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Pediatrics CRA
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SAU WAI CHEUNG
Concepts (676)
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Concepts are derived automatically from a person's publications.
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Categories
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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.
14-3-3 Proteins
1-Alkyl-2-acetylglycerophosphocholine Esterase
3' Untranslated Regions
3-Phosphoinositide-Dependent Protein Kinases
Abnormal Karyotype
Abnormalities, Multiple
Abortion, Habitual
Abortion, Spontaneous
Acoustic Stimulation
Actin-Related Protein 2-3 Complex
Actins
Acyl-CoA Dehydrogenase, Long-Chain
Adaptor Proteins, Signal Transducing
Adolescent
Adult
Age of Onset
Aged
Aged, 80 and over
Agenesis of Corpus Callosum
Aging
Aging, Premature
Alagille Syndrome
Algorithms
Alkynes
Alleles
Allelic Imbalance
alpha7 Nicotinic Acetylcholine Receptor
Alu Elements
Amino Acid Sequence
Amino Acid Substitution
Amniocentesis
Amniotic Fluid
Anal Canal
Analysis of Variance
Anemia, Diamond-Blackfan
Anesthesia
Anesthetics, Inhalation
Aneuploidy
Angelman Syndrome
Animals
Animals, Genetically Modified
Antigens, CD
Antigens, Neoplasm
Antigens, Nuclear
Antitubercular Agents
Anus, Imperforate
Aorta, Thoracic
Aortic Coarctation
Aortography
Apoptosis Regulatory Proteins
Aryl Hydrocarbon Hydroxylases
Asialoglycoprotein Receptor
Attention Deficit Disorder with Hyperactivity
Auditory Cortex
Auditory Threshold
Autism Spectrum Disorder
Autistic Disorder
Autoantigens
Azoospermia
Azure Stains
Bacterial Infections
Basal Cell Nevus Syndrome
Base Composition
Base Sequence
Bayes Theorem
Behavior, Animal
Benzoxazines
Binomial Distribution
Biological Evolution
Biological Variation, Population
Biomarkers
Biopsy
Bipolar Disorder
Bisbenzimidazole
Bladder Exstrophy
Blastocyst
Blepharoptosis
Body Dysmorphic Disorders
Body Height
Bone and Bones
Bone Diseases, Metabolic
Bone Morphogenetic Protein 2
Bone Morphogenetic Protein Receptors, Type I
Brain
Brain Neoplasms
Branchio-Oto-Renal Syndrome
Bromodeoxyuridine
Bronchopulmonary Dysplasia
Calcium-Binding Proteins
Capillaries
Cardiovascular Abnormalities
Cardiovascular Diseases
Carrier Proteins
Case-Control Studies
Catenins
Cats
CD11b Antigen
Cell Adhesion Molecules, Neuronal
Cell Cycle Proteins
Cell Division
Cell Line
Cell Line, Tumor
Cell-Free Nucleic Acids
Cells, Cultured
Cerebellum
Charcot-Marie-Tooth Disease
Chemical and Drug Induced Liver Injury
Child
Child Behavior
Child Behavior Disorders
Child Development Disorders, Pervasive
Child, Preschool
Chi-Square Distribution
Choanal Atresia
Cholesterol
Cholesterol Esters
Chondroitin Sulfate Proteoglycans
Chorionic Gonadotropin, beta Subunit, Human
Chorionic Villi
Chorionic Villi Sampling
Chromatin
Chromatin Assembly and Disassembly
Chromatography, High Pressure Liquid
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Banding
Chromosome Breakage
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Inversion
Chromosome Mapping
Chromosome Painting
Chromosomes
Chromosomes, Artificial, Bacterial
Chromosomes, Human
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 12
Chromosomes, Human, Pair 13
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 19
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 21
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 9
Chromosomes, Human, X
Chromosomes, Human, Y
Ciprofloxacin
Classical Lissencephalies and Subcortical Band Heterotopias
Cleavage And Polyadenylation Specificity Factor
Cleft Palate
