Harvard Catalyst Profiles

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Matthew Lebo, Ph.D.

Concepts (251)

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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 Testing25202435371.720 Why?
Genetic Variation25202365671.100 Why?
Sequence Analysis, DNA14202047401.060 Why?
Genome, Human19202444250.980 Why?
Genomics24202458210.960 Why?
Computational Biology10202235170.740 Why?
Pathology, Molecular420223280.710 Why?
High-Throughput Nucleotide Sequencing13202036390.690 Why?
Noonan Syndrome220171200.650 Why?
Protein Tyrosine Phosphatase, Non-Receptor Type 11320172230.580 Why?
Leukemia, Myelomonocytic, Juvenile12017250.560 Why?
Genetic Predisposition to Disease242024179040.540 Why?
Genetic Counseling520246270.530 Why?
Databases, Genetic10202117420.520 Why?
Software8202044340.520 Why?
Information Dissemination5202111260.500 Why?
Prion Diseases120161000.470 Why?
Blood Group Antigens320221840.470 Why?
GTP Phosphohydrolases220175170.460 Why?
Prions120161800.460 Why?
Cardiomyopathy, Hypertrophic6202213100.450 Why?
Hyperlipoproteinemia Type II320243950.430 Why?
Genetic Diseases, Inborn420206040.410 Why?
Disease Susceptibility1201917870.400 Why?
Germ-Line Mutation3201718580.400 Why?
Genome-Wide Association Study62024126900.380 Why?
Penetrance320233830.350 Why?
Metamorphosis, Biological22009370.350 Why?
Multifactorial Inheritance4202413870.340 Why?
Disease320216720.330 Why?
DNA Copy Number Variations2201520200.330 Why?
Rh-Hr Blood-Group System22020630.320 Why?
Sexual Development12009400.320 Why?
Antigens, Human Platelet22019410.320 Why?
Blood Grouping and Crossmatching220191000.310 Why?
Mutation, Missense3201925710.300 Why?
Algorithms72019140320.300 Why?
Laboratories320234580.290 Why?
Biological Specimen Banks420217830.290 Why?
Diabetes Mellitus, Type 242024121490.270 Why?
Hypercholesterolemia2202411410.270 Why?
Workflow320228510.260 Why?
Drosophila melanogaster3201017120.260 Why?
Neonatal Screening420245970.240 Why?
Cardiomyopathies4202019640.230 Why?
Genes, BRCA2220176010.230 Why?
BRCA2 Protein220198050.220 Why?
Genes, BRCA1220177640.220 Why?
Vinculin22020590.210 Why?
Humans7820247615780.200 Why?
Alleles4202368640.200 Why?
Pharmacogenetics320226750.200 Why?
Quality Improvement1201738010.200 Why?
BRCA1 Protein2201911580.200 Why?
Risk Assessment42023239960.190 Why?
Heart Diseases1201427810.180 Why?
MNSs Blood-Group System1202070.180 Why?
Membrane Proteins2201778590.180 Why?
Cardiomyopathy, Dilated320208290.180 Why?
Genetics, Medical120233340.170 Why?
Sexual Behavior, Animal220101200.160 Why?
Genes, Insect220102640.160 Why?
Biotinidase12018170.160 Why?
RNA, Messenger12013127940.150 Why?
Polymorphism, Restriction Fragment Length120197670.150 Why?
Oligonucleotide Array Sequence Analysis5201637790.150 Why?
Canada3202121220.150 Why?
Research Design3202061800.150 Why?
Electronic Health Records5201848110.140 Why?
Gene Expression Profiling2201094200.130 Why?
Herpes Zoster120182530.130 Why?
Colorectal Neoplasms, Hereditary Nonpolyposis120203800.130 Why?
Health120193980.130 Why?
Primary Health Care3202346860.130 Why?
ABO Blood-Group System120183800.130 Why?
Arrhythmogenic Right Ventricular Dysplasia120171620.130 Why?
Infant, Newborn102024261980.120 Why?
Government Programs120172790.120 Why?
Guidelines as Topic2201813860.120 Why?
