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Wen-Hann Tan, M.D.
Concepts (333)
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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.
Abnormalities, Multiple
Activities of Daily Living
Adaptor Proteins, Signal Transducing
Adipose Tissue
Adolescent
Adult
Age Factors
Age of Onset
Aged
Alleles
Amino Acid Metabolism, Inborn Errors
Amino Acid Transport Systems, Acidic
Angelman Syndrome
Animals
Anti-Bacterial Agents
Anticonvulsants
Antiporters
Anxiety
Arabs
Arteriovenous Fistula
Ataxia
Autistic Disorder
Basal Cell Nevus Syndrome
Base Pairing
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
Bayes Theorem
Beckwith-Wiedemann Syndrome
Beta Rhythm
Biopsy
Bipolar Disorder
Birth Order
Blood Flow Velocity
Blood Vessels
Bone and Bones
Bone Diseases, Developmental
Bone Marrow Neoplasms
Boston
Brain
Brain Diseases
Brain Diseases, Metabolic, Inborn
Brain Waves
Calcinosis
Calcium
Calcium-Calmodulin-Dependent Protein Kinase Type 2
Carcinoma, Basal Cell
Cardiac Myosins
Cardiomyopathies
Caregivers
Carrier Proteins
Case Management
Case-Control Studies
Cataplexy
Cataract
Cause of Death
Cell Adhesion Molecules
Cell Cycle Proteins
Cell Proliferation
Cerebellar Ataxia
Cerebellar Cortex
Cerebral Cortex
Cerebral Hemorrhage
Checklist
Child
Child Development
Child Development Disorders, Pervasive
Child Language
Child, Preschool
Chorea
Chromosome Aberrations
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 5
Cleft Lip
Cleft Palate
Clinical Trials as Topic
Cockayne Syndrome
Codon, Initiator
Cognition
Cohort Studies
Coloboma
Comparative Genomic Hybridization
Congenital Abnormalities
Consanguinity
Conserved Sequence
Co-Repressor Proteins
Craniosynostoses
Cross-Sectional Studies
Cyclin-Dependent Kinase Inhibitor p16
Cysteine
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
Cytoskeletal Proteins
Data Collection
Databases, Genetic
Deep Brain Stimulation
Delivery of Health Care
Delta Rhythm
Dentin
Developmental Disabilities
Diagnosis, Differential
Dietary Supplements
Diffusion Magnetic Resonance Imaging
Disease Management
Disease Models, Animal
Disease Progression
Disease Susceptibility
DNA Copy Number Variations
DNA Helicases
DNA Methylation
DNA Mutational Analysis
DNA-Binding Proteins
Dose-Response Relationship, Drug
Double-Blind Method
Down Syndrome
Drug Administration Schedule
Dystonic Disorders
Ear
Early Diagnosis
Echocardiography
Ectodermal Dysplasia
Electroencephalography
Endosomal Sorting Complexes Required for Transport
Ependyma
Epigenesis, Genetic
Epilepsies, Myoclonic
Epilepsies, Partial
Epilepsy
Epilepsy, Generalized
Esophageal Atresia
Esophagus
Facies
Failure to Thrive
Family
Family Health
Fatal Outcome
Female
Fetus
Fibroblasts
Fingers
Follow-Up Studies
Forecasting
Frameshift Mutation
GABA Agonists
GABA Plasma Membrane Transport Proteins
Galactosyltransferases
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression Profiling
Gene Expression Regulation, Developmental
Gene Silencing
Genes, Recessive
Genetic Association Studies
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Heterogeneity
Genetic Linkage
Genetic Loci
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomics
Genotype
Gestational Age
Globus Pallidus
Glucuronosyltransferase
Growth Disorders
Hamartoma Syndrome, Multiple
Haploinsufficiency
Head
Health Care Costs
Heart Defects, Congenital
HEK293 Cells
Hemangioma
Hereditary Central Nervous System Demyelinating Diseases
Hereditary Sensory and Autonomic Neuropathies
Homozygote
Hospitalization
Humans
Hyperkinesis
Hyperventilation
Hypoxia-Ischemia, Brain
