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WILLIAM CRAIGEN
Concepts (823)
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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.
1,4-alpha-Glucan Branching Enzyme
2-Aminoadipic Acid
3T3 Cells
4-Aminobutyrate Transaminase
Abnormalities, Multiple
Acetylation
Acetyltransferases
Acidosis, Lactic
Actins
Acute Kidney Injury
Acyl Coenzyme A
Acyl-CoA Dehydrogenase, Long-Chain
Acyltransferases
Adaptor Proteins, Signal Transducing
Adenosine Diphosphate
Adenosine Triphosphatases
Adenosine Triphosphate
Adipose Tissue
Adolescent
Adrenal Glands
Adrenal Insufficiency
Adult
Age of Onset
Aged
Aged, 80 and over
Agenesis of Corpus Callosum
Aging
Alanine Transaminase
Alcohol Oxidoreductases
Aldehyde Dehydrogenase
Algorithms
Alleles
alpha-Glucosidases
Alternative Splicing
Alzheimer Disease
Amidinotransferases
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acids, Branched-Chain
Amino Acyl-tRNA Synthetases
Ammonia
Anesthesia
Aneuploidy
Animals
Anions
Aniridia
Anodontia
Antibody Specificity
Antigens, CD
Anus, Imperforate
Aorta
Apoptosis
Arginase
Arginine
Argininosuccinate Lyase
Argininosuccinate Synthase
Argininosuccinic Acid
Argininosuccinic Aciduria
Arsenicals
Aryl Hydrocarbon Hydroxylases
Attention Deficit Disorder with Hyperactivity
Autism Spectrum Disorder
Autistic Disorder
Autophagy
Axonemal Dyneins
Aziridines
Bacterial Outer Membrane Proteins
Bacterial Proteins
Basal Ganglia Diseases
Base Sequence
bcl-2 Homologous Antagonist-Killer Protein
bcl-2-Associated X Protein
Behavior, Animal
BH3 Interacting Domain Death Agonist Protein
Binding Sites
Biological Transport
Biomarkers
Biopolymers
Biopsy
Bladder Exstrophy
Blindness
Blotting, Northern
Blotting, Southern
Blotting, Western
Body Patterning
Bone Density
Brain
Brain Chemistry
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Bridged Bicyclo Compounds, Heterocyclic
Caenorhabditis elegans
Calcification, Physiologic
Calcium
Carbamoyl-Phosphate Synthase (Ammonia)
Carbohydrate Metabolism, Inborn Errors
Carbon Dioxide
Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone
Carcinoma, Renal Cell
Cardiac Myosins
Cardiomyopathies
Cardiomyopathy, Dilated
Cardiomyopathy, Hypertrophic
Cardiovascular Abnormalities
Cardiovascular Diseases
Carnitine
Carrier Proteins
Case-Control Studies
Caspases
Catalytic Domain
Cataract
Cations, Divalent
Cell Cycle Proteins
Cell Death
Cell Line
Cell Line, Tumor
Cell Membrane
Cell Membrane Permeability
Cell Nucleolus
Cell Respiration
Cell Size
Cell Survival
Cell Transdifferentiation
Cells, Cultured
Cellular Senescence
Central Nervous System
Cerebellar Ataxia
Cerebral Ventricles
Child
Child, Preschool
Chloramphenicol O-Acetyltransferase
Chloride Channels
Choanal Atresia
Cholesterol
Chorea
Chromatin
Chromatin Immunoprecipitation
Chromatography, Gas
Chromatography, Thin Layer
Chromosome Aberrations
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosome Segregation
Chromosomes
Chromosomes, Bacterial
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 9
Chromosomes, Human, X
Cilia
Citrate (si)-Synthase
Citrulline
Citrullinemia
Clinical Trials as Topic
Cloaca
Cloning, Molecular
Codon
Codon, Nonsense
Cohort Studies
Collagen
Coloboma
Colon
Coma
Comparative Genomic Hybridization
Computational Biology
Computer Simulation
