CoMPaSS-NMD2025-08-05T09:54:17+00:00 Empowering clinicians with artificial intelligence in hereditary neuromuscular disorders
CoMPaSS-NMD2026-07-07T10:31:18+00:00 Exome sequencing in undiagnosed congenital myopathy reveals new genes and refines genes–phenotypes correlations
CoMPaSS-NMD2026-07-07T10:42:52+00:00 OBSCN undergoes extensive alternative splicing during human cardiac and skeletal muscle development
CoMPaSS-NMD2026-07-07T10:42:14+00:00 Optimizing 2D in vitro differentiation conditions for C2C12 murine myoblasts on gelatin hydrogel
CoMPaSS-NMD2026-07-08T10:28:27+00:00 Novel Mutations in Titin Exon 363 With Different Phenotypes Including a Founder Mutation in Eastern Europe
CoMPaSS-NMD2026-07-08T10:32:12+00:00 The burden of TTN variants in the genomic era: Analysis of 18,462 individuals from the Solve-RD consortium and general recommendations
CoMPaSS-NMD2026-07-08T10:51:38+00:00 A comprehensive framework for the interpretation of TTN missense variants
CoMPaSS-NMD2026-07-08T12:30:13+00:00 Poly(A)+ selection limits detection of long and alternatively spliced transcripts compared with rRNA depletion in RNA-Sequencing
CoMPaSS-NMD2026-07-08T12:33:28+00:00 Over-Representation of TTN Truncating Variants in a Finnish Cohort of Patients With Axial Myopathy
CoMPaSS-NMD2026-07-14T12:41:18+00:00 The CoMPaSS-NMD Neuromuscular Genome Atlas: a new AI-based platform for advanced deep phenotyping and stratification in hereditary neuromuscular disorders
