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  • Showing 1-11 of 11 Results
2016
A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases.Han, B., Pouget JG, Slowikowski K., Stahl E., Lee CH, Diogo D., Hu X., Park YR, Kim E., Gregersen PK, Dahlqvist SR, Worthington J., Martin J., Eyre S., Klareskog L., Huizinga T., Chen WM, Onengut-Gumuscu S., Rich SS, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, et al. Nature genetics, 2016/05/16, (2016) Read More / View Supplemental Materials
Abstract
Exome Sequencing of Familial Bipolar Disorder.Goes, FS, Pirooznia M., Parla JS, Kramer M., Ghiban E., Mavruk S., Chen YC, Monson ET, Willour VL, Karchin R., Flickinger M., Locke AE, Levy SE, Scott LJ, Boehnke M., Stahl E., Moran JL, Hultman CM, Landén M., Purcell SM, et al. JAMA psychiatry, 2016/04/27, (2016) Read More / View Supplemental Materials
Abstract
2015
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
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.Vilhjálmsson, BJ, Yang J., Finucane HK, Gusev A., Lindström S., Ripke S., Genovese G., Loh PR, Bhatia G., Do R., Hayeck T., Won HH, and of in study Schizophrenia Working Group of the Psychiatric Genomics Consortium, Discovery Biology Risk Inherited Variants Breast Cancer(DRIVE), Kathiresan S., Pato M., Pato C., Tamimi R., Stahl E., Zaitlen N., Pasaniuc B., et al. American journal of human genetics, 2015/10/01, Volume 97, Issue 4, p.576-92, (2015) Read More / View Supplemental Materials
Abstract
Partitioning heritability by functional annotation using genome-wide association summary statistics.Finucane, HK, Bulik-Sullivan B., Gusev A., Trynka G., Reshef Y., Loh PR, Anttila V., Xu H., Zang C., Farh K., Ripke S., Day FR, ReproGen Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, RACI Consortium, Purcell S., Stahl E., Lindstrom S., Perry JR, Okada Y., et al. Nature genetics, 2015/09/28, (2015) Read More / View Supplemental Materials
Abstract
2014
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.Gusev, A., Lee SH, Trynka G., Finucane H., Vilhjálmsson BJ, Xu H., Zang C., Ripke S., Bulik-Sullivan B., Stahl E., Schizophrenia Working Group of the Psychiatric Genomics Consortium, SWE-SCZ Consortium, Kähler AK, Hultman CM, Purcell SM, McCarroll SA, Daly M., Pasaniuc B., Sullivan PF, Neale BM, et al. American journal of human genetics, 2014/11/06, Volume 95, Issue 5, p.535-52, (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
Allele-specific methylation occurs at genetic variants associated with complex disease.Hutchinson, JN, Raj T., Fagerness J., Stahl E., Viloria FT, Gimelbrant A., Seddon J., Daly M., Chess A., and Plenge R. PloS one, 2014/01/01, Volume 9, Issue 6, p.e98464, (2014) Read More / View Supplemental Materials
Abstract
2013
Human genetics in rheumatoid arthritis guides a high-throughput drug screen of the CD40 signaling pathway.Li, G., Diogo D., Wu D., Spoonamore J., Dancik V., Franke L., Kurreeman F., Rossin EJ, Duclos G., Hartland C., Zhou X., Li K., Liu J., De Jager PL, Siminovitch KA, Zhernakova A., Raychaudhuri S., Bowes J., Eyre S., Padyukov L., et al. PLoS genetics, 2013/05/01, Volume 9, Issue 5, p.e1003487, (2013) Read More / View Supplemental Materials
Abstract
2011
Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records.Kurreeman, F., Liao K., Chibnik L., Hickey B., Stahl E., Gainer V., Li G., Bry L., Mahan S., Ardlie K., Thomson B., Szolovits P., Churchill S., Murphy SN, Cai T., Raychaudhuri S., Kohane I., Karlson E., and Plenge RM American journal of human genetics, 2011/01/07, Volume 88, Issue 1, p.57-69, (2011) Read More / View Supplemental Materials
Abstract
2007
Genome-wide detection and characterization of positive selection in human populations.Sabeti, PC, Varilly P., Fry B., Lohmueller J., Hostetter E., Cotsapas C., Xie X., Byrne EH, McCarroll SA, Gaudet R., Schaffner SF, Lander E. S., International HapMap Consortium, Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, et al. Nature, 2007/10/18, Volume 449, Issue 7164, p.913-8, (2007) Read More / View Supplemental Materials
Abstract
  • Showing 1-11 of 11 Results