5 July 2019 | Clinically-relevant postzygotic mosaicism in parents and children with developmental disorders in trio exome sequencing data
| Wright, C; Prigmore, E; Rajan, D; et al. |
1 August 2016 | Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
| Sifrim, A; Hitz, M-P; Wilsdon, A; et al. |
10 October 2019 | Finding Diagnostically Useful Patterns in Quantitative Phenotypic Data
| Aitken, S; Firth, HV; McRae, J; et al. |
11 November 2013 | The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.
| Köhler, S; Doelken, SC; Mungall, CJ; et al. |
11 January 2018 | Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders.
| Wright, CF; McRae, JF; Clayton, S; et al. |
7 December 2018 | Quantifying the contribution of recessive coding variation to developmental disorders
| Gallone, G; Bruntraeger, M; McRae, JF; et al. |
24 February 2017 | Returning genome sequences to research participants: Policy and practice.
| Wright, CF; Middleton, A; Barrett, JC; et al. |