Harvard Catalyst Profiles

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

Matthew Sampson, M.D.

Concepts (242)

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 Syndrome2120233825.840 Why?
Glomerulosclerosis, Focal Segmental1520243363.850 Why?
Kidney Glomerulus620215691.440 Why?
Genomics11202359161.260 Why?
Kidney Diseases7202321031.070 Why?
Urinary Tract520193051.060 Why?
Kidney13202370630.900 Why?
Alleles11202168920.800 Why?
Genome-Wide Association Study152023127750.780 Why?
Renal Insufficiency, Chronic6202322950.710 Why?
Multiple Endocrine Neoplasia Type 2a12019400.670 Why?
Nephrology220202700.640 Why?
Proto-Oncogene Proteins c-ret120192280.580 Why?
Nephrosis, Lipoid42024450.560 Why?
Podocytes520234040.550 Why?
Genetic Testing5202035870.540 Why?
Access to Information120193170.530 Why?
Apolipoproteins220233280.470 Why?
Proteinuria520236130.450 Why?
Glomerulonephritis, Membranous42024870.440 Why?
Genetics, Population220159420.430 Why?
Kidney Tubules120154480.430 Why?
Genotype152023130380.420 Why?
Quantitative Trait Loci4202221270.420 Why?
Genetic Variation6202166060.390 Why?
Polymorphism, Single Nucleotide142023160270.380 Why?
Microfluidics120166740.360 Why?
Lipoproteins, HDL120156820.360 Why?
Premature Birth2202318140.340 Why?
Selection, Genetic120138770.320 Why?
Chromosomes, Human, Pair 16120103440.320 Why?
Hirschsprung Disease120101630.310 Why?
Genetic Predisposition to Disease132023180470.300 Why?
Sequence Deletion2201514960.280 Why?
Haplotypes4202327240.280 Why?
High-Throughput Nucleotide Sequencing2201636660.280 Why?
Software3202044520.260 Why?
Ubiquitins220183670.240 Why?
Child202024808940.230 Why?
DNA Copy Number Variations3201920460.230 Why?
Glomerulonephritis220183330.220 Why?
Glomerular Filtration Rate5202322260.220 Why?
Humans6020247682980.210 Why?
Bayes Theorem2202323530.210 Why?
Hematuria120232330.200 Why?
Chromatin2202329670.180 Why?
Phenotype82018167160.180 Why?
Adenosine Deaminase120222520.180 Why?
Age of Onset2201733450.170 Why?
Angiogenic Proteins120191010.160 Why?
Kidney Failure, Chronic3202224910.160 Why?
Regulatory Sequences, Nucleic Acid120227920.160 Why?
Membrane Proteins6202178850.160 Why?
Urogenital Abnormalities220182550.160 Why?
Interferon Type I120225690.150 Why?
HLA-DQ Antigens120181900.150 Why?
Genetics, Medical120203340.150 Why?
Adolescent122024891820.150 Why?
Adaptor Proteins, Signal Transducing2201929110.140 Why?
Glomerulonephritis, Membranoproliferative12017410.140 Why?
Diacylglycerol Kinase12017470.140 Why?
Steroids220209360.140 Why?
HLA-DR Antigens120186070.130 Why?
Vesicular Transport Proteins120193770.130 Why?
Sequence Analysis, DNA5202247740.130 Why?
Young Adult82023600480.130 Why?
PHEX Phosphate Regulating Neutral Endopeptidase12015170.130 Why?
Chemokine CXCL1112015430.130 Why?
Chromosome Deletion2201813900.130 Why?
Genetic Association Studies4201927410.120 Why?
Chemokine CXCL9120151370.120 Why?
DiGeorge Syndrome120171870.120 Why?
Rare Diseases220246300.120 Why?
Cohort Studies102024417910.120 Why?
Pedigree3201945450.120 Why?
Vesico-Ureteral Reflux120184330.120 Why?
Haploinsufficiency120173360.120 Why?
High-Throughput Screening Assays120209370.120 Why?
Child, Preschool72024426540.120 Why?
Case-Control Studies82020222920.110 Why?
RNA Splice Sites120152120.110 Why?
Adult1620232236220.110 Why?
Fetal Development120197710.110 Why?
Risk Factors82023749540.100 Why?
Epidermal Growth Factor120156980.100 Why?
Autoantibodies1202121260.100 Why?
Congenital Abnormalities120177080.100 Why?
Female2520243970500.100 Why?
Introns120159680.100 Why?
Reference Values2201649410.100 Why?
HEK293 Cells1202142860.100 Why?
Mucins120155710.100 Why?
Biopsy5201568080.100 Why?
Gene Deletion1201926730.090 Why?
Genetic Diseases, X-Linked120153860.090 Why?
Infant, Newborn52023264100.090 Why?
Genes, Recessive120136250.090 Why?
Male2320243648700.090 Why?
Atrophy1201516480.090 Why?
Ear120101720.090 Why?
Point Mutation1201515950.090 Why?
Prognosis62023300200.080 Why?
Mutation42020302300.080 Why?
Genetic Loci1201926300.080 Why?
Gene Frequency1201636150.080 Why?
Exons1201523920.080 Why?
Fibrosis1201520760.070 Why?
Mutation, Missense1201625930.070 Why?
Polymerase Chain Reaction1201660840.070 Why?
Databases, Genetic1201317480.070 Why?
Internet2201631070.070 Why?
Gene Expression Profiling2202095080.060 Why?
Reproducibility of Results22022202240.060 Why?
Graft Rejection1201945050.060 Why?
Neoplasm Proteins1201736090.060 Why?
Predictive Value of Tests22020154550.060 Why?
Middle Aged920232234630.060 Why?
RNA, Messenger22022128010.060 Why?
Pregnancy Complications1201929710.060 Why?
