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Tim W. Yu, M.D., Ph.D.
Concepts (394)
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Concepts are derived automatically from a person's publications.
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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
Academic Medical Centers
Aconitate Hydratase
Adaptor Proteins, Signal Transducing
Adenosine Triphosphatases
Adolescent
Adult
Age of Onset
Aged
Algorithms
Alleles
Allelic Imbalance
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acyl-tRNA Synthetases
Aminoacylation
AMP-Activated Protein Kinases
Anemia, Diamond-Blackfan
Animals
Animals, Genetically Modified
Antibiotics, Antineoplastic
Anticonvulsants
Ataxia
Ataxia Telangiectasia
Attention Deficit Disorder with Hyperactivity
Attitude to Health
Autistic Disorder
Axons
Base Sequence
Binding Sites
Bioethical Issues
Biopsy
Biotinidase
Bipolar Disorder
Blepharophimosis
Blotting, Western
Body Dysmorphic Disorders
Body Weights and Measures
Brain
Brain Damage, Chronic
Brain Diseases
Brain Ischemia
Bromodeoxyuridine
Cadherins
Caenorhabditis elegans
Caenorhabditis elegans Proteins
Calcium-Binding Proteins
Calmodulin-Binding Proteins
Cardiomegaly
Case Management
Case-Control Studies
Cell Adhesion Molecules
Cell Adhesion Molecules, Neuronal
Cell Communication
Cell Cycle Proteins
Cell Differentiation
Cell Division
Cell Line
Cell Movement
Cell Nucleus
Cell Proliferation
Cells, Cultured
Central Nervous System
Centrioles
Cerebellum
Cerebral Angiography
Cerebral Cortex
Cerebral Revascularization
Child
Child Development
Child Development Disorders, Pervasive
Child, Preschool
Chromatin
Chromatin Assembly and Disassembly
Chromosomal Proteins, Non-Histone
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 19
Chromosomes, Human, Pair 7
Chromosomes, Human, X
Cilia
Class I Phosphatidylinositol 3-Kinases
Classical Lissencephalies and Subcortical Band Heterotopias
Clathrin Heavy Chains
Clinical Clerkship
Clinical Trials as Topic
Cognition Disorders
Cohort Studies
Coloboma
Colorectal Neoplasms
Combined Modality Therapy
Comparative Genomic Hybridization
Computational Biology
Computer Simulation
Congenital Abnormalities
Congenital Hypothyroidism
Consanguinity
Conserved Sequence
Contractile Proteins
Craniofacial Abnormalities
Critical Illness
Crohn Disease
Cues
Cyclin-Dependent Kinase 2
Cytokines
Cytoplasm
Cytoskeletal Proteins
Data Collection
Databases, Genetic
Dentate Gyrus
Depressive Disorder, Major
Developmental Disabilities
Disease
Disease Models, Animal
Distal Myopathies
DNA
DNA Copy Number Variations
DNA Methylation
DNA Modification Methylases
DNA Mutational Analysis
DNA Repair
DNA Replication
DNA-Binding Proteins
Doxorubicin
Drosophila melanogaster
Drug Discovery
Drug Resistance
Drugs, Investigational
Dystroglycans
Education
Education, Medical, Graduate
Education, Medical, Undergraduate
Electric Stimulation
Electroencephalography
Embolization, Therapeutic
Embryo, Mammalian
Embryonic Development
Epigenesis, Genetic
Epilepsy
Exons
Facies
Family
Family Health
Fatal Outcome
Female
Fibroblasts
Financing, Organized
Focus Groups
Fragile X Syndrome
Frameshift Mutation
GA-Binding Protein Transcription Factor
Gene Deletion
Gene Duplication
Gene Expression
Gene Expression Profiling
Gene Expression Regulation, Developmental
Gene Knockdown Techniques
Gene Order
Gene Rearrangement
Gene Silencing
Genes, DCC
Genes, Helminth
Genes, Recessive
Genes, Suppressor
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Heterogeneity
Genetic Linkage
Genetic Loci
Genetic Predisposition to Disease
Genetic Privacy
Genetic Research
Genetic Testing
Genetic Variation
Genetics, Medical
Genome, Human
Genome-Wide Association Study
Genomic Instability
Genomic Structural Variation
Genomics
Genotype
Germ-Line Mutation
Glucose
Glucose Clamp Technique
Glucose Transporter Type 1
Glycogen Storage Disease Type II
Glycosylation
Glycosyltransferases
Green Fluorescent Proteins
Growth Cones
Gyrus Cinguli
Haploinsufficiency
Head
Health
Health Care Costs
Health Personnel
Heart Defects, Congenital
Heart Ventricles
Hedgehog Proteins
Helminth Proteins
Heterozygote
High-Throughput Nucleotide Sequencing
Histone Acetyltransferases
Homozygote
Hospital Mortality
Humans
Hypertrichosis
Immunoprecipitation
Indicators and Reagents
Infant
Infant Mortality
Infant, Newborn
Information Dissemination
Informed Consent
