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Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease.

PloS one | 2019

Late onset Alzheimer's disease is the most common form of dementia for which about 30 susceptibility loci have been reported. The aim of the current study is to identify novel genes associated with Alzheimer's disease using the largest up-to-date reference single nucleotide polymorphism (SNP) panel, the most accurate imputation software and a novel gene-based analysis approach which tests for patterns of association within genes, in the powerful genome-wide association dataset of the International Genomics of Alzheimer's Project Consortium, comprising over 7 million genotypes from 17,008 Alzheimer's cases and 37,154 controls. In addition to earlier reported genes, we detected three novel gene-wide significant loci PPARGC1A (p = 2.2 × 10-6), RORA (p = 7.4 × 10-7) and ZNF423 (p = 2.1 × 10-6). PPARGC1A and RORA are involved in circadian rhythm; circadian disturbances are one of the earliest symptoms of Alzheimer's disease. PPARGC1A is additionally linked to energy metabolism and the generation of amyloid beta plaques. RORA is involved in a variety of functions apart from circadian rhythm, such as cholesterol metabolism and inflammation. The ZNF423 gene resides in an Alzheimer's disease-specific protein network and is likely involved with centrosomes and DNA damage repair.

Pubmed ID: 31283791 RIS Download

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Associated grants

  • Agency: Medical Research Council, United Kingdom
    Id: MC_PC_17112
  • Agency: Medical Research Council, United Kingdom
    Id: MC_U123160651
  • Agency: NIA NIH HHS, United States
    Id: U24 AG021886
  • Agency: Medical Research Council, United Kingdom
    Id: MC_UU_00024/1
  • Agency: NIA NIH HHS, United States
    Id: U24 AG056270
  • Agency: Medical Research Council, United Kingdom
    Id: MC_UU_00024/8
  • Agency: Medical Research Council, United Kingdom
    Id: G1100540
  • Agency: Medical Research Council, United Kingdom
    Id: G0600237
  • Agency: Medical Research Council, United Kingdom
    Id: MR/J004758/1
  • Agency: NIA NIH HHS, United States
    Id: U01 AG052409
  • Agency: Medical Research Council, United Kingdom
    Id: G0901254
  • Agency: NIA NIH HHS, United States
    Id: U01 AG049505
  • Agency: Medical Research Council, United Kingdom
    Id: MR/K01417X/1
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS017950
  • Agency: Medical Research Council, United Kingdom
    Id: G0902227
  • Agency: NIA NIH HHS, United States
    Id: R01 AG054076
  • Agency: Medical Research Council, United Kingdom
    Id: MR/L023784/1
  • Agency: Medical Research Council, United Kingdom
    Id: G1001253
  • Agency: NIA NIH HHS, United States
    Id: U01 AG032984
  • Agency: Medical Research Council, United Kingdom
    Id: MR/L501542/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/M009076/1
  • Agency: Medical Research Council, United Kingdom
    Id: MC_UP_1604/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/L010305/1
  • Agency: Parkinson's UK, United Kingdom
    Id: G-1307
  • Agency: Medical Research Council, United Kingdom
    Id: MR/K013041/1
  • Agency: Medical Research Council, United Kingdom
    Id: G0300429
  • Agency: Medical Research Council, United Kingdom
    Id: G0900652
  • Agency: Medical Research Council, United Kingdom
    Id: G0400074
  • Agency: Wellcome Trust, United Kingdom
  • Agency: NIA NIH HHS, United States
    Id: P30 AG010129
  • Agency: Medical Research Council, United Kingdom
    Id: MR/L023784/2
  • Agency: Medical Research Council, United Kingdom
    Id: G0701075
  • Agency: Medical Research Council, United Kingdom
    Id: MR/L501517/1
  • Agency: Medical Research Council, United Kingdom
    Id: G0502157

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OMIM (tool)

RRID:SCR_006437

Online catalog of human genes and genetic disorders, for clinical features, phenotypes and genes. Collection of human genes and genetic phenotypes, focusing on relationship between phenotype and genotype. Referenced overviews in OMIM contain information on all known mendelian disorders and variety of related genes. It is updated daily, and entries contain copious links to other genetics resources.

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GENCODE (tool)

RRID:SCR_014966

Human and mouse genome annotation project which aims to identify all gene features in the human genome using computational analysis, manual annotation, and experimental validation.

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