Matthieu Joseph Miossec

Currently working at the Centre for Human Genetics at Oxford. Previously at Andres Bello. Completed a BHF-funded PhD in genomic medicine studying rare genetic variants predisposing to congenital heart disease using whole-exome sequencing. Most important publication to date is "Whole Exome Sequencing Reveals the Major Contributors to Non-syndromic Tetralogy of Fallot". This work has been used as a case study for reproducibility in Terra in workshops held with and by the Broad Institute.