Emily Baker
Gene-Based Analysis in HRC Imputed Genome Wide Association Data Identifies Three Novel Genes For Alzheimer’s Disease
Baker, Emily; Sims, Rebecca; Leonenko, Ganna; Frizzati, Aura; Harwood, Janet; Grozeva, Detelina; Genetic and Environmental Risk in Alzheimer's Disease (GERAD) Consortium; PERADES consortium; IGAP consortia; Morgan, Kevin; Passmore, Peter; Holmes, Clive; Powell, John; Brayne, Carol; Gill, Michael; Mead, Simon; Heun, Reiner; Bossù, Paola; Spalletta, Gianfranco; Goate, Alison; Cruchaga, Carlos; van Duijn, Cornelia; Maier, Wolfgang; Ramirez, Alfredo; Jones, Lesley; Hardy, John; Ivanov, Dobril; Hill, Matthew; Holmans, Peter; Allen, Nicholas; Morgan, Paul; GERAD/PERADES; Williams, Julie; Escott-Price, Valentina; GERAD Consortium; ADGC Consortium; CHARGE Consortium; EADI Consortium
Authors
Rebecca Sims
Ganna Leonenko
Aura Frizzati
Janet Harwood
Detelina Grozeva
Genetic and Environmental Risk in Alzheimer's Disease (GERAD) Consortium
PERADES consortium
IGAP consortia
Kevin Morgan
Peter Passmore
Clive Holmes
John Powell
Carol Brayne
Michael Gill
Simon Mead
Reiner Heun
Paola Bossù
Gianfranco Spalletta
Alison Goate
Carlos Cruchaga
Cornelia van Duijn
Wolfgang Maier
Alfredo Ramirez
Lesley Jones
John Hardy
Dobril Ivanov
Matthew Hill
Peter Holmans
Nicholas Allen
Paul Morgan
GERAD/PERADES
Julie Williams
Valentina Escott-Price
GERAD Consortium
ADGC Consortium
CHARGE Consortium
EADI Consortium
Abstract
A novel POLARIS gene-based analysis approach was employed to compute gene-based polygenic risk score (PRS) for all individuals in the latest HRC imputed GERAD (N cases=3332 and N controls=9,832) data using the International Genomics of Alzheimer's Project summary statistics (N cases=13676 and N controls= 27322, excluding GERAD subjects) to identify the SNPs and weight their risk alleles for the PRS score. SNPs were assigned to known, protein coding genes using GENCODE (v19). SNPs are assigned using both 1) no window around the gene and 2) a window of 35kb upstream and 10kb downstream to include transcriptional regulatory elements. The overall association of a gene is determined using a logistic regression model, adjusting for population covariates. Three novel gene wide significant genes were determined for the POLARIS gene-based analysis using a gene window; PPARGC1A, RORA and ZNF423. The ZNF432 gene resides in an Alzheimer's disease (AD) specific protein network which also includes other AD-related genes. The PPARGC1A gene has been linked to energy metabolism and the generation of amyloid beta plaques and the RORA has strong links with genes which are differentially expressed in the hippocampus. We also demonstrate no enrichment for genes in either loss of function intolerant or conserved noncoding sequence regions.
Citation
Baker, E., Sims, R., Leonenko, G., Frizzati, A., Harwood, J., Grozeva, D., Genetic and Environmental Risk in Alzheimer's Disease (GERAD) Consortium, PERADES consortium, IGAP consortia, Morgan, K., Passmore, P., Holmes, C., Powell, J., Brayne, C., Gill, M., Mead, S., Heun, R., Bossù, P., Spalletta, G., Goate, A., …EADI Consortium. Gene-Based Analysis in HRC Imputed Genome Wide Association Data Identifies Three Novel Genes For Alzheimer’s Disease
Working Paper Type | Working Paper |
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Deposit Date | Sep 6, 2018 |
Publicly Available Date | Sep 6, 2018 |
Public URL | https://nottingham-repository.worktribe.com/output/1062489 |
Publisher URL | https://www.biorxiv.org/content/10.1101/374876v1 |
Additional Information | This is a bioRxiv preprint. |
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