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SARAH ELSEA
Concepts (658)
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Concepts are derived automatically from a person's publications.
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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.
12-Hydroxy-5,8,10,14-eicosatetraenoic Acid
Abnormalities, Multiple
Acetylcholine
Acetylserotonin O-Methyltransferase
Acid Ceramidase
Acid Sensing Ion Channels
Acidosis, Lactic
Actins
Acyl-CoA Dehydrogenase, Long-Chain
Acyltransferases
Adaptation, Psychological
Adaptor Proteins, Signal Transducing
Adolescent
Adult
Age Factors
Aged
Aged, 80 and over
Aggression
Algorithms
Alleles
alpha-MSH
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acid Substitution
Amino Acids
Ammonia
Amniotic Fluid
Amsacrine
Anemia, Macrocytic
Anemia, Sickle Cell
Anemia, Sideroblastic
Animals
Anti-Anxiety Agents
Antigens, Neoplasm
Anti-Infective Agents
Antineoplastic Agents
Anxiety
Aorta, Thoracic
Apoptosis
Apyrase
Arachidonate 12-Lipoxygenase
Arginase
Arginine
Arginine-tRNA Ligase
Argininosuccinate Lyase
Argininosuccinate Synthase
Argininosuccinic Aciduria
Aromatic-L-Amino-Acid Decarboxylases
Aspirin
Ataxia Telangiectasia
Attitude to Health
Autism Spectrum Disorder
Autistic Disorder
Automation
Autonomic Nervous System Diseases
Autophagy
Base Sequence
Behavior
Behavior, Animal
Benzamides
Benzofurans
Binding Sites
Binding, Competitive
Biomarkers
Bipolar Disorder
Blood Chemical Analysis
Blood Glucose
Blood Specimen Collection
Blotting, Southern
Blotting, Western
B-Lymphocytes
Body Composition
Body Fat Distribution
Body Mass Index
Body Weight
Brachydactyly
Brain
Brain Diseases
Brain Diseases, Metabolic, Inborn
Brain-Derived Neurotrophic Factor
Bulbar Palsy, Progressive
Carbidopa
Carbohydrate Metabolism, Inborn Errors
Carcinoma, Pancreatic Ductal
Cardiomyopathies
Caregivers
Carnitine
Carrier Proteins
Case-Control Studies
Cattle
CCAAT-Enhancer-Binding Proteins
Cell Cycle
Cell Cycle Proteins
Cell Death
Cell Differentiation
Cell Line
Cell Line, Tumor
Cell Movement
Cell Proliferation
Cell Survival
Cells, Cultured
Cerebellar Neoplasms
Cerebrospinal Fluid
Cerebrospinal Fluid Proteins
Chemistry Techniques, Analytical
Chemokines
Child
Child Behavior Disorders
Child Development
Child Development Disorders, Pervasive
Child, Preschool
Chile
CHO Cells
Cholesterol
Cholesterol, HDL
Cholesterol, LDL
Chondrogenesis
Chromatin
Chromatography, High Pressure Liquid
Chromatography, Liquid
Chromosome Aberrations
Chromosome Banding
Chromosome Breakage
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Mapping
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 5
Ciprofloxacin
Circadian Rhythm
Citric Acid
Citric Acid Cycle
Citrulline
Citrullinemia
Clinical Chemistry Tests
Clinical Trials as Topic
CLOCK Proteins
Cloning, Molecular
Codon
Coenzymes
Cohort Studies
Combined Modality Therapy
Comparative Genomic Hybridization
Computational Biology
Computer Graphics
Computer Simulation
Consanguinity
Consensus
Conserved Sequence
COP9 Signalosome Complex
COS Cells
CpG Islands
Craniofacial Abnormalities
Cricetinae
CRISPR-Cas Systems
Crosses, Genetic
Cross-Over Studies
Cross-Sectional Studies
Cryptochromes
Cyclohexanones
Cyclopropanes
Cysteine
Cytochrome P-450 CYP1A2
Databases, Factual
De Lange Syndrome
DEAD Box Protein 58
Degenerin Sodium Channels
