Harvard Catalyst Profiles

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Eric Vallabh Minikel, Ph.D.

Concepts (170)

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?
Prion Diseases162024995.220 Why?
Prions920241772.290 Why?
Oligonucleotides, Antisense420234611.570 Why?
Genes, Essential220201850.790 Why?
Neurodegenerative Diseases5202210940.740 Why?
Age of Onset2201933460.670 Why?
Drug Discovery3202410680.640 Why?
Penetrance320193860.620 Why?
Drug Approval120248210.550 Why?
Anticipation, Genetic1201450.490 Why?
Benzimidazoles120208640.480 Why?
Small Molecule Libraries120207420.470 Why?
Creutzfeldt-Jakob Syndrome12014920.450 Why?
Genetic Diseases, Inborn220166060.430 Why?
Molecular Targeted Therapy2202428300.410 Why?
Mass Spectrometry1201922040.400 Why?
Clinical Trials as Topic2202480550.350 Why?
Gene Frequency4202436260.350 Why?
Bicycling120111770.340 Why?
Environment Design120111740.340 Why?
Transportation120112170.330 Why?
Genetic Variation6202066110.300 Why?
Safety1201111610.270 Why?
Exons2202423950.270 Why?
Accidents, Traffic120118190.250 Why?
Heterozygote5202427980.210 Why?
Brain62024274530.210 Why?
RNA Splice Sites120242130.210 Why?
Urban Population1201120460.210 Why?
PrPC Proteins12021350.190 Why?
Multiple Sclerosis1201632500.190 Why?
Cerebrospinal Fluid120235450.170 Why?
Oligonucleotides120235630.170 Why?
Mutation62020302660.170 Why?
Gene Silencing2202415050.170 Why?
Sample Size220208480.160 Why?
Tissue Distribution1202322980.160 Why?
Dependovirus120247210.160 Why?
Central Nervous System Diseases120235210.160 Why?
Probability1202424830.160 Why?
Consanguinity120204600.150 Why?
Treatment Failure1202426640.150 Why?
Automation120205890.140 Why?
Macaca fascicularis120199130.140 Why?
Treatment Outcome12024654800.140 Why?
Mice72024820720.140 Why?
Jews120183590.130 Why?
Genome, Human3202044560.130 Why?
Genotype22022130480.130 Why?
Autoantigens120208910.130 Why?
Gene Knockdown Techniques1202016080.130 Why?
Rare Diseases220186310.120 Why?
Humans3120247689700.120 Why?
RNA2202327270.120 Why?
Enzyme-Linked Immunosorbent Assay2201938130.120 Why?
Homozygote1202017800.120 Why?
Drug Evaluation, Preclinical1202013400.120 Why?
Alleles2202469010.120 Why?
Genetic Predisposition to Disease42024180680.120 Why?
Animals1120241693350.120 Why?
Histones1202426030.110 Why?
tau Proteins2202421460.110 Why?
Craniosynostoses120174160.100 Why?
Pyrazoles1202320290.100 Why?
Artifacts1202019420.090 Why?
Autoantibodies1202021200.090 Why?
Databases, Genetic4202017580.090 Why?
Genome1201917540.090 Why?
Acceleration120111900.090 Why?
Magnetic Resonance Spectroscopy1202037820.090 Why?
DNA Methylation1202444320.080 Why?
Reproducibility of Results42020202450.080 Why?
Cell Line22020156040.080 Why?
Motor Vehicles120112800.080 Why?
Child Development Disorders, Pervasive120145990.080 Why?
Kaplan-Meier Estimate1201965470.080 Why?
Germ-Line Mutation1201718870.080 Why?
Genetic Association Studies1201727480.070 Why?
Cardiomyopathies2201720570.070 Why?
California1201114430.070 Why?
Mice, Inbred C57BL32020223790.070 Why?
Pedigree1201445450.070 Why?
Risk Factors42021749760.070 Why?
Sequence Analysis, DNA1201747850.060 Why?
Repressor Proteins1201729860.060 Why?
Crohn Disease1201822940.060 Why?
Choice Behavior120118480.060 Why?
