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Pediatrics CRA
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WEIMIN BI
Concepts (393)
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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.
1-Alkyl-2-acetylglycerophosphocholine Esterase
Abnormal Karyotype
Abnormalities, Multiple
Actin Cytoskeleton
Actins
Adaptor Proteins, Signal Transducing
Adaptor Proteins, Vesicular Transport
Adenosine Triphosphatases
Adolescent
Adult
Aging
Algorithms
Alleles
alpha7 Nicotinic Acetylcholine Receptor
Amino Acid Sequence
Amino Acid Substitution
Amniocentesis
Amniotic Fluid
Anal Canal
Aneuploidy
Angelman Syndrome
Animals
Antigens, Nuclear
Anxiety
Arteries
Arthralgia
ATPases Associated with Diverse Cellular Activities
Atrophy
Attention Deficit Disorder with Hyperactivity
Autism Spectrum Disorder
Autistic Disorder
Bardet-Biedl Syndrome
Base Composition
Base Sequence
Bayes Theorem
Behavior, Animal
Biological Variation, Population
Blotting, Northern
Blotting, Southern
Body Weight
Bone and Bones
Brain
Calcineurin
Cardiomyopathies
Cardiomyopathy, Dilated
Carrier Proteins
Cell Cycle Proteins
Cell Division
Cell Line
Cell Line, Transformed
Cell-Free Nucleic Acids
Cells, Cultured
Central Nervous System
Cerebellar Diseases
Chaperonins
Charcot-Marie-Tooth Disease
Child
Child, Preschool
Chorionic Villi Sampling
Chromatin
Chromogranins
Chromosomal Instability
Chromosomal Proteins, Non-Histone
Chromosome Aberrations
Chromosome Banding
Chromosome Breakage
Chromosome Breakpoints
Chromosome Deletion
Chromosome Disorders
Chromosome Duplication
Chromosome Inversion
Chromosome Mapping
Chromosomes
Chromosomes, Artificial, Bacterial
Chromosomes, Artificial, P1 Bacteriophage
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 12
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 18
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 8
Chromosomes, Human, X
Chromosomes, Mammalian
Classical Lissencephalies and Subcortical Band Heterotopias
Clinical Laboratory Techniques
Cloning, Molecular
Codon, Nonsense
Cohort Studies
Comparative Genomic Hybridization
Computational Biology
Congenital Abnormalities
Congenital Hypothyroidism
Conserved Sequence
Contig Mapping
Craniofacial Abnormalities
Cri-du-Chat Syndrome
Critical Care
Crossing Over, Genetic
Cytogenetic Analysis
Cytoskeletal Proteins
Databases as Topic
Databases, Genetic
De Lange Syndrome
Developmental Disabilities
Diet, High-Fat
DiGeorge Syndrome
Disease Management
Disease Models, Animal
DNA
DNA Copy Number Variations
DNA Damage
DNA Fingerprinting
DNA Methylation
DNA Mutational Analysis
DNA Primers
DNA Repair
DNA Replication
DNA, Complementary
DNA-Binding Proteins
Down Syndrome
Drosophila melanogaster
Drug Resistant Epilepsy
Dwarfism
Electroencephalography
Electrophoresis, Gel, Pulsed-Field
Electrophysiology
Embryo, Mammalian
Endopeptidases
Epilepsy
Esophageal Atresia
Esophagus
Evolution, Molecular
Exome
Exons
Eye Abnormalities
Facies
Failure to Thrive
Family
Fanconi Anemia
Fanconi Anemia Complementation Group Proteins
Fatal Outcome
Feasibility Studies
Female
Fetus
Fibroblasts
Frameshift Mutation
Fungal Proteins
Gametogenesis
Gene Deletion
Gene Dosage
Gene Duplication
Gene Expression
Gene Expression Regulation, Developmental
Gene Frequency
Gene Order
Gene Rearrangement
Gene Targeting
Gene Transfer Techniques
Genes, Dominant
Genes, Recessive
Genetic Association Studies
Genetic Counseling
Genetic Diseases, Inborn
Genetic Engineering
Genetic Heterogeneity
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Genetic Variation
Genetic Vectors
Genome
Genome, Human
Genome-Wide Association Study
Genomic Instability
Genomics
Genotype
Genotyping Techniques
Germ Cells
Germ-Line Mutation
Glycine-tRNA Ligase
GTP-Binding Protein alpha Subunits, Gs
GTP-Binding Protein beta Subunits
Guanine Nucleotide Exchange Factors
Hand Deformities, Congenital
Haploinsufficiency
Haplotypes
Heart
Heart Defects, Congenital
Heterotaxy Syndrome
Heterozygote
High-Throughput Nucleotide Sequencing
Homeodomain Proteins
Homologous Recombination
Homozygote
Humans
Hyperphagia
Hypertension, Pulmonary
Immunohistochemistry
In Situ Hybridization, Fluorescence
INDEL Mutation
Infant
Infant Care
Infant, Newborn
Inflammation
Inheritance Patterns
Insulin
Intellectual Disability
Intensive Care Units, Pediatric
