Multimodal ultra-high-field MRI, clinical, cognitive, and genetic profiles across the ALS-FTD spectrum.
Overview
18 affiliations
- School of Electrical Engineering and Computer Science, The University of Queensland, Brisbane, Australia
- Centre for Advanced Imaging, Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, Australia
- Royal Brisbane and Women’s Hospital, Neurology Dept., Brisbane, Australia
- Queensland Digital Health Centre, The University of Queensland, Brisbane, Australia
- Australian e-Health Research Centre, CSIRO Health and Biosecurity, Herston, Queensland Australia
- School of Biomedical Sciences, The University of Queensland, Brisbane, Australia
- School of Psychology, The University of Queensland, Brisbane, Australia
- Queensland Brain Institute, The University of Queensland, Brisbane, Australia
- QIMR Berghofer Medical Research Institute, Brisbane, Australia
- Ametris, Pensacola, FL USA
- Centre for Clinical Research, The University of Queensland, Brisbane, Australia
- Sydney Medical School, School of Biomedical Engineering, The University of Sydney, Sydney, Australia
- Brain and Mind Centre, The University of Sydney, Sydney, Australia
- Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, Australia
- Siemens Healthcare Pty Ltd, Brisbane, Australia
- High Field MR Center, Department for Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, Vienna, Austria
- Christian Doppler Laboratory for MR Imaging Biomarkers, Department for Biomedical Imaging and Image-Guided Therapy, Medical University of Vienna, Vienna, Austria
- Queensland University of Technology, Brisbane, Australia
Abstract
The abstract is not reproduced here: the paper's license (CC BY-NC-ND) does not allow it. Read it in the paper, at the publisher or on Europe PMC.
Code
The paper links to its data, not to its authors' code: see the Data section.
Code availability statement
The paper has a code availability statement. Its license (CC BY-NC-ND) does not allow reproducing it here; in short, from what the harvester recognized in it:
- no repository, dataset or request procedure was recognized in it
Read it in the paper: doi.org/10.1038/s41597-026-07461-3.
Tracing map
A tracing map links a paper to the code its authors published: this paper has none, so it has no map.
Data
Datasets cited
- doi:10.18112/
openneuro.ds007036.v1.1. , at OpenNeuro; found in the references0 - doi:10.18112/
openneuro.ds007036.v1.1. , at OpenNeuro; found in “Data availability”3
Data availability statement
The paper has a data availability statement. Its license (CC BY-NC-ND) does not allow reproducing it here; in short, from what the harvester recognized in it:
- it points to a dataset: OpenNeuro 10.18112/
openneuro.ds007036.v1.1. 3
Read it in the paper: doi.org/10.1038/s41597-026-07461-3.
Versions
The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.
Version 1, 28 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 25 authors, 5 MeSH terms, 14 funders, 69 references.
Cite
This paper
Shaw, T. B., Al Najjar, A., Barth, M., Bollmann, S., Bourgeat, P., Chang, J., Dempsey-Jones, H., Fazlollahi, A., Fripp, J., Garden, N., Guo, C. C., Henderson, R. D., Kuan, E., Lv, J., McCombe, P. A., Narayanan, A., Ngo, S. T., Nguyen, V., O’Brien, K., . . . Bollmann, S. (2026). Multimodal ultra-high-field MRI, clinical, cognitive, and genetic profiles across the ALS-FTD spectrum. Scientific data, 13(1), 1152. https://
BibTeX
@article{shaw2026multimo
author = {Shaw, Thomas B and Al Najjar, Aiman and Barth, Markus and Bollmann, Steffen and Bourgeat, Pierrick and Chang, Jeryn and Dempsey-Jones, Harriet and Fazlollahi, Amir and Fripp, Jurgen and Garden, Natalie and Guo, Christine C and Henderson, Robert D and Kuan, Elaine and Lv, Jinglei and McCombe, Pamela A and Narayanan, Aswin and Ngo, Shyuan T and Nguyen, Vinh and O’Brien, Kieran and Robinson, Gail and Robinson, Simon and Salvado, Olivier and Stewart, Ashley and Steyn, Frederik J and Bollmann, Saskia},
title = {{Multimodal ultra-high-field MRI, clinical, cognitive, and genetic profiles across the ALS-FTD spectrum}},
journal = {Scientific data},
year = {2026},
month = may,
volume = {13},
number = {1},
pages = {1152},
publisher = {Nature Publishing Group},
issn = {2052-4463},
doi = {10.1038/
url = {https://
pmid = {42156779},
pmcid = {PMC13454292}
}
RIS
TY - JOUR
AU - Shaw, Thomas B
AU - Al Najjar, Aiman
AU - Barth, Markus
AU - Bollmann, Steffen
AU - Bourgeat, Pierrick
AU - Chang, Jeryn
AU - Dempsey-Jones, Harriet
AU - Fazlollahi, Amir
AU - Fripp, Jurgen
AU - Garden, Natalie
AU - Guo, Christine C
AU - Henderson, Robert D
AU - Kuan, Elaine
AU - Lv, Jinglei
AU - McCombe, Pamela A
AU - Narayanan, Aswin
AU - Ngo, Shyuan T
AU - Nguyen, Vinh
AU - O’Brien, Kieran
AU - Robinson, Gail
AU - Robinson, Simon
AU - Salvado, Olivier
AU - Stewart, Ashley
AU - Steyn, Frederik J
AU - Bollmann, Saskia
TI - Multimodal ultra-high-field MRI, clinical, cognitive, and genetic profiles across the ALS-FTD spectrum
