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Cynthia Curry
Concepts (363)
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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.
14-3-3 Proteins
1-Alkyl-2-acetylglycerophosphocholine Esterase
46, XX Disorders of Sex Development
Abnormalities, Multiple
Aborted Fetus
Acetyltransferases
Acrocephalosyndactylia
Acro-Osteolysis
Adolescent
Adolescent Medicine
ADP-Ribosylation Factors
Adult
Age of Onset
Aged
Aged, 80 and over
Agenesis of Corpus Callosum
Alleles
Alopecia
Alternative Splicing
Alveolar Bone Loss
Amino Acid Sequence
Anal Canal
Aneuploidy
Animals
Anophthalmos
Anthropometry
Antibodies, Antiphospholipid
Antigens
Antithrombin III
Anus, Imperforate
Aortic Aneurysm
Apoptosis
Arachnodactyly
Arthrogryposis
Autistic Disorder
Autoimmunity
Basal Ganglia Diseases
Base Sequence
beta-Transducin Repeat-Containing Proteins
Birth Weight
Bladder Exstrophy
Blepharophimosis
Blood
Body Height
Bone and Bones
Bone Diseases, Developmental
Brain
Brain Diseases
Brain Stem
Calcinosis
California
Canada
Candida
Candidiasis
Catheterization
Cell Cycle Proteins
Cell Line
Cells, Cultured
Centrosome
Cerebellar Diseases
Cerebellum
Cerebral Arteries
Cerebral Palsy
Child
Child Behavior Disorders
Child Development Disorders, Pervasive
Child, Preschool
Chondrocytes
Chondrodysplasia Punctata
Chondroitin Sulfate Proteoglycans
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Breakage
Chromosome Deletion
Chromosomes, Artificial, Bacterial
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 12
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 21
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Class Ia Phosphatidylinositol 3-Kinase
Cleft Palate
Cloaca
Clubfoot
Cohort Studies
Collagen
Collagen Type III
Collagen Type V
Comparative Genomic Hybridization
Congenital Abnormalities
Connective Tissue
Connective Tissue Diseases
Consanguinity
Contracture
Coronary Disease
COS Cells
Craniofacial Abnormalities
Craniosynostoses
Curriculum
Cyclin-Dependent Kinase 5
Cytogenetic Analysis
De Lange Syndrome
Developmental Disabilities
Diagnosis, Differential
Diagnostic and Statistical Manual of Mental Disorders
Diagnostic Tests, Routine
Disease
Disease Models, Animal
Diseases in Twins
DNA
DNA Copy Number Variations
DNA Methylation
DNA Mutational Analysis
DNA Primers
DNA-Binding Proteins
Drosophila melanogaster
Dwarfism
E2F3 Transcription Factor
Education, Medical
Ehlers-Danlos Syndrome
Endoplasmic Reticulum
Epiglottis
Epilepsy
Esophageal Atresia
Esophagus
Evolution, Molecular
Exome
Exons
Eye Abnormalities
Face
Facies
Factor V
Family
Family Health
Female
Fetal Death
Fetus
Fibroblast Growth Factors
Fibroblasts
Fibula
Fingers
Frameshift Mutation
Gene Dosage
Gene Duplication
Gene Expression Regulation
Genes, Dominant
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Carrier Screening
Genetic Predisposition to Disease
Genetic Testing
Genetics, Medical
Genome, Human
Genomics
Genotype
Gestational Age
Golgi Apparatus
Growth Disorders
GTPase-Activating Proteins
Hamartoma
Hand Deformities, Congenital
Heart Defects, Congenital
Hernia, Umbilical
Heterozygote
High-Throughput Nucleotide Sequencing
Histone Demethylases
History, 20th Century
History, 21st Century
Holoprosencephaly
Homeodomain Proteins
Homozygote
Human Genetics
Humans
Hybrid Cells
Hydatidiform Mole
Hydrops Fetalis
Hypercalcemia
Hyperhomocysteinemia
Hypertelorism
Hypertension, Pulmonary
Hypospadias
Hypothalamic Diseases
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Infant, Newborn, Diseases
Inheritance Patterns
Inhibitor of Differentiation Proteins
Intellectual Disability
Intestines
Intracranial Thrombosis
Ion Channels
Joints
Jumonji Domain-Containing Histone Demethylases
Karyotyping
Kidney
Kruppel-Like Transcription Factors
