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Stephan Sanders
Concepts (534)
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)
Abnormalities, Multiple
Absorptiometry, Photon
Action Potentials
Acute Disease
Adaptor Proteins, Signal Transducing
Adenosine
Adenosine Deaminase
Adipose Tissue
Adolescent
Adult
Age of Onset
Aged
Aged, 80 and over
Aging
Algorithms
Alleles
alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid
Alternative Splicing
Altitude
Altitude Sickness
Alzheimer Disease
Amino Acid Sequence
Amino Acids, Branched-Chain
Analysis of Variance
Angelman Syndrome
Animals
Ankyrins
Antineoplastic Combined Chemotherapy Protocols
Antiviral Agents
Anxiety
Anxiety Disorders
Apolipoproteins E
Arginine
Artificial Intelligence
Astrocytes
Atlases as Topic
Attention Deficit Disorder with Hyperactivity
Autism Spectrum Disorder
Autistic Disorder
Base Sequence
Bayes Theorem
beta Catenin
Bias
Binding Sites
Biological Ontologies
Biological Psychiatry
Biomarkers
Biomedical Research
Bipolar Disorder
Body Composition
Body Water
Body Weights and Measures
Bone and Bones
Boronic Acids
Bortezomib
Brain
Brain Diseases
Brain Mapping
Cadherins
Calcium Signaling
Calcium-Binding Proteins
Calcium-Calmodulin-Dependent Protein Kinase Type 2
Carboplatin
Cardiac Myosins
Carnitine
Carrier Proteins
Case-Control Studies
Cataract
Catenins
Causality
Cell Adhesion Molecules, Neuronal
Cell Communication
Cell Cycle Proteins
Cell Differentiation
Cell Line
Cell Lineage
Cell Proliferation
Cells, Cultured
Cerebellar Ataxia
Cerebral Cortex
Child
Child Development Disorders, Pervasive
Child, Preschool
Chromatin
Chromatin Assembly and Disassembly
Chromosome Aberrations
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Inversion
Chromosome Mapping
Chromosomes, Human
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 7
Chromosomes, Human, X
Chromothripsis
Cluster Analysis
Clustered Regularly Interspaced Short Palindromic Repeats
Codon, Nonsense
Cognition
Cognition Disorders
Cohort Studies
Coitus
Communication Disorders
Comparative Genomic Hybridization
Computational Biology
Computer Simulation
Condoms
Confidence Intervals
Congenital Abnormalities
Conserved Sequence
Contactins
COUP Transcription Factor I
COUP Transcription Factor II
Cricetinae
CRISPR-Cas Systems
Crohn Disease
Cross-Sectional Studies
Cytomegalovirus
Cytomegalovirus Infections
Data Collection
Data Mining
Database Management Systems
Databases, Genetic
Demography
Dendrites
Dendritic Spines
Depression
Depressive Disorder
Depressive Disorder, Major
Developmental Disabilities
Diagnosis, Differential
Diarrhea
Diet
Dietary Carbohydrates
Dietary Supplements
DiGeorge Syndrome
Disease Models, Animal
Disease Susceptibility
DNA
DNA Copy Number Variations
DNA Mutational Analysis
DNA Repair
DNA-Binding Proteins
Down-Regulation
Drosophila melanogaster
Drosophila Proteins
Educational Status
Electroencephalography
Electronic Health Records
Embryo, Mammalian
Energy Intake
Energy Metabolism
Enhancer Elements, Genetic
Epigenesis, Genetic
Epigenomics
Epilepsy
Epilepsy, Benign Neonatal
Epileptic Syndromes
Epistasis, Genetic
Epithelial Cells
Etoposide
Euchromatin
Evolution, Molecular
Exome
Exons
Facies
Family
Family Health
Female
Ferritins
Fetal Growth Retardation
Fetal Therapies
Fetus
Fever
Fibronectins
Forecasting
Fragile X Mental Retardation Protein
Frameshift Mutation
GABA Plasma Membrane Transport Proteins
Gain of Function Mutation
gamma-Aminobutyric Acid
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Frequency
