USC Home
About USC
Keck Hospital of USC
USC Norris Cancer Hospital
Powered by SC CTSI
Find more Research Resources
Home
About
Help/FAQs
History (0)
Search Options
UC Davis
UCI
UCLA
UCSD
UCSF
All UC Health
USC
All
Everything
Research
Concepts
Awards
People
UC Health People
UC Davis People
UCI People
UCLA People
UCSD People
UCSF People
USC People
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Matthew Deardorff
Concepts (586)
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.
Abnormalities, Multiple
Acetylation
Acetyltransferases
Acylation
ADAMTS Proteins
Adaptor Proteins, Signal Transducing
Adenomatous Polyposis Coli Protein
Adenosine Triphosphate
Adolescent
Adult
Age Factors
Aged
Agenesis of Corpus Callosum
Aging
Aging, Premature
Algorithms
Alleles
alpha-Fetoproteins
Amino Acid Sequence
Amino Acid Substitution
Ammonia
Anaphase
Aneuploidy
Animals
Anterior Cruciate Ligament
Anthropometry
Arrhythmogenic Right Ventricular Dysplasia
Arteries
Arthrogryposis
ATPases Associated with Diverse Cellular Activities
ATP-Dependent Proteases
Autistic Disorder
Autopsy
Axin Protein
Axonemal Dyneins
Axoneme
Base Pairing
Base Sequence
Basement Membrane
Basic Helix-Loop-Helix Transcription Factors
Beckwith-Wiedemann Syndrome
Benzamides
beta Catenin
Binding Sites
Biomarkers, Tumor
Biopsy
Bodily Secretions
Body Patterning
Bone and Bones
Bone Diseases, Developmental
Bone Morphogenetic Protein 4
Bone Morphogenetic Proteins
Brachydactyly
Brain
Brain Diseases
Brain Neoplasms
Branchio-Oto-Renal Syndrome
Calcium
Calcium Channels
Calcium-Binding Proteins
Calcium-Calmodulin-Dependent Protein Kinase Type 2
Calcium-Calmodulin-Dependent Protein Kinases
California
Canada
Capillaries
Cardiomyopathy, Hypertrophic
Carrier Proteins
Case-Control Studies
Catalysis
Catalytic Domain
Cataract
Cause of Death
Cell Cycle Proteins
Cell Differentiation
Cell Line
Cell Line, Tumor
Cell Membrane
Cell Survival
Cells, Cultured
Cerebral Cortex
Child
Child, Preschool
Chimerism
Chondroitin Sulfate Proteoglycans
Chromatin
Chromatin Assembly and Disassembly
Chromatin Immunoprecipitation
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 12
Chromosomes, Human, Pair 13
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 6
Chromosomes, Human, X
Cilia
Ciliary Motility Disorders
Class I Phosphatidylinositol 3-Kinases
Cleft Palate
Clinical Competence
Clinical Decision-Making
Cloning, Molecular
Codon
Codon, Nonsense
Cognition Disorders
Cohort Studies
Collagen Type IV
Comet Assay
Comparative Genomic Hybridization
Computational Biology
Computer Simulation
Confidentiality
Congenital Abnormalities
Congenital Disorders of Glycosylation
Congenital Hyperinsulinism
Connective Tissue
Connexin 26
Connexins
Consanguinity
Consensus
Contracture
Core Binding Factor Alpha 2 Subunit
Corpus Callosum
Costello Syndrome
CpG Islands
Cranial Fontanelles
Craniofacial Abnormalities
Craniosynostoses
Cross-Sectional Studies
Crystallography, X-Ray
Cyclin-Dependent Kinase Inhibitor p57
Cytogenetic Analysis
Cytokines
Cytoskeletal Proteins
Data Accuracy
Databases, Genetic
Databases, Nucleic Acid
De Lange Syndrome
Death, Sudden, Cardiac
Delivery of Health Care
Developmental Disabilities
Diagnosis, Differential
Diagnostic Errors
Disease Management
Disease Models, Animal
Disease Progression
Disease Resistance
Diseases in Twins
DNA
DNA Copy Number Variations
DNA Damage
DNA Helicases
DNA Methylation
DNA Mutational Analysis
DNA Primers
DNA Replication
DNA, Mitochondrial
DNA-Binding Proteins
DNA-Directed RNA Polymerases
Dogs
Drosophila
Drosophila melanogaster
Dyneins
E1A-Associated p300 Protein
Ear
Early Detection of Cancer
Ectromelia
Electronic Health Records
Embryo, Nonmammalian
Embryonic Development
Embryonic Induction
Enzyme Activation
Enzyme Stability
Epidemiological Monitoring
Epigenesis, Genetic
Epigenomics
Epilepsy
Esophagus
Exome
Exons
Extracellular Matrix Proteins
Eye
Eye Abnormalities
Eye Proteins
Face
Facies
Factor Analysis, Statistical
Family
Family Health
Fatal Outcome
Feeding Behavior
Female
