Harvard Catalyst Profiles

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

Matthew Sampson, M.D.

Concepts (203)

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?
Nephrotic Syndrome1820213735.990 Why?
Glomerulosclerosis, Focal Segmental920213322.900 Why?
Kidney Glomerulus520197171.460 Why?
Genomics10202149211.440 Why?
Urinary Tract520192821.330 Why?
Kidney11202167441.010 Why?
Alleles10202171400.880 Why?
Renal Insufficiency, Chronic5202117300.840 Why?
Nephrology220202160.810 Why?
Multiple Endocrine Neoplasia Type 2a12019450.810 Why?
Kidney Diseases6202120990.800 Why?
Proto-Oncogene Proteins c-ret120192150.690 Why?
Genetic Testing4202032300.640 Why?
Podocytes420214080.620 Why?
Access to Information120193140.610 Why?
African Americans4201851440.540 Why?
Apolipoproteins120152930.510 Why?
Kidney Tubules120155340.490 Why?
Genetics, Population2201510010.490 Why?
Quantitative Trait Loci3202119530.480 Why?
Microfluidics120165410.450 Why?
Genotype122021130730.430 Why?
Genetic Variation6202167720.430 Why?
Lipoproteins, HDL120156220.420 Why?
Hirschsprung Disease120101420.390 Why?
Chromosomes, Human, Pair 16120103330.380 Why?
Selection, Genetic120139070.360 Why?
Nephrosis, Lipoid22021470.360 Why?
Premature Birth1201713070.350 Why?
Sequence Deletion2201515850.320 Why?
High-Throughput Nucleotide Sequencing2201635570.320 Why?
Genome-Wide Association Study112021110190.320 Why?
Software3202043140.300 Why?
Proteinuria320196090.290 Why?
Polymorphism, Single Nucleotide102021152960.280 Why?
Ubiquitins220184170.280 Why?
DNA Copy Number Variations3201917700.280 Why?
Glomerulonephritis220183810.260 Why?
Glomerular Filtration Rate4201920370.240 Why?
Phenotype82018160910.210 Why?
Child142021713610.210 Why?
Genetic Predisposition to Disease82021170710.200 Why?
Humans4520216866630.200 Why?
Urogenital Abnormalities220182220.200 Why?
Age of Onset2201733730.200 Why?
Angiogenic Proteins120191070.190 Why?
Genetics, Medical120203230.180 Why?
Membrane Proteins6202182620.170 Why?
HLA-DQ Antigens120182440.170 Why?
Glomerulonephritis, Membranoproliferative12017360.170 Why?
Diacylglycerol Kinase12017470.170 Why?
Steroids220208300.160 Why?
Haplotypes3202129130.160 Why?
Adaptor Proteins, Signal Transducing2201930060.160 Why?
HLA-DR Antigens120187290.160 Why?
Vesicular Transport Proteins120194070.150 Why?
PHEX Phosphate Regulating Neutral Endopeptidase12015190.150 Why?
Chemokine CXCL1112015430.150 Why?
Chemokine CXCL9120151270.150 Why?
Chromosome Deletion2201813850.150 Why?
Vesico-Ureteral Reflux120184180.150 Why?
DiGeorge Syndrome120171750.150 Why?
Haploinsufficiency120172890.140 Why?
Genetic Association Studies4201927220.140 Why?
RNA Splice Sites120151880.140 Why?
High-Throughput Screening Assays120209340.140 Why?
Adolescent82018849570.140 Why?
Young Adult62018560520.130 Why?
Pedigree2201947920.130 Why?
Fetal Development120197290.130 Why?
Autoantibodies1202119250.120 Why?
Child, Preschool62021411590.120 Why?
Congenital Abnormalities120176990.120 Why?
Epidermal Growth Factor120157490.120 Why?
Introns1201510550.120 Why?
Case-Control Studies72019216840.120 Why?
Mucins120155380.120 Why?
Sequence Analysis, DNA4201750440.120 Why?
Reference Values2201651340.120 Why?
Adult1120212114000.110 Why?
Bayes Theorem1201818480.110 Why?
Genetic Diseases, X-Linked120153810.110 Why?
Atrophy1201514470.110 Why?
Rare Diseases120154870.110 Why?
Genes, Recessive120136730.110 Why?
Cohort Studies72021387320.110 Why?
Biopsy4201568490.110 Why?
Gene Deletion1201929220.100 Why?
Female1820213754590.100 Why?
Ear120101790.100 Why?
Infant, Newborn42019239530.100 Why?
Point Mutation1201517070.100 Why?
Mutation42020288480.100 Why?
Gene Frequency1201637130.090 Why?
Genetic Loci1201925750.090 Why?
Exons1201525190.090 Why?
Fibrosis1201517980.090 Why?
Kidney Failure, Chronic2201824670.090 Why?
Male1720213524650.090 Why?
Prognosis52020289230.080 Why?
Mutation, Missense1201625700.080 Why?
Databases, Genetic1201318180.080 Why?
