Concepts (149)
Concepts are derived automatically from a person's publications.
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.
- Abnormalities, Multiple
- Adenosine Triphosphatases
- Adipose Tissue, White
- Adolescent
- Adult
- Alleles
- Amino Acid Sequence
- Animals
- Animals, Genetically Modified
- Antibodies
- Arabs
- Arrhythmias, Cardiac
- Ataxia
- ATPases Associated with Diverse Cellular Activities
- Autism Spectrum Disorder
- Axons
- Base Sequence
- Caenorhabditis elegans
- Calcium Channels
- Cardiomyopathies
- CDC2 Protein Kinase
- Cell Cycle Proteins
- Central Nervous System
- Cerebellar Ataxia
- Child
- Child, Preschool
- Chromosome Deletion
- Chromosome Mapping
- Chromosomes, Human, Pair 5
- Circadian Rhythm
- Computational Biology
- Critical Care
- Cyclic AMP
- Cyclic AMP-Dependent Protein Kinases
- Developmental Disabilities
- Disease Management
- DNA Copy Number Variations
- DNA-Binding Proteins
- Drosophila melanogaster
- Endocytosis
- Endoplasmic Reticulum Stress
- Endosomes
- Exome
- Exons
- Face
- Family
- Fasting
- Female
- Fetal Growth Retardation
- Fetus
- Fibrillin-1
- Fibroblasts
- Fluorescent Dyes
- Fluorometry
- Gene Deletion
- Gene Dosage
- Genetic Carrier Screening
- Genetic Counseling
- Genetic Diseases, Inborn
- Genetic Testing
- Genetic Variation
- Genitalia
- Genome, Human
- Genome-Wide Association Study
- Genomics
- Genotyping Techniques
- Glucose
- Glutathione
- Golgi Apparatus
- GTP-Binding Protein beta Subunits
- Haploinsufficiency
- Heart Defects, Congenital
- HeLa Cells
- High-Throughput Nucleotide Sequencing
- Homozygote
| - Humans
- Incidental Findings
- Infant
- Infant Care
- Infant, Newborn
- Inheritance Patterns
- Insulin
- Intellectual Disability
- Intensive Care Units, Pediatric
- Kidney Diseases
- Kinetics
- Language Development Disorders
- Length of Stay
- Liver
- Loss of Function Mutation
- Male
- Membrane Proteins
- Metalloendopeptidases
- Mice
- Mice, Inbred C57BL
- Mice, Obese
- Microfilament Proteins
- Microscopy, Electron, Transmission
- Mitochondria
- Mitochondrial Diseases
- Mitochondrial Proteins
- Molecular Diagnostic Techniques
- Molecular Sequence Data
- Muscle Hypotonia
- Muscle Weakness
- Muscles
- Muscular Atrophy, Spinal
- Mutation
- Mutation, Missense
- Myelin Sheath
- Nervous System Diseases
- Neurodegenerative Diseases
- Neurodevelopmental Disorders
- Neuroimaging
- Neurons
- Nuclear Proteins
- Optic Atrophy
- Pedigree
- Peptide Fragments
- Peptide Hormones
- Phenotype
- Phosphoprotein Phosphatases
- Pilot Projects
- Point Mutation
- Polymorphism, Single Nucleotide
- Problem Behavior
- Progeria
- Proteins
- Recombinant Proteins
- Referral and Consultation
- Reproducibility of Results
- Retrospective Studies
- Rhabdomyolysis
- RNA Splice Sites
- Seizures
- Sensitivity and Specificity
- Sequence Alignment
- Sequence Analysis, DNA
- Single-Cell Analysis
- Speech Disorders
- Survival of Motor Neuron 1 Protein
- Survival of Motor Neuron 2 Protein
- Syndrome
- Texas
- Transcription Factors
- Transferrin
- Ultrasonography, Prenatal
- Young Adult
- Zinc Fingers
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Concepts
(149)
Derived automatically from this person's publications.
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Co-Authors
(66)
People in Profiles who have published with this person.
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Similar People
(60)
People who share similar concepts with this person.
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Same Department
People who are also in this person's primary department.
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People whose addresses are nearby this person.
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