Evidence map›Paper›PMID 37225732›Full record

ArticleNPJ genomic medicine2023

Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.

Giuliana Giannuzzi, Nicolas Chatron, Katrin Mannik, Chiara Auwerx, Sylvain Pradervand, Gilles Willemin, Kendra Hoekzema, Xander Nuttle, Jacqueline Chrast, Marie C Sadler and 8 more

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

Article in NPJ genomic medicine, 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

18 authors.

Giuliana GiannuzziCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland. giuliana.giannuzzi@unimi.it.
Nicolas ChatronCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.ORCID http://orcid.org/0000-0003-0538-0981
Katrin MannikCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
Chiara AuwerxCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.ORCID http://orcid.org/0000-0003-3613-8450
Sylvain PradervandCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
Gilles WilleminCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
Kendra HoekzemaDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Xander NuttleCenter for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
Jacqueline ChrastCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
Marie C SadlerDepartment of Computational Biology, University of Lausanne, Lausanne, Switzerland.
Eleonora PorcuCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
16p11.2 Consortium
Yann HeraultUniversity of Strasbourg, CNRS, INSERM, PHENOMIN-ICS, Institute of Genetics and Molecular and Cellular Biology, Illkirch, France.ORCID http://orcid.org/0000-0001-7049-6900
Bertrand IsidorService de Génétique Médicale, CHU de Nantes, Nantes, France.
Brigitte Gilbert-DussardierService de Génétique, CHU de Poitiers, Poitiers, France.
Evan E EichlerDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Zoltan KutalikDepartment of Computational Biology, University of Lausanne, Lausanne, Switzerland.
Alexandre ReymondCenter for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.ORCID http://orcid.org/0000-0003-1030-8327

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID37225732
PMCPMC10209113

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.