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LINDSAY BURRAGE
Concepts (468)
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Concepts are derived automatically from a person's publications.
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Categories
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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.
14-3-3 Proteins
1-Alkyl-2-acetylglycerophosphocholine Esterase
3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)
Abnormalities, Multiple
Acidosis
Acidosis, Lactic
Actins
Acyl-CoA Dehydrogenase, Long-Chain
Acyl-CoA Oxidase
Adaptor Proteins, Signal Transducing
Adipose Tissue
Adiposity
Adolescent
Adult
Age of Onset
Aged
Agenesis of Corpus Callosum
Alanine Transaminase
Alleles
Alopecia
Alveolar Epithelial Cells
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acid Substitution
Amino Acid Transport System y+L
Amino Acids
Amino Acids, Branched-Chain
Amino Acids, Essential
Ammonia
Androgen-Insensitivity Syndrome
Anemia, Sideroblastic
Animals
Animals, Congenic
Aniridia
Anti-Bacterial Agents
Antibodies, Bacterial
Anxiety
Aorta, Thoracic
Arginase
Arginine
Argininosuccinate Lyase
Argininosuccinic Aciduria
Arthrogryposis
Ascorbic Acid
Ataxia
Autism Spectrum Disorder
Autistic Disorder
Axons
Bartonella henselae
Base Sequence
Biomarkers
Blood Pressure
Blood-Brain Barrier
Body Mass Index
Body Size
Body Weight
Bone and Bones
Bone Development
Bone Diseases, Developmental
Brachydactyly
Brain
Brain Diseases
Caenorhabditis elegans
Caenorhabditis elegans Proteins
Calcium Channels, L-Type
Calcium Channels, R-Type
Carbohydrate Metabolism, Inborn Errors
Cardiovascular Diseases
Cardiovascular System
Carnitine
Carrier Proteins
Cataract
Cation Transport Proteins
Cat-Scratch Disease
Cell Cycle
Cell Differentiation
Cell Lineage
Cell Membrane
Cell Respiration
Cells, Cultured
Central Nervous System
Cerebellar Ataxia
Child
Child Development
Child, Preschool
Chondrodysplasia Punctata
Chromatin Assembly and Disassembly
Chromosomal Instability
Chromosomal Proteins, Non-Histone
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Mammalian
Chronic Disease
Cilia
Claudins
Cleidocranial Dysplasia
Coat Protein Complex I
Coatomer Protein
Cognition
Cohort Studies
Collagen Type I
Collagen Type II
Comparative Genomic Hybridization
Computer Simulation
Congenital Abnormalities
Congenital Hyperinsulinism
Congenital Microtia
Corpus Callosum
Craniofacial Abnormalities
C-Reactive Protein
Critical Care
Crosses, Genetic
Cross-Sectional Studies
Cyclin-Dependent Kinase 8
Cyclin-Dependent Kinases
Cytokine Receptor gp130
Cytokines
Cytoskeletal Proteins
Databases, Factual
Developmental Disabilities
Diabetes Mellitus
Diabetes Mellitus, Type 2
Diagnosis, Computer-Assisted
Diagnosis, Differential
Diet
Diet, Fat-Restricted
Dietary Fats
Disease
Disease Management
Disease Models, Animal
DNA Copy Number Variations
DNA Damage
DNA Helicases
DNA Mutational Analysis
DNA, Mitochondrial
DNA-Binding Proteins
Down-Regulation
Drosophila
Drosophila melanogaster
Drosophila Proteins
Dwarfism
Ectodermal Dysplasia
eIF-2 Kinase
Elasticity Imaging Techniques
Electroencephalography
Embryo, Nonmammalian
Endopeptidases
Endoplasmic Reticulum
Endothelial Cells
Endothelium, Vascular
Enzyme Activation
