Evidence map›Paper›PMID 36341503›Full record

ArticleNeuropathology and applied neurobiology2023

Recurrent posterior fossa group A (PFA) ependymoma in a young child with constitutional mismatch repair deficiency (CMMRD).

Mayen Briggs, Anirban Das, Helen Firth, Adrian Levine, Santiago Sánchez-Ramírez, Logine Negm, Ayse B Ercan, Jill Chung, Vanessa Bianchi, Ibrahim Jalloh and 10 more

Open access · hybridAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Neuropathology and applied neurobiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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  5. Update on Cancer Predisposition Syndromes and Surveillance Guidelines for Childhood Brain Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
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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 at 5 institutions in 2 countries.

Mayen BriggsDepartment of Neuropathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Anirban DasThe International Replication Repair Deficiency Consortium (IRRDC), Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada.
Helen FirthDepartment of Genetics, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Adrian LevineThe International Replication Repair Deficiency Consortium (IRRDC), Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada.
Santiago Sánchez-RamírezThe International Replication Repair Deficiency Consortium (IRRDC), Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada.
Logine NegmThe International Replication Repair Deficiency Consortium (IRRDC), Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada.
Ayse B ErcanThe International Replication Repair Deficiency Consortium (IRRDC), Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada.
Jill ChungThe International Replication Repair Deficiency Consortium (IRRDC), Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada.
Vanessa BianchiThe International Replication Repair Deficiency Consortium (IRRDC), Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada.
Ibrahim JallohDepartment of Neurosurgery, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Poe PhyuDepartment of Radiology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Nicky ThorpDepartment of Radiation Oncology, The Christie Proton Beam Therapy Centre, Manchester, UK.
Richard G GrundyChildren's Brain Tumour Research Centre, Biodiscovery Unit, University of Nottingham, Nottingham, UK.
Cynthia HawkinsDivision of Neuropathology, The Hospital for Sick Children, Toronto, ON, Canada.
Jamie TrotmanEast-Genomics Laboratory Hub (GLH) Genetics Laboratory, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Patrick TarpeyEast-Genomics Laboratory Hub (GLH) Genetics Laboratory, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Uri TaboriThe International Replication Repair Deficiency Consortium (IRRDC), Division of Haematology/Oncology, The Hospital for Sick Children, Toronto, ON, Canada.
Kieren AllinsonDepartment of Neuropathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Matthew J MurrayDepartment of Pathology, University of Cambridge, Cambridge, UK.ORCID https://orcid.org/0000-0002-4480-1147
Genomics England Research Consortium
Hospital for Sick Children · CACambridge University Hospitals NHS Foundation Trust · GBProton (United Kingdom) · GBUniversity of Cambridge · GBUniversity of Nottingham · GB

Funding

Cancer Research UKHold'em for Life FoundationKai Slockers Pediatric Cancer Research FundMedical Research CouncilNational Institute for Health and Care ResearchNHS EnglandNIHR Cambridge Biomedical Research Centre BRC-1215-20014Stand Up To Cancer Maverick AwardSt Baldrick's Foundation International Scholars ProgramThe Wellcome Trust
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Brain NeoplasmsColorectal NeoplasmsEpendymomaNeoplastic Syndromes, HereditaryChildHumansMutationCMMRDcongenital mismatch repair deficiencyependymomaLynch syndromePMS2

Identifiers

PMID36341503
PMCPMC10099894
OpenAlexW4308372087

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.