Evidence map›Paper›PMID 37654076›Full record

ArticleAmerican journal of medical genetics. Part C, Seminars in medical genetics2023

Integration of EpiSign, facial phenotyping, and likelihood ratio interpretation of clinical abnormalities in the re-classification of an ARID1B missense variant.

Caitlin Forwood, Katie Ashton, Ying Zhu, Futao Zhang, Kerith-Rae Dias, Krystle Standen, Carey-Anne Evans, Louise Carey, Michael Cardamone, Carolyn Shalhoub and 10 more

Open access · hybridAbstract readCase Reports
In one paragraph

Article in American journal of medical genetics. Part C, Seminars in medical genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 8 institutions in 4 countries.

Caitlin ForwoodNSW Health Pathology Randwick Genomics, Prince of Wales Hospital, Sydney, Australia.
Katie AshtonNSW Health Pathology Randwick Genomics, Prince of Wales Hospital, Sydney, Australia.
Ying ZhuNSW Health Pathology Randwick Genomics, Prince of Wales Hospital, Sydney, Australia.
Futao ZhangNSW Health Pathology Randwick Genomics, Prince of Wales Hospital, Sydney, Australia.
Kerith-Rae DiasNeuroscience Research Australia (NeuRA), University of New South Wales, Sydney, Australia.
Krystle StandenNSW Health Pathology Randwick Genomics, Prince of Wales Hospital, Sydney, Australia.
Carey-Anne EvansNeuroscience Research Australia (NeuRA), University of New South Wales, Sydney, Australia.
Louise CareyNSW Health Pathology Randwick Genomics, Prince of Wales Hospital, Sydney, Australia.
Michael CardamoneSydney Children's Hospital, Randwick, Australia.
Carolyn ShalhoubCentre for Clinical Genetics, Sydney Children's Hospital, Randwick, Australia.
Hala KatfSydney Children's Hospital, Randwick, Australia.
Carlos RiverosBioinformatics, Hunter Medical Research Institute, Newcastle, Australia.
Tzung-Chien HsiehInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Bonn, Germany.
Peter KrawitzInstitute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Bonn, Germany.
Peter N RobinsonJAX Center for Precision Genetics, The JAX Cancer Center, Farmington, Connecticut, USA.
Tracy Dudding-BythGenetics of Learning Disability (GoLD) Service, Waratah, Australia.
Bekim SadikovicLondon Health Sciences Centre, Verspeeten Clinical Genome Centre, Western University, London, Canada.
Jason PinnerCentre for Clinical Genetics, Sydney Children's Hospital, Randwick, Australia.
Michael F BuckleyNSW Health Pathology Randwick Genomics, Prince of Wales Hospital, Sydney, Australia.
Tony RoscioliNSW Health Pathology Randwick Genomics, Prince of Wales Hospital, Sydney, Australia.ORCID 0000-0003-1502-5000
Prince of Wales Hospital · AUUNSW Sydney · AUSydney Children's Hospital · AUUniversity Hospital Bonn · DECancer Genetics (United States) · USHunter Genetics · AUHunter Medical Research Institute · AUWestern University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heterozygous ARID1B variants result in Coffin-Siris syndrome. Features may include hypoplastic nails, slow growth, characteristic facial features, hypotonia, hypertrichosis, and sparse scalp hair. Most reported cases are due to ARID1B loss of function variants. We report a boy with developmental delay, feeding difficulties, aspiration, recurrent respiratory infections, slow growth, and hypotonia without a clinical diagnosis, where a previously unreported ARID1B missense variant was classified as a variant of uncertain significance. The pathogenicity of this variant was refined through combined methodologies including genome-wide methylation signature analysis (EpiSign), Machine Learning (ML) facial phenotyping, and LIRICAL. Trio exome sequencing and EpiSign were performed. ML facial phenotyping compared facial images using FaceMatch and GestaltMatcher to syndrome-specific libraries to prioritize the trio exome bioinformatic pipeline gene list output. Phenotype-driven variant prioritization was performed with LIRICAL. A de novo heterozygous missense variant, ARID1B p.(Tyr1268His), was reported as a variant of uncertain significance. The ACMG classification was refined to likely pathogenic by a supportive methylation signature, ML facial phenotyping, and prioritization through LIRICAL. The ARID1B genotype-phenotype has been expanded through an extended analysis of missense variation through genome-wide methylation signatures, ML facial phenotyping, and likelihood-ratio gene prioritization.

Indexed as

Abnormalities, MultipleHand Deformities, CongenitalIntellectual DisabilityMicrognathismDNA-Binding ProteinsFaceHumansMaleMuscle HypotoniaNeckTranscription FactorsARID1B protein, humanDNA-Binding ProteinsTranscription FactorsARID1BCoffin-Siris syndromeepisignatureFaceMatchGestaltMatcherLIRICAL

Identifiers

PMID37654076
PMCPMC10952833
OpenAlexW4386346829

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.