Harvard Catalyst Profiles

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

Emily Margaret Place, M.S.

Concepts (233)

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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 Degeneration1020244131.250 Why?
Retinitis Pigmentosa1020243971.080 Why?
Retinal Dystrophies42022650.620 Why?
Night Blindness32024560.580 Why?
Eye Diseases, Hereditary520241220.540 Why?
Pedigree14202445420.510 Why?
Rare Diseases320246220.460 Why?
Mitochondrial Diseases520183430.460 Why?
Retinal Diseases420247050.380 Why?
Myopia320242530.350 Why?
Rhodopsin220212030.340 Why?
Electroretinography420245250.300 Why?
High-Throughput Nucleotide Sequencing8202436390.300 Why?
Leber Congenital Amaurosis32020360.290 Why?
Mutation192024300530.280 Why?
Hyperbilirubinemia12007740.280 Why?
Plasmapheresis120072060.270 Why?
Genetic Testing9202435370.260 Why?
Sequence Analysis, DNA10202447400.260 Why?
Homozygote4202417760.250 Why?
DNA Copy Number Variations4202420200.240 Why?
De Lange Syndrome12024210.230 Why?
Chondroitinsulfatases12023160.220 Why?
Machado-Joseph Disease12022260.210 Why?
Codon, Nonsense120242850.210 Why?
Genetic Variation4202465670.210 Why?
Spinocerebellar Ataxias120221050.190 Why?
Alagille Syndrome12021450.190 Why?
Turner Syndrome120221290.190 Why?
Epstein-Barr Virus Infections120076120.180 Why?
Eye Proteins320236330.180 Why?
Vitamin A120236130.170 Why?
Visual Field Tests520214110.170 Why?
Codon120216010.170 Why?
Retina3202226590.170 Why?
Hereditary Sensory and Motor Neuropathy12019210.160 Why?
Alcohol Oxidoreductases120201690.160 Why?
Genes, Dominant120218520.160 Why?
cis-trans-Isomerases12018440.160 Why?
Hexokinase120191240.160 Why?
Mitochondrial Proton-Translocating ATPases12018530.160 Why?
Genetic Diseases, X-Linked220243860.150 Why?
Phenotype82024165920.150 Why?
Adrenal Cortex Hormones1200718810.150 Why?
DNA, Intergenic120181050.150 Why?
Leigh Disease12018890.140 Why?
Retinopathy of Prematurity120224390.140 Why?
Macular Degeneration2202210070.140 Why?
Optic Disk120214210.140 Why?
Renal Tubular Transport, Inborn Errors12016110.140 Why?
Genome, Human5202444250.140 Why?
Ribonuclease P12016180.130 Why?
Hypercalciuria12016310.130 Why?
Mitochondria5201836240.130 Why?
3-Hydroxyacyl CoA Dehydrogenases12016590.130 Why?
Nephrocalcinosis12016520.130 Why?
Calcium Channels, L-Type120172420.130 Why?
Claudins120161170.130 Why?
Mutation, Missense3202025710.130 Why?
Exons3201823910.120 Why?
Peroxisomal Disorders12014120.120 Why?
Microtubule-Associated Proteins1202010760.120 Why?
Visual Acuity5202426720.120 Why?
Usher Syndromes12014560.120 Why?
DNA Mutational Analysis6202041110.120 Why?
Bardet-Biedl Syndrome12014510.110 Why?
GTP Phosphohydrolases120175170.110 Why?
Lysosomal Storage Diseases12014790.110 Why?
Genetic Markers1202026010.110 Why?
Pyruvate Dehydrogenase Complex Deficiency Disease12013150.110 Why?
Optic Nerve Diseases120173420.110 Why?
Mitochondrial Encephalomyopathies12013400.110 Why?
Genetic Association Studies2202027350.110 Why?
Atrophy3202416330.110 Why?
Myosins120144050.110 Why?
Nicotinamide-Nucleotide Adenylyltransferase12012120.100 Why?
Pyruvic Acid120132040.100 Why?
Haplotypes3202427130.100 Why?
Point Mutation1201715950.100 Why?
RNA, Transfer, Amino Acyl12012460.100 Why?
Induced Pluripotent Stem Cells1202318600.100 Why?
Visual Fields4202110620.100 Why?
PAX2 Transcription Factor12012860.100 Why?
Tomography, Optical Coherence5202429170.100 Why?
Coloboma12012590.100 Why?
Genome, Mitochondrial12011660.090 Why?
Humans4920247615960.090 Why?
Heterozygote3202427870.090 Why?
Amino Acids, Branched-Chain120132690.090 Why?
Diagnostic Errors1201712650.090 Why?
Fundus Oculi220225560.090 Why?
Genetic Predisposition to Disease52020179040.080 Why?
Erythrocytes1201924130.080 Why?
Genetic Diseases, Inborn220246040.080 Why?
Alleles4202468640.080 Why?
Eye Diseases120146530.080 Why?
Child152024801580.080 Why?
Male2720243608460.080 Why?
Polymorphism, Single Nucleotide32024159360.080 Why?
Frameshift Mutation220223920.070 Why?
Vesico-Ureteral Reflux120124370.070 Why?
Adult1920242212100.070 Why?
GTP-Binding Proteins220229510.070 Why?
Mitochondrial Proteins120139760.070 Why?
Developmental Disabilities1201615090.070 Why?
Fluorescein Angiography2202410590.070 Why?
Female2420243927050.070 Why?
Proteins2201860320.070 Why?
Computational Biology2202435170.070 Why?
Renal Insufficiency120128090.060 Why?
Child, Preschool92024422320.060 Why?
Adolescent112024883260.060 Why?
Cataract120128320.060 Why?
Databases, Genetic1201217420.060 Why?
