World's Best Scientists 2026 revealed!
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Molecular Biology
Australia
2026
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Chemistry
Australia
2025

D-Index & Metrics

Chemistry

D-Index
93
Citations
27632
World Ranking
1815
National Ranking
48

Molecular Biology

D-Index
113
Citations
68826
World Ranking
326
National Ranking
6

Research.com Recognitions

  • 2026 - Research.com Molecular Biology in Australia Leader Award
  • 2025 - Research.com Chemistry in Australia Leader Award
  • 2025 - Research.com Molecular Biology in Australia Leader Award
  • 2023 - Research.com Molecular Biology in Australia Leader Award
  • 2022 - Research.com Chemistry in Australia Leader Award

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • Amino acid

Michael W. Parker spends much of his time researching Biochemistry, Protein structure, Stereochemistry, Cell biology and Glutathione. His Biophysics research extends to Biochemistry, which is thematically connected. He has researched Protein structure in several fields, including Superoxide dismutase, Glutathione S-transferase, Amyloid precursor protein, Förster resonance energy transfer and Lipid bilayer.

His Stereochemistry research is multidisciplinary, incorporating elements of Crystallography, Tetramer and Substrate. His research investigates the link between Cell biology and topics such as Common gamma chain that cross with problems in Cytokine receptor. Michael W. Parker combines subjects such as Alanine, Cooperative binding and Transferase with his study of Glutathione.

His most cited work include:

  • Origin of the West Nile Virus Responsible for an Outbreak of Encephalitis in the Northeastern United States (1339 citations)
  • Large-scale discovery of novel genetic causes of developmental disorders (661 citations)
  • Structure and function of glutathione S-transferases (493 citations)

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

Michael W. Parker mostly deals with Biochemistry, Stereochemistry, Protein structure, Cell biology and Enzyme. Glutathione, Binding site, Active site, Plasma protein binding and Aminopeptidase are among the areas of Biochemistry where the researcher is concentrating his efforts. As part of his studies on Stereochemistry, Michael W. Parker often connects relevant areas like Crystal structure.

His studies deal with areas such as Crystallography, Biophysics and Peptide sequence as well as Protein structure. His research investigates the connection between Biophysics and topics such as Membrane that intersect with issues in Cholesterol-dependent cytolysin. His research in Cell biology intersects with topics in Receptor, Interleukin-21 receptor and Cytokine.

He most often published in these fields:

  • Biochemistry (45.82%)
  • Stereochemistry (21.84%)
  • Protein structure (22.84%)

What were the highlights of his more recent work (between 2015-2021)?

  • Cell biology (23.69%)
  • Receptor (12.06%)
  • Biochemistry (45.82%)

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

His main research concerns Cell biology, Receptor, Biochemistry, Biophysics and Protein structure. His research in Cell biology focuses on subjects like Monoubiquitination, which are connected to DNA Repair Pathway. His Receptor study integrates concerns from other disciplines, such as Endocrinology, Erythropoietin, Interleukin, Cytokine and Beta.

Binding site, Allosteric regulation, Active site, Mutagenesis and Glutathione are among the areas of Biochemistry where Michael W. Parker concentrates his study. The study incorporates disciplines such as Membrane and Cholesterol-dependent cytolysin in addition to Biophysics. The Protein structure study combines topics in areas such as Drug discovery and Dihydrodipicolinate synthase.

Between 2015 and 2021, his most popular works were:

  • Inhibitors of histone acetyltransferases KAT6A/B induce senescence and arrest tumour growth (74 citations)
  • Inhibitors of histone acetyltransferases KAT6A/B induce senescence and arrest tumour growth (74 citations)
  • Transitional changes in the CRP structure lead to the exposure of proinflammatory binding sites (68 citations)

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

  • Gene
  • Enzyme
  • DNA

The scientist’s investigation covers issues in Cell biology, Plasma protein binding, Biochemistry, Biophysics and Protein structure. His Cell biology study combines topics from a wide range of disciplines, such as Pharmacophore, Receptor, Sialic acid and Protein subunit. His Plasma protein binding study combines topics in areas such as Inflammation, Structural biology, Complement factor I and Small molecule.

