Evidence map›Paper›PMID 33168987›Full record

ArticleEuropean journal of human genetics : EJHG2021

Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.

Lilian Downie, Jane Halliday, Rachel Burt, Sebastian Lunke, Elly Lynch, Melissa Martyn, Zeffie Poulakis, Clara Gaff, Valerie Sung, Melissa Wake and 9 more

Open access · bronzeAbstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in European journal of human genetics : EJHG, 2021. 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, top 76% of its field
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, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 5 institutions in 2 countries.

Lilian DownieVictorian Clinical Genetics Services, Melbourne, VIC, Australia.
Jane HallidayMurdoch Children's Research Institute, Melbourne, VIC, Australia.
Rachel BurtMurdoch Children's Research Institute, Melbourne, VIC, Australia.
Sebastian LunkeVictorian Clinical Genetics Services, Melbourne, VIC, Australia.
Elly LynchVictorian Clinical Genetics Services, Melbourne, VIC, Australia.
Melissa MartynMurdoch Children's Research Institute, Melbourne, VIC, Australia.
Zeffie PoulakisMurdoch Children's Research Institute, Melbourne, VIC, Australia.
Clara GaffDepartment of Paediatrics, University of Melbourne, Melbourne, VIC, Australia.
Valerie SungMurdoch Children's Research Institute, Melbourne, VIC, Australia.
Melissa WakeMurdoch Children's Research Institute, Melbourne, VIC, Australia.
Matthew F HunterMonash Health, Melbourne, VIC, Australia.
Kerryn SaundersMonash Health, Melbourne, VIC, Australia.
Elizabeth RoseMurdoch Children's Research Institute, Melbourne, VIC, Australia.
Sharon LewisMurdoch Children's Research Institute, Melbourne, VIC, Australia.
Anna JarmolowiczVictorian Clinical Genetics Services, Melbourne, VIC, Australia.
Dean PhelanVictorian Clinical Genetics Services, Melbourne, VIC, Australia.
Heidi L RehmMassachusetts General Hospital and the Broad Institute of MIT and Harvard, Boston, MA, USA.
Melbourne Genomics Health Alliance
David J AmorVictorian Clinical Genetics Services, Melbourne, VIC, Australia. david.amor@mcri.edu.au.
The University of Melbourne · AURoyal Children's Hospital · AUVictorian Clinical Genetics Services · AUBroad Institute · USMonash Health · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID33168987
PMCPMC7868367
OpenAlexW3102169100

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.