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 Syndrome2120233915.870 Why?
Glomerulosclerosis, Focal Segmental1520243253.930 Why?
Kidney Glomerulus620215671.460 Why?
Genomics11202357881.290 Why?
Kidney Diseases7202320821.090 Why?
Urinary Tract520193071.070 Why?
Kidney13202370120.910 Why?
Alleles11202168940.810 Why?
Genome-Wide Association Study152023126010.800 Why?
Renal Insufficiency, Chronic6202322370.720 Why?
Multiple Endocrine Neoplasia Type 2a12019400.680 Why?
Nephrology220202630.650 Why?
Proto-Oncogene Proteins c-ret120192250.590 Why?
Nephrosis, Lipoid42024450.570 Why?
Podocytes520234020.560 Why?
Genetic Testing4202035290.540 Why?
Access to Information120193160.530 Why?
Apolipoproteins220233190.470 Why?
Proteinuria520235940.460 Why?
Glomerulonephritis, Membranous42024880.440 Why?
Genetics, Population220159290.440 Why?
Kidney Tubules120154490.430 Why?
Genotype142023129510.420 Why?
Quantitative Trait Loci4202221000.420 Why?
Genetic Variation6202165490.390 Why?
Polymorphism, Single Nucleotide142023157740.390 Why?
Microfluidics120166520.370 Why?
Lipoproteins, HDL120156640.360 Why?
Premature Birth2202317660.340 Why?
Chromosomes, Human, Pair 16120103420.320 Why?
Selection, Genetic120138680.320 Why?
Hirschsprung Disease120101630.310 Why?
Genetic Predisposition to Disease122023177670.290 Why?
Sequence Deletion2201514940.290 Why?
High-Throughput Nucleotide Sequencing2201636140.280 Why?
Haplotypes4202327640.280 Why?
Software3202044160.260 Why?
Ubiquitins220183660.250 Why?
Child202024797820.240 Why?
DNA Copy Number Variations3201920120.230 Why?
Glomerular Filtration Rate5202321520.220 Why?
Glomerulonephritis220183360.220 Why?
Humans5720247575660.210 Why?
Bayes Theorem2202323180.210 Why?
Hematuria120232330.200 Why?
Chromatin2202329380.190 Why?
Phenotype82018165330.180 Why?
Adenosine Deaminase120222510.180 Why?
Age of Onset2201732960.170 Why?
Kidney Failure, Chronic3202224550.160 Why?
Angiogenic Proteins120191010.160 Why?
Regulatory Sequences, Nucleic Acid120227880.160 Why?
Membrane Proteins6202178400.160 Why?
Urogenital Abnormalities220182560.160 Why?
Interferon Type I120225620.160 Why?
HLA-DQ Antigens120182110.150 Why?
Adolescent122024878190.150 Why?
Genetics, Medical120203360.150 Why?
Glomerulonephritis, Membranoproliferative12017400.140 Why?
Adaptor Proteins, Signal Transducing2201928910.140 Why?
Diacylglycerol Kinase12017480.140 Why?
Steroids220209260.140 Why?
HLA-DR Antigens120186300.140 Why?
Vesicular Transport Proteins120193740.130 Why?
Young Adult82023587550.130 Why?
Sequence Analysis, DNA5202247100.130 Why?
PHEX Phosphate Regulating Neutral Endopeptidase12015170.130 Why?
Chemokine CXCL1112015430.130 Why?
Chromosome Deletion2201813870.130 Why?
Genetic Association Studies4201927170.120 Why?
Chemokine CXCL9120151350.120 Why?
Rare Diseases220246180.120 Why?
Cohort Studies102024411900.120 Why?
DiGeorge Syndrome120171850.120 Why?
Haploinsufficiency120173270.120 Why?
Vesico-Ureteral Reflux120184370.120 Why?
High-Throughput Screening Assays120209330.120 Why?
Child, Preschool72024420450.120 Why?
Case-Control Studies82020220220.120 Why?
RNA Splice Sites120152110.110 Why?
Pedigree2201945780.110 Why?
Adult1520232197250.110 Why?
Fetal Development120197660.110 Why?
Risk Factors82023737080.110 Why?
Epidermal Growth Factor120156950.110 Why?
Autoantibodies1202121160.100 Why?
Congenital Abnormalities120177040.100 Why?
Female2220243899430.100 Why?
Reference Values2201649180.100 Why?
Introns120159780.100 Why?
HEK293 Cells1202142570.100 Why?
Mucins120155680.100 Why?
Gene Deletion1201926660.100 Why?
Genetic Diseases, X-Linked120153780.090 Why?
Infant, Newborn52023261760.090 Why?
Biopsy4201567570.090 Why?
Genes, Recessive120136260.090 Why?
Male2020243581800.090 Why?
Atrophy1201516270.090 Why?
Ear120101720.090 Why?
Prognosis62023294880.090 Why?
Point Mutation1201515940.090 Why?
Mutation42020299290.080 Why?
Genetic Loci1201926120.080 Why?
Gene Frequency1201636120.080 Why?
Exons1201523920.080 Why?
Fibrosis1201520380.080 Why?
Mutation, Missense1201625640.070 Why?
Polymerase Chain Reaction1201660700.070 Why?
Databases, Genetic1201317360.070 Why?
Internet2201630810.070 Why?
Gene Expression Profiling2202094030.070 Why?
