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Single nucleotide polymorphism in IL1B is associated with infection risk in paediatric acute myeloid leukaemia.
Sung L, Dix D, Cellot S, Gillmeister B, Ethier MC, Roslin NM, Johnston DL, Feusner J, Mitchell D, Lewis V, Aplenc R, Yanofsky R, Portwine C, Price V, Zelcer S, Silva M, Bowes L, Michon B, Stobart K, Traubici J, Allen U, Beyene J, den Hollander N, Paterson AD. Sung L, et al. Among authors: roslin nm. Clin Microbiol Infect. 2016 Jun;22(6):563.e9-563.e17. doi: 10.1016/j.cmi.2016.02.006. Epub 2016 Feb 27. Clin Microbiol Infect. 2016. PMID: 26932518 Free article.
Data integration in genetics and genomics: methods and challenges.
Hamid JS, Hu P, Roslin NM, Ling V, Greenwood CM, Beyene J. Hamid JS, et al. Among authors: roslin nm. Hum Genomics Proteomics. 2009 Jan 12;2009:869093. doi: 10.4061/2009/869093. Hum Genomics Proteomics. 2009. PMID: 20948564 Free PMC article.
Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancer.
Mrkonjic M, Roslin NM, Greenwood CM, Raptis S, Pollett A, Laird PW, Pethe VV, Chiang T, Daftary D, Dicks E, Thibodeau SN, Gallinger S, Parfrey PS, Younghusband HB, Potter JD, Hudson TJ, McLaughlin JR, Green RC, Zanke BW, Newcomb PA, Paterson AD, Bapat B. Mrkonjic M, et al. Among authors: roslin nm. PLoS One. 2010 Oct 13;5(10):e13314. doi: 10.1371/journal.pone.0013314. PLoS One. 2010. PMID: 20967208 Free PMC article.
OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium.
Vincent A, Forster N, Maynes JT, Paton TA, Billingsley G, Roslin NM, Ali A, Sutherland J, Wright T, Westall CA, Paterson AD, Marshall CR; FORGE Canada Consortium; Héon E. Vincent A, et al. Among authors: roslin nm. J Med Genet. 2014 Dec;51(12):797-805. doi: 10.1136/jmedgenet-2014-102620. Epub 2014 Oct 7. J Med Genet. 2014. PMID: 25293953
32 results