Harvard Catalyst Profiles

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

Emily Margaret Place, M.S.

Concepts (217)

Back to Profile
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 Degeneration1020244151.310 Why?
Retinitis Pigmentosa920233860.950 Why?
Retinal Dystrophies42022580.650 Why?
Eye Diseases, Hereditary420211170.510 Why?
Mitochondrial Diseases520183200.480 Why?
Night Blindness22022530.370 Why?
Retinal Diseases320226830.360 Why?
Rhodopsin220212030.360 Why?
Pedigree12202246440.350 Why?
Myopia220242540.320 Why?
Leber Congenital Amaurosis32020330.310 Why?
Mutation182022297860.290 Why?
Chondroitinsulfatases12023160.230 Why?
Machado-Joseph Disease12022260.220 Why?
Sequence Analysis, DNA8201948030.210 Why?
High-Throughput Nucleotide Sequencing7202135970.210 Why?
Genetic Testing6202134440.200 Why?
Spinocerebellar Ataxias12022910.200 Why?
Alagille Syndrome12021350.200 Why?
Turner Syndrome120221300.200 Why?
Visual Field Tests520213830.190 Why?
Eye Proteins320236460.180 Why?
Vitamin A120236150.180 Why?
Codon120216110.180 Why?
Retina3202226160.170 Why?
Hereditary Sensory and Motor Neuropathy12019210.170 Why?
Alcohol Oxidoreductases120201700.170 Why?
cis-trans-Isomerases12018440.170 Why?
Genes, Dominant120218800.170 Why?
Mitochondrial Proton-Translocating ATPases12018520.160 Why?
Hexokinase120191250.160 Why?
Rare Diseases120235530.160 Why?
DNA, Intergenic120181070.160 Why?
Leigh Disease12018750.150 Why?
Retinopathy of Prematurity120224210.150 Why?
Macular Degeneration220229800.150 Why?
Optic Disk120214000.150 Why?
Renal Tubular Transport, Inborn Errors12016120.140 Why?
Mitochondria5201835200.140 Why?
Ribonuclease P12016170.140 Why?
Hypercalciuria12016310.140 Why?
Nephrocalcinosis12016480.140 Why?
3-Hydroxyacyl CoA Dehydrogenases12016600.140 Why?
Calcium Channels, L-Type120172400.140 Why?
Claudins120161110.130 Why?
Genetic Variation3202065440.130 Why?
Exons3201824370.130 Why?
Mutation, Missense3202025640.130 Why?
Peroxisomal Disorders12014120.130 Why?
Microtubule-Associated Proteins1202010860.130 Why?
DNA Copy Number Variations3202019410.120 Why?
Usher Syndromes12014500.120 Why?
Bardet-Biedl Syndrome12014420.120 Why?
GTP Phosphohydrolases120175090.120 Why?
DNA Mutational Analysis6202041860.120 Why?
Pyruvate Dehydrogenase Complex Deficiency Disease1201370.120 Why?
Lysosomal Storage Diseases12014790.120 Why?
Optic Nerve Diseases120173270.120 Why?
Atrophy3202415830.120 Why?
Mitochondrial Encephalomyopathies12013370.120 Why?
Genetic Diseases, X-Linked120173720.120 Why?
Genetic Markers1202026340.110 Why?
Genetic Association Studies2202027030.110 Why?
Myosins120144090.110 Why?
Phenotype52022163650.110 Why?
Electroretinography320205090.110 Why?
Nicotinamide-Nucleotide Adenylyltransferase12012130.110 Why?
Pyruvic Acid120132000.110 Why?
RNA, Transfer, Amino Acyl12012460.110 Why?
Induced Pluripotent Stem Cells1202317360.110 Why?
Point Mutation1201716230.100 Why?
Visual Fields4202110470.100 Why?
PAX2 Transcription Factor12012800.100 Why?
Coloboma12012540.100 Why?
Visual Acuity4202125300.100 Why?
Genome, Mitochondrial12011710.100 Why?
Amino Acids, Branched-Chain120132510.090 Why?
Fundus Oculi220224730.090 Why?
Genome, Human3202044200.090 Why?
Diagnostic Errors1201712570.090 Why?
Genetic Predisposition to Disease52020174460.090 Why?
Erythrocytes1201924550.090 Why?
Eye Diseases120146690.080 Why?
Tomography, Optical Coherence4202426570.080 Why?
Fluorescein Angiography220249400.080 Why?
Humans4220247443430.080 Why?
Vesico-Ureteral Reflux120124270.080 Why?
Frameshift Mutation220223990.080 Why?
GTP-Binding Proteins220229700.080 Why?
Developmental Disabilities1201614560.070 Why?
Mitochondrial Proteins120139960.070 Why?
Proteins2201861030.070 Why?
Child132020777090.070 Why?
Renal Insufficiency120128040.070 Why?
Cataract120128340.070 Why?
Male2220233501180.060 Why?
Databases, Genetic1201217830.060 Why?
Adult1620232140550.060 Why?
Genes, Recessive220206410.060 Why?
Sendai virus12023210.060 Why?
Oxidative Phosphorylation220184810.060 Why?
HEK293 Cells3201942040.060 Why?
Amino Acid Transport System y+L12023170.060 Why?
Alleles3202069330.060 Why?
Cyclic Nucleotide Phosphodiesterases, Type 612022290.060 Why?
Child, Preschool82020410060.060 Why?
