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Joseph Shieh
Concepts (443)
Back to Profile
Concepts are derived automatically from a person's publications.
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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.
Abnormalities, Multiple
Actins
Adenosine Triphosphatases
Adenoviridae
Adolescent
Adult
Age of Onset
Aged
Agenesis of Corpus Callosum
Aging, Premature
AIDS Dementia Complex
Aldehyde Reductase
Alleles
Amino Acid Sequence
Amniocentesis
Aneurysm
Animals
Antibody Formation
Anticholesteremic Agents
Antigens, CD
Antigens, Differentiation, Myelomonocytic
Antihypertensive Agents
Aorta, Thoracic
Aortic Coarctation
Apoferritins
Arnold-Chiari Malformation
Arteriosclerosis
Arthrogryposis
Astrocytes
Astrocytoma
Ataxia
Autism Spectrum Disorder
Autistic Disorder
Bacterial Outer Membrane Proteins
Bacterial Proteins
Bacterial Vaccines
Base Sequence
Basilar Artery
Benzazepines
Biopsy
Birth Weight
Blood Platelets
Blood Pressure
Blood Pressure Monitoring, Ambulatory
Blotting, Northern
Blotting, Western
Brachiocephalic Trunk
Brain
Brain Diseases
Brain Neoplasms
Calcium Signaling
California
Capillaries
Cardiomyopathies
Carotid Arteries
Case-Control Studies
Cation Transport Proteins
CD4 Antigens
Cell Adhesion
Cell Cycle
Cell Cycle Proteins
Cell Fusion
Cell Line
Cell Line, Transformed
Cell Line, Tumor
Cell Polarity
Cell Proliferation
Cells, Cultured
Cerebellar Vermis
Cerebellum
Chemokine CCL4
Chemokine CCL5
Chemokines, CXC
Child
Child, Preschool
CHO Cells
Cholestasis
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Banding
Chromosome Deletion
Chromosome Duplication
Chromosome Mapping
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Cleft Lip
Cleft Palate
Coculture Techniques
Codon
Cohort Studies
Comorbidity
Comparative Genomic Hybridization
Computational Biology
Consanguinity
Constipation
Corpus Callosum
Coxsackie and Adenovirus Receptor-Like Membrane Protein
Craniofacial Abnormalities
Cricetinae
CRISPR-Cas Systems
Culture Media, Serum-Free
Cyclin-Dependent Kinase Inhibitor p15
Cyclin-Dependent Kinase Inhibitor p16
Cyclin-Dependent Kinase Inhibitor p18
Cystic Fibrosis
Cystic Fibrosis Transmembrane Conductance Regulator
Cytopathogenic Effect, Viral
Dasatinib
Data Interpretation, Statistical
Databases, Genetic
De Lange Syndrome
Developmental Disabilities
Diagnosis, Differential
Diagnostic Imaging
Disease Management
Disease Models, Animal
Diseases in Twins
Disks Large Homolog 4 Protein
DNA
DNA Copy Number Variations
DNA Helicases
DNA Mutational Analysis
DNA, Mitochondrial
DNA-Binding Proteins
Dogs
Drosophila
Drug Resistance, Neoplasm
Dyslipidemias
Early Diagnosis
Early Growth Response Protein 1
Early Growth Response Protein 2
Embryo, Mammalian
Endothelial Cells
Enzyme Activation
Enzyme-Linked Immunosorbent Assay
Epigenesis, Genetic
Epilepsy
ErbB Receptors
Erlotinib Hydrochloride
Exome
Exons
Eye Abnormalities
Face
Failure to Thrive
Female
Ferritins
Fetus
Fibroblasts
Fibrosis
Fluorescent Antibody Technique, Indirect
Forkhead Transcription Factors
Frameshift Mutation
Gene Deletion
Gene Expression
Gene Expression Profiling
Gene Knockout Techniques
Gene Products, env
Genes, Dominant
