Browsing by Author Jostins, Luke

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Issue DateTitleAuthor(s)Citation
2015Class II HLA interactions modulate genetic risk for multiple sclerosisBooth, David; Stewart, Graeme; Alfredsson, Lars; Anderson, Carl; Ban, Maria; Beecham, Ashley; Dilthey, Alexander T; et al, Various; Jostins, Luke; Moutsianas, Loukas; Patsopoulos, Nikolaos; Shah, Tejas S; Xifara, Dionysia; Western Clinical School: Westmead Institute for Medical Res; Western Clinical School: Westmead Institute for Medical ResClass II HLA interactions modulate genetic risk for multiple sclerosis, Nature Genetics, vol.47, 10, 2015,pp 1107-1113
2013Negligible impact of rare autoimmune-locus coding-region variants on missing heritabilityLek, Monkol; Ahmad, Tariq; Ban, Maria; Barker, Jonathan; Barrett, Jeffrey; Blackburn, Hannah; Bockett, Nicholas; Brand, Oliver; Burren, Oliver; Capon, Francesca; Compston, Alastair; et al, Various; Gough, Stephen; Hunt, Karen; Jostins, Luke; Kong, Yong; Lee, James; Mistry, Vanisha; Children's Hospital Westmead: Paediatrics & Child HealthNegligible impact of rare autoimmune-locus coding-region variants on missing heritability, Nature, vol.498, 7453, 2013,pp 232-235
2012A systematic survey of loss-of-function variants in human protein-coding genesMacArthur, Daniel; Albers, Cornelis A; Balasubramanian, Suganthi; et al, Various; Frankish, Adam; Habegger, Lukas; Huang, Ni; Jostins, Luke; Montgomery, Stephen B; Morris, James; Pickrell, Joseph; Walter, Klaudia; Children's Hospital Westmead: Paediatrics & Child HealthA systematic survey of loss-of-function variants in human protein-coding genes, Science, vol.335, 6070, 2012,pp 823-828