Intracellular Signaling Peptides and Proteins
Introns
Iris Diseases
Karyotyping
Kidney
Klinefelter Syndrome
Language Development Disorders
Learning
Length of Stay
Leptin
Limb Deformities, Congenital
Liver
Loss of Function Mutation
Lung Diseases
Lymphocytes
Lysosomes
Magnetic Resonance Imaging
Male
Megalencephaly
Meiosis
Membrane Proteins
Membrane Transport Proteins
Memory
Metal Metabolism, Inborn Errors
Metalloendopeptidases
Mice
Mice, Inbred C57BL
Mice, Knockout
Mice, Mutant Strains
Mice, Transgenic
Microarray Analysis
Microcephaly
Micrognathism
Microsatellite Repeats
Microtubule-Associated Proteins
Minor Histocompatibility Antigens
Mitochondrial Proteins
Mitochondrial Proton-Translocating ATPases
Models, Genetic
Models, Theoretical
Molecular Chaperones
Molecular Sequence Data
Mosaicism
Multigene Family
Muscle Hypotonia
Muscle Proteins
Muscle, Skeletal
Muscular Atrophy, Spinal
Musculoskeletal Abnormalities
Mutagenesis, Insertional
Mutation
Mutation, Missense
Myopathies, Nemaline
Neoplasms
Nerve Tissue Proteins
Nervous System Diseases
Neurodevelopmental Disorders
Neutropenia
NF-kappa B
Nuclear Proteins
Nucleic Acid Amplification Techniques
Nucleotide Motifs
Nucleotides
Obesity
Obesity, Morbid
Oligonucleotide Array Sequence Analysis
Oligonucleotide Probes
Organ Size
Osteochondrodysplasias
Oxidative Stress
Parents
Pathology, Molecular
Pediatric Obesity
Pedigree
Penetrance
Phenotype
Physical Chromosome Mapping
Physical Examination
Pilot Projects
Placenta
Point Mutation
Polycomb Repressive Complex 2
Polyhydramnios
Polymerase Chain Reaction
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Prader-Willi Syndrome
Predictive Value of Tests
Pregnancy
Preimplantation Diagnosis
Prenatal Diagnosis
Problem Behavior
Prognosis
Proline-Rich Protein Domains
Prospective Studies
Proteasome Endopeptidase Complex
Protein Structure, Tertiary
Proteins
Proton-Translocating ATPases
Proto-Oncogene Proteins
Pseudogenes
Pseudohypoparathyroidism
Psychomotor Disorders
Psychomotor Performance
Rare Diseases
Real-Time Polymerase Chain Reaction
Receptors, Cell Surface
Receptors, Glycine
Receptors, G-Protein-Coupled
Recurrence
Reference Standards
Repetitive Sequences, Nucleic Acid
Reproducibility of Results
Restriction Mapping
Retina
Retrospective Studies
Retroviridae
Rho Guanine Nucleotide Exchange Factors
Ring Chromosomes
Risk
Saccharomyces cerevisiae Proteins
Sarcomeres
Segmental Duplications, Genomic
Seizures
Sensitivity and Specificity
Sequence Alignment
Sequence Analysis, DNA
Sequence Analysis, RNA
Sequence Deletion
Sequence Homology, Nucleic Acid
Sex Characteristics
Sex Chromosome Aberrations
Sex Chromosome Disorders of Sex Development
Sex Chromosomes
Siblings
Single-Cell Analysis
Skin
Smith-Magenis Syndrome
Social Dominance
Software
Spinal Muscular Atrophies of Childhood
Spine
Stem Cells
Stroke
Survival of Motor Neuron 1 Protein
Syndrome
Syntaxin 16
Synteny
Tandem Repeat Sequences
Texas
Time Factors
Tissue Distribution
Trachea
Tracheoesophageal Fistula
Trans-Activators
Transcription Factors
Transcription, Genetic
Transcriptional Activation
Translocation, Genetic
Transposition of Great Vessels
Trinucleotide Repeats
Trisomy
Trisomy 13 Syndrome
Trisomy 18 Syndrome
Trophoblasts
Troponin T
Turner Syndrome
Ubiquitin-Protein Ligases
Ultrasonography, Prenatal
Uniparental Disomy
Up-Regulation
Whole Genome Sequencing
Williams Syndrome
Wolf-Hirschhorn Syndrome
X Chromosome Inactivation
Young Adult
Zebrafish
Zinc Fingers
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Concepts (393)
Derived automatically from this person's publications.
DNA Copy Number Variations
Comparative Genomic Hybridization
Oligonucleotide Array Sequence Analysis
Mosaicism
Intellectual Disability
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Co-Authors (107)
People in Profiles who have published with this person.
LUPSKI, JAMES
CHEUNG, SAU WAI
YUAN, BO
STANKIEWICZ, PAWEL
LALANI, SEEMA
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Similar People (58)
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.
LICHTARGE, OLIVIER
SABO, ANIKO
SHAW, CHAD
SI, YUE
SZAFRANSKI, PRZEMYSLAW
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Physical Neighbors
People whose addresses are nearby this person.
DE HARO, MARIA
KIM, JI-YOEN
ROGERS, JEFFREY
YUAN, BO
ZONG, CHENGHANG
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