Sylvia Sura‐Trueba

Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case

Aurore Carré, Gabor Szinnai, Mireille Castanet et al. · Human Molecular Genetics · 2009 · 209 citations · Full text

Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis

Aurore Carré, Mireille Castanet, Sylvia Sura‐Trueba et al. · Human Genetics · 2007 · 69 citations

Developmental Biology, Foxe1 Alanine Stretch, Genetic Disorder +8

Linkage and mutational analysis of familial thyroid dysgenesis demonstrate genetic heterogeneity implicating novel genes

Mireille Castanet, Sylvia Sura‐Trueba, Anne Chauty et al. · European Journal of Human Genetics · 2004 · 53 citations · Full text

Developmental Biology, Mutational Analysis, Genetic Disorder +7

Elevated expression of MeCP2 in cardiac and skeletal tissues is detrimental for normal development

Matías Alvarez-Saavedra, Loreto Carrasco, Sylvia Sura‐Trueba et al. · Human Molecular Genetics · 2010 · 53 citations · Full text

Cardiac Muscle, Congenital Heart Anomaly, Epigenetics +21

Suppressing IL-36-driven inflammation using peptide pseudosubstrates for neutrophil proteases

Graeme P. Sullivan, Conor M. Henry, Danielle M. Clancy et al. · Cell Death and Disease · 2018 · 43 citations · Full text