Congenital Abnormalities
Connectin
Conserved Sequence
Contractile Proteins
Corticosterone
COS Cells
Craniofacial Abnormalities
Creatine
Creatine Kinase, MM Form
Creatinine
Critical Care
Crosses, Genetic
Cyclic GMP
Cyclin T
Cyclin-Dependent Kinase 9
Cyclins
Cyclophilins
Cyclosporine
Cysts
Cytochromes c
Cytogenetic Analysis
Cytoskeleton
Cytosol
Databases, Genetic
Databases, Nucleic Acid
DAX-1 Orphan Nuclear Receptor
Deafness
Dehydrocholesterols
Developmental Disabilities
Diabetes Mellitus
Diagnosis, Differential
Dibenzocycloheptenes
Dicarboxylic Acids
Dichloroacetic Acid
Dietary Supplements
DiGeorge Syndrome
Dihydrolipoamide Dehydrogenase
Dilatation, Pathologic
Dioxins
Disease Management
Disease Models, Animal
Disease Progression
DNA
DNA Copy Number Variations
DNA Damage
DNA Helicases
DNA Methylation
DNA Mutational Analysis
DNA Polymerase gamma
DNA Primers
DNA Restriction Enzymes
DNA, Bacterial
DNA, Complementary
DNA, Mitochondrial
DNA-Binding Proteins
DNA-Directed DNA Polymerase
Down-Regulation
Drosophila melanogaster
Drosophila Proteins
Drug Resistance
Dyneins
Dystroglycans
Dystrophin
Ear, Inner
Ear, Middle
Echocardiography
Echocardiography, Doppler, Color
Ectodermal Dysplasia
Education, Medical
Ehlers-Danlos Syndrome
Ejaculation
Electrocardiography
Electroencephalography
Electron Transport
Electron Transport Chain Complex Proteins
Electron Transport Complex IV
Electrophysiology
Embryo Loss
Embryo, Mammalian
Embryonic Stem Cells
Endoglin
Enhancer Elements, Genetic
Enzyme Activation
Enzyme Inhibitors
Enzyme Replacement Therapy
Ependyma
Epidermal Cyst
Epidermis
Epilepsies, Myoclonic
Epilepsy
Epithelial-Mesenchymal Transition
Escherichia coli
Escherichia coli Proteins
Ethylmaleimide
Etoposide
Eukaryotic Cells
Evolution, Molecular
Exome
Exons
Expressed Sequence Tags
Eyelids
Facial Asymmetry
Facies
Failure to Thrive
Family Health
Fatal Outcome
Fathers
Fatty Acids
F-Box Proteins
Feedback
Female
Fetal Death
Fetal Growth Retardation
Fetus
Fibroblasts
Filamins
Fluorescent Antibody Technique
Follow-Up Studies
Forkhead Transcription Factors
Fractures, Spontaneous
Frameshift Mutation
Fucosyltransferases
Fungal Proteins
Gait
Galactitol
Galactose
Galactosemias
Galactosephosphates
gamma-Aminobutyric Acid
GATA4 Transcription Factor
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Expression Regulation, Enzymologic
Gene Frequency
Gene Knockdown Techniques
Gene Knock-In Techniques
Gene Knockout Techniques
Gene Library
Gene Ontology
Gene Order
Gene Rearrangement
Gene Silencing
Gene Targeting
Genes
Genes, Bacterial
Genes, Dominant
Genes, Mitochondrial
Genes, Recessive
Genes, Regulator
Genes, X-Linked
Genetic Association Studies
Genetic Carrier Screening
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Heterogeneity
Genetic Linkage
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetics, Medical
Genome
Genome, Human
Genome, Mitochondrial
Genomic Imprinting
Genomics
Genotype
Gestational Age
Glucans
Glucocorticoids
Gluconeogenesis
Glucose
Glucose Tolerance Test
Glutarates
Glycerol Kinase
Glycogen
Glycogen Debranching Enzyme System
Glycogen Storage Disease
Glycogen Storage Disease Type II
Glycogen Storage Disease Type IV
Glycolates
Glycolysis
Glycosylation
GRB10 Adaptor Protein
Growth Disorders
Guanidinoacetate N-Methyltransferase
