Items where authors include "Renieri, A."
Up a levelArticle
Zhang, S., Cooper-Knock, J. orcid.org/0000-0002-0873-8689, Weimer, A.K. et al. (17 more authors) (2022) Multiomic analysis reveals cell-type-specific molecular determinants of COVID-19 severity. Cell Systems, 13 (8). pp. 598-614. ISSN 2405-4712
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
McNeill, A., Amador, M.-D.-M., Bekker, H. et al. (11 more authors) (2022) Predictive genetic testing for motor neuron disease : time for a guideline? European Journal of Human Genetics, 30 (6). pp. 635-636. ISSN 1018-4813
McNeill, A., Iovino, E., Mansard, L. et al. (17 more authors) (2020) SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect. Brain, 143 (8). pp. 2380-2387. ISSN 0006-8950
Grozeva, D., Carss, K., Spasic-Boskovic, O. et al. (23 more authors) (2015) Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability. Human Mutation, 36 (12). pp. 1197-1204. ISSN 1059-7794