His study in Biochemistry is interdisciplinary in nature, drawing from both Infectivity and Bacteria. Michael W. Parker has included themes like Cell, Proteasome, Membrane, Plasmodium falciparum and Proteostasis in his Biophysics study. The concepts of his Protein structure study are interwoven with issues in Regulator, Hydrolase, Cryo-electron microscopy and Binding site.

Best Publications

  • A global reference for human genetic variation.

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • Fair Allocation of Scarce Medical Resources in the Time of Covid-19.

    Ezekiel J. Emanuel;Govind Persad;Ross Upshur;Beatriz Thome

  • International network of cancer genome projects

    Thomas J. Hudson;Thomas J. Hudson;Warwick Anderson;Axel Aretz;Anna D. Barker

  • A global reference for human genetic variation

    Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin

  • Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data

    Caroline F Wright;Tomas W Fitzgerald;Wendy D Jones;Stephen Clayton

  • Structure and function of glutathione S-transferases

    Matthew C.J. Wilce;Michael W. Parker

  • Replicon-Helper Systems from Attenuated Venezuelan Equine Encephalitis Virus: Expression of Heterologous Genes in Vitro and Immunization against Heterologous Pathogens in Vivo

    Peter Pushko;Michael Parker;George V. Ludwig;Nancy L. Davis

  • Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study

    Jenny Lord;Dominic J McMullan;Ruth Y Eberhardt;Gabriele Rinck

  • Structure of a cholesterol-binding, thiol-activated cytolysin and a model of its membrane form.

    Jamie Rossjohn;Susanne C Feil;William J McKinstry;Rodney K Tweten

  • Pore-forming protein toxins: from structure to function.

    Michael W. Parker;Susanne C. Feil

  • AMPK β Subunit Targets Metabolic Stress Sensing to Glycogen

    Galina Polekhina;Abhilasha Gupta;Belinda J Michell;Bryce Jw van Denderen

  • Structure of the Aeromonas toxin proaerolysin in its water-soluble and membrane-channel states.

    M. W. Parker;J. T. Buckley;J. P. M. Postma;A. D. Tucker

  • Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

    Alejandro Sifrim;Marc-Phillip Hitz;Anna Wilsdon;Jeroen Breckpot

  • Genome-wide and fine-resolution association analysis of malaria in West Africa

    Muminatou Jallow;Yik Ying Teo;Yik Ying Teo;Kerrin S. Small;Kerrin S. Small;Kirk A. Rockett;Kirk A. Rockett

  • Identification of a membrane-spanning domain of the thiol-activated pore-forming toxin Clostridium perfringens perfringolysin O: an alpha-helical to beta-sheet transition identified by fluorescence spectroscopy.

    Laura A. Shepard;Alejandro P. Heuck;Brian D. Hamman;Jamie Rossjohn

  • Mechanism of Activation of Protein Kinase JAK2 by the Growth Hormone Receptor

    Andrew J. Brooks;Wei Dai;Megan L. O’Mara;Daniel Abankwa

  • Model for growth hormone receptor activation based on subunit rotation within a receptor dimer

    Richard J Brown;Julian J Adams;Rebecca A Pelekanos;Yu Wan

  • The mechanism of membrane insertion for a cholesterol-dependent cytolysin: a novel paradigm for pore-forming toxins.

    Oleg Shatursky;Alejandro P Heuck;Laura A Shepard;Jamie Rossjohn

  • Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.

    Carmel Toomes;Helen M. Bottomley;Richard M. Jackson;Katherine V. Towns

  • Structure of the membrane-pore-forming fragment of colicin A.

    M. W. Parker;F. Pattus;A. D. Tucker;D. Tsernoglou

  • Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study

    Lord J;McMullan Dj;Eberhardt Ry;Rinck G

Frequent Co-Authors

Jamie Rossjohn
Jamie Rossjohn Monash University
Angel F. Lopez
Angel F. Lopez University of South Australia
Philip G. Board
Philip G. Board Australian National University
Roberto Cappai
Roberto Cappai University of Melbourne
Rodney K. Tweten
Rodney K. Tweten University of Oklahoma Health Sciences Center
Bruce E. Kemp
Bruce E. Kemp Australian Catholic University
David B. Ascher
David B. Ascher University of Queensland
Giorgio Federici
Giorgio Federici University of Rome Tor Vergata
Colin L. Masters
Colin L. Masters University of Melbourne
Kevin J. Barnham
Kevin J. Barnham Florey Institute of Neuroscience and Mental Health

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