Harvard Catalyst Profiles

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

Matthew Lebo, Ph.D.

Concepts (251)

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 Testing25202435911.690 Why?
Genetic Variation25202366111.090 Why?
Sequence Analysis, DNA14202047801.040 Why?
Genome, Human19202444410.970 Why?
Genomics24202459240.940 Why?
Computational Biology10202235670.730 Why?
Pathology, Molecular420223280.700 Why?
High-Throughput Nucleotide Sequencing13202036670.680 Why?
Noonan Syndrome220171220.640 Why?
Protein Tyrosine Phosphatase, Non-Receptor Type 11320172240.580 Why?
Leukemia, Myelomonocytic, Juvenile12017240.550 Why?
Genetic Predisposition to Disease242024180630.540 Why?
Genetic Counseling520246350.520 Why?
Databases, Genetic10202117580.510 Why?
Software8202044720.510 Why?
Information Dissemination5202111420.490 Why?
Prion Diseases12016990.470 Why?
Blood Group Antigens320221830.470 Why?
GTP Phosphohydrolases220175250.460 Why?
Prions120161770.450 Why?
Cardiomyopathy, Hypertrophic6202213370.440 Why?
Hyperlipoproteinemia Type II320243960.430 Why?
Genetic Diseases, Inborn420206060.400 Why?
Disease Susceptibility1201917910.400 Why?
Germ-Line Mutation3201718850.390 Why?
Genome-Wide Association Study62024127900.380 Why?
Penetrance320233880.340 Why?
Metamorphosis, Biological22009380.340 Why?
Multifactorial Inheritance4202414220.340 Why?
Disease320216750.330 Why?
DNA Copy Number Variations2201520470.330 Why?
Rh-Hr Blood-Group System22020640.320 Why?
Sexual Development12009390.320 Why?
Antigens, Human Platelet22019410.310 Why?
Blood Grouping and Crossmatching22019990.310 Why?
Mutation, Missense3201925920.300 Why?
Algorithms72019140980.300 Why?
Laboratories320234630.280 Why?
Biological Specimen Banks420217870.280 Why?
Diabetes Mellitus, Type 242024122500.270 Why?
Hypercholesterolemia2202411440.270 Why?
Workflow320228590.260 Why?
Drosophila melanogaster3201017220.260 Why?
Neonatal Screening420246200.240 Why?
Genes, BRCA2220175910.230 Why?
Cardiomyopathies4202020570.220 Why?
BRCA2 Protein220198020.220 Why?
Genes, BRCA1220177530.220 Why?
Vinculin22020580.210 Why?
Humans7820247670400.200 Why?
BRCA1 Protein2201911550.200 Why?
Alleles4202368930.200 Why?
Quality Improvement1201738540.190 Why?
Pharmacogenetics320226820.190 Why?
Risk Assessment42023242990.190 Why?
Heart Diseases1201428170.180 Why?
MNSs Blood-Group System1202070.180 Why?
Membrane Proteins2201778680.180 Why?
Cardiomyopathy, Dilated320208430.170 Why?
Genetics, Medical120233340.170 Why?
Sexual Behavior, Animal220101200.160 Why?
Genes, Insect220102650.160 Why?
Biotinidase12018170.160 Why?
RNA, Messenger12013127930.150 Why?
Polymorphism, Restriction Fragment Length120197660.150 Why?
Oligonucleotide Array Sequence Analysis5201637970.150 Why?
Canada3202121270.150 Why?
Research Design3202062100.150 Why?
Electronic Health Records5201848810.140 Why?
Gene Expression Profiling2201095320.130 Why?
Herpes Zoster120182520.130 Why?
Colorectal Neoplasms, Hereditary Nonpolyposis120203880.130 Why?
Health120193980.130 Why?
ABO Blood-Group System120183810.130 Why?
Primary Health Care3202347460.120 Why?
Arrhythmogenic Right Ventricular Dysplasia120171630.120 Why?
Infant, Newborn102024263960.120 Why?
Government Programs120172780.120 Why?
Guidelines as Topic2201813960.120 Why?
