Harvard Catalyst Profiles

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Matthew Lebo, Ph.D.

Concepts (248)

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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?
Genetic Testing23202334391.770 Why?
Genetic Variation25202365401.140 Why?
Sequence Analysis, DNA14202048011.080 Why?
Genome, Human18202344200.990 Why?
Genomics23202356920.910 Why?
Computational Biology10202235180.760 Why?
Pathology, Molecular420223250.740 Why?
High-Throughput Nucleotide Sequencing13202035850.720 Why?
Noonan Syndrome220171200.680 Why?
Protein Tyrosine Phosphatase, Non-Receptor Type 11320172340.610 Why?
Leukemia, Myelomonocytic, Juvenile12017200.590 Why?
Databases, Genetic10202117800.530 Why?
Software8202044340.530 Why?
Information Dissemination5202111000.520 Why?
Genetic Predisposition to Disease232023174000.520 Why?
Prion Diseases12016880.500 Why?
Blood Group Antigens320221790.500 Why?
GTP Phosphohydrolases220175080.480 Why?
Cardiomyopathy, Hypertrophic6202212630.480 Why?
Prions120161810.480 Why?
Hyperlipoproteinemia Type II320243730.450 Why?
Germ-Line Mutation3201717860.430 Why?
Genetic Diseases, Inborn420205870.430 Why?
Disease Susceptibility1201917800.420 Why?
Penetrance320233800.370 Why?
Metamorphosis, Biological22009370.360 Why?
DNA Copy Number Variations2201519400.350 Why?
Genome-Wide Association Study52022122200.340 Why?
Disease320216810.340 Why?
Rh-Hr Blood-Group System22020650.340 Why?
Sexual Development12009340.340 Why?
Antigens, Human Platelet22019430.330 Why?
Blood Grouping and Crossmatching220191060.320 Why?
Genetic Counseling320236000.320 Why?
Algorithms72019138530.320 Why?
Mutation, Missense3201925560.320 Why?
Biological Specimen Banks420217070.310 Why?
Laboratories320234610.300 Why?
Hypercholesterolemia2202411490.280 Why?
Workflow320228460.280 Why?
Drosophila melanogaster3201017040.270 Why?
Cardiomyopathies4202019120.240 Why?
Diabetes Mellitus, Type 232023116950.240 Why?
Genes, BRCA2220176170.240 Why?
Multifactorial Inheritance3202011900.240 Why?
BRCA2 Protein220197900.230 Why?
Genes, BRCA1220177800.230 Why?
Vinculin22020620.220 Why?
Neonatal Screening320235910.210 Why?
Quality Improvement1201737380.210 Why?
Alleles4202369310.210 Why?
BRCA1 Protein2201911450.210 Why?
Pharmacogenetics320226760.210 Why?
Humans7520247420880.200 Why?
Risk Assessment42023233200.200 Why?
MNSs Blood-Group System1202080.190 Why?
Heart Diseases1201427890.190 Why?
Membrane Proteins2201778730.190 Why?
Genetics, Medical120233370.180 Why?
Cardiomyopathy, Dilated320208510.180 Why?
Sexual Behavior, Animal220101130.170 Why?
Genes, Insect220102680.170 Why?
Biotinidase12018190.170 Why?
Polymorphism, Restriction Fragment Length120197680.160 Why?
RNA, Messenger12013130290.160 Why?
Canada3202120610.160 Why?
Oligonucleotide Array Sequence Analysis5201639200.160 Why?
Electronic Health Records5201844400.150 Why?
Research Design3202059790.150 Why?
Gene Expression Profiling2201094100.140 Why?
Herpes Zoster120182640.140 Why?
Colorectal Neoplasms, Hereditary Nonpolyposis120203790.130 Why?
Primary Health Care3202345510.130 Why?
ABO Blood-Group System120183670.130 Why?
Health120193900.130 Why?
Arrhythmogenic Right Ventricular Dysplasia120171610.130 Why?
Government Programs120172750.130 Why?
Guidelines as Topic2201814020.120 Why?
