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  • Showing 1-15 of 15 Results
2016
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.Zheng, J., Erzurumluoglu AM, Elsworth BL, Kemp JP, Howe L., Haycock PC, Hemani G., Tansey K., Laurin C., Early Genetics and Lifecourse Epidemiology(EAGLE) Eczema Consortium, Pourcain BS, Warrington NM, Finucane HK, Price AL, Bulik-Sullivan BK, Anttila V., Paternoster L., Gaunt TR, Evans DM, and Neale BM Bioinformatics (Oxford, England), 2016/09/22, (2016) Read More / View Supplemental Materials
Abstract
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.Gormley, P., Anttila V., Winsvold BS, Palta P., Esko T., Pers TH, Farh KH, Cuenca-Leon E., Muona M., Furlotte NA, Kurth T., Ingason A., McMahon G., Ligthart L., Terwindt GM, Kallela M., Freilinger TM, Ran C., Gordon SG, Stam AH, et al. Nature genetics, 2016/06/20, (2016) Read More / View Supplemental Materials
Abstract
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
Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept.Franke, B., Stein JL, Ripke S., Anttila V., Hibar DP, van Hulzen KJ, Arias-Vasquez A., Smoller JW, Nichols TE, Neale MC, McIntosh AM, Lee P., McMahon FJ, Meyer-Lindenberg A., Mattheisen M., Andreassen OA, Gruber O., Sachdev PS, Roiz-Santiañez R., Saykin AJ, et al. Nature neuroscience, 2016/03/01, Volume 19, Issue 3, p.420-31, (2016) Read More / View Supplemental Materials
Abstract
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas.Eising, E., Huisman SM, Mahfouz A., Vijfhuizen LS, Anttila V., Winsvold BS, Kurth T., Ikram MA, Freilinger T., Kaprio J., Boomsma DI, van Duijn CM, Järvelin MR, Zwart JA, Quaye L., Strachan DP, Kubisch C., Dichgans M., Davey Smith G., Stefansson K., et al. Human genetics, 2016/02/22, (2016) Read More / View Supplemental Materials
Abstract
Effect of endocannabinoid degradation on pain: role of FAAH polymorphisms in experimental and postoperative pain in women treated for breast cancer.Cajanus, K., Holmström EJ, Wessman M., Anttila V., Kaunisto MA, and Kalso E. Pain, 2016/02/01, Volume 157, Issue 2, p.361-9, (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
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
In silico phenotyping via co-training for improved phenotype prediction from genotype.Roqueiro, D., Witteveen MJ, Anttila V., Terwindt GM, van den Maagdenberg AM, and Borgwardt K. Bioinformatics (Oxford, England), 2015/06/15, Volume 31, Issue 12, p.i303-i310, (2015) Read More / View Supplemental Materials
Abstract
2014
Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder.Jacobsen, KK, Nievergelt CM, Zayats T., Greenwood TA, Anttila V., Akiskal HS, BiGS Consortium, IHG Consortium, include: BiGS Consortium Co-Authors, include: IHG Consortium Co-Authors, Haavik J., Bernt Fasmer O., Kelsoe JR, Johansson S., Oedegaard KJ, include BiGS Consortium Co-Authors, and include IHG Consortium Co-Authors Journal of affective disorders, 2014/10/12, Volume 172C, p.453-461, (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
Selectivity in Genetic Association with Sub-classified Migraine in Women.Chasman, DI, Anttila V., Buring JE, Ridker PM, Schürks M., Kurth T., and International Headache Genetics Consortium PLoS genetics, 2014/05/01, Volume 10, Issue 5, p.e1004366, (2014) Read More / View Supplemental Materials
Abstract
High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms.Kurki, MI, Gaál EI, Kettunen J., Lappalainen T., Menelaou A., Anttila V., van 't Hof FN, von Und Zu Fraunberg M., Helisalmi S., Hiltunen M., Lehto H., Laakso A., Kivisaari R., Koivisto T., Ronkainen A., Rinne J., Kiemeney LA, Vermeulen SH, Kaunisto MA, Eriksson JG, et al. PLoS genetics, 2014/01/01, Volume 10, Issue 1, p.e1004134, (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
2010
Integrating common and rare genetic variation in diverse human populations.International HapMap 3, Consortium, Altshuler DM, Gibbs RA, Peltonen L., Altshuler DM, Gibbs RA, Peltonen L., Dermitzakis E., Schaffner SF, Yu F., Peltonen L., Dermitzakis E., Bonnen PE, Altshuler DM, Gibbs RA, de Bakker PI, Deloukas P., Gabriel SB, Gwilliam R., Hunt S., et al. Nature, 2010/09/02, Volume 467, Issue 7311, p.52-8, (2010) Read More / View Supplemental Materials
Abstract
  • Showing 1-15 of 15 Results