Clinical Laboratory Techniques
Clinical Trials as Topic
Cloaca
Clone Cells
Cloning, Molecular
Cognition
Cognition Disorders
Cohort Studies
Coloboma
Color
Comparative Genomic Hybridization
Computational Biology
Congenital Abnormalities
Core Binding Factor Alpha 2 Subunit
CpG Islands
Craniofacial Abnormalities
CREB-Binding Protein
Cri-du-Chat Syndrome
Cross-Sectional Studies
Culture Media
Culture Techniques
Cyclopropanes
Cytochrome P-450 CYP2B6
Cytodiagnosis
Cytogenetic Analysis
Cytogenetics
Cytological Techniques
Cytoplasmic Dyneins
Cytoskeletal Proteins
Databases, Genetic
DAX-1 Orphan Nuclear Receptor
De Lange Syndrome
Decidua
Decision Making
Developmental Disabilities
Diagnosis
Diagnosis, Differential
Diaphragmatic Eventration
DiGeorge Syndrome
Disease
Disease Management
Disease Models, Animal
Diseases in Twins
Dishevelled Proteins
Disorders of Sex Development
DNA
DNA Breaks
DNA Copy Number Variations
DNA End-Joining Repair
DNA Helicases
DNA Methylation
DNA Mutational Analysis
DNA Probes
DNA Repair
DNA Replication
DNA-Binding Proteins
Dopamine beta-Hydroxylase
Down Syndrome
Doxorubicin
Drug Evaluation
Drug Therapy, Combination
Dwarfism
E1A-Associated p300 Protein
Echocardiography
Ectodysplasins
Electrocardiography
Electrophysiology
Embryo Transfer
Embryo, Mammalian
Embryo, Nonmammalian
Embryonic and Fetal Development
Embryonic Development
Endocrine System
Endogenous Retroviruses
Endoglin
Endopeptidases
Epigenesis, Genetic
Epigenomics
Epilepsy
Erythropoiesis
Esophagus
Estrogen Receptor alpha
Estrogens
Evolution, Molecular
Excitatory Postsynaptic Potentials
Exome
Exons
Eye Abnormalities
Eye Proteins
Face
Facies
Failure to Thrive
False Positive Reactions
Family
Family Health
Fatal Outcome
Fathers
Feasibility Studies
Female
Fertility
Fertilization in Vitro
Fetal Diseases
Fetal Growth Retardation
Fetus
Fibroblasts
Flow Cytometry
Fluorescent Dyes
Follow-Up Studies
Foot Deformities, Congenital
Forkhead Transcription Factors
Fractures, Bone
Fragile X Mental Retardation Protein
Fragile X Syndrome
Frameshift Mutation
Gametogenesis
GATA4 Transcription Factor
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Frequency
Gene Knockdown Techniques
Gene Order
Gene Rearrangement
Gene Silencing
Genes, Dominant
Genes, Duplicate
Genes, Recessive
Genes, Wilms Tumor
Genes, X-Linked
Genetic Association Studies
Genetic Background
Genetic Carrier Screening
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Heterogeneity
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genitalia
Genome
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomic Instability
Genomics
Genotype
Genotyping Techniques
Germ Cells
Germ-Line Mutation
Gestational Age
Globus Pallidus
Glycoproteins
Goldenhar Syndrome
Gonadal Dysgenesis, Mixed
Granulocyte-Macrophage Colony-Stimulating Factor
Growth and Development
GTPase-Activating Proteins
Guanine Nucleotide Exchange Factors
Guidelines as Topic
Hair Color
Hand Deformities, Congenital
Haploinsufficiency
Haplotypes
Hearing Loss
Hearing Loss, Sensorineural
Heart Defects, Congenital
Heart Ventricles
Hematologic Neoplasms
Hemophilia A
Hepatocyte Nuclear Factor 1-beta
Hernia, Diaphragmatic
Hernia, Umbilical
Hernias, Diaphragmatic, Congenital
Heterochromatin
Heterozygote
High Mobility Group Proteins
High-Throughput Nucleotide Sequencing
Hippocampus
Hirsutism
Histone-Lysine N-Methyltransferase
HIV Infections
HIV-1
Homeodomain Proteins
Homologous Recombination
Homozygote
Hong Kong
Horner Syndrome
Human Genome Project
Humans
Hydatidiform Mole
Hyperkinesis
Hypnotics and Sedatives
Hypoplastic Left Heart Syndrome
Hypotension, Orthostatic
Hypotrichosis
