Items where authors include "Clayton, S."

Article

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

Armstrong, I., Billings, C., Kiely, D.G. orcid.org/0000-0003-0184-6502 et al. (4 more authors) (2019) The patient experience of pulmonary hypertension : a large cross-sectional study of UK patients. BMC Pulmonary Medicine, 19 (1). 67.

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

Akawi, N., McRae, J., Ansari, M. et al. (40 more authors) (2015) Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families. Nature Genetics, 47 (11). pp. 1363-1369. ISSN 1061-4036

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

Clayton, S., Apperley, E., Hannon, F. et al. (3 more authors) (2014) A survey of birth order status of students studying for medical degree at the University of Sheffield. Journal of the Royal Society of Medicine Open, 5 (9). pp. 1-5. ISSN 0141-0768

Kuhn, S., Ingham, N., Pearson, S. et al. (4 more authors) (2012) Auditory Function in the Tc1 Mouse Model of Down Syndrome Suggests a Limited Region of Human Chromosome 21 Involved in Otitis Media. PLoS One, 7 (2). e31433.