Evidence map›Paper›PMID 37745577›Full record

ArticlebioRxiv : the preprint server for biology2023

Multi-OMIC analysis of Huntington disease reveals a neuroprotective astrocyte state.

Fahad Paryani, Ji-Sun Kwon, Chris W Ng, Nacoya Madden, Kenneth Ofori, Alice Tang, Hong Lu, Juncheng Li, Aayushi Mahajan, Shawn M Davidson and 10 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. 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, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 5 institutions in 1 country.

Fahad ParyaniDepartment of Neurology, Columbia University Irving Medical Center.
Ji-Sun KwonWashington University School of Medicine in St. Louis.
Chris W NgMassachusetts Institute of Technology, Department of Biological Engineering.
Nacoya MaddenDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center.
Kenneth OforiDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center.
Alice TangDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center.
Hong LuDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center.
Juncheng LiDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center.
Aayushi MahajanDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center.
Shawn M DavidsonPrinceton University, Lewis-Sigler Institute for Integrative Genomics.
Anna BasileNew York Genome Center.
Caitlin McHughNew York Genome Center.
Jean Paul VonsattelDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center.
Richard HickmanDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center.
Michael ZodyNew York Genome Center.
David E HousemanMassachusetts Institute of Technology, Department of Biological Engineering.
James E GoldmanDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center.
Andrew S YooWashington University School of Medicine in St. Louis.
Vilas MenonDepartment of Neurology, Columbia University Irving Medical Center.
Osama Al-DalahmahDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center.
Columbia University Irving Medical Center · USNew York Genome Center · USMassachusetts Institute of Technology · USWashington University in St. Louis · USPrinceton University · US

Funding

Research Education CoreP30AG066462 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PHILIP L DE JAGER · 2020 to 2026
$30.1M
Identifying shared and distinct cell type vulnerability across neurological diseases.R21AG075754 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI AL DALAHMAH, OSAMA, GOLDMAN, JAMES · 2022 to 2022
$446k
NIA NIH HHS P30 AG066462NIA NIH HHS R21 AG075754
6 · The paper itself

Abstract

Huntington disease (HD) is an incurable neurodegenerative disease characterized by neuronal loss and astrogliosis. One hallmark of HD is the selective neuronal vulnerability of striatal medium spiny neurons. To date, the underlying mechanisms of this selective vulnerability have not been fully defined. Here, we employed a multi-omic approach including single nucleus RNAseq (snRNAseq), bulk RNAseq, lipidomics,

Identifiers

PMID37745577
PMCPMC10515780
OpenAlexW4386624985

What OpenQuestion 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 OpenQuestion graph.