Evidence map›Paper›PMID 33452016›Full record

ArticleGenome research2021

Allele-specific alternative splicing and its functional genetic variants in human tissues.

Kofi Amoah, Yun-Hua Esther Hsiao, Jae Hoon Bahn, Yiwei Sun, Christina Burghard, Boon Xin Tan, Ei-Wen Yang, Xinshu Xiao

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Allele-specific splicing modulates protein isoforms and Alzheimer's risk.bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
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  8. Article
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  13. Long-read RNA sequencing reveals allele-specific NbioRxiv : the preprint server for biology · 2024
    Article
  14. Article
  15. Review
  16. Allele-specific RNAGenome research · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. Review
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

8 authors at 2 institutions in 1 country.

Kofi Amoah *Bioinformatics Interdepartmental Program, University of California, Los Angeles, California 90095, USA.
Yun-Hua Esther Hsiao *Department of Bioengineering, University of California, Los Angeles, California 90095, USA.
Jae Hoon Bahn *Department of Integrative Biology and Physiology, University of California, Los Angeles, California 90095, USA.
Yiwei SunDepartment of Integrative Biology and Physiology, University of California, Los Angeles, California 90095, USA.
Christina BurghardBioinformatics Interdepartmental Program, University of California, Los Angeles, California 90095, USA.
Boon Xin TanDepartment of Integrative Biology and Physiology, University of California, Los Angeles, California 90095, USA.
Ei-Wen YangDepartment of Integrative Biology and Physiology, University of California, Los Angeles, California 90095, USA.
Xinshu XiaoBioinformatics Interdepartmental Program, University of California, Los Angeles, California 90095, USA.ORCID 0000-0002-9362-8029
University of California, Los Angeles · USQB3 · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Analysis of functional genetic variants in RNA processing and expressionU01HG009417 · NHGRI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI XIAO, XINSHU GRACE · 2017 to 2021
$3.2M
Prioritization of splicing-altering genetic variants in Alzheimer's diseaseR01AG056476 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI XIAO, XINSHU GRACE · 2017 to 2021
$2.0M
NCI NIH HHS P30 CA016042NHGRI NIH HHS U01 HG009417NIA NIH HHS R01 AG056476
6 · The paper itself

Abstract

Alternative splicing is an RNA processing mechanism that affects most genes in human, contributing to disease mechanisms and phenotypic diversity. The regulation of splicing involves an intricate network of

Indexed as

AllelesGenetic VariationAlternative SplicingCell LineExonsFemaleGenome-Wide Association StudyHumansLinkage DisequilibriumMaleOrgan SpecificityPolymorphism, Single Nucleotide

Identifiers

PMID33452016
PMCPMC7919445
OpenAlexW3125158765

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.