Polymerase Chain Reaction1201664640.080 Why?
Graft Rejection1201943140.080 Why?
Internet2201630970.070 Why?
Predictive Value of Tests22020154070.070 Why?
Gene Expression Profiling2202096610.070 Why?
Pregnancy Complications1201928390.070 Why?
Kidney Transplantation1201940150.070 Why?
Risk Factors52019692780.070 Why?
Neoplasm Proteins1201739720.070 Why?
Risk1201699150.060 Why?
Heart Defects, Congenital1201941320.060 Why?
Biomedical Research1201932850.060 Why?
Middle Aged620182164680.060 Why?
Diagnosis, Differential12019136030.060 Why?
Alternative Splicing2202111370.060 Why?
DNA Mutational Analysis3201744150.060 Why?
Reproducibility of Results12020193080.060 Why?
Zebrafish3201929690.060 Why?
Hypertension1202179410.060 Why?
Gene Expression1201581820.060 Why?
Tumor Necrosis Factor Ligand Superfamily Member 1512020100.050 Why?
Nuclear Proteins1201760090.050 Why?
Oligonucleotide Array Sequence Analysis1201041290.050 Why?
Genome, Human1201344580.050 Why?
United States22017655790.050 Why?
RNA, Messenger12015134690.050 Why?
Africa, Northern12018660.050 Why?
Lithuania12017240.040 Why?
Prospective Studies32017490710.040 Why?
Clathrin120192640.040 Why?
Heredity120171640.040 Why?
Exocytosis120193790.040 Why?
Histocompatibility Testing120198320.040 Why?
Phosphorylation2201988960.040 Why?
France120184920.040 Why?
Spain120184680.040 Why?
Research Design1201358350.040 Why?
Amino Acid Motifs1201910050.040 Why?
Italy120188050.040 Why?
Chromosomes, Human, Pair 22120173480.040 Why?
Mendelian Randomization Analysis120218030.040 Why?
Cell Movement2201956710.040 Why?
Uncertainty120206150.040 Why?
Embryo, Nonmammalian120199630.040 Why?
Mutagenesis, Site-Directed1201918580.040 Why?
Base Composition120153210.040 Why?
Consensus Sequence120153980.040 Why?
Probability1202025080.040 Why?
Endocytosis1201910520.030 Why?
Computer Simulation2202061200.030 Why?
Genetic Heterogeneity120177600.030 Why?
Cell Line, Transformed1201510260.030 Why?
Chromosomes, Human, X120153230.030 Why?
Genetic Techniques120164520.030 Why?
Protein Transport1201921010.030 Why?
HLA Antigens1201917170.030 Why?
Glomerulonephritis, Membranous12013710.030 Why?
Homozygote1201718550.030 Why?
Meta-Analysis as Topic1201813630.030 Why?
Remission Induction1201523870.030 Why?
Tissue Donors1201920350.020 Why?
Heterozygote1201727870.020 Why?
Molecular Sequence Annotation120125630.020 Why?
Aged, 80 and over12015593310.020 Why?
Models, Animal1201722630.020 Why?
North America1201311690.020 Why?
India1201521960.020 Why?
Cell Membrane1201939820.020 Why?
Systems Biology120135000.020 Why?
Animals520191708490.020 Why?
Immunoglobulin G1201942970.020 Why?
DNA Methylation1202139870.020 Why?
Mice32019808030.020 Why?
Regeneration1201515560.020 Why?
Aged220151622710.020 Why?
Chromosome Aberrations1201217990.020 Why?
Infant22017339180.020 Why?
Cooperative Behavior1201315860.020 Why?
Blood Pressure1202185290.020 Why?
Sex Factors12019109260.020 Why?
Cell Line12019171370.020 Why?
Mice, Knockout12019155970.020 Why?
Mice, Transgenic12016100940.020 Why?
Apoptosis12019102610.010 Why?
Proportional Hazards Models12015125250.010 Why?
Mice, Inbred C57BL12019234390.010 Why?
Proteins1201562640.010 Why?
Pilot Projects1201377910.010 Why?
Algorithms12020135000.010 Why?
Cells, Cultured12016206200.010 Why?
Disease Progression12015132040.010 Why?
Incidence12017204960.010 Why?
Pregnancy12019257030.010 Why?
Cell Differentiation12015118330.010 Why?
Risk Assessment12019237390.010 Why?
Longitudinal Studies12013134440.010 Why?
Registries1201380330.010 Why?
Signal Transduction12019243510.010 Why?
Age Factors12013192950.010 Why?
Diabetes Mellitus, Type 212015100880.010 Why?
Time Factors12013422710.010 Why?
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Concepts (203)
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Co-Authors (24)
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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.