Epilepsies, Myoclonic
Epilepsy
Epilepsy, Generalized
Epileptic Syndromes
Epistasis, Genetic
Exome
Exons
Exosomes
Face
Facies
Fasting
Fatty Liver
F-Box Proteins
Female
Ferrets
Fibroblasts
Filamins
Flavoproteins
Follow-Up Studies
Food, Formulated
Fractures, Bone
Frameshift Mutation
Fucosyltransferases
Gait
Geminin
Gene Deletion
Gene Expression
Gene Expression Regulation
Gene Expression Regulation, Developmental
Genes, Dominant
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Carrier Screening
Genetic Counseling
Genetic Diseases, Inborn
Genetic Linkage
Genetic Predisposition to Disease
Genetic Testing
Genetic Therapy
Genetic Variation
Genetics, Medical
Genetics, Population
Genome
Genomics
Genotype
Gluconeogenesis
Glucose
Glutathione
Glutathione Synthase
Glycerol
Glycolysis
Glycosylation
Golgi Apparatus
Gonads
Growth Disorders
GTPase-Activating Proteins
Guanine Nucleotide Exchange Factors
Guanosine Diphosphate Fucose
Guanosine Diphosphate Mannose
Hand
Hand Deformities, Congenital
Haploinsufficiency
Hearing Loss, Sensorineural
Heart Defects, Congenital
Hedgehog Proteins
HEK293 Cells
Hematologic Diseases
Hep G2 Cells
Hereditary Central Nervous System Demyelinating Diseases
Hernias, Diaphragmatic, Congenital
Heterozygote
High-Throughput Nucleotide Sequencing
Hip Joint
Histidine
Histone Demethylases
Homeostasis
Homocystinuria
Homozygote
Hospitalization
Humans
Hydroxocobalamin
Hyperammonemia
Hyperargininemia
Hypertension
Hypertension, Pulmonary
Hypoglycemia
In Situ Hybridization, Fluorescence
INDEL Mutation
Infant
Infant Care
Infant Formula
Infant, Newborn
Information Dissemination
Inheritance Patterns
Inositol 1,4,5-Trisphosphate Receptors
Insulin Resistance
Insulin-Like Growth Factor I
Intellectual Disability
Intensive Care Units, Pediatric
Internationality
Introns
Job Syndrome
Karyotype
Kidney
Kinetics
Larynx
Length of Stay
Leukoencephalopathies
Ligases
Limb Deformities, Congenital
Lipid Metabolism, Inborn Errors
Liver
Liver Cirrhosis
Liver Diseases
Liver Function Tests
Liver Glycogen
Liver Transplantation
Long QT Syndrome
Longitudinal Studies
Loss of Function Mutation
Lung
Lung Diseases
Lung Diseases, Interstitial
Lung Transplantation
Macaca fascicularis
Magnetic Resonance Imaging
Male
Maple Syrup Urine Disease
Mass Spectrometry
Membrane Proteins
Mental Status and Dementia Tests
Metabolic Diseases
Metabolic Networks and Pathways
Metabolic Syndrome
Metabolism, Inborn Errors
Metabolomics
Metalloendopeptidases
Methylmalonic Acid
Mice
Mice, Congenic
Mice, Inbred A
Mice, Inbred C57BL
Mice, Knockout
Mice, Mutant Strains
Mice, Transgenic
Microcephaly
Microfilament Proteins
Micrognathism
Micronutrients
Microsatellite Repeats
Microtubule-Associated Proteins
Middle Aged
Mitochondria, Liver
Mitochondrial Diseases
Mitochondrial Myopathies
Mitochondrial Proton-Translocating ATPases
Models, Animal
Models, Biological
Models, Genetic
Molecular Sequence Data
Mosaicism
Movement Disorders
Multicenter Studies as Topic
Multifactorial Inheritance
Multiple Carboxylase Deficiency
Multiprotein Complexes
Muscle Hypotonia
Muscle Proteins
Muscle, Skeletal
Muscular Diseases
Musculoskeletal Abnormalities
Mutation
Mutation, Missense
Myopathies, Structural, Congenital
Myosins
Nails, Malformed
National Institutes of Health (U.S.)
