Evidence map›Paper›PMID 31030663›Full record

ArticleJournal of biomedical science2019

Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta.

Mehran Kausar, Saima Siddiqi, Muhammad Yaqoob, Sajid Mansoor, Outi Makitie, Asif Mir, Chiea Chuen Khor, Jia Nee Foo, Mariam Anees

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

Article in Journal of biomedical science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 7 institutions in 3 countries.

Mehran KausarDepartment of Biochemistry, Faculty of Biological Sciences, Quaid-i-AzamUniversity, University Road, Islamabad, 45320, Pakistan.
Saima SiddiqiInstitute of Biomedical and Genetic Engineering (IBGE) Islamabad, Islamabad, 44000, Pakistan.
Muhammad YaqoobDepartment of Genetics, Children Hospital, Lahore, Pakistan.
Sajid MansoorAtta-ur-Rehman School of Applied Biosciences, NUST, Islamabad, Pakistan.
Outi MakitieChildren's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Asif MirDepartment of Bioinformatics & Biotechnology, Faculty of Basic and Applied Sciences, International Islamic University (IIU), H-10, Islamabad, 44000, Pakistan.
Chiea Chuen KhorHuman Genetics, A*STAR, Genome Institute of Singapore, Singapore, 138672, Singapore.
Jia Nee FooHuman Genetics, A*STAR, Genome Institute of Singapore, Singapore, 138672, Singapore. foojn@gis.a-star.edu.sg.
Mariam AneesDepartment of Biochemistry, Faculty of Biological Sciences, Quaid-i-AzamUniversity, University Road, Islamabad, 45320, Pakistan. mariam@qau.edu.pk.
Agency for Science, Technology and Research · SGInstitute of Biomedical and Genetic Engineering · PKHelsinki University Hospital · FIInternational Islamic University, Islamabad · PKMayo Hospital · PKNational University of Sciences and Technology · PKQuaid-i-Azam University · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the original publication of this article [1], there are two errors in the article which the cDNA position of the pathogenic variant WNT1 p.Gly324Cys should be c.970G>T instead of c.1168G>T.

Identifiers

PMID31030663
PMCPMC6487057
OpenAlexW2945910533

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.