Harvard Catalyst Profiles

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Po-Ru Loh, Ph.D.

Concepts (214)

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?
Multifactorial Inheritance13202211092.200 Why?
Biological Specimen Banks1120216192.160 Why?
Mosaicism820214511.830 Why?
Clone Cells3202017911.300 Why?
Quantitative Trait Loci9202219791.060 Why?
Genome, Human8202244971.060 Why?
Antley-Bixler Syndrome Phenotype1202230.960 Why?
Genetics, Population9202010120.880 Why?
Polymorphism, Single Nucleotide292022155210.880 Why?
Minisatellite Repeats120211600.840 Why?
Hematopoiesis3202020070.790 Why?
Genome-Wide Association Study252021116220.760 Why?
Gene Frequency6202137080.710 Why?
Chromosome Aberrations4202118110.710 Why?
Linkage Disequilibrium13202120730.690 Why?
Phenotype192022162680.660 Why?
Models, Genetic16202135550.660 Why?
Genetic Association Studies6202127090.620 Why?
DNA Copy Number Variations3202218600.610 Why?
Genetic Predisposition to Disease172022173120.580 Why?
Chromosomes, Human, Y320211550.560 Why?
Selection, Genetic720198810.550 Why?
Inheritance Patterns220163430.540 Why?
Lung Diseases, Interstitial120227420.530 Why?
Haplotypes2202128920.510 Why?
Algorithms92019136240.510 Why?
Cystic Fibrosis1202211480.500 Why?
Disease420187050.410 Why?
Polymorphism, Genetic1202143820.400 Why?
Molecular Sequence Annotation420205470.380 Why?
Computational Biology5202035800.380 Why?
Alleles8202271210.360 Why?
Penetrance220223580.360 Why?
Quantitative Trait, Heritable420195560.360 Why?
Bayes Theorem1201519730.330 Why?
Genotype142021129460.310 Why?
Analysis of Variance1201565550.300 Why?
Alcohol Dehydrogenase220161280.300 Why?
Proteins1202161670.290 Why?
Chromosome Deletion2201913830.270 Why?
Genetic Diseases, Inborn220205980.260 Why?
Genetic Markers3202127020.250 Why?
Polynucleotide Adenylyltransferase12021110.230 Why?
Aggrecans12021860.220 Why?
Receptors, Atrial Natriuretic Factor12021570.220 Why?
Schizophrenia3201866680.210 Why?
Intermediate Filament Proteins120212770.200 Why?
Aging5202183070.200 Why?
Tissue Banks120211980.190 Why?
Hematologic Neoplasms3202116830.190 Why?
Muscular Atrophy, Spinal120222430.180 Why?
Chromosome Fragile Sites12018260.180 Why?
Humans5020227070670.180 Why?
Hair120214650.170 Why?
Chromosome Breakage120181720.170 Why?
Principal Component Analysis320169690.170 Why?
Chromosomes, Human120204780.170 Why?
Loss of Heterozygosity120206890.170 Why?
Lipoprotein(a)120213810.170 Why?
Chromosomes, Human, Pair 10120182910.160 Why?
Leukocytes3202121010.160 Why?
Autopsy120219790.160 Why?
Hematopoietic Stem Cells2202034440.160 Why?
Gene Pool22013380.160 Why?
Mucin-1120215300.160 Why?
Brain Chemistry1202110260.160 Why?
Linear Models2201860080.150 Why?
Antigens1202115330.140 Why?
Databases, Genetic6201918000.140 Why?
Child Development Disorders, Pervasive120216150.140 Why?
Cell Division2202047870.140 Why?
Prenatal Diagnosis1202211490.140 Why?
Cohort Studies72021395630.140 Why?
Genomic Instability120196980.140 Why?
Health120183980.140 Why?
Telomere120208240.140 Why?
Open Reading Frames120188420.140 Why?
Genes1201919820.130 Why?
Chromosome Mapping2202148480.130 Why?
Body Height1202115990.130 Why?
Menarche120174890.130 Why?
Blood Pressure3202184970.130 Why?
Ribonucleoproteins120173870.130 Why?
Puberty120174620.130 Why?
Fetus2202218230.130 Why?
Communicable Diseases120217910.120 Why?
Diabetes Mellitus, Type 252021107260.120 Why?
Germ-Line Mutation1202117230.120 Why?
Models, Theoretical2201535610.120 Why?
Membrane Proteins2202180920.110 Why?
Chromatin2202026740.110 Why?
Genetic Loci5202025790.100 Why?
Emigration and Immigration120143860.100 Why?
Gene Regulatory Networks1201917140.100 Why?
Hypersensitivity1201810130.100 Why?
Pneumonia1202120670.100 Why?
Intercellular Signaling Peptides and Proteins1201717580.090 Why?
Transcription Factors22020119680.090 Why?
Demography1201416130.090 Why?
Reference Values1201650690.090 Why?
Single-Cell Analysis1201921600.090 Why?
Family2201631210.090 Why?
Birth Weight1201618790.090 Why?
Adult1020212119890.080 Why?
