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Pediatrics CRA
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YANG, ESTHER
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CARLOS BACINO
Concepts (722)
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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.
14-3-3 Proteins
1-Alkyl-2-acetylglycerophosphocholine Esterase
Abnormal Karyotype
Abnormalities, Multiple
Abortion, Habitual
Absorptiometry, Photon
Acetyltransferases
Achondroplasia
Actins
Activities of Daily Living
ADAMTS Proteins
Adaptation, Physiological
Adaptor Proteins, Signal Transducing
Adenosine Deaminase
Adenosine Triphosphatases
Adenosine Triphosphate
Adiponectin
Adolescent
Adult
Age Factors
Age of Onset
Aged
Agenesis of Corpus Callosum
Aging, Premature
Aicardi Syndrome
Algorithms
Alleles
Allelic Imbalance
alpha7 Nicotinic Acetylcholine Receptor
alpha-Thalassemia
Alu Elements
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acid Substitution
Aminoglycosides
Amish
Amniocentesis
Amniotic Band Syndrome
Amniotic Fluid
Anal Canal
Analysis of Variance
Anemia, Sideroblastic
Aneuploidy
Angelman Syndrome
Animals
Animals, Genetically Modified
Anisotropy
Anophthalmos
Anthropometry
Antigens, Nuclear
Antiporters
Anus, Imperforate
Anxiety
Aorta, Thoracic
Arabs
Area Under Curve
Aromatic-L-Amino-Acid Decarboxylases
Arrhythmias, Cardiac
Arthrogryposis
Ataxia
ATPases Associated with Diverse Cellular Activities
Atrophy
Attention Deficit Disorder with Hyperactivity
Autism Spectrum Disorder
Autistic Disorder
Autoimmune Diseases of the Nervous System
Axons
Basal Ganglia Diseases
Base Composition
Base Sequence
Bayes Theorem
Behavior
beta Catenin
Betaine
Biomarkers
Biopsy
Blood Component Transfusion
Blood Vessels
Blotting, Southern
Blotting, Western
B-Lymphocytes
Body Height
Body Mass Index
Body Weight
Bone and Bones
Bone Density
Bone Development
Bone Diseases, Developmental
Bone Marrow Cells
Bone Marrow Diseases
Bone Morphogenetic Proteins
Bone Remodeling
Brachydactyly
Brain
Brain Diseases
Cadherins
Caenorhabditis elegans
Calcinosis
Calcium
Calcium Channels
Calcium-Binding Proteins
Calcium-Calmodulin-Dependent Protein Kinase Type 2
Cardiovascular Abnormalities
Cardiovascular Diseases
Caregivers
Cartilage
Cell Cycle
Cell Cycle Proteins
Cell Division
Cell Line
Cell Movement
Cell Proliferation
Cell Transdifferentiation
Cells, Cultured
Central Nervous System
Cerebellar Ataxia
Cerebral Cortex
Cerebral Palsy
Checklist
Chilblains
Child
Child Development
Child Language
Child, Preschool
CHO Cells
Choanal Atresia
Cholesterol
Chorionic Villi Sampling
Chromatin
Chromatin Assembly and Disassembly
Chromogranins
Chromosomal Instability
Chromosome Aberrations
Chromosome Banding
Chromosome Breakage
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Inversion
Chromosome Mapping
Chromosomes, Human
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
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 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, Y
Cilia
Class I Phosphatidylinositol 3-Kinases
Classical Lissencephalies and Subcortical Band Heterotopias
Cleft Lip
Cleft Palate
Clinical Laboratory Techniques
Clone Cells
Clubfoot
Codon, Terminator
Cognition
Cognition Disorders
Cohort Studies
Colitis
Collagen
Collagen Type II
Collagen Type X
Collagen Type XI
Coloboma
Colon
Common Variable Immunodeficiency
Comorbidity
Comparative Genomic Hybridization
Computational Biology
Computer Systems
Congenital Abnormalities
Congenital Disorders of Glycosylation
Consanguinity
Contractile Proteins
Corpus Callosum
CpG Islands
Craniofacial Abnormalities
Craniosynostoses
