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Fabiola Quintero-Rivera
Concepts (360)
Back to Profile
Concepts are derived automatically from a person's publications.
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Categories
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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.
5' Flanking Region
Abnormalities, Multiple
Acetylation
Acrocephalosyndactylia
Acyltransferases
Adaptor Proteins, Signal Transducing
Adolescent
Adolescent Psychiatry
ADP-ribosyl Cyclase 1
Adult
Aftercare
Aged
Aged, 80 and over
Aggression
Alleles
alpha-Thalassemia
Alstrom Syndrome
Amino Acid Motifs
Amino Acid Sequence
Amyotrophic Lateral Sclerosis
Aneuploidy
Animals
Animals, Newborn
Antibodies, Antinuclear
Antineoplastic Agents
Anxiety
Aortic Coarctation
Aortic Valve
ATPases Associated with Diverse Cellular Activities
Atrophy
Autism Spectrum Disorder
Autistic Disorder
Autopsy
Bias
Biomarkers
Biomarkers, Tumor
Biopsy
Bipolar Disorder
Blotting, Northern
Blotting, Southern
Blotting, Western
B-Lymphocytes
Brain
Brain Diseases
Calmodulin
Cardiomyopathies
Cardiomyopathy, Dilated
Carrier Proteins
Caspases
Cell Adhesion Molecules, Neuronal
Cell Cycle Proteins
Cell Death
Cell Line
Cell Proliferation
Cerebellar Ataxia
Child
Child Behavior Disorders
Child Psychiatry
Child, Preschool
Cholesterol
Chromatin Assembly and Disassembly
Chromosome Aberrations
Chromosome Banding
Chromosome Breakage
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Inversion
Chromosome Mapping
Chromosomes, Human
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 12
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 19
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 8
Chromosomes, Human, X
Chromosomes, Human, Y
Chromothripsis
Ciliopathies
Cleft Lip
Cleft Palate
Clinical Competence
Clinical Laboratory Techniques
Codon, Nonsense
Cohort Studies
Comparative Genomic Hybridization
Computational Biology
Congenital Abnormalities
Consensus
Constipation
Corpus Callosum
Cranial Fontanelles
Craniofacial Abnormalities
Craniofacial Dysostosis
Cultural Diversity
Curriculum
Cyclic AMP Response Element-Binding Protein
Cystinuria
Cytidine Deaminase
Databases, Genetic
De Lange Syndrome
DEAD-box RNA Helicases
Delivery of Health Care
Developmental Disabilities
Diagnosis, Differential
DiGeorge Syndrome
DNA Breaks, Double-Stranded
DNA Copy Number Variations
DNA Mutational Analysis
DNA Primers
DNA-Binding Proteins
Down Syndrome
Down-Regulation
Drosophila melanogaster
Ductus Arteriosus, Patent
Duodenal Obstruction
E2F1 Transcription Factor
Education, Medical, Undergraduate
Embryo, Mammalian
Endocardial Fibroelastosis
Epithelial-Mesenchymal Transition
Epstein-Barr Virus Infections
Evidence-Based Medicine
Exome
Exons
Exophthalmos
Eye Abnormalities
Face
Facial Asymmetry
Facies
Failure to Thrive
Fatal Outcome
Feasibility Studies
Female
Fetal Growth Retardation
Fetus
Fibroblasts
Fibromatosis, Gingival
Frontotemporal Dementia
GATA6 Transcription Factor
Gene Amplification
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Profiling
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Expression Regulation, Leukemic
Gene Frequency
Gene Knockdown Techniques
Gene Order
Gene Rearrangement
Gene Regulatory Networks
Gene Silencing
Genes, myc
Genes, X-Linked
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Loci
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetics, Medical
Genome
Genome, Human
Genomics
Germ-Line Mutation
Growth Disorders
Haploidy
Haploinsufficiency
Health Status Disparities
Hearing Loss
Heart Defects, Congenital
Heart Transplantation
Heart Valve Diseases
Heart Ventricles
HEK293 Cells
Hepatocyte Nuclear Factor 1-beta
Herpesvirus 4, Human
Heterozygote
High-Throughput Nucleotide Sequencing
Histone Acetyltransferases
Histone Deacetylases
Histone-Lysine N-Methyltransferase
Histones
Homozygote
Human Development
Human Genome Project
Humans
Hydrops Fetalis
Hypertelorism
Hypertrichosis
Hypoxia
Immunoglobulin Heavy Chains
Immunohistochemistry
