Harvard Catalyst Profiles

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

David J. Harris, M.D.

Concepts (90)

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?
Chromosomes, Human, Pair 8320094620.310 Why?
Translocation, Genetic3200714200.300 Why?
Chromosomes, Human, Pair 10120072870.280 Why?
Acyltransferases120072940.260 Why?
Viscera120051390.240 Why?
Testis120078000.230 Why?
Trisomy120052660.230 Why?
Abnormalities, Multiple3200714160.100 Why?
Chromosome Breakage220081730.090 Why?
Chromosomes, Human, Pair 2220083260.090 Why?
Autistic Disorder2200811850.080 Why?
Gingival Hyperplasia12007170.080 Why?
NFI Transcription Factors12007440.070 Why?
Diacylglycerol Kinase12007480.070 Why?
Haploidy120071360.070 Why?
Hypertrichosis12007250.070 Why?
Human Development120081240.070 Why?
Chromosomes, Human, Pair 7120073220.070 Why?
Chromosomes, Human, Pair 3120073230.070 Why?
Language Development Disorders120071960.070 Why?
Williams Syndrome120071870.060 Why?
Nervous System Malformations120072470.060 Why?
Chromosome Mapping3200847420.060 Why?
HMGA2 Protein120041230.060 Why?
Urogenital Abnormalities120072610.060 Why?
Craniofacial Abnormalities120073150.060 Why?
Fructose-Bisphosphate Aldolase12003520.060 Why?
Chromosome Aberrations2200818140.060 Why?
Anemia, Hemolytic, Congenital12003690.060 Why?
Chromosomes, Human, Pair 12120044620.060 Why?
Congenital Abnormalities120087070.050 Why?
Rhabdomyolysis120031500.050 Why?
Lipoma120043340.050 Why?
Neuropeptides120089420.050 Why?
Genetic Predisposition to Disease32008174490.050 Why?
Child Behavior120078380.050 Why?
Exons1200724390.050 Why?
Social Behavior1200711270.050 Why?
Developmental Disabilities1200914560.050 Why?
Glycoproteins1200822630.040 Why?
Cerebellar Neoplasms120045870.040 Why?
Quantitative Trait Loci1200720190.040 Why?
Esophagus1200510180.040 Why?
Genome, Human2200944200.040 Why?
Seizures1200728590.030 Why?
Radiography1200570220.030 Why?
Syndrome2200732500.020 Why?
In Situ Hybridization, Fluorescence2200726490.020 Why?
Oligonucleotide Array Sequence Analysis2200939210.020 Why?
Chromosomes, Human, Pair 22120093510.020 Why?
Comparative Genomic Hybridization120094960.020 Why?
Human Genome Project120081920.020 Why?
Infant22007351290.020 Why?
Nucleic Acid Hybridization1200713750.020 Why?
Calcium Channels, L-Type120072400.020 Why?
Chromosomes, Human, Pair 1120076580.020 Why?
Female720093801970.020 Why?
Infant, Newborn12005256180.020 Why?
Ureter120073740.020 Why?
Brain Neoplasms1200488600.010 Why?
Humans1120097442200.010 Why?
Wnt Proteins120077210.010 Why?
Gene Rearrangement1200711790.010 Why?
Embryo, Mammalian1200717010.010 Why?
Cytoskeletal Proteins1200713640.010 Why?
Protein Structure, Tertiary1200838460.010 Why?
Growth Disorders120046450.010 Why?
Child, Preschool32007409920.010 Why?
Male520073500270.010 Why?
Child42009776790.010 Why?
Spinal Cord1200718090.010 Why?
Face120049940.010 Why?
Mutation, Missense1200825630.010 Why?
Phenotype22007163650.010 Why?
Sequence Analysis, DNA1200848030.010 Why?
Adult220072140350.010 Why?
Fibroblasts1200741560.010 Why?
Adaptor Proteins, Signal Transducing1200729150.010 Why?
Gene Expression Regulation, Developmental1200736170.010 Why?
Proto-Oncogene Proteins1200745530.010 Why?
Erythrocytes1200324540.010 Why?
Cell Line12007159990.010 Why?
Electroencephalography1200761500.010 Why?
Amino Acid Sequence12003138170.010 Why?
Kidney1200771830.010 Why?
Molecular Sequence Data12003181160.010 Why?
Mice22007811780.010 Why?
Muscle, Skeletal1200349350.000 Why?
Animals220071687880.000 Why?
Mutation12007297840.000 Why?
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Concepts (90)
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Co-Authors (20)
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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.