Evidence map›Paper›PMID 39256535›Full record

ArticleEuropean journal of human genetics : EJHG2024

Correction: Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlations.

Eva Vanbelleghem, Tim Van Damme, Aude Beyens, Sofie Symoens, Kathleen Claes, Julie De Backer, Ilse Meerschaut, Floris Vanommeslaeghe, Sigurd E Delanghe, Jenneke van den Ende and 23 more

Abstract readPublished Erratum
PubMed 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. 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

33 authors.

Eva Vanbelleghem *Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0000-0001-6380-2471
Tim Van Damme *Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0000-0002-6424-4421
Aude BeyensCenter for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Sofie SymoensCenter for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Kathleen ClaesCenter for Medical Genetics, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0000-0003-0841-7372
Julie De BackerCenter for Medical Genetics, Ghent University Hospital, Ghent, Belgium.ORCID http://orcid.org/0000-0001-8878-1507
Ilse MeerschautDepartment of Pediatric Cardiology, University Hospital Brussels, Brussels, Belgium.ORCID http://orcid.org/0000-0001-5502-0568
Floris VanommeslaegheDepartment of Nephrology, Ghent University Hospital, Ghent, Belgium.
Sigurd E DelangheDepartment of Nephrology, Ghent University Hospital, Ghent, Belgium.
Jenneke van den EndeDepartment of Medical Genetics, Antwerp University Hospital and University of Antwerp, Antwerp, Belgium.
Tessi BeyltjensDepartment of Medical Genetics, Antwerp University Hospital and University of Antwerp, Antwerp, Belgium.
Eleanor R ScimoneDepartment of Pediatrics, Genetics Unit, MassGeneral for Children, Boston, MA, USA.
Mark E LindsayCardiovascular Genetics Program, Cardiology Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Lisa A SchimmentiDepartment of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.
Alicia M HinzeDivision of Rheumatology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0002-6635-0383
Emily DunnDepartment of Pediatrics, Division of Medical Genetic, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0009-0003-2246-3778
Natalia Gomez-OspinaDepartment of Pediatrics, Division of Medical Genetic, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-6740-1154
Isabelle VandernootULB Center of Human Genetics, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.
Thomas DelgusteULB Center of Human Genetics, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.
Sandra CoppensULB Center of Human Genetics, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.
Valérie Cormier-DaireParis Cité University, Centre of Reference for Constitutional Bone Diseases (MOC), Department of Genetics, INSERM UMR 1163, Imagine Institute, Necker-Enfants Malades Hospital, Paris, France.ORCID http://orcid.org/0000-0002-2839-9856
Marco TartagliaMolecular Genetics and Functional Genomics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID http://orcid.org/0000-0001-7736-9672
Livia GaravelliMedical Genetics Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.ORCID http://orcid.org/0000-0002-7684-3982
Joseph ShiehInstitute for Human Genetics and Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA.ORCID http://orcid.org/0000-0003-0746-6084
Şenol DemirDepartment of Medical Genetics, School of Medicine, Marmara University, Istanbul, Turkey.ORCID http://orcid.org/0000-0002-8374-0359
Esra Arslan AteşDepartment of Medical Genetics, Faculty of Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.ORCID http://orcid.org/0000-0001-5552-8134
Martin ZenkerInstitute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.ORCID http://orcid.org/0000-0003-1618-9269
Mersedeh RohanizadeganDepartment of Medicine, Division of Translational Medicine & Human Genetics, University of Pennsylvania, Philadelphia, PA, USA.
Greysha Rivera-CruzDivision of Reproductive Endocrinology and Infertility, Stanford University School of Medicine, Stanford, CA, USA.
Sofia DouzgouDepartment of Medical Genetics, Haukeland University Hospital, Bergen, Norway.ORCID http://orcid.org/0000-0001-8890-7544
Myhre Syndrome Foundation
Angela E LinDepartment of Pediatrics, Genetics Unit, MassGeneral for Children, Boston, MA, USA.
Bert CallewaertCenter for Medical Genetics, Ghent University Hospital, Ghent, Belgium. bert.callewaert@ugent.be.ORCID http://orcid.org/0000-0002-9743-4205

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID39256535

What OpenQuestion holds

Textmetadata
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.