Sepsis1202124320.080 Why?
Genetic Variation3201866730.080 Why?
Female1620223766420.080 Why?
Carrier Proteins1202151730.080 Why?
Computer Simulation6201560470.080 Why?
Evolution, Molecular1201619670.080 Why?
Databases, Factual1202277750.080 Why?
Male1520213512630.070 Why?
Aged920211623200.070 Why?
Kidney1202168440.070 Why?
Japan2202013520.070 Why?
Calibration220188010.070 Why?
Genomic Imprinting220173480.070 Why?
Europe3201633570.070 Why?
Multiple Sclerosis2201529070.070 Why?
Sequence Analysis, DNA1201649480.070 Why?
Gene Expression1201880680.070 Why?
Africa, Southern22014500.060 Why?
Genomics2201652220.060 Why?
High-Throughput Nucleotide Sequencing1201637050.060 Why?
Middle Aged820212151660.060 Why?
Cardiovascular Diseases22020140030.060 Why?
Neoplasms32020203170.060 Why?
Risk Factors62021700660.060 Why?
Sample Size220158040.060 Why?
Cell Differentiation12019117360.050 Why?
Trisomy120222610.050 Why?
Case-Control Studies42021218250.050 Why?
Models, Statistical1201550560.050 Why?
Leukemia, T-Cell120201140.050 Why?
Digestive System Diseases120211350.050 Why?
Atrial Fibrillation1201743610.050 Why?
Binding Sites2202063390.050 Why?
Asthma1201858280.050 Why?
Chromosomes120226080.050 Why?
Aneuploidy120224600.050 Why?
Receptor, IGF Type 1120213970.050 Why?
Urogenital Abnormalities120212370.040 Why?
Risk Assessment12021234840.040 Why?
Jurkat Cells120198020.040 Why?
Coronary Artery Disease1201661100.040 Why?
Phylogeography12016870.040 Why?
Genetic Fitness120171130.040 Why?
Far East12016910.040 Why?
Protein Binding2202096880.040 Why?
Blood Chemical Analysis120184670.040 Why?
Blood Cells120183180.040 Why?
Glycogen120162680.040 Why?
False Positive Reactions1201810100.040 Why?
Medical History Taking120208020.040 Why?
Immune System Diseases120182660.040 Why?
Mutation12020291930.040 Why?
Regression Analysis2201565150.030 Why?
Africa, Eastern12014720.030 Why?
Insulin-Like Growth Factor Binding Protein 3120164230.030 Why?
Insulin2202166260.030 Why?
Placenta1202214840.030 Why?
Gene Flow12014980.030 Why?
Tissue Distribution1201824410.030 Why?
Genome1202117170.030 Why?
Linguistics12013930.030 Why?
Probability1201824930.030 Why?
Child12021737070.030 Why?
Multigene Family1201611730.030 Why?
Methylation1201511200.030 Why?
Chromatin Assembly and Disassembly120166190.030 Why?
Calcium-Binding Proteins1201711020.030 Why?
DNA Mutational Analysis1202143250.030 Why?
Anthropometry1201613790.030 Why?
History, Ancient120122850.030 Why?
Geography120136860.030 Why?
Lysine1201510250.030 Why?
Cell Lineage1202026340.030 Why?
Chi-Square Distribution1201735920.030 Why?
Aged, 80 and over32021586650.030 Why?
Gene Expression Regulation22020124630.020 Why?
Erythrocytes1201924760.020 Why?
HEK293 Cells1201943310.020 Why?
Population Dynamics120123120.020 Why?
Body Mass Index22018123990.020 Why?
Adaptation, Physiological1201613320.020 Why?
Leukemia, Lymphocytic, Chronic, B-Cell1202015220.020 Why?
Blood Platelets1201924890.020 Why?
Phylogeny1201628090.020 Why?
DNA1202272620.020 Why?
Base Sequence12019134170.020 Why?
Ubiquitin-Protein Ligases1201718440.020 Why?
India1201319900.020 Why?
Signal Transduction22021239660.020 Why?
Histones1201525750.020 Why?
Software1201943490.020 Why?
Epigenesis, Genetic1201834370.020 Why?
Cluster Analysis1201227430.020 Why?
Glucose1201642260.020 Why?
Arthritis, Rheumatoid1201836440.020 Why?
Gene Expression Profiling1201895510.010 Why?
Pregnancy12022267480.010 Why?
Adolescent22021851590.010 Why?
Reproducibility of Results12018194380.010 Why?
Bipolar Disorder1201851760.010 Why?
Age Factors12017189330.010 Why?
Neurons1201893930.010 Why?
Prognosis12015290370.010 Why?
Young Adult12021560580.010 Why?
Mice12019807950.010 Why?
Brain12018248750.010 Why?
Time Factors12013412510.010 Why?
United States12016670260.010 Why?
Retrospective Studies12016708570.010 Why?
Animals120191703560.010 Why?
Loh's Networks
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Concepts (214)
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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.