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  • Showing 1-9 of 9 Results
2016
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.Robinson, EB, St Pourcain B., Anttila V., Kosmicki JA, Bulik-Sullivan B., Grove J., Maller J., Samocha KE, Sanders SJ, Ripke S., Martin J., Hollegaard MV, Werge T., Hougaard DM, iPSYCH-SSI-Broad Autism Group, Neale BM, Evans DM, Skuse D., Mortensen PB, Børglum AD, et al. Nature genetics, 2016/03/21, (2016) Read More / View Supplemental Materials
Abstract
2015
An atlas of genetic correlations across human diseases and traits.Bulik-Sullivan, B., Finucane HK, Anttila V., Gusev A., Day FR, Loh PR, ReproGen Consortium, Psychiatric Genomics Consortium, Genetic Consortium for Anorexia Nervosa of the Wellcome Trust Case Control Consortium 3, Duncan L., Perry JR, Patterson N., Robinson EB, Daly M. J., Price AL, and Neale BM Nature genetics, 2015/09/28, (2015) Read More / View Supplemental Materials
Abstract
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.Sanders, SJ, He X., Willsey AJ, Ercan-Sencicek AG, Samocha KE, Cicek AE, Murtha MT, Bal VH, Bishop SL, Dong S., Goldberg AP, Jinlu C., Keaney JF 3rd, Klei L., Mandell JD, Moreno-De-Luca D., Poultney CS, Robinson EB, Smith L., Solli-Nowlan T., et al. Neuron, 2015/09/23, Volume 87, Issue 6, p.1215-33, (2015) Read More / View Supplemental Materials
Abstract
Genetic research in autism spectrum disorders.Robinson, EB, Neale BM, and Hyman SE Current opinion in pediatrics, 2015/09/18, (2015) Read More / View Supplemental Materials
Abstract
A longitudinal twin study of the association between childhood autistic traits and psychotic experiences in adolescence.Taylor, MJ, Robinson EB, Happé F., Bolton P., Freeman D., and Ronald A. Molecular autism, 2015/01/01, Volume 6, p.44, (2015) Read More / View Supplemental Materials
Abstract
2014
Autism spectrum disorder severity reflects the average contribution of de novo and familial influences.Robinson, EB, Samocha KE, Kosmicki JA, McGrath L., Neale BM, Perlis RH, and Daly M. J. Proceedings of the National Academy of Sciences of the United States of America, 2014/10/21, Volume 111, Issue 42, p.15161-5, (2014) Read More / View Supplemental Materials
Abstract
A framework for the interpretation of de novo mutation in human disease.Samocha, KE, Robinson EB, Sanders SJ, Stevens C., Sabo A., McGrath LM, Kosmicki JA, Rehnström K., Mallick S., Kirby A., Wall DP, Macarthur DG, Gabriel SB, DePristo M., Purcell SM, Palotie A., Boerwinkle E., Buxbaum JD, Cook EH Jr, Gibbs RA, et al. Nature genetics, 2014/08/03, (2014) Read More / View Supplemental Materials
Abstract
The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort.Robinson, EB, Kirby A., Ruparel K., Yang J., McGrath L., Anttila V., Neale BM, Merikangas K., Lehner T., Sleiman PM, Daly M. J., Gur R., Gur R., and Hakonarson H. Molecular psychiatry, 2014/07/15, (2014) Read More / View Supplemental Materials
Abstract
2013
Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'Robinson, EB, Howrigan D., Yang J., Ripke S., Anttila V., Duncan LE, Jostins L., Barrett JC, Medland SE, Macarthur DG, Breen G., O'Donovan MC, Wray NR, Devlin B., Daly M. J., Visscher PM, Sullivan PF, and Neale BM Molecular psychiatry, 2013/10/22, (2013) Read More / View Supplemental Materials
  • Showing 1-9 of 9 Results