Gene Knockdown Techniques
Gene Library
Gene Ontology
Gene Order
Gene Rearrangement
Gene Regulatory Networks
Genes
Genes, Developmental
Genes, Dominant
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Code
Genetic Complementation Test
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Linkage
Genetic Loci
Genetic Markers
Genetic Pleiotropy
Genetic Predisposition to Disease
Genetic Testing
Genetic Therapy
Genetic Variation
Genetics, Behavioral
Genetics, Medical
Genetics, Population
Genome
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Genotyping Techniques
Germ Cells
Germ-Line Mutation
Gestational Age
Glutamate Plasma Membrane Transport Proteins
Glutamic Acid
Glycogen Synthase Kinase 3
Gonadal Steroid Hormones
Gonadotropin-Releasing Hormone
Growth Differentiation Factor 1
GTP-Binding Proteins
Haploinsufficiency
Haplotypes
Head
Health Status Indicators
Health Surveys
Heart Defects, Congenital
Heart Diseases
Heart Rate
HEK293 Cells
Hemochromatosis
Hernias, Diaphragmatic, Congenital
Heterosexuality
Heterozygote
High-Throughput Nucleotide Sequencing
High-Throughput Screening Assays
Hippocampus
Histidine Decarboxylase
Histones
Homeostasis
Homologous Recombination
Homozygote
Humans
Hydrocephalus
Hydrops Fetalis
Hypothalamus
Image Processing, Computer-Assisted
Imaging, Three-Dimensional
Immune System Phenomena
Immune Tolerance
Immunohistochemistry
In Situ Hybridization, Fluorescence
In Vitro Techniques
INDEL Mutation
India
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Inheritance Patterns
Inhibitory Postsynaptic Potentials
Inosine
Intellectual Disability
Intelligence
Intelligence Tests
Interpersonal Relations
Intracellular Signaling Peptides and Proteins
Introns
K562 Cells
Kidney
Kidney Diseases
Language
Language Development Disorders
Language Disorders
Language Tests
Larva
Leptin
Life Style
Likelihood Functions
Linkage Disequilibrium
Loss of Function Mutation
Loss of Heterozygosity
Lysine
Magnetic Resonance Imaging
Male
Masturbation
Maze Learning
Melphalan
Membrane Potentials
Membrane Proteins
Mental Disorders
Mental Health
Metabolism, Inborn Errors
Methylation
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Mice, Knockout
Mice, Transgenic
Microarray Analysis
Microcephaly
Microsatellite Repeats
Microscopy, Confocal
Middle Aged
Miniature Postsynaptic Potentials
Mitoxantrone
Mixed Function Oxygenases
Models, Genetic
Models, Neurological
Models, Theoretical
Molecular Sequence Annotation
Molecular Sequence Data
Motor Skills
Multifactorial Inheritance
Multigene Family
Multiple Myeloma
Mutation
Mutation Rate
Mutation, Missense
Myeloablative Agonists
Myosin Heavy Chains
NAV1.1 Voltage-Gated Sodium Channel
NAV1.2 Voltage-Gated Sodium Channel
NAV1.3 Voltage-Gated Sodium Channel
NAV1.6 Voltage-Gated Sodium Channel
Neocortex
Nepal
Nerve Net
Nerve Tissue Proteins
Nervous System
Nervous System Diseases
Nervous System Malformations
Neural Cell Adhesion Molecules
Neural Pathways
Neural Stem Cells
Neurobiology
Neuroblastoma
Neurodevelopmental Disorders
Neurogenesis
Neuroimaging
Neuronal Plasticity
Neurons
Neuropsychiatry
N-Methylaspartate
Nonverbal Communication
Nuclear Proteins
Nuclear Receptor Subfamily 1, Group F, Member 1
Nucleotide Motifs
Obsessive-Compulsive Disorder
Odds Ratio
Oligonucleotide Array Sequence Analysis
Oligonucleotides, Antisense
Open Reading Frames
Oxidoreductases
Oxygen
Parents
Parturition
Patch-Clamp Techniques
Paternal Age
Pedigree
Penetrance
Peripheral Blood Stem Cell Transplantation
