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Raymond Wang
Concepts (349)
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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.
2-Hydroxypropyl-beta-cyclodextrin
Abnormalities, Multiple
Acidosis, Lactic
Acyl Coenzyme A
Acyl-CoA Dehydrogenase
Acyl-CoA Dehydrogenase, Long-Chain
Acyl-CoA Oxidase
Adenoidectomy
Adipose Tissue, Brown
Administration, Oral
Adolescent
Adrenal Insufficiency
Adult
Age Factors
Age of Onset
Aged
Aged, 80 and over
Algorithms
alpha-Galactosidase
alpha-Glucosidases
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acids, Branched-Chain
Aminopeptidases
Amyloid beta-Protein Precursor
Anal Canal
Anemia
Anemia, Sideroblastic
Animals
Antibodies
Antibodies, Monoclonal, Murine-Derived
Antibodies, Neutralizing
Aorta
Aortic Diseases
Asymptomatic Diseases
ATPases Associated with Diverse Cellular Activities
Autoantibodies
Base Sequence
Bile Acids and Salts
Biomarkers
Biopsy
Blood Glucose
Blood Pressure
Blood Vessels
Blood-Brain Barrier
Blotting, Western
Body Fluids
Bone Diseases, Metabolic
Bortezomib
Brain
Brain Diseases, Metabolic, Inborn
Brain Mapping
Cachexia
California
Cardiomegaly
Cardiomyopathies
Cardiomyopathy, Dilated
Cardiomyopathy, Hypertrophic
Cardiopulmonary Bypass
Cardiovascular Diseases
Career Choice
Carnitine
Carotid Arteries
Carotid Intima-Media Thickness
Cartilage, Articular
Case-Control Studies
Cats
Cells, Cultured
Cervical Vertebrae
Child
Child, Preschool
Chondrocytes
Chondroitin Sulfates
Chondroitinsulfatases
Chromatin
Chromatography, Liquid
Clinical Laboratory Techniques
Clinical Trials as Topic
Clusterin
Codon, Nonsense
Cognitive Dysfunction
Cohort Studies
Congenital Abnormalities
Congenital Disorders of Glycosylation
Congresses as Topic
Consanguinity
Consensus
Coronary Artery Disease
Coronary Vessels
Corpus Callosum
Cough
CRISPR-Cas Systems
Cross Reactions
Cross-Over Studies
Cross-Sectional Studies
Deglutition
Deglutition Disorders
Developmental Disabilities
Diabetes Mellitus
Diet, Ketogenic
Diet, Protein-Restricted
Diffusion Tensor Imaging
Dilatation, Pathologic
Dipeptidyl-Peptidases and Tripeptidyl-Peptidases
Disability Evaluation
Disease Management
Disease Models, Animal
DNA Mutational Analysis
DNA, Mitochondrial
Dogs
Dose-Response Relationship, Drug
Dried Blood Spot Testing
Early Diagnosis
Ehlers-Danlos Syndrome
Elasticity
Electron Transport Complex I
Electron Transport Complex III
Endocrine System
Energy Metabolism
Enzyme Replacement Therapy
Epigenesis, Genetic
Epilepsy
Exercise Test
Exome
Exons
Fabry Disease
Fatal Outcome
Fatty Acids
Female
Follow-Up Studies
Galactosylceramidase
Gastroesophageal Reflux
Gene Deletion
Gene Expression
Gene Expression Regulation
Gene Knock-In Techniques
Gene Regulatory Networks
Genes, Lethal
Genetic Association Studies
Genetic Linkage
Genetic Testing
Genetic Therapy
Genetics, Medical
Genomics
Genotype
Glucan 1,4-alpha-Glucosidase
Glucuronidase
Glyceric Acids
Glycine
Glycogen
Glycogen Storage Disease Type II
Glycosaminoglycans
Glycosylation
Granuloma, Pyogenic
Head Movements
Health Services Accessibility
Health Surveys
Hearing Loss
Heart Defects, Congenital
Heart Diseases
Heart Rate
Heart Valve Diseases
HEK293 Cells
Hematopoietic Stem Cell Transplantation
Heterozygote
Homeodomain Proteins
Homozygote
Hormone Replacement Therapy
Humans
Hydrolases
Hyperammonemia
Hyperglycemia
Hyperoxaluria, Primary
Hypertriglyceridemia
Hypoglycemia
Iduronidase
Image Processing, Computer-Assisted
Immunoglobulins
Immunoglobulins, Intravenous
Immunomodulation
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Inflammation
Infusion Pumps
Infusions, Intraventricular
Injections, Subcutaneous
Insulin
Intellectual Disability
Interdisciplinary Communication