Immunohistochemistry
In Situ Hybridization, Fluorescence
In Vitro Techniques
INDEL Mutation
Infant
Infant, Newborn
Infertility, Male
Inheritance Patterns
Inhibitory Postsynaptic Potentials
Intellectual Disability
Intercellular Signaling Peptides and Proteins
Internationality
Interspersed Repetitive Sequences
Intracellular Signaling Peptides and Proteins
Introns
Inverted Repeat Sequences
Isochromosomes
Isoflurane
Jagged-1 Protein
Karyotype
Karyotyping
Kidney
Klebsiella Infections
Klinefelter Syndrome
Language Development Disorders
Language Disorders
Leukemia, Lymphocytic, Chronic, B-Cell
Leukemia, Myeloid, Acute
Leukoencephalopathies
Limb Deformities, Congenital
Limit of Detection
Lipoproteins, HDL
Lipoproteins, LDL
Lipoproteins, VLDL
Lithium
Long Interspersed Nucleotide Elements
Longitudinal Studies
Loss of Heterozygosity
Lyases
Lymphocytes
MADS Domain Proteins
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
MAP Kinase Kinase 6
Maternal Age
MEF2 Transcription Factors
Megakaryocytes
Megalencephaly
Membrane Proteins
Menotropins
Mental Disorders
Mental Retardation, X-Linked
Mesencephalon
Metaphase
Methyl-CpG-Binding Protein 2
Methyltransferases
Mice
Mice, Transgenic
Microarray Analysis
Microcephaly
Microdissection
Microfilament Proteins
Micrognathism
Microsatellite Repeats
Microtubule-Associated Proteins
Middle Aged
Minisatellite Repeats
Mitochondria
Mitochondrial Diseases
Mitosis
Mitotic Index
Models, Animal
Models, Genetic
Models, Theoretical
Molecular Chaperones
Molecular Diagnostic Techniques
Molecular Sequence Data
Monocytes
Monosomy
Mosaicism
Mothers
Multifactorial Inheritance
Multigene Family
Multiple Trauma
Munc18 Proteins
Muscle Hypotonia
Mutagenesis, Insertional
Mutation
Mutation Rate
Mutation, Missense
Mutism
Mycobacterium tuberculosis
Myelin Proteins
Myelin Proteolipid Protein
Myogenic Regulatory Factors
NADPH Oxidases
Nails, Malformed
Natural Cytotoxicity Triggering Receptor 3
NAV1.2 Voltage-Gated Sodium Channel
NAV1.3 Voltage-Gated Sodium Channel
Neck
Neoplasm Proteins
Neoplasms
Nerve Growth Factors
Nerve Net
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Neural Cell Adhesion Molecules
Neurodevelopmental Disorders
Neurofibromatosis 1
Neurofibromatosis 2
Neurons
Neurons, Afferent
Nuchal Translucency Measurement
Nuclear Proteins
Nucleic Acid Amplification Techniques
Nucleic Acid Hybridization
Nucleotide Motifs
Obesity
Ofloxacin
Oligonucleotide Array Sequence Analysis
Oligonucleotide Probes
Oligospermia
Oncogene Proteins
Organ Size
Otx Transcription Factors
Ovulation Induction
Paired Box Transcription Factors
Parents
Patched Receptors
Patched-1 Receptor
Pathology, Molecular
PAX6 Transcription Factor
Pedigree
Pelizaeus-Merzbacher Disease
Penetrance
Pentobarbital
Peptide Termination Factors
Phenotype
Phosphoproteins
Physical Chromosome Mapping
Pierre Robin Syndrome
Pilot Projects
Placenta
Pleural Effusion
Point Mutation
Polyadenylation
Polyhydramnios
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Prader-Willi Syndrome
Predictive Value of Tests
Pregnancy
Pregnancy Outcome
Pregnancy Trimester, First
Pregnancy Trimester, Second
Pregnancy, High-Risk
Pregnancy, Twin
Pregnancy-Associated Plasma Protein-A
Preimplantation Diagnosis
Prenatal Diagnosis
Probability
Problem Behavior
Prognosis
Prospective Studies
Proteasome Endopeptidase Complex
Protein Array Analysis
Protein Interaction Maps
Protein Isoforms
Protein Tyrosine Phosphatase, Non-Receptor Type 11
Protein Tyrosine Phosphatases
Proteins
Proto-Oncogene Proteins
Pseudogenes
Psychological Tests
Psychomotor Performance
Pulmonary Alveolar Proteinosis
Pulmonary Alveoli
Pulmonary Surfactants
