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Pediatrics CRA
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VERNON SUTTON
Concepts (754)
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Concepts are derived automatically from a person's publications.
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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
3-Oxo-5-alpha-Steroid 4-Dehydrogenase
46, XX Disorders of Sex Development
Abnormalities, Multiple
Absorptiometry, Photon
Acetylgalactosamine
Acidosis
Acids
Aconitate Hydratase
Acyl-CoA Dehydrogenase, Long-Chain
Acyltransferases
Adaptor Proteins, Signal Transducing
Adenosine Triphosphatases
Adenosine Triphosphate
Adipose Tissue
Adipose Tissue, White
Administration, Oral
Adolescent
Adrenal Hyperplasia, Congenital
Adult
Age Factors
Age of Onset
Aged
Agenesis of Corpus Callosum
Aicardi Syndrome
Alcohol Oxidoreductases
Alleles
alpha-Fetoproteins
alpha-Mannosidosis
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acid Substitution
Amino Acids
Ammonia
Amniocentesis
Amniotic Fluid
Androgen-Insensitivity Syndrome
Androgens
Anemia, Macrocytic
Anemia, Megaloblastic
Animals
Anthropometry
Antibiotics, Antineoplastic
Antibodies
Antibodies, Neutralizing
Antineoplastic Combined Chemotherapy Protocols
Apoptosis
Appetite Depressants
Appetite Regulation
Apyrase
Arginase
Arginine
Argininosuccinate Lyase
Argininosuccinate Synthase
Argininosuccinic Acid
Argininosuccinic Aciduria
Aromatic-L-Amino-Acid Decarboxylases
Arteriovenous Malformations
Arthrogryposis
Arylsulfatases
Ascorbic Acid
Aspartate Carbamoyltransferase
Ataxia
ATPases Associated with Diverse Cellular Activities
Autism Spectrum Disorder
Autistic Disorder
Autopsy
Base Sequence
Binding Sites
Biocatalysis
Biological Clocks
Biological Transport
Biomarkers
Biopsy
Birth Weight
Blindness, Cortical
Blood Chemical Analysis
Blood Transfusion
Blood-Brain Barrier
Blotting, Southern
Body Composition
Body Height
Body Mass Index
Body Weight
Bone and Bones
Bone Density
Bone Density Conservation Agents
Bone Development
Bone Diseases, Developmental
Bone Marrow
Bone Marrow Cells
Bone Neoplasms
Bradycardia
Brain
Brain Diseases, Metabolic, Inborn
Bulbar Palsy, Progressive
Caenorhabditis elegans
Calcium-Calmodulin-Dependent Protein Kinase Type 2
Camurati-Engelmann Syndrome
Canada
Capillaries
Carbamoyl-Phosphate Synthase (Ammonia)
Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing)
Carbohydrate Metabolism, Inborn Errors
Cardiomyopathy, Hypertrophic
Cardiomyopathy, Restrictive
Cardiovascular Abnormalities
Carnitine
Carnitine O-Palmitoyltransferase
Carrier Proteins
Cartilage
Caspase Inhibitors
Cathepsin A
CCCTC-Binding Factor
Cell Cycle
Cell Cycle Proteins
Cell Differentiation
Cell Line
Cell Nucleolus
Cell Nucleus
Cell Shape
Cell Transdifferentiation
Cells, Cultured
Cellular Reprogramming
Central Nervous System Cysts
Cerebellum
Certification
Cesarean Section
Child
Child Development
Child, Preschool
China
Choanal Atresia
Cholic Acids
Chondroitin Sulfate Proteoglycans
Chondroitinsulfatases
Choroid Diseases
Chromatography, Liquid
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Banding
Chromosome Breakage
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosome Segregation
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 12
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 19
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 7
Chromosomes, Human, X
Chronic Pain
Circadian Rhythm
Citrulline
Citrullinemia
Class I Phosphatidylinositol 3-Kinases
Cleft Lip
Cleft Palate
Clinical Decision-Making
Coat Protein Complex I
Coatomer Protein
Codon, Nonsense
Coffin-Lowry Syndrome
Cohort Studies
Collagen Type I
Comparative Genomic Hybridization
Computational Biology
Computer Simulation
Confidentiality
Congenital Abnormalities
Congenital Disorders of Glycosylation
Connective Tissue
