Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Wai-Man Chan, A.L.M.

Concepts (237)

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 Syndrome92017591.060 Why?
Chimerin 152017130.790 Why?
Tubulin820196920.760 Why?
Ocular Motility Disorders620191440.720 Why?
Mobius Syndrome72017410.660 Why?
Ophthalmoplegia1120191680.620 Why?
Mutation, Missense10201325670.550 Why?
Oculomotor Muscles1020164060.510 Why?
Eye Diseases, Hereditary620151220.480 Why?
Pedigree23201945370.420 Why?
Fibrosis13201920510.390 Why?
Strabismus320123170.350 Why?
Mutation172019300060.340 Why?
Oculomotor Nerve42014720.290 Why?
Amino Acid Substitution9201917370.290 Why?
Homeodomain Proteins9201424130.280 Why?
Pyramidal Tracts220192510.240 Why?
Receptors, Immunologic3200914080.220 Why?
DNA Mutational Analysis10201941090.210 Why?
Malformations of Cortical Development220151760.200 Why?
Scoliosis220067900.190 Why?
Fovea Centralis220131260.190 Why?
Axons6201416710.190 Why?
Genetic Linkage7201923400.170 Why?
Nerve Tissue Proteins4200744050.170 Why?
Synkinesis12019230.170 Why?
Receptors, CXCR12019520.170 Why?
Kallmann Syndrome320191390.160 Why?
Myogenic Regulatory Factor 512018260.160 Why?
Genes, Dominant220138500.150 Why?
Receptor, EphA412017170.140 Why?
Esotropia12018990.140 Why?
Hearing Loss220167820.140 Why?
MafB Transcription Factor12016250.130 Why?
Ribs120182600.130 Why?
Embryo, Mammalian3201716680.130 Why?
Myoblasts120172310.130 Why?
Amino Acid Sequence92019134040.130 Why?
Pierre Robin Syndrome120171170.120 Why?
Abnormalities, Multiple2201314220.120 Why?
Labyrinth Diseases120161510.120 Why?
Morphogenesis220177410.120 Why?
Loss of Heterozygosity120176630.120 Why?
Corpus Callosum120197500.120 Why?
Phenotype132018165720.110 Why?
Blepharoptosis420141440.110 Why?
Molecular Sequence Data82015175980.110 Why?
Nystagmus, Congenital1201390.110 Why?
Malignant Hyperthermia12013710.110 Why?
Muscular Diseases120175520.100 Why?
Paired Box Transcription Factors120132060.100 Why?
Arthrogryposis12013680.100 Why?
Ryanodine Receptor Calcium Release Channel120131810.100 Why?
Pons120132400.100 Why?
Endocrine System Diseases120152490.100 Why?
Muscle Proteins1201711490.100 Why?
Transcription Factors82014120960.100 Why?
Motor Neurons120178690.100 Why?
Klippel-Feil Syndrome12011190.100 Why?
Metalloendopeptidases120133890.100 Why?
Albinism, Oculocutaneous12011190.090 Why?
Color Vision Defects12011280.090 Why?
Psychomotor Performance1201918810.090 Why?
Syndrome6201932690.090 Why?
Spine1201811280.090 Why?
Iris Diseases12011370.090 Why?
Polymorphism, Single Nucleotide62019159150.090 Why?
Zebrafish Proteins1201710120.090 Why?
Base Sequence32012124040.090 Why?
Eye Proteins120136320.080 Why?
Vomiting120136510.080 Why?
Motor Activity1201927120.080 Why?
Exotropia22014640.080 Why?
Eye Abnormalities120112410.080 Why?
Cerebral Cortex3201957770.080 Why?
Polymerase Chain Reaction4201460670.080 Why?
Consanguinity420134570.080 Why?
Facial Paralysis120123460.080 Why?
Movement Disorders120114590.070 Why?
Child172019801340.070 Why?
Eye Movements420145110.070 Why?
Chromatography, High Pressure Liquid1201115350.070 Why?
Cataract120138320.070 Why?
Receptors, Cell Surface4201728020.070 Why?
Male3320193606750.070 Why?
Hearing Loss, Sensorineural120127810.060 Why?
Gene Expression Regulation, Developmental1201735980.060 Why?
Developmental Disabilities3201515100.060 Why?
Heterozygote4201927780.060 Why?
Female3120193924580.060 Why?
Inheritance Patterns120073410.060 Why?
Sequence Homology, Amino Acid3201727410.060 Why?
Cardiovascular Abnormalities120051430.060 Why?
Rhombencephalon12004800.060 Why?
Nuclear Proteins1201857810.050 Why?
Sequence Alignment2201821750.050 Why?
Humans4120197610980.050 Why?
Visual Acuity2201126770.050 Why?
Exons3201823800.050 Why?
Protein Structure, Tertiary2200737790.050 Why?
Genetic Predisposition to Disease42019178890.050 Why?
Chromosomes, Human, Pair 20120021270.050 Why?
Repressor Proteins1201329740.050 Why?
Lod Score320136000.050 Why?
Homozygote3201317750.050 Why?
Codon, Nonsense120032840.050 Why?
Child, Preschool92018422170.050 Why?
Muscle, Skeletal1201749470.050 Why?
Neurons4201794350.050 Why?
Chromosomes, Human, Pair 12120034300.050 Why?
Alleles3201968570.050 Why?
Deafness120054590.050 Why?
Abducens Nerve22011280.040 Why?
Chromosomes, Human, Pair 16120023430.040 Why?
Membrane Proteins1201778440.040 Why?
Brain Stem120058580.040 Why?
Protein Transport2201919590.040 Why?
Chromosomes, Human, Pair 2220113130.040 Why?
