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Record W3092502073 · doi:10.1002/ajmg.a.61907

Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrum

2020· article· en· W3092502073 on OpenAlexaff
Yanick J. Crow, Heather Marshall, Gillian Rice, Luís Seabra, Emma M. Jenkinson, Kristin Barañano, Roberta Battini, Andrea Berger, Edward Blair, Thomas Blauwblomme, François V. Bolduc, N. Boddaert, Johannes Buckard, Heather E. Burnett, Sophie Calvert, Roseline Caumes, Andy Cheuk‐Him Ng, Diana Chiang, David B. Clifford, Duccio Maria Cordelli, Anna de Burca, Natasha Demic, Isabelle Desguerre, Liesbeth De Waele, Alessio Di Fonzo, Steven Dunham, Sarah Dyack, Frances Elmslie, Mickaël Ferrand, Gemma Fisher, Ehsan Ghayoor Karimiani, Jamal Ghoumid, Frances Gibbon, Himanshu Goel, Hilde Tveitan Hilmarsen, Imelda Hughes, Anu Jacob, Elizabeth A. Jones, Ram Kumar, Richard J. Leventer, Shelley MacDonald, Reza Maroofian, Sarju Mehta, Imke Metz, Edoardo Monfrini, Daniela Neumann, Michael J. Noetzel, Mary O’Driscoll, Katrin Õunap, Axel Panzer, Sumit Parikh, Prab Prabhakar, Francis Ramond, Richard Sandford, Russell P. Saneto, Calvin Soh, Chloe Stutterd, Gopinath M. Subramanian, Kevin Talbot, Rhys H. Thomas, Camilo Toro, Renaud Touraine, Emma Wakeling, Evangeline Wassmer, Andrea Whitney, John H. Livingston, Raymond T. O’Keefe, Andrew P. Badrock

Bibliographic record

VenueAmerican Journal of Medical Genetics Part A · 2020
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicRNA regulation and disease
Canadian institutionsIzaak Walton Killam Health CentreDalhousie UniversityUniversity of Alberta
FundersEstonian Research Competency CouncilEesti TeadusagentuurAgence Nationale de la RechercheGreat Ormond Street Hospital Charity
KeywordsBiologyGeneticsProbandPhenotypeLeukoencephalopathyCompound heterozygosityGenotypeAlleleMutationGeneDiseasePathologyMedicine

Abstract

fetched live from OpenAlex

Biallelic mutations in SNORD118, encoding the small nucleolar RNA U8, cause leukoencephalopathy with calcifications and cysts (LCC). Given the difficulty in interpreting the functional consequences of variants in nonprotein encoding genes, and the high allelic polymorphism across SNORD118 in controls, we set out to provide a description of the molecular pathology and clinical spectrum observed in a cohort of patients with LCC. We identified 64 affected individuals from 56 families. Age at presentation varied from 3 weeks to 67 years, with disease onset after age 40 years in eight patients. Ten patients had died. We recorded 44 distinct, likely pathogenic, variants in SNORD118. Fifty two of 56 probands were compound heterozygotes, with parental consanguinity reported in only three families. Forty nine of 56 probands were either heterozygous (46) or homozygous (three) for a mutation involving one of seven nucleotides that facilitate a novel intramolecular interaction between the 5' end and 3' extension of precursor-U8. There was no obvious genotype-phenotype correlation to explain the marked variability in age at onset. Complementing recently published functional analyses in a zebrafish model, these data suggest that LCC most often occurs due to combinatorial severe and milder mutations, with the latter mostly affecting 3' end processing of precursor-U8.

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: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.433
Threshold uncertainty score0.325

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 head0.009
GPT teacher head0.247
Teacher spread0.238 · 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 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

Citations29
Published2020
Admission routes1
Has abstractyes

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