Polymorphism, Single Nucleotide62024159360.120 Why?
Exons1202023910.110 Why?
Male3320243608410.110 Why?
ras Proteins1201910540.110 Why?
Cardiomyopathy, Restrictive12014610.110 Why?
Medical History Taking120177740.110 Why?
Mutation52021300540.110 Why?
Skin Diseases, Genetic12014490.110 Why?
Science120162390.110 Why?
Erythrocytes2201924130.110 Why?
Female3420243926880.100 Why?
Diagnostic Techniques, Cardiovascular120141480.100 Why?
Ehlers-Danlos Syndrome12014930.100 Why?
Communicable Diseases120218750.100 Why?
Gene Deletion1202026650.100 Why?
Arthrogryposis12013680.100 Why?
Genotype62023129900.100 Why?
Data Interpretation, Statistical2201926910.100 Why?
Risk Factors102024742120.100 Why?
Marfan Syndrome120142360.100 Why?
Decision Trees120135040.100 Why?
Chromosome Aberrations2202117680.100 Why?
Death, Sudden, Cardiac1201915550.090 Why?
Comparative Genomic Hybridization120124730.090 Why?
Chromosome Mapping4202146150.090 Why?
Peer Review, Research120143400.090 Why?
Rare Diseases120166220.090 Why?
Polymorphism, Genetic1202042430.080 Why?
Base Sequence32017124410.080 Why?
Pupa12009420.080 Why?
Pneumonia1202121430.080 Why?
Receptors, Steroid120091560.080 Why?
Arteries1201411230.080 Why?
Delivery of Health Care, Integrated120169420.080 Why?
Coronary Disease1202359140.080 Why?
Databases, Factual2202179670.080 Why?
Genetic Association Studies4202027350.080 Why?
Body Weight1201946180.080 Why?
Middle Aged1920242209170.080 Why?
Vascular Malformations120144680.080 Why?
Ion Channels1201310400.080 Why?
Atherosclerosis1202434070.070 Why?
Mechanotransduction, Cellular120135290.070 Why?
Ultrasonography, Prenatal1201617550.070 Why?
Pedigree3202045420.070 Why?
Cardiovascular Diseases22024155020.070 Why?
Adult1820242212000.070 Why?
Aortic Aneurysm, Thoracic120146960.070 Why?
Larva120095080.070 Why?
Sepsis1202125850.070 Why?
Coronary Artery Disease2202464030.070 Why?
Randomized Controlled Trials as Topic52024102120.070 Why?
Early Detection of Cancer2201832010.070 Why?
Medical Informatics120137330.070 Why?
Joint Instability120148010.070 Why?
RNA Splicing220229180.060 Why?
Reproducibility of Results32021200990.060 Why?
Bayes Theorem2202423300.060 Why?
Phenotype52022165920.060 Why?
Cohort Studies62024414930.060 Why?
Decision Support Systems, Clinical1201311750.060 Why?
Arrhythmias, Cardiac1201422440.060 Why?
Epilepsy1201932900.060 Why?
Gene Frequency2202336060.060 Why?
Atrial Fibrillation1202251270.050 Why?
Health Surveys1201340610.050 Why?
Prospective Studies32022544230.050 Why?
Aged1220241693080.050 Why?
Heterozygote2202027870.050 Why?
Duty to Recontact12021190.050 Why?
Aging1202187110.050 Why?
Cluster Analysis1200927070.050 Why?
Gene Expression Regulation, Developmental2200936120.050 Why?
Molecular Sequence Data12013176350.050 Why?
Prostatic Neoplasms12023111220.050 Why?
Genetic Research120211710.050 Why?
Infant52024361930.040 Why?
Biomedical Research1201634290.040 Why?
Heart Defects, Congenital2201446710.040 Why?
Drosophila Proteins1200916990.040 Why?
Young Adult62024592540.040 Why?
North America1202312760.040 Why?
Digestive System Diseases120211510.040 Why?
Multicenter Studies as Topic1202417020.040 Why?
Aged, 80 and over62021589830.040 Why?
Sex Characteristics1200926390.040 Why?
