Harvard Catalyst Profiles

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

Matthew Sampson, M.D.

Concepts (225)

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 Syndrome2120233915.900 Why?
Glomerulosclerosis, Focal Segmental1520243253.940 Why?
Kidney Glomerulus620215681.460 Why?
Genomics11202357751.290 Why?
Kidney Diseases7202320921.090 Why?
Urinary Tract520193091.070 Why?
Kidney13202370660.900 Why?
Alleles11202168970.820 Why?
Genome-Wide Association Study152023125800.800 Why?
Renal Insufficiency, Chronic6202322860.710 Why?
Multiple Endocrine Neoplasia Type 2a12019400.680 Why?
Nephrology220202620.650 Why?
Proto-Oncogene Proteins c-ret120192250.590 Why?
Nephrosis, Lipoid42024450.570 Why?
Podocytes520234020.560 Why?
Genetic Testing4202035310.550 Why?
Access to Information120193200.540 Why?
Apolipoproteins220233200.480 Why?
Proteinuria520235940.470 Why?
Glomerulonephritis, Membranous42024880.440 Why?
Genetics, Population220159240.440 Why?
Kidney Tubules120154490.440 Why?
Quantitative Trait Loci4202220830.430 Why?
Genotype142023129400.430 Why?
Genetic Variation6202165310.400 Why?
Polymorphism, Single Nucleotide142023157500.390 Why?
Microfluidics120166550.370 Why?
Lipoproteins, HDL120156670.360 Why?
Premature Birth2202317650.350 Why?
Chromosomes, Human, Pair 16120103420.320 Why?
Selection, Genetic120138720.320 Why?
Hirschsprung Disease120101630.320 Why?
Genetic Predisposition to Disease122023177500.300 Why?
Sequence Deletion2201514940.290 Why?
High-Throughput Nucleotide Sequencing2201636150.280 Why?
Haplotypes4202327620.280 Why?
Software3202044210.260 Why?
Ubiquitins220183700.250 Why?
Child202024796230.240 Why?
DNA Copy Number Variations3201920120.230 Why?
Glomerular Filtration Rate5202321680.230 Why?
Glomerulonephritis220183370.220 Why?
Humans5720247592550.210 Why?
Bayes Theorem2202323220.210 Why?
Hematuria120232330.200 Why?
Chromatin2202329390.190 Why?
Phenotype82018165320.180 Why?
Adenosine Deaminase120222510.180 Why?
Age of Onset2201733010.170 Why?
Kidney Failure, Chronic3202224690.160 Why?
Angiogenic Proteins120191010.160 Why?
Regulatory Sequences, Nucleic Acid120227880.160 Why?
Membrane Proteins6202178510.160 Why?
Urogenital Abnormalities220182560.160 Why?
Interferon Type I120225570.160 Why?
HLA-DQ Antigens120182110.150 Why?
Adolescent122024875600.150 Why?
Genetics, Medical120203360.150 Why?
Glomerulonephritis, Membranoproliferative12017400.150 Why?
Diacylglycerol Kinase12017480.150 Why?
Adaptor Proteins, Signal Transducing2201928960.150 Why?
Steroids220209280.140 Why?
HLA-DR Antigens120186300.140 Why?
Vesicular Transport Proteins120193740.130 Why?
Young Adult82023584830.130 Why?
Sequence Analysis, DNA5202247160.130 Why?
PHEX Phosphate Regulating Neutral Endopeptidase12015170.130 Why?
Chemokine CXCL1112015430.130 Why?
Chromosome Deletion2201813870.130 Why?
Genetic Association Studies4201927120.130 Why?
Chemokine CXCL9120151350.130 Why?
Rare Diseases220246190.120 Why?
DiGeorge Syndrome120171860.120 Why?
Cohort Studies102024412470.120 Why?
Haploinsufficiency120173290.120 Why?
Vesico-Ureteral Reflux120184380.120 Why?
Child, Preschool72024419350.120 Why?
High-Throughput Screening Assays120209430.120 Why?
Case-Control Studies82020219880.120 Why?
RNA Splice Sites120152110.120 Why?
Pedigree2201945720.120 Why?
Adult1520232193900.110 Why?
Fetal Development120197650.110 Why?
Risk Factors82023741670.110 Why?
Epidermal Growth Factor120156950.110 Why?
Autoantibodies1202121160.110 Why?
Congenital Abnormalities120177040.100 Why?
Introns120159760.100 Why?
Reference Values2201649180.100 Why?
Female2220243902400.100 Why?
HEK293 Cells1202142620.100 Why?
Mucins120155690.100 Why?
Gene Deletion1201926670.100 Why?
Genetic Diseases, X-Linked120153770.100 Why?
Infant, Newborn52023261090.090 Why?
Biopsy4201567720.090 Why?
Genes, Recessive120136250.090 Why?
Male2020243587190.090 Why?
Atrophy1201516250.090 Why?
Ear120101720.090 Why?
Point Mutation1201515940.090 Why?
Prognosis62023295610.090 Why?
Mutation42020298770.080 Why?
Genetic Loci1201926170.080 Why?
Gene Frequency1201636030.080 Why?
Exons1201523890.080 Why?
Fibrosis1201520410.080 Why?
Mutation, Missense1201625590.070 Why?
Polymerase Chain Reaction1201660700.070 Why?
Databases, Genetic1201317400.070 Why?
Internet2201630730.070 Why?
