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 Syndrome2120233805.780 Why?
Glomerulosclerosis, Focal Segmental1520243333.820 Why?
Kidney Glomerulus620215681.420 Why?
Genomics11202359291.250 Why?
Kidney Diseases7202320981.060 Why?
Urinary Tract520193051.040 Why?
Kidney13202370660.890 Why?
Alleles11202168970.800 Why?
Genome-Wide Association Study152023128070.770 Why?
Renal Insufficiency, Chronic6202323100.700 Why?
Multiple Endocrine Neoplasia Type 2a12019400.660 Why?
Nephrology220202700.640 Why?
Proto-Oncogene Proteins c-ret120192280.570 Why?
Nephrosis, Lipoid42024450.560 Why?
Podocytes520233910.560 Why?
Genetic Testing5202035950.530 Why?
Access to Information120193170.520 Why?
Apolipoproteins220233270.460 Why?
Proteinuria520236070.450 Why?
Glomerulonephritis, Membranous42024840.430 Why?
Genetics, Population220159430.430 Why?
Kidney Tubules120154530.420 Why?
Genotype152023130240.420 Why?
Quantitative Trait Loci4202221400.410 Why?
Genetic Variation6202166100.390 Why?
Polymorphism, Single Nucleotide142023160470.380 Why?
Microfluidics120166510.360 Why?
Lipoproteins, HDL120156740.360 Why?
Premature Birth2202318290.330 Why?
Selection, Genetic120138780.310 Why?
Chromosomes, Human, Pair 16120103400.310 Why?
Hirschsprung Disease120101640.310 Why?
Genetic Predisposition to Disease132023180710.300 Why?
Sequence Deletion2201514950.280 Why?
Haplotypes4202327280.280 Why?
High-Throughput Nucleotide Sequencing2201636550.280 Why?
Software3202044620.260 Why?
Ubiquitins220183650.240 Why?
Child202024805640.230 Why?
DNA Copy Number Variations3201920450.230 Why?
Glomerulonephritis220183320.220 Why?
Glomerular Filtration Rate5202322330.210 Why?
Humans6020247659680.210 Why?
Bayes Theorem2202323540.200 Why?
Hematuria120232300.200 Why?
Chromatin2202329800.180 Why?
Phenotype82018167210.180 Why?
Adenosine Deaminase120222510.170 Why?
Age of Onset2201733440.160 Why?
Kidney Failure, Chronic3202224950.160 Why?
Membrane Proteins6202178510.160 Why?
Angiogenic Proteins120191010.160 Why?
Regulatory Sequences, Nucleic Acid120227920.160 Why?
Urogenital Abnormalities220182550.160 Why?
Interferon Type I120225670.150 Why?
HLA-DQ Antigens120181900.150 Why?
Genetics, Medical120203340.140 Why?
Adolescent122024888350.140 Why?
Adaptor Proteins, Signal Transducing2201929000.140 Why?
Glomerulonephritis, Membranoproliferative12017410.140 Why?
Diacylglycerol Kinase12017470.140 Why?
Steroids220209330.130 Why?
HLA-DR Antigens120186080.130 Why?
Vesicular Transport Proteins120193760.130 Why?
Sequence Analysis, DNA5202247720.130 Why?
Young Adult82023598890.130 Why?
PHEX Phosphate Regulating Neutral Endopeptidase12015170.130 Why?
Chemokine CXCL1112015430.130 Why?
Chromosome Deletion2201813850.130 Why?
Genetic Association Studies4201927410.120 Why?
Chemokine CXCL9120151370.120 Why?
DiGeorge Syndrome120171870.120 Why?
Cohort Studies102024416490.120 Why?
Rare Diseases220246350.120 Why?
Pedigree3201945260.120 Why?
Vesico-Ureteral Reflux120184340.120 Why?
Haploinsufficiency120173340.120 Why?
High-Throughput Screening Assays120209380.120 Why?
Child, Preschool72024425000.120 Why?
Case-Control Studies82020222230.110 Why?
RNA Splice Sites120152120.110 Why?
Adult1620232230440.110 Why?
Fetal Development120197770.110 Why?
Risk Factors82023748400.100 Why?
Autoantibodies1202121130.100 Why?
Epidermal Growth Factor120156980.100 Why?
Female2520243961120.100 Why?
Congenital Abnormalities120177040.100 Why?
Introns120159660.100 Why?
Reference Values2201649080.100 Why?
HEK293 Cells1202142600.100 Why?
Mucins120155670.100 Why?
Biopsy5201567630.100 Why?
Gene Deletion1201926660.090 Why?
Genetic Diseases, X-Linked120153850.090 Why?
Infant, Newborn52023263460.090 Why?
Genes, Recessive120136240.090 Why?
Male2320243636980.090 Why?
Atrophy1201516350.080 Why?
Point Mutation1201515900.080 Why?
Ear120101720.080 Why?
Prognosis62023299220.080 Why?
Mutation42020301980.080 Why?
Genetic Loci1201926310.080 Why?
Gene Frequency1201636240.080 Why?
Exons1201523910.080 Why?
Fibrosis1201520700.070 Why?
Mutation, Missense1201625890.070 Why?
Polymerase Chain Reaction1201660690.070 Why?
Databases, Genetic1201317510.070 Why?
Internet2201631060.070 Why?
Gene Expression Profiling2202095250.060 Why?
Reproducibility of Results22022201240.060 Why?
Graft Rejection1201944990.060 Why?
Neoplasm Proteins1201735960.060 Why?
Predictive Value of Tests22020153980.060 Why?
Middle Aged920232230090.060 Why?
RNA, Messenger22022127680.060 Why?
