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  • Showing 1-6 of 6 Results
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 1-6 of 6 Results