CREB-Binding Protein
Cricetulus
CRISPR-Cas Systems
Critical Care
Cutis Laxa
Cyclic GMP
Cyclic Nucleotide Phosphodiesterases, Type 3
Cyclic Nucleotide Phosphodiesterases, Type 4
Cyclin-Dependent Kinase 8
Cyclin-Dependent Kinases
Cytogenetic Analysis
Cytoskeletal Proteins
Data Collection
Deafness
Developmental Disabilities
Diabetes Mellitus, Type 2
Diagnosis, Differential
Diet
Diet Surveys
Dietary Supplements
Diffusion Tensor Imaging
Dihydroxyphenylalanine
Disease Management
Disease Models, Animal
Disease Progression
Diseases in Twins
DNA
DNA Breaks
DNA Copy Number Variations
DNA Damage
DNA Helicases
DNA Methylation
DNA Mutational Analysis
DNA Primers
DNA Probes
DNA Repair
DNA Replication
DNA, Complementary
DNA, Mitochondrial
DNA-Binding Proteins
Dopa Decarboxylase
Dosage Compensation, Genetic
Dose-Response Relationship, Drug
Double-Blind Method
Down-Regulation
Drosophila
Drosophila melanogaster
Drosophila Proteins
Drug Combinations
Ductus Arteriosus, Patent
Dwarfism
Dynamins
Dyskinesias
Dysostoses
Early Growth Response Protein 2
Ectodermal Dysplasia
Ectromelia
Ehlers-Danlos Syndrome
Electroencephalography
Embryo, Mammalian
Embryonic Development
Endoplasmic Reticulum Stress
Energy Intake
Energy Metabolism
Enhancer Elements, Genetic
Enteritis
Environment
Eosinophilia
Epilepsy
Epilepsy, Generalized
Ergometry
Esophageal Atresia
Esophagus
Exercise
Exercise Test
Exercise Tolerance
Exocrine Pancreatic Insufficiency
Exodeoxyribonucleases
Exome
Exons
Exosomes
Extracellular Matrix
Eye Abnormalities
Eye Movements
Eyelids
Facial Asymmetry
Facial Bones
Facies
Failure to Thrive
Family
Family Health
Fanconi Anemia
Fanconi Anemia Complementation Group Proteins
Fasting
Fatal Outcome
F-Box Proteins
Feedback
Feeding and Eating Disorders
Female
Ferrets
Fertilization in Vitro
Fetal Diseases
Fetal Growth Retardation
Fetal Movement
Fibrillin-1
Fibroblasts
Fibroma
Fibronectins
Filamins
Fingers
Fluorescent Antibody Technique
Folic Acid
Folic Acid Deficiency
Follow-Up Studies
Food Hypersensitivity
Foot
Foot Deformities, Congenital
Forkhead Transcription Factors
Fractures, Bone
Frameshift Mutation
Functional Laterality
Gait
Gametogenesis
Gastritis
Gastroenteritis
Gastrointestinal Agents
GATA4 Transcription Factor
Gene Deletion
Gene Dosage
Gene Duplication
Gene Editing
Gene Expression
Gene Expression Regulation
Gene Expression Regulation, Developmental
Gene Library
Gene Rearrangement
Gene-Environment Interaction
Genes, Dominant
Genes, Lethal
Genes, Recessive
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Heterogeneity
Genetic Linkage
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genitalia
Genome, Human
Genome-Wide Association Study
Genomic Imprinting
Genomic Instability
Genomics
Genotype
Genotyping Techniques
Germ Cells
Germ-Line Mutation
Golgi Apparatus
Gonadoblastoma
Gonads
Growth
Growth Charts
Growth Disorders
GTP Phosphohydrolases
GTP-Binding Protein alpha Subunits, Gs
GTP-Binding Protein beta Subunits
GTP-Binding Proteins
Hand
Hand Deformities, Congenital
Haploinsufficiency
Haplotypes
Health Care Costs
Health Services Accessibility
Health Surveys
Hearing Loss
Hearing Loss, Sensorineural
Heart Defects, Congenital
Hedgehog Proteins
HEK293 Cells
Hemoglobin H
Hemoglobins, Abnormal
Hepatoblastoma
Hereditary Sensory and Motor Neuropathy
Hernia, Diaphragmatic
Hernias, Diaphragmatic, Congenital
Heterogeneous-Nuclear Ribonucleoproteins
Heterozygote
High-Throughput Nucleotide Sequencing
Hirschsprung Disease
Hirsutism
Histidine
Histones
Homeodomain Proteins
Homeostasis
Homologous Recombination
Homozygote
Humans
Hydrogen Peroxide
Hyperphagia
Hypertrichosis
Hypertriglyceridemia