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Inpatients
Intellectual Disability
Intestinal Atresia
Intestinal Diseases
Intestines
Ion Channels
Karyotype
Karyotyping
Kidney
Kidney Diseases
Kidney Diseases, Cystic
Language Development Disorders
Latin America
Leucine
Leukemia, Lymphocytic, Chronic, B-Cell
Leukemia, Myeloid, Acute
Liver
Liver Diseases
Liver Transplantation
Loss of Function Mutation
Loss of Heterozygosity
Lupus Erythematosus, Systemic
Lymphoma, Non-Hodgkin
Lymphoproliferative Disorders
Magnetic Resonance Imaging
Male
Mandibulofacial Dysostosis
Medical History Taking
Membrane Proteins
Merozoite Surface Protein 1
Mice
Mice, Inbred C57BL
Microarray Analysis
Microcephaly
Middle Aged
Models, Molecular
Molecular Conformation
Molecular Diagnostic Techniques
Molecular Sequence Data
Mosaicism
Mothers
Multicenter Studies as Topic
Multiple Myeloma
Mutagenesis, Insertional
Mutation
Mutation, Missense
Myelodysplastic Syndromes
Myeloid-Lymphoid Leukemia Protein
Myeloproliferative Disorders
Myocardium
Myositis, Inclusion Body
Nerve Tissue Proteins
Nervous System Malformations
Neurodevelopmental Disorders
NFI Transcription Factors
Nuclear Matrix-Associated Proteins
Nucleotides
Oligonucleotide Array Sequence Analysis
Olivopontocerebellar Atrophies
Oncogene Proteins, Fusion
Ornithine Carbamoyltransferase
Ornithine Carbamoyltransferase Deficiency Disease
Osteitis Deformans
Pancreatitis
Paternal Age
Paternal Inheritance
Patient Discharge
Pedigree
Penetrance
Peptide Elongation Factors
Personnel Selection
Phenotype
Pierre Robin Syndrome
Point Mutation
Polymorphism, Single Nucleotide
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Pregnancy
Pregnancy Complications
Pregnancy Outcome
Prenatal Diagnosis
Prognosis
Proprotein Convertase 9
Proprotein Convertases
Protein Structure, Secondary
Protein Structure, Tertiary
Proteins
Protein-Tyrosine Kinases
Proto-Oncogene Proteins c-bcl-2
Proto-Oncogene Proteins c-bcl-6
Psychotic Disorders
PTEN Phosphohydrolase
Rare Diseases
Receptor, Fibroblast Growth Factor, Type 2
Receptor, Fibroblast Growth Factor, Type 3
Receptors, Cytokine
Receptors, Immunologic
Recurrence
Repetitive Sequences, Nucleic Acid
Repressor Proteins
Retrospective Studies
Reverse Transcriptase Polymerase Chain Reaction
Ribonucleoprotein, U5 Small Nuclear
Ribosomal Protein S6 Kinases, 90-kDa
Ring Chromosomes
RNA Helicases
RNA Splicing
RNA Splicing Factors
RNA-Binding Proteins
Segmental Duplications, Genomic
Seizures
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Serine Endopeptidases
Signal Transduction
Sotos Syndrome
SOX9 Transcription Factor
Spinal Cord
Spliceosomes
Strabismus
Students
Substance-Related Disorders
Surveys and Questionnaires
Synapses
Synaptotagmins
Syndrome
Testis
Tetralogy of Fallot
Tomography, X-Ray Computed
TOR Serine-Threonine Kinases
Tourette Syndrome
Transcriptome
Translocation, Genetic
Treatment Outcome
Trisomy
Ultrasonography, Prenatal
United States
Ureter
Urinary Tract
Urogenital Abnormalities
Valosin Containing Protein
Vesico-Ureteral Reflux
Wnt Proteins
X Chromosome Inactivation
Young Adult
ZAP-70 Protein-Tyrosine Kinase
Zebrafish
Fabiola's Networks
Concepts (360)
Derived automatically from this person's publications.
Abnormalities, Multiple
Chromosome Deletion
Intellectual Disability
Chromosome Disorders
Histone-Lysine N-Methyltransferase
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Co-Authors (68)
People in Profiles who have published with this person.
Martinez, Julian
UCLA
Gallant, Natalie
UCI
Nelson, Stanley
UCLA
Ji, Jianling
USC
Kimonis, Virginia
UCI
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_
Similar People (60)
People who share similar concepts with this person.
Gleeson, Joseph
UCSD
Norton, Mary
UCSF
Kimonis, Virginia
UCI
Sherr, Elliott
UCSF
Martinez, Julian
UCLA
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Same Department
Head, Elizabeth
Lipkova, Jana
Peterson, Ellena
Rahmatpanah, Farahnaz
Ramzy, Ibrahim
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