Pulmonary Veins
Quantitative Trait Loci
Quantitative Trait, Heritable
Radiography
Reaction Time
Real-Time Polymerase Chain Reaction
Receptor Tyrosine Kinase-like Orphan Receptors
Receptor, IGF Type 1
Receptors, Androgen
Receptors, Cell Surface
Receptors, G-Protein-Coupled
Receptors, Granulocyte-Macrophage Colony-Stimulating Factor
Receptors, Nicotinic
Receptors, Odorant
Receptors, Retinoic Acid
Receptors, Transforming Growth Factor beta
Recombination, Genetic
Recurrence
Reference Standards
Reference Values
Regulatory Sequences, Nucleic Acid
Repetitive Sequences, Nucleic Acid
Repressor Proteins
Reproducibility of Results
Retrospective Studies
Rett Syndrome
Reverse Transcriptase Inhibitors
Reverse Transcriptase Polymerase Chain Reaction
Rho Guanine Nucleotide Exchange Factors
Ribonucleoproteins, Small Nuclear
Ring Chromosomes
Risk
Risk Factors
RNA, Long Noncoding
RNA, Messenger
RNA, Small Nucleolar
R-SNARE Proteins
Rubinstein-Taybi Syndrome
Schizophrenia
Scoliosis
Segmental Duplications, Genomic
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Sequence Homology, Nucleic Acid
Serrate-Jagged Proteins
Sex Characteristics
Sex Chromosome Aberrations
Sex Chromosome Disorders
Sex Chromosome Disorders of Sex Development
Sex Chromosomes
Sex Determination Analysis
Sex Factors
Sexual Development
Short Rib-Polydactyly Syndrome
Short Stature Homeobox Protein
Siblings
Signal Transduction
Single-Cell Analysis
Sister Chromatid Exchange
Skin Pigmentation
SMARCB1 Protein
Smith-Magenis Syndrome
snRNP Core Proteins
Social Behavior
Sodium Channels
SOX9 Transcription Factor
SOXB1 Transcription Factors
Spasms, Infantile
Speech Disorders
Spermatozoa
Spine
Syndactyly
Syndrome
T-Box Domain Proteins
Telomere
Templates, Genetic
Terminal Repeat Sequences
Tetraspanins
Texas
Thoracic Injuries
Thrombocytopenia
Time Factors
Tomography, X-Ray Computed
Trachea
Trans-Activators
Transcription Factors
Transcription, Genetic
Translocation, Genetic
Trisomy
Trisomy 13 Syndrome
Trisomy 18 Syndrome
Trophoblasts
Tuberculosis
Tuberculosis, Pulmonary
Turner Syndrome
Twins
Twins, Dizygotic
Twins, Monozygotic
Ubiquitin Thiolesterase
Ubiquitin-Protein Ligases
Ultrasonography
Ultrasonography, Prenatal
Uniparental Disomy
Up-Regulation
Urinary Bladder
Urogenital Abnormalities
Urogenital System
Uterus
Vacuolar Proton-Translocating ATPases
Valproic Acid
Vascular System Injuries
Vesicular Acetylcholine Transport Proteins
WAGR Syndrome
Whole Genome Sequencing
Williams Syndrome
Wolff-Parkinson-White Syndrome
Wolf-Hirschhorn Syndrome
Wounds, Stab
WT1 Proteins
X Chromosome
X Chromosome Inactivation
Xenopus laevis
Y Chromosome
Young Adult
Zebrafish
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Concepts (676)
Derived automatically from this person's publications.
Chromosome Aberrations
Chromosome Deletion
Comparative Genomic Hybridization
Oligonucleotide Array Sequence Analysis
DNA Copy Number Variations
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Co-Authors (90)
People in Profiles who have published with this person.
STANKIEWICZ, PAWEL
LUPSKI, JAMES
BI, WEIMIN
NAGAMANI, SANDESH
BACINO, CARLOS
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
STANKIEWICZ, PAWEL
BOERWINKLE, ERIC
GIBBS, RICHARD
BACINO, CARLOS
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Same Department
People who are also in this person's primary department.
BACINO, CARLOS
DUDCHENKO, OLGA
KAIPPARETTU, BENNY
KETKAR, SHAMIKA
WANG, BAIPING
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People whose addresses are nearby this person.
EVANS, GINA
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