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Cruz Rodriguez, Benjamin
Cuccurazzu, Bruna
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Marilyn Jones
Concepts (286)
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Concepts are derived automatically from a person's publications.
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Categories
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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
Acyltransferases
Adaptor Proteins, Signal Transducing
Adolescent
Adult
Aged
Agenesis of Corpus Callosum
Algorithms
Alleles
Amino Acid Motifs
Anesthesia
Animals
Arteriovenous Malformations
Arthrogryposis
Attitude to Health
Audiometry, Pure-Tone
Autoimmune Diseases
Base Sequence
Beckwith-Wiedemann Syndrome
Blepharoptosis
Body Weights and Measures
Brain
Brain Diseases
California
Capillaries
CD8-Positive T-Lymphocytes
Cell Cycle Proteins
Cell Line
Cells, Cultured
Cerebellar Ataxia
Child
Child, Preschool
China
Chorion
Chromosome Aberrations
Chromosome Deletion
Chromosomes, Human, Pair 20
Chromosomes, Human, Pair 9
Cleft Lip
Cleft Palate
Clinical Competence
Clinical Protocols
Codon, Terminator
Cognition
Cohort Studies
Congenital Abnormalities
Constipation
Continuity of Patient Care
Corneal Diseases
Corpus Callosum
Counseling
Craniofacial Abnormalities
Craniosynostoses
Critical Illness
Cyclophilins
Cytokines
De Lange Syndrome
Death, Sudden, Cardiac
Decision Making
Delayed Diagnosis
Developmental Disabilities
Diabetes, Gestational
Diagnosis, Differential
Diaphragm
DiGeorge Syndrome
Disease Management
Disease Models, Animal
Diseases in Twins
Disorders of Sex Development
DNA Copy Number Variations
DNA Mutational Analysis
DNA-Binding Proteins
Drosophila melanogaster
Embryo, Nonmammalian
Entropion
Epilepsy, Generalized
Exome
Exons
Eye Abnormalities
Eye Diseases
Eyelids
Face
Facial Paralysis
Facies
Failure to Thrive
Fatal Outcome
Fellowships and Scholarships
Female
Femur Head
Fetal Diseases
Fetus
Follow-Up Studies
Frameshift Mutation
Gastrointestinal Diseases
Gene Deletion
Gene Expression
Gene Expression Regulation, Enzymologic
Gene Rearrangement
Genes, Dominant
Genes, Lethal
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Predisposition to Disease
Genetic Research
Genetic Testing
Genetic Variation
Genome-Wide Association Study
Genomic Imprinting
Genomics
Genotype
Gestational Age
Growth Charts
Growth Disorders
Hand Deformities, Congenital
Haploinsufficiency
Hearing Loss
Heart Defects, Congenital
HEK293 Cells
Hematologic Diseases
Hepatocyte Nuclear Factor 1-beta
Hernia, Hiatal
Hernias, Diaphragmatic, Congenital
Heterogeneous-Nuclear Ribonucleoprotein K
High-Throughput Nucleotide Sequencing
Histone Deacetylases
Histone Demethylases
Histone-Lysine N-Methyltransferase
Holoprosencephaly
Homozygote
Hospitals, Pediatric
Humans
Hydrops Fetalis
Hypertrichosis
Hypotrichosis
Image Enhancement
Image Interpretation, Computer-Assisted
Imaging, Three-Dimensional
Immunoblotting
Immunohistochemistry
Immunologic Deficiency Syndromes
In Situ Hybridization
In Situ Hybridization, Fluorescence
Incidence
Infant
Infant, Newborn
Infant, Newborn, Diseases
Inorganic Pyrophosphatase
Intellectual Disability
Intestinal Neoplasms
Intestines
Jacobsen Distal 11q Deletion Syndrome
Joint Instability
Jurkat Cells
