Evidence map›Paper›PMID 37770543›Full record

ArticleScientific reports2023

Publisher Correction: Whole genome sequencing resolves 10 years diagnostic odyssey in familiar myxoma.

Sára Pálla, Judit Tőke, Anikó Bozsik, Henriett Butz, János Papp, István Likó, Enikő Kuroli, András Bánvölgyi, Mátyás Hamar, Jerome Bertherat and 2 more

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

Article in Scientific reports, 2023. 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
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.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Sára Pálla *Department of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Judit Tőke *Department of Internal Medicine and Oncology, Semmelweis University, Budapest, Hungary.
Anikó Bozsik *Department of Molecular Genetics, National Institute of Oncology, Ráth György U. 7-9, 1122, Budapest, Hungary.
Henriett ButzDepartment of Molecular Genetics, National Institute of Oncology, Ráth György U. 7-9, 1122, Budapest, Hungary.
János PappDepartment of Molecular Genetics, National Institute of Oncology, Ráth György U. 7-9, 1122, Budapest, Hungary.
István LikóHereditary Cancers Research Group, Eötvös Loránd Research Network, Semmelweis University, Budapest, Hungary.
Enikő KuroliDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
András BánvölgyiDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Mátyás HamarDepartment of Surgery, Transplantation and Gastroenterology, Semmelweis University, Budapest, Hungary.
Jerome BertheratUniversité Paris Cité, Institut Cochin, Inserm U1016, Paris, France.
Márta MedveczDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Attila PatócsENDO-ERN HCP Semmelweis University, Budapest, Hungary. patocs.attila@med.semmelweis-univ.hu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID37770543
PMCPMC10539426

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.