Infant72019351360.050 Why?
Infant, Newborn52023256250.050 Why?
Female1920233801940.050 Why?
Antiporters120232770.050 Why?
INDEL Mutation120222790.050 Why?
Monosaccharide Transport Proteins120234400.050 Why?
Adolescent92021857810.050 Why?
Homozygote2201617850.050 Why?
Genotype32023129510.050 Why?
Carrier Proteins1201450210.050 Why?
Cytoskeletal Proteins2201813640.050 Why?
DNA, Mitochondrial220178170.040 Why?
Computational Biology1201135210.040 Why?
Automation120215840.040 Why?
Chromosome Mapping2201847400.040 Why?
Vitamin E120238690.040 Why?
X Chromosome120228140.040 Why?
Neonatal Screening120235910.040 Why?
Blindness120226170.040 Why?
Genetic Loci2202025750.040 Why?
Retinal Vessels120247720.040 Why?
Carrier State120225180.040 Why?
Founder Effect120181890.040 Why?
Guanine Nucleotide Exchange Factors120225810.040 Why?
RNA Splice Sites120182090.040 Why?
Zebrafish2202229940.040 Why?
Chromosome Aberrations1202318130.040 Why?
Nystagmus, Pathologic12017960.040 Why?
Dimerization120188930.040 Why?
Leukocytes, Mononuclear1202318360.040 Why?
Jews120183850.040 Why?
Cohort Studies52020405610.040 Why?
Gene Library1201910740.030 Why?
Canada1202220650.030 Why?
Refractive Errors120171420.030 Why?
Gene Expression Profiling3202094380.030 Why?
Virulence1202013330.030 Why?
Medical Records1202114130.030 Why?
Genes, X-Linked120161280.030 Why?
Alu Elements120151190.030 Why?
Comparative Genomic Hybridization120164960.030 Why?
Amino Acid Substitution1202017910.030 Why?
Cell Line22023159970.030 Why?
Young Adult62020564300.030 Why?
Middle Aged820232133830.030 Why?
Forecasting1202229510.030 Why?
RNA, Transfer120163160.030 Why?
Mutagenesis, Insertional120156550.030 Why?
Internationality1201810030.030 Why?
Fibroblasts2201341610.030 Why?
Membrane Proteins2202278800.030 Why?
Electron Transport120132110.030 Why?
Base Sequence22015127970.030 Why?
Subcellular Fractions120135470.030 Why?
Retrospective Studies42024774490.030 Why?
Chromosomes, Human, Pair 6120133800.030 Why?
Adenosine Triphosphate1201820250.030 Why?
Haplotypes1201827790.030 Why?
F-Box Proteins120131970.030 Why?
Siblings120168540.030 Why?
Gene Frequency1201835880.020 Why?
Family Health1201612820.020 Why?
Mutant Proteins120135000.020 Why?
3' Untranslated Regions120135130.020 Why?
Sequence Alignment1201522560.020 Why?
RNA Splicing120169070.020 Why?
Dependovirus120167060.020 Why?
Cilia120144660.020 Why?
Dietary Supplements1202332970.020 Why?
Vision Disorders1201710580.020 Why?
DNA, Complementary1201320500.020 Why?
Multienzyme Complexes120136860.020 Why?
Parents1202334070.020 Why?
Prenatal Diagnosis1201612360.020 Why?
Heterozygote1201528040.020 Why?
Gene Deletion1201627510.020 Why?
Muscle, Skeletal2201349310.020 Why?
Genome1201618080.020 Why?
Glutamic Acid1201311690.020 Why?
Protein Transport1201319880.020 Why?
Software1202144430.020 Why?
Syndrome1201332510.020 Why?
Nuclear Proteins1202258530.020 Why?
Animals520221687570.020 Why?
History, 21st Century1201315340.020 Why?
Age of Onset1201332710.020 Why?
Cell Differentiation12023114830.020 Why?
Polymorphism, Single Nucleotide22016155190.020 Why?
Genetic Vectors1201634200.020 Why?
Diagnosis, Differential12021129590.020 Why?
History, 20th Century1201327400.020 Why?
Ubiquitin-Protein Ligases1201318610.010 Why?
Aged, 80 and over22023577760.010 Why?
Adaptor Proteins, Signal Transducing1201429160.010 Why?
Amino Acid Sequence12015138150.010 Why?
Genomics1201957200.010 Why?
Models, Biological1201995830.010 Why?
Molecular Sequence Data12015181110.010 Why?
Family1201231470.010 Why?
Kidney Transplantation1201642510.010 Why?
Gene Expression Regulation12019120720.010 Why?
Aged320231632800.010 Why?
Sensitivity and Specificity12014147220.010 Why?
Cells, Cultured12014192290.010 Why?
Rats12014242600.010 Why?
Cross-Sectional Studies12018250430.010 Why?
Reproducibility of Results12014199050.010 Why?
Brain12022263850.010 Why?
Case-Control Studies12012217460.010 Why?
Signal Transduction12013234030.010 Why?
Prospective Studies12014532880.010 Why?
Place's Networks
Click the
Explore
buttons for more information and interactive visualizations!
Concepts (217)
Explore
_
Co-Authors (64)
Explore
_
Similar People (60)
Explore
_
Same Department 
Explore
_
© 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.