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Massively parallel sequencing in hereditary prostate cancer families reveals a rare risk variant in the DNA repair gene, RAD51C.
Marthick JR, Raspin K, Foley GR, Blackburn NB, Banks A, Donovan S, Malley RC, Field MA, Stanford JL, Ostrander EA, FitzGerald LM, Dickinson JL. Marthick JR, et al. Among authors: blackburn nb. Eur J Cancer. 2021 Dec;159:52-55. doi: 10.1016/j.ejca.2021.09.038. Epub 2021 Nov 1. Eur J Cancer. 2021. PMID: 34736042 No abstract available.
Rediscovering the value of families for psychiatric genetics research.
Glahn DC, Nimgaonkar VL, Raventós H, Contreras J, McIntosh AM, Thomson PA, Jablensky A, McCarthy NS, Charlesworth JC, Blackburn NB, Peralta JM, Knowles EEM, Mathias SR, Ament SA, McMahon FJ, Gur RC, Bucan M, Curran JE, Almasy L, Gur RE, Blangero J. Glahn DC, et al. Among authors: blackburn nb. Mol Psychiatry. 2019 Apr;24(4):523-535. doi: 10.1038/s41380-018-0073-x. Epub 2018 Jun 28. Mol Psychiatry. 2019. PMID: 29955165 Free PMC article. Review.
Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descent.
Lucas SEM, Zhou T, Blackburn NB, Mills RA, Ellis J, Leo P, Souzeau E, Ridge B, Charlesworth JC, Lindsay R, Craig JE, Burdon KP. Lucas SEM, et al. Among authors: blackburn nb. PLoS One. 2018 Jun 20;13(6):e0199178. doi: 10.1371/journal.pone.0199178. eCollection 2018. PLoS One. 2018. PMID: 29924831 Free PMC article.
Rare, Potentially Pathogenic Variants in ZNF469 Are Not Enriched in Keratoconus in a Large Australian Cohort of European Descent.
Lucas SEM, Zhou T, Blackburn NB, Mills RA, Ellis J, Leo P, Souzeau E, Ridge B, Charlesworth JC, Brown MA, Lindsay R, Craig JE, Burdon KP. Lucas SEM, et al. Among authors: blackburn nb. Invest Ophthalmol Vis Sci. 2017 Dec 1;58(14):6248-6256. doi: 10.1167/iovs.17-22417. Invest Ophthalmol Vis Sci. 2017. PMID: 29228253 Free article.
37 results