Proportional Hazards Models12019125620.060 Why?
Transcription Factors12023121740.050 Why?
Research Design1201962140.050 Why?
Rats12019237860.050 Why?
Genetic Testing1201635910.050 Why?
5' Untranslated Regions120242550.050 Why?
Gene Expression Regulation22024119320.050 Why?
Male1020243652030.050 Why?
Time Factors12024402610.050 Why?
Female1120243975150.050 Why?
Glial Fibrillary Acidic Protein120245640.050 Why?
Phenotype52020167310.050 Why?
Case-Control Studies22020222960.050 Why?
Neurofilament Proteins120243370.050 Why?
Introns120249690.050 Why?
Computer Simulation1201462910.050 Why?
Transgenes1202410160.040 Why?
Protein Structure, Quaternary120214260.040 Why?
Cohort Studies32020418080.040 Why?
Proteins1201560110.040 Why?
Young Adult22019601310.040 Why?
Primates120225220.040 Why?
Models, Statistical1201451100.040 Why?
Adult620242238510.040 Why?
RNA Splicing120249050.040 Why?
Aged, 80 and over32020597390.040 Why?
Child22019809600.040 Why?
Adolescent22019892440.040 Why?
Wounds and Injuries1201125170.040 Why?
Middle Aged520242237370.040 Why?
Aged420201717860.040 Why?
alpha-Synuclein120247740.040 Why?
Crystallography, X-Ray1202119520.030 Why?
Facies120172240.030 Why?
Polyradiculoneuropathy12016650.030 Why?
Molecular Epidemiology120184730.030 Why?
Longitudinal Studies22024147940.030 Why?
Chromosomes, Mammalian120161480.030 Why?
Brain Chemistry120199590.030 Why?
Biological Specimen Banks120207890.030 Why?
HeLa Cells1201930760.030 Why?
Endonucleases120163710.030 Why?
Genetics, Population120189440.030 Why?
Embryonic Stem Cells1202012510.030 Why?
Open Reading Frames120168180.030 Why?
Amino Acid Substitution1201717420.030 Why?
Longevity1202010770.030 Why?
Lymphocytes1202026140.020 Why?
Kinetics1201963320.020 Why?
Haplotypes1201827250.020 Why?
Disease Models, Animal22023183540.020 Why?
Nerve Degeneration120167500.020 Why?
Myocytes, Cardiac1202016820.020 Why?
Mice, Transgenic1202395650.020 Why?
Phagocytosis1201615300.020 Why?
Recombinant Proteins1201965120.020 Why?
Alternative Splicing1201511050.020 Why?
Genome-Wide Association Study22020128010.020 Why?
Gene Deletion1201626740.020 Why?
Models, Genetic1201834490.020 Why?
Sequence Analysis, RNA1201620410.020 Why?
DNA Mutational Analysis1201641240.020 Why?
Protein Binding1201993440.020 Why?
Disease Progression12024136740.020 Why?
Trans-Activators1201628580.020 Why?
Proteome1201618910.020 Why?
Parkinson Disease1202028950.020 Why?
Retrospective Studies12014819030.020 Why?
RNA, Messenger12020128060.020 Why?
Survival Rate12019128730.020 Why?
Base Sequence12016124300.010 Why?
Computational Biology1201635620.010 Why?
High-Throughput Nucleotide Sequencing1201636710.010 Why?
Sensitivity and Specificity12019147520.010 Why?
Molecular Sequence Data12016176290.010 Why?
Prevalence12019158790.010 Why?
Macrophages1201658010.010 Why?
Gene Expression Profiling1201595490.010 Why?
Polymorphism, Single Nucleotide12018160530.010 Why?
Algorithms12018142010.010 Why?
Infant12017365560.010 Why?
Cardiovascular Diseases12020156610.010 Why?
Child, Preschool12017426830.010 Why?
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Concepts (170)
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Co-Authors (33)
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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.