Concepts (152)
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
- Adolescent
- Adult
- Aflatoxin B1
- Aflatoxins
- Aged
- alpha-Synuclein
- Animals
- Apoptosis Regulatory Proteins
- Ataxia Telangiectasia Mutated Proteins
- Biological Variation, Population
- Bloom Syndrome
- Brain
- Brain Abscess
- BRCA2 Protein
- Carcinogenesis
- Carcinoma, Hepatocellular
- Cell Cycle Checkpoints
- Cell Line
- Cell Line, Transformed
- Cell Proliferation
- Cell Survival
- Cells, Cultured
- Child
- Child, Preschool
- Chromosomal Instability
- Chromosome Aberrations
- Chromosome Deletion
- Chromosome Fragile Sites
- Chromosomes, Human
- Chromosomes, Human, Pair 3
- Chromosomes, Human, Pair 5
- Chromothripsis
- Cohort Studies
- Congenital Disorders of Glycosylation
- Cytidine
- Cytokines
- Developmental Disabilities
- DNA
- DNA Adducts
- DNA Breaks, Double-Stranded
- DNA Copy Number Variations
- DNA Damage
- DNA End-Joining Repair
- DNA Glycosylases
- DNA Repair
- DNA Repair Enzymes
- DNA Replication
- DNA-Binding Proteins
- DNA-Directed DNA Polymerase
- Exome
- Exons
- Eye Proteins
- Fanconi Anemia
- Fanconi Anemia Complementation Group A Protein
- Fanconi Anemia Complementation Group D2 Protein
- Fanconi Anemia Complementation Group Proteins
- Female
- Fibroblasts
- Formaldehyde
- Galactosemias
- Gene Expression
- Gene Expression Profiling
- Gene Expression Regulation
- Genes, X-Linked
- Genetic Association Studies
- Genetic Counseling
- Genetic Predisposition to Disease
- Genetic Testing
- Genetic Variation
- Genetics, Medical
- Genome, Human
- Genomic Instability
- Genomics
- Genotype
- Glycolipids
| - Guanine
- Haploinsufficiency
- Health Services Accessibility
- Hearing Loss, Sensorineural
- Heart Defects, Congenital
- Hemangioma, Cavernous, Central Nervous System
- Hemiplegia
- Herpesvirus 4, Human
- High-Throughput Nucleotide Sequencing
- Homeodomain Proteins
- Humans
- In Situ Hybridization, Fluorescence
- Incidental Findings
- Infant
- Inflammation
- Intellectual Disability
- Intracellular Signaling Peptides and Proteins
- Lewy Bodies
- Lewy Body Disease
- Liver Neoplasms
- Loss of Function Mutation
- Lymphocytes
- Male
- Medically Underserved Area
- MEF2 Transcription Factors
- Membrane Proteins
- Mice
- Mice, Hairless
- Mice, Inbred C57BL
- Mice, Knockout
- Middle Aged
- Monte Carlo Method
- Mouth Mucosa
- Mutagenesis
- Mutation
- Mutation, Missense
- Neurodevelopmental Disorders
- Neurons
- Neutropenia
- Neutrophil Infiltration
- Oligonucleotide Array Sequence Analysis
- Oxidative Stress
- Parkinson Disease
- Pedigree
- Phenotype
- Phosphorylation
- Polysaccharides
- Proto-Oncogene Proteins
- Proto-Oncogene Proteins c-ets
- Pyrimidines
- Reactive Oxygen Species
- Recombinant Proteins
- RecQ Helicases
- Repressor Proteins
- Retinitis Pigmentosa
- RNA
- RNA Interference
- RNA-Binding Proteins
- Scimitar Syndrome
- Sister Chromatid Exchange
- Skin
- Skin Neoplasms
- Sodium-Potassium-Exchanging ATPase
- Suppressor of Cytokine Signaling 1 Protein
- Suppressor of Cytokine Signaling Proteins
- Tetralogy of Fallot
- Thymine
- Transcription Factors
- Tumor Suppressor p53-Binding Protein 1
- UDPglucose 4-Epimerase
- Ultraviolet Rays
- Uracil
- Vulnerable Populations
- Young Adult
- Zebrafish
- Zebrafish Proteins
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Concepts
(152)
Derived automatically from this person's publications.
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Co-Authors
(41)
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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