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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.
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.
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.
Rapid Point-of-Care Genotyping to Avoid Aminoglycoside-Induced Ototoxicity in Neonatal Intensive Care.
McDermott JH, Mahaveer A, James RA, Booth N, Turner M, Harvey KE, Miele G, Beaman GM, Stoddard DC, Tricker K, Corry RJ, Garlick J, Ainsworth S, Beevers T, Bruce IA, Body R, Ulph F, MacLeod R, Roberts PL, Wilson PM, Newman WG; PALOH Study Team. McDermott JH, et al. Among authors: macleod r. JAMA Pediatr. 2022 May 1;176(5):486-492. doi: 10.1001/jamapediatrics.2022.0187. JAMA Pediatr. 2022. PMID: 35311942 Free PMC article.
Exploring NICU nurses' views of a novel genetic point-of-care test identifying neonates at risk of antibiotic-induced ototoxicity: A qualitative study.
Brown G, Warrington N, Ulph F, Booth N, Harvey K, James R, Tricker K, Wilson P, Newman W, Mcdermott JH, Stoddard D, Mahaveer A, Turner M, Corry R, Garlick J, Miele G, Ainsworth S, Kemp L, Bruce I, Body R, Roberts P, Macleod R. Brown G, et al. Among authors: macleod r. J Adv Nurs. 2024 Jan 7. doi: 10.1111/jan.16045. Online ahead of print. J Adv Nurs. 2024. PMID: 38186205
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.
The role of genetic counsellors in genomic healthcare in the United Kingdom: a statement by the Association of Genetic Nurses and Counsellors.
Middleton A, Marks P, Bruce A, Protheroe-Davies LK, King C, Claber O, Houghton C, Giffney C, Macleod R, Dolling C, Kenwrick S, Scotcher D, Hall G, Patch C, Boyes L. Middleton A, et al. Among authors: macleod r. Eur J Hum Genet. 2017 Mar 22;25(6):659-661. doi: 10.1038/ejhg.2017.28. Epub 2017 Mar 22. Eur J Hum Genet. 2017. PMID: 28327572 Free PMC article.
1,166 results