1. GENECHOC study: genetic markers of arrhythmic risk in heart failure. (25th November 2020) Authors: Anys, S; Rigade, S; Rigade, S; Baron, E; Baron, E; Lecointe, S; Lecointe, S; Guyomarch, B; Guyomarch, B; Klug, D; Klug, D; Babuty, D; Babuty, D; Mansourati, J; Mansourati, J; Bordachar, P; Bordachar, P; Mabo, P; Mabo, P; Thollet, A 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) ↗
2. Genome-wide association study identifies 18 new susceptibility variants loci associated with Brugada Syndrome. (25th November 2020) Authors: Barc, J; Trados, R; Glinge, C; Simonet, F; Chiang, D; Jouni, M; Jurgens, S; The Brugada Syndrome Genetic Consortium, B.R.S; Tanck, M; Dina, C; Probst, V; Wilde, A; Redon, R; Schott, J.J; Bezzina, C 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) ↗
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) ↗
4. P333HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy. (15th July 2014) Authors: Milano, A; Vermeer, AMC; Lodder, ER; Barc, J; Verkerk, AO; Van Der Bilt, IAC; Pinto, Y; Christiaans, I; Wilde, AA; Bezzina, CR Journal: Cardiovascular research Issue: Volume 103(2014)Supplement 1 Page Start: S60 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. 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) ↗