Consanguinity
Consensus
Consensus Sequence
Consent Forms
Coroners and Medical Examiners
Craniofacial Abnormalities
Creatine
Critical Care
Cross-Over Studies
Cross-Sectional Studies
Cyclic AMP
Cyclic AMP-Dependent Protein Kinases
Cyclic GMP
Cyclophosphamide
Cytogenetic Analysis
Cytosol
Cytotoxicity, Immunologic
Databases, Factual
Databases, Genetic
De Lange Syndrome
DEAD-box RNA Helicases
Deafness
Decision Making
Delivery of Health Care, Integrated
Delphi Technique
Dental Caries
Dependovirus
Developmental Disabilities
Dexamethasone
Diagnosis, Differential
Diagnostic Errors
Diet
Diet, Protein-Restricted
Dietary Supplements
DiGeorge Syndrome
Dihydroorotase
Dihydroxyphenylalanine
Diphosphonates
Disclosure
Disease Management
Disease Models, Animal
Disease Progression
Dishevelled Proteins
Disorders of Excessive Somnolence
Disorders of Sex Development
DNA
DNA Copy Number Variations
DNA Methylation
DNA Mutational Analysis
DNA Primers
DNA Replication
DNA, Complementary
DNA, Mitochondrial
DNA-Binding Proteins
Dopa Decarboxylase
Dose-Response Relationship, Drug
Double-Blind Method
Down-Regulation
Doxorubicin
Drug Administration Schedule
Dwarfism
Dysarthria
Early Diagnosis
Ectodermal Dysplasia
Educational Measurement
Ehlers-Danlos Syndrome
Elastin
Electroencephalography
Embryo, Nonmammalian
Emergency Medical Services
Endocrinology
Endoplasmic Reticulum
Enzyme Activation
Enzyme Replacement Therapy
Enzyme Therapy
Epilepsies, Myoclonic
Epilepsy
Epilepsy, Generalized
Estriol
Estrogens
Ethics, Medical
Ethics, Professional
Etoposide
Evidence-Based Medicine
Evidence-Based Practice
Exercise Test
Exome
Exons
Exonucleases
Extracellular Matrix
Extracellular Matrix Proteins
Extracorporeal Membrane Oxygenation
Extremities
Eye
Eye Abnormalities
Eye Diseases, Hereditary
Eye Movements
Eyelids
Facial Bones
Facial Paralysis
Facies
Failure to Thrive
Family
Family Characteristics
Family Health
fas Receptor
Fasting
Fatal Outcome
Fear
Female
Femoral Artery
Femur
Fertilization in Vitro
Fetal Alcohol Spectrum Disorders
Fetal Growth Retardation
Fetus
Fibrillar Collagens
Fibrillin-1
Fibroblasts
Fibronectins
Flow Cytometry
Focal Dermal Hypoplasia
Follow-Up Studies
Foot
Forecasting
Forkhead Transcription Factors
Founder Effect
Fracture Fixation
Fractures, Bone
Fragile X Mental Retardation Protein
Frameshift Mutation
Gastroesophageal Reflux
Gastrostomy
Gaucher Disease
Gender Identity
Gene Components
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Frequency
Gene Library
Gene Order
Gene Rearrangement
Genes
Genes, Dominant
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Carrier Screening
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Heterogeneity
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Therapy
Genetic Variation
Genetic Vectors
Genetics
Genetics, Medical
Genitalia
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomic Structural Variation
Genomics
Genotype
Genotyping Techniques
Global Health
Glucose
Glucuronidase
Glutamic Acid
Glutamine
Glutarates
Glutathione
Glutathione Synthase
Glycerol
Glycine
Glycoproteins
Glycosaminoglycans
Glycosylation
Glypicans
Golgi Apparatus
Gonadal Dysgenesis, 46,XY
Gonads
Granzymes
Growth Disorders
GTP-Binding Protein beta Subunits
Guidelines as Topic
Hamartoma Syndrome, Multiple
Hand
Hand Deformities, Congenital
Haploinsufficiency
Health Planning Guidelines
Health Status
Health Surveys
Hearing Loss
Hearing Loss, Sensorineural
Heart Defects, Congenital
Heart Function Tests
Heart Rate
Heart Ventricles
HEK293 Cells
Hematologic Tests
Hepatocyte Nuclear Factor 1-beta
Hepatocytes
Hernia, Inguinal
Hernias, Diaphragmatic, Congenital
Heterozygote
High-Throughput Nucleotide Sequencing
Hip Dislocation
Histidine
Histone Deacetylases
Histone-Lysine N-Methyltransferase
History, 20th Century
History, 21st Century
Homocystinuria
Homozygote
Hormones
Hospitalization