Karyotyping
Kidney
Kidney Diseases
Kidney Diseases, Cystic
Killer Cells, Natural
Lacrimal Apparatus Diseases
Language Development
Limb Deformities, Congenital
LIM-Homeodomain Proteins
Lipomatosis
Loss of Function Mutation
Lymphedema
Magnetic Resonance Imaging
Male
Marfan Syndrome
Mass Screening
Matrix Attachment Region Binding Proteins
Mexico
Mice
Mice, 129 Strain
Mice, Inbred C57BL
Mice, Inbred Strains
Mice, Knockout
Microcephaly
Micrognathism
Middle Ear Ventilation
Mitochondrial Proteins
Models, Molecular
Molecular Sequence Data
Mosaicism
Multicenter Studies as Topic
Muscle Hypotonia
Mutation
Mutation, Missense
Myeloid-Lymphoid Leukemia Protein
Myosin-Light-Chain Phosphatase
Nail-Patella Syndrome
Nails, Malformed
Neck
Nephrosis
Nerve Tissue Proteins
Nervous System Malformations
Neurocognitive Disorders
Neurocutaneous Syndromes
Neurodevelopmental Disorders
Nuchal Translucency Measurement
Nuclear Proteins
Oculomotor Muscles
Organ Size
Orthognathic Surgical Procedures
Osteochondrodysplasias
Osteotomy, Le Fort
Otitis Media with Effusion
p120 GTPase Activating Protein
Palliative Care
Pancreas
Patella
Patient Care Team
Pedigree
Penis
Peptidylprolyl Isomerase
Phenotype
Physician-Patient Relations
Pierre Robin Syndrome
Placenta
Polyhydramnios
Polymorphism, Single Nucleotide
Port-Wine Stain
Postoperative Complications
Practice Guidelines as Topic
Pregnancy
Pregnancy Outcome
Pregnancy Trimester, First
Pregnancy, High-Risk
Pregnant Women
Prenatal Care
Prenatal Diagnosis
Prognosis
Prospective Studies
Protein Conformation
Protein Structure, Tertiary
Proteins
Proto-Oncogene Protein c-ets-1
Purine-Nucleoside Phosphorylase
Pyrophosphatases
Rare Diseases
Referral and Consultation
Repetitive Sequences, Nucleic Acid
Repressor Proteins
Reproducibility of Results
Reproductive Techniques, Assisted
Retinitis Pigmentosa
Retrospective Studies
Reverse Transcriptase Polymerase Chain Reaction
Rhabdomyosarcoma
Risk Factors
RNA Precursors
RNA Splicing
Seizures
Sensitivity and Specificity
Septum Pellucidum
Sequence Deletion
Siblings
Signal Transduction
Situs Inversus
Skin Abnormalities
Smoothened Receptor
SOXF Transcription Factors
Spine
Spliceosomes
Syndactyly
Syndrome
Telangiectasis
Tomography, X-Ray Computed
Transcription Factors
Transcriptional Elongation Factors
Translocation, Genetic
Treatment Outcome
Trisomy
Twins, Dizygotic
Ubiquitin-Protein Ligases
Ultrasonography
Ultrasonography, Prenatal
United States
Urethra
Urogenital Abnormalities
Vesico-Ureteral Reflux
Vestibular Diseases
Vocal Cord Paralysis
Whole Genome Sequencing
Workload
Young Adult
Marilyn's Networks
Concepts (286)
Derived automatically from this person's publications.
Limb Deformities, Congenital
Abnormalities, Multiple
Craniofacial Abnormalities
Intellectual Disability
Syndactyly
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Co-Authors (49)
People in Profiles who have published with this person.
Wigby, Kristen
UCSD
Wigby, Kristen
UC Davis
Pretorius, Dolores
UCSD
Gosman, Amanda
UCSD
Bird, Lynne
UCSD
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_
Similar People (60)
People who share similar concepts with this person.
Gleeson, Joseph
UCSD
Magee, William
USC
Lee, Justine
UCLA
Anderson, Peter
UCI
Deardorff, Matthew
USC
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