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Elizabeth Carson Engle, M.D.
Concepts (480)
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Concepts are derived automatically from a person's publications.
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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.
Abducens Nerve
Abducens Nerve Diseases
Abnormalities, Multiple
Accommodation, Ocular
Acrocephalosyndactylia
Action Potentials
Acute Disease
Adaptor Proteins, Signal Transducing
Adenosine Triphosphatases
Adolescent
Adult
Age Factors
Age of Onset
Aged
Aged, 80 and over
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Alleles
Alternative Splicing
Amblyopia
Amino Acid Motifs
Amino Acid Sequence
Amino Acid Substitution
Aminocoumarins
Amyotrophic Lateral Sclerosis
Anal Canal
Animals
Animals, Genetically Modified
Animals, Newborn
Anisotropy
Anti-Bacterial Agents
Anti-HIV Agents
Apraxias
Arginine
Arthrogryposis
Ataxia
Autistic Disorder
Axons
Axotomy
Basal Ganglia
Base Sequence
Benzylamines
Binding Sites
Biopsy
Blepharoptosis
Blinking
Bone Morphogenetic Proteins
Boston
Brain
Brain Diseases
Brain Neoplasms
Brain Stem
Brazil
Carboxy-Lyases
Cardiovascular Abnormalities
Carotid Artery, Internal
Carpal Tunnel Syndrome
Carrier Proteins
Case-Control Studies
Cataract
Cation Transport Proteins
Cell Count
Cell Culture Techniques
Cell Cycle Proteins
Cell Differentiation
Cell Fusion
Cell Line
Cell Membrane
Cell Movement
Cell Nucleus
Cell Survival
Central Nervous System
Cerebellar Ataxia
Cerebral Angiography
Cerebral Arteries
Cerebral Cortex
Cerebral Veins
Cerebrovascular Disorders
Chemokine CXCL12
Chick Embryo
Chickenpox
Child
Child Development Disorders, Pervasive
Child Welfare
Child, Preschool
Chimerin 1
China
Chromatin
Chromatography, High Pressure Liquid
Chromosome Aberrations
Chromosome Deletion
Chromosome Mapping
Chromosomes, Artificial, Bacterial
Chromosomes, Bacterial
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 12
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 20
Cilia
Cluster Analysis
Codon, Nonsense
Cognition Disorders
Cohort Studies
Cold Temperature
Coloboma
Color Vision Defects
Colorectal Neoplasms
Comparative Genomic Hybridization
Congenital Abnormalities
Conjunctival Diseases
Consanguinity
Conserved Sequence
Contig Mapping
Contracture
Convergence, Ocular
Corpus Callosum
Coumarins
Cranial Nerve Diseases
Cranial Nerves
Cranial Sutures
Craniosynostoses
Cross-Sectional Studies
Culture Media
Cytokines
Cytoskeletal Proteins
Cytoskeleton
Databases, Genetic
Deafness
Developmental Biology
Developmental Disabilities
Diagnosis, Differential
Diagnostic Errors
Diffusion Magnetic Resonance Imaging
Diffusion Tensor Imaging
Disease Models, Animal
Disease Progression
Diseases in Twins
DNA
DNA Copy Number Variations
DNA Mutational Analysis
DNA Primers
DNA Replication
DNA, Bacterial
DNA, Complementary
DNA, Satellite
DNA, Viral
DNA-Binding Proteins
Duane Retraction Syndrome
Dura Mater
Dystrophin
Ear, Inner
Electromyography
Electrooculography
Electroretinography
Embryo, Mammalian
Embryo, Nonmammalian
Emotions
Encephalitis, Viral
Endocrine System Diseases
Endophenotypes
Enhancer Elements, Genetic
Epigenomics
Escherichia coli
Esophagus
Esotropia
Evoked Potentials, Motor
Evoked Potentials, Somatosensory
Evoked Potentials, Visual
Exons
Exotropia
Eye Abnormalities
Eye Diseases
Eye Diseases, Hereditary
Eye Movements
Eye Proteins
Eyelids
Face
Facial Expression
Facial Muscles
Facial Paralysis
Facies
Family
Family Health
Female
Fibrosis
Fingers
Fluorescent Antibody Technique
Follow-Up Studies
Forkhead Transcription Factors
Founder Effect
Fovea Centralis
Frameshift Mutation
Functional Laterality
gamma-Crystallins
Ganglia, Spinal
GATA2 Transcription Factor
Gene Components
Gene Duplication
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Frequency
Genes
Genes, Bacterial
Genes, DCC
Genes, Dominant
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Complementation Test
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Heterogeneity
Genetic Linkage
Genetic Markers
Genetic Predisposition to Disease
Genetic Variation
Genome-Wide Association Study
Genotype
Glioma
Glutamic Acid
Green Fluorescent Proteins
Growth Cones
Haplotypes
Hearing Loss
Hearing Loss, Sensorineural
Heart Defects, Congenital
Heart Septal Defects, Atrial
HEK293 Cells
Herpesvirus 3, Human
Heterocyclic Compounds
Heterozygote
Histidine
Homeodomain Proteins
Homozygote
Humans
Hybrid Cells
Immunohistochemistry
IMP Dehydrogenase
In Situ Hybridization
In Situ Hybridization, Fluorescence
Incidence
India
Indians, North American
Infant
Infant, Newborn
Inheritance Patterns
Intracellular Signaling Peptides and Proteins
Introns
Iran
Iris Diseases
Japan
Jaw Abnormalities
Kallmann Syndrome
Kidney
Kinetics
Klippel-Feil Syndrome
Labyrinth Diseases
