Items where authors include "Mansour, S"
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Vezyroglou, A, Akilapa, R, Barwick, K et al. (26 more authors) (2022) The phenotypic continuum of ATP1A3-related disorders. Neurology, 99 (14). e1511-e1526. ISSN 1526-632X
Lee, MJ, Drake, TM, Sayers, AE et al. (532 more authors) (2020) Outcomes of obstructed abdominal wall hernia: results from the UK national small bowel obstruction audit. BJS Open, 4 (5). pp. 924-934. ISSN 2474-9842
Drake, TM, Lee, MJ orcid.org/0000-0001-9971-1635, Sayers, AE et al. (533 more authors) (2019) Outcomes following small bowel obstruction due to malignancy in the national audit of small bowel obstruction. European Journal of Surgical Oncology, 45 (12). pp. 2319-2324. ISSN 0748-7983
Aitken, S, Firth, HV, McRae, J et al. (280 more authors) (2019) Finding diagnostically useful patterns in quantitative phenotypic data. The American Journal of Human Genetics, 105 (5). pp. 933-946. ISSN 0002-9297
Bengani, H, Handley, M orcid.org/0000-0001-7200-747X, Alvi, M et al. (31 more authors) (2017) Clinical and molecular consequences of disease-associated de novo mutations in SATB2. Genetics in Medicine, 19 (8). pp. 900-908. ISSN 1098-3600
McRae, JF, Clayton, S, Fitzgerald, TW et al. (299 more authors) (2017) Prevalence and architecture of de novo mutations in developmental disorders. Nature, 542. pp. 433-438. ISSN 0028-0836
McRae, JF, Clayton, S, Fitzgerald, TW et al. (298 more authors) (2016) Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study. bioRxiv. (Submitted)