Evidence map›Paper›PMID 38826370›Full record

ArticlebioRxiv : the preprint server for biology2024

Causal network perturbation analysis identifies known and novel type-2 diabetes driver genes.

Yue Zhao, Ansarullah, Parveen Kumar, J Matthew Mahoney, Hao He, Candice Baker, Joshy George, Sheng Li

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Yue ZhaoThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
AnsarullahCenter for Biometric Analysis, The Jackson Laboratory, Bar Harbor, ME, USA.
Parveen KumarThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
J Matthew MahoneyThe Jackson Laboratory for Mouse Genetics, Bar Harbor, ME, USA.
Hao HeThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Candice BakerThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.ORCID 0009-0008-7793-3008
Joshy GeorgeThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Sheng LiThe Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI Paul Robson · 1985 to 2026
$61.9M
The Jackson Laboratory Senescence Tissue Mapping Center (JAX-Sen TMC) - Data Analysis CoreU54AG079753 · NIA · JACKSON LABORATORY · PI ROSENTHAL, NADIA A · 2022 to 2025
$11.0M
An Integrative Computational Framework for DNA Hydroxymethylation Data Mining and InterpretationR35GM133562 · NIGMS · JACKSON LABORATORY · PI LI, SHENG · 2019 to 2023
$2.4M
Multi-omic phenotyping of human transcriptional regulatorsU01HG013175 · NHGRI · JACKSON LABORATORY · PI Brian S White · 2023 to 2026
$2.2M
The impact of reduction of cellular senescence on age-related epigenetic heterogeneityU01CA271830 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI DEGREGORI, JAMES V, LI, SHENG · 2021 to 2025
$1.9M
3D Genome Reorganization and Epigenome Dynamics of Clonal HematopoiesisR56AG071766 · NIA · JACKSON LABORATORY · PI LI, SHENG, OGURO, HIDEYUKI · 2022 to 2022
$343k
NCI NIH HHS P30 CA034196NCI NIH HHS U01 CA271830NHGRI NIH HHS U01 HG013175NIA NIH HHS R56 AG071766NIA NIH HHS U54 AG079753NIGMS NIH HHS R35 GM133562
6 · The paper itself

Abstract

The molecular pathogenesis of diabetes is multifactorial, involving genetic predisposition and environmental factors that are not yet fully understood. However, pancreatic β-cell failure remains among the primary reasons underlying the progression of type-2 diabetes (T2D) making targeting β-cell dysfunction an attractive pathway for diabetes treatment. To identify genetic contributors to β-cell dysfunction, we investigated single-cell gene expression changes in β-cells from healthy (C57BL/6J) and diabetic (NZO/HlLtJ) mice fed with normal or high-fat, high-sugar diet (HFHS). Our study presents an innovative integration of the causal network perturbation assessment (ssNPA) framework with meta-cell transcriptome analysis to explore the genetic underpinnings of type-2 diabetes (T2D). By generating a reference causal network and

Indexed as

causal network perturbationmeta-cellssNPAtype-2 diabetesβ-cell

Identifiers

PMID38826370
PMCPMC11142180

What OpenQuestion holds

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Registered trials

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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.