Hilary J Vernon

Assistant Professor

19992018
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Medicine & Life Sciences

Barth Syndrome
Mitochondrial Diseases
Mutation
Inborn Errors Metabolism
Cardiolipins
Exome
Phenotype
Chromosome Deletion
Leukoencephalopathies
Neurology
Adenine Phosphoribosyltransferase
Ornithine Carbamoyltransferase Deficiency Disease
Methylmalonic Acid
Metabolomics
Yeast Artificial Chromosomes
Amino Acids
Genetic Association Studies
Chromosomes, Human, Pair 21
Sphingolipids
Phenylketonurias
Osteopontin
Muscle Hypotonia
Lyases
Kidney Calculi
Congenital Heart Defects
Neuroimaging
Kidney Diseases
Alagille Syndrome
Preschool Children
Ataxia
Coenzyme A
Standard of Care
Natural History
Blood-Brain Barrier
Knockout Mice
Liver Transplantation
Kidney Transplantation
Serine
Chromatin
Autistic Disorder
Phenylalanine
Renal Dialysis
Therapeutics
Cardiac Arrhythmias
Siblings
Exons
Inborn Urea Cycle Disorder
Genes
Brain
Genotype

Chemical Compounds

Plasmas
Fuzzy filters
Metabolism
Cardiolipins
Ornithine Carbamoyltransferase
Acyl-CoA Dehydrogenase
Clinical laboratories
Amino Acids
Genes
Phenylalanine
Metabolites
Chemical activation
Urea
Arginine
Health
Poly I-C
Citrulline
Kinetics
Transfer RNA
Cholesterol
Screening
Enzyme activity
Information systems
Nutrition
Glutamine
Ammonia
Amino Acyl-tRNA Synthetases
Exons
Animals
Gene encoding
Fatty Acids
Control systems
Messenger RNA
Biogenic Amines
Nitrobenzene
Nitric Oxide Synthase Type III
Biosynthesis
Defects
Liquid chromatography
Biomarkers