Evidence map›Paper›PMID 38698204›Full record

ArticleScientific reports2024

Author Correction: Analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases.

Daniel Moynihan, Sean Monaco, Teck Wah Ting, Kaavya Narasimhalu, Jenny Hsieh, Sylvia Kam, Jiin Ying Lim, Weng Khong Lim, Sonia Davila, Yasmin Bylstra and 9 more

Abstract readPublished Erratum
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Daniel MoynihanCurtin University, Perth, Australia.
Sean MonacoHealth Catalyst, Utah, USA.
Teck Wah TingGenetics Service, Department of Paediatrics, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore, 229899, Singapore.
Kaavya NarasimhaluSingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.
Jenny HsiehSingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.
Sylvia KamGenetics Service, Department of Paediatrics, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore, 229899, Singapore.
Jiin Ying LimGenetics Service, Department of Paediatrics, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore, 229899, Singapore.
Weng Khong LimSingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.
Sonia DavilaSingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.
Yasmin BylstraSingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.
Iswaree Devi BalakrishnanSingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.
Mark HengSingHealth Office of Insights and Analytics, Singapore, Singapore.
Elian ChiaSingHealth Office of Insights and Analytics, Singapore, Singapore.
Khung Keong YeoNational Heart Centre Singapore, Singapore, Singapore.
Bee Keow GohData Analytics Office, KK Women's and Children's Hospital, Singapore, Singapore.
Ritu GuptaCurtin University, Perth, Australia.
Tele TanCurtin University, Perth, Australia.
Gareth BaynamRare Care Centre, Perth Children's Hospital, Perth, WA, Australia.
Saumya Shekhar JamuarGenetics Service, Department of Paediatrics, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore, 229899, Singapore. saumya.s.jamuar@singhealth.com.sg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID38698204
PMCPMC11066083

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.