Article in Proceedings of the National Academy of Sciences of the United States of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
0numbers the graph read from it
0cells of the map it votes in
2citing 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.
Juan D Rodriguez *Department of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.
Monica N Reeves *Department of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.ORCID 0000-0002-6222-4865
Sindy R ChavezDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.
Hsiao-Lin V WangDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322.
Jaely Z ChavezDepartment of Molecular and Cellular Biology, Kennesaw State University, Kennesaw, GA 30322.ORCID 0009-0008-2063-9393
Rhea RastogiDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.ORCID 0009-0004-5154-8452
Liyang I SunDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.
Mackenzie S RobersonDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.ORCID 0009-0003-2422-3751
Elicia A PrestonDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.
Zaynab MassenburgDepartment of Molecular and Cellular Biology, Kennesaw State University, Kennesaw, GA 30322.
Kiani N CruzDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.ORCID 0009-0001-6129-0967
Madhav S ChadhaDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.ORCID 0009-0007-2760-6888
Emily J HillDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322.
Miguel L SoaresDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.ORCID 0000-0002-1812-6117
Victor G CorcesDepartment of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322.ORCID 0000-0001-5140-4337
Brandon S CarpenterDepartment of Molecular and Cellular Biology, Kennesaw State University, Kennesaw, GA 30322.ORCID 0000-0001-9939-1926
Karen L SchmeichelDepartment of Biology, Oglethorpe University, Brookhaven, GA 30319.
John I MurrayDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.ORCID 0000-0003-4026-584X
David J KatzDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.ORCID 0000-0002-3040-1142
Funding
PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM008490 · NIGMS · EMORY UNIVERSITY · PI BOSS, JEREMY M. · 1993 to 2022
$8.0M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Genetics Predoctoral Training ProgramT32GM149422 · NIGMS · EMORY UNIVERSITY · PI TAMARA J. CASPARY · 2023 to 2026
$2.2M
Decoding lineage and fate specification in the C. elegans embryoR35GM127093 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI MURRAY, JOHN ISAAC · 2018 to 2022
$2.0M
Decoding lineage and fate specification in the C. elegans embryoR35GM153497 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI John Isaac Murray · 2024 to 2026
$1.3M
Elucidating the mechanisms by which ectopically expressed genes and piRNAs perturb somatic cell function when histone methylation is inappropriately regulatedR15GM148887 · NIGMS · KENNESAW STATE UNIVERSITY · PI CARPENTER, BRANDON SCOTT · 2023 to 2023
$432k
Investigating How Defects in The Maternal Germline Reprogramming of Histone Methylation Contribute to Inherited DiseaseR56NS122964 · NINDS · EMORY UNIVERSITY · PI KATZ, DAVID JOHN · 2022 to 2022
$387k
Regulation of embryonic cell fate decision by histone methylationF31HD100145 · NICHD · EMORY UNIVERSITY · PI RODRIGUEZ, JUAN D · 2019 to 2023
$162k
Understanding how defects in the maternal epigenetic reprogramming function of LSD1/KDM1A contribute to inherited phenotypesF31HD116544 · NICHD · EMORY UNIVERSITY · PI Monica Reeves · 2025 to 2026
$100k
HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) 3F31HD100145-03S1HHS | NIH | National Institute of General Medical Sciences (NIGMS) R35GM127093HHS | NIH | National Institute of General Medical Sciences (NIGMS) R35GM153497HHS | NIH | National Institute of General Medical Sciences (NIGMS) T32GM008490-21HHS | NIH | National Institute of General Medical Sciences (NIGMS) T32GM008490-30HHS | NIH | National Institute of General Medical Sciences (NIGMS) T32GM149422-01NICHD NIH HHS F31 HD100145NICHD NIH HHS F31 HD116544NIGMS NIH HHS R15 GM148887NIGMS NIH HHS R35 GM127093NIGMS NIH HHS R35 GM153497NIGMS NIH HHS T32 GM008490NIGMS NIH HHS T32 GM149422NIH HHS P40 OD010440NINDS NIH HHS R56 NS122964NSF (NSF) IOS 1931697-03
6 · The paper itself
Abstract
How mutations in histone modifying enzymes lead to neurodevelopmental defects is unknown. To address this question, we took advantage of the invariant embryonic lineage and adult nervous system in
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.
Ectopic transcription due to inherited histone methylation may interfere with the ongoing function of differentiated neurons. · full record | OpenQuestion