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Matthew State
Concepts (536)
Back to Profile
Concepts are derived automatically from a person's publications.
Cloud
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.
3' Untranslated Regions
3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)
Abducens Nerve
Abnormalities, Multiple
Adaptor Proteins, Signal Transducing
Adolescent
Adult
Age Factors
Aged
Aged, 80 and over
Alleles
Alternative Splicing
Amino Acid Sequence
Amino Acid Substitution
Amino Acids, Branched-Chain
Amphetamine
Angelman Syndrome
Animals
Animals, Genetically Modified
Animals, Newborn
Aniridia
Anti-Arrhythmia Agents
Antidepressive Agents
Antineoplastic Combined Chemotherapy Protocols
Antipsychotic Agents
Arachnoid Cysts
Arginine
Arginine Vasopressin
Arnold-Chiari Malformation
Arrhythmias, Cardiac
Attention Deficit Disorder with Hyperactivity
Autism Spectrum Disorder
Autistic Disorder
Bacteriophage lambda
Basal Ganglia
Base Sequence
Bayes Theorem
Binding Sites
Biological Psychiatry
Biomarkers
Bipolar Disorder
Blood Pressure
Blood Specimen Collection
Body Weights and Measures
Bone and Bones
Brain
Brain Diseases
Brain Neoplasms
Cadherins
Calcium-Binding Proteins
Calcium-Calmodulin-Dependent Protein Kinase Type 2
Carboplatin
Carrier Proteins
Case-Control Studies
Catenins
Causality
Cell Adhesion
Cell Adhesion Molecules, Neuronal
Cell Cycle
Cell Cycle Proteins
Cell Differentiation
Cell Line
Cell Lineage
Cell Polarity
Cell Proliferation
Cell Survival
Cells, Cultured
Cerebellar Ataxia
Cerebral Cortex
Child
Child Behavior Disorders
Child Development Disorders, Pervasive
Child Psychiatry
Child, Preschool
Chromatin
Chromatin Assembly and Disassembly
Chromosome Aberrations
Chromosome Banding
Chromosome Breakage
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Inversion
Chromosome Mapping
Chromosomes, Artificial, Bacterial
Chromosomes, Human
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 13
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 9
Chromosomes, Human, X
Cilia
Clinical Trials as Topic
Cluster Analysis
Codon, Nonsense
Cognition Disorders
Cohort Studies
Combined Modality Therapy
Comorbidity
Comparative Genomic Hybridization
Computational Biology
Congenital Abnormalities
Consanguinity
Consensus Sequence
Conserved Sequence
Contactins
Cooperative Behavior
Corpus Striatum
Craniofacial Abnormalities
Crohn Disease
Cytogenetic Analysis
Cytogenetics
Data Mining
Databases, Genetic
Demography
Dendritic Spines
Depressive Disorder
Depressive Disorder, Major
Developmental Disabilities
Diagnosis, Differential
Diagnostic and Statistical Manual of Mental Disorders
Diagnostic Imaging
Diet
Disease Models, Animal
Diseases in Twins
DNA
DNA Copy Number Variations
DNA Mutational Analysis
DNA Replication
DNA Transposable Elements
DNA, Circular
DNA, Complementary
DNA, Viral
DNA-Binding Proteins
Dopamine Agonists
Dopamine Antagonists
Down Syndrome
Drosophila Proteins
Drug Discovery
Drug Evaluation, Preclinical
Drug Resistance
Drug Therapy, Combination
Duane Retraction Syndrome
Ductus Arteriosus, Patent
Dystrophin
Electrocardiography
Electrocardiography, Ambulatory
Electroconvulsive Therapy
Embryo, Mammalian
Embryo, Nonmammalian
Embryonic Development
Enhancer Elements, Genetic
Environment
Epigenesis, Genetic
Epigenomics
Epilepsy
Estrogens
Etoposide
Euchromatin
Europe
Evolution, Molecular
Exome
Exons
Exploratory Behavior
Eye Proteins
Family
Family Health
Feeding and Eating Disorders
Feeding Behavior
Female
Fetus
Fibrillar Collagens
Fibronectins
Fluvoxamine
Follow-Up Studies
Forecasting
Founder Effect
Fragile X Mental Retardation Protein
Fragile X Syndrome
Frameshift Mutation
