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Deep sequencing reveals persistence of cell-associated mumps vaccine virus in chronic encephalitis.
Morfopoulou S, Mee ET, Connaughton SM, Brown JR, Gilmour K, Chong WK, Duprex WP, Ferguson D, Hubank M, Hutchinson C, Kaliakatsos M, McQuaid S, Paine S, Plagnol V, Ruis C, Virasami A, Zhan H, Jacques TS, Schepelmann S, Qasim W, Breuer J. Morfopoulou S, et al. Among authors: plagnol v. Acta Neuropathol. 2017 Jan;133(1):139-147. doi: 10.1007/s00401-016-1629-y. Epub 2016 Oct 21. Acta Neuropathol. 2017. PMID: 27770235 Free PMC article.
Human Coronavirus OC43 Associated with Fatal Encephalitis.
Morfopoulou S, Brown JR, Davies EG, Anderson G, Virasami A, Qasim W, Chong WK, Hubank M, Plagnol V, Desforges M, Jacques TS, Talbot PJ, Breuer J. Morfopoulou S, et al. Among authors: plagnol v. N Engl J Med. 2016 Aug 4;375(5):497-8. doi: 10.1056/NEJMc1509458. N Engl J Med. 2016. PMID: 27518687 Free article. No abstract available.
Bayesian mixture analysis for metagenomic community profiling.
Morfopoulou S, Plagnol V. Morfopoulou S, et al. Among authors: plagnol v. Bioinformatics. 2015 Sep 15;31(18):2930-8. doi: 10.1093/bioinformatics/btv317. Epub 2015 May 21. Bioinformatics. 2015. PMID: 26002885 Free PMC article.
Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing.
Lopes LR, Zekavati A, Syrris P, Hubank M, Giambartolomei C, Dalageorgou C, Jenkins S, McKenna W; Uk10k Consortium; Plagnol V, Elliott PM. Lopes LR, et al. Among authors: plagnol v. J Med Genet. 2013 Apr;50(4):228-39. doi: 10.1136/jmedgenet-2012-101270. Epub 2013 Feb 8. J Med Genet. 2013. PMID: 23396983 Free PMC article.
Common variable immunodeficiency and natural killer cell lymphopenia caused by Ets-binding site mutation in the IL-2 receptor γ (IL2RG) gene promoter.
Chandra A, Zhang F, Gilmour KC, Webster D, Plagnol V, Kumararatne DS, Burns SO, Nejentsev S, Thrasher AJ. Chandra A, et al. Among authors: plagnol v. J Allergy Clin Immunol. 2016 Mar;137(3):940-2.e4. doi: 10.1016/j.jaci.2015.08.049. Epub 2015 Oct 31. J Allergy Clin Immunol. 2016. PMID: 26525228 Free PMC article. No abstract available.
TRNT1 deficiency: clinical, biochemical and molecular genetic features.
Wedatilake Y, Niazi R, Fassone E, Powell CA, Pearce S, Plagnol V, Saldanha JW, Kleta R, Chong WK, Footitt E, Mills PB, Taanman JW, Minczuk M, Clayton PT, Rahman S. Wedatilake Y, et al. Among authors: plagnol v. Orphanet J Rare Dis. 2016 Jul 2;11(1):90. doi: 10.1186/s13023-016-0477-0. Orphanet J Rare Dis. 2016. PMID: 27370603 Free PMC article.
238 results