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The RUDY study: using digital technologies to enable a research partnership.
Teare HJA, Hogg J, Kaye J, Luqmani R, Rush E, Turner A, Watts L, Williams M, Javaid MK. Teare HJA, et al. Among authors: kaye j. Eur J Hum Genet. 2017 Jun;25(7):816-822. doi: 10.1038/ejhg.2017.57. Epub 2017 Apr 26. Eur J Hum Genet. 2017. PMID: 28443622 Free PMC article.
Managing clinically significant findings in research: the UK10K example.
Kaye J, Hurles M, Griffin H, Grewal J, Bobrow M, Timpson N, Smee C, Bolton P, Durbin R, Dyke S, Fitzpatrick D, Kennedy K, Kent A, Muddyman D, Muntoni F, Raymond LF, Semple R, Spector T; UK 10K. Kaye J, et al. Eur J Hum Genet. 2014 Sep;22(9):1100-4. doi: 10.1038/ejhg.2013.290. Epub 2014 Jan 15. Eur J Hum Genet. 2014. PMID: 24424120 Free PMC article.
The RUDY study platform - a novel approach to patient driven research in rare musculoskeletal diseases.
Javaid MK, Forestier-Zhang L, Watts L, Turner A, Ponte C, Teare H, Gray D, Gray N, Popert R, Hogg J, Barrett J, Pinedo-Villanueva R, Cooper C, Eastell R, Bishop N, Luqmani R, Wordsworth P, Kaye J. Javaid MK, et al. Among authors: kaye j. Orphanet J Rare Dis. 2016 Nov 8;11(1):150. doi: 10.1186/s13023-016-0528-6. Orphanet J Rare Dis. 2016. PMID: 27825362 Free PMC article.
Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasia.
Forestier-Zhang L, Watts L, Turner A, Teare H, Kaye J, Barrett J, Cooper C, Eastell R, Wordsworth P, Javaid MK, Pinedo-Villanueva R. Forestier-Zhang L, et al. Among authors: kaye j. Orphanet J Rare Dis. 2016 Nov 28;11(1):160. doi: 10.1186/s13023-016-0538-4. Orphanet J Rare Dis. 2016. PMID: 27894323 Free PMC article.
1,583 results