Harvard Catalyst Profiles

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Emily Margaret Place, M.S.

Concepts (228)

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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 Degeneration1020244131.270 Why?
Retinitis Pigmentosa920233920.920 Why?
Retinal Dystrophies42022620.630 Why?
Eye Diseases, Hereditary420211180.500 Why?
Rare Diseases320246110.470 Why?
Mitochondrial Diseases520183330.470 Why?
Night Blindness22022520.360 Why?
Retinal Diseases320226890.350 Why?
Rhodopsin220212060.340 Why?
Pedigree12202245550.340 Why?
Myopia220242460.310 Why?
Leber Congenital Amaurosis32020360.300 Why?
Mutation192024296140.290 Why?
Hyperbilirubinemia12007750.290 Why?
Plasmapheresis120072020.270 Why?
Genetic Testing8202434770.240 Why?
DNA Copy Number Variations4202419980.240 Why?
Sequence Analysis, DNA9202447030.230 Why?
De Lange Syndrome12024200.230 Why?
Chondroitinsulfatases12023160.220 Why?
Machado-Joseph Disease12022260.220 Why?
Genetic Variation4202464530.210 Why?
High-Throughput Nucleotide Sequencing7202136090.200 Why?
Spinocerebellar Ataxias12022990.200 Why?
Alagille Syndrome12021450.190 Why?
Turner Syndrome120221300.190 Why?
Epstein-Barr Virus Infections120075970.180 Why?
Visual Field Tests520213940.180 Why?
Eye Proteins320236270.180 Why?
Vitamin A120236100.180 Why?
Codon120216020.170 Why?
Retina3202226150.170 Why?
Hereditary Sensory and Motor Neuropathy12019210.170 Why?
Alcohol Oxidoreductases120201670.170 Why?
Genes, Dominant120218670.160 Why?
cis-trans-Isomerases12018430.160 Why?
Hexokinase120191250.160 Why?
Mitochondrial Proton-Translocating ATPases12018520.160 Why?
Adrenal Cortex Hormones1200718670.150 Why?
DNA, Intergenic120181040.150 Why?
Leigh Disease12018870.150 Why?
Retinopathy of Prematurity120224260.150 Why?
Macular Degeneration220229970.140 Why?
Phenotype72024162450.140 Why?
Optic Disk120214170.140 Why?
Renal Tubular Transport, Inborn Errors12016120.140 Why?
Mitochondria5201835230.140 Why?
Ribonuclease P12016160.140 Why?
Hypercalciuria12016300.140 Why?
Nephrocalcinosis12016490.130 Why?
3-Hydroxyacyl CoA Dehydrogenases12016590.130 Why?
Calcium Channels, L-Type120172350.130 Why?
Claudins120161130.130 Why?
Exons3201823870.130 Why?
Mutation, Missense3202025400.130 Why?
Peroxisomal Disorders12014120.120 Why?
Microtubule-Associated Proteins1202010820.120 Why?
Usher Syndromes12014520.120 Why?
Bardet-Biedl Syndrome12014450.120 Why?
DNA Mutational Analysis6202041190.120 Why?
GTP Phosphohydrolases120175020.120 Why?
Genome, Human4202443560.120 Why?
Lysosomal Storage Diseases12014780.120 Why?
Pyruvate Dehydrogenase Complex Deficiency Disease1201380.110 Why?
Optic Nerve Diseases120173350.110 Why?
Genetic Markers1202025930.110 Why?
Genetic Diseases, X-Linked120173680.110 Why?
Mitochondrial Encephalomyopathies12013400.110 Why?
Atrophy3202416130.110 Why?
Genetic Association Studies2202026780.110 Why?
Myosins120144020.110 Why?
Electroretinography320205110.110 Why?
Nicotinamide-Nucleotide Adenylyltransferase12012120.110 Why?
Pyruvic Acid120131920.100 Why?
RNA, Transfer, Amino Acyl12012460.100 Why?
Induced Pluripotent Stem Cells1202317820.100 Why?
Point Mutation1201716000.100 Why?
Visual Fields4202110380.100 Why?
PAX2 Transcription Factor12012810.100 Why?
Coloboma12012560.100 Why?
Genome, Mitochondrial12011680.100 Why?
Visual Acuity4202125740.090 Why?
Amino Acids, Branched-Chain120132570.090 Why?
Fundus Oculi220225320.090 Why?
Diagnostic Errors1201712550.090 Why?
Humans4620247460440.090 Why?
Genetic Predisposition to Disease52020174340.090 Why?
Erythrocytes1201923970.080 Why?
Eye Diseases120146420.080 Why?
Tomography, Optical Coherence4202428050.080 Why?
Frameshift Mutation220223890.080 Why?
Vesico-Ureteral Reflux120124380.080 Why?
GTP-Binding Proteins220229460.070 Why?
Child142024784560.070 Why?
Fluorescein Angiography2202410190.070 Why?
Mitochondrial Proteins120139770.070 Why?
Developmental Disabilities1201614940.070 Why?
Male2420243510930.070 Why?
Proteins2201860000.070 Why?
Renal Insufficiency120127860.070 Why?
Adolescent112024862020.070 Why?
Cataract120128270.060 Why?
Adult1720242149580.060 Why?
Female2220243821090.060 Why?
Databases, Genetic1201217310.060 Why?
Genes, Recessive220206200.060 Why?
Cohort Studies72024405030.060 Why?
Sendai virus12023220.060 Why?
Oxidative Phosphorylation220184880.060 Why?
HEK293 Cells3201941780.060 Why?
Chondroitin Sulfate Proteoglycans120241280.060 Why?
Amino Acid Transport System y+L12023170.060 Why?
