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DARYL SCOTT
Concepts (319)
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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.
Abnormalities, Multiple
Aconitate Hydratase
Actins
Acyl Coenzyme A
Adaptor Proteins, Signal Transducing
Adolescent
Adult
Age of Onset
Algorithms
Alleles
alpha7 Nicotinic Acetylcholine Receptor
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acid Substitution
Anal Canal
Anemia, Diamond-Blackfan
Animals
Anophthalmos
Anorectal Malformations
Antigens, Neoplasm
Apoptosis
Ascorbic Acid
Atrophy
Attention Deficit Disorder with Hyperactivity
Autism Spectrum Disorder
Autistic Disorder
Base Composition
Base Sequence
Basic Helix-Loop-Helix Transcription Factors
Blotting, Western
Body Weight
Bone and Bones
Bone Marrow Transplantation
Brain
Cardiovascular Abnormalities
Cardiovascular Diseases
Carrier Proteins
Cell Cycle Proteins
Cell Movement
Cell Proliferation
Cerebellum
Child
Child, Preschool
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Banding
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Mapping
Chromosomes
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 9
Chromosomes, Human, X
Cleft Lip
Cleft Palate
Clinical Decision-Making
Coat Protein Complex I
Coatomer Protein
Cognition
Cognition Disorders
Cohort Studies
Collagen Type I
Coloboma
Comparative Genomic Hybridization
Congenital Abnormalities
Congenital Microtia
Consanguinity
Craniofacial Abnormalities
Critical Care
Cytoskeletal Proteins
Developmental Disabilities
Diaphragm
Diaphragmatic Eventration
Dietary Supplements
Disease Management
Disease Models, Animal
Disorders of Sex Development
DNA Breaks
DNA Copy Number Variations
DNA Helicases
DNA Mutational Analysis
DNA Repair Enzymes
DNA Replication
DNA, Mitochondrial
DNA-Binding Proteins
Drosophila melanogaster
Drosophila Proteins
Embryo, Mammalian
Embryo, Nonmammalian
Embryonic Development
Endocardial Cushions
Endocardium
Endoplasmic Reticulum
Epilepsy
Epistasis, Genetic
Epithelial-Mesenchymal Transition
Epithelium
Esophageal Atresia
Esophagus
Essential Hypertension
Ethylnitrosourea
Exome
Extracellular Matrix Proteins
Face
Failure to Thrive
Fatal Outcome
Female
Fertilization in Vitro
Fibrillin-1
Fibrillins
Fibroblast Growth Factor 10
Fibroblasts
Forkhead Transcription Factors
Frameshift Mutation
GATA4 Transcription Factor
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Genes, Dominant
Genes, Duplicate
Genes, Lethal
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genome, Human
Genomic Instability
Genotype
Gestational Age
Golgi Apparatus
Gonadal Dysgenesis, 46,XY
Gonads
Growth Disorders
Hand Deformities, Congenital
Haploinsufficiency
Hartnup Disease
Hearing Loss
Heart
Heart Defects, Congenital
Heart Septal Defects, Ventricular
Heart Ventricles
Hedgehog Proteins
Hematopoietic Stem Cell Transplantation
Hemizygote
Hepatocyte Nuclear Factor 1-beta
Hernia, Diaphragmatic
Hernias, Diaphragmatic, Congenital
Heterozygote
Hippocampus
Histone Acetyltransferases
Histone Deacetylases
Histone-Lysine N-Methyltransferase
Homeodomain Proteins
Homologous Recombination
Homozygote
Humans
Hypertension, Pulmonary
Immunohistochemistry
In Situ Hybridization, Fluorescence
Infant
Infant Care
Infant, Newborn
Infant, Newborn, Diseases
Intellectual Disability
Intensive Care Units, Pediatric
Intracellular Signaling Peptides and Proteins
Karyotyping
Kidney
Kidney Diseases
Language Development Disorders
Length of Stay
LIM Domain Proteins