Graft Rejection1201944270.060 Why?
Reproducibility of Results22022200370.060 Why?
Predictive Value of Tests22020152070.060 Why?
Neoplasm Proteins1201736080.060 Why?
Pregnancy Complications1201929400.060 Why?
RNA, Messenger22022127610.060 Why?
Middle Aged720232191920.060 Why?
Risk1201695900.060 Why?
Kidney Transplantation1201942140.060 Why?
Biomedical Research1201934150.060 Why?
Neptune1202320.060 Why?
Diagnosis, Differential12019129510.060 Why?
DNA Mutational Analysis3201741070.050 Why?
Alternative Splicing2202110910.050 Why?
Gene Expression1201575840.050 Why?
Heart Defects, Congenital1201946730.050 Why?
Zebrafish3201929920.050 Why?
Inosine120221300.050 Why?
Oligonucleotide Array Sequence Analysis1201037740.050 Why?
Nuclear Proteins1201757860.050 Why?
RNA Editing120221510.050 Why?
RNA, Double-Stranded120222950.050 Why?
Hypertension1202185020.050 Why?
Tumor Necrosis Factor Ligand Superfamily Member 1512020120.050 Why?
Genome, Human1201344140.040 Why?
3' Untranslated Regions120225140.040 Why?
Receptors, Phospholipase A212020330.040 Why?
NF-kappa B p50 Subunit120201030.040 Why?
United States22017719020.040 Why?
Interferon Regulatory Factors120202600.040 Why?
Africa, Northern12018860.040 Why?
Infant, Low Birth Weight120238580.040 Why?
Phosphorylation2201982960.040 Why?
Clathrin120192570.040 Why?
Adenosine120228020.040 Why?
Exocytosis120193190.040 Why?
Lithuania12017130.040 Why?
Prospective Studies32017540920.040 Why?
Histocompatibility Testing120197170.040 Why?
Heredity120171480.040 Why?
Cell Movement2201951960.040 Why?
France120184970.030 Why?
Spain120184880.030 Why?
Research Design1201361520.030 Why?
Amino Acid Motifs120199290.030 Why?
Italy120188380.030 Why?
Chromosomes, Human, Pair 22120173460.030 Why?
Mutagenesis, Site-Directed1201916930.030 Why?
Embryo, Nonmammalian120199000.030 Why?
Uncertainty120207500.030 Why?
Mendelian Randomization Analysis120219880.030 Why?
Probability1202024620.030 Why?
Base Composition120152890.030 Why?
Endocytosis120199580.030 Why?
Consensus Sequence120153650.030 Why?
Birth Weight1202320950.030 Why?
Computer Simulation2202061980.030 Why?
Genome1202217390.030 Why?
Interferon-gamma1202231540.030 Why?
Genetic Heterogeneity120177230.030 Why?
Cell Line, Transformed120158690.030 Why?
Genetic Techniques120164270.030 Why?
HLA Antigens1201913680.030 Why?
Protein Transport1201919630.030 Why?
Chromosomes, Human, X120153210.030 Why?
Longitudinal Studies22024144730.030 Why?
Meta-Analysis as Topic1201813730.030 Why?
Homozygote1201717880.030 Why?
Animals620221677180.030 Why?
Mice42022810660.020 Why?
Aged, 80 and over12015585580.020 Why?
Models, Animal1201721100.020 Why?
Molecular Sequence Annotation120125240.020 Why?
Heterozygote1201727970.020 Why?
Remission Induction1201523900.020 Why?
Models, Molecular1202054060.020 Why?
Cell Membrane1201936800.020 Why?
Tissue Donors1201923110.020 Why?
North America1201312730.020 Why?
Systems Biology120134820.020 Why?
India1201523280.020 Why?
Amino Acid Sequence12020134420.020 Why?
Time Factors22023398110.020 Why?
Immunoglobulin G1201945400.020 Why?
DNA Methylation1202143720.020 Why?
Regeneration1201515050.020 Why?
Prevalence12023156400.020 Why?
Aged220151678900.020 Why?
Chromosome Aberrations1201217640.020 Why?
Cooperative Behavior1201315020.020 Why?
Blood Pressure1202184530.020 Why?
Sex Factors12019104950.020 Why?
Cell Line12019155870.020 Why?
Infant22017360450.020 Why?
Gene Expression Regulation12022118900.010 Why?
Mice, Knockout12019143450.010 Why?
Mice, Transgenic1201695140.010 Why?
Apoptosis1201994660.010 Why?
Proportional Hazards Models12015123970.010 Why?
Mice, Inbred C57BL12019219900.010 Why?
Proteins1201560240.010 Why?
Cells, Cultured12016189360.010 Why?
Algorithms12020139520.010 Why?
Pilot Projects1201385500.010 Why?
Incidence12017212170.010 Why?
Disease Progression12015134630.010 Why?
Cell Differentiation12015114690.010 Why?
Risk Assessment12019238160.010 Why?
Pregnancy12019297120.010 Why?
Registries1201381640.010 Why?
Age Factors12013183260.010 Why?
Signal Transduction12019233350.010 Why?
Diabetes Mellitus, Type 212015120780.010 Why?
Sampson's Networks
Click the
Explore
buttons for more information and interactive visualizations!
Concepts (225)
Explore
_
Co-Authors (31)
Explore
_
Similar People (60)
Explore
_
Same Department 
Explore
_
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.