Fetal Growth Retardation
Fetus
Fibroblasts
Fingers
Fluorescein Angiography
Foot
Foot Bones
Foot Deformities, Congenital
Fovea Centralis
Frizzled Receptors
Gait
Ganglioglioma
Gastrula
Gene Conversion
Gene Deletion
Gene Dosage
Gene Expression
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Expression Regulation, Enzymologic
Gene Frequency
Gene Order
Gene Rearrangement
Genes, Dominant
Genes, Recessive
Genes, Regulator
Genes, X-Linked
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Heterogeneity
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetics, Medical
Genetics, Population
Genome
Genome, Human
Genome, Mitochondrial
Genome-Wide Association Study
Genomic Imprinting
Genomic Instability
Genomics
Genotype
Germ-Line Mutation
Glutamic Acid
Glycogen Synthase Kinase 3
Glycogen Synthase Kinases
Glycosylation
Granulomatous Disease, Chronic
Growth and Development
Growth Disorders
Growth Hormone
Guidelines as Topic
Hand Deformities, Congenital
Haploinsufficiency
Haplotypes
Health Surveys
Hearing Loss
Hearing Loss, Sensorineural
Heart Defects, Congenital
Heart Septum
HEK293 Cells
HeLa Cells
Hemangioma
Hemangioma, Capillary
Hepatoblastoma
Heredity
Heterozygote
High-Throughput Nucleotide Sequencing
Hip Dislocation, Congenital
Histone Deacetylase Inhibitors
Histone Deacetylases
Histone-Lysine N-Methyltransferase
Histones
History, 20th Century
History, 21st Century
Holoprosencephaly
Homeodomain Proteins
Homozygote
Hospitals, Pediatric
Humans
Hydrocephalus
Hydrogen Bonding
Hyperammonemia
Hyperbilirubinemia, Hereditary
Hyperinsulinism
Hyperparathyroidism
Hyperplasia
Hypertelorism
Hypertrophy
Hypoglycemia
Hypospadias
Hypotrichosis
Hypoxia, Brain
Image Processing, Computer-Assisted
Immunologic Deficiency Syndromes
Immunologic Tests
In Situ Hybridization
In Situ Hybridization, Fluorescence
Incidence
INDEL Mutation
Infant
Infant, Newborn
Intellectual Disability
Intensive Care Units
Intensive Care Units, Neonatal
Intercellular Signaling Peptides and Proteins
Interdisciplinary Communication
Intracellular Signaling Peptides and Proteins
Ion Transport
Isochromosomes
Joint Instability
Kartagener Syndrome
KATP Channels
Kidney Neoplasms
Knee Joint
Language Development Disorders
LEOPARD Syndrome
Leukemia, Myeloid, Acute
Limb Deformities, Congenital
Linkage Disequilibrium
Lipoma
Lithium
Liver Neoplasms
Lower Extremity Deformities, Congenital
Lymphocyte Activation
Macula Lutea
Macular Degeneration
Magnetic Resonance Imaging
Male
MAP Kinase Signaling System
Mass Screening
Mass Spectrometry
Maternal Inheritance
Maternal-Fetal Exchange
Matrix Metalloproteinase 13
Medical Audit
Medicine
Meiosis
Melanocytes
Melorheostosis
Membrane Proteins
Mendelian Randomization Analysis
Mesencephalon
Mesoderm
Metabolic Diseases
Metabolism, Inborn Errors
Methionine
Mice
Mice, Inbred C57BL
Mice, Knockout
Microarray Analysis
Microcephaly
Microfilament Proteins
Micrognathism
Microinjections
Micronucleus Tests
Microscopy, Electron, Transmission
Microtubule Proteins
Microtubule-Associated Proteins
Middle Aged
Mitochondria
Mitochondrial Proteins
Models, Animal
Models, Biological
Models, Genetic
Models, Molecular
Molecular Biology
Molecular Diagnostic Techniques
Molecular Dynamics Simulation
Molecular Mimicry
Molecular Sequence Data
Monosomy
Morphogenesis
Mosaicism
Multidrug Resistance-Associated Proteins
Multiprotein Complexes
Muscle Hypotonia
Muscle Stretching Exercises
Muscles
Muscular Atrophy
Musculoskeletal Abnormalities
Mutant Proteins
Mutation
Mutation, Missense
Myelodysplastic Syndromes
N-Acetylglucosaminyltransferases
Neck
Neoplasm Proteins
Neoplasms
Nerve Tissue Proteins
Netherlands
Neural Crest
Neurodevelopmental Disorders
Neurons
Nevus
NFATC Transcription Factors
Noonan Syndrome
Notochord
N-Terminal Acetyltransferase A
N-Terminal Acetyltransferase E
Nuclear Proteins
Nucleotide Transport Proteins
Oligonucleotide Array Sequence Analysis
Oligonucleotides, Antisense
Opportunistic Infections
Organ Size
Ornithine Carbamoyltransferase
