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Emily Margaret Place, M.S.
Concepts (228)
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Concepts are derived automatically from a person's publications.
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Categories
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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.
3' Untranslated Regions
3-Hydroxyacyl CoA Dehydrogenases
Acute Disease
Adaptor Proteins, Signal Transducing
Adenosine Triphosphate
Adolescent
Adrenal Cortex Hormones
Adult
Age of Onset
Aged
Aged, 80 and over
Alagille Syndrome
Alcohol Oxidoreductases
Alleles
Alu Elements
Amino Acid Sequence
Amino Acid Substitution
Amino Acid Transport System y+L
Amino Acids, Branched-Chain
Animals
Antiporters
Atrophy
Automation
Bardet-Biedl Syndrome
Base Sequence
Blindness
Brain
Calcium Channels, L-Type
Canada
Carrier Proteins
Carrier State
Case-Control Studies
Cataract
Cell Cycle Proteins
Cell Differentiation
Cell Line
Cells, Cultured
Child
Child, Preschool
Chondroitin Sulfate Proteoglycans
Chondroitinsulfatases
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Mapping
Chromosomes, Human, Pair 6
Cilia
cis-trans-Isomerases
Claudins
Codon
Cohort Studies
Coloboma
Comparative Genomic Hybridization
Computational Biology
Cross-Sectional Studies
Cyclic Nucleotide Phosphodiesterases, Type 6
Cytoskeletal Proteins
Databases, Genetic
De Lange Syndrome
Dependovirus
Developmental Disabilities
Diagnosis, Differential
Diagnostic Errors
Dietary Supplements
Dimerization
DNA Copy Number Variations
DNA Mutational Analysis
DNA, Complementary
DNA, Intergenic
DNA, Mitochondrial
Electron Transport
Electroretinography
Epstein-Barr Virus Infections
Erythrocytes
Exons
Eye Diseases
Eye Diseases, Hereditary
Eye Proteins
Family
Family Health
F-Box Proteins
Female
Fibroblasts
Fluorescein Angiography
Forecasting
Founder Effect
Frameshift Mutation
Fundus Oculi
Gene Deletion
Gene Expression Profiling
Gene Expression Regulation
Gene Frequency
Gene Library
Genes, Dominant
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetic Vectors
Genome
Genome, Human
Genome, Mitochondrial
Genomics
Genotype
Glutamic Acid
GTP Phosphohydrolases
GTP-Binding Proteins
Guanine Nucleotide Exchange Factors
Haplotypes
HEK293 Cells
Hereditary Sensory and Motor Neuropathy
Heterozygote
Hexokinase
High-Throughput Nucleotide Sequencing
History, 20th Century
History, 21st Century
Homozygote
Humans
Hyperbilirubinemia
Hypercalciuria
INDEL Mutation
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Internationality
Jews
Kidney Transplantation
Leber Congenital Amaurosis
Leigh Disease
Leukocytes, Mononuclear
Lysosomal Storage Diseases
Machado-Joseph Disease
Macular Degeneration
Male
Medical Records
Membrane Proteins
Microtubule-Associated Proteins
Middle Aged
Mitochondria
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Mitochondrial Proteins
Mitochondrial Proton-Translocating ATPases
Models, Biological
Molecular Sequence Data
Monosaccharide Transport Proteins
Multienzyme Complexes
Muscle, Skeletal
Mutagenesis, Insertional
Mutant Proteins
Mutation
Mutation, Missense
Myopia
Myosins
Neonatal Screening
Nephrocalcinosis
Nicotinamide-Nucleotide Adenylyltransferase
Night Blindness
Nuclear Proteins
Nystagmus, Pathologic
Optic Disk
Optic Nerve Diseases
Oxidative Phosphorylation
Parents
PAX2 Transcription Factor
Pedigree
Peroxisomal Disorders
Phenotype
Plasmapheresis
Point Mutation
Polymorphism, Single Nucleotide
Prenatal Diagnosis
Prospective Studies
Protein Transport
Proteins
Pyruvate Dehydrogenase Complex Deficiency Disease
Pyruvic Acid
Rare Diseases
Rats
Refractive Errors
Renal Insufficiency
Renal Tubular Transport, Inborn Errors
Reproducibility of Results
Retina
Retinal Degeneration
Retinal Diseases
Retinal Dystrophies
Retinal Vessels
Retinitis Pigmentosa
Retinopathy of Prematurity
Retrospective Studies
Rhodopsin
Ribonuclease P
RNA Splice Sites
RNA Splicing
RNA, Transfer
RNA, Transfer, Amino Acyl
Sendai virus
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Siblings
Signal Transduction
Software
Spinocerebellar Ataxias
Subcellular Fractions
Syndrome
Tomography, Optical Coherence
Treatment Outcome
Turner Syndrome
Ubiquitin-Protein Ligases
Usher Syndromes
Vesico-Ureteral Reflux
Virulence
Vision Disorders
Visual Acuity
Visual Field Tests
Visual Fields
Vitamin A
Vitamin E
X Chromosome
Young Adult
Zebrafish
Place's Networks
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Concepts (228)
Derived automatically from this person's publications.
Retinal Degeneration
Retinitis Pigmentosa
Pedigree
Retinal Dystrophies
Eye Diseases, Hereditary
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Co-Authors (65)
People in Profiles who have published with this person.
Sangermano, Riccardo
Huckfeldt, Rachel
Pierce, Eric
Bujakowska, Kinga
Comander, Jason
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Similar People (60)
People who share similar concepts with this person.
Pierce, Eric
Cepko, Constance
Alkuraya, Fowzan
Dryja, Thaddeus
Chung, Wendy
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_
Same Department
People in same department with this person.
Azad, Amee
Blanco, Tomas
Gilmore, Michael
Lester, Ethan
Vavvas, Demetrios
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