D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Biology and Biochemistry D-index 48 Citations 9,906 113 World Ranking 11373 National Ranking 4916

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • DNA
  • Genome

Genetics, Molecular biology, Antigen, Virology and Virus are his primary areas of study. His Molecular biology research is multidisciplinary, relying on both Retinoblastoma protein, Clone, Gene product, Ribosome and Adenocarcinoma. His Antigen research is multidisciplinary, incorporating elements of Carcinogenesis, SV40 large T antigen and Cell cycle.

His study looks at the intersection of SV40 large T antigen and topics like DNA-binding protein with E2F. His work in the fields of Virology, such as Capsid, overlaps with other areas such as Medical school. As part of the same scientific family, he usually focuses on Virus, concentrating on Viral evolution and intersecting with Metagenomics, Human virome, Genomics, Plant virus and Genetic diversity.

His most cited work include:

  • SV40-encoded microRNAs regulate viral gene expression and reduce susceptibility to cytotoxic T cells (555 citations)
  • SV40 large T antigen targets multiple cellular pathways to elicit cellular transformation (400 citations)
  • The retinoblastoma susceptibility gene product undergoes cell cycle-dependent dephosphorylation and binding to and release from SV40 large T. (328 citations)

What are the main themes of his work throughout his whole career to date?

James M. Pipas mostly deals with Antigen, Virology, Molecular biology, Virus and Cell biology. His Antigen research incorporates elements of SV40 large T antigen, Mutation, Virion assembly, Mutant and Cytotoxic T cell. Many of his studies on Virology apply to Viral evolution as well.

His Molecular biology study also includes fields such as

  • DNA replication which is related to area like Viral replication and Chaperone,
  • Cell culture and related Cell type. His Virus study is concerned with Genetics in general. James M. Pipas has researched Cell biology in several fields, including Cell cycle, Genetically modified mouse, Cell division and Cell growth.

He most often published in these fields:

  • Antigen (32.31%)
  • Virology (31.54%)
  • Molecular biology (28.46%)

What were the highlights of his more recent work (between 2015-2020)?

  • Virus (26.92%)
  • Genetics (16.92%)
  • Gene (14.62%)

In recent papers he was focusing on the following fields of study:

James M. Pipas focuses on Virus, Genetics, Gene, Virology and Genome. His study looks at the relationship between Virus and topics such as Whole genome sequencing, which overlap with Open reading frame and Metagenomics. His Viral metagenomics, E2F and DNA Tumor Virus study in the realm of Gene connects with subjects such as Biological classification.

James M. Pipas combines subjects such as Carcinogenesis, Cell and Liver cancer with his study of Virology. His study in Cell is interdisciplinary in nature, drawing from both Tumor necrosis factor alpha and Antigen. His Genome study combines topics from a wide range of disciplines, such as Computational biology and DNA sequencing.

Between 2015 and 2020, his most popular works were:

  • The Ancient Evolutionary History of Polyomaviruses. (136 citations)
  • Merkel Cell Polyomavirus Exhibits Dominant Control of the Tumor Genome and Transcriptome in Virus-Associated Merkel Cell Carcinoma. (62 citations)
  • Viral sequences in human cancer (46 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • DNA
  • Genome

His primary areas of investigation include Genome, Cancer research, Gene, Virus and Immunology. His studies in Genome integrate themes in fields like Virology, Carcinogenesis, Computational biology, DNA sequencing and Metagenomics. James M. Pipas has included themes like Merkel cell, Merkel cell carcinoma and Merkel cell polyomavirus in his Virology study.

His Cancer research study incorporates themes from Cancer and E2F, Gene expression. His work on Viral evolution, Phylogenetic tree and Viral metagenomics as part of general Gene research is often related to Biological classification, thus linking different fields of science. His Virus research is multidisciplinary, relying on both Liver cancer, Cell culture, Human virome and IRF3.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

SV40-encoded microRNAs regulate viral gene expression and reduce susceptibility to cytotoxic T cells

Christopher S. Sullivan;Adam T. Grundhoff;Satvir Tevethia;James M. Pipas.
Nature (2005)

808 Citations

SV40 large T antigen targets multiple cellular pathways to elicit cellular transformation

Deepika Ahuja;M Teresa Sáenz-Robles;James M Pipas.
Oncogene (2005)

613 Citations

The retinoblastoma susceptibility gene product undergoes cell cycle-dependent dephosphorylation and binding to and release from SV40 large T.

John W. Ludlow;John Shon;James M. Pipas;David M. Livingston.
Cell (1990)

457 Citations

Specific repression of TATA-mediated but not initiator-mediated transcription by wild-type p53

David H. Mack;Jai Vartikar;James M. Pipas;Laimonis A. Laimins;Laimonis A. Laimins.
Nature (1993)

436 Citations

pp60c-src activation in human colon carcinoma.

C A Cartwright;M P Kamps;A I Meisler;J M Pipas.
Journal of Clinical Investigation (1989)

351 Citations

Common and unique features of T antigens encoded by the polyomavirus group.

J M Pipas.
Journal of Virology (1992)

310 Citations

The amino-terminal transforming region of simian virus 40 large T and small t antigens functions as a J domain.

Ashok Srinivasan;Amie J. Mcclellan;Jai Vartikar;Ian Marks.
Molecular and Cellular Biology (1997)

296 Citations

T Antigens of Simian Virus 40: Molecular Chaperones for Viral Replication and Tumorigenesis

Christopher S. Sullivan;James M. Pipas.
Microbiology and Molecular Biology Reviews (2002)

288 Citations

Ribosomal protein genes are overexpressed in colorectal cancer : isolation of a cDNA clone encoding the human S3 ribosomal protein

Kay Pogue-Geile;John R. Geiser;Min Shu;Carla Miller.
Molecular and Cellular Biology (1991)

287 Citations

DnaJ/hsp40 chaperone domain of SV40 large T antigen promotes efficient viral DNA replication.

K S Campbell;K P Mullane;I A Aksoy;H Stubdal.
Genes & Development (1997)

266 Citations

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