Limb Deformities, Congenital
LIM-Homeodomain Proteins
Loss of Function Mutation
Lung
Lung Diseases
Lyases
Male
Marfan Syndrome
Maternal Inheritance
Membrane Glycoproteins
Membrane Proteins
Mental Disorders
Mesoderm
Methyltransferases
Mice
Mice, 129 Strain
Mice, Inbred C57BL
Mice, Knockout
Mice, Transgenic
Microcephaly
Microfilament Proteins
Micrognathism
Microphthalmos
Microscopy, Confocal
Microtubule-Associated Proteins
Minor Histocompatibility Antigens
Mitochondria
Mitochondrial Diseases
Models, Genetic
Molecular Sequence Data
Mosaicism
Mutation
Mutation, Missense
Myocardium
Neck
Neoplasm Proteins
Nerve Tissue Proteins
Neural Crest
Neurodevelopmental Disorders
Neuroglia
Neurons
NIH 3T3 Cells
Nose
Nose Diseases
Nuclear Matrix-Associated Proteins
Nuclear Proteins
Nucleic Acid Hybridization
Nucleotide Motifs
Octamer Transcription Factors
Oligonucleotide Array Sequence Analysis
Optic Atrophy
Optic Nerve
Organogenesis
Osteoporosis
Patella
Paternal Inheritance
Pathology, Molecular
PAX2 Transcription Factor
PAX5 Transcription Factor
Pedigree
Peptide Termination Factors
Phenotype
Phosphoric Monoester Hydrolases
Polymorphism, Single Nucleotide
Pregnancy
Prenatal Diagnosis
Primary Myelofibrosis
Prognosis
Protein Binding
Protein Tyrosine Phosphatases
Pulmonary Veins
Purkinje Cells
Radiography
Receptor, Fibroblast Growth Factor, Type 2
Receptor, Fibroblast Growth Factor, Type 5
Receptors, Cytoplasmic and Nuclear
Receptors, Interleukin
Repressor Proteins
Retina
Retinal Degeneration
Retrospective Studies
rhoA GTP-Binding Protein
Risk Factors
RNA, Long Noncoding
RNA, Messenger
RNA, Small Interfering
RNA-Binding Proteins
Rubinstein-Taybi Syndrome
Scimitar Syndrome
Segmental Duplications, Genomic
Sensitivity and Specificity
Sequence Alignment
Sequence Deletion
Sequence Homology, Amino Acid
Severity of Illness Index
Sibling Relations
Siblings
Signal Transduction
Sorting Nexins
SOXB1 Transcription Factors
SOXF Transcription Factors
Spine
Steroidogenic Factor 1
Succinate-CoA Ligases
Syndactyly
Syndrome
T-Box Domain Proteins
Telomere
Tetralogy of Fallot
Texas
Trachea
Tracheoesophageal Fistula
Transcription Factors
Transcription Factors, General
Trisomy
Tumor Suppressor Proteins
Uncertainty
United States
Urogenital Abnormalities
Vena Cava, Inferior
Vesico-Ureteral Reflux
Vesicular Transport Proteins
Vitamin B Complex
Wnt1 Protein
X Chromosome Inactivation
Young Adult
Zebrafish
Zebrafish Proteins
Zinc Fingers
SCOTT's Networks
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Concepts (319)
Derived automatically from this person's publications.
Hernias, Diaphragmatic, Congenital
Intellectual Disability
Chromosome Deletion
Abnormalities, Multiple
Nerve Tissue Proteins
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Co-Authors (91)
People in Profiles who have published with this person.
LALANI, SEEMA
SHAW, CHAD
Pendleton, Katherine
LUPSKI, JAMES
KAO, ERIC
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
ZOGHBI, HUDA
STANKIEWICZ, PAWEL
CHEUNG, SAU WAI
GIBBS, RICHARD
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Same Department
People who are also in this person's primary department.
FRANCISKOVICH, RACHEL
GINGRAS, MARIE-CLAUDE
GKOUNTAROULIS, DIMOS
PARK, DONGSU
QIN, XIANG
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Physical Neighbors
People whose addresses are nearby this person.
ARENKIEL, BENJAMIN
NAGAMANI, SANDESH
ROSENBERG, SUSAN
SHAULSKY, GAD
SUTTON, VERNON
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