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  • Showing 1-6 of 6 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
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.Power, RA, Tansey KE, Buttenschøn HN, Cohen-Woods S., Bigdeli T., Hall LS, Kutalik Z., Lee SH, Ripke S., Steinberg S., Teumer A., Viktorin A., Wray NR, Arolt V., Baune BT, Boomsma DI, Børglum AD, Byrne EM, Castelao E., Craddock N., et al. Biological psychiatry, 2016/05/24, (2016) Read More / View Supplemental Materials
Abstract
2015
Association of a brain methylation site with clinical outcomes in depression does not replicate across populations.Uher, R., Ripke S., Müller-Myhsok B., Lewis CM, and Perlis RH The American journal of psychiatry, 2015/04/01, Volume 172, Issue 4, p.395-7, (2015) Read More / View Supplemental Materials
2014
A Novel MMP12 Locus Is Associated with Large Artery Atherosclerotic Stroke Using a Genome-Wide Age-at-Onset Informed Approach.Traylor, M., Mäkelä KM, Kilarski LL, Holliday EG, Devan WJ, Nalls MA, Wiggins KL, Zhao W., Cheng YC, Achterberg S., Malik R., Sudlow C., Bevan S., Raitoharju E., METASTROKE, International Stroke Genetics Consortium Wellcome Trust Case Consortium(WTCCC2) 2, Oksala N., Thijs V., Lemmens R., Lindgren A., Slowik A., et al. PLoS genetics, 2014/07/01, Volume 10, Issue 7, p.e1004469, (2014) Read More / View Supplemental Materials
Abstract
2013
Genome-wide association analysis identifies 13 new risk loci for schizophrenia.Ripke, S., O'Dushlaine C., Chambert K., Moran JL, Kähler AK, Akterin S., Bergen SE, Collins AL, Crowley JJ, Fromer M., Kim Y., Lee SH, Magnusson PK, Sanchez N., Stahl EA, Williams S., Wray NR, Xia K., Bettella F., Borglum AD, et al. Nature genetics, 2013/10/01, Volume 45, Issue 10, p.1150-9, (2013) Read More / View Supplemental Materials
Abstract
2005
Association of DLG5 R30Q variant with inflammatory bowel disease.Daly, M. J., Pearce AV, Farwell L., Fisher SA, Latiano A., Prescott NJ, Forbes A., Mansfield J., Sanderson J., Langelier D., Cohen A., Bitton A., Wild G., Lewis CM, Annese V., Mathew CG, and Rioux JD European journal of human genetics : EJHG, 2005/07/01, Volume 13, Issue 7, p.835-9, (2005) Read More / View Supplemental Materials
Abstract
  • Showing 1-6 of 6 Results