Guanine Nucleotide Exchange Factors
Guanosine Diphosphate Fucose
Guanosine Diphosphate Mannose
Hair Cells, Auditory
Haploinsufficiency
Haplotypes
HCT116 Cells
Health Personnel
Hearing Loss
Heart
Heart Defects, Congenital
Heart Failure
Heart Septal Defects, Atrial
Heart Septal Defects, Ventricular
Heart Ventricles
HeLa Cells
Hemizygote
Hepatic Encephalopathy
Hepatocyte Nuclear Factor 1-beta
Hernia, Umbilical
Heterozygote
Hexokinase
High-Throughput Nucleotide Sequencing
Hippocampus
Histone Deacetylase Inhibitors
Histones
Homeostasis
Homocystinuria
Homozygote
Hospitalization
Humans
Hydrocephalus
Hydroxocobalamin
Hyperammonemia
Hyperpigmentation
Hypertension
Hypocalcemia
Hypoglycemia
Hypogonadism
Hypotrichosis
Ilium
Immune Tolerance
Immunoblotting
Immunohistochemistry
In Situ Hybridization, Fluorescence
In Vitro Techniques
Incidental Findings
Infant
Infant Care
Infant, Newborn
Infant, Newborn, Diseases
Infant, Premature
Infertility, Male
Information Dissemination
Infusions, Parenteral
Inheritance Patterns
Inositol 1,4,5-Trisphosphate Receptors
Insect Proteins
Insulin
Insulin Resistance
Intellectual Disability
Intensive Care Units, Pediatric
Intestinal Mucosa
Intestine, Small
Intracellular Membranes
Intracellular Signaling Peptides and Proteins
Introns
Ion Channel Gating
Ion Channels
Ischemia
Isochromosomes
Isoenzymes
Isolated Noncompaction of the Ventricular Myocardium
Isoleucine
Isotope Labeling
Jurkat Cells
Kartagener Syndrome
Karyotyping
Kearns-Sayre Syndrome
Keratoderma, Palmoplantar
Kidney
Kidney Cortex
Kidney Function Tests
Kidney Neoplasms
Klebsiella Infections
Lactate Dehydrogenases
Lactates
Lactic Acid
Lactose
Language Development Disorders
Larva
Learning
Leigh Disease
Length of Stay
Leptin
Leucine
LIM Domain Proteins
Limb Deformities, Congenital
Lipid Bilayers
Lipid Metabolism, Inborn Errors
Lipodystrophy
Liposomes
Liver
Liver Failure
Liver Function Tests
Liver Transplantation
L-Lactate Dehydrogenase
Lod Score
Longitudinal Studies
Long-Term Care
Loss of Heterozygosity
Lymphocytes
Lysosomal Storage Diseases
Lysosomes
Magnetic Resonance Imaging
Magnetic Resonance Imaging, Cine
Male
Mannosyltransferases
Mass Spectrometry
Megalencephaly
MELAS Syndrome
Membrane Potential, Mitochondrial
Membrane Proteins
Membrane Transport Proteins
Memory
Mendelian Randomization Analysis
Mental Retardation, X-Linked
Metabolic Networks and Pathways
Metabolism, Inborn Errors
Metabolomics
Methylation
Methyl-CpG-Binding Protein 2
Methylmalonic Acid
Mice
Mice, Inbred C57BL
Mice, Inbred Strains
Mice, Knockout
Mice, Mutant Strains
Mice, Obese
Mice, Transgenic
Microcephaly
Microfilament Proteins
Microinjections
Microsatellite Repeats
Microscopy, Electron
Middle Aged
Mitochondria
Mitochondria, Heart
Mitochondria, Liver
Mitochondria, Muscle
Mitochondrial ADP, ATP Translocases
Mitochondrial Diseases
Mitochondrial Dynamics
Mitochondrial Encephalomyopathies
Mitochondrial Membrane Transport Proteins
Mitochondrial Membranes
Mitochondrial Myopathies
Mitochondrial Proteins
Mitochondrial Proton-Translocating ATPases
Mitochondrial Swelling
Models, Biological
Models, Genetic
Models, Molecular
Molecular Diagnostic Techniques
Molecular Sequence Data
Mononuclear Phagocyte System
Mosaicism
Mothers
Motor Activity
Movement Disorders
Multifunctional Enzymes
Multigene Family
Muridae
Muscle Hypotonia
