Harvard Catalyst Profiles

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Wai-Man Chan, A.L.M.

Concepts (237)

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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?
Duane Retraction Syndrome92017601.100 Why?
Chimerin 152017140.820 Why?
Tubulin820196950.790 Why?
Ocular Motility Disorders620191350.750 Why?
Mobius Syndrome72017400.690 Why?
Ophthalmoplegia1120191660.650 Why?
Mutation, Missense10201325660.570 Why?
Oculomotor Muscles1020163700.550 Why?
Eye Diseases, Hereditary620151170.500 Why?
Pedigree23201946430.440 Why?
Fibrosis13201920300.420 Why?
Strabismus320122830.380 Why?
Mutation172019297770.360 Why?
Oculomotor Nerve42014730.300 Why?
Amino Acid Substitution9201917930.290 Why?
Homeodomain Proteins9201424190.290 Why?
Pyramidal Tracts220192550.250 Why?
Receptors, Immunologic3200914230.230 Why?
DNA Mutational Analysis10201941830.210 Why?
Scoliosis220067250.210 Why?
Fovea Centralis220131190.200 Why?
Malformations of Cortical Development220152000.200 Why?
Axons6201416850.200 Why?
Genetic Linkage7201924190.180 Why?
Synkinesis12019240.170 Why?
Receptors, CXCR12019520.170 Why?
Nerve Tissue Proteins4200744630.170 Why?
Kallmann Syndrome320191400.170 Why?
Myogenic Regulatory Factor 512018250.160 Why?
Genes, Dominant220138800.150 Why?
Receptor, EphA412017180.150 Why?
Esotropia12018900.150 Why?
Ribs120182520.140 Why?
Hearing Loss220167650.140 Why?
MafB Transcription Factor12016250.140 Why?
Embryo, Mammalian3201717020.140 Why?
Myoblasts120172380.140 Why?
Pierre Robin Syndrome120171130.130 Why?
Amino Acid Sequence92019138090.130 Why?
Abnormalities, Multiple2201314160.130 Why?
Labyrinth Diseases120161500.130 Why?
Morphogenesis220177510.130 Why?
Loss of Heterozygosity120176840.120 Why?
Corpus Callosum120197360.120 Why?
Phenotype132018163610.120 Why?
Blepharoptosis420141430.120 Why?
Nystagmus, Congenital1201370.120 Why?
Malignant Hyperthermia12013730.120 Why?
Molecular Sequence Data82015181070.120 Why?
Ryanodine Receptor Calcium Release Channel120131750.110 Why?
Muscular Diseases120175550.110 Why?
Arthrogryposis12013720.110 Why?
Paired Box Transcription Factors120132140.110 Why?
Endocrine System Diseases120152470.110 Why?
Pons120132440.110 Why?
Motor Neurons120178410.100 Why?
Klippel-Feil Syndrome12011190.100 Why?
Muscle Proteins1201711580.100 Why?
Transcription Factors82014122090.100 Why?
Metalloendopeptidases120133960.100 Why?
Albinism, Oculocutaneous12011170.100 Why?
Color Vision Defects12011280.100 Why?
Syndrome6201932490.100 Why?
Polymorphism, Single Nucleotide62019155180.100 Why?
Psychomotor Performance1201918950.100 Why?
Iris Diseases12011400.100 Why?
Spine1201811440.100 Why?
Zebrafish Proteins1201710050.090 Why?
Base Sequence32012127980.090 Why?
Eye Proteins120136450.090 Why?
Vomiting120136360.090 Why?
Motor Activity1201927140.080 Why?
Exotropia22014550.080 Why?
Eye Abnormalities120112460.080 Why?
Consanguinity420134550.080 Why?
Cerebral Cortex3201956920.080 Why?
Polymerase Chain Reaction4201461700.080 Why?
Facial Paralysis120123380.080 Why?
Movement Disorders120114480.080 Why?
Child172019776370.080 Why?
Eye Movements420145000.070 Why?
Male3320193497760.070 Why?
Chromatography, High Pressure Liquid1201115740.070 Why?
Cataract120138340.070 Why?
Receptors, Cell Surface4201728650.070 Why?
Hearing Loss, Sensorineural120127700.070 Why?
Developmental Disabilities3201514520.070 Why?
Female3120193800200.070 Why?
Gene Expression Regulation, Developmental1201736220.070 Why?
Heterozygote4201928030.060 Why?
Inheritance Patterns120073390.060 Why?
Sequence Homology, Amino Acid3201728390.060 Why?
Cardiovascular Abnormalities120051440.060 Why?
Visual Acuity2201125250.060 Why?
Rhombencephalon12004850.060 Why?
Humans4120197438110.060 Why?
Nuclear Proteins1201858540.060 Why?
Sequence Alignment2201822560.060 Why?
Exons3201824380.060 Why?
Genetic Predisposition to Disease42019174390.050 Why?
Protein Structure, Tertiary2200738470.050 Why?
Chromosomes, Human, Pair 20120021330.050 Why?
Homozygote3201317870.050 Why?
Child, Preschool92018409640.050 Why?
Codon, Nonsense120032810.050 Why?
Lod Score320136130.050 Why?
Repressor Proteins1201330240.050 Why?
Muscle, Skeletal1201749250.050 Why?
Neurons4201793360.050 Why?
Chromosomes, Human, Pair 12120034620.050 Why?
Alleles3201969340.050 Why?
Deafness120054580.050 Why?
Abducens Nerve22011280.050 Why?
Chromosomes, Human, Pair 16120023520.050 Why?
Membrane Proteins1201778800.050 Why?
Brain Stem120058440.050 Why?
Protein Transport2201919880.040 Why?
Chromosomes, Human, Pair 2220113260.040 Why?
Turkey220132370.040 Why?
