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Developing an intervention to facilitate family communication about inherited genetic conditions, and training genetic counsellors in its delivery.
Socio-Psychological Research in Genomics (SPRinG) Collaboration:; Eisler I, Ellison M, Flinter F, Grey J, Hutchison S, Jackson C, Longworth L, MacLeod R, McAllister M, Metcalfe A, Murrells T, Patch C, Pritchard S, Robert G, Rowland E, Ulph F. Socio-Psychological Research in Genomics (SPRinG) Collaboration:, et al. Among authors: macleod r. Eur J Hum Genet. 2016 Jun;24(6):794-802. doi: 10.1038/ejhg.2015.215. Epub 2015 Oct 7. Eur J Hum Genet. 2016. PMID: 26443265 Free PMC article.
Training Genetic Counsellors to Deliver an Innovative Therapeutic Intervention: their Views and Experience of Facilitating Multi-Family Discussion Groups.
Eisler I, Flinter F, Grey J, Hutchison S, Jackson C, Longworth L, MacLeod R, McAllister M, Metcalfe A, Patch C, Cope B, Robert G, Rowland E, Ulph F. Eisler I, et al. Among authors: macleod r. J Genet Couns. 2017 Apr;26(2):199-214. doi: 10.1007/s10897-016-0008-0. Epub 2016 Oct 10. J Genet Couns. 2017. PMID: 27722995 Free PMC article.
Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences.
Quarrell OW, Clarke AJ, Compton C, de Die-Smulders CEM, Fryer A, Jenkins S, Lahiri N, MacLeod R, Miedzybrodzka Z, Morrison PJ, Musgrave H, O'Driscoll M, Strong M, van Belzen MJ, Vermeer S, Verschuuren-Bemelmans CC, Bijlsma EK. Quarrell OW, et al. Among authors: macleod r. Am J Med Genet B Neuropsychiatr Genet. 2018 Jan;177(1):35-39. doi: 10.1002/ajmg.b.32582. Epub 2017 Nov 2. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 29095566 Free article.
A case-note review of continued pregnancies found to be at a high risk of Huntington's disease: considerations for clinical practice.
Wadrup F, Holden S, MacLeod R, Miedzybrodzka Z, Németh AH, Owens S, Pasalodos S, Quarrell O, Clarke AJ; UK Huntington’s Disease Predictive Testing Consortium. Wadrup F, et al. Among authors: macleod r. Eur J Hum Genet. 2019 Aug;27(8):1215-1224. doi: 10.1038/s41431-019-0375-8. Epub 2019 Mar 19. Eur J Hum Genet. 2019. PMID: 30890781 Free PMC article. Review.
Diagnosing and Preventing Hearing Loss in the Genomic Age.
McDermott JH, Molina-Ramírez LP, Bruce IA, Mahaveer A, Turner M, Miele G, Body R, Mahood R, Ulph F, MacLeod R, Harvey K, Booth N, Demain LAM, Wilson P, Black GC, Morton CC, Newman WG. McDermott JH, et al. Among authors: macleod r. Trends Hear. 2019 Jan-Dec;23:2331216519878983. doi: 10.1177/2331216519878983. Trends Hear. 2019. PMID: 31621509 Free PMC article. Review.
Pharmacogenetics to Avoid Loss of Hearing (PALOH) trial: a protocol for a prospective observational implementation trial.
McDermott JH, Mahood R, Stoddard D, Mahaveer A, Turner MA, Corry R, Garlick J, Miele G, Ainsworth S, Kemp L, Bruce I, Body R, Ulph F, Macleod R, Harvey K, Booth N, Roberts P, Wilson P, Newman WG. McDermott JH, et al. Among authors: macleod r. BMJ Open. 2021 Jun 16;11(6):e044457. doi: 10.1136/bmjopen-2020-044457. BMJ Open. 2021. PMID: 34135034 Free PMC article.
1,166 results