Evidence map›Paper›PMID 37156914›Full record

ArticleNature biotechnology2023

Multimodal spatiotemporal phenotyping of human retinal organoid development.

Philipp Wahle, Giovanna Brancati, Christoph Harmel, Zhisong He, Gabriele Gut, Jacobo Sarabia Del Castillo, Aline Xavier da Silveira Dos Santos, Qianhui Yu, Pascal Noser, Jonas Simon Fleck and 17 more

Open access · hybridAbstract read
In one paragraph

Article in Nature biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
18.2field-weighted citation impact, top 1% of its field
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

84 citing papers in PubMed, 119 citations in OpenAlex.

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  18. Spatial architecture of development and disease.Nature reviews. Genetics · 2026
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24 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors at 6 institutions in 1 country.

Philipp Wahle *Department of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.ORCID 0000-0002-4728-806X
Giovanna Brancati *Department of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.ORCID 0000-0002-8589-3463
Christoph Harmel *Institute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.ORCID 0000-0002-4915-4399
Zhisong He *Department of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.ORCID 0000-0002-1502-4801
Gabriele GutDepartment of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.
Jacobo Sarabia Del CastilloDepartment of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.ORCID 0000-0001-9656-1416
Aline Xavier da Silveira Dos SantosInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
Qianhui YuInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
Pascal NoserDepartment of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.
Jonas Simon FleckDepartment of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.
Bruno GjetaInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
Dinko PavlinićInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
Simone PicelliInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.ORCID 0000-0002-1747-614X
Max HessDepartment of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.ORCID 0000-0001-9528-4445
Gregor W SchmidtDepartment of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.
Tom T A LummenDepartment of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland.
Yanyan HouInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
Patricia GallikerInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
David GoldblumInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
Marton BaloghInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
Cameron S CowanInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
Hendrik P N SchollInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
Botond RoskaInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.ORCID 0000-0002-9559-1450
Magdalena RennerInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland.
Lucas PelkmansDepartment of Molecular Life Sciences, University of Zurich, Zurich, Switzerland. lucas.pelkmans@imls.uzh.ch.ORCID 0000-0002-6754-9730
Barbara TreutleinDepartment of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland. barbara.treutlein@bsse.ethz.ch.ORCID 0000-0002-3299-5597
J Gray CampInstitute of Molecular and Clinical Ophthalmology Basel, Basel, Switzerland. jarrettgrayson.camp@unibas.ch.ORCID 0000-0003-3295-1225
University of Basel · CHETH Zurich · CHRoche (Switzerland) · CHUniversity of Zurich · CHInstitute of Molecular and Clinical Ophthalmology Basel · CHLife Science Zurich · CH

Funding

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Swiss National Science Foundation) 310030_84795
6 · The paper itself

Abstract

Organoids generated from human pluripotent stem cells provide experimental systems to study development and disease, but quantitative measurements across different spatial scales and molecular modalities are lacking. In this study, we generated multiplexed protein maps over a retinal organoid time course and primary adult human retinal tissue. We developed a toolkit to visualize progenitor and neuron location, the spatial arrangements of extracellular and subcellular components and global patterning in each organoid and primary tissue. In addition, we generated a single-cell transcriptome and chromatin accessibility timecourse dataset and inferred a gene regulatory network underlying organoid development. We integrated genomic data with spatially segmented nuclei into a multimodal atlas to explore organoid patterning and retinal ganglion cell (RGC) spatial neighborhoods, highlighting pathways involved in RGC cell death and showing that mosaic genetic perturbations in retinal organoids provide insight into cell fate regulation.

Indexed as

Pluripotent Stem CellsRetinaCell DifferentiationHumansOrganoidsRetinal Ganglion CellsTranscriptome

Identifiers

PMID37156914
PMCPMC10713453
OpenAlexW4375858779

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.