Neonatal Screening
Neoplasm Proteins
Neovascularization, Pathologic
Nerve Degeneration
Nerve Tissue Proteins
Nervous System Malformations
Neurodevelopmental Disorders
Neuroglia
Neuromuscular Junction
NF-kappa B
NIH 3T3 Cells
Nitric Acid
Nitric Oxide
Nuclear Proteins
Nucleotide Transport Proteins
Obesity
Oligonucleotide Array Sequence Analysis
Organ Transplantation
Osteoblasts
Osteochondrodysplasias
Osteogenesis
Osteogenesis Imperfecta
Osteoporosis
Ovary
Overweight
Oxidative Phosphorylation
Oxidative Stress
Patella
Pathology, Molecular
Patient Care Team
Pedigree
Phenotype
Phenylalanine
Phenylbutyrates
Phenylketonurias
Phosphatidylinositol Phosphates
Phosphoprotein Phosphatases
Phosphoric Monoester Hydrolases
Phosphotransferases (Alcohol Group Acceptor)
Pneumonectomy
Point Mutation
Polymerase Chain Reaction
Prader-Willi Syndrome
Precision Medicine
Pregnancy
Prevalence
Primary Ovarian Insufficiency
Problem Behavior
Prognosis
Propionic Acidemia
Prospective Studies
Proteasome Endopeptidase Complex
Protein Binding
Protein Precursors
Protein Stability
Proteolysis
Proteomics
Pulmonary Surfactant-Associated Protein C
Pulmonary Surfactant-Associated Proteins
Pulmonary Surfactants
Quality of Life
Quantitative Trait Loci
Quantitative Trait, Heritable
rab5 GTP-Binding Proteins
Radiography
Random Allocation
Rare Diseases
Rats
Recombinant Proteins
Renal Replacement Therapy
Reproducibility of Results
Respiratory Insufficiency
Retrospective Studies
RNA Splicing
RNA, Small Interfering
Seizures
Sensitivity and Specificity
Separase
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Amino Acid
Serologic Tests
Severity of Illness Index
Sex Determination Processes
Sex Factors
Sexual Development
Sexual Maturation
Signal Transduction
Skin
Smith-Magenis Syndrome
Spasms, Infantile
Spectrin
Status Epilepticus
Steroid Isomerases
Steroidogenic Factor 1
Sterols
Sudden Infant Death
Symptom Assessment
Syndactyly
Syndrome
Tandem Mass Spectrometry
T-Box Domain Proteins
Testis
Texas
Th2 Cells
Tibial Fractures
Time Factors
Toes
TOR Serine-Threonine Kinases
Trans-Activators
Transcription Factors
Transposases
Treatment Outcome
Triglycerides
Trisomy
Ubiquitin
Ubiquitin-Protein Ligases
Ubiquitins
Ultrasonography
Uniparental Disomy
United States
Up-Regulation
Urea
Urea Cycle Disorders, Inborn
Vestibular Diseases
Vitamin B 12 Deficiency
Weight Gain
White Matter
Whole Genome Sequencing
X-Ray Microtomography
Young Adult
Zebrafish
BURRAGE's Networks
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Concepts (468)
Derived automatically from this person's publications.
Urea Cycle Disorders, Inborn
Amino Acid Metabolism, Inborn Errors
Intellectual Disability
Osteochondrodysplasias
Argininosuccinate Lyase
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Co-Authors (131)
People in Profiles who have published with this person.
NAGAMANI, SANDESH
LEE, BRENDAN
BACINO, CARLOS
ELSEA, SARAH
EMRICK, LISA
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
ELSEA, SARAH
GIBBS, RICHARD
BOERWINKLE, ERIC
STANKIEWICZ, PAWEL
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Same Department
People who are also in this person's primary department.
MATHUR, VEENA
RICONDA, DANIEL
SHAULSKY, GAD
WORLEY, KIM
ZHANG, BING
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Physical Neighbors
People whose addresses are nearby this person.
BAJIC, ALEKSANDAR
LEWIS, RICHARD
NASSEF, SALMA
NEHRING, RALF
SUN, QIN
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