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Katherine Rauen
Concepts (459)
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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
Achievement
Adaptation, Psychological
Adaptor Proteins, Signal Transducing
Adenosine Diphosphate
Adenoviridae
Adolescent
Adult
Age Distribution
Age Factors
Age of Onset
Aged
Aged, 80 and over
Alleles
alpha-Fetoproteins
Ameloblasts
Amino Acid Sequence
Amino Acid Substitution
Amniocentesis
Aneuploidy
Animals
Ankyrins
Antineoplastic Agents
Antiviral Agents
Apoptosis
Arrhythmias, Cardiac
Astrocytes
Autism Spectrum Disorder
Autistic Disorder
Base Sequence
Benzamides
Benzenesulfonates
Binding Sites
Biomarkers
Biomarkers, Tumor
Biomedical Research
Biotin
Blotting, Western
Bone Neoplasms
Brain
Breast
Breast Neoplasms
Cadherins
Cafe-au-Lait Spots
Calcium
California
Capital Financing
Carcinoma, Transitional Cell
Cardiomyopathy, Hypertrophic
Cardiovascular Abnormalities
Case-Control Studies
Cataract
Cell Communication
Cell Count
Cell Culture Techniques
Cell Differentiation
Cell Line
Cell Line, Tumor
Cell Polarity
Cell Proliferation
Cell Separation
Cell Transformation, Neoplastic
Cells, Cultured
Cellular Reprogramming
Cerebral Ventricles
Chick Embryo
Chickens
Child
Child, Preschool
CHO Cells
Choanal Atresia
Chondroitin Sulfates
Chorionic Gonadotropin
Choristoma
Chromatography, High Pressure Liquid
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Banding
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes, Artificial, Bacterial
Chromosomes, Human
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 12
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 19
Chromosomes, Human, Pair 20
Chromosomes, Human, Pair 21
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 8
Chromosomes, Human, X
Cleft Palate
Clinical Trials as Topic
Clinical Trials, Phase I as Topic
Clinical Trials, Phase II as Topic
Cloning, Molecular
Clubfoot
Codon
Cognition Disorders
Cohort Studies
Comparative Genomic Hybridization
Congenital Abnormalities
Conjunctival Neoplasms
Consensus
COS Cells
Cost of Illness
Costello Syndrome
Coxsackie and Adenovirus Receptor-Like Membrane Protein
CpG Islands
Craniofacial Abnormalities
Cricetinae
Critical Care
Critical Illness
Cross-Sectional Studies
Cytogenetic Analysis
Cytogenetics
Cytopathogenic Effect, Viral
Dental Enamel
Dental Enamel Hypoplasia
Dermoid Cyst
Dermoscopy
Developmental Disabilities
Diagnosis, Differential
Diaphragmatic Eventration
DiGeorge Syndrome
Diphenylamine
Disease Management
Disease Models, Animal
DNA
DNA Methylation
DNA Mutational Analysis
DNA Primers
DNA, Complementary
DNA-Binding Proteins
Down-Regulation
Drosophila Proteins
Drug Design
Ectodermal Dysplasia
Embryo, Mammalian
Embryo, Nonmammalian
Enterovirus
Enzyme Activation
Enzyme Assays
Enzyme Inhibitors
Epilepsy, Complex Partial
Epistasis, Genetic
Estriol
Exons
Extracellular Matrix
Extracellular Signal-Regulated MAP Kinases
Face
Facies
Failure to Thrive
Family
Family Characteristics
Farnesyltranstransferase
Female
Fetal Macrosomia
Fetus
Fibroblasts
Flow Cytometry
Follow-Up Studies
Foot Dermatoses
Ganciclovir
Gastrointestinal Neoplasms
Gene Components
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Regulation
Gene Expression Regulation, Neoplastic
Gene Frequency
Gene Transfer Techniques
Gene-Environment Interaction
Genes, Dominant
Genes, Modifier
Genes, ras
Genetic Association Studies
Genetic Diseases, Inborn
Genetic Engineering
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Therapy
Genetic Variation
Genome
Genome, Human
Genome-Wide Association Study
Genomics
Genotype
Germ Cells
Germ-Line Mutation
Gingival Hyperplasia
Glial Fibrillary Acidic Protein
Goldenhar Syndrome
Growth Disorders
Guidelines as Topic
Hair
Hair Diseases
Hand Dermatoses
Hand Strength
Hearing Loss, Bilateral
Hearing Loss, Sensorineural
Heart
Heart Defects, Congenital
HEK293 Cells
Helminth Proteins
Hernia, Diaphragmatic
Hernias, Diaphragmatic, Congenital
Heterozygote
High-Throughput Nucleotide Sequencing
Hippocampus
Histidine
Histological Techniques
Hospitals, Pediatric
Human Development
Human Growth Hormone
Humans
Hydra
Hydrops Fetalis
Imidazoles
Immunohistochemistry
In Situ Hybridization, Fluorescence
Incidence
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Information Dissemination
Inheritance Patterns
Integrin alphaV
Integrin alphaVbeta3
Integrins
Intellectual Disability
Intercellular Junctions
Intersectoral Collaboration
Intracellular Signaling Peptides and Proteins
Introns
Karyotyping
LEOPARD Syndrome
Leukemia
Leukemia, Myelomonocytic, Juvenile
Lipoma
Longitudinal Studies
Loss of Heterozygosity
Magnetic Resonance Imaging
Male
Malocclusion
MAP Kinase Kinase 1
MAP Kinase Kinase 2
MAP Kinase Kinase Kinase 1
MAP Kinase Kinase Kinases
MAP Kinase Signaling System
Mass Spectrometry
Matrix Metalloproteinases
Medicaid
Megalencephaly
Melanoma
Membrane Proteins
Metalloendopeptidases
Methyltransferases
Mice
Mice, Inbred C57BL
Mice, Mutant Strains
Mice, Transgenic
Microsatellite Repeats
Microscopy, Electron, Scanning
Middle Aged
Mitogen-Activated Protein Kinase Kinases
Mitogen-Activated Protein Kinases
Mitral Valve
Models, Biological
Models, Genetic
Models, Molecular
Models, Organizational
Molecular Diagnostic Techniques
Molecular Sequence Data
Molecular Targeted Therapy
Mosaicism
Motor Skills Disorders
Muscle Development
Muscle Hypotonia
Muscle Weakness
Muscle, Skeletal
Muscular Diseases
Musculoskeletal Abnormalities
Mutant Proteins
Mutation
Mutation, Missense
Myocytes, Cardiac
National Cancer Institute (U.S.)