Exons1202024310.120 Why?
ras Proteins1201910600.120 Why?
Cardiomyopathy, Restrictive12014600.120 Why?
Infant, Newborn92023255750.120 Why?
Skin Diseases, Genetic12014400.110 Why?
Mutation52021297170.110 Why?
Medical History Taking120177830.110 Why?
Science120162410.110 Why?
Polymorphism, Single Nucleotide52019154940.110 Why?
Ehlers-Danlos Syndrome12014890.110 Why?
Erythrocytes2201924520.110 Why?
Diagnostic Techniques, Cardiovascular120141530.110 Why?
Male3020243495380.110 Why?
Communicable Diseases120218780.110 Why?
Arthrogryposis12013720.110 Why?
Gene Deletion1202027510.100 Why?
Genotype62023129460.100 Why?
Marfan Syndrome120142400.100 Why?
Data Interpretation, Statistical2201927140.100 Why?
Decision Trees120135060.100 Why?
Chromosome Aberrations2202118110.100 Why?
Female3120243795920.100 Why?
Death, Sudden, Cardiac1201915410.100 Why?
Comparative Genomic Hybridization120124960.100 Why?
Peer Review, Research120143290.100 Why?
Rare Diseases120165540.100 Why?
Chromosome Mapping4202147420.090 Why?
Risk Factors92024721450.090 Why?
Pupa12009370.090 Why?
Polymorphism, Genetic1202043280.090 Why?
Pneumonia1202121170.090 Why?
Base Sequence32017127970.090 Why?
Databases, Factual2202177160.080 Why?
Receptors, Steroid120091550.080 Why?
Arteries1201411180.080 Why?
Delivery of Health Care, Integrated120169410.080 Why?
Genetic Association Studies4202026990.080 Why?
Vascular Malformations120144500.080 Why?
Coronary Disease1202360780.080 Why?
Body Weight1201946640.080 Why?
Ion Channels1201310560.080 Why?
Ultrasonography, Prenatal1201616940.080 Why?
Atherosclerosis1202434280.080 Why?
Mechanotransduction, Cellular120135410.080 Why?
Pedigree3202046460.070 Why?
Cardiovascular Diseases22024151080.070 Why?
Larva120095170.070 Why?
Aortic Aneurysm, Thoracic120146850.070 Why?
Sepsis1202125890.070 Why?
Early Detection of Cancer2201830700.070 Why?
Coronary Artery Disease2202464540.070 Why?
Middle Aged1720242131270.070 Why?
Medical Informatics120137420.070 Why?
Joint Instability120147920.070 Why?
RNA Splicing220229070.070 Why?
Adult1620232137120.060 Why?
Reproducibility of Results32021198620.060 Why?
Phenotype52022163310.060 Why?
Decision Support Systems, Clinical1201311620.060 Why?
Arrhythmias, Cardiac1201422670.060 Why?
Gene Frequency2202335870.060 Why?
Epilepsy1201933010.060 Why?
Atrial Fibrillation1202250190.060 Why?
Health Surveys1201340300.060 Why?
Prospective Studies32022531870.060 Why?
Heterozygote2202027900.050 Why?
Randomized Controlled Trials as Topic4202399410.050 Why?
Aging1202186260.050 Why?
Duty to Recontact12021200.050 Why?
Cluster Analysis1200927130.050 Why?
Cohort Studies52024404500.050 Why?
Gene Expression Regulation, Developmental2200936170.050 Why?
Genetic Research120211740.050 Why?
Prostatic Neoplasms12023110390.050 Why?
Biomedical Research1201633060.050 Why?
Molecular Sequence Data12013181120.050 Why?
Heart Defects, Congenital2201445660.050 Why?
Drosophila Proteins1200916990.040 Why?
North America1202312490.040 Why?
Digestive System Diseases120211470.040 Why?
Aged1020211629440.040 Why?
Aged, 80 and over62021576830.040 Why?
Sex Characteristics1200925850.040 Why?
Heart Failure12022108560.040 Why?
Mosaicism120214400.040 Why?