Polymorphism, Single Nucleotide62024160360.120 Why?
Exons1202023910.110 Why?
Male3320243642030.110 Why?
ras Proteins1201910540.110 Why?
Cardiomyopathy, Restrictive12014610.110 Why?
Medical History Taking120177790.110 Why?
Mutation52021302110.110 Why?
Skin Diseases, Genetic12014490.110 Why?
Science120162340.110 Why?
Erythrocytes2201924110.100 Why?
Communicable Diseases120218720.100 Why?
Female3420243966600.100 Why?
Ehlers-Danlos Syndrome12014940.100 Why?
Diagnostic Techniques, Cardiovascular120141530.100 Why?
Gene Deletion1202026680.100 Why?
Arthrogryposis12013690.100 Why?
Genotype62023130350.100 Why?
Data Interpretation, Statistical2201926980.100 Why?
Risk Factors102024748860.100 Why?
Chromosome Aberrations2202117760.100 Why?
Marfan Syndrome120142370.100 Why?
Decision Trees120135080.100 Why?
Death, Sudden, Cardiac1201915670.090 Why?
Comparative Genomic Hybridization120124740.090 Why?
Chromosome Mapping4202146160.090 Why?
Peer Review, Research120143430.090 Why?
Rare Diseases120166300.090 Why?
Polymorphism, Genetic1202042470.080 Why?
Base Sequence32017124140.080 Why?
Pneumonia1202121590.080 Why?
Pupa12009420.080 Why?
Receptors, Steroid120091570.080 Why?
Arteries1201411230.080 Why?
Delivery of Health Care, Integrated120169510.080 Why?
Coronary Disease1202359140.080 Why?
Genetic Association Studies4202027440.080 Why?
Databases, Factual2202180680.080 Why?
Body Weight1201946270.080 Why?
Vascular Malformations120144690.080 Why?
Middle Aged1920242232330.070 Why?
Ion Channels1201310430.070 Why?
Atherosclerosis1202434180.070 Why?
Mechanotransduction, Cellular120135390.070 Why?
Ultrasonography, Prenatal1201617720.070 Why?
Pedigree3202045390.070 Why?
Cardiovascular Diseases22024156450.070 Why?
Aortic Aneurysm, Thoracic120147070.070 Why?
Adult1820242233170.070 Why?
Larva120095120.070 Why?
Sepsis1202126050.070 Why?
Coronary Artery Disease2202465730.070 Why?
Randomized Controlled Trials as Topic52024103930.070 Why?
Early Detection of Cancer2201832360.070 Why?
Joint Instability120148030.070 Why?
Medical Informatics120137440.070 Why?
RNA Splicing220229030.060 Why?
Reproducibility of Results32021201690.060 Why?
Bayes Theorem2202423530.060 Why?
Phenotype52022167180.060 Why?
Decision Support Systems, Clinical1201311780.060 Why?
Cohort Studies62024417180.060 Why?
Arrhythmias, Cardiac1201422570.060 Why?
Epilepsy1201933170.050 Why?
Gene Frequency2202336210.050 Why?
Atrial Fibrillation1202251800.050 Why?
Health Surveys1201340560.050 Why?
Prospective Studies32022548860.050 Why?
Aged1220241713190.050 Why?
Heterozygote2202027940.050 Why?
Aging1202187290.050 Why?
Duty to Recontact12021190.050 Why?
Cluster Analysis1200927210.050 Why?
Gene Expression Regulation, Developmental2200936100.050 Why?
Molecular Sequence Data12013176080.050 Why?
Prostatic Neoplasms12023110970.050 Why?
Genetic Research120211730.040 Why?
Biomedical Research1201634640.040 Why?
Infant52024364850.040 Why?
Heart Defects, Congenital2201447130.040 Why?
Drosophila Proteins1200917050.040 Why?
Young Adult62024599800.040 Why?
North America1202312870.040 Why?
Digestive System Diseases120211520.040 Why?
Multicenter Studies as Topic1202417330.040 Why?
Aged, 80 and over62021595480.040 Why?
Sex Characteristics1200926470.040 Why?