Hypopigmentation
Hypoplastic Left Heart Syndrome
Hypothyroidism
In Situ Hybridization, Fluorescence
Incidence
INDEL Mutation
Infant
Infant Care
Infant, Newborn
Infant, Premature
Infant, Premature, Diseases
Inheritance Patterns
Injection Site Reaction
Injections, Subcutaneous
Intellectual Disability
Intensive Care Units, Pediatric
Intercellular Signaling Peptides and Proteins
Interferon Type I
Intestinal Pseudo-Obstruction
Intracellular Signaling Peptides and Proteins
Introns
Inverted Repeat Sequences
Iran
Isochromosomes
Joints
Karyotype
Karyotyping
Kidney
Lactic Acid
Language Development Disorders
Language Disorders
Larva
Larynx
Length of Stay
Leucovorin
Leukoencephalopathies
Levodopa
LIM Domain Proteins
Limb Deformities, Congenital
Limit of Detection
Lipomatosis
Lipotropic Agents
Lissencephaly
Liver Neoplasms
Lod Score
Long Interspersed Nucleotide Elements
Longitudinal Studies
Long-Term Potentiation
Losartan
Loss of Heterozygosity
Lung Diseases
Lymphangiectasis, Intestinal
Lymphedema
Lymphocytosis
Lysosomes
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Matrix Attachment Region Binding Proteins
Medically Underserved Area
MEF2 Transcription Factors
Megalencephaly
Membrane Potential, Mitochondrial
Membrane Proteins
Mental Disorders
Metabolic Diseases
Metabolism, Inborn Errors
Metabolomics
Metalloendopeptidases
Methyl-CpG-Binding Protein 2
Mice
Mice, Knockout
Microarray Analysis
Microcephaly
Microfibrils
Microfilament Proteins
Microsatellite Repeats
Microscopy, Electron, Transmission
Microtubule-Associated Proteins
Middle Aged
Minor Histocompatibility Antigens
Mitochondria
Mitochondrial Dynamics
Mitochondrial Proteins
Mitomycin
Models, Animal
Models, Biological
Models, Genetic
Models, Molecular
Models, Theoretical
Molecular Diagnostic Techniques
Molecular Sequence Data
Monosaccharide Transport Proteins
Monosomy
Mosaicism
Motor Activity
Motor Skills
Movement Disorders
Muscle Contraction
Muscle Hypotonia
Muscle Weakness
Muscle, Skeletal
Muscle, Smooth
Muscular Diseases
Musculoskeletal Abnormalities
Mutagenesis, Insertional
Mutation
Mutation, Missense
Myosins
NAD
NADP
National Institutes of Health (U.S.)
Natriuretic Peptide, C-Type
Neoplasms
Nerve Fibers, Myelinated
Nerve Growth Factors
Nerve Net
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Neural Pathways
Neurocutaneous Syndromes
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neuroimaging
Neuromuscular Junction
Neurons
Neuropsychological Tests
Neutropenia
NF-kappa B
Noonan Syndrome
Nose
Nuclear Proteins
Nucleic Acid Heteroduplexes
Nucleic Acid Hybridization
Nucleotide Motifs
Obesity
Obesity, Morbid
Oligonucleotide Array Sequence Analysis
Oligonucleotide Probes
Ophthalmoplegia, Chronic Progressive External
Optic Atrophy, Autosomal Dominant
Organ Size
Organogenesis
Osteochondrodysplasias
Osteogenesis
Osteogenesis Imperfecta
Osteopetrosis
Osteoporosis
Oxidative Stress
p120 GTPase Activating Protein
Pancreatic Diseases
Pancytopenia
Pandemics
PAX5 Transcription Factor
Pediatric Obesity
Pedigree
Penetrance
Peptide Elongation Factors
Peroxisomes
Persistent Fetal Circulation Syndrome
Personality Assessment
Phenotype
Phosphatidylinositol 3-Kinases
Phosphatidylinositols
Phosphoglycerate Kinase
Phosphoproteins
Phosphoric Monoester Hydrolases
Physical Chromosome Mapping
Pigmentation Disorders
Pilot Projects
Placebos
Point Mutation
Polydactyly
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Polymorphism, Single-Stranded Conformational
Practice Patterns, Physicians'
Prader-Willi Syndrome
Predictive Value of Tests
Pregnancy
Pregnancy Trimester, Second
Preimplantation Diagnosis
Prenatal Diagnosis
Prevalence
