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Record W4402945101 · doi:10.1016/j.gim.2024.101283

Microduplications of ARID1A and ARID1B cause a novel clinical and epigenetic distinct BAFopathy

2024· article· en· W4402945101 on OpenAlexafffund
Pleuntje J. van der Sluijs, Sébastien Moutton, Alexander J.M. Dingemans, Denisa Weis, Michael A. Levy, Kym M. Boycott, Claudia Arberas, Margherita Baldassarri, Claire Bénéteau, Alfredo Brusco, Charles Coutton, Tabib Dabir, Maria Lisa Dentici, Koenraad Devriendt, Laurence Faivre, Mieke M. van Haelst, Khadijé Jizi, Marlies Kempers, Jennifer Kerkhof, Mira Kharbanda, Katherine Lachlan, Nathalie Marle, Haley McConkey, Maria Antonietta Mencarelli, David Mowat, Marcello Niceta, Claire Nicolas, Antonio Novelli, Valeria Orlando, Olivier Pichon, Julia Rankin, Raissa Relator, Fabienne G. Ropers, Jill A. Rosenfeld, Rani Sachdev, Sarah A. Sandaradura, Elena Shukarova-Angelovska, Duco Steenbeek, Marco Tartaglia, Matthew A Tedder, Slavica Trajkova, Norbert Winer, Jeremy D. Woods, Bert de Vries, Bekim Sadiković, Mariëlle Alders, Gijs W.E. Santen

Bibliographic record

VenueGenetics in Medicine · 2024
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicChromatin Remodeling and Cancer
Canadian institutionsWestern UniversityCentre Hospitalier Universitaire Sainte-JustineChildren's Hospital of Eastern OntarioLondon Health Sciences Centre
FundersFaculty of Medicine and Health, University of SydneyStichting DondersfondsCentre Hospitalier Universitaire de NantesCentre hospitalier universitaire Sainte-JustineUniversità degli Studi di TorinoUniversity Hospital Southampton NHS Foundation TrustUniversiteit LeidenLeids Universitair Medisch CentrumUniversiteit MaastrichtZonMwUniversity of New South WalesUniversiteit van AmsterdamUniversity of SouthamptonMinistero della SaluteInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'EnvironnementAmsterdam University Medical CentersMaastricht Universitair Medisch Centrum
KeywordsARID1AEpigeneticsGeneticsBiologyComputational biologyMedicineGeneMutation

Abstract

fetched live from OpenAlex

PURPOSE: ARID1A/ARID1B haploinsufficiency leads to Coffin-Siris syndrome, duplications of ARID1A lead to a distinct clinical syndrome, whilst ARID1B duplications have not yet been linked to a phenotype. METHODS: We collected patients with duplications encompassing ARID1A and ARID1B duplications. RESULTS: 16 ARID1A and 13 ARID1B duplication cases were included with duplication sizes ranging from 0.1 to 1.2 Mb (1-44 genes) for ARID1A and 0.9 to 10.3 Mb (2-101 genes) for ARID1B. Both groups shared features, with ARID1A patients having more severe intellectual disability, growth delay, and congenital anomalies. DNA methylation analysis showed that ARID1A patients had a specific methylation pattern in blood, which differed from controls and from patients with ARID1A or ARID1B loss-of-function variants. ARID1B patients appeared to have a distinct methylation pattern, similar to ARID1A duplication patients, but further research is needed to validate these results. Five cases with duplications including ARID1A or ARID1B initially annotated as duplications of uncertain significance were evaluated using PhenoScore and DNA methylation reanalysis, resulting in the reclassification of 2 ARID1A and 2 ARID1B duplications as pathogenic. CONCLUSION: Our findings reveal that ARID1B duplications manifest a clinical phenotype, and ARID1A duplications have a distinct episignature that overlaps with that of ARID1B duplications, providing further evidence for a distinct and emerging BAFopathy caused by whole-gene duplication rather than haploinsufficiency.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.785
Threshold uncertainty score0.385

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.039
GPT teacher head0.367
Teacher spread0.328 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations6
Published2024
Admission routes2
Has abstractyes

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