All Stories

  1. Characterization of intrinsically disordered regions in proteins informed by human genetic diversity
  2. Characterization of the GABRB2 ‐Associated Neurodevelopmental Disorders
  3. Comprehensive characterization of amino acid positions in protein structures reveals molecular effect of missense variants
  4. Current knowledge of SLC6A1-related neurodevelopmental disorders
  5. Predicting functional effects of missense variants in voltage-gated sodium and calcium channels
  6. MISCAST: MIssense variant to protein StruCture Analysis web SuiTe
  7. Time to move beyond genetics towards biomedical data-driven translational genomic research in severe paediatric epilepsies
  8. Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation
  9. Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical Review
  10. PBRpredict-Suite: a suite of models to predict peptide-recognition domain residues from protein sequence
  11. Estimation of Position Specific Energy as a Feature of Protein Residues from Sequence Alone for Structural Classification
  12. DisPredict: A Predictor of Disordered Protein Using Optimized RBF Kernel