Evidence map›Paper›PMID 34011527›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2021

Single-Nucleus RNA-Seq Reveals Dysregulation of Striatal Cell Identity Due to Huntington's Disease Mutations.

Sonia Malaiya, Marcia Cortes-Gutierrez, Brian R Herb, Sydney R Coffey, Samuel R W Legg, Jeffrey P Cantle, Carlo Colantuoni, Jeffrey B Carroll, Seth A Ament

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 74 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Sonia MalaiyaInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland 21201.
Marcia Cortes-GutierrezInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland 21201 sament@som.umaryland.edu.
Brian R HerbInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland 21201.
Sydney R CoffeyDepartment of Psychology, Western Washington University, Bellingham, Washington 98225.
Samuel R W LeggDepartment of Psychology, Western Washington University, Bellingham, Washington 98225.
Jeffrey P CantleDepartment of Psychology, Western Washington University, Bellingham, Washington 98225.
Carlo ColantuoniInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland 21201.
Jeffrey B CarrollDepartment of Psychology, Western Washington University, Bellingham, Washington 98225.
Seth A AmentInstitute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland 21201 sament@som.umaryland.edu.
University of Maryland, Baltimore · USWestern Washington University · USJohns Hopkins University · US

Funding

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
NIMH NIH HHS R24 MH114815
6 · The paper itself

Abstract

Huntington's disease (HD) is a dominantly inherited neurodegenerative disorder caused by a trinucleotide expansion in exon 1 of the huntingtin (

Indexed as

AnimalsCorpus StriatumHuntington DiseaseMaleMiceMice, Inbred C57BLMutationNeuronsPolycomb Repressive Complex 2RNA-SeqPolycomb Repressive Complex 2gene regulationHuntington's diseasepolycomb repressive complex 2single-nucleus RNA-seqstriatum

Identifiers

PMID34011527
PMCPMC8221598
OpenAlexW3160595780

What OpenQuestion holds

Textmetadata
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.