Browsing by Author Nurnberg, Peter

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Showing results 1 to 4 of 4
Issue DateTitleAuthor(s)Citation
2010Demographic History of Oceania Inferred from Genome-wide DataTrent, Ronald; Becker, Christian; Brauer, Silke; Kayser, Manfred; Lao, Oscar; Nurnberg, Peter; Stoneking, Mark; Wollstein, Andreas; Central Clinical School: MedicineDemographic History of Oceania Inferred from Genome-wide Data, Current Biology, vol.20, 22,pp 1983-1992
2008Genome-wide Analysis Indicates More Asian than Melanesian Ancestry of PolynesiansTrent, Ronald; Brauer, Silke; Kayser, Manfred; Lao, Oscar; Nurnberg, Peter; Saar, Kathrin; Stoneking, Mark; Wang, Xingyu; Central Clinical School: MedicineGenome-wide Analysis Indicates More Asian than Melanesian Ancestry of Polynesians, American Journal of Human Genetics, vol.82, 1, 2008,pp 194-198
2013A novel OPA3 mutation revealed by exome sequencing: An example of reverse phenotypingKumar, Kishore Raj; Arif, Beenish; Bruggemann, Anne; et al, Various; Fatima, Amara; Jamil, Ahmad Zeeshan; Nurnberg, Gudrun; Nurnberg, Peter; Seibler, Philip; Thiele, Holger; Vulinovic, Franca; Winkler, Susen; Northern Clinical School: Kolling InstituteA novel OPA3 mutation revealed by exome sequencing: An example of reverse phenotyping, JAMA Neurology (formerly Archives of Neurology), vol.70, 6, 2013,pp 783-787
2011U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutationBarthelmes, Daniel; Berger, Wolfgang; Fliegauf, Manfred; Gaspar, Harald; Glaus, Esther; Neidhardt, John; Nurnberg, Gudrun; Nurnberg, Peter; Omran, Heymut; Schmid, Fabian; Central Clinical School: Ophthalmology & Eye HealthU1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation, Human Mutation, vol.32, 7, 2011,pp 815-824