Christopher Barnett
Women's and Children's Hospital(AU)Women's and Children's Health Network(AU)The University of Adelaide(AU)
Publications by Year
Research Areas
Genomics and Rare Diseases, Gastroesophageal reflux and treatments, Genetics and Neurodevelopmental Disorders, RNA modifications and cancer, Neonatal Respiratory Health Research
Most-Cited Works
- → Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases(2017)571 cited
- → Gain-of-Function Mutations in RIT1 Cause Noonan Syndrome, a RAS/MAPK Pathway Syndrome(2013)329 cited
- → Mechanisms of gastro-oesophageal reflux in preterm and term infants with reflux disease(2002)246 cited
- → Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System(2020)231 cited
- → Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848(2017)205 cited
- → Prediction of Late Death or Disability at Age 5 Years Using a Count of 3 Neonatal Morbidities in Very Low Birth Weight Infants(2015)198 cited