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Comparative Effectiveness Research
NEWMARK, MICHAEL
Upper Gastrointestinal Tract
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BO YUAN
Concepts (248)
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Concepts are derived automatically from a person's publications.
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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.
14-3-3 Proteins
A549 Cells
Abnormalities, Multiple
Acromegaly
Actins
Adaptor Proteins, Signal Transducing
Adenoma
Adenosine Triphosphatases
Adolescent
Adult
Aged
Algorithms
Alleles
Alternative Splicing
Alu Elements
Amino Acid Sequence
Aneuploidy
Animals
Antibodies, Monoclonal, Humanized
Antigens, Nuclear
Artificial Intelligence
ATPases Associated with Diverse Cellular Activities
Autism Spectrum Disorder
Axons
Base Sequence
Basic Helix-Loop-Helix Transcription Factors
Biological Variation, Population
Bipolar Disorder
Brain
Campomelic Dysplasia
Carcinoma, Squamous Cell
Cardiomyopathies
Carrier Proteins
Cation Transport Proteins
CD8-Positive T-Lymphocytes
Cell Cycle Proteins
Cell Division
Cell Line, Transformed
Cell Movement
Cell Proliferation
Charcot-Marie-Tooth Disease
Child
Child, Preschool
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Breakage
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Inversion
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 9
Chromosomes, Human, X
Clone Cells
Cohort Studies
Comparative Genomic Hybridization
Computational Biology
Consanguinity
COS Cells
Cytokines
Cytoskeletal Proteins
Databases, Genetic
Datasets as Topic
De Lange Syndrome
Developmental Disabilities
Disease Models, Animal
DNA
DNA Copy Number Variations
DNA Methylation
DNA Replication
DNA-Binding Proteins
Drosophila melanogaster
Drosophila Proteins
Embryonic Development
Evolution, Molecular
Exome
Exons
Facies
Failure to Thrive
Female
Fibrillar Collagens
Fibroblasts
Fibula
Fingers
Follow-Up Studies
Foot Deformities, Congenital
Founder Effect
Gain of Function Mutation
Gametogenesis
Gene Deletion
Gene Dosage
Gene Duplication
Gene Frequency
Gene Rearrangement
Gene Regulatory Networks
Genes, Dominant
Genes, p53
Genes, ras
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genome, Human
Genomic Imprinting
Genomic Instability
Genomic Structural Variation
Genomics
Genotype
Germ Cells
Germ-Line Mutation
Gigantism
Hand Deformities, Congenital
Haploinsufficiency
Haplotypes
Head and Neck Neoplasms
Heart Defects, Congenital
HeLa Cells
Hemizygote
Hereditary Autoinflammatory Diseases
High-Throughput Nucleotide Sequencing
Homeodomain Proteins
Homologous Recombination
Homozygote
Humans
Immunologic Deficiency Syndromes
In Situ Hybridization, Fluorescence
INDEL Mutation
Induced Pluripotent Stem Cells
Infant
Infant, Newborn
Information Storage and Retrieval
Inheritance Patterns
Intellectual Disability
Interleukin-1beta
Intracellular Signaling Peptides and Proteins
Karyotyping
Kidney Diseases, Cystic
Knowledge Bases
Language Development Disorders
Lung Neoplasms
Male
Matrix Metalloproteinase 2
Megalencephaly
Membrane Proteins
Mendelian Randomization Analysis
Mice
Microcephaly
Micrognathism
Microscopy, Confocal
Middle Aged
Mitochondria
Mitochondrial Proteins
Models, Genetic
Molecular Sequence Data
Molecular Targeted Therapy
Mosaicism
Mouth Neoplasms
Muscle Hypotonia
Muscles
Muscular Diseases
Mutation
Mutation, Missense
Myelin Proteins
Myelin Proteolipid Protein
Nervous System Diseases
Neural Stem Cells
Neurodevelopmental Disorders
Neuroglia
Neurons
Neutrophils
Nuclear Proteins
Nucleotides
Optic Atrophy
Osteochondrodysplasias
Pedigree
Pelizaeus-Merzbacher Disease
Pharmacogenetics
Pharmacogenomic Testing
Phenotype
Pituitary Neoplasms
Plasminogen Activator Inhibitor 1
Polymorphism, Single Nucleotide
Population Health
Precision Medicine
Pregnancy
Primates
Prognosis
Prospective Studies
Prostaglandins F
Protein Binding
Protein Inhibitors of Activated STAT
Protein Isoforms
Proto-Oncogene Proteins
Proto-Oncogene Proteins p21(ras)
Psychotic Disorders
Puerto Rico
Radiography
Rare Diseases
Recombinant Fusion Proteins
Recombination, Genetic
Recurrence
Reproducibility of Results
Retrospective Studies
Ring Chromosomes
Risk
RNA-Binding Proteins
Seizures
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology, Amino Acid
Sex Characteristics
Signal Transduction
Smith-Magenis Syndrome
Spastic Paraplegia, Hereditary
Spastin
Spheroids, Cellular
SUMO-1 Protein
Sumoylation
Syndactyly
Syndrome
Tibia
Toes
Trans-Activators
Transcription Factors
Transforming Growth Factor beta
Translocation, Genetic
Tumor Microenvironment
Tumor Necrosis Factor alpha-Induced Protein 3
Tumor Suppressor Protein p53
Tumor Suppressor Proteins
Ubiquitin-Protein Ligases
United States
Whole Genome Sequencing
Workflow
Young Adult
Zebrafish
Zebrafish Proteins
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Concepts (248)
Derived automatically from this person's publications.
DNA Copy Number Variations
Myelin Proteins
Hand Deformities, Congenital
INDEL Mutation
Chromosomal Proteins, Non-Histone
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Co-Authors (89)
People in Profiles who have published with this person.
LUPSKI, JAMES
BI, WEIMIN
LIU, PENGFEI
ENG, CHRISTINE
CHEUNG, SAU WAI
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_
Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
GIBBS, RICHARD
STANKIEWICZ, PAWEL
CHEUNG, SAU WAI
BOERWINKLE, ERIC
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_
Same Department
People who are also in this person's primary department.
BAURI, DIANNE
GKOUNTAROULIS, DIMOS
GU, YANGHONG
LIU, NING
ZHANG, BING
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Physical Neighbors
People whose addresses are nearby this person.
BAE, YANGJIN
DE HARO, MARIA
GIBBS, RICHARD
HARRIS, RONALD
MATHUR, VEENA
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