What is he best known for?
The fields of study he is best known for:
- Antibody
- Gene
- Immune system
His primary areas of investigation include Antibody, Virology, Immunology, Virus and Antigen.
His study looks at the intersection of Antibody and topics like Vaccination with Antibody Repertoire.
The concepts of his Virology study are interwoven with issues in Epitope and Immunoglobulin G.
His study looks at the relationship between Immunoglobulin G and topics such as Orthomyxoviridae, which overlap with Original antigenic sin and Neutralizing antibody.
His Antigen study combines topics in areas such as Clonal deletion, Molecular biology, Naive B cell and Immunoglobulin heavy chain.
Patrick C. Wilson combines subjects such as In vitro, Fc receptor and In vivo with his study of Influenza A virus.
His most cited work include:
- Rapid cloning of high-affinity human monoclonal antibodies against influenza virus (851 citations)
- Rapid cloning of high-affinity human monoclonal antibodies against influenza virus (851 citations)
- Broadly cross-reactive antibodies dominate the human B cell response against 2009 pandemic H1N1 influenza virus infection (668 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Antibody, Virology, Immunology, Virus and Antigen.
His research investigates the connection between Antibody and topics such as Molecular biology that intersect with issues in Immunoglobulin light chain.
His research integrates issues of Epitope and Monoclonal antibody in his study of Virology.
His Virus research includes themes of Immunogenicity and Polyclonal antibodies.
His research investigates the link between Antigen and topics such as B-1 cell that cross with problems in Receptor editing.
His research in Influenza A virus intersects with topics in Influenza A virus subtype H5N1 and Neutralizing antibody.
He most often published in these fields:
- Antibody (58.99%)
- Virology (49.44%)
- Immunology (32.58%)
What were the highlights of his more recent work (between 2018-2021)?
- Virology (49.44%)
- Antibody (58.99%)
- Virus (33.15%)
In recent papers he was focusing on the following fields of study:
Patrick C. Wilson mainly focuses on Virology, Antibody, Virus, Epitope and Hemagglutinin.
The Virology study combines topics in areas such as Memory B cell, Humoral immunity, Antigen, Polyclonal antibodies and Monoclonal antibody.
His research investigates the connection with Antigen and areas like B cell which intersect with concerns in Pathogen.
The concepts of his Antibody study are interwoven with issues in Nucleoprotein, Computational biology and Convalescent plasma.
His studies in Virus integrate themes in fields like Immunogenicity, Immunity and Vaccination.
Patrick C. Wilson interconnects Fc receptor, Isotype and Effector in the investigation of issues within Hemagglutinin.
Between 2018 and 2021, his most popular works were:
- Antibiotics-Driven Gut Microbiome Perturbation Alters Immunity to Vaccines in Humans. (128 citations)
- Influenza Virus Vaccination Elicits Poorly Adapted B Cell Responses in Elderly Individuals. (61 citations)
- Mapping person-to-person variation in viral mutations that escape polyclonal serum targeting influenza hemagglutinin. (49 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Antibody
- Immune system
His primary scientific interests are in Virology, Virus, Vaccination, Antibody and Antigenic drift.
His biological study spans a wide range of topics, including Humoral immunity, Monoclonal antibody, Memory B cell and Severe acute respiratory syndrome coronavirus 2.
In his study, Microbiome, Cytokine, Pathogenesis and Immunosenescence is inextricably linked to Immunity, which falls within the broad field of Virus.
To a larger extent, Patrick C. Wilson studies Immunology with the aim of understanding Vaccination.
His primary area of study in Antibody is in the field of Antibody titer.
His study in Antigenic drift is interdisciplinary in nature, drawing from both Epitope, Inactivated vaccine, Immunogenicity and Polyclonal antibodies.
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