Procollagen N-Endopeptidase
Progeria
Prospective Studies
Proteasome Endopeptidase Complex
Protein Conformation
Protein Domains
Protein Interaction Maps
Protein Structure, Tertiary
Protein Transport
Protein Tyrosine Phosphatases
Proteins
Pseudohypoparathyroidism
Psychological Tests
Psychometrics
Psychomotor Disorders
Pulmonary Alveoli
Pulmonary Veins
Quantitative Trait Loci
Racemases and Epimerases
Radiography
Radius
Rare Diseases
Receptor Tyrosine Kinase-like Orphan Receptors
Receptor, Melanocortin, Type 4
Receptors, Cell Surface
Receptors, Glycine
Receptors, Lipoprotein
Receptors, Nicotinic
Receptors, Notch
Recombination, Genetic
Recovery of Function
Recurrence
Reduced Folate Carrier Protein
Reference Values
Repressor Proteins
Reproducibility of Results
Retrospective Studies
Rett Syndrome
Rhabdomyolysis
Ribonuclease H
Ribonucleoprotein, U5 Small Nuclear
Risk
Risk Factors
RNA Processing, Post-Transcriptional
RNA Splice Sites
RNA, Double-Stranded
RNA, Long Noncoding
RNA, Messenger
RNA, Ribosomal
RNA-Binding Proteins
Rubinstein-Taybi Syndrome
Schizophrenia
Scoliosis
Segmental Duplications, Genomic
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Sequence Homology, Amino Acid
Sex Characteristics
Sex Chromosome Aberrations
Sex Factors
Short Bowel Syndrome
Siblings
Signal Transduction
Single-Cell Analysis
Skin
Skin Pigmentation
Skull
Sleep Wake Disorders
Smith-Magenis Syndrome
Social Behavior
SOXD Transcription Factors
Spasms, Infantile
Speech Disorders
Spine
Standard of Care
Statistics as Topic
Statistics, Nonparametric
Structure-Activity Relationship
Sucking Behavior
Sudden Infant Death
Syndrome
Syntaxin 16
Syringomyelia
T-Box Domain Proteins
Telomere
Templates, Genetic
Testis
Tetrahydrofolates
Tetralogy of Fallot
Tetraspanins
Texas
Thrombocytopenia
Thumb
Time Factors
Toes
Tooth Abnormalities
TOR Serine-Threonine Kinases
Trachea
Tracheoesophageal Fistula
Trans-Activators
Transcription Factors
Transcription Factors, General
Transcription, Genetic
Transcriptome
Transforming Growth Factor beta
Translocation, Genetic
Transposases
Treatment Outcome
Trisomy
TRPV Cation Channels
Tumor Suppressor Proteins
Turner Syndrome
Twins, Monozygotic
Tyrosine
Ubiquitin-Protein Ligases
Ultrasonography, Prenatal
Uniparental Disomy
United States
Uridine Diphosphate Galactose
Urinary Bladder
Vacuolar Proton-Translocating ATPases
Vesicular Acetylcholine Transport Proteins
Vitamin B Complex
Vulnerable Populations
Waardenburg Syndrome
Weight Gain
Whole Genome Sequencing
Wolf-Hirschhorn Syndrome
X Chromosome
X Chromosome Inactivation
Y Chromosome
Young Adult
Zebrafish
Zinc Fingers
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Concepts (722)
Derived automatically from this person's publications.
Angelman Syndrome
Chromosome Deletion
Intellectual Disability
Neurodevelopmental Disorders
Abnormalities, Multiple
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Co-Authors (144)
People in Profiles who have published with this person.
CHEUNG, SAU WAI
WANGLER, MICHAEL
LALANI, SEEMA
STANKIEWICZ, PAWEL
BI, WEIMIN
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
STANKIEWICZ, PAWEL
CHEUNG, SAU WAI
GIBBS, RICHARD
BOERWINKLE, ERIC
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Same Department
People who are also in this person's primary department.
ASMUSSEN, JENNIFER
FONG, JAMIE
FONSECA, CLAUDIA
HALLIDAY, JENNIFER
IRA, GRZEGORZ
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Physical Neighbors
People whose addresses are nearby this person.
BEKHEIRNIA, MIR REZA
EBLE, TANYA
ROSENBERG, SUSAN
SCAGLIA, FERNANDO
WORLEY, KIM
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