Internationality
Intracellular Signaling Peptides and Proteins
Ireland
Isoenzymes
Isoleucine
Kaplan-Meier Estimate
Ketosis
Laser Therapy
Leigh Disease
Leucine
Leukodystrophy, Globoid Cell
Lipid Metabolism
Lipid Metabolism, Inborn Errors
Longitudinal Studies
Lung
Lung Diseases, Obstructive
Lysosomal Storage Diseases
Lysosomes
Magnetic Resonance Imaging
Male
Malonates
Mannosyltransferases
Maple Syrup Urine Disease
Medical Records
Membrane Proteins
Methotrexate
Methyltransferases
Mice
Mice, Inbred C57BL
Mice, Transgenic
Middle Aged
Mitochondria
Mitochondrial Diseases
Mitochondrial Proteins
Molecular Sequence Data
Motor Disorders
Movement Disorders
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis II
Mucopolysaccharidosis III
Mucopolysaccharidosis IV
Mucopolysaccharidosis VI
Mucopolysaccharidosis VII
Muscle Hypotonia
Muscle Weakness
Muscle, Skeletal
Muscular Diseases
Mutation
Mutation, Missense
Myelin Proteins
Myelin Sheath
Myocardium
N-Acetylglucosaminyltransferases
N-Acetylneuraminic Acid
Neonatal Screening
Nervous System Diseases
Neural Stem Cells
Neurodevelopmental Disorders
Neuroimaging
Neuronal Ceroid-Lipofuscinoses
Neurosurgical Procedures
Niemann-Pick Disease, Type C
Organic Anion Transporters
Oxidation-Reduction
Oxidative Phosphorylation
Oxysterols
Pain
Pain Measurement
Palliative Care
Patient Care Team
Patient Compliance
Pedigree
Pentosan Sulfuric Polyester
Peptide Elongation Factor G
Periodontitis
Phenotype
Phosphorylcholine
Phosphotransferases (Alcohol Group Acceptor)
Physical Therapy Modalities
Plasma Cells
Pneumonia
Polymorphism, Single Nucleotide
Polysaccharides
Polysomnography
Practice Guidelines as Topic
Pregnancy
Prevalence
Problem Behavior
Prognosis
Prospective Studies
Protein Conformation
Pulmonary Fibrosis
Quality of Life
Radiography
Rare Diseases
Rats
Receptors, GABA-A
Recombinant Proteins
Rectum
Recurrence
Respiratory Function Tests
Retrospective Studies
Risk Assessment
Risk Factors
Rituximab
RNA Splice Sites
RNA, Messenger
Sacrum
Safety
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Serine Proteases
Severity of Illness Index
Sialic Acid Storage Disease
Siblings
Sickness Impact Profile
Signal Transduction
Skin
Sleep Apnea, Obstructive
Social Class
Social Determinants of Health
Spasms, Infantile
Speech Disorders
Stem Cell Transplantation
Succinates
Surveys and Questionnaires
Survival Analysis
Survivors
Symporters
Syndrome
Synovial Fluid
Synovial Membrane
Tandem Mass Spectrometry
Tennessee
Time Factors
Tomography, X-Ray Computed
Tonsillectomy
Trachea
Transcription Factors
Transfection
Transferrin
Treatment Outcome
Triglycerides
Trihexosylceramides
Triolein
Ubiquitin
Ubiquitination
United States
Vacuolar Proton-Translocating ATPases
Vascular Stiffness
Vesicular Transport Proteins
Vomiting
Whole Genome Sequencing
X Chromosome Inactivation
Young Adult
Raymond's Networks
Concepts (349)
Derived automatically from this person's publications.
Glycogen Storage Disease Type II
Mucopolysaccharidosis I
alpha-Glucosidases
Enzyme Replacement Therapy
Neuronal Ceroid-Lipofuscinoses
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Co-Authors (28)
People in Profiles who have published with this person.
Abdenur, Jose
UCI
Harmatz, Paul
UCSF
Esko, Jeffrey
UCSD
Gallant, Natalie
UCI
Gordts, Philip
UCSD
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_
Similar People (60)
People who share similar concepts with this person.
Harmatz, Paul
UCSF
Budoff, Matthew
UCLA
Polgreen, Lynda
UCLA
Kakkis, Emil
UCLA
Mozaffar, Tahseen
UCI
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Same Department
Blanco, Kirsten
Kiciman, Nafiz
Kimonis, Virginia
Ovunc, Bugsu
Przekop, Allison
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