Evidence map›Paper›PMID 31253706›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Regulation of nuclear epigenome by mitochondrial DNA heteroplasmy.

Piotr K Kopinski, Kevin A Janssen, Patrick M Schaefer, Sophie Trefely, Caroline E Perry, Prasanth Potluri, Jesus A Tintos-Hernandez, Larry N Singh, Kelly R Karch, Sydney L Campbell and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 3 pooled it
7.6field-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

101 citing papers in PubMed, 3 syntheses or guidelines pooled it, 155 citations in OpenAlex.

  1. Pooled it
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  3. Pooled it
  4. Trial
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  7. Review
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  12. Review
  13. Mitochondrial tRNAHuman mutation · 2026
    Article
  14. Article
  15. Article
  16. Spectrum and Impact of Mitochondrial DNA Mutations in Ovarian Cancer.International journal of molecular sciences · 2025
    Review
  17. Article
  18. Article
  19. Article
  20. Review

41 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 3 institutions in 1 country.

Piotr K KopinskiHoward Hughes Medical Institute, University of Pennsylvania, Philadelphia, PA 19104.
Kevin A JanssenEpigenetics Institute, University of Pennsylvania, Philadelphia, PA 19104.
Patrick M SchaeferCenter for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 19104.
Sophie TrefelyDepartment of Cancer Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
Caroline E PerryCenter for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 19104.
Prasanth PotluriCenter for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 19104.
Jesus A Tintos-HernandezCenter for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 19104.
Larry N SinghCenter for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 19104.
Kelly R KarchEpigenetics Institute, University of Pennsylvania, Philadelphia, PA 19104.
Sydney L CampbellDepartment of Cancer Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
Mary T DoanA.J. Drexel Autism Institute, Drexel University, Philadelphia, PA 19104.
Helen JiangA.J. Drexel Autism Institute, Drexel University, Philadelphia, PA 19104.
Itzhak NissimDepartment of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
Eiko Nakamaru-OgisoDepartment of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
Kathryn E WellenDepartment of Cancer Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
Nathaniel W SnyderA.J. Drexel Autism Institute, Drexel University, Philadelphia, PA 19104.
Benjamin A GarciaEpigenetics Institute, University of Pennsylvania, Philadelphia, PA 19104.
Douglas C WallaceCenter for Mitochondrial and Epigenomic Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 19104; WallaceD1@email.chop.edu.ORCID 0000-0002-7480-8278
Children's Hospital of Philadelphia · USUniversity of Pennsylvania · USDrexel University · US

Funding

Shared Resources Core 2: Quantitative Proteomics CoreP01CA196539 · NCI · ROCKEFELLER UNIVERSITY · PI MUIR, TOM · 2015 to 2024
$17.6M
MITOCHONDRIAL INBORN ERRORS OF METABOLISMR01NS021328 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI WALLACE, DOUGLAS C · 1985 to 2017
$6.5M
The Intellectual and Developmental Disabilities Research Center at CHOP/PennU54HD086984 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI YUDKOFF, MARC · 2016 to 2020
$6.3M
Viral modulation of epitranscriptomic mechanismsR01AI118891 · NIAID · WASHINGTON UNIVERSITY · PI GARCIA, BENJAMIN A, WEITZMAN, MATTHEW D. · 2015 to 2025
$5.4M
A MITOCHONDRIAL-INTERNEURONAL HYPOTHESIS OF AUTISMR01MH108592 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI WALLACE, DOUGLAS C · 2016 to 2020
$3.1M
Mouse models for mitochondrial disorders caused by mutations in mtDNAR01OD010944 · OD · UNIVERSITY OF SOUTH ALABAMA · PI ALEXEYEV, MIKHAIL F., WALLACE, DOUGLAS C · 2012 to 2020
$2.6M
Understanding the Role of Combinatorial Histone PTM PatternsR01GM110174 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI GARCIA, BENJAMIN A · 2014 to 2017
$1.3M
Howard Hughes Medical InstituteNCI NIH HHS P01 CA196539NIAID NIH HHS R01 AI118891NICHD NIH HHS U54 HD086984NIGMS NIH HHS R01 GM110174NIH HHS R01 OD010944NIMH NIH HHS R01 MH108592NINDS NIH HHS R01 NS021328
6 · The paper itself

Abstract

Diseases associated with mitochondrial DNA (mtDNA) mutations are highly variable in phenotype, in large part because of differences in the percentage of normal and mutant mtDNAs (heteroplasmy) present within the cell. For example, increasing heteroplasmy levels of the mtDNA tRNA

Indexed as

EpigenomeAcetyl Coenzyme ACell LineCell NucleusDNA, MitochondrialHistonesHumansMetabolomeMitochondriaNADTranscription, GeneticAcetyl Coenzyme ADNA, MitochondrialHistonesNADcommon diseasesepigeneticsmetabolismmitochondriatranscription

Identifiers

PMID31253706
PMCPMC6689928
OpenAlexW2955398568

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.