% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Hausmann:274053,
author = {Hausmann, Fabian and Caldi Gomes, Lucas and Hänzelmann,
Sonja and Khatri, Robin and Oller, Sergio and Gebelin, Marie
and Parvaz, Mojan and Tzeplaeff, Laura and Pasetto, Laura
and Zhou, Qihui and Zelina, Pavol and Edbauer, Dieter and
Pasterkamp, R Jeroen and Rehrauer, Hubert and Schlapbach,
Ralph and Carapito, Christine and Bonetto, Valentina and
Bonn, Stefan and Lingor, Paul},
title = {{A} dataset profiling the multiomic landscape of the
prefrontal cortex in amyotrophic lateral sclerosis.},
journal = {GigaScience},
volume = {13},
issn = {2047-217X},
address = {Oxford},
publisher = {Oxford University Press},
reportid = {DZNE-2025-00034},
pages = {giae100},
year = {2024},
abstract = {Amyotrophic lateral sclerosis (ALS) is the most common
motor neuron disease, which still lacks effective
disease-modifying therapies. Similar to other
neurodegenerative disorders, such as Alzheimer and Parkinson
disease, ALS pathology is presumed to propagate over time,
originating from the motor cortex and spreading to other
cortical regions. Exploring early disease stages is crucial
to understand the causative molecular changes underlying the
pathology. For this, we sampled human postmortem prefrontal
cortex (PFC) tissue from Brodmann area 6, an area that
exhibits only moderate pathology at the time of death, and
performed a multiomic analysis of 51 patients with sporadic
ALS and 50 control subjects. To compare sporadic disease to
genetic ALS, we additionally analyzed PFC tissue from 4
transgenic ALS mouse models (C9orf72-, SOD1-, TDP-43-, and
FUS-ALS) using the same methods. This multiomic data
resource includes transcriptome, small RNAome, and proteome
data from female and male samples, aimed at elucidating
early and sex-specific ALS mechanisms, biomarkers, and drug
targets.},
keywords = {Amyotrophic Lateral Sclerosis: genetics / Amyotrophic
Lateral Sclerosis: metabolism / Prefrontal Cortex:
metabolism / Prefrontal Cortex: pathology / Humans / Female
/ Mice / Male / Animals / Mice, Transgenic / Transcriptome /
Proteome / Disease Models, Animal / Aged / Gene Expression
Profiling: methods / Middle Aged / amyotrophic lateral
sclerosis (Other) / early disease mechanisms (Other) /
multiomics analysis (Other) / neurodegeneration (Other) /
prefrontal cortex (Other) / Proteome (NLM Chemicals)},
cin = {Clinical Research (Munich) / AG Zhou / AG Edbauer},
ddc = {610},
cid = {I:(DE-2719)1111015 / I:(DE-2719)5000080 /
I:(DE-2719)1110004},
pnm = {353 - Clinical and Health Care Research (POF4-353) / 352 -
Disease Mechanisms (POF4-352)},
pid = {G:(DE-HGF)POF4-353 / G:(DE-HGF)POF4-352},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:39693632},
pmc = {pmc:PMC11653894},
doi = {10.1093/gigascience/giae100},
url = {https://pub.dzne.de/record/274053},
}