Functional Laterality
GABA Plasma Membrane Transport Proteins
Gait Ataxia
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Frequency
Gene Knockdown Techniques
Gene Ontology
Gene Rearrangement
Gene Regulatory Networks
Gene-Environment Interaction
Genes
Genes, Developmental
Genes, Dominant
Genes, Neurofibromatosis 2
Genes, Recessive
Genetic Association Studies
Genetic Code
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Linkage
Genetic Loci
Genetic Markers
Genetic Pleiotropy
Genetic Predisposition to Disease
Genetic Research
Genetic Testing
Genetic Therapy
Genetic Variation
Genetics, Population
Genistein
Genome
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomic Instability
Genomics
Genotype
Genotyping Techniques
Germ Cells
Germ-Line Mutation
Gestational Age
Glass
Glutamic Acid
Green Fluorescent Proteins
Growth Disorders
GTP-Binding Proteins
Haplotypes
Head
Heart Conduction System
Heart Defects, Congenital
Heart Diseases
HEK293 Cells
Hemangioma, Cavernous, Central Nervous System
Hemorrhage
Hereditary Sensory and Autonomic Neuropathies
Heterozygote
High-Throughput Nucleotide Sequencing
Hippocampus
Histamine
Histidine Decarboxylase
Histones
Homeodomain Proteins
Homologous Recombination
Homozygote
Human Genome Project
Human Growth Hormone
Humans
Hypertension
Hypothalamic Diseases
Immunohistochemistry
In Situ Hybridization
In Situ Hybridization, Fluorescence
In Vitro Techniques
INDEL Mutation
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Inheritance Patterns
Inhibitory Postsynaptic Potentials
Intellectual Disability
Intelligence
Intelligence Tests
International Classification of Diseases
International Cooperation
Interneurons
Intracellular Signaling Peptides and Proteins
Intracranial Aneurysm
Introns
Ion Channel Gating
Japan
Judaism
Karyotyping
Kidney
Kidney Diseases
Kruppel-Like Transcription Factors
Language Disorders
Larva
Likelihood Functions
Limb Deformities, Congenital
Linkage Disequilibrium
Lissencephaly
Lithium
Lod Score
Long QT Syndrome
Longitudinal Studies
Loss of Heterozygosity
Luminescent Proteins
Lysine
Macaca
Macaca mulatta
Magnetic Resonance Imaging
Male
Maze Learning
Measles-Mumps-Rubella Vaccine
Membrane Proteins
Meningeal Neoplasms
Meningioma
Mental Disorders
Meta-Analysis as Topic
Methylation
Methylphenidate
Mexiletine
Mice
Mice, Inbred C57BL
Mice, Knockout
Mice, Transgenic
Microcephaly
Microsatellite Repeats
Microtubules
Middle Aged
Mitoxantrone
Mixed Function Oxygenases
Models, Biological
Models, Genetic
Models, Neurological
Models, Theoretical
Molecular Epidemiology
Molecular Sequence Annotation
Molecular Sequence Data
Molecular Weight
Motor Activity
Multifactorial Inheritance
Muscle Proteins
Muscular Dystrophy, Duchenne
Mutation
Mutation, Missense
NAV1.2 Voltage-Gated Sodium Channel
NAV1.5 Voltage-Gated Sodium Channel
Neocortex
Neoplasm Grading
Nerve Net
Nerve Tissue Proteins
Nervous System
Nervous System Diseases
Neural Cell Adhesion Molecules
Neural Pathways
Neural Stem Cells
Neurobiology
Neurodevelopmental Disorders
Neurogenesis
Neuroimaging
Neurons
Neuropsychiatry
Neurosciences
Nucleic Acid Conformation
Nucleic Acid Hybridization
Nucleotide Motifs
Obsessive-Compulsive Disorder
Odds Ratio
Oligonucleotide Array Sequence Analysis
Olivopontocerebellar Atrophies
Open Reading Frames
Organ Size
Organ Specificity
Organogenesis
Oxazines
Oxytocin
Paired Box Transcription Factors
Pan troglodytes
Parent-Child Relations
Parents
Parkinsonian Disorders
Patch-Clamp Techniques
Patient Advocacy
PAX6 Transcription Factor
Pedigree
Penetrance
Phenotype
Phosphoproteins
Phosphorylation
Phylogeny
Phytoestrogens
Piperazines
Point Mutation
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Postmortem Changes
