Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Emily Margaret Place, M.S.

Concepts (214)

Concepts are derived automatically from a person's publications.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
Name Number of Publications Most Recent Publication Publications by All Authors Concept Score Why?
Retinal Degeneration1020244221.320 Why?
Retinitis Pigmentosa920233860.960 Why?
Retinal Dystrophies42022590.660 Why?
Eye Diseases, Hereditary420211160.520 Why?
Mitochondrial Diseases520183150.490 Why?
Night Blindness22022520.370 Why?
Retinal Diseases320226860.360 Why?
Rhodopsin220212040.360 Why?
Pedigree12202246370.350 Why?
Myopia220242540.320 Why?
Leber Congenital Amaurosis32020330.310 Why?
Mutation182022297360.290 Why?
Chondroitinsulfatases12023160.230 Why?
Sequence Analysis, DNA8201947960.210 Why?
High-Throughput Nucleotide Sequencing7202136290.210 Why?
Genetic Testing6202134530.200 Why?
Alagille Syndrome12021350.200 Why?
Turner Syndrome120221300.200 Why?
Visual Field Tests520213740.190 Why?
Eye Proteins320236450.180 Why?
Vitamin A120236240.180 Why?
Codon120216120.180 Why?
Hereditary Sensory and Motor Neuropathy12019220.170 Why?
Alcohol Oxidoreductases120201710.170 Why?
cis-trans-Isomerases12018440.170 Why?
Genes, Dominant120218820.170 Why?
Mitochondrial Proton-Translocating ATPases12018530.160 Why?
Hexokinase120191260.160 Why?
Rare Diseases120235470.160 Why?
DNA, Intergenic120181070.160 Why?
Leigh Disease12018750.160 Why?
Retinopathy of Prematurity120224220.150 Why?
Retina2202126200.150 Why?
Macular Degeneration220229780.150 Why?
Optic Disk120213990.150 Why?
Renal Tubular Transport, Inborn Errors12016110.150 Why?
Ribonuclease P12016170.140 Why?
Hypercalciuria12016310.140 Why?
Mitochondria5201835590.140 Why?
Nephrocalcinosis12016460.140 Why?
3-Hydroxyacyl CoA Dehydrogenases12016600.140 Why?
Calcium Channels, L-Type120172390.140 Why?
Claudins120161040.130 Why?
Genetic Variation3202065210.130 Why?
Exons3201824290.130 Why?
Mutation, Missense3202025420.130 Why?
Peroxisomal Disorders12014120.130 Why?
Microtubule-Associated Proteins1202010840.130 Why?
Usher Syndromes12014500.120 Why?
DNA Copy Number Variations3202019540.120 Why?
Bardet-Biedl Syndrome12014420.120 Why?
GTP Phosphohydrolases120175150.120 Why?
Pyruvate Dehydrogenase Complex Deficiency Disease1201370.120 Why?
Lysosomal Storage Diseases12014780.120 Why?
DNA Mutational Analysis6202042200.120 Why?
Optic Nerve Diseases120173240.120 Why?
Atrophy3202415670.120 Why?
Genetic Diseases, X-Linked120173670.120 Why?
Mitochondrial Encephalomyopathies12013370.120 Why?
Genetic Markers1202026360.120 Why?
Genetic Association Studies2202026920.110 Why?
Myosins120144100.110 Why?
Phenotype52022162870.110 Why?
Electroretinography320205110.110 Why?
Nicotinamide-Nucleotide Adenylyltransferase12012130.110 Why?
Induced Pluripotent Stem Cells1202316920.110 Why?
Pyruvic Acid120131930.110 Why?
RNA, Transfer, Amino Acyl12012470.110 Why?
Point Mutation1201716250.100 Why?
Visual Fields4202110460.100 Why?
PAX2 Transcription Factor12012800.100 Why?
Coloboma12012540.100 Why?
Visual Acuity4202125280.100 Why?
Genome, Mitochondrial12011700.100 Why?
Amino Acids, Branched-Chain120132490.100 Why?
Fundus Oculi220224740.090 Why?
Genome, Human3202044220.090 Why?
Diagnostic Errors1201712550.090 Why?
Genetic Predisposition to Disease52020173840.090 Why?
Erythrocytes1201924580.090 Why?
Eye Diseases120146670.080 Why?
Vesico-Ureteral Reflux120123830.080 Why?
Tomography, Optical Coherence4202426020.080 Why?
Fluorescein Angiography220249390.080 Why?
Frameshift Mutation220223980.080 Why?
Humans4120247363980.080 Why?
GTP-Binding Proteins220229710.080 Why?
Developmental Disabilities1201614370.080 Why?
Mitochondrial Proteins120139940.070 Why?
Proteins2201860940.070 Why?
Renal Insufficiency120127960.070 Why?
Child132020766620.070 Why?
Cataract120128220.070 Why?
Databases, Genetic1201217770.060 Why?
Male2220233487590.060 Why?
Adult1620232131840.060 Why?
Genes, Recessive220206480.060 Why?
Sendai virus12023220.060 Why?
Oxidative Phosphorylation220184820.060 Why?
Amino Acid Transport System y+L12023170.060 Why?
HEK293 Cells3201941770.060 Why?
