Harvard Catalyst Profiles

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Riccardo Sangermano, Ph.D.

Concepts (128)

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?
ATP-Binding Cassette Transporters920205632.010 Why?
Retinal Degeneration320234131.370 Why?
Macular Degeneration7202210071.090 Why?
RNA Splice Sites420202110.960 Why?
Night Blindness12022560.830 Why?
Lactoferrin220201000.800 Why?
Kidney Diseases, Cystic120231830.750 Why?
Eye Abnormalities120232420.710 Why?
Tooth Discoloration12019150.690 Why?
Oligonucleotides, Antisense320194610.680 Why?
Iron Metabolism Disorders12019240.670 Why?
Pedigree12202445420.640 Why?
Exons6202023910.630 Why?
RNA Splicing320209180.560 Why?
RNA Precursors120172120.540 Why?
Dental Caries120194270.500 Why?
Photoreceptor Cells, Vertebrate220182030.500 Why?
Abnormalities, Multiple1202314230.500 Why?
Protein Isoforms1201916990.450 Why?
Anti-Infective Agents120199830.390 Why?
Alternative Splicing1201610930.360 Why?
Retinal Dystrophies22022650.340 Why?
Introns420199810.310 Why?
Retinitis Pigmentosa220243970.270 Why?
Gastritis, Hypertrophic2201790.250 Why?
Cyclic Nucleotide Phosphodiesterases, Type 612022270.210 Why?
Stem Cells1201635240.210 Why?
RNA, Messenger22018127940.200 Why?
INDEL Mutation120222660.190 Why?
HEK293 Cells4202042810.190 Why?
Mutation72023300530.190 Why?
Retinal Diseases220247050.190 Why?
Frameshift Mutation120223920.180 Why?
Polymorphism, Single Nucleotide42024159360.170 Why?
Electroretinography320185250.170 Why?
Haplotypes3202427130.160 Why?
Blindness120225840.160 Why?
Dental Plaque120192090.150 Why?
Mouth120203810.140 Why?
High-Throughput Nucleotide Sequencing3202436390.140 Why?
Genes, Recessive120196230.130 Why?
Stomach Diseases120171340.130 Why?
Cerebellum1202315010.120 Why?
Saliva120198280.120 Why?
Fluorescein Angiography2201810590.110 Why?
Genetic Markers1202026010.110 Why?
Visual Acuity3201926720.110 Why?
Transforming Growth Factor alpha120121350.100 Why?
Receptors, Notch120177440.100 Why?
Retina1202326590.100 Why?
Genome, Human2202444250.090 Why?
DNA Mutational Analysis2201641110.090 Why?
Genes, Dominant120128520.090 Why?
Alleles4202468640.080 Why?
Visual Fields1201610620.080 Why?
Membrane Transport Proteins1201410350.080 Why?
Reverse Transcriptase Polymerase Chain Reaction1201645760.080 Why?
Stomach120126960.080 Why?
Transfection1201657740.070 Why?
Humans2120247615960.070 Why?
Adult920242212100.070 Why?
Genetic Variation2202065670.070 Why?
Gene Frequency3201936060.070 Why?
Mutation, Missense1201725710.070 Why?
Ubiquitin-Protein Ligases1201718990.070 Why?
Child52024801580.070 Why?
Ventricular Dysfunction, Left1201721180.060 Why?
Male1420243608460.060 Why?
Young Adult42024592600.060 Why?
Fibroblasts1201641420.060 Why?
Genetic Association Studies1201527350.060 Why?
Female1420243927050.060 Why?
Cardiomyopathies1201719640.060 Why?
Sequence Analysis, DNA3202447400.060 Why?
Induced Pluripotent Stem Cells1201618600.060 Why?
Phenotype42024165920.050 Why?
Computational Biology2202435170.050 Why?
Republic of Korea120245900.050 Why?
Anti-Bacterial Agents1202074060.050 Why?
Genetic Testing2202435370.050 Why?
Middle Aged720242209210.050 Why?
Genetic Diseases, Inborn120246040.040 Why?
Homozygote1202417760.040 Why?
Dystrophin120202830.040 Why?
Guanine Nucleotide Exchange Factors120225690.040 Why?
Administration, Topical120207040.040 Why?
Proteins1201260320.040 Why?
Heterozygote1202427870.040 Why?
Genetic Complementation Test120185550.040 Why?
Pregnancy12019298900.040 Why?
Atrophy1202216330.030 Why?
Penetrance120183830.030 Why?
Canada1202221220.030 Why?
Biofilms120206270.030 Why?
Membrane Proteins2202478590.030 Why?
Adolescent22024883260.030 Why?
Siblings120188250.030 Why?
Aged420191693100.030 Why?
Tomography, Optical Coherence2201829170.030 Why?
Visual Field Tests120144110.020 Why?
Ubiquitination1201710070.020 Why?
Animals, Newborn1201726770.020 Why?
Genetic Heterogeneity120157320.020 Why?
Age of Onset1201833060.020 Why?
Sequence Deletion1201514940.020 Why?
Gastric Mucosa120126040.020 Why?
Hyperplasia1201211520.020 Why?
Bacteria1202021990.020 Why?
Kaplan-Meier Estimate1201964840.020 Why?
Genomics1202458210.020 Why?
Myocytes, Cardiac1201716680.020 Why?
Case-Control Studies22017221760.020 Why?
Base Sequence12018124410.020 Why?
Child, Preschool22024422320.020 Why?
Computer Simulation1201862410.010 Why?
Gene Expression Profiling1202094200.010 Why?
Family1201231950.010 Why?
Retrospective Studies22022806470.010 Why?
Cells, Cultured12017189660.010 Why?
Rats12017237410.010 Why?
Inflammation12020107740.010 Why?
Prospective Studies12024544230.010 Why?
Gene Expression Regulation12017119040.010 Why?
Animals220201684750.010 Why?
Cohort Studies12019414950.010 Why?
Genome-Wide Association Study12014126900.010 Why?
Signal Transduction12017234470.010 Why?
Genetic Predisposition to Disease12015179040.010 Why?
Sangermano's Networks
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Concepts (128)
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Co-Authors (10)
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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.