Human Growth Hormone
Humans
Huntington Disease
Hydroxocobalamin
Hydroxylation
Hyperammonemia
Hyperplasia
Hypertelorism
Hypoglycemia
Hypospadias
Hypothalamus
Ifosfamide
In Situ Hybridization, Fluorescence
Incidence
Induced Pluripotent Stem Cells
Infant
Infant Care
Infant Formula
Infant Mortality
Infant, Newborn
Infant, Newborn, Diseases
Informed Consent
Inheritance Patterns
Injections, Intramuscular
Insulin
Intellectual Disability
Intensive Care Units, Neonatal
Intensive Care Units, Pediatric
Internet
Internship and Residency
Intracellular Signaling Peptides and Proteins
Isochromosomes
Isoleucine
Jews
Keratan Sulfate
Laboratories
Language Development Disorders
Leg
Length of Stay
Limb Deformities, Congenital
Limit of Detection
Lipid Metabolism, Inborn Errors
Lipoma
Liver
Liver Function Tests
Liver Neoplasms, Experimental
Liver Transplantation
Logistic Models
Lower Extremity Deformities, Congenital
Lumbar Vertebrae
Lysine
Lysosomal Storage Diseases
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Malocclusion
Maple Syrup Urine Disease
Mass Screening
Mass Spectrometry
Medical Informatics
Meglutol
Membrane Glycoproteins
Membrane Proteins
Mental Retardation, X-Linked
Metabolic Networks and Pathways
Metabolism, Inborn Errors
Metabolome
Metabolomics
Metalloendopeptidases
Methylmalonic Acid
Mice
Mice, Inbred C57BL
Mice, Inbred Strains
Mice, Knockout
Mice, Obese
Mice, Transgenic
Microcephaly
Microfilament Proteins
Microsatellite Repeats
Microscopy, Fluorescence
Middle Aged
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Mitochondrial Proteins
Mobility Limitation
Mobius Syndrome
Models, Animal
Models, Molecular
Molecular Chaperones
Molecular Sequence Data
Monosomy
Mosaicism
Motor Activity
Mouth Abnormalities
Mucopolysaccharidosis IV
Mucopolysaccharidosis VII
Muridae
Muscle Hypotonia
Muscle Strength
Muscle, Skeletal
Muscular Diseases
Musculoskeletal Abnormalities
Mutation
Mutation, Missense
Myeloid-Lymphoid Leukemia Protein
National Institutes of Health (U.S.)
Neonatal Screening
Neoplasm Proteins
Neoplasms
Nerve Tissue Proteins
Nervous System
Nervous System Malformations
Neurocognitive Disorders
Neurodevelopmental Disorders
Neuroimaging
Neurons
Neuropsychological Tests
Nevus
NIH 3T3 Cells
Nitric Oxide
Nitrogen
Nondisjunction, Genetic
Noonan Syndrome
North America
N-Terminal Acetyltransferase A
N-Terminal Acetyltransferase E
Nuclear Envelope
Nuclear Proteins
Nucleic Acid Amplification Techniques
Nucleic Acid Conformation
Nucleic Acid Hybridization
Nutritional Physiological Phenomena
Obesity
Ocular Motility Disorders
Oligonucleotide Array Sequence Analysis
Ophthalmoplegia
Optic Atrophy
Optic Nerve Diseases
Oral Health
Orbital Diseases
Organ Specificity
Ornithine Carbamoyltransferase
Ornithine Carbamoyltransferase Deficiency Disease
Osteochondrodysplasias
Osteogenesis Imperfecta
Osteopetrosis
Osteoporosis
Osteosclerosis
Otorhinolaryngologic Diseases
Overweight
Oxidoreductases
Pain Management
Paraplegia
Pathology, Molecular
Patient Care Team
Patient Reported Outcome Measures
Patient Rights
Patient Safety
Pediatrics
Pedigree
Pentose Phosphate Pathway
Peptide Fragments
Peptide Hormones
Perforin
Periventricular Nodular Heterotopia
Peroxisomal Disorders
Phenotype
Phenylacetates
Phenylalanine
Phenylalanine Hydroxylase
Phenylbutyrates
Phenylketonurias
Phosphatidylcholines
Phosphatidylinositol 3-Kinases
Phosphatidylinositols
Phosphoglycerate Dehydrogenase
Phosphoproteins
Phosphorylation
Pilot Projects
Plasma Membrane Neurotransmitter Transport Proteins
Platybasia
Point Mutation
Polyhydramnios
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Polymorphism, Single Nucleotide
Polysomnography
Pore Forming Cytotoxic Proteins
Practice Guidelines as Topic
Prader-Willi Syndrome
Pregnancy
Pregnancy Complications
Prenatal Diagnosis
Prevalence
Progeria
Prognosis
Promoter Regions, Genetic