Muscle Proteins
Muscle, Skeletal
Muscle, Smooth
Muscle, Striated
Muscular Diseases
Muscular Dystrophy, Duchenne
Mutagenesis, Insertional
Mutation
Mutation Rate
Mutation, Missense
Myocardium
Myoclonic Epilepsies, Progressive
Myocytes, Cardiac
Myosin Heavy Chains
NAD
Nail Diseases
Neonatal Screening
Nephrolithiasis
Nerve Tissue Proteins
Nervous System Diseases
Neurodevelopmental Disorders
Neuromuscular Diseases
Neuronal Plasticity
Neurons
NF-E2-Related Factor 1
NIH 3T3 Cells
NIMA-Related Kinase 1
Nitric Oxide
Nitric Oxide Synthase Type III
Nodal Protein
Noonan Syndrome
Nuclear Proteins
Nuclear Respiratory Factor 1
Nuclear Respiratory Factors
Nucleic Acid Hybridization
Nucleosides
Nucleotide Transport Proteins
Nucleotides
Oculocerebrorenal Syndrome
Oligonucleotide Array Sequence Analysis
Oocytes
Open Reading Frames
Ophthalmoplegia, Chronic Progressive External
Organ Size
Organ Specificity
Ornithine Carbamoyltransferase
Ornithine Decarboxylase
Osmotic Pressure
Osteogenesis Imperfecta
Osteopetrosis
Oxidation-Reduction
Oxidative Phosphorylation
Oxidative Stress
Oxo-Acid-Lyases
Oxygen Consumption
p21-Activated Kinases
Patch-Clamp Techniques
Pathology, Molecular
PAX2 Transcription Factor
Pedigree
Peptide Chain Termination, Translational
Peptide Termination Factors
Peripheral Nervous System
Peristalsis
Permeability
Phenotype
Phenylacetates
Phenylalanine Hydroxylase
Phosphoenolpyruvate Carboxykinase (ATP)
Phospholipids
Phosphoric Monoester Hydrolases
Phosphorylation
Phosphotransferases
Phosphotransferases (Alcohol Group Acceptor)
Photochemistry
Phylogeny
Physical Conditioning, Animal
Placenta
Plasma Membrane Neurotransmitter Transport Proteins
Plasmids
Ploidies
Point Mutation
Poly (ADP-Ribose) Polymerase-1
Poly A
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Polymorphism, Single Nucleotide
Porins
Porosity
Precision Medicine
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Predictive Value of Tests
Pregnancy
Pregnanolone
Prenatal Diagnosis
Procollagen
Prognosis
Promoter Regions, Genetic
Propionic Acidemia
Prospective Studies
Proteasome Endopeptidase Complex
Protein Binding
Protein Biosynthesis
Protein Conformation
Protein Domains
Protein Isoforms
Protein Kinases
Protein Structure, Quaternary
Protein Structure, Secondary
Protein Structure, Tertiary
Protein Transport
Protein Tyrosine Phosphatase, Non-Receptor Type 11
Protein Tyrosine Phosphatases
Proteins
Proton-Translocating ATPases
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-bcl-2
Pseudohypoparathyroidism
Psychomotor Disorders
PubMed
Puerperal Disorders
Pulmonary Artery
Pulmonary Valve Stenosis
Pyridoxine
Pyruvate Dehydrogenase Complex
Quadriplegia
Rabbits
Radiochemistry
Radiography
Rats
Rats, Sprague-Dawley
Reactive Nitrogen Species
Reactive Oxygen Species
Receptors, Cell Surface
Receptors, GABA
Receptors, GABA-A
Receptors, G-Protein-Coupled
Receptors, Retinoic Acid
Recombinant Fusion Proteins
Recombinant Proteins
Recovery of Function
Recurrence
Reference Values
Referral and Consultation
Remission, Spontaneous
Repressor Proteins
Reproducibility of Results
Respiratory Mucosa
Restriction Mapping
Retroelements
Retrospective Studies
Retroviridae Proteins
Rett Syndrome
Reverse Transcriptase Polymerase Chain Reaction
Review Literature as Topic
rho GTP-Binding Proteins