Language Development Disorders
Lens, Crystalline
Ligands
Limb Deformities, Congenital
Lissencephaly
Lod Score
Loss of Heterozygosity
Lower Extremity Deformities, Congenital
Lupus Erythematosus, Systemic
Lymphocytes
Lysine
MafB Transcription Factor
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Malignant Hyperthermia
Mandible
Manometry
Markov Chains
Mastication
Maze Learning
Median Nerve
Medulla Oblongata
Membrane Glycoproteins
Membrane Proteins
Menkes Kinky Hair Syndrome
Mesoderm
Metalloendopeptidases
Mexico
Mice
Mice, Inbred C57BL
Mice, Knockout
Mice, Mutant Strains
Mice, Transgenic
Microcephaly
Microfilament Proteins
Microsatellite Repeats
Microscopy, Confocal
Microtubule-Associated Proteins
Microtubules
Middle Aged
Mobius Syndrome
Models, Animal
Models, Biological
Models, Molecular
Molecular Sequence Data
Morphogenesis
Motor Activity
Motor Neuron Disease
Motor Neurons
Movement Disorders
Muscle Denervation
Muscle Proteins
Muscle, Skeletal
Muscles
Muscular Atrophy
Muscular Diseases
Musculoskeletal Abnormalities
Mutation
Mutation, Missense
Myoblasts
MyoD Protein
Myogenic Regulatory Factor 5
Neoplasm Proteins
Nerve Fibers
Nerve Regeneration
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Netherlands
Neural Crest
Neural Pathways
Neurogenesis
Neuromuscular Junction
Neuronal Plasticity
Neurons
Neurons, Afferent
Neurons, Efferent
Neuropsychological Tests
Neurosciences
New Hampshire
Nuclear Family
Nuclear Pore Complex Proteins
Nuclear Proteins
Nystagmus, Congenital
Ocular Motility Disorders
Oculomotor Muscles
Oculomotor Nerve
Oculomotor Nerve Diseases
Odds Ratio
Ontario
Ophthalmic Nerve
Ophthalmologic Surgical Procedures
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Ophthalmoscopy
Optic Disk
Optic Nerve
Oral Health
Orbit
Organ Culture Techniques
Organ Size
Osteoblasts
Osteochondrodysplasias
Oxolinic Acid
Paired Box Transcription Factors
Papain
Paracrine Communication
Pedigree
Peptide Hydrolases
Perception
Peripheral Nervous System Diseases
Phenotype
Pierre Robin Syndrome
Point Mutation
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Pons
Portugal
Pregnancy
Prognosis
Prospective Studies
Protein Binding
Protein Conformation
Protein Isoforms
Protein Structure, Tertiary
Protein Transport
Proteins
Psychomotor Performance
Psychotic Disorders
Pupil
Pursuit, Smooth
Pyramidal Tracts
Quality of Life
rac GTP-Binding Proteins
Radial Neuropathy
Rare Diseases
Receptor, EphA4
Receptors, Cell Surface
Receptors, CXCR
Receptors, CXCR4
Receptors, Immunologic
Recombination, Genetic
Recurrence
Reflex, Abnormal
Reflex, Pupillary
Repetitive Sequences, Nucleic Acid
Repressor Proteins
Retina
Retinal Degeneration
Retinal Diseases
Retinal Ganglion Cells
Retrospective Studies
Reverse Transcriptase Polymerase Chain Reaction
Rhombencephalon
Ribs
Risk Factors
RNA Splice Sites
RNA, Messenger
Ryanodine Receptor Calcium Release Channel
Saudi Arabia
Schizophrenia
Scoliosis
Self Mutilation
Self-Injurious Behavior
Sequence Alignment
Sequence Analysis, DNA
Sequence Analysis, Protein
Sequence Deletion
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Severity of Illness Index
Sex Characteristics
Siblings
Signal Transduction
Single-Cell Analysis
Skull
Skull Base
Social Perception
Spinal Canal
Spinal Cord
Spine
Stem Cells
Strabismus
Syndrome
Synkinesis
Temperature
Time-Lapse Imaging
Tomography, Optical Coherence
Tomography, X-Ray Computed
Toothbrushing
Topoisomerase II Inhibitors
Trachea
Transcription Factors
Transcription, Genetic
Transcriptional Activation
Transverse Sinuses
Treatment Outcome
Trochlear Nerve
Tubulin
Tumor Suppressor Proteins
Turkey
Twins, Dizygotic
Ubiquitin
Ubiquitin-Protein Ligases
Ubiquitins
Upper Extremity Deformities, Congenital
Vision Disorders
Visual Acuity
Vomiting
Young Adult
Zebrafish
Zebrafish Proteins
Zinc
Zinc Fingers
Engle's Networks
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Concepts (480)
Derived automatically from this person's publications.
Fibrosis
Tubulin
Ophthalmoplegia
Oculomotor Muscles
Duane Retraction Syndrome
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_
Co-Authors (67)
People in Profiles who have published with this person.
MacKinnon, Sarah
Chan, Wai-Man
Hunter, David
Whitman, Mary
Lee, Arthur
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Similar People (60)
People who share similar concepts with this person.
Dagi, Linda
Alkuraya, Fowzan
Hunter, David
Chung, Wendy
Whitman, Mary
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Same Department
People in same department with this person.
Aria, Francesca
LaFortune, Lauren
Lehman, Laura
Libenson, Mark
Peek, Carrie
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Physical Neighbors
People whose addresses are nearby this person.
Pinto, Anna
Bergin, Ann Marie
Anselm, Irina
Rollins, Caitlin
Hameed, Mustafa
_