Phenotype harmonization and cross-study collaboration in GWAS consortia: The GENEVA experience

by Bennett, S.N., Caporaso, N., Fitzpatrick, A.L., Agrawal, A., Barnes, K., Boyd, H.A., Cornelis, M.C., Hansel, N.N., Heiss, G., Heit, J.A., Kang, J.H., Kittner, S.J., Kraft, P., Lowe, W., Marazita, M.L., Monroe, K.R., Pasquale, L.R., Ramos, E.M., van Dam, R.M., Udren, J., Williams, K.
Published 2014

Molecular genetic aetiology of general cognitive function is enriched in evolutionarily conserved regions

by Hill, W.D, Davies, G, Harris, S.E, Hagenaars, S.P, Liewald, D.C, Penke, L, Gale, C.R, Deary, I.J, Debette, S, Verbaas, C.I, Bressler, J, Schuur, M, Smith, A.V, Bis, J.C, Bennett, D.A, Ikram, M.A, Launer, L.J, Fitzpatrick, A.L, Seshadri, S, Van Duijn, C.M, Mosley, T.H
Published 2020

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

by Jakobsdottir J., van der Lee S.J., Bis J.C., Chouraki V., Li-Kroeger D., Yamamoto S., Grove M.L., Naj A., Vronskaya M., Salazar J.L., DeStefano A.L., Brody J.A., Smith A.V., Amin N., Sims R., Ibrahim-Verbaas C.A., Choi S.-H., Satizabal C.L., Lopez O.L., Beiser A., Ikram M.A., Garcia M.E., Hayward C., Varga T.V., Ripatti S., Franks P.W., Hallmans G., Rolandsson O., Jansson J.-H., Porteous D.J., Salomaa V., Eiriksdottir G., Rice K.M., Bellen H.J., Levy D., Uitterlinden A.G., Emilsson V., Rotter J.I., Aspelund T., O?Donnell C.J., Fitzpatrick A.L., Launer L.J., Hofman A., Wang L.-S., Williams J., Schellenberg G.D., Boerwinkle E., Psaty B.M., Seshadri S.
Published 2019