Rho Guanine Nucleotide Exchange Factors
Ribosomes
Risk Factors
RNA
RNA Helicases
RNA Interference
RNA Polymerase II
RNA Splice Sites
RNA Splicing
RNA, Messenger
RNA, Ribosomal, 16S
RNA, Small Interfering
RNA, Transfer
RNA, Transfer, Leu
Saccharomyces cerevisiae
Segmental Duplications, Genomic
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Analysis, Protein
Sequence Analysis, RNA
Sequence Deletion
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Sequence Tagged Sites
Severity of Illness Index
Sex Chromosome Aberrations
Sexual Behavior, Animal
SH2 Domain-Containing Protein Tyrosine Phosphatases
Siblings
Signal Transduction
Situs Inversus
Skin
Smad2 Protein
Smad3 Protein
Smith-Lemli-Opitz Syndrome
Societies, Medical
Software
Spasms, Infantile
Species Specificity
Speech Disorders
Sperm Count
Sperm Motility
Spine
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Spiro Compounds
Spleen
src Homology Domains
Status Epilepticus
Staurosporine
Steroids
Stress, Physiological
Stroke Volume
Structure-Activity Relationship
Succinate-CoA Ligases
Sulfur Radioisotopes
Surveys and Questionnaires
Survival Analysis
Survival Rate
Symptom Assessment
Synapses
Synapsins
Syndrome
Systole
Tandem Mass Spectrometry
Telangiectasia, Hereditary Hemorrhagic
Testis
Texas
Thymidine Kinase
Thymidine Phosphorylase
Time Factors
Tissue Distribution
Tomography, X-Ray Computed
Trans-Activators
Transaminases
Transcription Factors
Transcription, Genetic
Transcriptome
Transfection
Transition to Adult Care
Treatment Failure
Treatment Outcome
Tropomyosin
Tryptophan-tRNA Ligase
Tunicamycin
Tyrosine Transaminase
Ubiquinone
Ubiquitin
Ubiquitination
Ubiquitin-Protein Ligases
Uncoupling Agents
Uniparental Disomy
United States
Urea
Urea Cycle Disorders, Inborn
Urinary Bladder
Urogenital Abnormalities
Valerates
Vascular Cell Adhesion Molecule-1
Ventricular Dysfunction, Left
Ventricular Remodeling
Vesico-Ureteral Reflux
Viscera
Vision, Low
Vitamin B 12 Deficiency
Voltage-Dependent Anion Channel 1
Voltage-Dependent Anion Channel 2
Voltage-Dependent Anion Channels
Von Hippel-Lindau Tumor Suppressor Protein
Walker-Warburg Syndrome
Water-Electrolyte Balance
Whole Genome Sequencing
X Chromosome
X Chromosome Inactivation
Yeasts
Young Adult
YY1 Transcription Factor
Zebrafish
Zinc Fingers
CRAIGEN's Networks
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Concepts (823)
Derived automatically from this person's publications.
Mitochondria
Porins
Mitochondrial Diseases
Voltage-Dependent Anion Channels
Voltage-Dependent Anion Channel 1
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Co-Authors (90)
People in Profiles who have published with this person.
SCAGLIA, FERNANDO
BURRAGE, LINDSAY
LALANI, SEEMA
BELMONT, JOHN
EMRICK, LISA
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
SCAGLIA, FERNANDO
GIBBS, RICHARD
BELLEN, HUGO
BOERWINKLE, ERIC
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Same Department
People who are also in this person's primary department.
ALI, SAIMA
LICHTARGE, OLIVIER
LUPSKI, JAMES
ROSENBERG, SUSAN
SEDLAZECK, FRITZ
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Physical Neighbors
People whose addresses are nearby this person.
BEKHEIRNIA, MIR REZA
BOTAS, JUAN
DHAR, SHWETA
SUTTON, VERNON
WORLEY, KIM
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