Follow-up of loci from the International Genomics of Alzheimer’s Disease Project identifies TRIP4 as a novel susceptibility gene
Translational Psychiatry2014Vol. 4(2), pp. e358–e358
Citations Over TimeTop 10% of 2014 papers
Agustı́n Ruiz, Stefanie Heilmann‐Heimbach, Tim Becker, Isabel Hernández, Holger Wagner, M. Thelen, Ana Mauleón, Maitée Rosende‐Roca, Céline Bellenguez, Joshua C. Bis, Denise Harold, Amy Gerrish, Rebecca Sims, Óscar Sotolongo‐Grau, Ana Espinosa, Montserrat Alegret, J. López Arrieta, André Lacour, Markus Leber, Jessica Becker, A. Lafuente, Susana Ruiz, Liliana Vargas, Octavio Rodríguez, Gemma Ortega, M-A Dominguez, IGAP, Richard Mayeux, Jonathan L. Haines, Margaret A. Pericak‐Vance, Lindsay A. Farrer, Gerard D. Schellenberg, Vincent Chouraki, Lenore J. Launer, Cornelia M. van Duijn, Sudha Seshadri, Carmen Antúnez, Monique M.B. Breteler, Manuel Serrano‐Ríos, Frank Jessen, Lluís Tárraga, Markus M. Nöthen, W. Maier, Merçé Boada, Alfredo Ramı́rez
Abstract
To follow-up loci discovered by the International Genomics of Alzheimer's Disease Project, we attempted independent replication of 19 single nucleotide polymorphisms (SNPs) in a large Spanish sample (Fundació ACE data set; 1808 patients and 2564 controls). Our results corroborate association with four SNPs located in the genes INPP5D, MEF2C, ZCWPW1 and FERMT2, respectively. Of these, ZCWPW1 was the only SNP to withstand correction for multiple testing (P=0.000655). Furthermore, we identify TRIP4 (rs74615166) as a novel genome-wide significant locus for Alzheimer's disease risk (odds ratio=1.31; confidence interval 95% (1.19-1.44); P=9.74 × 10(-)(9)).
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