Evidence map›Paper›PMID 36833203›Full record

ArticleGenes2023

Molecular Genetic Characteristics of

Caitlin T Fierheller, Wejdan M Alenezi, Corinne Serruya, Timothée Revil, Setor Amuzu, Karine Bedard, Deepak N Subramanian, Eleanor Fewings, Jeffrey P Bruce, Stephenie Prokopec and 11 more

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

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. The Genetic and Molecular Analyses of Rare Candidate GermlineInternational journal of molecular sciences · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Most Fanconi anemia heterozygotes are not at increased cancer risk: A genome-first DiscovEHR cohort population study.Genetics in medicine : official journal of the American College of Medical Genetics · 2024
    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

21 authors at 10 institutions in 4 countries.

Caitlin T FierhellerDepartment of Human Genetics, McGill University, Montreal, QC H3A 0C7, Canada.
Wejdan M AleneziDepartment of Human Genetics, McGill University, Montreal, QC H3A 0C7, Canada.ORCID 0000-0002-2882-7267
Corinne SerruyaCancer Research Program, The Research Institute of the McGill University Health Centre, Montreal, QC H4A 3J1, Canada.
Timothée RevilDepartment of Human Genetics, McGill University, Montreal, QC H3A 0C7, Canada.ORCID 0000-0003-1210-7748
Setor AmuzuDepartment of Human Genetics, McGill University, Montreal, QC H3A 0C7, Canada.ORCID 0000-0003-3244-7475
Karine BedardLaboratoire de Diagnostic Moléculaire, Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, QC H2X 3E4, Canada.
Deepak N SubramanianCancer Genetics Laboratory, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia.
Eleanor FewingsDepartment of Medical Genetics, National Institute for Health Research Cambridge Biomedical Research Centre, University of Cambridge, Cambridge CB2 1TN, UK.
Jeffrey P BrucePrincess Margaret Cancer Centre, University Health Network, Toronto, ON M5G 2C1, Canada.ORCID 0000-0001-5509-9990
Stephenie ProkopecPrincess Margaret Cancer Centre, University Health Network, Toronto, ON M5G 2C1, Canada.ORCID 0000-0001-7936-8577
Luigi BouchardDepartment of Biochemistry and Functional Genomics, Université de Sherbrooke, Sherbrooke, QC J1K 2R1, Canada.
Diane ProvencherCentre de Recherche du Centre Hospitalier de l'Université de Montréal and Institut du Cancer de Montréal, Montreal, QC H2X 0A9, Canada.ORCID 0000-0003-1902-3256
William D FoulkesDepartment of Human Genetics, McGill University, Montreal, QC H3A 0C7, Canada.
Zaki El HaffafCentre de Recherche du Centre Hospitalier de l'Université de Montréal, Montreal, QC H2X 0A9, Canada.
Anne-Marie Mes-MassonCentre de Recherche du Centre Hospitalier de l'Université de Montréal and Institut du Cancer de Montréal, Montreal, QC H2X 0A9, Canada.ORCID 0000-0002-6498-266X
Marc TischkowitzDepartment of Medical Genetics, National Institute for Health Research Cambridge Biomedical Research Centre, University of Cambridge, Cambridge CB2 1TN, UK.ORCID 0000-0002-7880-0628
Ian G CampbellCancer Genetics Laboratory, Peter MacCallum Cancer Centre, Melbourne, VIC 3000, Australia.ORCID 0000-0002-7773-4155
Trevor J PughPrincess Margaret Cancer Centre, University Health Network, Toronto, ON M5G 2C1, Canada.ORCID 0000-0002-8073-5888
Celia M T GreenwoodDepartment of Human Genetics, McGill University, Montreal, QC H3A 0C7, Canada.ORCID 0000-0002-2427-5696
Jiannis RagoussisDepartment of Human Genetics, McGill University, Montreal, QC H3A 0C7, Canada.ORCID 0000-0002-8515-0934
Patricia N ToninDepartment of Human Genetics, McGill University, Montreal, QC H3A 0C7, Canada.
Centre Hospitalier de l’Université de Montréal · CAMcGill University Health Centre · CAMcGill Genome Centre · CAUniversity Health Network · CAUniversity of Cambridge · GBJewish General Hospital · CAPeter MacCallum Cancer Centre · AUTaibah University · SAThe University of Melbourne · AUUniversité de Sherbrooke · CA

Funding

CIHR MOP-115071CIHR PCC-156736CIHR PJT-152989CIHR PJT-156124Department of Health BRC-1215-20014
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Fanconi Anemia Complementation Group ProteinsGenetic Predisposition to DiseaseOvarian NeoplasmsFanconi AnemiaFemaleGenes, BRCA2HumansMolecular BiologyMutationFANCI protein, humanFanconi Anemia Complementation Group Proteinscancer predisposing geneFANCIFanconi anemia pathwayhereditary cancerovarian cancerTCGAwhole exome sequencing

Identifiers

PMID36833203
PMCPMC9956348
OpenAlexW4317930439

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.