Evidence map›Paper›PMID 32698189›Full record

ArticleNature2020

MeCP2 links heterochromatin condensates and neurodevelopmental disease.

Charles H Li, Eliot L Coffey, Alessandra Dall'Agnese, Nancy M Hannett, Xin Tang, Jonathan E Henninger, Jesse M Platt, Ozgur Oksuz, Alicia V Zamudio, Lena K Afeyan and 10 more

Open access · greenAbstract read
In one paragraph

Article in Nature, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 132 papers.

0numbers the graph read from it
0cells of the map it votes in
132citing papers in PubMed
19.4field-weighted citation impact, top 1% 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

132 citing papers in PubMed, 197 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. MECP2Science China. Life sciences · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

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

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

20 authors at 5 institutions in 2 countries.

Charles H Li *Whitehead Institute for Biomedical Research, Cambridge, MA, USA.ORCID http://orcid.org/0000-0001-8091-6112
Eliot L Coffey *Whitehead Institute for Biomedical Research, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-6579-6527
Alessandra Dall'AgneseWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Nancy M HannettWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Xin TangWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Jonathan E HenningerWhitehead Institute for Biomedical Research, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-9604-2007
Jesse M PlattWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Ozgur OksuzWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Alicia V ZamudioWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Lena K AfeyanWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Jurian SchuijersWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
X Shawn LiuWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Styliani MarkoulakiWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Tenzin LungjangwaWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Gary LeRoyDepartment of Biochemistry and Molecular Pharmacology, New York University School of Medicine, New York, NY, USA.
Devon S SvobodaWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Emile WogramWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Tong Ihn LeeWhitehead Institute for Biomedical Research, Cambridge, MA, USA.
Rudolf JaenischWhitehead Institute for Biomedical Research, Cambridge, MA, USA. jaenisch@wi.mit.edu.ORCID http://orcid.org/0000-0002-2540-7099
Richard A YoungWhitehead Institute for Biomedical Research, Cambridge, MA, USA. young@wi.mit.edu.ORCID http://orcid.org/0000-0001-8855-8647
Whitehead Institute for Biomedical Research · USColumbia University Irving Medical Center · USMassachusetts General Hospital · USNew York University · USUniversity Medical Center Utrecht · NL

Funding

PRE-DOCTORAL TRAINING IN THE BIOLOGICAL SCIENCEST32GM007287 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BELL, STEPHEN P., KEATING, AMY E · 1985 to 2019
$40.8M
RESEARCH TRAINING IN DIGESTIVE DISEASES AND NUTRITIONT32DK007191 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1986 to 2026
$14.6M
GENOMIC IMPRINTING AND THE CLONING OF MICER37CA084198 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI JAENISCH, RUDOLF · 2000 to 2008
$9.2M
Transcriptional condensates, epigenetic editing and Rett SyndromeR01MH104610 · NIMH · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI JAENISCH, RUDOLF, YOUNG, RICHARD · 2014 to 2023
$7.4M
Graduate Training in Computational and Systems BiologyT32GM087237 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BURGE, CHRISTOPHER B · 2009 to 2023
$4.6M
Transcriptional regulatory networks in living cellsR01GM123511 · NIGMS · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI YOUNG, RICHARD · 2017 to 2020
$3.6M
Role of the Rett Syndrome-causing gene MeCP2 in 3D chromosomal organization and rescue of cellular disease phenotypesR00MH113813 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI LIU, X. SHAWN · 2020 to 2022
$735k
Role of the Rett Syndrome-causing gene MeCP2 in 3D chromosomal organization and rescue of cellular disease phenotypesK99MH113813 · NIMH · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI LIU, X. SHAWN · 2018 to 2019
$261k
NCI NIH HHS R37 CA084198NIDDK NIH HHS T32 DK007191NIGMS NIH HHS R01 GM123511NIGMS NIH HHS T32 GM007287NIGMS NIH HHS T32 GM087237NIH HHS 2 R01 MH104610-20NIH HHS T32 5T3DK007191-45NIMH NIH HHS K99 MH113813NIMH NIH HHS R00 MH113813NIMH NIH HHS R01 MH104610
6 · The paper itself

Abstract

Methyl CpG binding protein 2 (MeCP2) is a key component of constitutive heterochromatin, which is crucial for chromosome maintenance and transcriptional silencing

Indexed as

MutationAdaptive ImmunityAnimalsFemaleHeterochromatinImmunity, InnateIntellectual DisabilityMethyl-CpG-Binding Protein 2MiceNeuronsPhenotypeRett SyndromeHeterochromatinMECP2 protein, humanMethyl-CpG-Binding Protein 2

Identifiers

PMID32698189
PMCPMC7735819
OpenAlexW3045466751

What OpenQuestion holds

Textmetadata
LicenceTDM
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.