Genes, Lethal
Genes, Reporter
Genes, X-Linked
Genetic Association Studies
Genetic Carrier Screening
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Loci
Genetic Pleiotropy
Genetic Predisposition to Disease
Genetic Privacy
Genetic Research
Genetic Services
Genetic Testing
Genetic Variation
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomic Structural Variation
Genomics
Genotype
Genotyping Techniques
Germ-Line Mutation
Gestational Age
Giant Cells
Gitelman Syndrome
Glioblastoma
Glioma
Glutamic Acid
Growth Disorders
GTP-Binding Protein alpha Subunits
GTP-Binding Protein alpha Subunits, Gq-G11
Guanosine Diphosphate
Guanosine Triphosphate
Haemophilus influenzae
Headache
Health Services Accessibility
Heart
Heart Defects, Congenital
Heart Septal Defects, Ventricular
Heart Ventricles
Hedgehog Proteins
Heterogeneous Nuclear Ribonucleoprotein A1
Heterozygote
High-Throughput Nucleotide Sequencing
Hirschsprung Disease
Histone-Lysine N-Methyltransferase
HIV
HIV-1
Homeodomain Proteins
Homozygote
Humans
Hyalin
Hypertension
Hypertension, Pulmonary
Hypertrichosis
Imaging, Three-Dimensional
Imatinib Mesylate
Immunity
Immunization
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Information Dissemination
Insurance Coverage
Integrin alphaXbeta2
Intellectual Disability
Intensive Care Units, Neonatal
Interleukin-2
Internet
Intracranial Aneurysm
Intracranial Arteriovenous Malformations
Intracranial Hemorrhages
Iron
Iron Metabolism Disorders
Jumonji Domain-Containing Histone Demethylases
Karyotype
Karyotyping
Kidney Diseases, Cystic
Kinetics
Language Development Disorders
Leukocyte Common Antigens
Leukocytes, Mononuclear
Leukoencephalopathies
Lipopolysaccharide Receptors
Liver Failure, Acute
Loss of Function Mutation
Loss of Heterozygosity
Luciferases
Lung
Lung Diseases, Interstitial
Lung Transplantation
Lymphocyte Activation
Macaca mulatta
Macrophage Inflammatory Proteins
Macrophages
Magnetic Resonance Angiography
Magnetic Resonance Imaging
Male
MAP Kinase Signaling System
Megalencephaly
Melanoma
Membrane Fusion
Membrane Potentials
Membrane Proteins
Metabolism, Inborn Errors
Mice
Mice, Inbred BALB C
Mice, Inbred C3H
Mice, Transgenic
Microglia
MicroRNAs
Microscopy, Confocal
Microscopy, Electron
Microscopy, Electron, Transmission
Microscopy, Fluorescence
Middle Aged
Mitogen-Activated Protein Kinase Kinases
Mitogens
Molecular Sequence Data
Monocytes
Mosaicism
Muscle Hypotonia
Muscle, Skeletal
Mutation
Mutation, Missense
Myeloid-Lymphoid Leukemia Protein
Myocardium
Myocytes, Cardiac
Myofibromatosis
Myopathies, Structural, Congenital
Myosin Heavy Chains
Neisseria meningitidis
Neonatal Screening
Neoplasm Recurrence, Local
Neoplasm Transplantation
Nephrotic Syndrome
Nervous System Malformations
Nervous System Neoplasms
Neuroaxonal Dystrophies
Neurocutaneous Syndromes
Neurodevelopmental Disorders
Neurofibromatosis 1
Neurogenesis
Neurons
Nonsense Mediated mRNA Decay
Nuchal Translucency Measurement
Nuclear Proteins
Nuclear Respiratory Factor 1
Nucleic Acid Hybridization
Nucleotide Transport Proteins
Oligodendroglia
Oligonucleotide Array Sequence Analysis
Oncogene Fusion
Organ Specificity
Organogenesis
Osteochondrodysplasias
Oxidative Stress