T2 - Scientific data
J2 - Sci Data
PY - 2026
DA - 2026/
VL - 13
IS - 1
SP - 1152
SN - 2052-4463
PB - Nature Publishing Group
DO - 10.1038/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1038/
"type": "article-journal",
"title": "Multimodal ultra-high-field MRI, clinical, cognitive, and genetic profiles across the ALS-FTD spectrum",
"container-title": "Scientific data",
"author": [
{
"family": "Shaw",
"given": "Thomas B"
},
{
"family": "Al Najjar",
"given": "Aiman"
},
{
"family": "Barth",
"given": "Markus"
},
{
"family": "Bollmann",
"given": "Steffen"
},
{
"family": "Bourgeat",
"given": "Pierrick"
},
{
"family": "Chang",
"given": "Jeryn"
},
{
"family": "Dempsey-Jones",
"given": "Harriet"
},
{
"family": "Fazlollahi",
"given": "Amir"
},
{
"family": "Fripp",
"given": "Jurgen"
},
{
"family": "Garden",
"given": "Natalie"
},
{
"family": "Guo",
"given": "Christine C"
},
{
"family": "Henderson",
"given": "Robert D"
},
{
"family": "Kuan",
"given": "Elaine"
},
{
"family": "Lv",
"given": "Jinglei"
},
{
"family": "McCombe",
"given": "Pamela A"
},
{
"family": "Narayanan",
"given": "Aswin"
},
{
"family": "Ngo",
"given": "Shyuan T"
},
{
"family": "Nguyen",
"given": "Vinh"
},
{
"family": "O’Brien",
"given": "Kieran"
},
{
"family": "Robinson",
"given": "Gail"
},
{
"family": "Robinson",
"given": "Simon"
},
{
"family": "Salvado",
"given": "Olivier"
},
{
"family": "Stewart",
"given": "Ashley"
},
{
"family": "Steyn",
"given": "Frederik J"
},
{
"family": "Bollmann",
"given": "Saskia"
}
],
"container-title-short":
"volume": "13",
"issue": "1",
"page": "1152",
"DOI": "10.1038/
"PMID": "42156779",
"PMCID": "PMC13454292",
"ISSN": "2052-4463",
"publisher": "Nature Publishing Group",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
5,
19
]
]
}
}
Similar papers
The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.
- [1] doi:10.1093/braincomms/fcag127 [code]
- Individualized phenotyping of functional amyotrophic lateral sclerosis pathology in sensorimotor cortex.Journal: Brain communicationsIn common: other condition, 5 references
- [2] doi:10.1186/s40478-026-02341-8 [code]
- Intrathecal (G&
lt;sub& gt;4& lt;/ sub& gt;C& lt;sub& gt;2& lt;/ sub& gt;)& lt;sub& gt;149& lt;/ sub& gt; delivery in C9orf72-deficient mice yields mild motor dysfunction and ALS/ FTD pathological hallmarks. Journal: Acta neuropathologica communicationsIn common: Alzheimer's / dementia, other condition, 5 references - [3] doi:10.1186/s12916-026-04948-z [code]
- Putative glymphatic dysfunction links extracellular fluid dysregulation to white matter degeneration and clinical impairment in amyotrophic lateral sclerosis.Journal: BMC medicineIn common: structural MRI / diffusion, other condition, 4 references
- [4] doi:10.1007/s00415-026-14134-z
- What do ALS motor phenotypes measure? A population-based decomposition of their prognostic dimensions.Journal: Journal of neurologyIn common: other condition, 4 references
- [5] doi:10.1136/bmjopen-2025-110906
- Strategic Amyotrophic Lateral Sclerosis Australia-Systems Genomics Consortium (SALSA-SGC): cohort profile.Journal: BMJ openIn common: other condition, 4 references
- [6] doi:10.1002/hbm.70621 [code]
- Optimising 7T-fMRI for Imaging Regions of Magnetic Susceptibility.Journal: Human brain mappingIn common: 4 references
- [7] doi:10.1002/mrm.70366 [code]
- Mesoscale Whole-Brain T&
lt;sub& gt;2& lt;/ sub& gt;*-Weighted and Associated Quantitative MRI in Humans at 10.5 T. Journal: Magnetic resonance in medicineIn common: structural MRI / diffusion, 3 references - [8] doi:10.1002/mrm.70336 [code]
- Offline Reconstruction of Diffusion MRI Acquisitions for Comparison Between Complex PCA-Based and AI-Based Denoising.Journal: Magnetic resonance in medicineIn common: methods / tools, structural MRI / diffusion, 3 references
- [9] doi:10.1162/netn.a.547 [code]
- An evaluation of the efficacy of single-echo and multi-echo fMRI denoising strategies.Journal: Network neuroscience (Cambridge, Mass.)In common: 4 references
- [10] doi:10.3348/kjr.2026.0103 [code]
- Deep Learning-Based Automated Detection and Burden Assessment of Paramagnetic Rim Lesions on Quantitative Susceptibility Mapping in Patients With Multiple Sclerosis.Journal: Korean journal of radiologyIn common: structural MRI / diffusion, 3 references
Contribute
The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.
Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.
Claim this paper
Correct its record
Say what each link of this record is, remove the ones that are not the paper's, add the ones that are missing. The correction becomes a new version of the record, in its Versions section.
Request its removal
To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).
Discussion, reproductions, activity
Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.
Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.
Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.
