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  • Showing 1-11 of 11 Results
2016
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.Okbay, A., Baselmans BM, De Neve JE, Turley P., Nivard MG, Fontana MA, Meddens SF, Linnér RK, Rietveld CA, Derringer J., Gratten J., Lee JJ, Liu JZ, de Vlaming R., Ahluwalia TS, Buchwald J., Cavadino A., Frazier-Wood AC, Furlotte NA, Garfield V., et al. Nature genetics, 2016/04/18, (2016) Read More / View Supplemental Materials
Abstract
Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci.Smith, DJ, Escott-Price V., Davies G., Bailey ME, Colodro-Conde L., Ward J., Vedernikov A., Marioni R., Cullen B., Lyall D., Hagenaars SP, Liewald DC, Luciano M., Gale CR, Ritchie SJ, Hayward C., Nicholl B., Bulik-Sullivan B., Adams M., Couvy-Duchesne B., et al. Molecular psychiatry, 2016/04/12, (2016) Read More / View Supplemental Materials
Abstract
2015
ENIGMA and the Individual: Predicting Factors that Affect the Brain in 35 Countries Worldwide.Thompson, PM, Andreassen OA, Arias-Vasquez A., Bearden CE, Boedhoe PS, Brouwer RM, Buckner RL, Buitelaar JK, Bulaeva KB, Cannon DM, Cohen RA, Conrod PJ, Dale AM, Deary IJ, Dennis EL, de Reus MA, Desrivieres S., Dima D., Donohoe G., Fisher SE, et al. NeuroImage, 2015/12/04, (2015) Read More / View Supplemental Materials
Abstract
Genome-wide autozygosity is associated with lower general cognitive ability.Howrigan, DP, Simonson MA, Davies G., Harris SE, Tenesa A., Starr JM, Liewald DC, Deary IJ, McRae A., Wright MJ, Montgomery GW, Hansell N., Martin NG, Payton A., Horan M., Ollier WE, Abdellaoui A., Boomsma DI, DeRosse P., Knowles EE, et al. Molecular psychiatry, 2015/09/22, (2015) Read More / View Supplemental Materials
Abstract
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.Kato, N., Loh M., Takeuchi F., Verweij N., Wang X., Zhang W., Kelly TN, Saleheen D., Lehne B., Leach IM, Drong AW, Abbott J., Wahl S., Tan ST, Scott WR, Campanella G., Chadeau-Hyam M., Afzal U., Ahluwalia TS, Bonder MJ, et al. Nature genetics, 2015/09/21, (2015) Read More / View Supplemental Materials
Abstract
Directional dominance on stature and cognition in diverse human populations.Joshi, PK, Esko T., Mattsson H., Eklund N., Gandin I., Nutile T., Jackson AU, Schurmann C., Smith AV, Zhang W., Okada Y., Stančáková A., Faul JD, Zhao W., Bartz TM, Concas MP, Franceschini N., Enroth S., Vitart V., Trompet S., et al. Nature, 2015/07/01, (2015) Read More / View Supplemental Materials
Abstract
Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949).Davies, G., Armstrong N., Bis JC, Bressler J., Chouraki V., Giddaluru S., Hofer E., Ibrahim-Verbaas CA, Kirin M., Lahti J., van der Lee SJ, Le Hellard S., Liu T., Marioni RE, Oldmeadow C., Postmus I., Smith AV, Smith JA, Thalamuthu A., Thomson R., et al. Molecular psychiatry, 2015/02/03, (2015) Read More / View Supplemental Materials
Abstract
Modulation of genetic associations with serum urate levels by body-mass-index in humans.Huffman, JE, Albrecht E., Teumer A., Mangino M., Kapur K., Johnson T., Kutalik Z., Pirastu N., Pistis G., Lopez LM, Haller T., Salo P., Goel A., Li M., Tanaka T., Dehghan A., Ruggiero D., Malerba G., Smith AV, Nolte IM, et al. PloS one, 2015/01/01, Volume 10, Issue 3, p.e0119752, (2015) Read More / View Supplemental Materials
Abstract
2014
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method.Rietveld, CA, Esko T., Davies G., Pers TH, Turley P., Benyamin B., Chabris CF, Emilsson V., Johnson AD, Lee JJ, de Leeuw C., Marioni RE, Medland SE, Miller MB, Rostapshova O., van der Lee SJ, Vinkhuyzen AA, Amin N., Conley D., Derringer J., et al. Proceedings of the National Academy of Sciences of the United States of America, 2014/09/08, (2014) Read More / View Supplemental Materials
Abstract
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.Peloso, GM, Auer PL, Bis JC, Voorman A., Morrison AC, Stitziel NO, Brody JA, Khetarpal SA, Crosby JR, Fornage M., Isaacs A., Jakobsdottir J., Feitosa MF, Davies G., Huffman JE, Manichaikul A., Davis B., Lohman K., Joon AY, Smith AV, et al. American journal of human genetics, 2014/02/06, Volume 94, Issue 2, p.223-32, (2014) Read More / View Supplemental Materials
Abstract
Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function.Tang, W., Kowgier M., Loth DW, Soler Artigas M., Joubert BR, Hodge E., Gharib SA, Smith AV, Ruczinski I., Gudnason V., Mathias RA, Harris TB, Hansel NN, Launer LJ, Barnes KC, Hansen JG, Albrecht E., Aldrich MC, Allerhand M., Barr RG, et al. PloS one, 2014/01/01, Volume 9, Issue 7, p.e100776, (2014) Read More / View Supplemental Materials
Abstract
  • Showing 1-11 of 11 Results