Delivery of Health Care
Developmental Disabilities
Diabetes, Gestational
Diagnosis, Computer-Assisted
Diagnosis, Differential
Diet, High-Fat
Diet, Ketogenic
Dietary Carbohydrates
Dietary Supplements
Dihydropteridine Reductase
Dihydroxyphenylalanine
Dilatation
Disease Management
Disease Models, Animal
Disease Progression
Disease Susceptibility
DNA
DNA Copy Number Variations
DNA Damage
DNA Methylation
DNA Mutational Analysis
DNA Primers
DNA Replication
DNA Topoisomerases, Type I
DNA Topoisomerases, Type II
DNA, Complementary
DNA, Superhelical
DNA-Binding Proteins
Dopa Decarboxylase
Dopamine
Dopamine Agonists
Dose-Response Relationship, Drug
Dose-Response Relationship, Radiation
Double-Blind Method
Down Syndrome
Drosophila melanogaster
Drug Combinations
Drug Interactions
Drug Resistance
Drug Resistance, Microbial
Dynamins
Dysarthria
Edetic Acid
Electroencephalography
Electron Transport
Electron Transport Complex IV
Electrophoresis, Agar Gel
Electrophoresis, Polyacrylamide Gel
Ellipticines
Endophenotypes
Energy Metabolism
Enoyl-CoA Hydratase
Enzyme Activation
Enzyme Inhibitors
Epidermal Growth Factor
Epidermis
Epigenesis, Genetic
Epilepsy
Epilepsy, Generalized
Epileptic Syndromes
Epithelial Sodium Channels
Erythrocytes
Escherichia coli
Esophageal Motility Disorders
Etoposide
Exome
Exons
Exostoses, Multiple Hereditary
Expressed Sequence Tags
Facial Bones
Facies
Family
Family Health
Farber Lipogranulomatosis
Fasting
Fatty Acids
Feeding Behavior
Female
Fetus
Fever
Fibroblasts
Fingers
Fluoroquinolones
Foot Deformities, Congenital
Fragile X Mental Retardation Protein
Fragile X Syndrome
Frameshift Mutation
gamma-Aminobutyric Acid
Gene Amplification
Gene Deletion
Gene Dosage
Gene Duplication
Gene Editing
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Frequency
Gene Knockdown Techniques
Gene Regulatory Networks
Gene Targeting
Genes, Bacterial
Genes, Dominant
Genes, Fungal
Genes, Recessive
Genetic Association Studies
Genetic Carrier Screening
Genetic Counseling
Genetic Diseases, Inborn
Genetic Linkage
Genetic Markers
Genetic Pleiotropy
Genetic Predisposition to Disease
Genetic Services
Genetic Testing
Genetic Therapy
Genetic Variation
Genistein
Genome, Human
Genome-Wide Association Study
Genotype
Gestational Age
Glucosephosphate Dehydrogenase Deficiency
Glutamine
Glutathione
Glycerol
Glycine
Glycine Hydroxymethyltransferase
Grenada
Growth Charts
Growth Disorders
GTP Phosphohydrolases
GTP-Binding Proteins
Guinea Pigs
Hand Deformities, Congenital
Haploidy
Haploinsufficiency
Haplotypes
Health Knowledge, Attitudes, Practice
Health Services Accessibility
Hearing Loss
Hearing Loss, Sensorineural
Heart Failure
Hedgehog Proteins
HEK293 Cells
Hematopoietic Stem Cell Transplantation
Hemochromatosis
Hemochromatosis Protein
Hepatocytes
Hereditary Central Nervous System Demyelinating Diseases
Heterozygote
High-Throughput Nucleotide Sequencing
Histidine
Histocompatibility Antigens Class I
Histone Deacetylases
History, 20th Century
HLA Antigens
Homocysteine
Homologous Recombination
Homozygote
Humans
Hunger
Hybrid Cells
Hydrolases
Hyperammonemia
Hyperargininemia
Hypercholesterolemia
Hyperphagia
Hypertension, Pulmonary
Hyperventilation
Hypoglycemia
Hypothalamic Diseases
Hypothalamus
Ileum
Immunoglobulin Class Switching
Immunologic Deficiency Syndromes
Immunologic Memory
In Situ Hybridization, Fluorescence
In Vitro Techniques
