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 40 Citations 6,481 62 World Ranking 3388 National Ranking 305

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Genetics
  • Bacteria

The scientist’s investigation covers issues in Plasmodium falciparum, Cell biology, Virology, Rhoptry and Malaria. Apical membrane antigen 1 is the focus of his Plasmodium falciparum research. Jake Baum combines subjects such as Membrane protein and Ligand with his study of Cell biology.

His work in Rhoptry addresses issues such as Immunoprecipitation, which are connected to fields such as Protein family and Epidermal growth factor. His research in Malaria is mostly focused on Plasmodium. His biological study spans a wide range of topics, including Acquired immune system, Dendritic cell, Molecular motor, Actin cytoskeleton and Cell membrane.

His most cited work include:

  • Cell-Cell Communication between Malaria-Infected Red Blood Cells via Exosome-like Vesicles (317 citations)
  • Cell-Cell Communication between Malaria-Infected Red Blood Cells via Exosome-like Vesicles (317 citations)
  • A conserved molecular motor drives cell invasion and gliding motility across malaria life cycle stages and other apicomplexan parasites. (292 citations)

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

Plasmodium falciparum, Cell biology, Malaria, Plasmodium and Actin are his primary areas of study. Jake Baum works in the field of Plasmodium falciparum, focusing on Rhoptry in particular. He has researched Cell biology in several fields, including Actin cytoskeleton and Cytoskeleton.

The various areas that Jake Baum examines in his Malaria study include In vitro and Pharmacology. His Plasmodium study combines topics from a wide range of disciplines, such as Apicomplexa, Disease, Organelle and Intracellular parasite. He studied Actin and Drug discovery that intersect with Drug.

He most often published in these fields:

  • Plasmodium falciparum (88.62%)
  • Cell biology (76.65%)
  • Malaria (41.92%)

What were the highlights of his more recent work (between 2018-2021)?

  • Plasmodium falciparum (88.62%)
  • Malaria (41.92%)
  • Cell biology (76.65%)

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

His scientific interests lie mostly in Plasmodium falciparum, Malaria, Cell biology, Plasmodium and Drug discovery. His Plasmodium falciparum study combines topics in areas such as In vitro, Gene, Natural product, Drug and Myosin. His studies deal with areas such as Computational biology, Pharmacology and Virology as well as Malaria.

In the subject of general Cell biology, his work in Actin and Motility is often linked to Basigin, thereby combining diverse domains of study. His studies in Plasmodium integrate themes in fields like Parasitic life cycles, Molecular motor and Growth inhibition. Jake Baum works mostly in the field of Drug discovery, limiting it down to topics relating to Actin cytoskeleton and, in certain cases, Antimalarial Agent and Escherichia coli, as a part of the same area of interest.

Between 2018 and 2021, his most popular works were:

  • Lysyl-tRNA synthetase as a drug target in malaria and cryptosporidiosis (37 citations)
  • Plasmodium myosin A drives parasite invasion by an atypical force generating mechanism (24 citations)
  • Quantitative and rapid Plasmodium falciparum malaria diagnosis and artemisinin-resistance detection using a CMOS Lab-on-Chip platform. (23 citations)

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

  • Gene
  • Bacteria
  • Genetics

Jake Baum focuses on Plasmodium falciparum, Malaria, Drug discovery, Cell biology and Myosin. His Plasmodium falciparum research includes themes of Mode of action and Synthetic biology. His Malaria research integrates issues from Transcriptome, Computational biology, Gene and In vivo.

Jake Baum has included themes like Blood stage, High content imaging and Transmission blocking in his Drug discovery study. His work on Actin is typically connected to Motor protein as part of general Cell biology study, connecting several disciplines of science. His research in Plasmodium intersects with topics in Molecular motor, Parasitic life cycles, Protein phosphorylation and Gliding motility, Motility.

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

Cell-Cell Communication between Malaria-Infected Red Blood Cells via Exosome-like Vesicles

Neta Regev-Rudzki;Danny W Wilson;Danny W Wilson;Teresa G Carvalho;Teresa G Carvalho;Xavier Sisquella;Xavier Sisquella.
Cell (2013)

478 Citations

The cellular and molecular basis for malaria parasite invasion of the human red blood cell.

Alan F. Cowman;Drew Berry;Jake Baum.
Journal of Cell Biology (2012)

461 Citations

A conserved molecular motor drives cell invasion and gliding motility across malaria life cycle stages and other apicomplexan parasites.

Jake Baum;Dave Richard;Julie Healer;Melanie Rug.
Journal of Biological Chemistry (2006)

399 Citations

Super-Resolution Dissection of Coordinated Events during Malaria Parasite Invasion of the Human Erythrocyte

David T Riglar;Dave Richard;Danny W Wilson;Michelle J. Boyle;Michelle J. Boyle.
Cell Host & Microbe (2011)

356 Citations

The Dendritic Cell Receptor Clec9A Binds Damaged Cells via Exposed Actin Filaments

Jian Guo Zhang;Jian Guo Zhang;Peter E. Czabotar;Peter E. Czabotar;Antonia N. Policheni;Antonia N. Policheni;Irina Caminschi;Irina Caminschi;Irina Caminschi.
Immunity (2012)

295 Citations

Isolation of viable Plasmodium falciparum merozoites to define erythrocyte invasion events and advance vaccine and drug development

Michelle J Boyle;Danny W Wilson;Jack S Richards;David T Riglar.
Proceedings of the National Academy of Sciences of the United States of America (2010)

262 Citations

Cryo-EM structure of the Plasmodium falciparum 80S ribosome bound to the anti-protozoan drug emetine

Wilson Wong;Xiao Chen Bai;Alan Brown;Israel S. Fernandez.
eLife (2014)

254 Citations

Interaction between Plasmodium falciparum apical membrane antigen 1 and the rhoptry neck protein complex defines a key step in the erythrocyte invasion process of malaria parasites

Dave Richard;Christopher A. MacRaild;David T. Riglar;Jo-Anne Chan.
Journal of Biological Chemistry (2010)

253 Citations

Reticulocyte-binding protein homologue 5 – An essential adhesin involved in invasion of human erythrocytes by Plasmodium falciparum

Jake Baum;Lin Chen;Julie Healer;Sash Lopaticki.
International Journal for Parasitology (2009)

245 Citations

Host-cell invasion by malaria parasites: insights from Plasmodium and Toxoplasma

Jake Baum;Tim-Wolf Gilberger;Freddy Frischknecht;Markus Meissner.
Trends in Parasitology (2008)

235 Citations

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