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, Human8202144250.620 Why?
Molecular Sequence Annotation320205220.490 Why?
Gene Rearrangement5201711250.480 Why?
Quantitative Trait Loci3202021160.430 Why?
Genetic Variation7202065670.420 Why?
Chromosome Breakage220121590.410 Why?
Sequence Analysis, DNA5201747400.370 Why?
Software3202044340.270 Why?
High-Throughput Nucleotide Sequencing3202136390.250 Why?
Germ-Line Mutation1201218580.220 Why?
Sequence Deletion4201914940.210 Why?
Genomic Structural Variation12021680.180 Why?
Gene Expression Regulation12017119040.160 Why?
Chromosome Aberrations2201617680.150 Why?
Chromosome Breakpoints22014930.140 Why?
Choanal Atresia12017410.140 Why?
Child Development Disorders, Pervasive220126000.140 Why?
Microphthalmos12017580.140 Why?
Genetic Predisposition to Disease62019179040.130 Why?
INDEL Mutation120172660.130 Why?
Aneuploidy120185520.120 Why?
Chromosome Inversion220121200.120 Why?
Muscular Dystrophies120173900.120 Why?
Chromosomes, Human, Pair 2220123130.110 Why?
Chromosomes, Human220184410.110 Why?
Mitral Valve Prolapse120152120.110 Why?
Nose120175210.110 Why?
Inverted Repeat Sequences12013600.110 Why?
Organ Specificity1201719680.100 Why?
Translocation, Genetic3201213930.100 Why?
Congenital Abnormalities120167090.100 Why?
DNA Copy Number Variations3202120200.100 Why?
Chromosomal Proteins, Non-Histone120177270.100 Why?
Cell Adhesion Molecules, Neuronal120132630.090 Why?
Models, Genetic3201834420.090 Why?
Cadherins120159030.090 Why?
Workflow120158510.090 Why?
Genetic Markers1201626010.090 Why?
Exons2201323910.090 Why?
Huntington Disease1201711440.090 Why?
Genetic Association Studies1201927350.090 Why?
Genome-Wide Association Study42017126900.080 Why?
Finland220216070.080 Why?
Chromosome Mapping1201746150.080 Why?
Mutation42018300530.070 Why?
Genome1201517400.070 Why?
Animals, Genetically Modified1201215610.070 Why?
Linear Models1201758720.070 Why?
Polymorphism, Single Nucleotide22017159360.070 Why?
Oligonucleotide Array Sequence Analysis2201237790.070 Why?
DNA Mutational Analysis1201441110.060 Why?
Molecular Sequence Data32013176350.060 Why?
Alleles3202168640.060 Why?
Gene Expression Profiling2201794200.060 Why?
Mice, Transgenic1201795420.060 Why?
Gene Deletion1201126650.060 Why?
Developmental Disabilities1201215090.060 Why?
Genomics2201758210.050 Why?
Chromosomes, Human, Pair 11220154100.050 Why?
Pyruvate Dehydrogenase (Lipoamide)-Phosphatase1202140.050 Why?
Phenotype52018165920.040 Why?
Pyruvic Acid120212040.040 Why?
Nerve Tissue Proteins1201344150.040 Why?
Humans2020217615960.040 Why?
Gene Frequency2201836060.040 Why?
Anaphase120181140.040 Why?
Proteins1201360320.040 Why?
Zebrafish Proteins2201510150.040 Why?
Disease Models, Animal12017182550.040 Why?
Chromosomal Instability120181780.040 Why?
Endpoint Determination120195900.030 Why?
Neoplasms32015221730.030 Why?
Algorithms12017140330.030 Why?
Xenopus120187110.030 Why?
Epilepsy1201132900.030 Why?
Chromosome Painting12015260.030 Why?
Syndrome2201332670.030 Why?
Phylogeography12015720.030 Why?
Gene Dosage1202012180.030 Why?
Genetics, Population120209370.030 Why?
Cardiovascular Diseases12021155020.030 Why?
Mitochondrial Proteins120219760.030 Why?
Genotype22021129900.030 Why?
Embryo, Nonmammalian120189060.030 Why?
DNA-Binding Proteins1201196100.030 Why?
Animals620181684750.030 Why?
Protein Stability120155780.030 Why?
Terminal Repeat Sequences12013700.030 Why?
Mental Disorders1201368450.030 Why?
Mitosis1201811880.030 Why?
Epigenesis, Genetic2202038010.030 Why?
Cholesterol, HDL1201918140.030 Why?
Neural Cell Adhesion Molecules120131220.030 Why?
Suppression, Genetic120131900.030 Why?
Major Histocompatibility Complex120158700.030 Why?
Gene Order120121690.030 Why?
Zebrafish2201530080.030 Why?
Cluster Analysis1201927070.030 Why?
Facies120132220.020 Why?
Cholesterol1202129050.020 Why?
Female1120213927050.020 Why?
Base Sequence22013124410.020 Why?
Computational Biology2201535170.020 Why?
DNA Breaks12011470.020 Why?
Interspersed Repetitive Sequences12011530.020 Why?
Multifactorial Inheritance1201913870.020 Why?
DNA, Single-Stranded120133550.020 Why?
Body Patterning120156320.020 Why?
Breast Neoplasms12018210190.020 Why?
DNA Barcoding, Taxonomic120111320.020 Why?
Male920213608460.020 Why?
Promoter Regions, Genetic1202157900.020 Why?
Sequence Analysis, RNA1201720210.020 Why?
Bayes Theorem1201723300.020 Why?
Homozygote1201417760.020 Why?
Karyotyping1201111710.020 Why?
Nervous System120125450.020 Why?
Genomic Instability120137090.020 Why?
Case-Control Studies22020221760.020 Why?
Gene Library1201110590.020 Why?
Calcium-Binding Proteins1201310690.020 Why?
Protein Isoforms1201316990.020 Why?
Phylogeny1201528110.020 Why?
Pedigree1201545420.020 Why?
Alternative Splicing1201210930.020 Why?
Chromosome Deletion1201213860.020 Why?
Cytoskeletal Proteins1201313420.020 Why?
Evolution, Molecular1201518860.020 Why?
Mitral Valve1201514650.020 Why?
Child, Preschool32017422320.020 Why?
CpG Islands1201112300.020 Why?
ROC Curve1201435780.020 Why?
Transcription Factors22018121300.020 Why?
DNA Replication1201314180.020 Why?
Neural Stem Cells120128880.020 Why?
Adolescent42017883260.020 Why?
Child42017801580.020 Why?
Lymphocytes1201226120.010 Why?
Transcription, Genetic1201875930.010 Why?
Cell Movement1201552050.010 Why?
Infant22017361930.010 Why?
Autistic Disorder1201212200.010 Why?
Reproducibility of Results12019201000.010 Why?
Amino Acid Sequence12013134460.010 Why?
RNA, Messenger12015127940.010 Why?
Models, Statistical1201450790.010 Why?
Mice22017815390.010 Why?
Schizophrenia1201269370.010 Why?
Cohort Studies12013414950.010 Why?
Signal Transduction12012234470.000 Why?
Adult220132212100.000 Why?
Young Adult12013592600.000 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.