Pregnancy Complications1201929750.060 Why?
Risk1201695910.060 Why?
Kidney Transplantation1201942700.060 Why?
Biomedical Research1201934580.050 Why?
Diagnosis, Differential12019129760.050 Why?
Neptune1202320.050 Why?
DNA Mutational Analysis3201741080.050 Why?
Alternative Splicing2202111070.050 Why?
Gene Expression1201575840.050 Why?
Heart Defects, Congenital1201946970.050 Why?
Nuclear Proteins1201757830.050 Why?
Zebrafish3201930360.050 Why?
Oligonucleotide Array Sequence Analysis1201037970.050 Why?
Inosine120221290.050 Why?
RNA Editing120221480.050 Why?
RNA, Double-Stranded120222920.050 Why?
Hypertension1202186260.050 Why?
Tumor Necrosis Factor Ligand Superfamily Member 1512020120.040 Why?
Insulin, Long-Acting12000590.040 Why?
Genome, Human1201344480.040 Why?
3' Untranslated Regions120225150.040 Why?
Receptors, Phospholipase A212020310.040 Why?
NF-kappa B p50 Subunit120201030.040 Why?
United States22017729030.040 Why?
Chromosomes, Human, Pair 1120016400.040 Why?
Interferon Regulatory Factors120202710.040 Why?
Africa, Northern12018850.040 Why?
Infant, Low Birth Weight120238710.040 Why?
Phosphorylation2201982780.040 Why?
Clathrin120192590.040 Why?
Adenosine120228060.040 Why?
Exocytosis120193230.040 Why?
Lithuania12017130.040 Why?
Prospective Studies32017548020.040 Why?
Histocompatibility Testing120197260.040 Why?
Heredity120171490.030 Why?
Cell Movement2201951940.030 Why?
Hepatitis, Viral, Human119971410.030 Why?
France120184950.030 Why?
Research Design1201362090.030 Why?
Spain120184830.030 Why?
Amino Acid Motifs120199240.030 Why?
Italy120188540.030 Why?
Mutagenesis, Site-Directed1201916790.030 Why?
Chromosomes, Human, Pair 22120173480.030 Why?
Embryo, Nonmammalian120199070.030 Why?
Uncertainty120207610.030 Why?
Mendelian Randomization Analysis1202110440.030 Why?
Probability1202024750.030 Why?
Base Composition120152910.030 Why?
Birth Weight1202321210.030 Why?
Consensus Sequence120153620.030 Why?
Endocytosis120199510.030 Why?
Computer Simulation2202062550.030 Why?
Genome1202217530.030 Why?
Lidocaine119975500.030 Why?
Interferon-gamma1202231600.030 Why?
Genetic Heterogeneity120177350.030 Why?
Cell Line, Transformed120158580.030 Why?
HLA Antigens1201913390.030 Why?
Genetic Techniques120164290.030 Why?
Protein Transport1201919390.030 Why?
Chromosomes, Human, X120153190.030 Why?
Longitudinal Studies22024147510.030 Why?
Meta-Analysis as Topic1201813700.030 Why?
Homozygote1201717750.030 Why?
Animals620221687640.020 Why?
Mice42022818190.020 Why?
Diabetes Mellitus, Type 232015122400.020 Why?
Models, Animal1201721200.020 Why?
Aged, 80 and over12015594890.020 Why?
Molecular Sequence Annotation120125230.020 Why?
Heterozygote1201727940.020 Why?
Models, Molecular1202053790.020 Why?
Remission Induction1201524110.020 Why?
Cell Membrane1201936340.020 Why?
Tissue Donors1201923950.020 Why?
North America1201312850.020 Why?
Systems Biology120134810.020 Why?
India1201523340.020 Why?
Blood Pressure2202185320.020 Why?
Amino Acid Sequence12020134000.020 Why?
Time Factors22023400650.020 Why?
Immunoglobulin G1201945280.020 Why?
DNA Methylation1202144240.020 Why?
Regeneration1201515170.020 Why?
Prevalence12023158420.020 Why?
Chromosome Aberrations1201217740.020 Why?
Aged220151711170.020 Why?
Cooperative Behavior1201315090.020 Why?
Cell Line12019155430.020 Why?
Sex Factors12019106030.020 Why?
Infant22017363860.010 Why?
Gene Expression Regulation12022118880.010 Why?
Mice, Knockout12019144480.010 Why?
Mice, Transgenic1201695500.010 Why?
Apoptosis1201995140.010 Why?
Liver1199775620.010 Why?
Proportional Hazards Models12015125090.010 Why?
Proteins1201559950.010 Why?
Mice, Inbred C57BL12019223320.010 Why?
Cells, Cultured12016189730.010 Why?
Algorithms12020140710.010 Why?
Pilot Projects1201387330.010 Why?
Incidence12017214800.010 Why?
Disease Progression12015136320.010 Why?
Cell Differentiation12015116410.010 Why?
Risk Assessment12019242820.010 Why?
Pregnancy12019302600.010 Why?
Registries1201382970.010 Why?
Age Factors12013183800.010 Why?
Liver Function Tests119975250.010 Why?
Signal Transduction12019236010.010 Why?
Cross-Over Studies1200021080.010 Why?
Hypoglycemia120008960.010 Why?
Chromosome Mapping1200146180.010 Why?
Drug Administration Schedule1200048500.010 Why?
Body Weight1200046220.010 Why?
Circadian Rhythm1200025920.000 Why?
Molecular Sequence Data12001175940.000 Why?
Hypoglycemic Agents1200031100.000 Why?
Blood Glucose1200064240.000 Why?
Comorbidity12000105630.000 Why?
Chronic Disease1199793470.000 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.