Genes, Recessive220206230.060 Why?
Sendai virus12023220.060 Why?
Cohort Studies72024414950.060 Why?
Oxidative Phosphorylation220184960.060 Why?
Photophobia12024750.060 Why?
HEK293 Cells3201942810.060 Why?
Amino Acid Transport System y+L12023170.060 Why?
Chondroitin Sulfate Proteoglycans120241410.060 Why?
Cyclic Nucleotide Phosphodiesterases, Type 612022270.050 Why?
Retinal Cone Photoreceptor Cells120241840.050 Why?
Retinal Rod Photoreceptor Cells120242040.050 Why?
Infant72019361930.050 Why?
Infant, Newborn52023262020.050 Why?
Antiporters120232770.050 Why?
INDEL Mutation120222660.050 Why?
Young Adult82024592600.050 Why?
Monosaccharide Transport Proteins120234360.050 Why?
Carrier Proteins1201449370.050 Why?
Genotype32023129900.050 Why?
Cytoskeletal Proteins2201813420.050 Why?
Membrane Proteins3202478590.040 Why?
Calcium-Binding Proteins1202410690.040 Why?
DNA, Mitochondrial220178650.040 Why?
Automation120215860.040 Why?
Chromosome Mapping2201846150.040 Why?
Vitamin E120238720.040 Why?
X Chromosome120228160.040 Why?
Blindness120225840.040 Why?
Chromosomal Proteins, Non-Histone120247270.040 Why?
Neonatal Screening120235970.040 Why?
Genetic Loci2202026320.040 Why?
Carrier State120225230.040 Why?
Founder Effect120181860.040 Why?
Guanine Nucleotide Exchange Factors120225690.040 Why?
Retinal Vessels120248520.040 Why?
RNA Splice Sites120182110.040 Why?
Zebrafish2202230080.040 Why?
Chromosome Aberrations1202317680.040 Why?
Dimerization120188910.030 Why?
Sensitivity and Specificity22014146650.030 Why?
Leukocytes, Mononuclear1202318440.030 Why?
Jews120183560.030 Why?
Nystagmus, Pathologic120171050.030 Why?
Gene Library1201910590.030 Why?
Acute Disease1200772370.030 Why?
Canada1202221220.030 Why?
Gene Expression Profiling3202094200.030 Why?
Genomics2202458210.030 Why?
Virulence1202013030.030 Why?
Refractive Errors120171470.030 Why?
Medical Records1202114080.030 Why?
Genes, X-Linked120161280.030 Why?
Amino Acid Substitution1202017390.030 Why?
Cell Line22023156010.030 Why?
Alu Elements120151150.030 Why?
Comparative Genomic Hybridization120164730.030 Why?
Forecasting1202229280.030 Why?
RNA, Transfer120162920.030 Why?
Middle Aged820232209210.030 Why?
Base Sequence22015124410.030 Why?
Mutagenesis, Insertional120156560.030 Why?
Internationality1201810010.030 Why?
Fibroblasts2201341420.030 Why?
Electron Transport120132100.030 Why?
Subcellular Fractions120135320.030 Why?
Cell Cycle Proteins1202434490.030 Why?
Chromosomes, Human, Pair 6120133670.030 Why?
Retrospective Studies42024806470.030 Why?
Adenosine Triphosphate1201819890.020 Why?
Siblings120168250.020 Why?
F-Box Proteins120132010.020 Why?
Family Health1201612570.020 Why?
Mutant Proteins120134910.020 Why?
Gene Frequency1201836060.020 Why?
Sequence Alignment1201521800.020 Why?
3' Untranslated Regions120135190.020 Why?
RNA Splicing120169180.020 Why?
Dependovirus120167180.020 Why?
Dietary Supplements1202334150.020 Why?
Cilia120144950.020 Why?
DNA, Complementary1201319910.020 Why?
Vision Disorders1201710880.020 Why?
Multienzyme Complexes120136660.020 Why?
Parents1202335630.020 Why?
Prenatal Diagnosis1201612650.020 Why?
Gene Deletion1201626650.020 Why?
Genome1201617400.020 Why?
Muscle, Skeletal2201349480.020 Why?
Protein Transport1201319670.020 Why?
Glutamic Acid1201311760.020 Why?
Software1202144340.020 Why?
Nuclear Proteins1202257990.020 Why?
Syndrome1201332670.020 Why?
Animals520221684750.020 Why?
History, 21st Century1201315670.020 Why?
Age of Onset1201333060.020 Why?
Cell Differentiation12023115300.020 Why?
Genetic Vectors1201633960.020 Why?
Diagnosis, Differential12021129730.020 Why?
History, 20th Century1201327670.020 Why?
Adaptor Proteins, Signal Transducing1201428980.010 Why?
Amino Acid Sequence12015134460.010 Why?
Ubiquitin-Protein Ligases1201318990.010 Why?
Aged, 80 and over22023589840.010 Why?
Models, Biological1201994690.010 Why?
Molecular Sequence Data12015176350.010 Why?
Family1201231950.010 Why?
Gene Expression Regulation12019119040.010 Why?
Kidney Transplantation1201642350.010 Why?
Aged320231693100.010 Why?
Treatment Outcome12007646850.010 Why?
Cells, Cultured12014189660.010 Why?
Rats12014237410.010 Why?
Cross-Sectional Studies12018261290.010 Why?
Reproducibility of Results12014201000.010 Why?
Brain12022271210.010 Why?
Case-Control Studies12012221760.010 Why?
Signal Transduction12013234470.010 Why?
Prospective Studies12014544230.010 Why?
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© 2025 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.