Ornithine Carbamoyltransferase Deficiency Disease
Osteochondrodysplasias
Osteopoikilosis
Osteosarcoma
Otx Transcription Factors
Oxidative Stress
Paired Box Transcription Factors
Palate
Pancreas
Parents
Pathology, Molecular
Patient Selection
PAX6 Transcription Factor
Pediatrics
Pedigree
Pennsylvania
Phenotype
Phenylthiourea
Pheochromocytoma
Philadelphia
Phosphoproteins
Phosphorylation
Placenta
Polycomb-Group Proteins
Polymerase Chain Reaction
Polymicrogyria
Polymorphism, Restriction Fragment Length
Polymorphism, Single Nucleotide
Posterior Cruciate Ligament
Postural Balance
Potassium Channels, Tandem Pore Domain
Potassium Channels, Voltage-Gated
Practice Guidelines as Topic
Prader-Willi Syndrome
Precision Medicine
Pregnancy
Prenatal Diagnosis
Prevalence
Primary Cell Culture
Privacy
Procollagen-Proline Dioxygenase
Prognosis
Prolyl Hydroxylases
Promoter Regions, Genetic
Prophase
Prospective Studies
Protein Binding
Protein Biosynthesis
Protein Conformation
Protein Domains
Protein Interaction Domains and Motifs
Protein Interaction Maps
Protein Stability
Protein Structure, Tertiary
Proteins
Proteolysis
Proteome
Proteomics
Proteus Syndrome
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-akt
Proto-Oncogene Proteins c-ets
Proto-Oncogene Proteins c-myc
Pseudoxanthoma Elasticum
Radiography
Radius
Rare Diseases
ras Proteins
Receptors, Cell Surface
Receptors, G-Protein-Coupled
Receptors, Neurotransmitter
Recombination, Genetic
Recurrence
Remote Consultation
Repetitive Sequences, Nucleic Acid
Repressor Proteins
Reproducibility of Results
Research Personnel
Retina
Retinal Diseases
Retinal Neoplasms
Retinal Pigment Epithelium
Retinitis Pigmentosa
Retinoic Acid 4-Hydroxylase
Retrospective Studies
Rett Syndrome
Reverse Transcriptase Polymerase Chain Reaction
RGS Proteins
Risk Factors
RNA Stability
RNA, Messenger
Rubinstein-Taybi Syndrome
Saccharomyces cerevisiae
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Serine Proteases
Severity of Illness Index
Sex Chromosomes
Sex Factors
Siblings
Signal Transduction
Sister Chromatid Exchange
Skin
Skin Neoplasms
Skull
Sleep
Sleep Apnea Syndromes
Smith-Magenis Syndrome
Snail Family Transcription Factors
snRNP Core Proteins
Software
Somites
Sotos Syndrome
Spasms, Infantile
Stroke Volume
Structure-Activity Relationship
Sturge-Weber Syndrome
Surveys and Questionnaires
Syndactyly
Syndrome
Synostosis
T-Box Domain Proteins
Telomere Homeostasis
Tendons
Tetrasomy
Thiourea
Thrombocytopenia
Tibia
Time Factors
T-Lymphocyte Subsets
Tomography, Optical Coherence
Tooth Abnormalities
Trans-Activators
Transcription Factors
Transcription, Genetic
Transcriptional Elongation Factors
Trinucleotide Repeat Expansion
Trisomy
TRPV Cation Channels
Truncus Arteriosus
Tumor Cells, Cultured
Twins, Dizygotic
Twins, Monozygotic
Two-Dimensional Difference Gel Electrophoresis
Two-Hybrid System Techniques
Ubiquitin-Protein Ligases
Ulna
Ultrasonography
Uniparental Disomy
United States
Upper Extremity Deformities, Congenital
Urea
Vacuolar Proton-Translocating ATPases
Vascular Calcification
Vascular Malformations
Vesicular Transport Proteins
Weill-Marchesani Syndrome
Wilms Tumor
Wnt Proteins
Wnt Signaling Pathway
Wnt1 Protein
X Chromosome Inactivation
Xenopus
Xenopus laevis
Xenopus Proteins
Young Adult
Zebrafish
Zebrafish Proteins
Zinc Fingers
Matthew's Networks
Concepts (586)
Derived automatically from this person's publications.
De Lange Syndrome
Intellectual Disability
Beckwith-Wiedemann Syndrome
Chromosomal Proteins, Non-Histone
Abnormalities, Multiple
Explore
_
Co-Authors (32)
People in Profiles who have published with this person.
Nagiel, Aaron
USC
Bird, Lynne
UCSD
Saitta, Sulagna
UCLA
Iyengar, Rahul
USC
Biswas, Sawona
UCSF
Explore
_
Similar People (60)
People who share similar concepts with this person.
Gleeson, Joseph
UCSD
Kimonis, Virginia
UCI
Cleveland, Don
UCSD
Moore, Anthony
UCSF
Yokomori, Kyoko
UCI
Explore
_
Same Department
Buffenn, Angela
Deavenport-Saman, Alexis
Gillette, Kelley
Lin, Chuan-Hao
Rosenthal, Leslie
Search Department
_