Scientific Publications

Search by Keyword(s)
Found 13 results

Filters: Author is Lage, K  [Clear All Filters]

Search Results

  • Showing 1-13 of 13 Results
2016
52 Genetic Loci Influencing Myocardial Mass.van der Harst, P., van Setten J., Verweij N., Vogler G., Franke L., Maurano MT, Wang X., Mateo Leach I., Eijgelsheim M., Sotoodehnia N., Hayward C., Sorice R., Meirelles O., Lyytikäinen LP, Polašek O., Tanaka T., Arking DE, Ulivi S., Trompet S., Müller-Nurasyid M., et al. Journal of the American College of Cardiology, 2016/09/27, Volume 68, Issue 13, p.1435-48, (2016) Read More / View Supplemental Materials
Abstract
Systematic functional interrogation of rare cancer variants identifies oncogenic alleles.Kim, E., Ilic N., Shrestha Y., Zou L., Kamburov A., Zhu C., Yang X., Lubonja R., Tran N., Nguyen C., Lawrence MS, Piccioni F., Bagul M., Doench JG, Chouinard CR, Wu X., Hogstrom L., Natoli T., Tamayo P., Horn H., et al. Cancer discovery, 2016/05/04, (2016) Read More / View Supplemental Materials
Abstract
CD44 Splice Variant v8-10 as a Marker of Serous Ovarian Cancer Prognosis.Sosulski, A., Horn H., Zhang L., Coletti C., Vathipadiekal V., Castro CM, Birrer MJ, Nagano O., Saya H., Lage K., Donahoe PK, and Pépin D. PloS one, 2016/01/01, Volume 11, Issue 6, p.e0156595, (2016) Read More / View Supplemental Materials
Abstract
2015
Comprehensive assessment of cancer missense mutation clustering in protein structures.Kamburov, A., Lawrence MS, Polak P., Leshchiner I., Lage K., Golub T. R., Lander E. S., and Getz G. Proceedings of the National Academy of Sciences of the United States of America, 2015/10/06, Volume 112, Issue 40, p.E5486-95, (2015) Read More / View Supplemental Materials
Abstract
Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.Won, HH, Natarajan P., Dobbyn A., Jordan DM, Roussos P., Lage K., Raychaudhuri S., Stahl E., and Do R. PLoS genetics, 2015/10/01, Volume 11, Issue 10, p.e1005622, (2015) Read More / View Supplemental Materials
Abstract
2014
Molecular pathogenesis of congenital diaphragmatic hernia revealed by exome sequencing, developmental data, and bioinformatics.Longoni, M., High FA, Russell MK, Kashani A., Tracy AA, Coletti CM, Hila R., Shamia A., Wells J., Ackerman KG, Wilson JM, Bult CJ, Lee C., Lage K., Pober BR, and Donahoe PK Proceedings of the National Academy of Sciences of the United States of America, 2014/08/08, (2014) Read More / View Supplemental Materials
Abstract
Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics.Lundby, A., Rossin EJ, Steffensen AB, Acha MR, Newton-Cheh C., Pfeufer A., Lynch SN, The QT Interval International GWAS Consortium(QT-IGC), Olesen SP, Brunak S., Ellinor PT, Jukema JW, Trompet S., Ford I., Macfarlane PW, Krijthe BP, Hofman A., Uitterlinden AG, Stricker BH, Nathoe HM, et al. Nature methods, 2014/06/22, (2014) Read More / View Supplemental Materials
Abstract
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.Arking, DE, Pulit SL, Crotti L., van der Harst P., Munroe PB, Koopmann TT, Sotoodehnia N., Rossin EJ, Morley M., Wang X., Johnson AD, Lundby A., Gudbjartsson DF, Noseworthy PA, Eijgelsheim M., Bradford Y., Tarasov KV, Dörr M., Müller-Nurasyid M., Lahtinen AM, et al. Nature genetics, 2014/06/22, (2014) Read More / View Supplemental Materials
Abstract
Protein-protein interactions and genetic diseases: The Interactome.Lage, K. Biochimica et biophysica acta, 2014/05/31, (2014) Read More / View Supplemental Materials
Abstract
2013
MetaRanker 2.0: a web server for prioritization of genetic variation data.Pers, TH, Dworzynski P., Thomas CE, Lage K., and Brunak S. Nucleic acids research, 2013/07/01, Volume 41, Issue W1, p.W104-W108, (2013) Read More / View Supplemental Materials
Abstract
2012
Proteomic analysis of lysine acetylation sites in rat tissues reveals organ specificity and subcellular patterns.Lundby, A., Lage K., Weinert BT, Bekker-Jensen DB, Secher A., Skovgaard T., Kelstrup CD, Dmytriyev A., Choudhary C., Lundby C., and Olsen JV Cell reports, 2012/08/30, Volume 2, Issue 2, p.419-31, (2012) Read More / View Supplemental Materials
Abstract
Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries.Talkowski, ME, Rosenfeld JA, Blumenthal I., Pillalamarri V., Chiang C., Heilbut A., Ernst C., Hanscom C., Rossin E., Lindgren AM, Pereira S., Ruderfer D., Kirby A., Ripke S., Harris DJ, Lee JH, Ha K., Kim HG, Solomon BD, Gropman AL, et al. Cell, 2012/04/27, Volume 149, Issue 3, p.525-37, (2012) Read More / View Supplemental Materials
Abstract
2011
Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology.Rossin, EJ, Lage K., Raychaudhuri S., Xavier RJ, Tatar D., Benita Y., International Inflammatory Bowel Disease Genetics Constortium, Cotsapas C., and Daly M. J. PLoS genetics, 2011/01/13, Volume 7, Issue 1, p.e1001273, (2011) Read More / View Supplemental Materials
Abstract
  • Showing 1-13 of 13 Results