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Record W2914075307 · doi:10.1186/s11689-019-9263-3

Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders

2019· article· en· W2914075307 on OpenAlexafffund
Gregory Costain, Susan Walker, Bob Argiropoulos, Danielle Baribeau, Anne S. Bassett, Erik Boot, Koenraad Devriendt, Barbara Kellam, Christian R. Marshall, Aparna Prasad, Moises Serrano, Dimitri J. Stavropoulos, Hope Twede, Joris Vermeesch, Jacob Vorstman, Stephen W. Scherer

Bibliographic record

VenueJournal of Neurodevelopmental Disorders · 2019
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenomic variations and chromosomal abnormalities
Canadian institutionsToronto General HospitalUniversity of CalgarySickKids FoundationHospital for Sick ChildrenUniversity of Toronto
FundersNational Institute on Drug AbuseNational Eye InstituteNational Institute on AgingCanadian Institutes of Health ResearchNational Heart, Lung, and Blood InstituteHospital for Sick ChildrenNational Human Genome Research InstituteWellcome TrustGenome CanadaJohns Hopkins UniversityCanadian Institute for Advanced ResearchNational Cancer InstituteNational Institute on Alcohol Abuse and AlcoholismAutism SpeaksUniversity of TorontoNational Institutes of HealthMcLaughlin Centre, University of TorontoGlaxoSmithKlineCentre for Applied GenomicsGovernment of Ontario
KeywordsCopy-number variationGeneticsBiologyAutism spectrum disorderMissense mutationAutismWhole genome sequencingGeneHuman geneticsIntellectual disabilityPhenotypeGenomeMedicinePsychiatry

Abstract

fetched live from OpenAlex

BACKGROUND: Ultra-rare genetic variants, including non-recurrent copy number variations (CNVs) affecting important dosage-sensitive genes, are important contributors to the etiology of neurodevelopmental disorders (NDDs). Pairing family-based whole-genome sequencing (WGS) with detailed phenotype data can enable novel gene associations in NDDs. METHODS: We performed WGS of six members from a three-generation family, where three individuals each had a spectrum of features suggestive of a NDD. CNVs and sequence-level variants were identified and further investigated in disease and control databases. RESULTS: We identified a novel 252-kb deletion at 15q21 that overlaps the synaptic gene DMXL2 and the gene GLDN. The microdeletion segregated in NDD-affected individuals. Additional rare inherited and de novo sequence-level variants were found that may also be involved, including a missense change in GRIK5. Multiple CNVs and loss-of-function sequence variants affecting DMXL2 were discovered in additional unrelated individuals with a range of NDDs. CONCLUSIONS: Disruption of DMXL2 may predispose to NDDs including autism spectrum disorder. The robust interpretation of private variants requires a multifaceted approach that incorporates multigenerational pedigrees and genome-wide and population-scale data.

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 machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.005

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

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 head0.005
GPT teacher head0.210
Teacher spread0.205 · 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 source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
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

Citations16
Published2019
Admission routes2
Has abstractyes

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