Items where authors include "Roche, M."

Article

Hartill, V. orcid.org/0000-0003-2537-8205, Kabir, M., Best, S. et al. (16 more authors) (2025) Molecular diagnoses and candidate gene identification in the congenital heart disease cohorts of the 100,000 genomes project. European Journal of Human Genetics, 33. pp. 793-802. ISSN 1018-4813

Hartill, V., Kabir, M., Best, S. et al. (16 more authors) (2024) Molecular diagnoses and candidate gene identification in the congenital heart disease cohorts of the 100,000 genomes project. European Journal of Human Genetics. ISSN 1018-4813

Best, S., Yu, J., Lord, J. orcid.org/0000-0002-0539-9343 et al. (16 more authors) (2022) Uncovering the burden of hidden ciliopathies in the 100 000 Genomes Project: a reverse phenotyping approach. Journal of Medical Genetics, 59. pp. 1151-1164. ISSN 0022-2593

Elsharif, M., Roche, M., Wilson, D. et al. (11 more authors) (2021) Hepatectomy risk assessment with functional magnetic resonance imaging (HEPARIM). BMC Cancer, 21 (1). 1139.

Conference or Workshop Item

Best, S., Lord, J., Roche, M. et al. (10 more authors) (2022) Molecular diagnoses in the congenital malformations caused by ciliopathies cohort of the 100 000 genomes project. In: 2021 European Association for Vision and Eye Research Festival, 27 Sep - 02 Oct 2021, Online.