Items where authors include "Stewart, H."

Article

Copeland, H., Low, K.J., Wynn, S.L. et al. (89 more authors) (2024) Large-scale evaluation of outcomes after a genetic diagnosis in children with severe developmental disorders. Genetics in Medicine Open, 2. 101864. ISSN 2949-7744

Wardrope, A. orcid.org/0000-0003-3614-6346 and Stewart, H. (2024) Epistemic privilege, phenomenology and symptomatology in functional/dissociative seizures. Social Epistemology, 39 (2). pp. 134-149. ISSN 0269-1728

Griffen, E.J., Boulet, P., Albrecht, R. et al. (365 more authors) (2024) Enabling equitable and affordable access to novel therapeutics for pandemic preparedness and response via creative intellectual property agreements. Wellcome Open Research, 9. 374. ISSN 2398-502X

Pagnamenta, A.T. orcid.org/0000-0001-7334-0602, Yu, J., Walker, S. et al. (65 more authors) (2024) The impact of inversions across 33,924 families with rare disease from a national genome sequencing project. The American Journal of Human Genetics, 111 (6). pp. 1140-1164. ISSN 0002-9297

Stewart, H. orcid.org/0000-0003-1438-1089, Palmulli, R. orcid.org/0000-0003-2271-3186, Johansen, K.H. orcid.org/0000-0002-7711-9451 et al. (12 more authors) (2023) Tetherin antagonism by SARS-CoV-2 ORF3a and spike protein enhances virus release. EMBO reports, 24 (12). ISSN 1469-221X

Lee, S., Ochoa, E., Badura-Stronka, M. et al. (12 more authors) (2023) Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome. European Journal of Human Genetics, 31 (9). pp. 1040-1047. ISSN 1018-4813

Parker, M.D., Stewart, H., Shehata, O.M. et al. (36 more authors) (2022) Altered subgenomic RNA abundance provides unique insight into SARS-CoV-2 B.1.1.7/Alpha variant infections. Communications Biology, 5. 666. ISSN 2399-3642

Wright, C.F., Quaife, N.M., Ramos-Hernández, L. et al. (31 more authors) (2021) Non-coding region variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanisms. American Journal of Human Genetics, 108 (6). pp. 1083-1094. ISSN 0002-9297

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

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

Monograph

Stowell, A., Hardy, J.G., Cass, N. orcid.org/0000-0003-2652-1931 et al. (1 more author) (2020) Organic Electronics: barriers, benefits and opportunities. Report. Zenodo

Preprint

Copeland, H., Low, K.J., Wynn, S. et al. (89 more authors) (2023) Large-scale evaluation of outcomes following a genetic diagnosis in children with severe developmental disorders. [Preprint] (Submitted)