Urogenital Abnormalities120212610.040 Why?
Pregnancy22017290870.040 Why?
DNA2202272890.040 Why?
Case-Control Studies32020217190.040 Why?
Galactosyltransferases120182630.040 Why?
Pennsylvania120186130.040 Why?
Young Adult52024563500.040 Why?
Obesity12019127050.040 Why?
Neoplasms22017215960.040 Why?
Chromosomes, Human120184570.040 Why?
Gene Duplication120173300.030 Why?
SOS1 Protein12016410.030 Why?
Nerve Tissue Proteins1200944650.030 Why?
Molecular Diagnostic Techniques120216020.030 Why?
Infant42021350700.030 Why?
Nuclear Proteins1201158510.030 Why?
Disclosure120217360.030 Why?
INDEL Mutation120162790.030 Why?
Proto-Oncogene Proteins c-raf120162030.030 Why?
Principal Component Analysis120189390.030 Why?
Informed Consent120219910.030 Why?
United States52023696930.030 Why?
Breast Neoplasms22020207740.030 Why?
Counseling1202315210.030 Why?
Virulence1201813280.030 Why?
Cholesterol, LDL1202423540.030 Why?
MAP Kinase Kinase 1120163370.030 Why?
Asymptomatic Diseases120175520.030 Why?
Bayes Theorem1202223030.030 Why?
Desmoplakins12014620.030 Why?
Adolescent52021856490.030 Why?
Homozygote1201817770.030 Why?
Connective Tissue Diseases120162640.030 Why?
Myopathies, Structural, Congenital120141020.030 Why?
Child52021774780.030 Why?
Prognosis12013290100.030 Why?
Sequence Analysis120132560.030 Why?
Financing, Organized120142020.030 Why?
Carrier Proteins2201750190.030 Why?
Gene Expression Regulation12010120710.030 Why?
Hypolipidemic Agents120166040.030 Why?
Haplotypes1201827810.030 Why?
Age of Onset1201932660.030 Why?
Evidence-Based Practice120165000.030 Why?
Drug Design1201610780.020 Why?
Incidental Findings120166880.020 Why?
Time Factors22010400540.020 Why?
National Institutes of Health (U.S.)120137800.020 Why?
Transcription Factors12009121640.020 Why?
Hematologic Neoplasms1202118200.020 Why?
Hearing Loss120167650.020 Why?
Costs and Cost Analysis1201516790.020 Why?
Dissection120102940.020 Why?
Olfactory Receptor Neurons12009920.020 Why?
Proto-Oncogene Proteins p21(ras)1201616830.020 Why?
Sensitivity and Specificity22015147200.020 Why?
Family1201931440.020 Why?
Insect Proteins120092580.020 Why?
Odds Ratio1202098460.020 Why?
Blood Platelets1201825060.020 Why?
DNA Mutational Analysis1201641870.020 Why?
Proto-Oncogene Proteins B-raf1201620280.020 Why?
Organ Specificity1201020030.020 Why?
Lipids1201633020.020 Why?
Health Behavior1201726300.020 Why?
Proportional Hazards Models12020123440.020 Why?
Molecular Targeted Therapy1201627230.020 Why?
Child, Preschool22020409550.020 Why?
Head120108780.020 Why?
Health Personnel1201832100.020 Why?
Referral and Consultation1201735270.020 Why?
Mass Screening1202052380.010 Why?
Pilot Projects1201782970.010 Why?
Health Care Costs1201732030.010 Why?
Brain12010263430.010 Why?
Patient Acceptance of Health Care1201730140.010 Why?
Longitudinal Studies12019139210.010 Why?
Animals320101685610.010 Why?
Body Mass Index12019126950.010 Why?
Severity of Illness Index12019155300.010 Why?
Colorectal Neoplasms1202067540.010 Why?
Prevalence12017151940.010 Why?
Retrospective Studies22021770980.010 Why?
Cell Line12013159940.010 Why?
Cross-Sectional Studies12018249130.010 Why?
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Concepts (248)
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© 2024 President and Fellows of Harvard College
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.