Heterozygote2202427640.060 Why?
Alleles3202068310.060 Why?
Cyclic Nucleotide Phosphodiesterases, Type 612022280.050 Why?
Child, Preschool82020413760.050 Why?
Infant72019354440.050 Why?
Infant, Newborn52023257520.050 Why?
Antiporters120232760.050 Why?
INDEL Mutation120222650.050 Why?
Monosaccharide Transport Proteins120234410.050 Why?
Genotype32023127730.050 Why?
Homozygote2201617670.050 Why?
Carrier Proteins1201449260.050 Why?
Cytoskeletal Proteins2201813480.050 Why?
DNA, Mitochondrial220178350.040 Why?
Genetic Diseases, Inborn120245920.040 Why?
Computational Biology1201134840.040 Why?
Automation120215790.040 Why?
Chromosome Mapping2201846120.040 Why?
Vitamin E120238690.040 Why?
X Chromosome120228110.040 Why?
Blindness120225820.040 Why?
Chromosomal Proteins, Non-Histone120247100.040 Why?
Young Adult72024571060.040 Why?
Neonatal Screening120235910.040 Why?
Genetic Loci2202025540.040 Why?
Carrier State120225200.040 Why?
Founder Effect120181850.040 Why?
Guanine Nucleotide Exchange Factors120225630.040 Why?
Retinal Vessels120248240.040 Why?
RNA Splice Sites120182020.040 Why?
Zebrafish2202229790.040 Why?
Chromosome Aberrations1202317710.040 Why?
Sensitivity and Specificity22014145370.040 Why?
Dimerization120188860.040 Why?
Jews120183600.040 Why?
Nystagmus, Pathologic120171040.030 Why?
Leukocytes, Mononuclear1202318220.030 Why?
Gene Library1201910630.030 Why?
Acute Disease1200771160.030 Why?
Canada1202220880.030 Why?
Gene Expression Profiling3202093100.030 Why?
Virulence1202012920.030 Why?
Refractive Errors120171380.030 Why?
Medical Records1202113900.030 Why?
Genes, X-Linked120161280.030 Why?
Alu Elements120151140.030 Why?
Amino Acid Substitution1202017430.030 Why?
Comparative Genomic Hybridization120164750.030 Why?
Cell Line22023156310.030 Why?
RNA, Transfer120162840.030 Why?
Middle Aged820232144120.030 Why?
Forecasting1202229050.030 Why?
Fibroblasts2201340360.030 Why?
Internationality120189790.030 Why?
Mutagenesis, Insertional120156500.030 Why?
Base Sequence22015124470.030 Why?
Membrane Proteins2202277850.030 Why?
Electron Transport120132090.030 Why?
Subcellular Fractions120135300.030 Why?
Retrospective Studies42024782970.030 Why?
Cell Cycle Proteins1202434080.030 Why?
Chromosomes, Human, Pair 6120133750.030 Why?
Adenosine Triphosphate1201819800.030 Why?
Haplotypes1201827220.030 Why?
Siblings120168190.030 Why?
F-Box Proteins120132000.020 Why?
Gene Frequency1201835320.020 Why?
Family Health1201612550.020 Why?
Mutant Proteins120134910.020 Why?
Sequence Alignment1201521940.020 Why?
3' Untranslated Regions120135200.020 Why?
RNA Splicing120169060.020 Why?
Dependovirus120167010.020 Why?
Dietary Supplements1202333240.020 Why?
Cilia120144880.020 Why?
Vision Disorders1201710640.020 Why?
DNA, Complementary1201319930.020 Why?
Multienzyme Complexes120136640.020 Why?
Parents1202334620.020 Why?
Prenatal Diagnosis1201612560.020 Why?
Gene Deletion1201626620.020 Why?
Genome1201617440.020 Why?
Muscle, Skeletal2201348610.020 Why?
Glutamic Acid1201311540.020 Why?
Protein Transport1201319600.020 Why?
Software1202143990.020 Why?
Nuclear Proteins1202257460.020 Why?
Animals520221663310.020 Why?
Syndrome1201332450.020 Why?
History, 21st Century1201315380.020 Why?
Age of Onset1201332410.020 Why?
Cell Differentiation12023113840.020 Why?
Polymorphism, Single Nucleotide22016153660.020 Why?
Genetic Vectors1201633460.020 Why?
Diagnosis, Differential12021128390.020 Why?
History, 20th Century1201327390.020 Why?
Ubiquitin-Protein Ligases1201318530.010 Why?
Aged, 80 and over22023575570.010 Why?
Adaptor Proteins, Signal Transducing1201428810.010 Why?
Amino Acid Sequence12015134940.010 Why?
Genomics1201956940.010 Why?
Models, Biological1201994430.010 Why?
Molecular Sequence Data12015176750.010 Why?
Family1201231560.010 Why?
Kidney Transplantation1201640910.010 Why?
Gene Expression Regulation12019118390.010 Why?
Aged320231642360.010 Why?
Treatment Outcome12007636610.010 Why?
Cells, Cultured12014188910.010 Why?
Rats12014236800.010 Why?
Cross-Sectional Studies12018251770.010 Why?
Reproducibility of Results12014198040.010 Why?
Brain12022265960.010 Why?
Case-Control Studies12012216730.010 Why?
Prospective Studies12014532180.010 Why?
Signal Transduction12013231120.010 Why?
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Concepts (228)
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© 2024 President and Fellows of Harvard College
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.