Oxidoreductases
PAX2 Transcription Factor
Pedigree
Penetrance
Persistent Fetal Circulation Syndrome
Phenotype
Phosphorylation
Phosphotransferases (Alcohol Group Acceptor)
Polydactyly
Polymerase Chain Reaction
Polymicrogyria
Polymorphism, Single Nucleotide
Polysaccharides, Bacterial
Pre-B-Cell Leukemia Transcription Factor 1
Precipitin Tests
Precision Medicine
Predictive Value of Tests
Pregnancy
Prevalence
Propranolol
Prospective Studies
Protein Binding
Protein C
Protein Domains
Protein Kinase Inhibitors
Protein Phosphatase 2C
Protein Tyrosine Phosphatases, Non-Receptor
Proteomics
Proto-Oncogene Proteins
Proto-Oncogene Proteins B-raf
Proto-Oncogene Proteins c-fos
Proto-Oncogene Proteins p21(ras)
Public Health
Pulmonary Alveoli
Pulmonary Artery
Pulmonary Embolism
Pulmonary Surfactant-Associated Protein C
Pulmonary Veins
Radioimmunoassay
raf Kinases
ral GTP-Binding Proteins
Real-Time Polymerase Chain Reaction
Receptor, Platelet-Derived Growth Factor beta
Receptors, CCR3
Receptors, CCR5
Receptors, Chemokine
Receptors, CXCR4
Receptors, Cytoplasmic and Nuclear
Receptors, HIV
Receptors, Peptide
Receptors, Virus
Recombination, Genetic
Registries
Renal Insufficiency
Repressor Proteins
Reproducibility of Results
Retina
Retinal Dehydrogenase
Retrospective Studies
Reverse Transcriptase Polymerase Chain Reaction
Risk
Risk Factors
RNA, Messenger
RNA-Binding Proteins
Secondary Prevention
Seizures
Sequence Analysis, DNA
Sequence Deletion
Serotyping
Severity of Illness Index
Siblings
Signal Transduction
Skin
Skin Abnormalities
Software
SOXD Transcription Factors
Spectrin
Spleen
Subclavian Vein
Synapses
Synaptic Transmission
Synaptosomal-Associated Protein 25
Syndrome
Tandem Mass Spectrometry
T-Box Domain Proteins
Telangiectasia, Hereditary Hemorrhagic
Telangiectasis
Telomerase
Temporal Lobe
Tight Junctions
Time Factors
Time-Lapse Imaging
T-Lymphocytes
T-Lymphocytes, Helper-Inducer
Tomography, X-Ray Computed
Trans-Activators
Transcription Factors
Transcriptome
Transfection
Travel
Trichothiodystrophy Syndromes
Tripartite Motif-Containing Protein 28
Truncus Arteriosus, Persistent
Tubulin
Tumor Cells, Cultured
Tumor Microenvironment
Tumor Suppressor Protein p53
Tumor Suppressor Proteins
Twins, Monozygotic
United States
Valine
Vascular Patency
Vascular Resistance
Vesicular Transport Proteins
Virus Diseases
Virus Replication
Whole Genome Sequencing
World Health Organization
X Chromosome Inactivation
Xenograft Model Antitumor Assays
Young Adult
Zebrafish
Zebrafish Proteins
Zinc
Zinc Finger E-box Binding Homeobox 2
Joseph's Networks
Concepts (443)
Derived automatically from this person's publications.
Growth Disorders
Intellectual Disability
Genetic Diseases, Inborn
Abnormalities, Multiple
Diseases in Twins
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_
Co-Authors (109)
People in Profiles who have published with this person.
Phillips, Joanna
UCSF
Srivastava, Deepak
UCSF
Kwok, Pui-Yan
UCSF
Blair, David
UCSF
Klein, Ophir
UCSF
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_
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People who share similar concepts with this person.
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