0003-2261-3820
Gregorius P M LuytenDepartment of Ophthalmology, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Maartje NielsenDepartment of Clinical Genetics, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands. m.nielsen@lumc.nl.

Funding

Algemene Nederlandse Vereniging ter voorkoming van Blindheid UitZicht 2018-3Landelijke Stichting voor Blinden en Slechtzienden UitZicht 2018-3Oogfonds 2018-11Wealtheon x
6 · The paper itself

Abstract

Germline pathogenic variants in the BRCA1-associated protein-1 (

Indexed as

BAP1BAP1 tumor predisposition syndromegermlinereferral guidelines

Identifiers

PMID31382694
PMCPMC6721807

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.