Propionic Acidemia
Prospective Studies
Protein Array Analysis
Protein Binding
Protein Processing, Post-Translational
Protein Structure, Tertiary
Protein Tyrosine Phosphatase, Non-Receptor Type 11
Proteins
Proteomics
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-akt
Psychometrics
Psychomotor Disorders
Puberty
Pupil Disorders
Qualitative Research
Quality of Life
Radiography
Rare Diseases
Rats
Receptor Tyrosine Kinase-like Orphan Receptors
Receptors, Androgen
Receptors, G-Protein-Coupled
Recombinant Proteins
Recurrence
Referral and Consultation
Regulatory Sequences, Nucleic Acid
Repressor Proteins
Reproducibility of Results
Respiratory Function Tests
Respiratory Insufficiency
Respiratory Tract Diseases
Retinal Diseases
Retrospective Studies
Rett Syndrome
Riboflavin
Riboflavin Deficiency
Ribosomal Protein S6 Kinases, 90-kDa
Risk Assessment
Risk Factors
RNA Helicases
RNA Splice Sites
RNA, Long Noncoding
RNA, Messenger
RNA, Small Interfering
Saccharomyces cerevisiae
Sarcoma, Ewing
Scoliosis
Segmental Duplications, Genomic
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology
Sequence Homology, Amino Acid
Serine
Serine Endopeptidases
Serpins
Severity of Illness Index
Sex
Sex Chromosome Aberrations
Sex Chromosome Disorders
Sex Factors
Sex Reassignment Procedures
Sexual Development
Siblings
Signal Transduction
Sinoatrial Node
Sirolimus
Skin
Skin Pigmentation
Skull
Sleep Apnea Syndromes
Sodium-Calcium Exchanger
Software
Spasms, Infantile
Spastic Paraplegia, Hereditary
Species Specificity
Spectral Karyotyping
Sphingomyelins
Spine
Steroids
Steryl-Sulfatase
Sudden Infant Death
Sulfites
Surveys and Questionnaires
Survival Analysis
Syndrome
Tacrolimus Binding Proteins
Tandem Mass Spectrometry
Tay-Sachs Disease
T-Box Domain Proteins
Telomere
Teriparatide
Terminology as Topic
Testis
Texas
Thrombotic Microangiopathies
Thyroxine-Binding Globulin
Time Factors
T-Lymphocytes, Cytotoxic
Tomography, X-Ray Computed
TOR Serine-Threonine Kinases
Trans-Activators
Transaldolase
Transaminases
Transcription Factors
Transcription, Genetic
Transcriptome
Transduction, Genetic
Transfection
Transforming Growth Factor beta
Transketolase
Translocation, Genetic
Transposases
Treatment Outcome
Tretinoin
Trisomy
Tubulin
Tumor Cells, Cultured
Tumor Suppressor Proteins
Tyrosine
Ubiquitin Thiolesterase
Ultrasonography
Ultrasonography, Prenatal
Uncertainty
Uniparental Disomy
United States
Upper Extremity
Urea
Urea Cycle Disorders, Inborn
Uridine
Urogenital Abnormalities
Uterus
Vascular Malformations
Vasoplegia
Vesicular Transport Proteins
Vincristine
Viral Proteins
Virilism
Vitamin B 12 Deficiency
Walking
Weight Gain
White Matter
Whole Genome Sequencing
Williams Syndrome
Wnt Proteins
Wnt Signaling Pathway
Wnt-5a Protein
X Chromosome Inactivation
Young Adult
Zebrafish
Zebrafish Proteins
Zellweger Syndrome
SUTTON's Networks
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Concepts (754)
Derived automatically from this person's publications.
Osteogenesis Imperfecta
Metabolism, Inborn Errors
Phenotype
Abnormalities, Multiple
Craniofacial Abnormalities
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Co-Authors (146)
People in Profiles who have published with this person.
LUPSKI, JAMES
ELSEA, SARAH
MCCANN-CROSBY, BONNIE
GIBBS, RICHARD
POSEY, JENNIFER
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
GIBBS, RICHARD
BOERWINKLE, ERIC
ELSEA, SARAH
STANKIEWICZ, PAWEL
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Same Department
People who are also in this person's primary department.
GRIGORENKO, ELENA
HALLIDAY, JENNIFER
NEHRING, RALF
ROGERS, JEFFREY
YUAN, BO
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Physical Neighbors
People whose addresses are nearby this person.
BALLABIO, ANDREA
CRAIGEN, WILLIAM
EBLE, TANYA
NAGAMANI, SANDESH
SCOTT, DARYL
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