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@ARTICLE{Bressan:257318,
author = {Bressan, Elisangela and Reed, Xylena and Bansal, Vikas and
Hutchins, Elizabeth and Cobb, Melanie M and Webb, Michelle G
and Alsop, Eric and Grenn, Francis P and Illarionova,
Anastasia and Savytska, Natalia and Violich, Ivo and Bröer,
Stefanie and Alves Fernandes, Noemia Rita and Sivakumar,
Ramiyapriya and Beilina, Alexandra and Billingsley,
Kimberley J and Berghausen, Joos and Pantazis, Caroline B
and Pitz, Vanessa and Patel, Dhairya and Daida, Kensuke and
Meechoovet, Bessie and Reiman, Rebecca and Courtright-Lim,
Amanda and Logemann, Amber and Antone, Jerry and Barch,
Mariya and Kitchen, Robert and Li, Yan and Dalgard, Clifton
L and Rizzu, Patrizia and Hernandez, Dena Michelle Godwin
and Hjelm, Brooke E and Nalls, Mike and Gibbs, J Raphael and
Finkbeiner, Steven and Cookson, Mark R and Van
Keuren-Jensen, Kendall and Craig, David W and Singleton,
Andrew B and Heutink, Peter and Blauwendraat, Cornelis},
collaboration = {Center, American Genome},
title = {{T}he {F}oundational {D}ata {I}nitiative for {P}arkinson
{D}isease: {E}nabling efficient translation from genetic
maps to mechanism.},
journal = {Cell genomics},
volume = {3},
number = {3},
issn = {2666-979X},
address = {Amsterdam},
publisher = {Elsevier},
reportid = {DZNE-2023-00387},
pages = {100261},
year = {2023},
note = {CC BY},
abstract = {The Foundational Data Initiative for Parkinson Disease
(FOUNDIN-PD) is an international collaboration producing
fundamental resources for Parkinson disease (PD). FOUNDIN-PD
generated a multi-layered molecular dataset in a cohort of
induced pluripotent stem cell (iPSC) lines differentiated to
dopaminergic (DA) neurons, a major affected cell type in PD.
The lines were derived from the Parkinson's Progression
Markers Initiative study, which included participants with
PD carrying monogenic PD variants, variants with
intermediate effects, and variants identified by genome-wide
association studies and unaffected individuals. We generated
genetic, epigenetic, regulatory, transcriptomic, and
longitudinal cellular imaging data from iPSC-derived DA
neurons to understand molecular relationships between
disease-associated genetic variation and proximate molecular
events. These data reveal that iPSC-derived DA neurons
provide a valuable cellular context and foundational atlas
for modeling PD genetic risk. We have integrated these data
into a FOUNDIN-PD data browser as a resource for
understanding the molecular pathogenesis of PD.},
keywords = {Parkinson disease (Other) / dopaminergic neurons (Other) /
genetic risk (Other) / induced pluripotent stem cell (Other)
/ omics single-cell RNA sequencing single-cell ATAC
sequencing SNCA LRRK2 GBA1 (Other)},
cin = {AG Heutink 1 / AG Rizzu / Core ICRU},
ddc = {610},
cid = {I:(DE-2719)1210002 / I:(DE-2719)1210009 /
I:(DE-2719)1240005},
pnm = {354 - Disease Prevention and Healthy Aging (POF4-354)},
pid = {G:(DE-HGF)POF4-354},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:36950378},
pmc = {pmc:PMC10025424},
doi = {10.1016/j.xgen.2023.100261},
url = {https://pub.dzne.de/record/257318},
}