1. Dynamic transcriptomic analysis reveals suppression of PGC1α/ERRα drives perturbed myogenesis in facioscapulohumeral muscular dystrophy. (6th December 2018) Authors: Banerji, Christopher R S; Panamarova, Maryna; Pruller, Johanna; Figeac, Nicolas; Hebaishi, Husam; Fidanis, Efthymios; Saxena, Alka; Contet, Julian; Sacconi, Sabrina; Severini, Simone; Zammit, Peter S Journal: Human molecular genetics Issue: Volume 28:Number 8(2019) Page Start: 1244 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Monosomy 18p is a risk factor for facioscapulohumeral dystrophy. Issue 7 (21st March 2018) Authors: Balog, Judit; Goossens, Remko; Lemmers, Richard J L F; Straasheijm, Kirsten R; van der Vliet, Patrick J; Heuvel, Anita van den; Cambieri, Chiara; Capet, Nicolas; Feasson, Léonard; Manel, Veronique; Contet, Julian; Kriek, Marjolein; Donlin-Smith, Colleen M; Ruivenkamp, Claudia A L; Heard, Patricia... Journal: Journal of medical genetics Issue: Volume 55:Issue 7(2018) Page Start: 469 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