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Topics Covered
- Alzheimer’s disease
- Neuropathology
- Molecular basis of AD
- Integrated multimodal cell atlas
Biography
Dr. Michael J. Hawrylycz is a Senior Investigator in Informatics and Data Science at the Allen Institute for Brain Science in Seattle, USA. He earned his Ph.D. in Applied Mathematics from Massachusetts Institute of Technology and previously worked in computational biology and applied mathematics. At the Allen Institute, he leads data integration and analysis efforts for large-scale brain atlasing projects such as the Allen Brain Atlas and BrainSpan, advancing understanding of brain organisation and gene expression.
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Talk Citation
Hawrylycz, M. (2025, December 31). Integrated multimodal cell atlas of Alzheimer’s disease [Audio file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 31, 2025, from https://doi.org/10.69645/TYXK1457.Export Citation (RIS)
Publication History
- Published on December 31, 2025
Financial Disclosures
- Dr. Michael Hawrylycz has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Other Talks in the Playlist: Research and Clinical Interviews
Transcript
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0:00
Interviewer: We're joined today
by Professor Michael Hawrylycz
from the Allen
Institute to discuss
his recent publication
in Nature Neuroscience
presenting an integrated
multimodal cell atlas
of Alzheimer's disease.
Professor Hawrylycz, thank you
very much for coming today.
Dr. Hawrylycz: Thank you.
I'm very happy to be here
as part of HSTalks.
Interviewer: To
start off, could you
start with a bit
of background on
what led your group to undertake
a multimodal approach for
studying Alzheimer's,
and what are the key
advantages of this approach
over previous research methods?
Dr. Hawrylycz: As we
know, Alzheimer's disease
is the most common cause of
dementia in older adults,
and it is a disease for which
progress has been limited
and treatments have been
somewhat ineffective.
Scientists now realize that
we really need to understand
the molecular basis of
the disease better.
Exactly how the associated
proteins accumulate.
What are the mechanisms
driving AD progression?
And what are vulnerable
cell populations
that are affected in the
course of the disease?
Several groups are now actually
pursuing this approach
by using single-cell
technologies
to explore vulnerabilities
of cell types.
What we did was essentially,
we had access to a
very strong team of
neuropathologists as well
as molecular scientists,
and we were able to
combine, essentially,
a deep profiling using
both neuropathology
classical approaches
to understanding
protein accumulations
and also the molecular basis
and alterations or what
goes wrong in the disease.