INDEL Mutation
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Information Theory
Intellectual Disability
Interleukin-8
Internationality
Intracellular Signaling Peptides and Proteins
Introns
Iodine Radioisotopes
Isoflavones
Kinetics
Language Development Disorders
Leigh Disease
Levodopa
Limit of Detection
Linear Models
Lipid Metabolism, Inborn Errors
Litter Size
Liver
Liver Transplantation
Longitudinal Studies
Loss of Heterozygosity
Luciferases
Lymphocytes
Lysosomal Storage Diseases
Macaca fascicularis
Machine Learning
Macromolecular Substances
Magnetic Resonance Imaging
Male
Mammals
Mass Screening
Mass Spectrometry
Maternal Behavior
Medulloblastoma
MELAS Syndrome
Melatonin
Membrane Proteins
Mental Disorders
Metabolic Diseases
Metabolic Networks and Pathways
Metabolism, Inborn Errors
Metabolome
Metabolomics
Methionine
Metoclopramide
Mice
Mice, Congenic
Mice, Inbred C57BL
Mice, Inbred Strains
Mice, Knockout
Mice, Transgenic
Michigan
Microarray Analysis
Microcephaly
Middle Aged
Mitochondria
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Mitochondrial Proteins
Models, Genetic
Models, Molecular
Models, Structural
Molecular Diagnostic Techniques
Molecular Probe Techniques
Molecular Sequence Annotation
Molecular Sequence Data
Molecular Structure
Molybdenum
Monosaccharide Transport Proteins
Mothers
Moyamoya Disease
Multigene Family
Muscle Contraction
Muscle Hypotonia
Muscle, Smooth
Muscles
Muscular Atrophy, Spinal
Muscular Diseases
Musculoskeletal Abnormalities
Mutagenesis, Site-Directed
Mutation
Mutation, Missense
Myelin Proteins
Myoclonic Epilepsies, Progressive
NAD
NADP
NAV1.3 Voltage-Gated Sodium Channel
Neonatal Screening
Neoplasm Proteins
Neoplasms, Experimental
Nerve Tissue Proteins
Neural Crest
Neural Stem Cells
Neurodevelopmental Disorders
Neuroectodermal Tumors, Primitive
Neurons
Neurotransmitter Agents
NF-kappa B
Niacin
Nitric Oxide Donors
Nitrobenzoates
Nitrogen
Nuclear Proteins
Nucleic Acid Amplification Techniques
Nucleic Acid Conformation
Nucleic Acid Hybridization
Nucleocytoplasmic Transport Proteins
Nucleotidyltransferases
Obesity
Obesity Hypoventilation Syndrome
Obesity, Morbid
Oligodeoxyribonucleotides
Oligonucleotide Array Sequence Analysis
Open Reading Frames
Ornithine Carbamoyltransferase Deficiency Disease
Oscillometry
Otitis
Overweight
Oxidoreductases
Pancreatic Neoplasms
Paraplegia
Parents
Patient Satisfaction
Pedigree
Penetrance
Pentose Phosphate Pathway
Period Circadian Proteins
Peripheral Nervous System Diseases
Peroxisomal Disorders
Peroxisomes
Phenotype
Phenylacetates
Phenylbutyrates
Phosphatidylcholines
Phosphoglycerate Dehydrogenase
Phylogeny
Physicians
Pierre Robin Syndrome
Pilot Projects
Plasma
Plasmids
Pneumonia
Point Mutation
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Practice Guidelines as Topic
Prader-Willi Syndrome
Precipitin Tests
Precision Medicine
Pre-Eclampsia
Pregnancy
Prenatal Diagnosis
Prevalence
Primary Cell Culture
Problem Behavior
Prognosis
Promoter Regions, Genetic
Prospective Studies
Proteasome Endopeptidase Complex
Protein Array Analysis
Protein Interaction Mapping
Protein Kinases
Protein Transport
Proteins
Pseudogenes
Psychomotor Disorders
Psychomotor Performance
Psychopathology
Purpura
Pyrroline Carboxylate Reductases
Pyruvate Dehydrogenase Complex Deficiency Disease
Quality of Life
Quinolones
Rabbits
Racemases and Epimerases
