Evidence map›Paper›PMID 36831303›Full record

ArticleCells2023

Sexually Dimorphic Alterations in the Transcriptome and Behavior with Loss of Histone Demethylase

Katherine M Bonefas, Christina N Vallianatos, Brynne Raines, Natalie C Tronson, Shigeki Iwase

Abstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Versatile JMJD proteins: juggling histones and much more.Trends in biochemical sciences · 2024
    Review
  9. 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

5 authors.

Katherine M BonefasDepartment of Human Genetics, Michigan Medicine, University of Michigan, Ann Arbor, MI 48109, USA.ORCID 0000-0002-1845-9050
Christina N VallianatosDepartment of Human Genetics, Michigan Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Brynne RainesDepartment of Psychology, College of LS&A, University of Michigan, Ann Arbor, MI 48109, USA.
Natalie C TronsonNeuroscience Graduate Program, University of Michigan, Ann Arbor, MI 48109, USA.ORCID 0000-0001-5676-1579
Shigeki IwaseDepartment of Human Genetics, Michigan Medicine, University of Michigan, Ann Arbor, MI 48109, USA.ORCID 0000-0003-2280-7422

Funding

PREDOCTORAL TRAINING IN GENETICST32GM007544 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MORAN, JOHN V. · 1985 to 2022
$11.3M
A Neuron-specific Methyl-histone Regulatory ComplexR01NS116008 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Shigeki Iwase · 2020 to 2026
$3.6M
Early Stage Training in the NeurosciencesT32NS076401 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Carol Fuzeti Elias, LESLIE S. SATIN · 2011 to 2026
$3.1M
Career Training in Reproductive BiologyT32HD079342 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Suzanne M MOENTER · 2014 to 2026
$2.3M
Neutralizing epigenomes in neurodevelopment disordersR01NS089896 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI IWASE, SHIGEKI · 2015 to 2019
$2.1M
Diurnal Experimental Models to Investigate Neural Mechanisms of Sleep Disturbance in Smith-Magenis SyndromeR21NS125449 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI IWASE, SHIGEKI, YAN, LILY · 2021 to 2021
$444k
Neuronal Activity-dependent Pomoter UsageR21MH127485 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI IWASE, SHIGEKI · 2022 to 2023
$418k
NICHD NIH HHS T32 HD079342NIGMS NIH HHS T32 GM007544NIH HHS R21NS125449NIMH NIH HHS R21 MH127485NINDS NIH HHS R01 NS089896NINDS NIH HHS R01 NS116008NINDS NIH HHS R21 NS125449NINDS NIH HHS T32 NS076401
6 · The paper itself

Abstract

Chromatin dysregulation has emerged as a major hallmark of neurodevelopmental disorders such as intellectual disability (ID) and autism spectrum disorders (ASD). The prevalence of ID and ASD is higher in males compared to females, with unknown mechanisms. Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type (MRXSCJ), is caused by loss-of-function mutations of lysine demethylase 5C (

Indexed as

Intellectual DisabilityTranscriptomeAnimalsChromatinFemaleHistone DemethylasesHumansMaleMiceMutationX-Linked Intellectual DisabilityChromatinHistone DemethylasesKDM5C protein, humanchromatin regulatorshistone demethylaselearning and memoryneurodevelopmental disordersx-linked intellectual disability

Identifiers

PMID36831303
PMCPMC9954040

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.