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Julian Martinez
Concepts (442)
Back to Profile
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
Active Transport, Cell Nucleus
Adaptor Protein Complex 1
Adenocarcinoma
Adolescent
Adolescent Psychiatry
Adrenal Hyperplasia, Congenital
Adrenal Insufficiency
Adult
Aftercare
Aged
Aged, 80 and over
Aggression
Aging
Aging, Premature
Algorithms
Alleles
Amino Acid Sequence
Amyloid beta-Protein Precursor
Aneuploidy
Aneurysm
Animals
Animals, Genetically Modified
Antennapedia Homeodomain Protein
Antigens, Nuclear
Antineoplastic Agents
Antineoplastic Combined Chemotherapy Protocols
Anxiety
Apoptosis
Apraxias
ATPases Associated with Diverse Cellular Activities
Attention Deficit Disorder with Hyperactivity
Autism Spectrum Disorder
Autistic Disorder
Base Sequence
Basic Helix-Loop-Helix Transcription Factors
Beckwith-Wiedemann Syndrome
Biomarkers
Biomarkers, Tumor
Biomedical Research
Bipolar Disorder
Bloom Syndrome
Body Size
Brain
Calcium-Binding Proteins
Calmodulin
Carcinoma, Squamous Cell
Cardiomyopathies
Carrier Proteins
Case-Control Studies
Caspases
Cataract
CCCTC-Binding Factor
Cell Adhesion Molecules, Neuronal
Cell Cycle
Cell Cycle Proteins
Cell Death
Cell Differentiation
Cell Division
Cell Hypoxia
Cell Line
Cell Line, Transformed
Cell Proliferation
Central Nervous System
Cerebellar Neoplasms
Chemotherapy, Adjuvant
Child
Child Behavior Disorders
Child Psychiatry
Child, Preschool
Chromatin
Chromatin Assembly and Disassembly
Chromogranins
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Deletion
Chromosome Disorders
Chromosome Inversion
Chromosome Mapping
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 5
Chromosomes, Human, X
Chromothripsis
Chronic Disease
Cleft Lip
Cleft Palate
Codon, Nonsense
Cognition
Cohort Studies
Communication
Comparative Genomic Hybridization
Computational Biology
Computer Simulation
Congenital Abnormalities
Consanguinity
Conserved Sequence
Cooperative Behavior
Corpus Callosum
Craniofacial Abnormalities
Craniofacial Dysostosis
Craniosynostoses
CRISPR-Cas Systems
Cyclic AMP-Dependent Protein Kinase RIbeta Subunit
Cyclin-Dependent Kinase Inhibitor p57
Cystinuria
Cysts
Data Collection
Databases, Factual
DEAD-box RNA Helicases
Deep Brain Stimulation
Developmental Disabilities
Diagnosis, Computer-Assisted
Diagnosis, Differential
DiGeorge Syndrome
Disease Models, Animal
Disease Progression
DNA
DNA Methylation
DNA Mutational Analysis
DNA Primers
DNA Repair Enzymes
DNA Replication
DNA, Mitochondrial
DNA-Binding Proteins
Down Syndrome
Down-Regulation
Drosophila
Drosophila melanogaster
Drosophila Proteins
Dystonic Disorders
Electroencephalography
Electromyography
Embryo, Nonmammalian
Endocrine System Diseases
Epigenesis, Genetic
Epigenomics
Epilepsy
Eukaryotic Initiation Factor-3
Exome
Exons
Exophthalmos
Extracellular Matrix
Eye Abnormalities
Eye Proteins
Face
Facial Asymmetry
Facies
Feasibility Studies
Female
Fetal Growth Retardation
Follow-Up Studies
Forkhead Transcription Factors
Fragile X Syndrome
Frameshift Mutation
Frizzled Receptors
Gait
Gait Disorders, Neurologic
GATA Transcription Factors
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Knockdown Techniques
Gene Order
Gene Rearrangement
Gene Regulatory Networks
Genes, Recessive
Genes, X-Linked
Genetic Association Studies
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Loci
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genome, Human
Genome, Insect
Genome-Wide Association Study
Genomic Imprinting
Genomic Structural Variation
Genomics
Genotype
Germ Cells
Germ-Line Mutation
Glomerulosclerosis, Focal Segmental
Glycerol Kinase
Glycogen Storage Disease Type IIb
Growth Disorders
GTP-Binding Protein alpha Subunits, Gs
Hamartoma Syndrome, Multiple
Haploinsufficiency
Heart Defects, Congenital
Hedgehog Proteins
HEK293 Cells
Hematopoiesis
Hematopoietic Stem Cells
Hematopoietic System
Hemocytes
Hemolymph
Hermanski-Pudlak Syndrome
Heterozygote
High-Throughput Nucleotide Sequencing
Histone-Lysine N-Methyltransferase
Histones
Homeostasis
Homozygote
Host-Parasite Interactions
Humans
Hypertelorism
Hypoadrenocorticism, Familial
Immunohistochemistry
In Situ Hybridization
In Situ Hybridization, Fluorescence
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Information Dissemination
Informed Consent
Inpatients
Intellectual Disability
Intelligence Tests
Intracellular Signaling Peptides and Proteins
Intracranial Aneurysm
Intranuclear Space
Kidney
Kidney Neoplasms
Language Development Disorders
Larva
Laryngeal Diseases
Leucine
Li-Fraumeni Syndrome
Linear Models
Lipid Metabolism
Lipomatosis
Liver
Liver Failure
Locomotion
Loss of Heterozygosity
Lung Diseases
Lymphatic System
Lymphoid Tissue
Lysosomal-Associated Membrane Protein 2
Magnetic Resonance Imaging
Male
Medical History Taking
Medical Records
Medulloblastoma
Megalencephaly
Melanoma
Membrane Proteins
Methylation
Mice
Mice, Inbred C57BL
Mice, Knockout
Microarray Analysis
Microcephaly
Micrognathism
MicroRNAs
Microscopy, Confocal
Middle Aged
Mitochondria
Mitochondrial Diseases
Mitochondrial Proteins
Models, Animal
Models, Biological
Molecular Biology
Molecular Diagnostic Techniques
Molecular Sequence Data
Mosaicism
Motor Skills
Mouth Mucosa
Multienzyme Complexes
Muscle Hypotonia
Muscular Diseases
Musculoskeletal Abnormalities
Mutation
Mutation, Missense
Myeloid Cells
National Institutes of Health (U.S.)
