Harvard Catalyst Profiles

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Colby Chiang, M.D.

Concepts (152)

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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?
Genome, Human8202144430.610 Why?
Molecular Sequence Annotation320205260.480 Why?
Gene Rearrangement5201711420.470 Why?
Quantitative Trait Loci3202021360.420 Why?
Genetic Variation7202066120.420 Why?
Chromosome Breakage220121590.400 Why?
Sequence Analysis, DNA5201747800.370 Why?
Software3202044660.260 Why?
High-Throughput Nucleotide Sequencing3202136660.240 Why?
Germ-Line Mutation1201218850.210 Why?
Sequence Deletion4201914940.210 Why?
Genomic Structural Variation12021800.180 Why?
Gene Expression Regulation12017119200.160 Why?
Chromosome Aberrations2201617760.150 Why?
Chromosome Breakpoints22014930.140 Why?
Choanal Atresia12017410.140 Why?
Child Development Disorders, Pervasive220125970.140 Why?
Microphthalmos12017580.130 Why?
INDEL Mutation120172660.130 Why?
Genetic Predisposition to Disease62019180750.130 Why?
Chromosome Inversion220121190.120 Why?
Aneuploidy120185730.120 Why?
Muscular Dystrophies120173930.120 Why?
Chromosomes, Human220184370.110 Why?
Chromosomes, Human, Pair 2220123130.110 Why?
Mitral Valve Prolapse120152130.110 Why?
Inverted Repeat Sequences12013590.100 Why?
Nose120175220.100 Why?
Organ Specificity1201719660.100 Why?
Translocation, Genetic3201213920.100 Why?
Congenital Abnormalities120167030.100 Why?
DNA Copy Number Variations3202120450.090 Why?
Chromosomal Proteins, Non-Histone120177230.090 Why?
Cell Adhesion Molecules, Neuronal120132620.090 Why?
Models, Genetic3201834500.090 Why?
Cadherins120159020.090 Why?
Workflow120158590.090 Why?
Genetic Markers1201626030.090 Why?
Exons2201323920.090 Why?
Genetic Association Studies1201927460.080 Why?
Huntington Disease1201711470.080 Why?
Genome-Wide Association Study42017128060.080 Why?
Finland220216080.080 Why?
Chromosome Mapping1201746190.080 Why?
Mutation42018302130.070 Why?
Genome1201517520.070 Why?
Animals, Genetically Modified1201215620.070 Why?
Linear Models1201758740.070 Why?
Polymorphism, Single Nucleotide22017160440.070 Why?
Oligonucleotide Array Sequence Analysis2201237960.070 Why?
DNA Mutational Analysis1201441140.060 Why?
Molecular Sequence Data32013176080.060 Why?
Alleles3202168950.060 Why?
Gene Expression Profiling2201795250.060 Why?
Mice, Transgenic1201795470.060 Why?
Gene Deletion1201126690.060 Why?
Developmental Disabilities1201215190.060 Why?
Genomics2201759230.050 Why?
Chromosomes, Human, Pair 11220154120.050 Why?
Pyruvate Dehydrogenase (Lipoamide)-Phosphatase1202140.050 Why?
Phenotype52018167240.040 Why?
Nerve Tissue Proteins1201344000.040 Why?
Pyruvic Acid120212050.040 Why?
Humans2020217667660.040 Why?
Gene Frequency2201836240.040 Why?
Anaphase120181120.040 Why?
Proteins1201360020.040 Why?
Zebrafish Proteins2201510180.040 Why?
Disease Models, Animal12017183300.040 Why?
Chromosomal Instability120181760.040 Why?
Endpoint Determination120195920.030 Why?
Neoplasms32015223500.030 Why?
Algorithms12017140720.030 Why?
Xenopus120187100.030 Why?
Epilepsy1201133170.030 Why?
Chromosome Painting12015260.030 Why?
Syndrome2201332710.030 Why?
Phylogeography12015720.030 Why?
Gene Dosage1202012110.030 Why?
Genetics, Population120209430.030 Why?
Cardiovascular Diseases12021156570.030 Why?
Mitochondrial Proteins120219800.030 Why?
Genotype22021130360.030 Why?
Embryo, Nonmammalian120189100.030 Why?
DNA-Binding Proteins1201196110.030 Why?
Animals620181689300.030 Why?
Protein Stability120155780.030 Why?
Terminal Repeat Sequences12013700.030 Why?
Mitosis1201811760.030 Why?
Mental Disorders1201368690.030 Why?
Epigenesis, Genetic2202038240.030 Why?
Neural Cell Adhesion Molecules120131220.030 Why?
Cholesterol, HDL1201918120.030 Why?
Suppression, Genetic120131900.030 Why?
Major Histocompatibility Complex120158800.030 Why?
Gene Order120121650.030 Why?
Zebrafish2201530350.030 Why?
Cluster Analysis1201927170.020 Why?
Facies120132240.020 Why?
Cholesterol1202129030.020 Why?
Base Sequence22013124150.020 Why?
Female1120213965200.020 Why?
Computational Biology2201535640.020 Why?
DNA Breaks12011470.020 Why?
DNA, Single-Stranded120133510.020 Why?
Interspersed Repetitive Sequences12011520.020 Why?
Body Patterning120156340.020 Why?
Multifactorial Inheritance1201914250.020 Why?
Breast Neoplasms12018211620.020 Why?
DNA Barcoding, Taxonomic120111340.020 Why?
Male920213641420.020 Why?
Promoter Regions, Genetic1202157890.020 Why?
Sequence Analysis, RNA1201720390.020 Why?
Homozygote1201417750.020 Why?
Bayes Theorem1201723540.020 Why?
Karyotyping1201111760.020 Why?
Nervous System120125420.020 Why?
Genomic Instability120137160.020 Why?
Case-Control Studies22020222480.020 Why?
Gene Library1201110650.020 Why?
Calcium-Binding Proteins1201310780.020 Why?
Protein Isoforms1201317160.020 Why?
Phylogeny1201528400.020 Why?
Pedigree1201545390.020 Why?
Alternative Splicing1201211030.020 Why?
Chromosome Deletion1201213840.020 Why?
Cytoskeletal Proteins1201313250.020 Why?
Evolution, Molecular1201518920.020 Why?
Mitral Valve1201514730.020 Why?
CpG Islands1201112080.020 Why?
Child, Preschool32017425770.020 Why?
ROC Curve1201436200.020 Why?
Transcription Factors22018121500.020 Why?
DNA Replication1201314260.020 Why?
Neural Stem Cells120128950.020 Why?
Adolescent42017889040.020 Why?
Child42017806680.020 Why?
Lymphocytes1201226050.010 Why?
Transcription, Genetic1201876090.010 Why?
Cell Movement1201551990.010 Why?
Infant22017364610.010 Why?
Autistic Disorder1201212380.010 Why?
Reproducibility of Results12019201440.010 Why?
Amino Acid Sequence12013134110.010 Why?
RNA, Messenger12015127910.010 Why?
Models, Statistical1201450910.010 Why?
Mice22017818890.010 Why?
Schizophrenia1201269760.010 Why?
Cohort Studies12013417100.010 Why?
Signal Transduction12012236190.000 Why?
Adult220132233070.000 Why?
Young Adult12013599390.000 Why?
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Concepts (152)
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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.