Gene Expression Profiling2202093740.070 Why?
Graft Rejection1201944180.070 Why?
Reproducibility of Results22022200310.060 Why?
Predictive Value of Tests22020152640.060 Why?
Neoplasm Proteins1201736130.060 Why?
Pregnancy Complications1201929400.060 Why?
RNA, Messenger22022127740.060 Why?
Middle Aged720232196530.060 Why?
Risk1201696230.060 Why?
Kidney Transplantation1201942160.060 Why?
Biomedical Research1201934160.060 Why?
Neptune1202320.060 Why?
Diagnosis, Differential12019129640.060 Why?
DNA Mutational Analysis3201741110.050 Why?
Alternative Splicing2202110910.050 Why?
Heart Defects, Congenital1201946630.050 Why?
Gene Expression1201575930.050 Why?
Zebrafish3201929960.050 Why?
Inosine120221300.050 Why?
Oligonucleotide Array Sequence Analysis1201037740.050 Why?
Nuclear Proteins1201757930.050 Why?
RNA Editing120221520.050 Why?
RNA, Double-Stranded120222940.050 Why?
Hypertension1202185940.050 Why?
Tumor Necrosis Factor Ligand Superfamily Member 1512020120.050 Why?
Genome, Human1201344120.040 Why?
3' Untranslated Regions120225220.040 Why?
Receptors, Phospholipase A212020330.040 Why?
NF-kappa B p50 Subunit120201060.040 Why?
United States22017722370.040 Why?
Interferon Regulatory Factors120202600.040 Why?
Africa, Northern12018860.040 Why?
Infant, Low Birth Weight120238530.040 Why?
Phosphorylation2201983130.040 Why?
Clathrin120192570.040 Why?
Lithuania12017130.040 Why?
Exocytosis120193220.040 Why?
Adenosine120228320.040 Why?
Prospective Studies32017542040.040 Why?
Histocompatibility Testing120197170.040 Why?
Heredity120171480.040 Why?
Cell Movement2201952090.040 Why?
France120185100.030 Why?
Spain120184860.030 Why?
Research Design1201361680.030 Why?
Amino Acid Motifs120199290.030 Why?
Italy120188400.030 Why?
Chromosomes, Human, Pair 22120173470.030 Why?
Mutagenesis, Site-Directed1201916940.030 Why?
Embryo, Nonmammalian120199000.030 Why?
Uncertainty120207540.030 Why?
Mendelian Randomization Analysis120219870.030 Why?
Probability1202024750.030 Why?
Base Composition120152900.030 Why?
Consensus Sequence120153670.030 Why?
Endocytosis120199600.030 Why?
Birth Weight1202320910.030 Why?
Computer Simulation2202061950.030 Why?
Genome1202217390.030 Why?
Genetic Heterogeneity120177210.030 Why?
Interferon-gamma1202231610.030 Why?
Cell Line, Transformed120158710.030 Why?
Genetic Techniques120164280.030 Why?
HLA Antigens1201913660.030 Why?
Protein Transport1201919660.030 Why?
Chromosomes, Human, X120153190.030 Why?
Longitudinal Studies22024144420.030 Why?
Homozygote1201717860.030 Why?
Meta-Analysis as Topic1201813750.030 Why?
Animals620221678380.030 Why?
Mice42022811380.030 Why?
Aged, 80 and over12015588670.020 Why?
Models, Animal1201721180.020 Why?
Molecular Sequence Annotation120125250.020 Why?
Heterozygote1201727960.020 Why?
Remission Induction1201523880.020 Why?
Models, Molecular1202054270.020 Why?
Cell Membrane1201936830.020 Why?
Tissue Donors1201923010.020 Why?
North America1201312820.020 Why?
Systems Biology120134790.020 Why?
India1201523430.020 Why?
Amino Acid Sequence12020134560.020 Why?
Time Factors22023401090.020 Why?
Immunoglobulin G1201945460.020 Why?
DNA Methylation1202143710.020 Why?
Regeneration1201515060.020 Why?
Prevalence12023156410.020 Why?
Aged220151686170.020 Why?
Chromosome Aberrations1201217710.020 Why?
Cooperative Behavior1201315010.020 Why?
Blood Pressure1202185230.020 Why?
Sex Factors12019105180.020 Why?
Cell Line12019156360.020 Why?
Infant22017359410.020 Why?
Gene Expression Regulation12022119080.010 Why?
Mice, Knockout12019143810.010 Why?
Mice, Transgenic1201695280.010 Why?
Apoptosis1201994920.010 Why?
Proportional Hazards Models12015125220.010 Why?
Mice, Inbred C57BL12019219810.010 Why?
Proteins1201560290.010 Why?
Cells, Cultured12016189680.010 Why?
Algorithms12020139460.010 Why?
Pilot Projects1201385400.010 Why?
Incidence12017213360.010 Why?
Disease Progression12015134790.010 Why?
Cell Differentiation12015114760.010 Why?
Risk Assessment12019240490.010 Why?
Pregnancy12019296580.010 Why?
Registries1201384340.010 Why?
Signal Transduction12019233620.010 Why?
Age Factors12013183940.010 Why?
Diabetes Mellitus, Type 212015122680.010 Why?
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Concepts (225)
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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.