Radiation Tolerance
Radiography
Rare Diseases
Rats
Rats, Inbred Strains
Receptor, Melanocortin, Type 4
Receptors, Cytoplasmic and Nuclear
Receptors, G-Protein-Coupled
Receptors, Immunologic
Receptors, Interleukin
Receptors, Interleukin-8B
Receptors, Prolactin
Recombinant Fusion Proteins
Recombinant Proteins
Recombination, Genetic
Referral and Consultation
Repressor Proteins
Reproducibility of Results
Restriction Mapping
Retrospective Studies
Reverse Transcriptase Polymerase Chain Reaction
Riboflavin
Riboflavin Deficiency
RNA
RNA, Messenger
RNA, Small Interfering
ROC Curve
Saccharomyces cerevisiae
Satiety Response
Schizophrenia
Seizures
Selection, Genetic
Self-Injurious Behavior
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Amino Acid
Sequence Tagged Sites
Serine
Serotonin
Severity of Illness Index
Sex Factors
Sheep
Sibling Relations
Siblings
Signal Transduction
Sinusitis
Skull
Sleep
Sleep Disorders, Circadian Rhythm
Sleep Initiation and Maintenance Disorders
Sleep Wake Disorders
Smith-Magenis Syndrome
Social Behavior
Social Support
Sodium Channels
Sodium Dodecyl Sulfate
Sodium-Calcium Exchanger
Somnambulism
Spasms, Infantile
Spastic Paraplegia, Hereditary
Species Specificity
Speech Disorders
Sphingomyelins
Spleen
Stereotyped Behavior
Sterol Esterase
Sterol Regulatory Element Binding Protein 1
Stress, Psychological
Stroke
Structure-Activity Relationship
Succinate-Semialdehyde Dehydrogenase
Sulfite Oxidase
Suppression, Genetic
Supratentorial Neoplasms
Symporters
Syndrome
Tandem Mass Spectrometry
Tandem Repeat Sequences
Tetrodotoxin
Thymidine
Thymidine Phosphorylase
Thymus Gland
Time
Time Factors
Topoisomerase II Inhibitors
TOR Serine-Threonine Kinases
Trans-Activators
Transaldolase
Transaminases
Transcription Factor 4
Transcription Factors
Transcription, Genetic
Transcriptional Activation
Transcriptome
Transgenes
trans-Golgi Network
Transketolase
Translocation, Genetic
Treatment Outcome
Tretinoin
Trichloroacetic Acid
Triglycerides
Trinucleotide Repeats
Trisomy
Tryptophan
Tyrosine
Tyrosinemias
Uncertainty
United States
Urea
Urea Cycle Disorders, Inborn
Urinalysis
Vanilmandelic Acid
Veterans
Waist Circumference
Weight Loss
West Indies
White Matter
Whole Genome Sequencing
Wolman Disease
Xenopus
Xenopus laevis
Xenopus Proteins
X-Rays
Young Adult
Zebrafish
Zellweger Syndrome
ELSEA's Networks
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Concepts (658)
Derived automatically from this person's publications.
Metabolomics
Smith-Magenis Syndrome
Intellectual Disability
Metabolism, Inborn Errors
Abnormalities, Multiple
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Co-Authors (84)
People in Profiles who have published with this person.
GLINTON, KEVIN
SCAGLIA, FERNANDO
SUTTON, VERNON
GIJAVANEKAR, CHARUL
Cappuccio, Gerarda
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
BOERWINKLE, ERIC
STANKIEWICZ, PAWEL
GIBBS, RICHARD
CHEUNG, SAU WAI
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Same Department
People who are also in this person's primary department.
ERWIN, GRAHAM
LEE, BRENDAN
NAKADA, DAISUKE
RETROUVEY, JEAN-MARC
SCHULZE, KATHARINA
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Physical Neighbors
People whose addresses are nearby this person.
BAJIC, ALEKSANDAR
BURRAGE, LINDSAY
ROBBINS-FURMAN, PATRICIA
SUN, QIN
WANG, YUE
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