Urogenital Abnormalities120212610.040 Why?
DNA2202272130.040 Why?
Heart Failure12022116710.040 Why?
Pregnancy22017298760.040 Why?
Mosaicism120214750.040 Why?
Case-Control Studies32020221760.040 Why?
Galactosyltransferases120182760.040 Why?
Pennsylvania120186130.040 Why?
Obesity12019129470.030 Why?
Chromosomes, Human120184410.030 Why?
Nerve Tissue Proteins1200944150.030 Why?
Neoplasms22017221720.030 Why?
Gene Duplication120173140.030 Why?
SOS1 Protein12016400.030 Why?
Molecular Diagnostic Techniques120216100.030 Why?
Nuclear Proteins1201157990.030 Why?
Disclosure120217480.030 Why?
INDEL Mutation120162660.030 Why?
Proto-Oncogene Proteins c-raf120162050.030 Why?
Principal Component Analysis120189450.030 Why?
Breast Neoplasms22020210190.030 Why?
Informed Consent1202110080.030 Why?
United States52023723350.030 Why?
Counseling1202315470.030 Why?
Virulence1201813030.030 Why?
Cholesterol, LDL1202423820.030 Why?
MAP Kinase Kinase 1120163320.030 Why?
Asymptomatic Diseases120175880.030 Why?
Desmoplakins12014610.030 Why?
Adolescent52021883230.030 Why?
Homozygote1201817760.030 Why?
Connective Tissue Diseases120162850.030 Why?
Myopathies, Structural, Congenital120141030.030 Why?
Child52021801570.030 Why?
Sequence Analysis120132400.030 Why?
Prognosis12013296290.030 Why?
Carrier Proteins2201749370.030 Why?
Gene Expression Regulation12010119040.030 Why?
Financing, Organized120142040.030 Why?
Haplotypes1201827130.030 Why?
Hypolipidemic Agents120166090.020 Why?
Evidence-Based Practice120164950.020 Why?
Age of Onset1201933060.020 Why?
Drug Design1201610480.020 Why?
Incidental Findings120166970.020 Why?
Time Factors22010399700.020 Why?
Decision Making1202439290.020 Why?
National Institutes of Health (U.S.)120137930.020 Why?
Health Knowledge, Attitudes, Practice1202440160.020 Why?
Transcription Factors12009121300.020 Why?
Hematologic Neoplasms1202118960.020 Why?
Hearing Loss120167830.020 Why?
Costs and Cost Analysis1201516680.020 Why?
Dissection120102980.020 Why?
Olfactory Receptor Neurons12009960.020 Why?
Sensitivity and Specificity22015146650.020 Why?
Family1201931940.020 Why?
Odds Ratio1202096460.020 Why?
Insect Proteins120092540.020 Why?
Proto-Oncogene Proteins p21(ras)1201617450.020 Why?
DNA Mutational Analysis1201641110.020 Why?
Blood Platelets1201824790.020 Why?
Proto-Oncogene Proteins B-raf1201620570.020 Why?
Organ Specificity1201019680.020 Why?
Health Behavior1201726440.020 Why?
Lipids1201633410.020 Why?
Proportional Hazards Models12020124630.020 Why?
Molecular Targeted Therapy1201628110.020 Why?
Child, Preschool22020422310.020 Why?
Health Personnel1201833350.010 Why?
Head120109240.010 Why?
Referral and Consultation1201736000.010 Why?
Mass Screening1202054280.010 Why?
Health Care Costs1201732420.010 Why?
Pilot Projects1201786330.010 Why?
Brain12010271210.010 Why?
Patient Acceptance of Health Care1201732050.010 Why?
Animals320101684750.010 Why?
Longitudinal Studies12019146070.010 Why?
Body Mass Index12019129530.010 Why?
Severity of Illness Index12019158430.010 Why?
Colorectal Neoplasms1202069380.010 Why?
Prevalence12017157320.010 Why?
Retrospective Studies22021806460.010 Why?
Cell Line12013156010.010 Why?
Cross-Sectional Studies12018261270.010 Why?
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Concepts (251)
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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.