Evidence map›Paper›PMID 38915580›Full record

ArticlebioRxiv : the preprint server for biology2024

Early Developmental Origins of Cortical Disorders Modeled in Human Neural Stem Cells.

Xoel Mato-Blanco, Suel-Kee Kim, Alexandre Jourdon, Shaojie Ma, Andrew T N Tebbenkamp, Fuchen Liu, Alvaro Duque, Flora M Vaccarino, Nenad Sestan, Carlo Colantuoni and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Xoel Mato-BlancoHospital del Mar Research Institute, Parc de Recerca Biomèdica de Barcelona (PRBB), 08003 Barcelona, Catalonia, Spain.
Suel-Kee KimDepartment of Neuroscience, Yale School of Medicine, New Haven, CT 06520, USA.ORCID 0000-0003-0240-9304
Alexandre JourdonChild Study Center, Yale University School of Medicine, New Haven, CT, USA.
Shaojie MaDepartment of Neuroscience, Yale School of Medicine, New Haven, CT 06520, USA.
Andrew T N TebbenkampDepartment of Neuroscience, Yale School of Medicine, New Haven, CT 06520, USA.
Fuchen LiuDepartment of Neuroscience, Yale School of Medicine, New Haven, CT 06520, USA.
Alvaro DuqueDepartment of Neuroscience, Yale School of Medicine, New Haven, CT 06520, USA.
Flora M VaccarinoChild Study Center, Yale University School of Medicine, New Haven, CT, USA.
Nenad SestanDepartment of Neuroscience, Yale School of Medicine, New Haven, CT 06520, USA.
Carlo ColantuoniDepts. of Neurology, Neuroscience, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Pasko RakicDepartment of Neuroscience, Yale School of Medicine, New Haven, CT 06520, USA.
Gabriel SantpereHospital del Mar Research Institute, Parc de Recerca Biomèdica de Barcelona (PRBB), 08003 Barcelona, Catalonia, Spain.
Nicola MicaliDepartment of Neuroscience, Yale School of Medicine, New Haven, CT 06520, USA.ORCID 0009-0002-2936-4708

Funding

A Multidisciplinary Center for Developing Human and Non-human Primate Brain Cell AtlasesUM1MH130991 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Hao Huang, ARNOLD KRIEGSTEIN · 2022 to 2026
$25.2M
Multispecies NHP dGTEx Research CenterU24HG012483 · NHGRI · OREGON HEALTH & SCIENCE UNIVERSITY · PI KRISTIN ARDLIE, DONALD F. CONRAD · 2022 to 2026
$17.0M
M-SCORCH: Methamphetamine use disorder data generation center for Single Cell Opioid Responses in the Context of HIVU01DA053628 · NIDA · YALE UNIVERSITY · PI HO, YA-CHI, SESTAN, NENAD · 2021 to 2025
$9.5M
Laboratory, Data Analysis, and Coordinating Center (LDACC) for the Developmental Human Genotype-Tissue Expression ProjectU24HG012108 · NHGRI · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, HUTTNER, ANITA JULIANE · 2021 to 2025
$8.7M
Origin of Cortical Species-specific Distinctions.R01DA023999 · NIDA · YALE UNIVERSITY · PI RAKIC, PASKO · 2008 to 2019
$7.9M
1/2 Cell Type and Region-Specific Regulatory Networks in Human Brain Development and DisordersU01MH116488 · NIMH · YALE UNIVERSITY · PI SESTAN, NENAD · 2018 to 2022
$6.5M
Origin of Cortical Species-specific DistinctionsR37DA023999 · NIDA · YALE UNIVERSITY · PI PASKO RAKIC · 2020 to 2026
$5.6M
Yale Macaque Brain ResourceR01MH113257 · NIMH · YALE UNIVERSITY · PI Alvaro Duque · 2017 to 2026
$4.3M
Neurobiology of Autism With MacrocephalyR01MH109648 · NIMH · YALE UNIVERSITY · PI VACCARINO, FLORA M · 2016 to 2021
$3.3M
Illuminating Neurodevelopment through Integrated Analysis and Vizualization of Multi-Omic DataR24MH114815 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI HERTZANO, RONNA, WHITE, OWEN R · 2018 to 2020
$2.3M
Identification of Genetic and Molecular Bases of Derived Phenotypes in Primate Brain DevelopmentR01HG010898 · NHGRI · YALE UNIVERSITY · PI SANTPERE BARO, GABRIEL, SESTAN, NENAD · 2020 to 2023
$2.2M
Engineering of organoid-based brain circuitsRF1MH123978 · NIMH · YALE UNIVERSITY · PI LEVCHENKO, ANDRE, VACCARINO, FLORA M · 2020 to 2020
$1.6M
NHGRI NIH HHS R01 HG010898NHGRI NIH HHS U24 HG012108NHGRI NIH HHS U24 HG012483NIDA NIH HHS R01 DA023999NIDA NIH HHS R37 DA023999NIDA NIH HHS U01 DA053628NIDCD NIH HHS R01 DC019370NIMH NIH HHS R01 MH109648NIMH NIH HHS R01 MH113257NIMH NIH HHS R24 MH114815NIMH NIH HHS RF1 MH123978NIMH NIH HHS U01 MH116488NIMH NIH HHS UM1 MH130991
6 · The paper itself

Abstract

The implications of the early phases of human telencephalic development, involving neural stem cells (NSCs), in the etiology of cortical disorders remain elusive. Here, we explored the expression dynamics of cortical and neuropsychiatric disorder-associated genes in datasets generated from human NSCs across telencephalic fate transitions in vitro and in vivo. We identified risk genes expressed in brain organizers and sequential gene regulatory networks across corticogenesis revealing disease-specific critical phases, when NSCs are more vulnerable to gene dysfunctions, and converging signaling across multiple diseases. Moreover, we simulated the impact of risk transcription factor (TF) depletions on different neural cell types spanning the developing human neocortex and observed a spatiotemporal-dependent effect for each perturbation. Finally, single-cell transcriptomics of newly generated autism-affected patient-derived NSCs in vitro revealed recurrent alterations of TFs orchestrating brain patterning and NSC lineage commitment. This work opens new perspectives to explore human brain dysfunctions at the early phases of development.

Indexed as

brain patterningcortical disordersneural stem cells

Identifiers

PMID38915580
PMCPMC11195173

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.