Tomography, Optical Coherence1201126570.040 Why?
Neural Pathways3201929710.040 Why?
Accommodation, Ocular12018480.040 Why?
Infant52017351220.040 Why?
Adult1420192138890.040 Why?
Magnetic Resonance Imaging82019354090.040 Why?
Mice, Knockout32018145630.040 Why?
MyoD Protein120181510.040 Why?
Endophenotypes120192500.040 Why?
Limb Deformities, Congenital120181360.040 Why?
Brain42019263450.040 Why?
Colorectal Neoplasms1201767730.040 Why?
Introns220109910.040 Why?
Genotype32019129440.040 Why?
Cell Fusion120172970.040 Why?
Genetic Complementation Test120175610.040 Why?
Diffusion Tensor Imaging2201923050.030 Why?
Eye Diseases120026680.030 Why?
Autistic Disorder1200511620.030 Why?
Anisotropy1201912630.030 Why?
Anal Canal120183760.030 Why?
Neurogenesis220128380.030 Why?
Gene Expression2201977930.030 Why?
Microtubules2201210870.030 Why?
Fluorescent Antibody Technique1201925030.030 Why?
Siblings120198530.030 Why?
Animals920191686600.030 Why?
Genes, Recessive120176410.030 Why?
Animals, Genetically Modified1201915520.030 Why?
Organ Size1201922410.030 Why?
Disease Models, Animal32019180270.030 Why?
Mice62019811540.030 Why?
Embryo, Nonmammalian120178950.030 Why?
Signal Transduction12017233980.030 Why?
Twins, Dizygotic120132350.030 Why?
Young Adult52019563920.030 Why?
Trachea1201810760.030 Why?
Chromosomes, Human, Pair 11120134170.030 Why?
Esophagus1201810190.030 Why?
Adolescent72018857290.030 Why?
Lower Extremity Deformities, Congenital12011120.030 Why?
Sequence Analysis, DNA3201348030.030 Why?
Founder Effect120121890.030 Why?
Upper Extremity Deformities, Congenital12011290.030 Why?
Diseases in Twins120134500.030 Why?
Ophthalmic Nerve12011430.020 Why?
Case-Control Studies22019217330.020 Why?
Cranial Nerve Diseases120111120.020 Why?
rac GTP-Binding Proteins120111640.020 Why?
Models, Molecular2201254450.020 Why?
Lysine1201510070.020 Why?
Genetic Association Studies1201927030.020 Why?
Age Factors22019183550.020 Why?
Cell Count1201418550.020 Why?
Muscle Denervation12009570.020 Why?
Central Nervous System1201713580.020 Why?
Disease Progression12006132730.020 Why?
Glutamic Acid1201511680.020 Why?
Microtubule-Associated Proteins1201410830.020 Why?
Spinal Cord1201718090.020 Why?
Heart Defects, Congenital2201845840.020 Why?
Animals, Newborn1201427250.020 Why?
Green Fluorescent Proteins1201420860.020 Why?
Heart Septal Defects, Atrial120114780.020 Why?
Genetic Variation1200365350.020 Why?
Optic Nerve120115540.020 Why?
Diffusion Magnetic Resonance Imaging1201927390.020 Why?
Haplotypes2200427790.020 Why?
Age of Onset1201332680.020 Why?
Chick Embryo120089830.020 Why?
Neuropsychological Tests1201969760.020 Why?
Transcriptional Activation1201217830.020 Why?
Zebrafish1201729950.020 Why?
Immunohistochemistry12019113600.020 Why?
Odds Ratio1201898480.020 Why?
Saudi Arabia120052090.020 Why?
HEK293 Cells1201442040.020 Why?
Gene Expression Regulation22014120660.020 Why?
Vision Disorders1201110550.010 Why?
Spinal Canal12003390.010 Why?
Ophthalmoscopy120031760.010 Why?
Carotid Artery, Internal120054450.010 Why?
Medulla Oblongata120042430.010 Why?
Evoked Potentials, Somatosensory120042430.010 Why?
Kidney1201871850.010 Why?
Middle Aged520182132410.010 Why?
Microsatellite Repeats120047990.010 Why?
Amino Acid Motifs120049360.010 Why?
Sequence Analysis, Protein120022580.010 Why?
Mice, Transgenic1201497310.010 Why?
Manometry120034450.010 Why?
Ear, Inner120054200.010 Why?
Evoked Potentials, Motor120044540.010 Why?
Aged420181631780.010 Why?
Iran120037090.010 Why?
DNA-Binding Proteins1201896480.010 Why?
Zinc Fingers120025830.010 Why?
Protein Binding1201293770.010 Why?
In Situ Hybridization1200419520.010 Why?
Cell Survival1201058810.010 Why?
Cell Movement1201152160.010 Why?
Genome-Wide Association Study12018122590.010 Why?
Japan1200313600.010 Why?
Alternative Splicing1200411170.010 Why?
Cell Membrane1200837490.010 Why?
Family Health1200312800.010 Why?
Transcription, Genetic1201277190.010 Why?
Functional Laterality1200422800.010 Why?
Reverse Transcriptase Polymerase Chain Reaction1200447490.010 Why?
Chromosome Mapping1200247370.010 Why?
Cell Line12008159930.010 Why?
Aged, 80 and over12018577440.010 Why?
Diagnosis, Differential12008129540.010 Why?
Gene Expression Profiling1200894400.010 Why?
Mice, Inbred C57BL12010218240.010 Why?
Cognition Disorders1200540410.010 Why?
Prospective Studies12014532500.010 Why?
Tomography, X-Ray Computed12009201210.000 Why?
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Concepts (237)
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© 2024 President and Fellows of Harvard College
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.