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Darrel J. Waggoner
Concepts (368)
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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
Acute-Phase Reaction
Adaptor Proteins, Signal Transducing
Adenosine Triphosphatases
Adolescent
Adult
Age Factors
Aged
Aged, 80 and over
Alcohol Oxidoreductases
Alleles
Alzheimer Disease
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amyloid beta-Peptides
Amyotrophic Lateral Sclerosis
Animals
Anticholesteremic Agents
Anti-Mullerian Hormone
Aortic Coarctation
Aortic Valve Stenosis
Arm
Arrhythmogenic Right Ventricular Dysplasia
Asparagine
Aspartic Acid
Asymptomatic Diseases
Ataxia
Bariatric Surgery
Base Sequence
Biomarkers
Bone and Bones
Brain
Calcinosis
Calcium
Calcium Signaling
Calibration
Canada
Cardiac Myosins
Carrier Proteins
Cation Transport Proteins
Cell Cycle Proteins
Cell Line
Certification
Ceruloplasmin
Child
Child Development Disorders, Pervasive
Child, Preschool
Cholesterol
Chondrodysplasia Punctata
Chromatin
Chromatin Assembly and Disassembly
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Banding
Chromosome Breakage
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 19
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, X
Chromosomes, Human, Y
Cleft Palate
Clinical Competence
Cohort Studies
Comparative Genomic Hybridization
Computational Biology
Congenital Abnormalities
Congenital Hyperinsulinism
Consanguinity
Consensus
Consumer Advocacy
Copper
Copper-transporting ATPases
Core Binding Factor Alpha 1 Subunit
Craniofacial Dysostosis
Craniosynostoses
C-Reactive Protein
Creatine Kinase
Cricetinae
Cri-du-Chat Syndrome
Curriculum
Cyclic AMP
Cystic Fibrosis
Cytogenetic Analysis
Cytokines
Databases, Genetic
Databases, Nucleic Acid
De Lange Syndrome
Dental Enamel
Desmocollins
Developmental Disabilities
Diagnostic Errors
DiGeorge Syndrome
Disclosure
Diseases in Twins
DNA Mutational Analysis
DNA Primers
DNA, Complementary
DNA-Binding Proteins
Dried Blood Spot Testing
Duodenal Diseases
Dystrophin
Education, Medical
Education, Medical, Undergraduate
Educational Measurement
Electron Transport Complex IV
Embryo, Mammalian
Embryonic and Fetal Development
Endocardium
Endoplasmic Reticulum
Epigenesis, Genetic
Epilepsy
Estradiol
Euchromatin
Exome
Exons
Ezetimibe
Face
Facies
Failure to Thrive
Family Health
Fanconi Anemia
Fatal Outcome
Fathers
Female
Fetal Growth Retardation
Fibroblasts
Fingers
Foot Deformities, Congenital
Founder Effect
Frameshift Mutation
Gene Amplification
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Regulation
Gene Frequency
Gene Knockdown Techniques
Gene Silencing
Genes, Dominant
Genes, Lethal
Genes, Recessive
Genetic Association Studies
Genetic Carrier Screening
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Linkage
Genetic Predisposition to Disease
Genetic Research
Genetic Testing
Genetics
Genetics, Medical
Genome, Human
Genomic Imprinting
Genomics
Genotype
Germany
Glycogen Storage Disease Type II
Glycoproteins
Golgi Apparatus
Green Fluorescent Proteins
Growth Disorders
Hamartoma Syndrome, Multiple
Hand Deformities, Congenital
Haplotypes
Head
Heart
Heart Defects, Congenital
Heart Diseases
HEK293 Cells
HeLa Cells
Hematologic Diseases
Hepatolenticular Degeneration
Heterozygote
High-Throughput Nucleotide Sequencing
Hippocampus
Histone Demethylases
Histone-Lysine N-Methyltransferase
Homeostasis
Homozygote
Humans
Hypercholesterolemia
Hypertrophy, Left Ventricular
Illinois
Immunohistochemistry
In Situ Hybridization, Fluorescence
Incidence
Incidental Findings
Inclusion Bodies
Infant
Infant, Newborn
Infant, Premature
Information Services
Intellectual Disability
Internet
Internship and Residency
Intestinal Diseases
Intracellular Signaling Peptides and Proteins
Karyotyping
Kinetics
Leukodystrophy, Globoid Cell
Licensure, Medical
Limb Deformities, Congenital