In Situ Hybridization, Fluorescence
Infant
Infant Mortality
Infant, Newborn
Inheritance Patterns
Intensive Care, Neonatal
International Classification of Diseases
Isoxazoles
Karyotyping
Kidney
Kv1.1 Potassium Channel
Language Development Disorders
Length of Stay
Levodopa
Longitudinal Studies
Long-Term Potentiation
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Male
Mammals
Mandibular Condyle
Maple Syrup Urine Disease
Marfan Syndrome
Medical History Taking
Melanosis
Membrane Proteins
Mental Disorders
Methionine
Mice
Microcephaly
Middle Aged
Minocycline
Mitochondria
Mitochondrial Diseases
Mitochondrial Proteins
Mitogen-Activated Protein Kinase 7
Models, Molecular
Mosaicism
Motor Skills
Muscle Hypotonia
Musculoskeletal Abnormalities
Mutation
Mutation, Missense
Myokymia
Myosin Heavy Chains
Neoplastic Syndromes, Hereditary
Nerve Tissue Proteins
Nervous System
Neural Stem Cells
Neurodegenerative Diseases
Neurons
Neuropsychological Tests
NIH 3T3 Cells
Nipples
Nuclear Proteins
Nuclear Receptor Subfamily 4, Group A, Member 2
Nucleic Acid Hybridization
Ocular Motility Disorders
Oligonucleotide Array Sequence Analysis
Oligoribonucleotides, Antisense
Oman
Optic Atrophy
Oxidation-Reduction
Pancreatitis
Paraplegia
Parenting
Patient Acceptance of Health Care
PAX2 Transcription Factor
Pediatrics
Pedigree
Phenotype
Physical Examination
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Practice Guidelines as Topic
Prader-Willi Syndrome
Pregnancy
Prenatal Diagnosis
Prevalence
Primary Health Care
Prognosis
Protein Conformation
Protein Isoforms
Proteins
Proteoglycans
Psychometrics
Psychomotor Disorders
PTEN Phosphohydrolase
Pyrroline Carboxylate Reductases
Quality of Life
Rare Diseases
Referral and Consultation
Registries
Renal Insufficiency
Repressor Proteins
Retrospective Studies
Rett Syndrome
Risk Factors
RNA, Messenger
Scalp
Schizophrenia
Seizures
Sepsis
Sequence Analysis, DNA
Sequence Deletion
Severity of Illness Index
Siblings
Skin
snRNP Core Proteins
Sodium Channel Blockers
Speech Disorders
Statistics as Topic
Statistics, Nonparametric
Stereotyped Behavior
Stress, Psychological
Structure-Activity Relationship
Sulfite Oxidase
Syndactyly
Syndrome
Theta Rhythm
Thioredoxins
Tight Junctions
Toes
Tomography, X-Ray Computed
Tooth, Supernumerary
Topoisomerase Inhibitors
Trachea
Transcription Factors
Treatment Outcome
Ubiquitin-Protein Ligases
Ultrasonography, Prenatal
Uniparental Disomy
United Arab Emirates
United States
Valproic Acid
Vancomycin
Vesico-Ureteral Reflux
Vesicular Transport Proteins
Vital Statistics
Wilms Tumor
Young Adult
Zebrafish
Zinc Fingers
Tan's Networks
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Concepts (333)
Derived automatically from this person's publications.
Angelman Syndrome
Developmental Disabilities
Ubiquitin-Protein Ligases
Genetic Diseases, Inborn
Basal Cell Nevus Syndrome
Explore
_
Co-Authors (89)
People in Profiles who have published with this person.
Rufo, Paul
Wojcik, Monica
Irons, Mira
Sadhwani, Anjali
Gold, Nina
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_
Similar People (60)
People who share similar concepts with this person.
Sadhwani, Anjali
Alkuraya, Fowzan
Keary, Christopher
Thibert, Ronald
Chung, Wendy
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_
Same Department
People in same department with this person.
An, Zheming
Bodamer, Olaf
Duyzend, Michael
Neilan, Edward
Stenton, Sarah
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_
Physical Neighbors
People whose addresses are nearby this person.
Beggs, Alan
Miller, David
Stoler, Joan
Picker, Jonathan
Neilan, Edward
_