Risk1201696350.060 Why?
Kidney Transplantation1201943000.060 Why?
Biomedical Research1201934640.060 Why?
Neptune1202320.060 Why?
Diagnosis, Differential12019130190.050 Why?
DNA Mutational Analysis3201741200.050 Why?
Alternative Splicing2202110930.050 Why?
Gene Expression1201575950.050 Why?
Heart Defects, Congenital1201947130.050 Why?
Zebrafish3201930370.050 Why?
Nuclear Proteins1201758020.050 Why?
Inosine120221290.050 Why?
Oligonucleotide Array Sequence Analysis1201037940.050 Why?
RNA Editing120221490.050 Why?
RNA, Double-Stranded120222930.050 Why?
Hypertension1202186150.050 Why?
Tumor Necrosis Factor Ligand Superfamily Member 1512020120.050 Why?
Insulin, Long-Acting12000590.040 Why?
Genome, Human1201344500.040 Why?
3' Untranslated Regions120225150.040 Why?
Receptors, Phospholipase A212020330.040 Why?
NF-kappa B p50 Subunit120201030.040 Why?
United States22017731440.040 Why?
Chromosomes, Human, Pair 1120016400.040 Why?
Interferon Regulatory Factors120202680.040 Why?
Africa, Northern12018860.040 Why?
Infant, Low Birth Weight120238750.040 Why?
Phosphorylation2201983260.040 Why?
Clathrin120192580.040 Why?
Lithuania12017130.040 Why?
Exocytosis120193230.040 Why?
Adenosine120228160.040 Why?
Prospective Studies32017549210.040 Why?
Histocompatibility Testing120197160.040 Why?
Heredity120171490.040 Why?
Hepatitis, Viral, Human119971410.030 Why?
Cell Movement2201952140.030 Why?
France120184970.030 Why?
Spain120184920.030 Why?
Research Design1201362090.030 Why?
Amino Acid Motifs120199280.030 Why?
Italy120188540.030 Why?
Chromosomes, Human, Pair 22120173480.030 Why?
Mutagenesis, Site-Directed1201916840.030 Why?
Embryo, Nonmammalian120199110.030 Why?
Uncertainty120207590.030 Why?
Mendelian Randomization Analysis1202110370.030 Why?
Probability1202024820.030 Why?
Base Composition120152910.030 Why?
Consensus Sequence120153630.030 Why?
Birth Weight1202321140.030 Why?
Endocytosis120199590.030 Why?
Genome1202217470.030 Why?
Computer Simulation2202062770.030 Why?
Lidocaine119975450.030 Why?
Interferon-gamma1202231640.030 Why?
Genetic Heterogeneity120177370.030 Why?
Cell Line, Transformed120158660.030 Why?
HLA Antigens1201913370.030 Why?
Genetic Techniques120164280.030 Why?
Chromosomes, Human, X120153200.030 Why?
Protein Transport1201919580.030 Why?
Meta-Analysis as Topic1201813640.030 Why?
Longitudinal Studies22024147830.030 Why?
Homozygote1201717790.030 Why?
Animals620221693220.030 Why?
Mice42022820040.020 Why?
Diabetes Mellitus, Type 232015122390.020 Why?
Models, Animal1201721240.020 Why?
Aged, 80 and over12015596830.020 Why?
Molecular Sequence Annotation120125250.020 Why?
Heterozygote1201727920.020 Why?
Models, Molecular1202054080.020 Why?
Remission Induction1201524070.020 Why?
Cell Membrane1201936630.020 Why?
Tissue Donors1201923890.020 Why?
North America1201312900.020 Why?
Systems Biology120134790.020 Why?
India1201523240.020 Why?
Blood Pressure2202185410.020 Why?
Amino Acid Sequence12020134250.020 Why?
Time Factors22023402670.020 Why?
Immunoglobulin G1201945700.020 Why?
DNA Methylation1202144190.020 Why?
Regeneration1201515250.020 Why?
Prevalence12023158680.020 Why?
Chromosome Aberrations1201217800.020 Why?
Aged220151715440.020 Why?
Cooperative Behavior1201315150.020 Why?
Cell Line12019155930.020 Why?
Sex Factors12019106560.020 Why?
Infant22017365120.010 Why?
Gene Expression Regulation12022119140.010 Why?
Mice, Knockout12019144810.010 Why?
Mice, Transgenic1201695630.010 Why?
Apoptosis1201995060.010 Why?
Liver1199775700.010 Why?
Proportional Hazards Models12015125570.010 Why?
Proteins1201560060.010 Why?
Mice, Inbred C57BL12019223550.010 Why?
Cells, Cultured12016190190.010 Why?
Algorithms12020141540.010 Why?
Pilot Projects1201387300.010 Why?
Incidence12017215440.010 Why?
Disease Progression12015136460.010 Why?
Cell Differentiation12015116590.010 Why?
Risk Assessment12019243160.010 Why?
Pregnancy12019301980.010 Why?
Registries1201383780.010 Why?
Liver Function Tests119975250.010 Why?
Age Factors12013184720.010 Why?
Signal Transduction12019236290.010 Why?
Cross-Over Studies1200021060.010 Why?
Hypoglycemia120008940.010 Why?
Chromosome Mapping1200146220.010 Why?
Drug Administration Schedule1200048590.010 Why?
Body Weight1200046300.010 Why?
Circadian Rhythm1200025880.000 Why?
Molecular Sequence Data12001176260.000 Why?
Hypoglycemic Agents1200031080.000 Why?
Blood Glucose1200064300.000 Why?
Comorbidity12000105880.000 Why?
Chronic Disease1199793800.000 Why?
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Concepts (242)
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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.