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Detection of novel germline mutations for breast cancer in non-BRCA1/2 families.
Aloraifi F, McDevitt T, Martiniano R, McGreevy J, McLaughlin R, Egan CM, Cody N, Meany M, Kenny E, Green AJ, Bradley DG, Geraghty JG, Bracken AP. Aloraifi F, et al. Among authors: mclaughlin r. FEBS J. 2015 Sep;282(17):3424-37. doi: 10.1111/febs.13352. Epub 2015 Jul 14. FEBS J. 2015. PMID: 26094658 Free article.
Patterns of cerebral and cerebellar white matter degeneration in ALS.
Bede P, Elamin M, Byrne S, McLaughlin RL, Kenna K, Vajda A, Fagan A, Bradley DG, Hardiman O. Bede P, et al. Among authors: mclaughlin rl. J Neurol Neurosurg Psychiatry. 2015 Apr;86(4):468-70. doi: 10.1136/jnnp-2014-308172. Epub 2014 Jul 21. J Neurol Neurosurg Psychiatry. 2015. PMID: 25053771 Free PMC article. No abstract available.
The population genomics of archaeological transition in west Iberia: Investigation of ancient substructure using imputation and haplotype-based methods.
Martiniano R, Cassidy LM, Ó'Maoldúin R, McLaughlin R, Silva NM, Manco L, Fidalgo D, Pereira T, Coelho MJ, Serra M, Burger J, Parreira R, Moran E, Valera AC, Porfirio E, Boaventura R, Silva AM, Bradley DG. Martiniano R, et al. Among authors: mclaughlin r. PLoS Genet. 2017 Jul 27;13(7):e1006852. doi: 10.1371/journal.pgen.1006852. eCollection 2017 Jul. PLoS Genet. 2017. PMID: 28749934 Free PMC article.
The multistep hypothesis of ALS revisited: The role of genetic mutations.
Chiò A, Mazzini L, D'Alfonso S, Corrado L, Canosa A, Moglia C, Manera U, Bersano E, Brunetti M, Barberis M, Veldink JH, van den Berg LH, Pearce N, Sproviero W, McLaughlin R, Vajda A, Hardiman O, Rooney J, Mora G, Calvo A, Al-Chalabi A. Chiò A, et al. Among authors: mclaughlin r. Neurology. 2018 Aug 14;91(7):e635-e642. doi: 10.1212/WNL.0000000000005996. Epub 2018 Jul 25. Neurology. 2018. PMID: 30045958 Free PMC article.
Proposed criteria for familial amyotrophic lateral sclerosis.
Byrne S, Bede P, Elamin M, Kenna K, Lynch C, McLaughlin R, Hardiman O. Byrne S, et al. Among authors: mclaughlin r. Amyotroph Lateral Scler. 2011 May;12(3):157-9. doi: 10.3109/17482968.2010.545420. Epub 2011 Jan 5. Amyotroph Lateral Scler. 2011. PMID: 21208036 No abstract available.
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis.
Dekker AM, Diekstra FP, Pulit SL, Tazelaar GHP, van der Spek RA, van Rheenen W, van Eijk KR, Calvo A, Brunetti M, Damme PV, Robberecht W, Hardiman O, McLaughlin R, Chiò A, Sendtner M, Ludolph AC, Weishaupt JH, Pardina JSM, van den Berg LH, Veldink JH. Dekker AM, et al. Among authors: mclaughlin r. Sci Rep. 2019 Apr 11;9(1):5931. doi: 10.1038/s41598-019-42091-3. Sci Rep. 2019. PMID: 30976013 Free PMC article.
936 results