Harvard Catalyst Profiles

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

Daniel Patrick Howrigan, Ph.D.

Concepts (131)

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?
Schizophrenia11202269290.540 Why?
Homozygote5201617760.480 Why?
DNA Copy Number Variations6202220200.460 Why?
Genetic Predisposition to Disease172023178780.430 Why?
Genome-Wide Association Study122023126610.390 Why?
Polymorphism, Single Nucleotide122022159080.350 Why?
Genetic Linkage1201123400.250 Why?
Genome, Human6202244210.210 Why?
Genes, Recessive220156230.190 Why?
Sequence Analysis, DNA1201147390.180 Why?
Synapses3201917550.180 Why?
Genetic Variation4202165610.170 Why?
Bipolar Disorder2202250910.170 Why?
Organelles120212660.170 Why?
Computational Biology1201135090.160 Why?
Cognition2202369870.160 Why?
Paternal Age12019870.160 Why?
Biological Specimen Banks120247780.160 Why?
Quantitative Trait, Heritable120215400.150 Why?
Genetic Loci2201826240.150 Why?
Post-Synaptic Density12017110.150 Why?
Epilepsy, Rolandic12017540.140 Why?
Heat-Shock Proteins120197950.130 Why?
Attention Deficit Disorder with Hyperactivity2202337080.130 Why?
Chromosome Mapping2201546110.120 Why?
Molecular Chaperones120197540.120 Why?
Epilepsy, Generalized120171780.120 Why?
Consanguinity120164560.120 Why?
Antisocial Personality Disorder120152240.110 Why?
Epilepsies, Partial120174310.110 Why?
Phenotype52024165710.110 Why?
Alleles4202268610.110 Why?
Chromosome Deletion1201713860.100 Why?
Immunity120189940.100 Why?
Algorithms22018140180.100 Why?
Impulsive Behavior120153460.100 Why?
Mutation42022300160.100 Why?
Family2202031930.090 Why?
Chromosomes, Human, Pair 18120112470.090 Why?
Genetic Markers1201626010.090 Why?
Chromosomes, Human, Pair 17120114180.080 Why?
Models, Genetic1201934310.080 Why?
Chromosomes, Human, Pair 9120115350.080 Why?
Amyotrophic Lateral Sclerosis1201914660.080 Why?
Child Development Disorders, Pervasive120136000.080 Why?
Obsessive-Compulsive Disorder1201714910.080 Why?
Epilepsy2202032880.070 Why?
Nerve Tissue Proteins2201744080.070 Why?
Humans3120247606170.070 Why?
Intracellular Signaling Peptides and Proteins1201728720.070 Why?
Denmark220197700.070 Why?
Linkage Disequilibrium1201119940.070 Why?
Case-Control Studies62022221480.070 Why?
Genetic Testing1201935330.070 Why?
Parents1202035630.060 Why?
Proteomics1201938360.060 Why?
Software1201944310.060 Why?
Gene Regulatory Networks1201317450.060 Why?
Transcription, Genetic1201875830.060 Why?
Male1620243603580.060 Why?
Gene Expression Regulation22018118740.060 Why?
Female1620243921480.050 Why?
Proteins1201760300.050 Why?
Aging1202186990.050 Why?
Regression Analysis1201163380.050 Why?
A Kinase Anchor Proteins12022570.050 Why?
Data Interpretation, Statistical1201126890.050 Why?
Multifactorial Inheritance2201913800.040 Why?
Risk Assessment22019239720.040 Why?
Haploinsufficiency120223360.040 Why?
Membrane Proteins1201778470.040 Why?
Synaptic Potentials12019440.040 Why?
Synaptosomes120191160.040 Why?
Haplotypes2201827130.040 Why?
Oxidative Phosphorylation120214950.040 Why?
Child42020800790.040 Why?
Knowledge Bases12019970.040 Why?
Brain32023271010.040 Why?
Substance-Related Disorders1201544160.040 Why?
Computer Simulation1201162330.040 Why?
Gene Dosage1202212170.040 Why?
Neural Cell Adhesion Molecules120171220.040 Why?
Alzheimer Disease1201886010.030 Why?
Genotype32016129780.030 Why?
Receptors, N-Methyl-D-Aspartate120228940.030 Why?
Adult420202209690.030 Why?
DNA, Mitochondrial120218650.030 Why?
Cell Adhesion Molecules, Neuronal120172630.030 Why?
Kruppel-Like Transcription Factors120185040.030 Why?
Social Class1202419920.030 Why?
Genomics2202258220.030 Why?
Education120165340.030 Why?
Sample Size120168380.030 Why?
Conduct Disorder120152450.030 Why?
Calcium-Binding Proteins1201710660.030 Why?
Apolipoproteins E1201814430.030 Why?
Task Performance and Analysis120167630.030 Why?
Databases, Genetic1201917420.030 Why?
Membrane Transport Proteins1201710340.020 Why?
Likelihood Functions120159910.020 Why?
Rare Diseases120166220.020 Why?
Cohort Studies32018414570.020 Why?
Risk-Taking1201510370.020 Why?
Heterozygote1201527800.020 Why?
Gene Frequency1201536010.020 Why?
Brain Diseases1201715450.020 Why?
Genetic Association Studies1201727340.020 Why?
Polymorphism, Genetic1201842420.020 Why?
DNA Mutational Analysis1201641100.020 Why?
Risk1201896040.020 Why?
Immunoglobulin G1201845330.020 Why?
Proteome1201618570.020 Why?
Child, Preschool22019421880.020 Why?
Adolescent32019882340.020 Why?
Amyloid beta-Peptides1201838390.020 Why?
Risk Factors32019741150.010 Why?
Mice, Transgenic1201795290.010 Why?
Gene Expression1201775680.010 Why?
Carrier Proteins1201749350.010 Why?
Signal Transduction22017234160.010 Why?
Alcoholism1201519720.010 Why?
Registries1201982070.010 Why?
Heart Defects, Congenital1201946710.010 Why?
Age Factors12019183810.010 Why?
Prevalence12019156890.010 Why?
Incidence12019213370.010 Why?
Disease Models, Animal12017182210.010 Why?
Middle Aged220242205840.010 Why?
Animals220191682010.010 Why?
Aged, 80 and over12018588940.010 Why?
Aged120181690420.000 Why?
Howrigan's Networks
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Concepts (131)
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Co-Authors (66)
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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.