Concepts (113)
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.
- Adaptor Proteins, Signal Transducing
- Adenosine Triphosphatases
- Adolescent
- Adult
- Agammaglobulinemia
- Aged
- Alleles
- Animals
- Antigens, Differentiation, T-Lymphocyte
- Antineoplastic Agents
- Autoantibodies
- Autoantigens
- Autoimmune Diseases
- Autoimmunity
- Base Sequence
- B-Lymphocytes
- Cardiomyopathy, Hypertrophic
- Carrier Proteins
- CD56 Antigen
- Cell Degranulation
- Cell Line
- Child
- Child, Preschool
- Chromosomes, Human, Pair 5
- Codon, Nonsense
- Cohort Studies
- Consanguinity
- Crohn Disease
- Cross-Sectional Studies
- Cytokines
- Cytotoxicity, Immunologic
- Data Collection
- Databases, Genetic
- Developmental Disabilities
- Disease Models, Animal
- Disease Susceptibility
- DNA Copy Number Variations
- Endoplasmic Reticulum Stress
- Exome
- Exons
- Family
- Female
- Frameshift Mutation
- Gain of Function Mutation
- Genetic Association Studies
- Genetic Predisposition to Disease
- Genetic Testing
- Genome, Human
- Genome-Wide Association Study
- Genomics
- Heart Defects, Congenital
- Hematopoietic Stem Cell Transplantation
- Hereditary Autoinflammatory Diseases
- Hereditary Sensory and Autonomic Neuropathies
- Herpesvirus 4, Human
- Heterozygote
- High-Throughput Nucleotide Sequencing
| - Humans
- Immunity
- Immunity, Innate
- Immunization
- Immunoglobulins, Intravenous
- Immunologic Deficiency Syndromes
- Immunophenotyping
- Infant
- Infant, Newborn
- Inflammation
- Intellectual Disability
- Interferon Type I
- Interferon-gamma
- Interleukin-18
- Interleukin-2
- Killer Cells, Natural
- Loss of Function Mutation
- Lupus Erythematosus, Systemic
- Lymphohistiocytosis, Hemophagocytic
- Lymphoma
- Lymphopenia
- Lymphoproliferative Disorders
- Macrophage Activation
- Magnetic Resonance Imaging
- Male
- Mice
- Mice, Inbred BALB C
- Mice, Inbred C57BL
- Middle Aged
- Models, Molecular
- Molecular Chaperones
- Multifactorial Inheritance
- Mutant Proteins
- Mutation
- Mutation, Missense
- Nerve Tissue Proteins
- Neuroimaging
- Neutropenia
- Nonsense Mediated mRNA Decay
- Pedigree
- Phenotype
- Proteasome Endopeptidase Complex
- Protein Conformation
- Pyrin
- Ribonucleoproteins
- RNA, Messenger
- Signal Transduction
- Survival Analysis
- Syndrome
- Systemic Inflammatory Response Syndrome
- T-Lymphocytes
- Tumor Microenvironment
- Unfolded Protein Response
- Uniparental Disomy
- Wiskott-Aldrich Syndrome Protein
- Young Adult
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Concepts
(113)
Derived automatically from this person's publications.
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Co-Authors
(38)
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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