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HONGZHENG DAI
Concepts (236)
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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.
4-Aminopyridine
Abnormalities, Multiple
Accreditation
Achondroplasia
Acidosis, Lactic
Acrocephalosyndactylia
Actins
Adenosine Triphosphatases
Adolescent
Adult
Age of Onset
Agenesis of Corpus Callosum
Alleles
Alveolar Epithelial Cells
Amino Acyl-tRNA Synthetases
Amish
Animals
Aniridia
Anus, Imperforate
Artificial Intelligence
Autism Spectrum Disorder
Base Sequence
Blepharophimosis
Blepharoptosis
Bone and Bones
Brain
Caenorhabditis elegans
Calcineurin
Calcium
Calcium Channels
Calcium Channels, L-Type
Calcium Channels, N-Type
Cardiomyopathy, Hypertrophic
Carrier Proteins
Cell Membrane
Cell-Free Nucleic Acids
Cells, Cultured
Cerebellar Ataxia
Certification
Child
Child, Preschool
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Disorders
Chromosome Inversion
Cleft Palate
Collagen Type I
Colorectal Neoplasms, Hereditary Nonpolyposis
Constipation
C-Reactive Protein
CRISPR-Cas Systems
Critical Care
Cryptorchidism
Cytokine Receptor gp130
Cytokines
De Lange Syndrome
DEAD-box RNA Helicases
Developmental Disabilities
Disease Management
DNA Copy Number Variations
DNA Methylation
DNA Mutational Analysis
DNA Repair Enzymes
DNA, Mitochondrial
DNA-Binding Proteins
Down-Regulation
Drosophila melanogaster
Drosophila Proteins
Drug Resistant Epilepsy
Education
Electronic Health Records
Epilepsy
Epilepsy, Generalized
Exome
Exons
Facies
Family
F-Box Proteins
Female
Fetus
Fibroblasts
Gain of Function Mutation
Gait
Gene Deletion
Gene Dosage
Gene Expression
Genes, Dominant
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Genetic Predisposition to Disease
Genetic Services
Genetic Testing
Genetic Variation
Genetics
Genetics, Population
Genome, Human
Genome-Wide Association Study
Genomics
Germ Cells
Germ-Line Mutation
Hand Deformities, Congenital
Haploinsufficiency
Health Services Accessibility
Healthcare Disparities
Heart Defects, Congenital
HEK293 Cells
Heredodegenerative Disorders, Nervous System
Hernias, Diaphragmatic, Congenital
High-Throughput Nucleotide Sequencing
Histidine
Homologous Recombination
Homozygote
Humans
Hydrops Fetalis
INDEL Mutation
Infant
Infant Care
Infant, Newborn
Inheritance Patterns
Inositol 1,4,5-Trisphosphate Receptors
Intellectual Disability
Intensive Care Units, Pediatric
Introns
Job Syndrome
Kaplan-Meier Estimate
Kinetics
Kv1.1 Potassium Channel
Laboratories
Length of Stay
Limit of Detection
Liver
Liver Diseases
Loss of Function Mutation
Lung
Lung Diseases, Interstitial
Lymphangioma, Cystic
Magnetic Resonance Imaging
Male
Mammals
Mediator Complex
Medically Underserved Area
Membrane Proteins
Mental Retardation, X-Linked
Mice
Microarray Analysis
Microcephaly
Micrognathism
Microscopy, Confocal
Middle Aged
Mismatch Repair Endonuclease PMS2
Mitochondria
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Mitochondrial Proteins
Models, Biological
Molecular Sequence Data
Movement Disorders
Multiplex Polymerase Chain Reaction
Muscle Hypotonia
Muscular Diseases
Muscular Dystrophy, Duchenne
Mutation
Mutation, Missense
Neoplasms
Neurodevelopmental Disorders
Neuroglia
Neurons
NIH 3T3 Cells
NIMA-Related Kinases
Nuchal Translucency Measurement
Nuclear Proteins
Osteogenesis Imperfecta
Ovarian Neoplasms
Oxidative Phosphorylation
Pan troglodytes
Paraplegia
Pedigree
Peripheral Nervous System Diseases
Phenotype
Phenylalanine
Phenylalanine-tRNA Ligase
Phosphoric Monoester Hydrolases
Polycystic Kidney, Autosomal Dominant
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Predictive Value of Tests
Pregnancy
Prenatal Diagnosis
Prospective Studies
Protein Binding
Protein Isoforms
Protein Precursors
Proteome
Proteomics
Pulmonary Surfactant-Associated Protein C
Pulmonary Surfactant-Associated Proteins
Pulmonary Surfactants
rab5 GTP-Binding Proteins
Rare Diseases
Retrospective Studies
Ribonuclease III
RNA Splice Sites
RNA, Long Noncoding
Scleroderma, Systemic
Seizures
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Sertoli-Leydig Cell Tumor
Signal Transduction
Skin
Structure-Activity Relationship
Sudden Infant Death
Symptom Assessment
Technology
Telemedicine
Testis
Texas
Th2 Cells
Thanatophoric Dysplasia
TOR Serine-Threonine Kinases
Transcription Factors
Transposases
TRPP Cation Channels
Tumor Suppressor Proteins
Ubiquitin-Protein Ligases
Ultrasonography, Prenatal
Uniparental Disomy
United States
Up-Regulation
Whole Genome Sequencing
Young Adult
Zebrafish
Zebrafish Proteins
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Concepts (236)
Derived automatically from this person's publications.
DNA Copy Number Variations
Muscle Hypotonia
Whole Genome Sequencing
Scleroderma, Systemic
Muscular Diseases
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Co-Authors (96)
People in Profiles who have published with this person.
BURRAGE, LINDSAY
ENG, CHRISTINE
LALANI, SEEMA
YUAN, BO
BI, WEIMIN
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
BOERWINKLE, ERIC
GIBBS, RICHARD
AMOS, CHRIS
STANKIEWICZ, PAWEL
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_
Same Department
People who are also in this person's primary department.
BAJIC, ALEKSANDAR
FONG, JAMIE
MENG, LINYAN
NASSEF, SALMA
RETROUVEY, JEAN-MARC
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