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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.
Cloud
Categories
Timeline
Details
In this concept 'cloud', the sizes of the concepts are based not only on the number of corresponding publications, but also how relevant the concepts are to the overall topics of the publications, how long ago the publications were written, whether the person was the first or senior author, and how many other people have written about the same topic. The largest concepts are those that are most unique to this person.
Abducens Nerve
Abnormalities, Multiple
Accommodation, Ocular
Adolescent
Adult
Age Factors
Age of Onset
Aged
Aged, 80 and over
Albinism, Oculocutaneous
Alleles
Alternative Splicing
Amino Acid Motifs
Amino Acid Sequence
Amino Acid Substitution
Anal Canal
Animals
Animals, Genetically Modified
Animals, Newborn
Anisotropy
Arthrogryposis
Autistic Disorder
Axons
Base Sequence
Blepharoptosis
Brain
Brain Stem
Cardiovascular Abnormalities
Carotid Artery, Internal
Case-Control Studies
Cataract
Cell Count
Cell Fusion
Cell Line
Cell Membrane
Cell Movement
Cell Survival
Central Nervous System
Cerebral Cortex
Chick Embryo
Child
Child, Preschool
Chimerin 1
Chromatography, High Pressure Liquid
Chromosome Mapping
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 12
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 20
Codon, Nonsense
Cognition Disorders
Color Vision Defects
Colorectal Neoplasms
Consanguinity
Corpus Callosum
Cranial Nerve Diseases
Deafness
Developmental Disabilities
Diagnosis, Differential
Diffusion Magnetic Resonance Imaging
Diffusion Tensor Imaging
Disease Models, Animal
Disease Progression
Diseases in Twins
DNA Mutational Analysis
DNA-Binding Proteins
Duane Retraction Syndrome
Ear, Inner
Embryo, Mammalian
Embryo, Nonmammalian
Endocrine System Diseases
Endophenotypes
Esophagus
Esotropia
Evoked Potentials, Motor
Evoked Potentials, Somatosensory
Exons
Exotropia
Eye Abnormalities
Eye Diseases
Eye Diseases, Hereditary
Eye Movements
Eye Proteins
Facial Paralysis
Family Health
Female
Fibrosis
Fluorescent Antibody Technique
Founder Effect
Fovea Centralis
Functional Laterality
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Genes, Dominant
Genes, Recessive
Genetic Association Studies
Genetic Complementation Test
Genetic Linkage
Genetic Predisposition to Disease
Genetic Variation
Genome-Wide Association Study
Genotype
Glutamic Acid
Green Fluorescent Proteins
Haplotypes
Hearing Loss
Hearing Loss, Sensorineural
Heart Defects, Congenital
Heart Septal Defects, Atrial
HEK293 Cells
Heterozygote
Homeodomain Proteins
Homozygote
Humans
Immunohistochemistry
In Situ Hybridization
Infant
Inheritance Patterns
Introns
Iran
Iris Diseases
Japan
Kallmann Syndrome
Kidney
Klippel-Feil Syndrome
Labyrinth Diseases
Limb Deformities, Congenital
Lod Score
Loss of Heterozygosity
Lower Extremity Deformities, Congenital
Lysine
MafB Transcription Factor
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Malignant Hyperthermia
Manometry
Medulla Oblongata
Membrane Proteins
Metalloendopeptidases
Mice
Mice, Inbred C57BL
Mice, Knockout
Mice, Transgenic
Microsatellite Repeats
Microtubule-Associated Proteins
Microtubules
Middle Aged
Mobius Syndrome
Models, Molecular
Molecular Sequence Data
Morphogenesis
Motor Activity
Motor Neurons
Movement Disorders
Muscle Denervation
Muscle Proteins
Muscle, Skeletal
Muscular Diseases
Mutation
Mutation, Missense
Myoblasts
MyoD Protein
Myogenic Regulatory Factor 5
Nerve Tissue Proteins
Neural Pathways
Neurogenesis
Neurons
Neuropsychological Tests
Nuclear Proteins
Nystagmus, Congenital
Ocular Motility Disorders
Oculomotor Muscles
Oculomotor Nerve
Odds Ratio
Ophthalmic Nerve
Ophthalmoplegia
Ophthalmoscopy
Optic Nerve
Organ Size
Paired Box Transcription Factors
Pedigree
Phenotype
Pierre Robin Syndrome
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Pons
Prospective Studies
Protein Binding
Protein Structure, Tertiary
Protein Transport
Psychomotor Performance
Pyramidal Tracts
rac GTP-Binding Proteins
Receptor, EphA4
Receptors, Cell Surface
Receptors, CXCR
Receptors, Immunologic
Repressor Proteins
Reverse Transcriptase Polymerase Chain Reaction
Rhombencephalon
Ribs
Ryanodine Receptor Calcium Release Channel
Saudi Arabia
Scoliosis
Sequence Alignment
Sequence Analysis, DNA
Sequence Analysis, Protein
Sequence Homology, Amino Acid
Siblings
Signal Transduction
Spinal Canal
Spinal Cord
Spine
Strabismus
Syndrome
Synkinesis
Tomography, Optical Coherence
Tomography, X-Ray Computed
Trachea
Transcription Factors
Transcription, Genetic
Transcriptional Activation
Tubulin
Turkey
Twins, Dizygotic
Upper Extremity Deformities, Congenital
Vision Disorders
Visual Acuity
Vomiting
Young Adult
Zebrafish
Zebrafish Proteins
Zinc Fingers
Chan's Networks
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Concepts (237)
Derived automatically from this person's publications.
Chimerin 1
Tubulin
Ocular Motility Disorders
Mobius Syndrome
Duane Retraction Syndrome
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Co-Authors (29)
People in Profiles who have published with this person.
MacKinnon, Sarah
Engle, Elizabeth
Robson, Caroline
Hunter, David
Whitman, Mary
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_
Similar People (60)
People who share similar concepts with this person.
Dagi, Linda
Engle, Elizabeth
Alkuraya, Fowzan
Hunter, David
Chung, Wendy
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_
Same Department
People in same department with this person.
Abbaspoor, Saman
Andzelm, Milena
Jiang, Qiufen
Joshi, Rasesh
Mohammadpour Touserkani, Fatemeh
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_