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
Microbiology D-index 70 Citations 13,882 147 World Ranking 1231 National Ranking 106

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • DNA

Michael J. Blackman mainly focuses on Plasmodium falciparum, Cell biology, Virology, Antigen and Protease. Michael J. Blackman is interested in Merozoite surface protein, which is a field of Plasmodium falciparum. His research integrates issues of Secretion, Plasmodium and Rhoptry in his study of Cell biology.

Michael J. Blackman usually deals with Virology and limits it to topics linked to Apical membrane antigen 1 and Microneme, Ectodomain, Heterologous, Immunofluorescence and Immunoglobulin G. His Protease course of study focuses on Proteases and Malaria. His Epitope research is multidisciplinary, incorporating elements of Malaria vaccine and Monoclonal antibody, Monoclonal.

His most cited work include:

  • A single fragment of a malaria merozoite surface protein remains on the parasite during red cell invasion and is the target of invasion-inhibiting antibodies. (494 citations)
  • A role for apical membrane antigen 1 during invasion of hepatocytes by Plasmodium falciparum sporozoites. (262 citations)
  • Subcellular discharge of a serine protease mediates release of invasive malaria parasites from host erythrocytes. (257 citations)

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

His primary scientific interests are in Plasmodium falciparum, Cell biology, Protease, Malaria and Virology. Merozoite surface protein is the focus of his Plasmodium falciparum research. His work deals with themes such as Proteases, Plasmodium and Rhoptry, which intersect with Cell biology.

His work on Serine protease as part of general Protease study is frequently linked to Sheddase, therefore connecting diverse disciplines of science. The concepts of his Malaria study are interwoven with issues in Red blood cell, Host, Computational biology and Microbiology. His Virology research includes themes of Humoral immunity and Malaria vaccine.

He most often published in these fields:

  • Plasmodium falciparum (81.25%)
  • Cell biology (75.96%)
  • Protease (30.29%)

What were the highlights of his more recent work (between 2017-2021)?

  • Cell biology (75.96%)
  • Plasmodium falciparum (81.25%)
  • Malaria (30.29%)

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

Cell biology, Plasmodium falciparum, Malaria, Protein kinase A and Plasmodium are his primary areas of study. His research in Cell biology intersects with topics in Red blood cell, Protease and Plasmodium berghei. Michael J. Blackman has researched Protease in several fields, including Proteases, Protein degradation and Protein precursor.

His research on Plasmodium falciparum also deals with topics like

  • Subtilisin most often made with reference to Gene,
  • Phenotype which intersects with area such as Computational biology and Allele. His Malaria research incorporates themes from Virology, Antigen, Microbiology, Host and Antibody. His studies in Plasmodium integrate themes in fields like Perforin and Organelle.

Between 2017 and 2021, his most popular works were:

  • A protease cascade regulates release of the human malaria parasite Plasmodium falciparum from host red blood cells. (60 citations)
  • A protease cascade regulates release of the human malaria parasite Plasmodium falciparum from host red blood cells. (60 citations)
  • The Actinomyosin Motor Drives Malaria Parasite Red Blood Cell Invasion but Not Egress. (38 citations)

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

  • Gene
  • Enzyme
  • DNA

Michael J. Blackman mostly deals with Plasmodium falciparum, Cell biology, Protein kinase A, Malaria and Plasmodium. In his study, which falls under the umbrella issue of Plasmodium falciparum, Cleavage, Complementation and Cytoskeleton is strongly linked to Protease. The study incorporates disciplines such as Transferase and Apicomplexa in addition to Cell biology.

As a member of one scientific family, Michael J. Blackman mostly works in the field of Protein kinase A, focusing on Phenotype and, on occasion, Mutant, Function, Allele and Computational biology. Michael J. Blackman interconnects Antibody, Antigen, Antigenic variation and Virology in the investigation of issues within Malaria. His biological study spans a wide range of topics, including Blood stage malaria and Parasitophorous vacuole.

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

A single fragment of a malaria merozoite surface protein remains on the parasite during red cell invasion and is the target of invasion-inhibiting antibodies.

M J Blackman;H G Heidrich;S Donachie;J S McBride.
Journal of Experimental Medicine (1990)

729 Citations

A role for apical membrane antigen 1 during invasion of hepatocytes by Plasmodium falciparum sporozoites.

Olivier Silvie;Jean-François Franetich;Stéphanie Charrin;Markus S. Mueller.
Journal of Biological Chemistry (2004)

385 Citations

Antibodies inhibit the protease-mediated processing of a malaria merozoite surface protein.

Michael J. Blackman;Terry J. Scott-Finnigan;Shafrira Shai;Anthony A. Holder.
Journal of Experimental Medicine (1994)

361 Citations

Subcellular discharge of a serine protease mediates release of invasive malaria parasites from host erythrocytes.

Sharon Yeoh;Rebecca A. O'Donnell;Konstantinos Koussis;Anton R. Dluzewski.
Cell (2007)

360 Citations

Naturally acquired cellular and humoral immune responses to the major merozoite surface antigen (PfMSP1) of Plasmodium falciparum are associated with reduced malaria morbidity.

E. M. Riley;S. J. Allen;J. G. Wheeler;M. J. Blackman;M. J. Blackman.
Parasite Immunology (1992)

348 Citations

Proteolytic processing of thePlasmodium falciparum merozoite surface protein-1 produces a membrane-bound fragment containing two epidermal growth factor-like domains

Michael J. Blackman;Irene T. Ling;Stephen C. Nicholls;Anthony A. Holder.
Molecular and Biochemical Parasitology (1991)

324 Citations

A Plant-Like Kinase in Plasmodium falciparum Regulates Parasite Egress from Erythrocytes

Jeffrey D. Dvorin;Jeffrey D. Dvorin;Derek C. Martyn;Saurabh D. Patel;Saurabh D. Patel;Joshua S. Grimley.
Science (2010)

317 Citations

Antibodies that Inhibit Malaria Merozoite Surface Protein–1 Processing and Erythrocyte Invasion Are Blocked by Naturally Acquired Human Antibodies

José A. Guevara Patiño;Anthony A. Holder;Jana S. McBride;Michael J. Blackman.
Journal of Experimental Medicine (1997)

288 Citations

Secondary processing of the Plasmodium falciparum merozoite surface protein-1 (MSP1) by a calcium-dependent membrane-bound serine protease: shedding of MSP133 as a noncovalently associated complex with other fragments of the MSP1.

Michael J. Blackman;Anthony A. Holder.
Molecular and Biochemical Parasitology (1992)

279 Citations

Malaria parasite cGMP-dependent protein kinase regulates blood stage merozoite secretory organelle discharge and egress.

Christine R. Collins;Fiona Hackett;Malcolm Strath;Maria Penzo.
PLOS Pathogens (2013)

256 Citations

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