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 8320094530.290 Why?
Translocation, Genetic3200713950.280 Why?
Chromosomes, Human, Pair 10120072770.270 Why?
Acyltransferases120073050.250 Why?
Viscera120051380.230 Why?
Testis120077830.220 Why?
Trisomy120052610.220 Why?
Abnormalities, Multiple3200714240.090 Why?
Chromosome Breakage220081590.090 Why?
Chromosomes, Human, Pair 2220083130.080 Why?
Autistic Disorder2200812400.070 Why?
NFI Transcription Factors12007420.070 Why?
Gingival Hyperplasia12007190.070 Why?
Diacylglycerol Kinase12007470.070 Why?
Haploidy120071270.070 Why?
Hypertrichosis12007310.070 Why?
Human Development120081230.070 Why?
Chromosomes, Human, Pair 7120073100.070 Why?
Language Development Disorders120071930.060 Why?
Chromosomes, Human, Pair 3120073230.060 Why?
Nervous System Malformations120072440.060 Why?
Williams Syndrome120071950.060 Why?
Chromosome Mapping3200846220.060 Why?
HMGA2 Protein120041010.060 Why?
Urogenital Abnormalities120072550.060 Why?
Craniofacial Abnormalities120073200.060 Why?
Chromosome Aberrations2200817810.060 Why?
Fructose-Bisphosphate Aldolase12003430.060 Why?
Anemia, Hemolytic, Congenital12003710.050 Why?
Chromosomes, Human, Pair 12120044310.050 Why?
Congenital Abnormalities120087080.050 Why?
Lipoma120042960.050 Why?
Rhabdomyolysis120031520.050 Why?
Neuropeptides120089500.050 Why?
Child Behavior120078620.050 Why?
Exons1200723920.050 Why?
Genetic Predisposition to Disease32008180480.050 Why?
Social Behavior1200711440.040 Why?
Developmental Disabilities1200915160.040 Why?
Glycoproteins1200822060.040 Why?
Cerebellar Neoplasms120045900.040 Why?
Quantitative Trait Loci1200721270.040 Why?
Esophagus1200510450.040 Why?
Genome, Human2200944530.040 Why?
Seizures1200729960.030 Why?
Radiography1200569950.030 Why?
In Situ Hybridization, Fluorescence2200725250.020 Why?
Syndrome2200732780.020 Why?
Oligonucleotide Array Sequence Analysis2200937940.020 Why?
Chromosomes, Human, Pair 22120093480.020 Why?
Comparative Genomic Hybridization120094740.020 Why?
Human Genome Project120082020.020 Why?
Infant22007364970.020 Why?
Nucleic Acid Hybridization1200713050.020 Why?
Calcium Channels, L-Type120072420.020 Why?
Chromosomes, Human, Pair 1120076400.010 Why?
Ureter120073700.010 Why?
Infant, Newborn12005263950.010 Why?
Female720093969430.010 Why?
Brain Neoplasms1200491820.010 Why?
Humans1120097684510.010 Why?
Wnt Proteins120077240.010 Why?
Gene Rearrangement1200711390.010 Why?
Embryo, Mammalian1200716740.010 Why?
Cytoskeletal Proteins1200713370.010 Why?
Protein Structure, Tertiary1200837900.010 Why?
Growth Disorders120046350.010 Why?
Child, Preschool32007426230.010 Why?
Spinal Cord1200718140.010 Why?
Child42009808630.010 Why?
Male520073647810.010 Why?
Face1200410310.010 Why?
Mutation, Missense1200825940.010 Why?
Phenotype22007167120.010 Why?
Sequence Analysis, DNA1200847800.010 Why?
Adaptor Proteins, Signal Transducing1200729100.010 Why?
Fibroblasts1200741800.010 Why?
Gene Expression Regulation, Developmental1200736120.010 Why?
Adult220072235420.010 Why?
Proto-Oncogene Proteins1200745340.010 Why?
Erythrocytes1200324220.010 Why?
Cell Line12007156090.010 Why?
Amino Acid Sequence12003134520.010 Why?
Kidney1200770640.010 Why?
Electroencephalography1200763090.010 Why?
Molecular Sequence Data12003176470.010 Why?
Mice22007820450.010 Why?
Muscle, Skeletal1200349840.000 Why?
Animals220071694180.000 Why?
Mutation12007302430.000 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.