Evidence map›Paper›PMID 38992656›Full record

ArticleBMC medicine2024

Correction: Olfactory bulb anomalies in KBG syndrome mouse model and patients.

Kara Goodkey, Anita Wischmeijer, Laurence Perrin, Adrianne E S Watson, Leenah Qureshi, Duccio Maria Cordelli, Francesco Toni, Maria Gnazzo, Francesco Benedicenti, Monique Elmaleh-Berges and 2 more

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

Article in BMC medicine, 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

12 authors.

Kara GoodkeyDepartment of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, T6G 2H7, Canada.
Anita WischmeijerClinical Genetics Service and Coordination Center for Rare Diseases, Department of Pediatrics, Regional Hospital of Bolzano, Bolzano, Italy.
Laurence PerrinClinical Genetics Unit, Hopital Robert-Debre, Paris, France.
Adrianne E S WatsonDepartment of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, T6G 2H7, Canada.
Leenah QureshiDepartment of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, T6G 2H7, Canada.
Duccio Maria CordelliIRCCS Istituto Delle Scienze Neurologiche Di Bologna, UOC Neuropsichiatria Dell'eta Pediatrica, Bologna, Italy.
Francesco ToniProgramma Di Neuroradiologia Con Tecniche Ad Elevata Complessita (PNTEC), IRCCS Istituto Delle Scienze Neurologiche Di Bologna, Bologna, Italy.
Maria GnazzoLaboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesu Children's Hospital, IRCCS, 00165, Rome, Italy.
Francesco BenedicentiClinical Genetics Service and Coordination Center for Rare Diseases, Department of Pediatrics, Regional Hospital of Bolzano, Bolzano, Italy.
Monique Elmaleh-BergesService d'Imagerie Pediatrique, Hopital Universitaire Robert Debre, Paris, France.
Karen J LowDepartment of Academic Child Health, Bristol Medical School, Population Health Sciences, University of Bristol, Bristol, UK.
Anastassia VoronovaDepartment of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, T6G 2H7, Canada. voronova@ualberta.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID38992656
PMCPMC11241786

What OpenQuestion holds

Textmetadata
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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.