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Record W4412940493 · doi:10.1136/jmg-2025-110783

Refined genotype–phenotype correlations in neurofibromatosis type 1 patients with <i>NF1</i> point variants

2025· article· en· W4412940493 on OpenAlexaff
Laurence Pacot, Marinus J. Blok, Dominique Vidaud, L. Fertitta, Ingrid Laurendeau, Audrey Coustier, Théodora Maillard, Cécile Barbance, Djihad Hadjadj, Manuela Ye, Dominique Lallemand, S. Ferkal, Benoît Funalot, Ariane Lunati, Bérénice Hebrard, Rakia Bhouri, Liesbeth Spruijt, D. Bessis, David Geneviève, Vivian Vernimmen, Martinus P. G. Broen, Sabine Sigaudy, Sylvie Odent, Léna Damaj, Chloé Quēlin, Laurent Pasquier, Valérie Layet, Brigitte Gilbert‐Dussardier, Gaël Nicolas, Anne‐Marie Guerrot, Bruno Leheup, A.‐C. Bursztejn, Florence Petit, Odile Boute‐Bénéjean, Yline Capri, Anne Guimier, Stanislas Lyonnet, Geneviève Baujat, E. Bourrat, Bertrand Isidor, Mathilde Nizon, S. Barbarot, Annick Toutain, Sophie Blesson, Julien Van‐Gils, Fanny Morice‐Picard, Séverine Audebert‐Bellanger, J. Mazereeuw‐Hautier, Alban Ziegler, Yves Alembik, Juliette Piard, Elise Brischoux‐Boucher, Léa Guerrini‐Rousseau, J. Morera, Véronique Paquis‐Flucklinger, Bruno Delobel, Jean‐Luc Alessandri, Béatrice Parfait, P. Wolkenstein, Éric Pasmant

Bibliographic record

VenueJournal of Medical Genetics · 2025
Typearticle
Languageen
FieldMedicine
TopicNeurofibromatosis and Schwannoma Cases
Canadian institutionsHotel Dieu Hospital
FundersZonMwAgence Nationale de la Recherche
KeywordsMissense mutationNeurofibromin 1NeurofibromatosisPenetranceGeneticsGenotypePhenotypeBiologyNeurofibromatosis type IPoint mutationGeneMutation

Abstract

fetched live from OpenAlex

Background Neurofibromatosis type 1 (NF1) is one of the most frequent genetic disorders. NF1 is caused by dominant loss-of-function pathogenic variants (PVs) of the tumour-suppressor gene NF1 , which encodes neurofibromin, a negative regulator of rat sarcoma proteins. NF1 is an autosomal dominant disorder with complete penetrance, but a highly variable expression. Identification of genotype–phenotype correlations is challenging because of the wide clinical variability, the progressive nature of the disorder and the extreme diversity of the mutation spectrum. Only a few NF1 point variants have been associated with a specific phenotype in NF1 patients. Methods We investigated a large, well-phenotyped NF1 cohort. Results We report analyses of genotype-phenotype correlations in 112 NF1 patients with specific NF1 point variants: p.Arg1809 missense variants were associated with a mild form of NF1 (n=24), while a more severe phenotype was associated with codons 844–848 (n=27), p.Arg1276 (n=25) and p.Lys1423 (n=35) missense variants. We describe a new correlation for p.Arg1204 missense variants (n=11), with no neurofibroma observed in patients. Functional studies will be critical for drawing conclusions on the potential hypomorphic or dominant-negative effects of these variants. Conclusion The current data confirms several genotype-phenotype correlations in NF1, which may be relevant to the management and surveillance of NF1 patients with specific NF1 PVs.

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)0.001
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 score0.039
Threshold uncertainty score0.454

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
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 head0.012
GPT teacher head0.263
Teacher spread0.251 · 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

Citations4
Published2025
Admission routes1
Has abstractyes

Explore more

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