Evidence map›Paper›PMID 42310027›Full record

ArticleNature communications2026

iSCORE-PD: an isogenic stem cell collection to research Parkinson's disease.

Oriol Busquets, Hanqin Li, Khaja Mohieddin Syed, Pilar Alvarez Jerez, Jesse Dunnack, Riana Lo Bu, Yogendra Verma, Gabriella R Pangilinan, Annika Martin, Jannes Straub and 18 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors.

Oriol Busquets *Dominick P. Purpura Department of Neuroscience, Rose F. Kennedy Center, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0002-1372-9699
Hanqin Li *Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.
Khaja Mohieddin Syed *Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.ORCID 0000-0002-7682-7608
Pilar Alvarez Jerez *Center for Alzheimer's and Related Dementias, National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-5812-1898
Jesse Dunnack *Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.ORCID 0000-0002-0387-0090
Riana Lo BuDominick P. Purpura Department of Neuroscience, Rose F. Kennedy Center, Albert Einstein College of Medicine, Bronx, NY, USA.
Yogendra VermaAligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.
Gabriella R PangilinanAligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.ORCID 0000-0003-2662-7883
Annika MartinDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.ORCID 0009-0006-3369-1495
Jannes StraubAligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.
YuXin DuAligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.
Vivien M SimonDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.
Steven PoserDominick P. Purpura Department of Neuroscience, Rose F. Kennedy Center, Albert Einstein College of Medicine, Bronx, NY, USA.
Zipporiah BushAligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.ORCID 0000-0002-6304-9579
Jessica DiazDominick P. Purpura Department of Neuroscience, Rose F. Kennedy Center, Albert Einstein College of Medicine, Bronx, NY, USA.
Atehsa SahagunAligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.ORCID 0000-0001-7521-3279
Jianpu GaoDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA, USA.
Samantha HongCenter for Alzheimer's and Related Dementias, National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.ORCID 0009-0001-8968-6461
Dena G HernandezLaboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
Kristin S LevineCenter for Alzheimer's and Related Dementias, National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
Nathalie PochetDominick P. Purpura Department of Neuroscience, Rose F. Kennedy Center, Albert Einstein College of Medicine, Bronx, NY, USA.
Ezgi O BoothAligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.ORCID 0000-0001-9213-8426
Marco BlanchetteLiftOff Biosolution, Santa Cruz, CA, USA.
Helen S BateupAligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.ORCID 0000-0002-0135-0972
Donald C RioAligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.ORCID 0000-0002-4775-3515
Cornelis BlauwendraatCenter for Alzheimer's and Related Dementias, National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0001-9358-8111
Dirk HockemeyerAligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA. hockemeyer@berkeley.edu.ORCID 0000-0002-5598-5092
Frank SoldnerDominick P. Purpura Department of Neuroscience, Rose F. Kennedy Center, Albert Einstein College of Medicine, Bronx, NY, USA. frank.soldner@einsteinmed.edu.ORCID 0000-0002-7102-8655

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI Ulrich Steidl · 1985 to 2026
$111.2M
The Role of Aberrant Histone Acetylation in the Pathogenesis of Parkinson’s Disease and Related Synucleinopathies.R01NS138402 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Frank Soldner · 2024 to 2026
$2.1M
The Role of GPNMB in Parkinson's Disease.R01NS133140 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Frank Soldner · 2024 to 2026
$2.0M
Dysregulation of Histone Acetylation in Parkinson's DiseaseR56NS128015 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SOLDNER, FRANK · 2023 to 2023
$624k
Dissecting GWAS Identified Risk Variants in Parkinson's Disease – Functional Role of GPNMB in the Pathogenesis of PDF31NS129265 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI LO BU, RIANA · 2023 to 2024
$97k
NCI NIH HHS P30 CA013330NINDS NIH HHS F31 NS129265NINDS NIH HHS R01 NS133140NINDS NIH HHS R01 NS138402NINDS NIH HHS R56 NS128015U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) 1R01NS133140U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) 1R01NS138402U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) 1R56NS128015U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) 5F31NS129265
6 · The paper itself

Abstract

Genome-edited human pluripotent stem cells (hPSCs) provide a powerful platform to study complex diseases such as Parkinson's disease (PD). Here, we describe iSCORE-PD, an isogenic collection of 65 genome-edited hPSC lines carrying disease-causing or high-risk variants in 11 PD-linked genes (SNCA, PRKN, PINK1, DJ1/PARK7, LRRK2, ATP13A2, FBXO7, DNAJC6, SYNJ1, VPS13C, and GBA1). All lines are derived from a well-characterized female hESC line and subjected to extensive quality control. Whole-genome sequencing reveals that genetic variation between lines, largely confined to non-coding regions, is minimal relative to inter-individual differences in patient-derived hiPSCs, with most variation arising from random mutations acquired during cell culture rather than genome-editing-induced off-target effects. Including multiple independently derived clones per mutation can control for this random genetic drift. Our systematic approach ensures high quality of this publicly available iSCORE-PD resource, highlights the advantages of prime editing over conventional CRISPR/Cas9 methods, and establishes best practices for generating disease-modeling hPSC collections.

Indexed as

Induced Pluripotent Stem CellsParkinson DiseasePluripotent Stem Cellsalpha-SynucleinCell LineCRISPR-Cas SystemsFemaleGene EditingGenetic VariationHumansMutationWhole Genome Sequencingalpha-Synuclein

Identifiers

PMID42310027
PMCPMC13434110

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.