Child, Preschool82020407260.060 Why?
Cyclic Nucleotide Phosphodiesterases, Type 612022290.060 Why?
Alleles3202069340.060 Why?
Infant72019348050.050 Why?
Infant, Newborn52023253740.050 Why?
Female1920233782590.050 Why?
Antiporters120232780.050 Why?
INDEL Mutation120222770.050 Why?
Monosaccharide Transport Proteins120234420.050 Why?
Adolescent92021852340.050 Why?
Homozygote2201617780.050 Why?
Genotype32023129370.050 Why?
Carrier Proteins1201450150.050 Why?
Cytoskeletal Proteins2201813770.050 Why?
DNA, Mitochondrial220178060.040 Why?
Computational Biology1201135130.040 Why?
Automation120215830.040 Why?
Chromosome Mapping2201847340.040 Why?
Vitamin E120238700.040 Why?
X Chromosome120228150.040 Why?
Neonatal Screening120235900.040 Why?
Blindness120226120.040 Why?
Genetic Loci2202025650.040 Why?
Retinal Vessels120247750.040 Why?
Carrier State120225170.040 Why?
Founder Effect120181910.040 Why?
Guanine Nucleotide Exchange Factors120225780.040 Why?
RNA Splice Sites120182070.040 Why?
Zebrafish2202229710.040 Why?
Nystagmus, Pathologic12017940.040 Why?
Chromosome Aberrations1202318210.040 Why?
Dimerization120188950.040 Why?
Leukocytes, Mononuclear1202318170.040 Why?
Cohort Studies52020402750.040 Why?
Jews120183850.040 Why?
Canada1202220110.040 Why?
Gene Library1201910760.040 Why?
Refractive Errors120171430.030 Why?
Gene Expression Profiling3202094090.030 Why?
Virulence1202013240.030 Why?
Genes, X-Linked120161250.030 Why?
Medical Records1202114200.030 Why?
Alu Elements120151180.030 Why?
Comparative Genomic Hybridization120165050.030 Why?
Amino Acid Substitution1202017950.030 Why?
Cell Line22023159950.030 Why?
Young Adult62020562300.030 Why?
Middle Aged820232129960.030 Why?
Forecasting1202229490.030 Why?
RNA, Transfer120163150.030 Why?
Mutagenesis, Insertional120156570.030 Why?
Internationality1201810020.030 Why?
Fibroblasts2201341360.030 Why?
Membrane Proteins2202278720.030 Why?
Electron Transport120132140.030 Why?
Retrospective Studies42024761810.030 Why?
Subcellular Fractions120135500.030 Why?
Base Sequence22015128320.030 Why?
Chromosomes, Human, Pair 6120133800.030 Why?
Adenosine Triphosphate1201820410.030 Why?
Haplotypes1201827810.030 Why?
F-Box Proteins120131970.030 Why?
Siblings120168540.030 Why?
Gene Frequency1201835800.030 Why?
Family Health1201612810.020 Why?
Mutant Proteins120135040.020 Why?
3' Untranslated Regions120135100.020 Why?
Sequence Alignment1201522580.020 Why?
RNA Splicing120169030.020 Why?
Dependovirus120167090.020 Why?
Cilia120144630.020 Why?
Dietary Supplements1202332760.020 Why?
Vision Disorders1201710460.020 Why?
DNA, Complementary1201320510.020 Why?
Multienzyme Complexes120136920.020 Why?
Parents1202333450.020 Why?
Prenatal Diagnosis1201612200.020 Why?
Heterozygote1201527920.020 Why?
Gene Deletion1201627660.020 Why?
Genome1201617940.020 Why?
Muscle, Skeletal2201349290.020 Why?
Glutamic Acid1201311730.020 Why?
Protein Transport1201319970.020 Why?
Software1202144260.020 Why?
Syndrome1201332390.020 Why?
Animals520221683680.020 Why?
Nuclear Proteins1202258510.020 Why?
History, 21st Century1201315330.020 Why?
Age of Onset1201332640.020 Why?
Cell Differentiation12023114670.020 Why?
Polymorphism, Single Nucleotide22016154910.020 Why?
Genetic Vectors1201634150.020 Why?
Diagnosis, Differential12021129840.020 Why?
History, 20th Century1201327390.020 Why?
Ubiquitin-Protein Ligases1201318420.010 Why?
Aged, 80 and over22023577230.010 Why?
Adaptor Proteins, Signal Transducing1201429170.010 Why?
Amino Acid Sequence12015138210.010 Why?
Genomics1201956670.010 Why?
Models, Biological1201996030.010 Why?
Molecular Sequence Data12015181440.010 Why?
Family1201231190.010 Why?
Kidney Transplantation1201642000.010 Why?
Gene Expression Regulation12019120670.010 Why?
Aged320231625900.010 Why?
Sensitivity and Specificity12014147390.010 Why?
Cells, Cultured12014192480.010 Why?
Rats12014242680.010 Why?
Cross-Sectional Studies12018245800.010 Why?
Reproducibility of Results12014197750.010 Why?
Case-Control Studies12012216860.010 Why?
Prospective Studies12014527930.010 Why?
Signal Transduction12013233680.010 Why?
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Concepts (214)
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.