Lipid Metabolism, Inborn Errors
Lipopolysaccharides
Liver
Lod Score
Luminescent Proteins
Lysophospholipids
Lysosomal Storage Diseases
Lysosomal-Associated Membrane Protein 2
Lysosomes
Malabsorption Syndromes
Male
Malformations of Cortical Development
Maple Syrup Urine Disease
Mass Screening
Medical Informatics
Medical Records
Membrane Glycoproteins
Membrane Proteins
Menkes Kinky Hair Syndrome
Mesocricetus
Methylmalonic Acid
Mice
Mice, Transgenic
Microarray Analysis
Microcephaly
Microphthalmos
Microsatellite Repeats
Middle Aged
Models, Biological
Models, Genetic
Molecular Sequence Data
Monosomy
Mosaicism
Movement Disorders
Multiprotein Complexes
Muscle Hypotonia
Muscular Diseases
Muscular Dystrophies
Muscular Dystrophies, Limb-Girdle
Mutation
Mutation, Missense
Myosin Heavy Chains
Neonatal Screening
Neoplasm Proteins
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neurofibroma, Plexiform
Neurofibromatosis 1
Neuronal Ceroid-Lipofuscinoses
New York
Niemann-Pick Disease, Type C
North America
Nuclear Proteins
Obesity, Morbid
Oligodeoxyribonucleotides, Antisense
Ophthalmoplegia
Ovary
Ovotesticular Disorders of Sex Development
Oxidoreductases
Parents
Pathology, Molecular
Patient Education as Topic
Pediatrics
Pedigree
Pentosyltransferases
Phenotype
Phosphatidate Phosphatase
Phosphorylation
Physicians
Phytosterols
Pierre Robin Syndrome
Pilot Projects
Polymorphism, Genetic
Precision Medicine
Pregnancy
Pregnancy Complications
Pregnancy, High-Risk
Prenatal Diagnosis
Prevalence
Prion Diseases
Prions
Prognosis
Propionates
Protein Binding
Protein Stability
Protein Transport
Proteins
PrPC Proteins
PrPSc Proteins
PTEN Phosphohydrolase
Puberty
Pyloric Stenosis
Radiography
Rare Diseases
Rats
Receptors, Cell Surface
Receptors, G-Protein-Coupled
Receptors, Lysophosphatidic Acid
Recombinant Fusion Proteins
Recombinant Proteins
Recurrence
Retrospective Studies
Risk Factors
RNA Splice Sites
RNA, Messenger
Sarcomeres
Schools, Medical
Seizures
Sensitivity and Specificity
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Amino Acid
Serum Amyloid A Protein
Sex Chromosome Aberrations
Sex Differentiation
Sex Factors
Signal Transduction
Sitosterols
Skin Abnormalities
Spine
Students, Medical
Subcellular Fractions
Superoxide Dismutase
Superoxide Dismutase-1
Synaptic Membranes
Syndrome
Syria
Tandem Mass Spectrometry
T-Box Domain Proteins
Telomere
Temporal Lobe
Terminal Repeat Sequences
Testis
Testosterone
Thiolester Hydrolases
Time Factors
Tracheoesophageal Fistula
Transcription Factors
Transcription, Genetic
Transfection
Translocation, Genetic
Treatment Outcome
Trisomy
Turner Syndrome
Ultrasonography
United States
Vesicular Transport Proteins
Vestibular Diseases
Vitamin B 12
Vitamin K Deficiency
X Chromosome Inactivation
Young Adult
Zebrafish
Zinc Fingers
Waggoner's Networks
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Concepts (368)
Derived automatically from this person's publications.
Genetics, Medical
Genetic Testing
Chromosome Deletion
Intellectual Disability
Chromosome Disorders
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Co-Authors (35)
People in Profiles who have published with this person.
Das, Soma
Yano, Sho
Schwab, Joel
Ross, Lainie
Del Gaudio, Daniela
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_
Similar People (60)
People who share similar concepts with this person.
Dobyns, William
Ross, Lainie
Arora, Vineet
Olopade, Olufunmilayo
Nakamura, Yusuke
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_
Same Department
People who are also in this person's primary department.
Das, Soma
Field, Yair
Novembre, John
Pantaleo, Ester
Thompson, Emma
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_
Physical Neighbors
People whose addresses are nearby this person.
Abney, Mark A.
Flutre, Timothee
Gilliam, T. Conrad
Nobrega, Marcelo A.
Thompson, Emma
_