Browsing Centre for Genomics and Child Health by Author "Edkins, S"
Now showing items 1-6 of 6
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Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data
Romagnoni, A; Jegou, S; Van Steen, K; Wainrib, G; Hugot, J-P; Peyrin-Biroulet, L; Chamaillard, M; Colombel, J-F; Cottone, M; D'Amato, M (2019-07-17) -
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
Trynka, G; Hunt, KA; Bockett, NA; Romanos, J; Mistry, V; Szperl, A; Bakker, SF; Bardella, MT; Bhaw-Rosun, L; Castillejo, G (2011) -
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Craddock, N; Hurles, ME; Cardin, N; Pearson, RD; Plagnol, V; Robson, S; Vukcevic, D; Barnes, C; Conrad, DF; Giannoulatou, E (2010-04-01) -
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
Tarpey, P; Thomas, S; Sarvananthan, N; Mallya, U; Lisgo, S; Talbot, CJ; Roberts, EO; Awan, M; Surendran, M; McLean, RJ (2006-11) -
Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis
Yang, Y; van der Klaauw, AA; Zhu, L; Cacciottolo, TM; He, Y; Stadler, LKJ; Wang, C; Xu, P; Saito, K; Hinton, A (2019-04-12) -
The UK10K project identifies rare variants in health and disease
Walter, K; Min, JL; Huang, J; Crooks, L; Memari, Y; McCarthy, S; Perry, JRB; Xu, C; Futema, M; Lawson, D (2015-10-01)