Evidence map›Paper›PMID 30970224›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2019

Epigenetic-genetic chromatin footprinting identifies novel and subject-specific genes active in prefrontal cortex neurons.

Fedor E Gusev, Denis A Reshetov, Amanda C Mitchell, Tatiana V Andreeva, Aslihan Dincer, Anastasia P Grigorenko, Gennady Fedonin, Tobias Halene, Maria Aliseychik, Andrey Y Goltsov and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

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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

16 authors at 7 institutions in 3 countries.

Fedor E GusevDepartment of Psychiatry, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Denis A ReshetovDepartment of Human Genetics and Genomics, Laboratory of Evolutionary Genomics, Vavilov Institute of General Genetics of Russian Academy of Science, Moscow, Russia.
Amanda C MitchellDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Tatiana V AndreevaDepartment of Human Genetics and Genomics, Laboratory of Evolutionary Genomics, Vavilov Institute of General Genetics of Russian Academy of Science, Moscow, Russia.
Aslihan DincerDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Anastasia P GrigorenkoDepartment of Psychiatry, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Gennady FedoninDepartment of Human Genetics and Genomics, Laboratory of Evolutionary Genomics, Vavilov Institute of General Genetics of Russian Academy of Science, Moscow, Russia.
Tobias HaleneDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Maria AliseychikDepartment of Human Genetics and Genomics, Laboratory of Evolutionary Genomics, Vavilov Institute of General Genetics of Russian Academy of Science, Moscow, Russia.
Andrey Y GoltsovDepartment of Human Genetics and Genomics, Laboratory of Evolutionary Genomics, Vavilov Institute of General Genetics of Russian Academy of Science, Moscow, Russia.
Victor SolovyevDepartment of Cell Biology, Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences (SB RAS), Novosibirsk, Russia.
Leonid BrizgalovCenter of Brain Neurobiology and Neurogenetics, Institute of Cytology and Genetics of Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia.
Elena FilippovaDepartment of Psychiatry, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Zhiping WengDepartment of Cell Biology, Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences (SB RAS), Novosibirsk, Russia.
Schahram AkbarianDepartment of Psychiatry, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Evgeny I RogaevDepartment of Psychiatry, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
Vavilov Institute of General Genetics · RUAllen Institute for Brain Science · USIcahn School of Medicine at Mount Sinai · USInstitute of Cytology and Genetics · RUSiberian Branch of the Russian Academy of Sciences · RUUniversity of Massachusetts Chan Medical School · USLomonosov Moscow State University · RU

Funding

REPRESSIVE HISTONE AND DNA METHYLATION IN RODENT DEPRESSION MODELSP50MH096890 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI TAMMINGA, CAROL A · 2012 to 2021
$20.2M
Higher Order Chromatin and Genetic Risk for SchizophreniaR01MH106056 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI AKBARIAN, SCHAHRAM, BRENNAND, KRISTEN JENNIFER · 2015 to 2023
$6.7M
Epigenetic-Genetic Modulations in Aging and Alzheimer's Disease NeuronsR01AG054712 · NIA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI ROGAEV, EVGENY I · 2017 to 2021
$3.3M
NIA NIH HHS R01 AG054712NIMH NIH HHS P50 MH096890NIMH NIH HHS R01 MH106056
6 · The paper itself

Abstract

Human prefrontal cortex (PFC) is associated with broad individual variabilities in functions linked to personality, social behaviors, and cognitive functions. The phenotype variabilities associated with brain functions can be caused by genetic or epigenetic factors. The interactions between these factors in human subjects is, as of yet, poorly understood. The heterogeneity of cerebral tissue, consisting of neuronal and nonneuronal cells, complicates the comparative analysis of gene activities in brain specimens. To approach the underlying neurogenomic determinants, we performed a deep analysis of open chromatin-associated histone methylation in PFC neurons sorted from multiple human individuals in conjunction with whole-genome and transcriptome sequencing. Integrative analyses produced novel unannotated neuronal genes and revealed individual-specific chromatin "blueprints" of neurons that, in part, relate to genetic background. Surprisingly, we observed gender-dependent epigenetic signals, implying that gender may contribute to the chromatin variabilities in neurons. Finally, we found epigenetic, allele-specific activation of the testis-specific gene nucleoporin 210 like (

Indexed as

AdolescentAdultAgedAged, 80 and overChildChild, PreschoolChromatinCognitionEpigenesis, GeneticFemaleGenetic LociHistonesHumansInfantInfant, NewbornMaleChromatinHistonesNuclear Pore Complex ProteinsNUP210 protein, humanbrainChIP-seqH3K4me3histone

Identifiers

PMID30970224
PMCPMC6593885
OpenAlexW2940302012

What OpenQuestion holds

Textmetadata
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.