Evidence map›Paper›PMID 34496934›Full record

ArticleHereditary cancer in clinical practice2021

Correction to: Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants.

Krithika Murali, Tanya M Dwarte, Mehrdad Nikfarjam, Katherine M Tucker, Rhys B Vaughan, Marios Efthymiou, Allison Collins, Allan D Spigelman, Lucinda Salmon, Amber L Johns and 4 more

Open access · goldAbstract readPublished Erratum
In one paragraph

Article in Hereditary cancer in clinical practice, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 86% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 7 institutions in 1 country.

Krithika MuraliDepartment of Clinical Genetics, Austin Health, Heidelberg, VIC, 3084, Australia.
Tanya M DwarteAustralian Pancreatic Cancer Genome Initiative, Garvan Institute of Medical Research, Darlinghurst, NSW, 2010, Australia.
Mehrdad NikfarjamDivision of Surgery, Austin Health, Heidelberg, VIC, 3084, Australia.
Katherine M TuckerHereditary Cancer Centre, Prince of Wales Hospital, Randwick, NSW, 2031, Australia.
Rhys B VaughanDepartment of Gastroenterology, Austin Health, Heidelberg, VIC, 3084, Australia.
Marios EfthymiouDepartment of Gastroenterology, Austin Health, Heidelberg, VIC, 3084, Australia.
Allison CollinsClinical Trials Unit, Olivia Newton John Cancer and Wellness Centre, Austin Health, Heidelberg, VIC, 3084, Australia.
Allan D SpigelmanUniversity of New South Wales, St Vincent's Clinical School and Prince of Wales Clinical School, Randwick, NSW, 2031, Australia.
Lucinda SalmonDepartment of Clinical Genetics, Austin Health, Heidelberg, VIC, 3084, Australia.
Amber L JohnsAustralian Pancreatic Cancer Genome Initiative, Garvan Institute of Medical Research, Darlinghurst, NSW, 2010, Australia.
David B WilliamsDepartment of Gastroenterology, St Vincent's Hospital, Darlinghurst, NSW, 2010, Australia.
Martin B DelatyckiDepartment of Clinical Genetics, Austin Health, Heidelberg, VIC, 3084, Australia.
Thomas JohnPeter MacCallum Cancer Centre, Parkville, VIC, 3000, Australia.
Alina StoitaDepartment of Gastroenterology, St Vincent's Hospital, Darlinghurst, NSW, 2010, Australia. alina.stoita@svha.org.au.
Austin Health · AUPrince of Wales Hospital · AUUNSW Sydney · AUGarvan Institute of Medical Research · AUOlivia Newton-John Cancer Wellness & Research Centre · AUPeter MacCallum Cancer Centre · AUSt Vincent's Hospital Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID34496934
PMCPMC8427826
OpenAlexW3198004058

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.