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Research project

Dr C Mercer Investigating a genetic cause of left vastricular outflow tract obstruction

Staff

Research outputs

Familial Ebstein’s anomaly
Catherine Mercer, Gaia Andreoletti, Aisling Carroll, Anthony P. Salmon, I. Karen Temple & Sarah Ennis, 2017, Circulation: Cardiovascular Genetics, 10(6)
DOI: 10.1161/circgenetics.116.001683
Type: article
Rare variants in NR2F2 cause congenital heart defects in humans
Saeed Al Turki, Ashok K. Manickaraj, Catherine L. Mercer, Sebastian S. Gerety, Marc-Phillip Hitz, Sarah Lindsay, Lisa C.A. D’Alessandro, G. Jawahar Swaminathan, Jamie Bentham, Anne-Karin Arndt, Jacoba Low, Jeroen Breckpot, Marc Gewillig, Bernard Thienpont, Hashim Abdul-Khaliq, Christine Harnack, Kirstin Hoff, Hans-Heiner Kramer, Stephan Schubert, Reiner Siebert, Okan Toka, Catherine Cosgrove, Hugh Watkins, Anneke M. Lucassen, Ita M. O’Kelly, Anthony P. Salmon, Frances A. Bu’Lock, Javier Granados-Riveron, Kerry Setchfield, Chris Thornborough, J. David Brook, Barbara Mulder, Sabine Klaassen, Shoumo Bhattacharya, Koen Devriendt, David F. FitzPatrick, David I. Wilson, Seema Mital & Matthew E. Hurles, 2014, The American Journal of Human Genetics, 94(4), 574-585
DOI: 10.1016/j.ajhg.2016.02.016
Type: article
Detailed clinical and molecular study of 20 females with Xq deletions with special reference to menstruation and fertility
2013, European Journal of Medical Genetics, 56(1), 1-6
DOI: 10.1016/j.ejmg.2012.08.012
Type: article