Literature DB >> 26496533

Common and Rare Genetic Variants Associated With Alzheimer's Disease.

Hany E Marei1, Asmaa Althani1,2, Jaana Suhonen3, Mohamed E El Zowalaty1, Mohammad A Albanna4, Carlo Cenciarelli5, Tengfei Wang6, Thomas Caceci7.   

Abstract

Alzheimer's disease (AD) is one of the most devastating disorders. Despite the continuing increase of its incidence among aging populations, no effective cure has been developed mainly due to difficulties in early diagnosis of the disease before damaging of the brain, and the failure to explore its complex underlying molecular mechanisms. Recent technological advances in genome-wide association studies (GWAS) and high throughput next generation whole genome, and exome sequencing had deciphered many of AD-related loci, and discovered single nucleotide polymorphisms (SNPs) that are associated with altered AD molecular pathways. Highlighting altered molecular pathways linked to AD pathogenesis is crucial to identify novel diagnostic and therapeutic AD targets.
© 2015 Wiley Periodicals, Inc.

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Year:  2015        PMID: 26496533     DOI: 10.1002/jcp.25225

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  8 in total

1.  Imaging-wide association study: Integrating imaging endophenotypes in GWAS.

Authors:  Zhiyuan Xu; Chong Wu; Wei Pan
Journal:  Neuroimage       Date:  2017-07-20       Impact factor: 6.556

2.  Disease-Specific Integration of Omics Data to Guide Functional Validation of Genetic Associations.

Authors:  Maya Shumyatcher; Rui Hong; Jessica Levin; Blanca E Himes
Journal:  AMIA Annu Symp Proc       Date:  2018-04-16

3.  Powerful and Adaptive Testing for Multi-trait and Multi-SNP Associations with GWAS and Sequencing Data.

Authors:  Junghi Kim; Yiwei Zhang; Wei Pan
Journal:  Genetics       Date:  2016-04-13       Impact factor: 4.562

Review 4.  Combination of RNA Interference and Stem Cells for Treatment of Central Nervous System Diseases.

Authors:  Xue-Qin Hou; Lei Wang; Fu-Gang Wang; Xiao-Min Zhao; Han-Ting Zhang
Journal:  Genes (Basel)       Date:  2017-05-06       Impact factor: 4.096

5.  Rare protein-coding variants implicate genes involved in risk of suicide death.

Authors:  Emily DiBlasi; Andrey A Shabalin; Eric T Monson; Brooks R Keeshin; Amanda V Bakian; Anne V Kirby; Elliott Ferris; Danli Chen; Nancy William; Eoin Gaj; Michael Klein; Leslie Jerominski; W Brandon Callor; Erik Christensen; Ken R Smith; Alison Fraser; Zhe Yu; Douglas Gray; Nicola J Camp; Eli A Stahl; Qingqin S Li; Anna R Docherty; Hilary Coon
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2021-05-27       Impact factor: 3.358

6.  CD11b-activated Src signal attenuates neuroinflammatory pain by orchestrating inflammatory and anti-inflammatory cytokines in microglia.

Authors:  Mei Yang; Wenyun Xu; Yiru Wang; Xin Jiang; Yingke Li; Yajuan Yang; Hongbin Yuan
Journal:  Mol Pain       Date:  2018-10-03       Impact factor: 3.395

7.  A Novel Three-Stage Framework for Association Analysis Between SNPs and Brain Regions.

Authors:  Juan Zhou; Yangping Qiu; Shuo Chen; Liyue Liu; Huifa Liao; Hongli Chen; Shanguo Lv; Xiong Li
Journal:  Front Genet       Date:  2020-09-24       Impact factor: 4.599

8.  A Correlation Analysis between SNPs and ROIs of Alzheimer's Disease Based on Deep Learning.

Authors:  Juan Zhou; Linfeng Hu; Yu Jiang; Liyue Liu
Journal:  Biomed Res Int       Date:  2021-02-09       Impact factor: 3.411

  8 in total

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