Genomics/Epigenomics 1

Genomics/Epigenomics 1

375 - Computational and Laboratory Identification of Risk-Driving Alleles on Juvenile Idiopathic Arthritis (JIA)-Associated Haplotypes

376 - Developmental Support for Infants with Genetic Syndromes

377 - Enhancing pediatric rare disease diagnosis by long-read HiFi-genome sequencing

378 - Family-Based Genomic Analysis Identifies Rare Variants Contributing to Pediatric ADHD

379 - Genetic testing for neonatal seizures: A necessary diagnostic tool?

380 - Implementation of First-tier Rapid Genome Sequencing in Pediatric Wards

381 - Implementation of first-tier rapid genome sequencing in the PICU and CICU

382 - Precision Medicine in Bronchiolitis: A Feasibility Study in the Pediatric Emergency Department

383 - Rapid whole genome sequencing in the NICU: A process time comparison

384 - Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome

385 - The Landscape of Genetic Testing and Associated Anomalies for Prenatally Identified Cystic Renal Malformations

386 - Unique Signatures of Highly Constrained Genes Across Publicly Available Genomic Databases

387 - Using genomic database analysis to characterize pathogenicity of IDS missense variants in Mucopolysaccharidosis Type II

388 - Utility of Genomic Autopsy for Infant Mortality

389 - Utilizing automated phenotype extraction for more timely whole genome sequencing