Neoplasm Invasiveness
Neoplasm Staging
Neoplasms
Nervous System Neoplasms
Neural Stem Cells
Neurilemmoma
Neurocutaneous Syndromes
Neurodevelopmental Disorders
Neurofibroma, Plexiform
Neurofibromatoses
Neurofibromatosis 1
Neurofibromatosis 2
Neurofibromin 1
Neurogenesis
Neuronal Plasticity
Neurons
Neuropsychological Tests
Nevus
Nevus, Pigmented
Niacinamide
Noonan Syndrome
Nucleic Acid Hybridization
Nucleolus Organizer Region
Obstetric Labor, Premature
Oligodendrocyte Transcription Factor 2
Oligonucleotide Array Sequence Analysis
Oncogene Protein p21(ras)
Organogenesis
Ovarian Neoplasms
Pallor
Papilloma
Paracrine Communication
Parents
Patient Advocacy
Patient Outcome Assessment
Pedigree
Personality
Personality Disorders
Phenotype
Phenylurea Compounds
Phosphatidylinositol 3-Kinases
Phosphoglycerate Kinase
Phosphoproteins
Phosphorylation
Physical Examination
Pigmentation Disorders
Plasmids
Point Mutation
Polyhydramnios
Polylysine
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Postmortem Changes
Practice Guidelines as Topic
Prader-Willi Syndrome
Precancerous Conditions
Precision Medicine
Pregnancy
Pregnancy Complications
Pregnancy Outcome
Prenatal Diagnosis
Prevalence
Prognosis
Promoter Regions, Genetic
Prospective Studies
Prostate
Prostatectomy
Prostate-Specific Antigen
Prostatic Neoplasms
Protein Conformation
Protein Kinase Inhibitors
Protein Tyrosine Phosphatase, Non-Receptor Type 11
Protein Tyrosine Phosphatases
Proteins
Protein-Tyrosine Kinases
Proteoglycans
Proto-Oncogene Proteins
Proto-Oncogene Proteins B-raf
Proto-Oncogene Proteins c-akt
Proto-Oncogene Proteins c-raf
Proto-Oncogene Proteins p21(ras)
Pseudoxanthoma Elasticum
Psychomotor Disorders
Public-Private Sector Partnerships
Pyridines
Quality of Life
Quantitative Trait, Heritable
Radiography
raf Kinases
Rare Diseases
ras Proteins
Rats
Receptors, G-Protein-Coupled
Receptors, Virus
Receptors, Vitronectin
Recombinant Proteins
Refractive Errors
Research Design
Research Report
Retrospective Studies
Reverse Transcriptase Polymerase Chain Reaction
Ring Chromosomes
RNA, Long Noncoding
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Sensitivity and Specificity
Sequence Analysis, DNA
Sequence Deletion
Sex Chromosome Aberrations
Sex Distribution
Sex Factors
Siblings
Signal Transduction
Simplexvirus
Skin Abnormalities
Skin Diseases
Skin Neoplasms
Small Molecule Libraries
SMARCB1 Protein
Smith-Magenis Syndrome
Snail Family Transcription Factors
Software
SOS1 Protein
Strabismus
Sulfhydryl Compounds
Surveys and Questionnaires
Symptom Assessment
Syndrome
Tandem Repeat Sequences
Terminology as Topic
Tetralogy of Fallot
Thymidine Kinase
Thyroid Neoplasms
Time Factors
Tooth
Tooth Abnormalities
Trans-Activators
Transcription Factors
Transduction, Genetic
Transfection
Transforming Growth Factor beta1
Translocation, Genetic
Treatment Outcome
Trisomy
Tumor Burden
Tumor Cells, Cultured
Tumor Suppressor Protein p53
Ubiquitin
Ubiquitination
Ultrasonography, Prenatal
Uniparental Disomy
United States
Up-Regulation
Urinary Bladder
Urinary Bladder Neoplasms
Whole Genome Sequencing
Xanthogranuloma, Juvenile
Young Adult
Zebrafish
Katherine's Networks
Concepts (459)
Derived automatically from this person's publications.
Costello Syndrome
Ectodermal Dysplasia
ras Proteins
Failure to Thrive
Abnormalities, Multiple
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Co-Authors (56)
People in Profiles who have published with this person.
Shankar, Suma
UC Davis
McCormick, Frank
UCSF
Kiuru, Maija
UC Davis
Klein, Ophir
UCSF
Weiss, Lauren
UCSF
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Similar People (60)
People who share similar concepts with this person.
McCormick, Frank
UCSF
Kiuru, Maija
UC Davis
Ribas, Antoni
UCLA
Gleeson, Joseph
UCSD
McMahon, Martin
UCSF
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