Evidence map›Paper›PMID 41702927›Full record

ArticleNature communications2026

Author Correction: Complex de novo structural variants are an underestimated cause of rare disorders.

Hyunchul Jung, Tsun-Po Yang, Susan Walker, Petr Danecek, O Isaac Garcia-Salinas, Matthew D C Neville, Joseph Christopher, Isidro Cortés-Ciriano, Helen Firth, Aylwyn Scally and 3 more

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

Article in Nature communications, 2026. 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

13 authors.

Hyunchul JungWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK. hj6@sanger.ac.uk.ORCID http://orcid.org/0000-0003-0450-2190
Tsun-Po YangWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
Susan WalkerGenomics England, London, UK.ORCID http://orcid.org/0000-0002-5016-6426
Petr DanecekWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
O Isaac Garcia-SalinasWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.ORCID http://orcid.org/0000-0003-2550-569X
Matthew D C NevilleWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.ORCID http://orcid.org/0000-0001-5816-7936
Joseph ChristopherWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
Isidro Cortés-CirianoWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.ORCID http://orcid.org/0000-0002-2036-494X
Helen FirthWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
Aylwyn ScallyDepartment of Genetics, University of Cambridge, Downing Street, Cambridge, UK.ORCID http://orcid.org/0000-0002-0807-1167
Matthew HurlesWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.ORCID http://orcid.org/0000-0002-2333-7015
Peter CampbellWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.ORCID http://orcid.org/0000-0002-3921-0510
Raheleh RahbariWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK. rr11@sanger.ac.uk.ORCID http://orcid.org/0000-0002-1839-7785

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID41702927
PMCPMC12914042

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.