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Biology and Biochemistry

D-Index
54
Citations
12117
World Ranking
15519
National Ranking
543

Overview

Holger Wille is affiliated with the University of Alberta in Canada, focusing research predominantly on biochemistry, genetics, and molecular biology, with additional work in medicine.

The scientist's main fields of study include:

  • Biochemistry, Genetics and Molecular Biology
  • Medicine

Subfields explored encompass:

  • Molecular Biology
  • Physiology
  • Neurology
  • Nutrition and Dietetics
  • Pharmacology

The research topics investigated cover various neurological and molecular conditions including:

  • Alzheimer's disease research and treatments
  • Prion Diseases and Protein Misfolding
  • Trace Elements in Health
  • Neurological diseases and metabolism
  • Cholinesterase and Neurodegenerative Diseases
  • Supramolecular Self-Assembly in Materials
  • Parkinson's Disease Mechanisms and Treatments

Frequent publication venues where the scientist's work appears include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • PLoS Pathogens
  • Scientific Reports
  • Bioactive Materials
  • Brain

Co-authors regularly collaborating with Holger Wille are:

  • Sara Amidian
  • Leonardo M. Cortez
  • Valerie L. Sim
  • Maria Stepanova
  • Satyabrata Kar

Recent papers authored or co-authored by Holger Wille include:

  • "Prion protein lowering is a disease-modifying therapy across prion disease stages, strains and endpoints" (2020), published in Nucleic Acids Research
  • "Significance of native PLGA nanoparticles in the treatment of Alzheimer's disease pathology" (2022), published in Bioactive Materials
  • "Unconjugated PLGA nanoparticles attenuate temperature-dependent β-amyloid aggregation and protect neurons against toxicity: implications for Alzheimer's disease pathology" (2022), published in Journal of Nanobiotechnology
  • "Mimosine functionalized gold nanoparticles (Mimo-AuNPs) suppress β-amyloid aggregation and neuronal toxicity" (2021), published in Bioactive Materials
  • "Homogeneous nanodiscs of native membranes formed by stilbene-maleic-acid copolymers" (2020), published in Nanoscale

Best Publications

  • Eight prion strains have PrP Sc molecules with different conformations

    Jiri Safar;Holger Wille;Vincenza Itri;Darlene Groth

  • Evidence for assembly of prions with left-handed β-helices into trimers

    Cédric Govaerts;Holger Wille;Stanley B. Prusiner;Fred E. Cohen

  • Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains

    Martin Vey;Susanne Pilkuhn;Holger Wille;Randal Nixon

  • Alzheimer-like paired helical filaments and antiparallel dimers formed from microtubule-associated protein tau in vitro.

    H Wille;G Drewes;J Biernat;E M Mandelkow

  • Structural studies of the scrapie prion protein by electron crystallography

    Holger Wille;Melissa D. Michelitsch;Vincent Guénebaut;Surachai Supattapone

  • Small-molecule aggregates inhibit amyloid polymerization

    Brian Y Feng;Brandon H Toyama;Holger Wille;David W Colby

  • Branched Polyamines Cure Prion-Infected Neuroblastoma Cells

    Surachai Supattapone;Holger Wille;Lisa Uyechi;Jiri Safar

  • Design and construction of diverse mammalian prion strains.

    David W. Colby;Kurt Giles;Giuseppe Legname;Holger Wille

  • Natural and synthetic prion structure from X-ray fiber diffraction

    Holger Wille;Wen Bian;Michele McDonald;Amy Kendall

  • Cytosolic Prion Protein in Neurons

    Alexander Mironov;Diane Latawiec;Holger Wille;Essia Bouzamondo-Bernstein

  • Prion Protein of 106 Residues Creates an Artificial Transmission Barrier for Prion Replication in Transgenic Mice

    Surachai Supattapone;Patrick Bosque;Tamaki Muramoto;Holger Wille

  • Conformational Diversity of Wild-type Tau Fibrils Specified by Templated Conformation Change

    Bess Frost;Julian Ollesch;Holger Wille;Marc I. Diamond

  • α-Synuclein strains target distinct brain regions and cell types

    Angus Lau;Raphaella W. L. So;Heather H. C. Lau;Jason C. Sang

  • Tau protein becomes long and stiff upon phosphorylation: correlation between paracrystalline structure and degree of phosphorylation.

    T Hagestedt;B Lichtenberg;H Wille;E M Mandelkow

  • Engineering a 2D Protein–DNA Crystal

    Jonathan Malo;James C. Mitchell;Catherine Vénien-Bryan;J. Robin Harris

  • Mechanisms of prion protein assembly into amyloid.

    Jan Stöhr;Nicole Weinmann;Holger Wille;Tina Kaimann

  • A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic mice.

    Kiyotoshi Kaneko;Haydn L. Ball;Holger Wille;Hong Zhang

  • The Structural Architecture of an Infectious Mammalian Prion Using Electron Cryomicroscopy.

    Ester Vázquez-Fernández;Matthijn R. Vos;Pavel Afanasyev;Lino Cebey

  • Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity.

    D Riesner;K Kellings;K Post;H Wille

  • Evolutionary Descent of Prion Genes from the ZIP Family of Metal Ion Transporters

    Gerold Schmitt-Ulms;Sepehr Ehsani;Joel C. Watts;Joel C. Watts;David Westaway

Frequent Co-Authors

Stanley B. Prusiner
Stanley B. Prusiner University of California, San Francisco
Fred E. Cohen
Fred E. Cohen University of California, San Francisco
Stephen J. DeArmond
Stephen J. DeArmond University of California, San Francisco
David Westaway
David Westaway University of Alberta
Peter J. Peters
Peter J. Peters Maastricht University
Michael A. Baldwin
Michael A. Baldwin University of California, San Francisco
Detlev Riesner
Detlev Riesner Heinrich Heine University Düsseldorf
Frederick Cohen
Frederick Cohen Nurix Therapeutics
Darlene Groth
Darlene Groth University of California, San Francisco
Eckhard Mandelkow
Eckhard Mandelkow German Center for Neurodegenerative Diseases

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