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  • Showing 1-7 of 7 Results
2015
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.Song, J., Bergen SE, Di Florio A., Karlsson R., Charney A., Ruderfer DM, Stahl EA, Members of the International Cohort Collection for Bipolar Disorder(ICCBD), Chambert KD, Moran JL, Gordon-Smith K., Forty L., Green EK, Jones I., Jones L., Scolnick EM, Sklar P., Smoller JW, Lichtenstein P., Hultman C., et al. Molecular psychiatry, 2015/10/27, (2015) Read More / View Supplemental Materials
Abstract
Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.Won, HH, Natarajan P., Dobbyn A., Jordan DM, Roussos P., Lage K., Raychaudhuri S., Stahl E., and Do R. PLoS genetics, 2015/10/01, Volume 11, Issue 10, p.e1005622, (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
Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.Rees, E., Kirov G., Walters JT, Richards AL, Howrigan D., Kavanagh DH, Pocklington AJ, Fromer M., Ruderfer DM, Georgieva L., Carrera N., Gormley P., Palta P., Williams H., Dwyer S., Johnson JS, Roussos P., Barker DD, Banks E., Milanova V., et al. Translational psychiatry, 2015/07/21, Volume 5, p.e607, (2015) Read More / View Supplemental Materials
Abstract
2014
A role for noncoding variation in schizophrenia.Roussos, P., Mitchell AC, Voloudakis G., Fullard JF, Pothula VM, Tsang J., Stahl EA, Georgakopoulos A., Ruderfer DM, Charney A., Okada Y., Siminovitch KA, Worthington J., Padyukov L., Klareskog L., Gregersen PK, Plenge RM, Raychaudhuri S., Fromer M., Purcell SM, et al. Cell reports, 2014/11/20, Volume 9, Issue 4, p.1417-29, (2014) Read More / View Supplemental Materials
Abstract
De novo mutations in schizophrenia implicate synaptic networks.Fromer, M., Pocklington AJ, Kavanagh DH, Williams HJ, Dwyer S., Gormley P., Georgieva L., Rees E., Palta P., Ruderfer DM, Carrera N., Humphreys I., Johnson JS, Roussos P., Barker DD, Banks E., Milanova V., Grant SG, Hannon E., Rose SA, et al. Nature, 2014/02/13, Volume 506, Issue 7487, p.179-84, (2014) Read More / View Supplemental Materials
Abstract
A polygenic burden of rare disruptive mutations in schizophrenia.Purcell, SM, Moran JL, Fromer M., Ruderfer D., Solovieff N., Roussos P., O'Dushlaine C., Chambert K., Bergen SE, Kähler A., Duncan L., Stahl E., Genovese G., Fernández E., Collins MO, Komiyama NH, Choudhary JS, Magnusson PK, Banks E., Shakir K., et al. Nature, 2014/02/13, Volume 506, Issue 7487, p.185-90, (2014) Read More / View Supplemental Materials
Abstract
  • Showing 1-7 of 7 Results