Evidence map›Paper›PMID 40195523›Full record

ArticleEuropean journal of human genetics : EJHG2025

Correction: Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes.

German Demidov, Steven Laurie, Annalaura Torella, Giulio Piluso, Marcello Scala, Manuela Morleo, Vincenzo Nigro, Holm Graessner, Siddharth Banka, Solve-RD consortium and 2 more

Abstract readPublished Erratum
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In one paragraph

Article in European journal of human genetics : EJHG, 2025. 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.

German DemidovInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany. German.Demidov@med.uni-tuebingen.de.ORCID http://orcid.org/0000-0001-9075-4276
Steven LaurieCentro Nacional de Análisis Genómico (CNAG), Barcelona, Spain.ORCID http://orcid.org/0000-0003-3913-5829
Annalaura TorellaDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Giulio PilusoDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.ORCID http://orcid.org/0000-0001-9418-125X
Marcello ScalaDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, Università Degli Studi di Genova, Genoa, Italy.ORCID http://orcid.org/0000-0003-2194-7239
Manuela MorleoDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Vincenzo NigroDepartment of Precision Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Holm GraessnerInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0001-9803-7183
Siddharth BankaDivision of Evolution & Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0002-8527-2210
Solve-RD consortium
Katja LohmannInstitute of Neurogenetics, University of Lübeck and University Hospital Schleswig-Holstein, Lübeck, Germany.ORCID http://orcid.org/0000-0002-5121-1460
Stephan OssowskiInstitute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.ORCID http://orcid.org/0000-0002-7416-9568

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID40195523

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.