Evidence map›Paper›PMID 31612310›Full record

ReviewMolecular genetics and genomics : MGG2020

Single nucleotide polymorphisms in piRNA-pathway genes: an insight into genetic determinants of human diseases.

Jyoti Roy, Kalyani Anand, Swati Mohapatra, Rojalin Nayak, Trisha Chattopadhyay, Bibekanand Mallick

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular genetics and genomics : MGG, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Advances in PIWI-piRNA function in female reproduction in mammals.Acta biochimica et biophysica Sinica · 2024
    Review
  7. Article
  8. Review
  9. Review
  10. Shaping the Trans-Scale Properties of SchizophreniaFrontiers in human neuroscience · 2021
    Review
  11. Article
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

6 authors at 3 institutions in 2 countries.

Jyoti RoyRNAi and Functional Genomics Lab, Department of Life Science, National Institute of Technology, Rourkela, Odisha, 769008, India.
Kalyani AnandDepartment of Life Zoology, University of Madras, Guindy Campus, Chennai, Tamil Nadu, 600025, India.
Swati MohapatraRNAi and Functional Genomics Lab, Department of Life Science, National Institute of Technology, Rourkela, Odisha, 769008, India.
Rojalin NayakRNAi and Functional Genomics Lab, Department of Life Science, National Institute of Technology, Rourkela, Odisha, 769008, India.
Trisha ChattopadhyayRNAi and Functional Genomics Lab, Department of Life Science, National Institute of Technology, Rourkela, Odisha, 769008, India.
Bibekanand MallickRNAi and Functional Genomics Lab, Department of Life Science, National Institute of Technology, Rourkela, Odisha, 769008, India. mallickb@nitrkl.ac.in.ORCID http://orcid.org/0000-0003-4311-0720
National Institute of Technology Rourkela · INThe University of Texas MD Anderson Cancer Center · USUniversity of Madras · IN

Funding

Department of Biotechnology , Ministry of Science and Technology BT/PR21128/MED/30/1756/2016
6 · The paper itself

Abstract

With the development of advanced high-throughput genotyping technologies, there has been a dramatic improvement in identifying millions of single nucleotide polymorphisms (SNPs) across the human genome. SNPs located within the genes involved in biogenesis and function of small regulatory RNAs such as PIWI-interacting RNAs (piRNAs) can alter physiological processes by affecting gene expression. The genetic variations within PIWI genes and their associated factors such as TDRDs, EIFs, and KIF17 etc. have shown significant association with dreadful human diseases such as Alzheimer's disease, cancer, and schizophrenia. In this review, we have attempted to survey and summarize the association of all the genetic variants reported in different piRNA-pathway genes with diseases and discern their potential in clinical manifestations which will serve as a cornerstone for subsequent studies to decrypt the molecular mechanisms of SNPs in developing diseases.

Indexed as

AnimalsDiseaseHumansPolymorphism, Single NucleotideRNA, Small InterferingSignal TransductionRNA, Small InterferingDiseasesGenetic variationpiRNAPIWILSNPs

Identifiers

PMID31612310
OpenAlexW2980736713

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.