Evidence map›Paper›PMID 38172175›Full record

ArticleEuropean journal of human genetics : EJHG2024

Publisher Correction: A 39 kb structural variant causing Lynch syndrome detected by optical genome mapping and nanopore sequencing.

Pål Marius Bjørnstad, Ragnhild Aaløkken, June Åsheim, Arvind Y M Sundaram, Caroline N Felde, G Henriette Østby, Marianne Dalland, Wenche Sjursen, Christian Carrizosa, Magnus D Vigeland and 5 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in European journal of human genetics : EJHG, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Pål Marius Bjørnstad *Department Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.ORCID http://orcid.org/0000-0001-6217-7467
Ragnhild Aaløkken *Department Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
June Åsheim *Department Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
Arvind Y M Sundaram *Department Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
Caroline N FeldeDepartment Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
G Henriette ØstbyDepartment Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
Marianne DallandDepartment Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.ORCID http://orcid.org/0000-0003-4105-1034
Wenche SjursenDepartment of Clinical & Molecular Medicine, NTNU and Department of Medical Genetics, St Olavs Hospital, Trondheim, Norway.
Christian CarrizosaDepartment Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
Magnus D VigelandDepartment Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
Hanne S SorteDepartment Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
Ying ShengDepartment Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
Sarah L AriansenDepartment Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
Eli Marie Grindedal *Department Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway.
Gregor D Gilfillan *Department Medical Genetics, Oslo University Hospital and University of Oslo, Oslo, Norway. gregorg@medisin.uio.no.ORCID http://orcid.org/0000-0001-8116-0134

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID38172175
PMCPMC11061170

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.