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 8320094520.300 Why?
Translocation, Genetic3200713880.290 Why?
Chromosomes, Human, Pair 10120072760.280 Why?
Acyltransferases120073050.250 Why?
Viscera120051380.230 Why?
Testis120077940.230 Why?
Trisomy120052600.220 Why?
Abnormalities, Multiple3200714150.090 Why?
Chromosome Breakage220081590.090 Why?
Chromosomes, Human, Pair 2220083130.080 Why?
Autistic Disorder2200812140.070 Why?
NFI Transcription Factors12007420.070 Why?
Gingival Hyperplasia12007190.070 Why?
Diacylglycerol Kinase12007480.070 Why?
Haploidy120071330.070 Why?
Hypertrichosis12007310.070 Why?
Human Development120081230.070 Why?
Chromosomes, Human, Pair 7120073110.070 Why?
Chromosomes, Human, Pair 3120073150.070 Why?
Language Development Disorders120071920.060 Why?
Nervous System Malformations120072440.060 Why?
Williams Syndrome120071930.060 Why?
Chromosome Mapping3200846260.060 Why?
HMGA2 Protein120041020.060 Why?
Urogenital Abnormalities120072560.060 Why?
Craniofacial Abnormalities120073150.060 Why?
Chromosome Aberrations2200817670.060 Why?
Fructose-Bisphosphate Aldolase12003510.060 Why?
Anemia, Hemolytic, Congenital12003710.050 Why?
Chromosomes, Human, Pair 12120044300.050 Why?
Congenital Abnormalities120087040.050 Why?
Lipoma120042920.050 Why?
Rhabdomyolysis120031550.050 Why?
Neuropeptides120089430.050 Why?
Child Behavior120078470.050 Why?
Exons1200723890.050 Why?
Genetic Predisposition to Disease32008177900.050 Why?
Social Behavior1200711310.050 Why?
Developmental Disabilities1200915040.040 Why?
Glycoproteins1200822080.040 Why?
Cerebellar Neoplasms120045860.040 Why?
Quantitative Trait Loci1200721010.040 Why?
Esophagus1200510230.040 Why?
Genome, Human2200944180.040 Why?
Seizures1200729170.030 Why?
Radiography1200569650.030 Why?
In Situ Hybridization, Fluorescence2200725050.020 Why?
Syndrome2200732800.020 Why?
Oligonucleotide Array Sequence Analysis2200937740.020 Why?
Chromosomes, Human, Pair 22120093460.020 Why?
Comparative Genomic Hybridization120094730.020 Why?
Human Genome Project120081990.020 Why?
Infant22007360530.020 Why?
Nucleic Acid Hybridization1200713040.020 Why?
Calcium Channels, L-Type120072400.020 Why?
Chromosomes, Human, Pair 1120076350.020 Why?
Infant, Newborn12005261790.010 Why?
Ureter120073750.010 Why?
Female720093912460.010 Why?
Brain Neoplasms1200489850.010 Why?
Humans1120097606130.010 Why?
Wnt Proteins120077190.010 Why?
Gene Rearrangement1200711220.010 Why?
Embryo, Mammalian1200716740.010 Why?
Cytoskeletal Proteins1200713440.010 Why?
Protein Structure, Tertiary1200838000.010 Why?
Growth Disorders120046530.010 Why?
Child, Preschool32007420560.010 Why?
Spinal Cord1200718170.010 Why?
Child42009797990.010 Why?
Male520073597180.010 Why?
Face1200410170.010 Why?
Mutation, Missense1200825670.010 Why?
Phenotype22007165480.010 Why?
Sequence Analysis, DNA1200847160.010 Why?
Fibroblasts1200740890.010 Why?
Adaptor Proteins, Signal Transducing1200728960.010 Why?
Adult220072200070.010 Why?
Gene Expression Regulation, Developmental1200736040.010 Why?
Proto-Oncogene Proteins1200744960.010 Why?
Erythrocytes1200324150.010 Why?
Cell Line12007156200.010 Why?
Amino Acid Sequence12003134510.010 Why?
Kidney1200770640.010 Why?
Electroencephalography1200761890.010 Why?
Molecular Sequence Data12003176240.010 Why?
Mice22007812090.010 Why?
Muscle, Skeletal1200349240.000 Why?
Animals220071679600.000 Why?
Mutation12007299570.000 Why?
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Concepts (90)
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Co-Authors (19)
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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.