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Article detail · 2013

The Identification of Pathway Markers in Intracranial Aneurysm Using Genome Wide Association Data from Two Different Populations

Journal

PLOS ONE

ISSN 1932-6203

YÖKSİS OpenAlex Open access · gold SJR Q1 JCR Q1 Citations 17 Percentile 81.5% FWCI 1.63
Year
2013
Type
article

Data source split

  • YÖKSİS YÖKSİS article record
  • YÖKSİS venue PLoS ONE
  • Catalog match (ISSN) PLOS ONE
  • OpenAlex OpenAlex enrichment (abstract, citations, topics)

Abstract

OpenAlex · English

The identification of significant individual factors causing complex diseases is challenging in genome-wide association studies (GWAS) since each factor has only a modest effect on the disease development mechanism. In this study, we hypothesize that the biological pathways that are targeted by these individual factors show higher conservation within and across populations. To test this hypothesis, we searched for the disease related pathways on two intracranial aneurysm GWAS in European and Japanese case-control cohorts. Even though there were a few significantly conserved SNPs within and between populations, seven of the top ten affected pathways were found significant in both populations. The probability of random occurrence of such an event is 2.44E-36. We therefore claim that even though each individual has a unique combination of factors involved in the mechanism of disease development, most targeted pathways that need to be altered by these factors are, for the most part, the same. These pathways can serve as disease markers. Individuals, for example, can be scanned for factors affecting the genes in marker pathways. Hence, individual factors of disease development can be determined; and this knowledge can be exploited for drug development and personalized therapeutic applications. Here, we discuss the potential avenues of pathway markers in medicine and their translation to preventive and individualized health care.

Topics

Citations

OpenAlex cited_by_count. Not a WoS or Scopus citation count; those sources have no separate column here.

17 citations

OpenAlex cited_by_count (cache / database)

16 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).

  1. pathfindR: An R Package for Comprehensive Identification of Enriched Pathways in Omics Data Through Active Subnetworks 2019 Citations 510 · OpenAlex
  2. PANOGA: a web server for identification of SNP-targeted pathways from genome-wide association study data 2014 Citations 35 · OpenAlex
  3. PANOGA a web server for identification of SNP targeted pathways from genome wide association study data 2014 Citations 35 · OpenAlex
  4. Identification of possible pathogenic pathways in Behçet s disease using genome wide association study data from two different populations 2015 Citations 30 · OpenAlex
  5. Identification of possible pathogenic pathways in Behçet’s disease using genome-wide association study data from two different populations 2014 Citations 30 · OpenAlex
  6. CSF Proteomics Identifies Specific and Shared Pathways for Multiple Sclerosis Clinical Subtypes 2015 Citations 23 · OpenAlex
  7. CSF Proteomics Identifies Specific and Shared Pathways for Multiple Sclerosis Clinical Subtypes 2015 Citations 23 · OpenAlex
  8. CSF Proteomics Identifies Specific and Shared Pathways for Multiple Sclerosis Clinical Subtypes 2015 Citations 23 · OpenAlex
  9. CSF Proteomics Identifies Specific and Shared Pathways for Multiple Sclerosis Clinical Subtypes 2015 Citations 23 · OpenAlex
  10. CSF Proteomics Identifies Specific and Shared Pathways for Multiple Sclerosis Clinical Subtypes 2015 Citations 23 · OpenAlex

Authors

  1. BURCU GÜNGÖR ABDULLAH GÜL ÜNİVERSİTESİ
  2. Sezerman Osman Ugur
  3. OSMAN UĞUR SEZERMAN ACIBADEM MEHMET ALİ AYDINLAR ÜNİVERSİTESİ