Items where authors include "Armstrong, R."

Article

McVeigh, T.P., Monahan, K.J., Christopher, J. et al. (86 more authors) (2024) Extent of investigation and management of cases of ‘unexplained’ mismatch repair deficiency (u-dMMR): a UK Cancer Genetics Group consensus. Journal of Medical Genetics, 61 (7). pp. 707-715. ISSN 0022-2593

Leta, T.H., Fenstad, A.M. orcid.org/0000-0002-6429-0153, Lygre, S.H.L. et al. (41 more authors) (2023) The use of antibiotic-loaded bone cement and systemic antibiotic prophylactic use in 2,971,357 primary total knee arthroplasties from 2010 to 2020: an international register-based observational study among countries in Africa, Europe, North America, and Oceania. Acta Orthopaedica, 94. pp. 416-425. ISSN 1745-3674

Boulton, C. orcid.org/0000-0001-9135-2674, Harrison, C., Wilton, T. et al. (4 more authors) (2022) Implementing large-scale data quality validation in a national arthroplasty registry to improve compliance. Bone & Joint Open, 3 (9). pp. 716-725. ISSN 2633-1462

Kousathanas, A. orcid.org/0000-0001-6265-6521, Pairo-Castineira, E. orcid.org/0000-0002-2423-3090, Rawlik, K. orcid.org/0000-0002-0010-370X et al. (2377 more authors) (2022) Whole-genome sequencing reveals host factors underlying critical COVID-19. Nature, 607. pp. 97-103. ISSN 0028-0836

Balasubramanian, M. orcid.org/0000-0003-1488-3695, Dingemans, A.J.M., Albaba, S. et al. (36 more authors) (2021) Comprehensive study of 28 individuals with SIN3A-related disorder underscoring the associated mild cognitive and distinctive facial phenotype. European Journal of Human Genetics, 29 (4). pp. 625-636. ISSN 1018-4813

Bownass, L., Abbs, S., Armstrong, R. et al. (24 more authors) (2019) PAPSS2‐related brachyolmia : clinical and radiological phenotype in 18 new cases. American Journal of Medical Genetics Part A, 179 (9). pp. 1884-1894. ISSN 1552-4825

Porter, M., Armstrong, R., Howard, P. et al. (2 more authors) (2019) Orthopaedic registries - the UK view (National Joint Registry) : impact on practice. EFORT Open Reviews, 4 (6). pp. 377-390. ISSN 2396-7544

McRae, J.F., Clayton, S., Fitzgerald, T.W. et al. (299 more authors) (2017) Prevalence and architecture of de novo mutations in developmental disorders. Nature, 542 (7642). pp. 433-438. ISSN 0028-0836

Fitzgerald, T.W., Gerety, S.S., Jones, W.D. et al. (263 more authors) (2015) Large-scale discovery of novel genetic causes of developmental disorders. Nature, 519. pp. 223-228. ISSN 0028-0836