Natural Language Processing
Neoadjuvant Therapy
Neonatal Screening
Neoplasm Proteins
Neoplasm Staging
Neoplasms
Neoplasms, Germ Cell and Embryonal
Nephrotic Syndrome
Nerve Tissue Proteins
Nervous System
Nervous System Diseases
Nervous System Malformations
Neural Stem Cells
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neurofibromatosis 1
Neuroimaging
Neurology
Neurons
Neuropeptides
Neuropsychological Tests
Nuclear Proteins
Nucleosomes
Octamer Transcription Factor-3
Oligonucleotide Array Sequence Analysis
Optic Nerve Glioma
Optic Nerve Neoplasms
Organelles
Ornithine Carbamoyltransferase Deficiency Disease
Osteochondrodysplasias
Osteochondroma
Oxidative Stress
Oxidoreductases Acting on Sulfur Group Donors
p21-Activated Kinases
Pain
Pancreatitis
Papilloma
Parents
Paternal Age
Paternal Inheritance
Pathology, Molecular
Patient Discharge
Pedigree
Peptide Initiation Factors
Phenotype
Phosphatidylinositol 3-Kinase
Phosphatidylinositol 3-Kinases
Phosphoric Monoester Hydrolases
Phylogeny
Podocytes
Polycystic Kidney Diseases
Polycystic Kidney, Autosomal Dominant
Polydactyly
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Polyneuropathies
Prader-Willi Syndrome
Precision Medicine
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
Pregnancy
Primary Cell Culture
Prognosis
Proliferating Cell Nuclear Antigen
Protein Binding
Protein Kinases
Protein Phosphatase 2C
Protein Structure, Tertiary
Proteins
Protein-Tyrosine Kinases
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-akt
Psychotic Disorders
PTEN Phosphohydrolase
Quality of Life
rac GTP-Binding Proteins
Rare Diseases
ras Proteins
Rats
Reactive Oxygen Species
Receptor Protein-Tyrosine Kinases
Receptor, Fibroblast Growth Factor, Type 2
Receptor, Platelet-Derived Growth Factor beta
Receptors, Cell Surface
Receptors, Fibroblast Growth Factor
Receptors, Notch
Repressor Proteins
Retrospective Studies
Ribonuclease III
Ribosomal Protein S6 Kinases
Ribosomal Protein S6 Kinases, 90-kDa
RNA Helicases
RNA Interference
RNA Polymerase II
RNA Processing, Post-Transcriptional
RNA Splicing
RNA Splicing Factors
RNA, Messenger
Saccharomyces cerevisiae
Seizures
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Serine-Arginine Splicing Factors
Severity of Illness Index
Signal Transduction
Sirolimus
Skin Abnormalities
Skin Neoplasms
snRNP Core Proteins
SOXB1 Transcription Factors
SOXD Transcription Factors
Spasms, Infantile
Spinocerebellar Degenerations
Spliceosomes
STAT Transcription Factors
Stem Cell Niche
Stem Cells
Stereotyped Behavior
Stomach Neoplasms
Strabismus
Structure-Activity Relationship
Substance-Related Disorders
Symptom Assessment
Synapses
Syndrome
Testicular Neoplasms
TOR Serine-Threonine Kinases
Tourette Syndrome
Trachea
Tracheotomy
Trans-Activators
Transcription Factors
Transcription, Genetic
Transcriptome
Translocation, Genetic
Treatment Outcome
Trisomy
TRPP Cation Channels
Tumor Suppressor Protein p53
Tumor Suppressor Proteins
United States
Vascular Endothelial Growth Factors
Vascular Malformations
Visual Pathways
Vocal Cord Paralysis
Vomiting
Wasps
Whole Genome Sequencing
Wilms Tumor
Wnt1 Protein
X Chromosome Inactivation
Xenopus laevis
Young Adult
Zebrafish
Zebrafish Proteins
Julian's Networks
Concepts (442)
Derived automatically from this person's publications.
Neurodevelopmental Disorders
Intellectual Disability
Developmental Disabilities
Megalencephaly
Drosophila Proteins
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_
Co-Authors (97)
People in Profiles who have published with this person.
Quintero-Rivera, Fabiola
UCI
Nelson, Stanley
UCLA
Besterman, Aaron
UCSD
Banerjee, Utpal
UCLA
Chang, Vivian
UCLA
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Similar People (60)
People who share similar concepts with this person.
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UCSD
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UCLA
Anderson, Peter
UCI
Hagerman, Randi
UC Davis
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UCSF
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