Turkey220132540.040 Why?
Neural Pathways3201930570.040 Why?
Accommodation, Ocular12018470.040 Why?
Infant52017361640.040 Why?
MyoD Protein120181410.040 Why?
Tomography, Optical Coherence1201129230.040 Why?
Adult1420192210830.040 Why?
Mice, Knockout32018143930.040 Why?
Magnetic Resonance Imaging82019364180.040 Why?
Endophenotypes120192550.040 Why?
Limb Deformities, Congenital120181360.040 Why?
Introns220109680.030 Why?
Colorectal Neoplasms1201769190.030 Why?
Brain42019270970.030 Why?
Genotype32019129830.030 Why?
Cell Fusion120172940.030 Why?
Genetic Complementation Test120175560.030 Why?
Eye Diseases120026530.030 Why?
Diffusion Tensor Imaging2201924010.030 Why?
Autistic Disorder1200512220.030 Why?
Anisotropy1201912840.030 Why?
Gene Expression2201975670.030 Why?
Neurogenesis220128610.030 Why?
Anal Canal120183740.030 Why?
Microtubules2201210710.030 Why?
Fluorescent Antibody Technique1201924680.030 Why?
Siblings120198240.030 Why?
Animals920191680830.030 Why?
Genes, Recessive120176220.030 Why?
Animals, Genetically Modified1201915590.030 Why?
Organ Size1201922530.030 Why?
Mice62019813240.030 Why?
Embryo, Nonmammalian120179040.030 Why?
Signal Transduction12017234150.030 Why?
Disease Models, Animal32019182170.030 Why?
Twins, Dizygotic120132360.030 Why?
Young Adult52019591990.030 Why?
Chromosomes, Human, Pair 11120134100.030 Why?
Sequence Analysis, DNA3201347390.030 Why?
Esophagus1201810330.020 Why?
Trachea1201810900.020 Why?
Lower Extremity Deformities, Congenital12011120.020 Why?
Adolescent72018882710.020 Why?
Founder Effect120121850.020 Why?
Diseases in Twins120134460.020 Why?
Upper Extremity Deformities, Congenital12011320.020 Why?
Ophthalmic Nerve12011420.020 Why?
Case-Control Studies22019221570.020 Why?
Models, Molecular2201254130.020 Why?
Cranial Nerve Diseases120111100.020 Why?
rac GTP-Binding Proteins120111620.020 Why?
Lysine120159830.020 Why?
Age Factors22019183850.020 Why?
Genetic Association Studies1201927310.020 Why?
Cell Count1201418310.020 Why?
Muscle Denervation12009600.020 Why?
Central Nervous System1201713330.020 Why?
Glutamic Acid1201511730.020 Why?
Disease Progression12006135060.020 Why?
Spinal Cord1201718070.020 Why?
Microtubule-Associated Proteins1201410740.020 Why?
Heart Septal Defects, Atrial120114510.020 Why?
Green Fluorescent Proteins1201420610.020 Why?
Animals, Newborn1201426660.020 Why?
Heart Defects, Congenital2201846730.020 Why?
Genetic Variation1200365650.020 Why?
Optic Nerve120115710.020 Why?
Diffusion Magnetic Resonance Imaging1201927870.020 Why?
Haplotypes2200427140.020 Why?
Chick Embryo120089770.020 Why?
Age of Onset1201333070.020 Why?
Neuropsychological Tests1201970430.020 Why?
Transcriptional Activation1201217510.020 Why?
Odds Ratio1201896480.020 Why?
Immunohistochemistry12019110660.020 Why?
Zebrafish1201730010.020 Why?
Saudi Arabia120052100.020 Why?
Gene Expression Regulation22014118560.010 Why?
HEK293 Cells1201442500.010 Why?
Vision Disorders1201110880.010 Why?
Spinal Canal12003400.010 Why?
Ophthalmoscopy120031710.010 Why?
Carotid Artery, Internal120054450.010 Why?
Kidney1201870340.010 Why?
Medulla Oblongata120042480.010 Why?
Evoked Potentials, Somatosensory120042470.010 Why?
Microsatellite Repeats120047820.010 Why?
Middle Aged520182208350.010 Why?
Amino Acid Motifs120049250.010 Why?
Sequence Analysis, Protein120022610.010 Why?
Mice, Transgenic1201495180.010 Why?
Ear, Inner120054250.010 Why?
Manometry120034530.010 Why?
DNA-Binding Proteins1201895660.010 Why?
Evoked Potentials, Motor120044640.010 Why?
Iran120037360.010 Why?
Aged420181692660.010 Why?
Zinc Fingers120025750.010 Why?
Protein Binding1201293000.010 Why?
In Situ Hybridization1200419000.010 Why?
Cell Survival1201057760.010 Why?
Cell Movement1201151950.010 Why?
Japan1200313730.010 Why?
Genome-Wide Association Study12018126700.010 Why?
Alternative Splicing1200410870.010 Why?
Cell Membrane1200836650.010 Why?
Family Health1200312550.010 Why?
Transcription, Genetic1201275740.010 Why?
Functional Laterality1200422560.010 Why?
Reverse Transcriptase Polymerase Chain Reaction1200445650.010 Why?
Cell Line12008155420.010 Why?
Chromosome Mapping1200246120.010 Why?
Aged, 80 and over12018589460.010 Why?
Diagnosis, Differential12008129750.010 Why?
Gene Expression Profiling1200894160.010 Why?
Mice, Inbred C57BL12010221290.010 Why?
Cognition Disorders1200539740.010 Why?
Prospective Studies12014544190.010 Why?
Tomography, X-Ray Computed12009206000.000 Why?
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Concepts (237)
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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.