Harvard Catalyst Profiles

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Arthur S Lee, Ph.D.

Concepts (75)

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?
Gene Dosage3200812720.360 Why?
Biological Evolution2200810870.280 Why?
Macaca mulatta1200824260.210 Why?
Genome1200817190.190 Why?
Arthrogryposis12019730.180 Why?
Conserved Sequence1201812450.140 Why?
Genome, Human2200845000.140 Why?
Zinc120186860.130 Why?
Ossification, Heterotopic120162330.130 Why?
Microfilament Proteins1201812110.120 Why?
Erythroblastosis, Fetal12012390.120 Why?
Rh-Hr Blood-Group System12012620.110 Why?
Basic Helix-Loop-Helix Transcription Factors1201611520.100 Why?
Intracellular Signaling Peptides and Proteins1201929950.090 Why?
Pan troglodytes120082350.090 Why?
alpha-Amylases12007370.090 Why?
Gene Duplication120083360.080 Why?
Nucleic Acid Hybridization1200814550.070 Why?
Cell Movement1201855290.070 Why?
Mutation32019291710.070 Why?
Genetic Variation3201166820.070 Why?
Zebrafish2201929920.070 Why?
Nuclear Proteins1201959730.060 Why?
DNA Copy Number Variations1201118600.060 Why?
Stem Cells1201635930.060 Why?
Evolution, Molecular2201219690.060 Why?
Oligonucleotide Array Sequence Analysis2200840890.050 Why?
Lissencephaly12018400.050 Why?
Genes, X-Linked120191350.050 Why?
Neurons1201893810.050 Why?
Comparative Genomic Hybridization220115110.040 Why?
Codon, Nonsense120192910.040 Why?
Frameshift Mutation120194010.040 Why?
Nervous System Malformations120182230.040 Why?
Ligaments120161250.040 Why?
Activin Receptors, Type I120161450.040 Why?
Genomics1201152060.040 Why?
Species Specificity2201126390.040 Why?
DNA Primers2201130420.040 Why?
Gene Knock-In Techniques120164460.030 Why?
Cilia120184520.030 Why?
Joints120163350.030 Why?
Sequence Deletion1201915510.030 Why?
Brain Stem120188480.030 Why?
Alleles2201671260.030 Why?
Microtubules1201811990.030 Why?
Pedigree1201947190.030 Why?
Bone Morphogenetic Proteins120168490.030 Why?
Animals620191702740.030 Why?
Phenotype22019162650.020 Why?
Mutation, Missense1201925000.020 Why?
Genotype22016129570.020 Why?
Ligands1201633170.020 Why?
Sex Characteristics1201924910.020 Why?
Disease Models, Animal22019183140.020 Why?
Base Sequence22012134640.020 Why?
Starch12007770.020 Why?
Cell Lineage1201626330.020 Why?
Chromosomes, Human120084780.020 Why?
Genetics, Population1201110130.020 Why?
Mice, Transgenic1201699580.020 Why?
Male420193511810.020 Why?
Female420193762490.010 Why?
In Situ Hybridization, Fluorescence1200826650.010 Why?
Humans720197060920.010 Why?
Sequence Analysis, DNA1201249490.010 Why?
Polymerase Chain Reaction1200863180.010 Why?
Polymorphism, Genetic1200843850.010 Why?
Genetic Predisposition to Disease12019173210.010 Why?
Cell Line12012167940.010 Why?
Child, Preschool12018411290.010 Why?
Child12018736230.010 Why?
Adolescent12018850930.010 Why?
Mice12016807230.010 Why?
Diet1200774770.010 Why?
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Concepts (75)
Co-Authors (6)
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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.