What is he best known for?
The fields of study he is best known for:
His primary areas of investigation include Virology, Virus, Antibody, Rotavirus and Immunology.
Serotype, Titer, Viral Vaccine and Viral replication are the subjects of his Virology studies.
His Serotype study also includes fields such as
- Viral shedding which connect with Antigen and Immunogen,
- Gene that intertwine with fields like Amino acid.
As part of his studies on Virus, R M Chanock often connects relevant areas like Immune system.
He works in the field of Antibody, namely Neutralizing antibody.
As part of the same scientific family, he usually focuses on Rotavirus, concentrating on Feces and intersecting with Outbreak, Viral infection, Electron microscopic and Enzyme.
His most cited work include:
- Enhancement of respiratory syncytial virus pulmonary pathology in cotton rats by prior intramuscular inoculation of formalin-inactiva ted virus. (261 citations)
- Dissociation between serum neutralizing and glycoprotein antibody responses of infants and children who received inactivated respiratory syncytial virus vaccine. (255 citations)
- Quantitative aspects of passive immunity to respiratory syncytial virus infection in infant cotton rats. (210 citations)
What are the main themes of his work throughout his whole career to date?
R M Chanock mainly focuses on Virology, Virus, Rotavirus, Antibody and Microbiology.
The various areas that R M Chanock examines in his Virology study include Gene and Antigen.
R M Chanock interconnects Cell culture, Respiratory tract, Mutant and Recombinant DNA in the investigation of issues within Virus.
The Reoviridae research R M Chanock does as part of his general Rotavirus study is frequently linked to other disciplines of science, such as Reassortment, therefore creating a link between diverse domains of science.
His Immunoglobulin G, Neutralizing antibody and Antibody titer study in the realm of Antibody interacts with subjects such as Blood serum.
His studies in Microbiology integrate themes in fields like Virus quantification, Rotavirus RNA and Viral rna.
He most often published in these fields:
- Virology (88.54%)
- Virus (54.17%)
- Rotavirus (31.25%)
What were the highlights of his more recent work (between 1986-1996)?
- Virology (88.54%)
- Rotavirus (31.25%)
- Virus (54.17%)
In recent papers he was focusing on the following fields of study:
His main research concerns Virology, Rotavirus, Virus, Serotype and Gene.
His specific area of interest is Virology, where R M Chanock studies Paramyxoviridae.
In Paramyxoviridae, R M Chanock works on issues like Antibody, which are connected to Cotton rat.
His Rotavirus study combines topics from a wide range of disciplines, such as Amino acid, Peptide sequence, Neutralization and Capsid.
His Virus study often links to related topics such as Recombinant virus.
His Serotype research is multidisciplinary, incorporating perspectives in Immunogen and Vaccination.
Between 1986 and 1996, his most popular works were:
- PROTECTION AGAINST SEVERE ROTAVIRUS DIARRHOEA BY RHESUS ROTAVIRUS VACCINE IN VENEZUELAN INFANTS (165 citations)
- Pathogenesis of adenovirus type 5 pneumonia in cotton rats (Sigmodon hispidus). (148 citations)
- Effectiveness of topically administered neutralizing antibodies in experimental immunotherapy of respiratory syncytial virus infection in cotton rats. (131 citations)
In his most recent research, the most cited papers focused on:
R M Chanock focuses on Virology, Rotavirus, Reoviridae, Paramyxoviridae and Antigen.
Titer, Viral replication, Virus and Nasal administration are the core of his Virology study.
His work carried out in the field of Virus brings together such families of science as Antibody and Immunotherapy.
His Rotavirus research includes themes of Amino acid, Nucleic acid sequence, Serotype and Pediatrics.
R M Chanock has researched Reoviridae in several fields, including Viral disease, Immunization and Vaccine efficacy, Vaccination.
The study incorporates disciplines such as Viral shedding, Immunogen, Microbiology and Passive immunity in addition to Antigen.
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