Concepts (224)
Concepts are derived automatically from a person's publications.
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
- Actin-Related Protein 2-3 Complex
- Actins
- Action Potentials
- Activity Cycles
- Adaptor Proteins, Signal Transducing
- Adolescent
- Adult
- Age of Onset
- Aged
- Aged, 80 and over
- Aggression
- Aging
- Alleles
- alpha-MSH
- Amino Acid Metabolism, Inborn Errors
- Amino Acid Sequence
- Amino Acid Substitution
- Animals
- Animals, Genetically Modified
- Anorexia
- Anticonvulsants
- Apolipoproteins E
- Autism Spectrum Disorder
- Autistic Disorder
- Base Sequence
- Basic Helix-Loop-Helix Transcription Factors
- Behavior
- Behavior, Animal
- Biomarkers
- Bipolar Disorder
- Body Composition
- Body Constitution
- Body Weight
- Brain
- Brain Waves
- Calcium Channel Blockers
- Calcium Channels, T-Type
- Caregivers
- Carrier Proteins
- Cell Differentiation
- Cell Enlargement
- Cell Line, Tumor
- Cell Size
- Cells, Cultured
- Cerebral Cortex
- Child
- Child Development
- Child, Preschool
- Chromosome Aberrations
- Chromosome Banding
- Chromosome Deletion
- Chromosome Disorders
- Chromosomes, Bacterial
- Chromosomes, Human, Pair 1
- Chromosomes, Human, Pair 14
- Chromosomes, Human, Pair 22
- Chromosomes, Human, Pair 5
- Chromosomes, Human, Pair 6
- Chromosomes, Human, X
- Circadian Rhythm
- Cloning, Molecular
- Cognition
- Cohort Studies
- Comparative Genomic Hybridization
- Craniofacial Abnormalities
- CRISPR-Cas Systems
- Cytoskeletal Proteins
- Databases, Factual
- DEAD-box RNA Helicases
- Dendrites
- Developmental Disabilities
- Diagnosis, Differential
- Diet
- Dietary Fats
- Disease Models, Animal
- Disease Progression
- DNA Methylation
- DNA Mutational Analysis
- DNA Primers
- DNA-Binding Proteins
- Down Syndrome
- Drosophila
- Eating
- Electroencephalography
- Electromyography
- Energy Metabolism
- Epigenesis, Genetic
- Epilepsy
- Evolution, Molecular
- Excitatory Postsynaptic Potentials
- Facies
- Feeding Behavior
- Female
- Fetal Development
- Gene Deletion
- Gene Dosage
- Gene Expression
- Gene Expression Regulation
- Genes, Duplicate
- Genetic Association Studies
- Genetic Counseling
- Genetic Diseases, Inborn
- Genetic Loci
- Genetic Predisposition to Disease
- Genomics
- Genotype
- Germ-Line Mutation
- Growth
- Growth and Development
- GTPase-Activating Proteins
- Haploinsufficiency
| - HEK293 Cells
- Helix-Loop-Helix Motifs
- Heterozygote
- Homeostasis
- Homologous Recombination
- Humans
- Hyperkinesis
- Hyperphagia
- Immunohistochemistry
- In Situ Hybridization, Fluorescence
- INDEL Mutation
- Infant
- Infant, Newborn
- Inhibitory Postsynaptic Potentials
- Intellectual Disability
- Internal Ribosome Entry Sites
- Isoxazoles
- Lithium
- Longitudinal Studies
- Magnetic Resonance Imaging
- Male
- Mammals
- Membrane Proteins
- Memory
- Mental Health
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Mice, Mutant Strains
- Mice, Transgenic
- Microfilament Proteins
- Middle Aged
- Mitogen-Activated Protein Kinase 1
- Mitogen-Activated Protein Kinase Kinases
- Models, Biological
- Molecular Sequence Data
- Muscle Hypotonia
- Mutation
- Mutation, Missense
- Nerve Net
- Nerve Tissue Proteins
- Nervous System
- Neurites
- Neurodevelopmental Disorders
- Neurofibromatosis 2
- Neurogenesis
- Neurons
- Obesity
- Oxidoreductases Acting on Sulfur Group Donors
- Pandemics
- Paraventricular Hypothalamic Nucleus
- Parent-Child Relations
- Parenting
- Parents
- Patch-Clamp Techniques
- Pedigree
- Peptides, Cyclic
- Phenotype
- Phosphorylation
- Physical Examination
- Pluripotent Stem Cells
- Point Mutation
- Post-Synaptic Density
- Pregnancy
- Prenatal Diagnosis
- Pro-Opiomelanocortin
- Prospective Studies
- Protein Biosynthesis
- Protein Stability
- Quality of Life
- Rare Diseases
- ras GTPase-Activating Proteins
- ras Proteins
- Rats
- Receptor, Melanocortin, Type 4
- Registries
- Repressor Proteins
- Retrospective Studies
- Reverse Transcriptase Polymerase Chain Reaction
- RNA
- RNA Interference
- RNA, Messenger
- RNA-Binding Proteins
- Seizures
- Sensation Disorders
- Sequence Deletion
- Sex Factors
- Signal Transduction
- Sleep
- Sleep Deprivation
- Sleep, REM
- Smith-Magenis Syndrome
- Sodium Channel Blockers
- Somatosensory Cortex
- Spasms, Infantile
- Stakeholder Participation
- Stiff-Person Syndrome
- Sulfite Oxidase
- Surveys and Questionnaires
- Synapses
- Syndrome
- Touch
- Touch Perception
- Transcription Factors
- Transcription Factors, General
- Transgenes
- Translocation, Genetic
- Up-Regulation
- Valproic Acid
- Wakefulness
- Wolf-Hirschhorn Syndrome
- Young Adult
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Concepts
(224)
Derived automatically from this person's publications.
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People in Profiles who have published with this person.
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(59)
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