Phenotype
Phodopus
Phosphoproteins
Phosphorylation
Photic Stimulation
Pilot Projects
Placenta
Point Mutation
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Precision Medicine
Prednisolone
Prefrontal Cortex
Pregnancy
Pregnancy Trimester, First
Prenatal Diagnosis
Prenatal Exposure Delayed Effects
Preoptic Area
Presynaptic Terminals
Prevalence
Primates
Probability
Prognosis
Promoter Regions, Genetic
Prospective Studies
Proteasome Endopeptidase Complex
Protein Binding
Protein Engineering
Protein Folding
Protein Interaction Maps
Protein Isoforms
Protein Structure, Tertiary
Protein Tyrosine Phosphatase, Non-Receptor Type 11
Proteins
Purkinje Cells
Pyramidal Cells
Pyrazines
Quantitative Trait Loci
Quantitative Trait, Heritable
Rape
Rare Diseases
Rats
Receptors, Cell Surface
Receptors, GABA
Receptors, Histamine H1
Receptors, Histamine H2
Reference Values
Registries
Regression Analysis
Regulatory Sequences, Nucleic Acid
Renal Insufficiency, Chronic
Repressor Proteins
Reproducibility of Results
Research Design
Respiratory Tract Diseases
Retrospective Studies
Ribonucleoproteins
Risk
Risk Factors
Risk-Taking
RNA Editing
RNA Precursors
RNA Recognition Motif Proteins
RNA Splice Sites
RNA Splicing
RNA Splicing Factors
RNA, Messenger
RNA, Small Nuclear
RNA-Binding Proteins
Sample Size
San Francisco
Schizophrenia
Schizophrenia, Childhood
Segmental Duplications, Genomic
Seizures
Semaphorins
Sensitivity and Specificity
Septal Nuclei
Sequence Alignment
Sequence Analysis
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Sequence Homology
Sex Characteristics
Sex Factors
Sexual Behavior
Sexually Transmitted Diseases
Siblings
Signal Transduction
Single-Cell Analysis
Sleep
Smith-Magenis Syndrome
Smoking
Social Behavior
Sodium Channel Blockers
Sodium Channels
Software
Software Design
Spasms, Infantile
Spatio-Temporal Analysis
Spliceosomes
Statistics as Topic
Structure-Activity Relationship
Students
Surveys and Questionnaires
Sweden
Synapses
Synaptic Transmission
Syndrome
Telencephalon
Thalidomide
Thymus Gland
Tissue Distribution
Tourette Syndrome
Transcription Factor 7-Like 2 Protein
Transcription Factors
Transcription, Genetic
Transcriptome
Translocation, Genetic
Transplantation Conditioning
Transplantation, Autologous
Trisomy
TRPC Cation Channels
TRPC6 Cation Channel
Tumor Suppressor Proteins
Ubiquitin Thiolesterase
Ubiquitin-Protein Ligases
Ubiquitin-Specific Peptidase 7
Ultrasonography, Prenatal
Uniparental Disomy
United States
United States Food and Drug Administration
Universities
Untranslated Regions
User-Computer Interface
Vascular Endothelial Growth Factor Receptor-3
Verbal Behavior
Viral Load
Viremia
Virus Activation
Visual Cortex
Vocabulary
Voltage-Gated Sodium Channels
White Matter
Whole Genome Sequencing
Williams Syndrome
Wnt Signaling Pathway
WT1 Proteins
WW Domain-Containing Oxidoreductase
Young Adult
Zebrafish
Stephan's Networks
Concepts (534)
Derived automatically from this person's publications.
Autism Spectrum Disorder
Child Development Disorders, Pervasive
NAV1.2 Voltage-Gated Sodium Channel
Autistic Disorder
DNA Copy Number Variations
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Co-Authors (129)
People in Profiles who have published with this person.
State, Matthew
UCSF
Willsey, Jeremy
UCSF
Ljungdahl, Alicia
UCSF
Dong, Shan
UCSF
Rubenstein, John
UCSF
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People who share similar concepts with this person.
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