Evidence map›Paper›PMID 37065064›Full record

ArticleACS omega2023

Integrative Genomic Analysis of m6a-SNPs Identifies Potential Functional Variants Associated with Alzheimer's Disease.

Syed Mansoor Jan, Aamir Fahira, Yongyong Shi, Mohammad Imran Khan, Alam Jamal, Arif Mahmood, Sulaiman Shams, Zahida Parveen, Junjian Hu, Muhammad Umair and 1 more

Open access · goldAbstract read
In one paragraph

Article in ACS omega, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Riboregulation: a non-canonical tau function.Molecular neurodegeneration · 2026
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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

11 authors at 6 institutions in 3 countries.

Syed Mansoor JanDepartment of Biochemistry, Abdul Wali Khan University, Mardan 23200, Pakistan.
Aamir FahiraBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Collaborative Innovation Center for Brain Science, Shanghai Jiao Tong University, Shanghai 200240, China.
Yongyong ShiBio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Collaborative Innovation Center for Brain Science, Shanghai Jiao Tong University, Shanghai 200240, China.
Mohammad Imran KhanDepartment of Biochemistry, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Alam JamalDepartment of Biochemistry, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Arif MahmoodCenter for Medical Genetics and Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha 410078, Hunan, China.ORCID https://orcid.org/0000-0002-0309-1230
Sulaiman ShamsDepartment of Biochemistry, Abdul Wali Khan University, Mardan 23200, Pakistan.
Zahida ParveenDepartment of Biochemistry, Abdul Wali Khan University, Mardan 23200, Pakistan.ORCID https://orcid.org/0000-0003-3846-3513
Junjian HuDepartment of Central Laboratory, SSL, Central Hospital of Gongguan City, Affiliated Dongguan Shilong People's Hospital of Southern Medical University, Dongguan 523000, China.
Muhammad UmairDepartment of Life Sciences, School of Science, University of Management and Technology (UMT), Lahore 54770, Pakistan.
Abdul WadoodDepartment of Biochemistry, Abdul Wali Khan University, Mardan 23200, Pakistan.ORCID https://orcid.org/0000-0002-3415-9277
Abdul Wali Khan University Mardan · PKKing Abdulaziz University · SAShanghai Jiao Tong University · CNCentral South University · CNDongguan People’s Hospital · CNUniversity of Management and Technology · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder that affects 35 million people worldwide. However, no potential therapeutics currently are available for AD because of the multiple factors involved in it, such as regulatory factors with their candidate genes, factors associated with the expression levels of its corresponding genes, and many others. To date, 29 novel loci from GWAS have been reported for AD by the Psychiatric Genomics Consortium (PGC2). Nevertheless, the main challenge of the post-GWAS era, namely to detect significant variants of the target disease, has not been conducted for AD. N6-methyladenosine (m6a) is reported as the most prevalent mRNA modification that exists in eukaryotes and that influences mRNA nuclear export, translation, splicing, and the stability of mRNA. Furthermore, studies have also reported m6a's association with neurogenesis and brain development. We carried out an integrative genomic analysis of AD variants from GWAS and m6a-SNPs from m6AVAR to identify the effects of m6a-SNPs on AD and identified the significant variants using the statistically significance value (

Identifiers

PMID37065064
PMCPMC10099436
OpenAlexW4361295149

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.