Evidence map›Paper›PMID 37377903›Full record

ArticleCancer research communications2023

Multiple Germline Events Contribute to Cancer Development in Patients with Li-Fraumeni Syndrome.

Vallijah Subasri, Nicholas Light, Nisha Kanwar, Jack Brzezinski, Ping Luo, Jordan R Hansford, Elizabeth Cairney, Carol Portwine, Christine Elser, Jonathan L Finlay and 15 more

Open access · goldAbstract read
In one paragraph

Article in Cancer research communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% of its field
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Guideline
  2. The Dynamic Alliance of p53 and Metabolism in the Tumor Microenvironment Shapes Tumor Evolution.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
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  4. Cancers · 2025
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Clustering ofiScience · 2024
    Article
  10. 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

25 authors at 13 institutions in 3 countries.

Vallijah SubasriDepartment of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-6584-877X
Nicholas LightProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0003-2021-3938
Nisha KanwarDepartment of Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0003-2829-7566
Jack BrzezinskiDivision of Haematology/Oncology, The Hospital for Sick Children, Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-9475-0077
Ping LuoPrincess Margaret Cancer Center, University Health Network, Toronto, Ontario, Canada.ORCID 0000-0002-0039-747X
Jordan R HansfordChildren's Cancer Centre, Royal Children's Hospital, Melbourne, Victoria, Australia.ORCID 0000-0001-7733-383X
Elizabeth CairneyDepartment of Paediatrics, London Health Sciences Centre and Western University, London, Ontario, Canada.ORCID 0000-0003-1569-8838
Carol PortwineDepartment of Paediatrics, McMaster University, Hamilton, Ontario, Canada.ORCID 0000-0002-1314-8691
Christine ElserDepartment of Medical Oncology, Princess Margaret Hospital and Mount Sinai Hospital, Toronto, Ontario, Canada.ORCID 0000-0003-0003-713X
Jonathan L FinlayNeuro-Oncology Program, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.ORCID 0000-0002-8312-6586
Kim E NicholsDepartment of Oncology, St Jude Children's Research Hospital, Memphis, Tennessee.ORCID 0000-0002-5581-6555
Noa AlonProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0001-9483-1785
Ledia BrungaProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0003-0343-937X
Jo AnsonHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah.ORCID 0000-0002-6847-6529
Wendy KohlmannHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah.ORCID 0000-0002-9134-9640
Kelvin C de AndradeClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, NCI, Bethesda, Maryland.ORCID 0000-0003-4651-996X
Payal P KhinchaClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, NCI, Bethesda, Maryland.ORCID 0000-0003-2473-7800
Sharon A SavageClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, NCI, Bethesda, Maryland.ORCID 0000-0001-6006-0740
Joshua D SchiffmanDepartment of Pediatrics, University of Utah, Salt Lake City, Utah.ORCID 0000-0002-6968-7694
Rosanna WeksbergProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0002-6501-4150
Trevor J PughDepartment of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-8073-5888
Anita VillaniDivision of Haematology/Oncology, The Hospital for Sick Children, Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0003-3283-2197
Adam ShlienProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0002-0368-5370
Anna GoldenbergProgram in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.ORCID 0000-0002-2416-833X
David MalkinDepartment of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0001-5752-9763
University of Toronto · CAHospital for Sick Children · CACancer Genetics (United States) · USUniversity of Utah · USHuntsman Cancer Institute · USMcMaster University · CAMount Sinai Hospital · CANationwide Children's Hospital · USOntario Institute for Cancer Research · CAPrincess Margaret Cancer Centre · CARoyal Children's Hospital · AUSt. Jude Children's Research Hospital · USWestern University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Li-Fraumeni syndrome (LFS) is an autosomal dominant cancer-predisposition disorder. Approximately 70% of individuals who fit the clinical definition of LFS harbor a pathogenic germline variant in the Significance: Our study clarifies the genomic basis for the phenotypic variability in LFS and highlights the immense benefits of expanding genetic and epigenetic testing of patients with LFS beyond

Indexed as

Li-Fraumeni SyndromeGenes, p53Genetic Predisposition to DiseaseGerm-Line MutationHumansTumor Suppressor Protein p53Tumor Suppressor Protein p53

Identifiers

PMID37377903
PMCPMC10150777
OpenAlexW4362577044

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.