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  • Showing 1-5 of 5 Results
2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.van Rheenen, W., Shatunov A., Dekker AM, McLaughlin RL, Diekstra FP, Pulit SL, van der Spek RA, Võsa U., de Jong S., Robinson MR, Yang J., Fogh I., van Doormaal PT, Tazelaar GH, Koppers M., Blokhuis AM, Sproviero W., Jones AR, Kenna KP, van Eijk KR, et al. Nature genetics, 2016/07/25, (2016) Read More / View Supplemental Materials
Abstract
2015
An integrated map of structural variation in 2,504 human genomes.Sudmant, PH, Rausch T., Gardner EJ, Handsaker RE, Abyzov A., Huddleston J., Zhang Y., Ye K., Jun G., Hsi-Yang Fritz M., Konkel MK, Malhotra A., Stütz AM, Shi X., Paolo Casale F., Chen J., Hormozdiari F., Dayama G., Chen K., Malig M., et al. Nature, 2015/10/01, Volume 526, Issue 7571, p.75-81, (2015) Read More / View Supplemental Materials
Abstract
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci.Betz, RC, Petukhova L., Ripke S., Huang H., Menelaou A., Redler S., Becker T., Heilmann S., Yamany T., Duvic M., Hordinsky M., Norris D., Price VH, Mackay-Wiggan J., de Jong A., DeStefano GM, Moebus S., Böhm M., Blume-Peytavi U., Wolff H., et al. Nature communications, 2015/01/22, Volume 6, p.5966, (2015) Read More / View Supplemental Materials
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2014
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'Deelen, P., Menelaou A., van Leeuwen EM, Kanterakis A., van Dijk F., Medina-Gomez C., Francioli LC, Hottenga JJ, Karssen LC, Estrada K., Kreiner-Møller E., Rivadeneira F., van Setten J., Gutierrez-Achury J., Westra HJ, Franke L., van Enckevort D., Dijkstra M., Byelas H., van Duijn CM, et al. European journal of human genetics : EJHG, 2014/06/04, (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
  • Showing 1-5 of 5 Results