Inheritance Patterns
Insulin Resistance
Intelligence
Intensive Care Units, Neonatal
Internship and Residency
Intracranial Aneurysm
Intracranial Thrombosis
Introns
Iodide Peroxidase
Joint Instability
KATP Channels
Kidney
Kruppel-Like Transcription Factors
Lipid Metabolism
Lissencephaly
Liver
Loss of Heterozygosity
Luminescent Proteins
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Mass Spectrometry
Membrane Transport Proteins
Mental Disorders
Mice
Mice, Knockout
Mice, Transgenic
Microarray Analysis
Microcephaly
Microfilament Proteins
Microglia
Microtubule-Associated Proteins
Microtubules
Middle Aged
Minority Groups
Mitochondrial Proton-Translocating ATPases
Models, Biological
Models, Molecular
Molecular Diagnostic Techniques
Molecular Sequence Data
Muscle Development
Muscle, Skeletal
Muscles
Muscular Dystrophies, Limb-Girdle
Muscular Dystrophy, Duchenne
Muscular Dystrophy, Facioscapulohumeral
Mutagenesis
Mutagenesis, Insertional
Mutation
Mutation, Missense
Myofibrils
Myopathies, Nemaline
Myopathies, Structural, Congenital
Neonatal Screening
Nerve Growth Factors
Nerve Net
Nerve Tissue Proteins
Nervous System
Nervous System Malformations
Neural Cell Adhesion Molecules
Neural Pathways
Neurology
Neuromuscular Diseases
Neuronal Ceroid-Lipofuscinoses
Neuronal Plasticity
Neurons
Neuropsychological Tests
Nuclear Proteins
Nucleic Acid Hybridization
Odds Ratio
Oligonucleotide Array Sequence Analysis
Oligonucleotides
Oligonucleotides, Antisense
Oncogene Proteins
Open Reading Frames
Osteochondrodysplasias
Parasympathomimetics
Parents
Patella
Patient Selection
Pedigree
Peer Review, Research
Periventricular Nodular Heterotopia
Pharmacogenetics
Phenotype
Phosphatidylinositol 3-Kinases
Pilocarpine
Pilot Projects
Point Mutation
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Postoperative Complications
Practice Guidelines as Topic
Predictive Value of Tests
Pregnancy
Prevalence
Promoter Regions, Genetic
Prospective Studies
Protein Binding
Protein Conformation
Protein Interaction Domains and Motifs
Protein Kinases
Protein Multimerization
Protein Structure, Tertiary
Protein Tyrosine Phosphatases
Proteins
Proto-Oncogene Proteins c-akt
Psychomotor Disorders
Psychotic Disorders
Public Health
Quantitative Trait, Heritable
rac GTP-Binding Proteins
Rare Diseases
Rats
Rats, Sprague-Dawley
Receptor-Like Protein Tyrosine Phosphatases
Receptors, Cell Surface
Receptors, Immunologic
Recombinant Fusion Proteins
Repressor Proteins
Research Design
Retina
Retinitis Pigmentosa
Retroelements
Retrospective Studies
Ribosomal Proteins
Risk Assessment
Risk Factors
RNA Splice Sites
RNA Splicing
RNA, Messenger
RNA, Small Interfering
Schizophrenia
Scrotum
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Homology
Severity of Illness Index
Siblings
Signal Transduction
Skin
Software
Status Epilepticus
Subarachnoid Hemorrhage
Surgical Instruments
Survival Analysis
Synapses
Syndrome
Tay-Sachs Disease
Teaching
Thiolester Hydrolases
Thrombectomy
Thrombopoietin
TOR Serine-Threonine Kinases
Transcription Factors
Transcription, Genetic
Treatment Outcome
Triiodothyronine
Two-Hybrid System Techniques
Ubiquitin Thiolesterase
Ubiquitination
Ubiquitin-Protein Ligases
Ultrasonography
United States
United States Food and Drug Administration
Urogenital Abnormalities
Ventricular Dysfunction
Walker-Warburg Syndrome
Williams Syndrome
Young Adult
Zebrafish
Yu's Networks
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Concepts (394)
Derived automatically from this person's publications.
RNA Splicing
Ataxia Telangiectasia
Oligonucleotides, Antisense
Autistic Disorder
Rare Diseases
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Co-Authors (116)
People in Profiles who have published with this person.
D'Gama, Alissa
Green, Robert
Beggs, Alan
Walsh, Christopher
Bodamer, Olaf
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_
Similar People (60)
People who share similar concepts with this person.
Walsh, Christopher
Rehm, Heidi
Faraone, Stephen
Alkuraya, Fowzan
Chung, Wendy
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_
Same Department
People in same department with this person.
Alkuraya, Fowzan
Amin, Mutaz
Mochida, Ganeshwaran
Song, Janet
Zhao, Boxun
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Physical Neighbors
People whose addresses are nearby this person.
Neumeyer, Ann
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