Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2023Differences in white matter detected by ex vivo 9.4T MRI are associated with axonal changes in the R6/1 model of Huntington's Disease1citations
  • 2022Mutation-related magnetization-transfer, not axon density, drives white matter differences in premanifest Huntington disease8citations
  • 2020Drumming Motor Sequence Training Induces Apparent Myelin Remodelling in Huntington's Disease16citations

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Metzler-Baddeley, Claudia
3 / 4 shared
Parker, Greg D.
3 / 3 shared
Lelos, Mariah
1 / 1 shared
Dion, Vincent
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Rosser, Anne E.
2 / 2 shared
Mills-Smith, Bella
1 / 1 shared
Ruhland, Christopher Von
1 / 1 shared
Jones, Derek K.
3 / 3 shared
Syed, Yasir Ahmed
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Murillo, Alvaro
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Kelly, Brendan
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Chamberland, Maxime
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Coulthard, Elizabeth
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Rickards, Hugh
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Berry, Samuel C.
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Laguna, Pedro L.
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Bells, Sonya
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Rosser, Anne
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Co-Authors (by relevance)

  • Metzler-Baddeley, Claudia
  • Parker, Greg D.
  • Lelos, Mariah
  • Dion, Vincent
  • Rosser, Anne E.
  • Mills-Smith, Bella
  • Ruhland, Christopher Von
  • Jones, Derek K.
  • Syed, Yasir Ahmed
  • Murillo, Alvaro
  • Kelly, Brendan
  • Chamberland, Maxime
  • Coulthard, Elizabeth
  • Rickards, Hugh
  • Berry, Samuel C.
  • Laguna, Pedro L.
  • Bourbon-Teles, Jose
  • Bells, Sonya
  • Rosser, Anne
OrganizationsLocationPeople

article

Mutation-related magnetization-transfer, not axon density, drives white matter differences in premanifest Huntington disease

  • Chamberland, Maxime
  • Metzler-Baddeley, Claudia
  • Parker, Greg D.
  • Coulthard, Elizabeth
  • Casella, Chiara
  • Rosser, Anne E.
  • Rickards, Hugh
  • Berry, Samuel C.
  • Jones, Derek K.
  • Laguna, Pedro L.
Abstract

<p>White matter (WM) alterations have been observed in Huntington disease (HD) but their role in the disease-pathophysiology remains unknown. We assessed WM changes in premanifest HD by exploiting ultra-strong-gradient magnetic resonance imaging (MRI). This allowed to separately quantify magnetization transfer ratio (MTR) and hindered and restricted diffusion-weighted signal fractions, and assess how they drove WM microstructure differences between patients and controls. We used tractometry to investigate region-specific alterations across callosal segments with well-characterized early- and late-myelinating axon populations, while brain-wise differences were explored with tract-based cluster analysis (TBCA). Behavioral measures were included to explore disease-associated brain-function relationships. We detected lower MTR in patients' callosal rostrum (tractometry: p =.03; TBCA: p =.03), but higher MTR in their splenium (tractometry: p =.02). Importantly, patients' mutation-size and MTR were positively correlated (all p-values &lt;.01), indicating that MTR alterations may directly result from the mutation. Further, MTR was higher in younger, but lower in older patients relative to controls (p =.003), suggesting that MTR increases are detrimental later in the disease. Finally, patients showed higher restricted diffusion signal fraction (FR) from the composite hindered and restricted model of diffusion (CHARMED) in the cortico-spinal tract (p =.03), which correlated positively with MTR in the posterior callosum (p =.033), potentially reflecting compensatory mechanisms. In summary, this first comprehensive, ultra-strong gradient MRI study in HD provides novel evidence of mutation-driven MTR alterations at the premanifest disease stage which may reflect neurodevelopmental changes in iron, myelin, or a combination of these.</p>

Topics
  • density
  • microstructure
  • cluster
  • composite
  • iron
  • magnetization