Harvard Catalyst Profiles

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Pier Francesco Palamara

Concepts (84)

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?
Genetics, Population820239311.820 Why?
Haplotypes8202327821.030 Why?
Multifactorial Inheritance6202311740.990 Why?
Linkage Disequilibrium5202319920.920 Why?
Genome3202317940.830 Why?
Quantitative Trait Loci3202320160.720 Why?
Models, Genetic10202334930.710 Why?
Genomics4202356520.700 Why?
Disease220186830.540 Why?
Biological Specimen Banks420236920.400 Why?
Genome, Human5202044190.380 Why?
Population Dynamics120123000.380 Why?
Polymorphism, Single Nucleotide112023155000.360 Why?
Selection, Genetic320209150.350 Why?
Population Density220231940.330 Why?
Recombination, Genetic3202315910.320 Why?
Jews520123850.310 Why?
Computer Simulation3202362370.310 Why?
Germ-Line Mutation1201517860.310 Why?
Quantitative Trait, Heritable220205450.290 Why?
Genome-Wide Association Study62023121780.250 Why?
Models, Theoretical1201636090.240 Why?
Molecular Sequence Annotation220185240.170 Why?
Phenotype52023163010.170 Why?
Algorithms52020138720.150 Why?
Benchmarking1202310340.140 Why?
Gene Conversion12016710.140 Why?
Genotype52023129510.140 Why?
Mosaicism120184420.130 Why?
Clone Cells1201816850.130 Why?
Genetic Variation3201765390.120 Why?
Gene Frequency3201935850.120 Why?
INDEL Mutation120152780.120 Why?
Inheritance Patterns120163390.120 Why?
Alleles4201969420.120 Why?
Population120121420.110 Why?
High-Throughput Screening Assays120189530.110 Why?
Founder Effect120121900.100 Why?
Chromosome Aberrations1201818120.100 Why?
Computational Biology2201635060.100 Why?
Epigenesis, Genetic1202336140.090 Why?
Humans2120237393980.090 Why?
Hematopoiesis1201820490.080 Why?
Pedigree2201246400.080 Why?
Heterozygote1201227980.070 Why?
Linear Models1201559480.060 Why?
Evolution, Molecular1201119360.050 Why?
Chromosome Fragile Sites12018270.040 Why?
Transcription Factors12018121200.040 Why?
Chromosome Breakage120181730.040 Why?
Chromosomes, Human, Pair 10120182870.040 Why?
Markov Chains120209700.040 Why?
Penetrance120183810.040 Why?
Blood Chemical Analysis120184410.040 Why?
Blood Cells120183090.040 Why?
Genetic Fitness120171210.040 Why?
Health120183900.030 Why?
Phylogeny2201227890.030 Why?
Judaism12012300.030 Why?
Mutation12016296580.030 Why?
Chi-Square Distribution1201735100.020 Why?
Africa120126660.020 Why?
Middle East120102190.020 Why?
Binding Sites1201861130.020 Why?
Emigration and Immigration120124020.020 Why?
Reference Values1201649830.020 Why?
Demography1201216500.020 Why?
Hematologic Neoplasms1201818000.020 Why?
Protein Binding1201893750.020 Why?
Cluster Analysis1201227110.020 Why?
Sequence Analysis, DNA1201647910.020 Why?
Animals120161683680.010 Why?
High-Throughput Nucleotide Sequencing1201635710.010 Why?
Cohort Studies22016403890.010 Why?
Oligonucleotide Array Sequence Analysis1201239220.010 Why?
Chromosome Mapping1201147430.010 Why?
Gene Expression Regulation12018120490.010 Why?
Genetic Predisposition to Disease12018173840.010 Why?
Risk Factors12018719740.010 Why?
Male220183490220.010 Why?
Female220183788530.010 Why?
Aged120181626980.000 Why?
Middle Aged120182128630.000 Why?
Adult120182133940.000 Why?
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Concepts (84)
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Co-Authors (19)
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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.