Leg
Leukoencephalopathies
Limb Deformities, Congenital
Lip
Lipoprotein(a)
Lod Score
Loeys-Dietz Syndrome
Loss of Function Mutation
Lung
Lung Diseases
Lupus Erythematosus, Systemic
Lymphocytes
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Mammals
Marfan Syndrome
Maternal Age
Matrix Attachment Region Binding Proteins
Membrane Proteins
Mentors
Metabolic Diseases
Methylenetetrahydrofolate Reductase (NADPH2)
Mice
Mice, Transgenic
Microcephaly
Microphthalmos
Microtubule-Associated Proteins
Middle Aged
Migraine with Aura
Mitosis
Mitosporic Fungi
Mixed Connective Tissue Disease
Models, Biological
Models, Molecular
Molecular Sequence Data
Monoacylglycerol Lipases
Mouth
Mouth Abnormalities
Mullerian Ducts
Mutation
Mutation, Missense
Mycoses
Myofibromatosis
Nephrocalcinosis
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Neurocutaneous Syndromes
Neurodevelopmental Disorders
Noonan Syndrome
Nuclear Proteins
Nucleic Acid Hybridization
Ocular Motility Disorders
Oligonucleotide Array Sequence Analysis
Ophthalmoplegia
Osteoblasts
Osteochondrodysplasias
Osteogenesis
Osteogenesis Imperfecta
Osteoporosis
Paired Box Transcription Factors
Pallister-Hall Syndrome
Parenteral Nutrition
Paternal Age
Pediatrics
Pedigree
Periodontitis
Phenotype
Phosphorylation
Placenta
Point Mutation
Polydactyly
Polymerase Chain Reaction
Polymicrogyria
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Practice Guidelines as Topic
Pre-Eclampsia
Pregnancy
Pregnancy Complications
Primates
Progeria
Prognosis
Prospective Studies
Protein C
Protein Isoforms
Protein Phosphatase 2C
Protein S
Prothrombin
Proto-Oncogene Proteins
rab GTP-Binding Proteins
Radiography
Radius
Real-Time Polymerase Chain Reaction
Receptor, Fibroblast Growth Factor, Type 2
Receptor, Platelet-Derived Growth Factor beta
Recurrence
Registries
Regression Analysis
Repressor Proteins
Retinal Diseases
Retrospective Studies
Review Literature as Topic
Rhombencephalon
Risk Factors
RNA Interference
RNA, Messenger
Scleroderma, Systemic
Segmental Duplications, Genomic
Sepsis
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Amino Acid
Severity of Illness Index
Sex Distribution
Signal Transduction
Skeleton
Skin
Skin Abnormalities
Smoothened Receptor
Social Support
Sodium-Potassium-Exchanging ATPase
SOS1 Protein
SOXC Transcription Factors
Spastic Paraplegia, Hereditary
Spindle Apparatus
Spine
Spondylolysis
Stroke
Syndactyly
Syndrome
Teaching
Terminology as Topic
Thinness
Thrombophilia
Tibia
Time Factors
Trachea
Tracheoesophageal Fistula
Transcription Factors
Transfection
Transforming Growth Factor beta
Translocation, Genetic
tRNA Methyltransferases
Twin Studies as Topic
Twins, Dizygotic
Twins, Monozygotic
Ubiquitin-Protein Ligases
Ulna
Uniparental Disomy
United States
Veins
Venous Thromboembolism
Vomiting
Wnt1 Protein
X Chromosome
Young Adult
Zebrafish
Zinc Finger Protein Gli3
Zinc Fingers
Cynthia's Networks
Concepts (363)
Derived automatically from this person's publications.
Intellectual Disability
Neurodevelopmental Disorders
Genetics, Medical
Limb Deformities, Congenital
Osteogenesis Imperfecta
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Co-Authors (20)
People in Profiles who have published with this person.
Hutchison, Terry
UCSF
Bird, Lynne
UCSD
Marco, Elysa
UCSF
Martinez, Julian
UCLA
Russell, Bianca
UCLA
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_
Similar People (60)
People who share similar concepts with this person.
Gleeson, Joseph
UCSD
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USC
Anderson, Peter
UCI
Geschwind, Daniel
UCLA
Martinez, Julian
UCLA
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Same Department
Brox, William
Foster, Steven
Keosheyan, Rhonda
Kido, Tamiko
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