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Renata Gallagher
Concepts (254)
Back to Profile
Concepts are derived automatically from a person's publications.
Cloud
Categories
Timeline
Details
In this concept 'cloud', the sizes of the concepts are based not only on the number of corresponding publications, but also how relevant the concepts are to the overall topics of the publications, how long ago the publications were written, whether the person was the first or senior author, and how many other people have written about the same topic. The largest concepts are those that are most unique to this person.
3-Hydroxyacyl CoA Dehydrogenases
Abnormalities, Multiple
Acetyl-CoA C-Acetyltransferase
Acyl Coenzyme A
Acyl-CoA Dehydrogenase
Adenosine Triphosphatases
Adenoviridae
Adolescent
Adult
Aged
Agenesis of Corpus Callosum
Aldehyde Dehydrogenase
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acids
Ammonia
Angelman Syndrome
Animals
Anticonvulsants
Antigens, CD
Antineoplastic Agents
Arginine
Attitude
Base Sequence
Biogenic Monoamines
Biomarkers
Brain
Brain Diseases
Brain Diseases, Metabolic
Canada
Carbon Monoxide
Carcinoma, Hepatocellular
Cardiomyopathies
Carnitine
Carnitine O-Palmitoyltransferase
Cell Cycle
Cell Division
Cell Nucleus
Cell Respiration
Cells, Cultured
Cerebrospinal Fluid
Cerebrovascular Circulation
Chemistry, Organic
Child
Child, Preschool
Chromosome Breakage
Chromosome Deletion
Chromosomes
Clinical Laboratory Techniques
Clinical Trials, Phase I as Topic
Codon, Terminator
Cohort Studies
Colorado
Comparative Genomic Hybridization
Cooperative Behavior
Craniofacial Abnormalities
Cross-Over Studies
Cross-Sectional Studies
Developmental Disabilities
Diet Therapy
Dietary Supplements
Diphosphates
Disease Management
DNA
DNA Footprinting
DNA Mutational Analysis
DNA Nucleotidylexotransferase
DNA Primers
DNA Replication
DNA, Mitochondrial
DNA, Protozoan
DNA, Ribosomal
DNA-Binding Proteins
Double-Blind Method
Drug Therapy, Combination
Dyskinesias
Electron Transport
Energy Metabolism
Enoyl-CoA Hydratase
Enzyme Replacement Therapy
Epilepsy
Exome
Facies
Fasting
Fatal Outcome
Female
Fetal Therapies
Fibroblasts
Follow-Up Studies
Gene Deletion
Gene Dosage
Gene Expression
Gene Expression Regulation
Gene Frequency
Gene Rearrangement
Genetic Association Studies
Genetic Diseases, Inborn
Genetic Predisposition to Disease
Genetic Testing
Genetic Therapy
Genetic Variation
Genetics, Medical
Genetics, Population
Genome, Human
Genomics
Genotype
Glutamine
Glutarates
Glutaryl-CoA Dehydrogenase
Glycerol
Glycogen Storage Disease Type II
Growth Disorders
Heart Arrest
HEK293 Cells
Heterozygote
Hirschsprung Disease
Homeodomain Proteins
Homocysteine
Humans
Hybrid Cells
Hyperammonemia
Hypoglycemia
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Intellectual Disability
Interinstitutional Relations
Laboratories
Language Development Disorders
Leigh Disease
Lentivirus
Leucovorin
Linear Models
Lipid Metabolism, Inborn Errors
Liver
Liver Diseases
Liver Failure, Acute
Liver Neoplasms
Longitudinal Studies
Lymphocytes
Lysine
Lysosomal Storage Diseases
Machine Learning
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Male
Mass Spectrometry
MELAS Syndrome
Mental Retardation, X-Linked
Metabolism, Inborn Errors
Methylmalonic Acid
Microcephaly
Middle Aged
Mitochondria
Mitochondrial Diseases
Models, Biological
Models, Molecular
Molecular Sequence Data
Multigene Family
Muscles
Mutation
Myocardium
Neonatal Screening
Nervous System Diseases
Neurodevelopmental Disorders
Neuropsychological Tests
Niemann-Pick Disease, Type A
Niemann-Pick Diseases
Nitrogenous Group Transferases
Nucleic Acid Amplification Techniques
Oligonucleotide Array Sequence Analysis
Oligonucleotides, Antisense
Open Reading Frames
Organ Specificity
Organic Cation Transport Proteins
Ornithine Carbamoyltransferase
Ornithine Carbamoyltransferase Deficiency Disease
Osmolar Concentration
Oxidative Phosphorylation
Parents
Pedigree
Pharmacogenetics
Phenotype
Phenylbutyrates
Pipecolic Acids
Plasmids
Point Mutation
Polymorphism, Genetic
Prader-Willi Syndrome
Precision Medicine
Predictive Value of Tests
Pregnancy
Prevalence
Promoter Regions, Genetic
Protein Binding
Protein Biosynthesis
Protein Conformation
Protein Structure, Secondary
Protein Subunits
Protein Transport
Pulmonary Artery
Pyridoxine
Quality of Life
Rare Diseases
Receptors, Cell Surface
Recombinant Fusion Proteins
Recombinant Proteins
Registries
Repetitive Sequences, Nucleic Acid
Replication Origin
Repressor Proteins
Reproducibility of Results
Retrospective Studies
Reverse Transcriptase Polymerase Chain Reaction
RNA Polymerase I
RNA Processing, Post-Transcriptional
RNA Splicing
RNA, Messenger
RNA, Protozoan
RNA, Ribosomal
RNA, Small Nucleolar
RNA, Transfer
RNA, Transfer, Leu
Saccharomyces cerevisiae
Seizures
Self Report
Sensitivity and Specificity
Sequence Alignment
Sequence Deletion
Solute Carrier Family 22 Member 5
Sphingomyelin Phosphodiesterase
Splenomegaly
Structure-Activity Relationship
Succinate-CoA Ligases
Surveys and Questionnaires
Syndrome
Tandem Mass Spectrometry
Telomere
Tetraethylammonium
Tetrahymena thermophila
Transcobalamins
Transcription Factors
Transcription, Genetic
Transformation, Genetic
Translocation, Genetic
Treatment Outcome
United States
Urea Cycle Disorders, Inborn
Urinalysis
Vitamin B 12
Vitamin B Complex
Vomiting
Young Adult
Zinc Finger E-box Binding Homeobox 2
Renata's Networks
Concepts (254)
Derived automatically from this person's publications.
Urea Cycle Disorders, Inborn
Lipid Metabolism, Inborn Errors
Ornithine Carbamoyltransferase Deficiency Disease
Neonatal Screening
Metabolism, Inborn Errors
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Co-Authors (47)
People in Profiles who have published with this person.
Shieh, Joseph
UCSF
Gelfand, Amy
UCSF
Norton, Mary
UCSF
Kwok, Pui-Yan
UCSF
Giacomini, Kathy
UCSF
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_
Similar People (60)
People who share similar concepts with this person.
Longo, Nicola
UCLA
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UCSD
Kimonis, Virginia
UCI
Abdenur, Jose
UCI
Puck, Jennifer
UCSF
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Same Department
Atkinson Mcevoy, Lee
Bokser, Seth
Judge, Luke
Kremen, Jess
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