1. Syndromic cardiac disorder is associated with a non-coding deletion that induces a 3D chromatin remodeling and PITX2 expression dysregulation. (3rd October 2022) Authors: Baudic, M; Murata, H; Bosada, F M; Souto Melo, U; Aizawa, T; Guedon, A; Lindenbaum, P; Gourraud, J B; Makita, N; Mundlos, S; Christoffels, V M; Makiyama, T; Probst, V; Schott, J J; Barc, J Journal: European heart journal Issue: Volume 43(2022)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. P336Exome sequencing of multiple affected individuals from an Irish family with Brugada Syndrome uncovers a novel locus for the disorder. (15th July 2014) Authors: Barc, J G; Marsman, RF; Marsman, RF; Le Scouarnec, S; Le Scouarnec, S; Mizusawa, Y; Mizusawa, Y; Lindenbaum, P; Lindenbaum, P; Carter, N; Carter, N; Redon, R; Redon, R; Wilde, AAM; Wilde, AAM; Mckeown, P; Mckeown, P; Bezzina, CR; Bezzina, CR Journal: Cardiovascular research Issue: Volume 103(2014)Supplement 1 Page Start: S61 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Molecular mechanism of a new cardiac syndrome associated with a regulatory element deletion of chromosome 4q25. (25th November 2020) Authors: Baudic, M; Murata, H; Le Scouarnec, S; Foucal, A; Lindenbaum, P; Ishikawa, T; Si-Tayeb, K; Gaborit, N; Makita, N; Makiyama, T; Shimizu, W; Vieyres, C; Probst, V; Schott, J.J; Barc, J Journal: European heart journal Issue: Volume 41:(2020)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