Evidence map›Paper›PMID 33351141›Full record

ArticleBrain : a journal of neurology2021

Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigree.

Nancy Vegas, Karen Low, Christopher C Y Mak, Jasmine L F Fung, Anne V Hing, Brian H Y Chung, Dan Doherty, Jeanne Amiel, Christopher T Gordon

Open access · bronzeAbstract readLetterComment
PubMed Publisher
In one paragraph

Article in Brain : a journal of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Iterative genetic testing identifiesJournal of human immunity · 2026
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  4. Frontiers in molecular neuroscience · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 6 institutions in 4 countries.

Nancy VegasLaboratory of Embryology and Genetics of Human Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) UMR 1163, Institut Imagine, Université de Paris, 75015 Paris, France.
Karen LowDepartment of Clinical Genetics, St Michaels Hospital, University Hospitals Bristol and Weston NHS Trust, Bristol BS2 8EJ, UK.
Christopher C Y MakDepartment of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
Jasmine L F FungDepartment of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
Anne V HingDivision of Craniofacial Medicine, Department of Pediatrics, University of Washington, Seattle, WA 98195, USA.
Brian H Y ChungDepartment of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.
Dan DohertyDepartment of Pediatrics, University of Washington, Seattle, WA 98195, USA.
Jeanne AmielLaboratory of Embryology and Genetics of Human Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) UMR 1163, Institut Imagine, Université de Paris, 75015 Paris, France.
Christopher T GordonLaboratory of Embryology and Genetics of Human Malformations, Institut National de la Santé et de la Recherche Médicale (INSERM) UMR 1163, Institut Imagine, Université de Paris, 75015 Paris, France.
University of Hong Kong · HKInserm · FRHôpital Necker-Enfants Malades · FRSeattle Children's Hospital · USUniversity Hospitals Bristol NHS Foundation Trust · GBUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Cleft PalateHumansMutationPedigreeTrans-ActivatorsTumor Suppressor ProteinsMN1 protein, humanTrans-ActivatorsTumor Suppressor Proteins

Identifiers

PMID33351141
OpenAlexW3151980522

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.