Elodie Tron

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 · 211 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

<i>NKX2-1</i>mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in “Brain-Lung-Thyroid Syndrome”

Loïc Guillot, Aurore Carré, Gabor Szinnai et al. · Human Mutation · 2009 · 130 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

A Novel <i>FOXE1</i> Mutation (R73S) in Bamforth–Lazarus Syndrome Causing Increased Thyroidal Gene Expression

Aurore Carré, Rasha T. Hamza, Dulanjalee Kariyawasam et al. · Thyroid · 2013 · 49 citations

Life Sciences, Genetics, Molecular Genetics +17

Hes1 Is Required for Appropriate Morphogenesis and Differentiation during Mouse Thyroid Gland Development

Aurore Carré, Latif Rachdi, Elodie Tron et al. · PLoS ONE · 2011 · 46 citations · Full text

Life Sciences, Endocrinology, Genetics +15

Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations

Helton Estrela Ramos, Aurore Carré, L. Chevrier et al. · European Journal of Endocrinology · 2014 · 45 citations · Full text

Life Sciences, Endocrinology, Genetics +17