Urogenital Abnormalities120212550.040 Why?
DNA2202272100.040 Why?
Pregnancy22017302380.040 Why?
Heart Failure12022118770.040 Why?
Mosaicism120214800.040 Why?
Case-Control Studies32020222540.040 Why?
Pennsylvania120186150.030 Why?
Galactosyltransferases120182830.030 Why?
Obesity12019130850.030 Why?
Chromosomes, Human120184370.030 Why?
Nerve Tissue Proteins1200944010.030 Why?
Neoplasms22017223500.030 Why?
Gene Duplication120173150.030 Why?
SOS1 Protein12016400.030 Why?
Molecular Diagnostic Techniques120216150.030 Why?
Nuclear Proteins1201157940.030 Why?
INDEL Mutation120162660.030 Why?
Disclosure120217550.030 Why?
Proto-Oncogene Proteins c-raf120162050.030 Why?
Principal Component Analysis120189500.030 Why?
Informed Consent1202110100.030 Why?
Breast Neoplasms22020211780.030 Why?
United States52023729710.030 Why?
Counseling1202315530.030 Why?
Virulence1201812940.030 Why?
Cholesterol, LDL1202423920.030 Why?
MAP Kinase Kinase 1120163300.030 Why?
Asymptomatic Diseases120175880.030 Why?
Desmoplakins12014630.030 Why?
Homozygote1201817740.030 Why?
Adolescent52021890460.030 Why?
Connective Tissue Diseases120162850.030 Why?
Myopathies, Structural, Congenital120141040.030 Why?
Child52021807710.030 Why?
Sequence Analysis120132400.030 Why?
Prognosis12013299630.030 Why?
Carrier Proteins2201749250.030 Why?
Financing, Organized120142020.030 Why?
Gene Expression Regulation12010119230.030 Why?
Hypolipidemic Agents120166090.020 Why?
Haplotypes1201827220.020 Why?
Evidence-Based Practice120164990.020 Why?
Drug Design1201610450.020 Why?
Age of Onset1201933440.020 Why?
Incidental Findings120166980.020 Why?
Time Factors22010401540.020 Why?
Decision Making1202439510.020 Why?
National Institutes of Health (U.S.)120137930.020 Why?
Health Knowledge, Attitudes, Practice1202440540.020 Why?
Transcription Factors12009121580.020 Why?
Hematologic Neoplasms1202119070.020 Why?
Hearing Loss120167850.020 Why?
Costs and Cost Analysis1201516660.020 Why?
Dissection120102980.020 Why?
Olfactory Receptor Neurons12009950.020 Why?
Sensitivity and Specificity22015146720.020 Why?
Family1201932100.020 Why?
Odds Ratio1202096600.020 Why?
Insect Proteins120092530.020 Why?
Proto-Oncogene Proteins p21(ras)1201617610.020 Why?
DNA Mutational Analysis1201641140.020 Why?
Blood Platelets1201824640.020 Why?
Proto-Oncogene Proteins B-raf1201620580.020 Why?
Organ Specificity1201019660.020 Why?
Health Behavior1201726500.020 Why?
Lipids1201633220.020 Why?
Proportional Hazards Models12020125360.020 Why?
Molecular Targeted Therapy1201628240.020 Why?
Child, Preschool22020426060.010 Why?
Head120109260.010 Why?
Health Personnel1201833870.010 Why?
Referral and Consultation1201736180.010 Why?
Health Care Costs1201732390.010 Why?
Mass Screening1202054560.010 Why?
Pilot Projects1201787320.010 Why?
Brain12010271630.010 Why?
Patient Acceptance of Health Care1201732320.010 Why?
Animals320101689650.010 Why?
Longitudinal Studies12019147660.010 Why?
Body Mass Index12019130480.010 Why?
Severity of Illness Index12019159250.010 Why?
Colorectal Neoplasms1202069660.010 Why?
Prevalence12017158510.010 Why?
Retrospective Studies22021816590.010 Why?
Cell Line12013155670.010 Why?
Cross-Sectional Studies12018263250.010 Why?
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Concepts (251)
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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.