Potassium Channels, Inwardly Rectifying
Practice Guidelines as Topic
Prader-Willi Syndrome
Precision Medicine
Prednisolone
Prefrontal Cortex
Pregnancy
Pregnancy Complications
Prevalence
Prognosis
Promoter Regions, Genetic
Prospective Studies
Protein Conformation
Protein Folding
Protein Interaction Maps
Protein Isoforms
Protein Structure, Tertiary
Proteins
Protein-Tyrosine Kinases
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-akt
Proto-Oncogene Proteins c-met
Psychiatric Status Rating Scales
Psychiatry
Psychopathology
Psychotic Disorders
Psychotropic Drugs
PubMed
Quality of Life
Quantitative Trait Loci
Quantitative Trait, Heritable
Raclopride
Radionuclide Imaging
Rats
Rats, Sprague-Dawley
Receptor, trkA
Receptor-Interacting Protein Serine-Threonine Kinases
Receptors, Cell Surface
Receptors, Drug
Receptors, GABA
Receptors, G-Protein-Coupled
Receptors, Growth Factor
Receptors, Histamine H1
Receptors, Histamine H2
Receptors, LDL
Reference Values
Repressor Proteins
Reproducibility of Results
Republic of Korea
Research Design
Retrospective Studies
Reverse Transcriptase Polymerase Chain Reaction
Risk
Risk Factors
RNA Splice Sites
RNA, Messenger
RNA, Small Interfering
Sample Size
Schizophrenia
Schizophrenia, Childhood
Schizophrenic Psychology
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Sequence Homology, Amino Acid
Severity of Illness Index
Sex Characteristics
Sex Factors
Siblings
Sick Sinus Syndrome
Signal Transduction
Single-Cell Analysis
Sleep Wake Disorders
Sleep-Wake Transition Disorders
Smith-Magenis Syndrome
Smoothened Receptor
Social Behavior
Social Environment
Sodium Channels
Sodium Chloride
Sodium-Potassium-Chloride Symporters
Solute Carrier Family 12, Member 1
Solute Carrier Family 12, Member 3
Spatio-Temporal Analysis
Species Specificity
Spindle Apparatus
Statistics, Nonparametric
Stereotyped Behavior
Sudden Infant Death
Symporters
Synapses
Syndrome
Systems Biology
T-Box Domain Proteins
Telencephalon
Telomere
Temporal Lobe
Thalamus
Thiazoles
Tic Disorders
Tics
Time Factors
Tomography, X-Ray Computed
Tooth Abnormalities
Tourette Syndrome
Transcription Factor AP-2
Transcription Factors
Transcription, Genetic
Transcriptome
Translocation, Genetic
Transposases
Treatment Failure
Treatment Outcome
Trisomy
TRPC Cation Channels
TRPC6 Cation Channel
Tryptophan
Tubulin
Tumor Necrosis Factor Receptor-Associated Peptides and Proteins
Turkey
Twin Studies as Topic
Ubiquitin Thiolesterase
Ubiquitin-Protein Ligases
Ubiquitin-Specific Peptidase 7
Uniparental Disomy
United States
Urinary Tract
Urogenital Abnormalities
Valproic Acid
Vesicular Glutamate Transport Protein 2
Whole Genome Sequencing
Williams Syndrome
Wnt Signaling Pathway
Xenopus
Xenopus Proteins
Young Adult
Zebrafish
Zinc Finger Protein Gli3
Matthew's Networks
Concepts (536)
Derived automatically from this person's publications.
Tourette Syndrome
Child Development Disorders, Pervasive
Autistic Disorder
Autism Spectrum Disorder
Genetic Predisposition to Disease
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Co-Authors (94)
People in Profiles who have published with this person.
Willsey, Jeremy
UCSF
Sanders, Stephan
UCSF
Willsey, Helen
UCSF
Geschwind, Daniel
UCLA
Rubenstein, John
UCSF
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Similar People (60)
People who share similar concepts with this person.
Geschwind, Daniel
UCLA
Piacentini, John
UCLA
Gleeson, Joseph
UCSD
Mathews, Carol
UCSF
Ozonoff, Sally
UC Davis
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Same Department
Glowinski, Anne
Patrick, Cory
Reus, Victor
Steinbuchel, Petra
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