Aurore Carré

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

Sodium/Iodide Symporter (NIS) Gene Expression Is the Limiting Step for the Onset of Thyroid Function in the Human Fetus

Gabor Szinnai, Ludovic Lacroix, Aurore Carré et al. · The Journal of Clinical Endocrinology & Metabolism · 2006 · 95 citations · Full text

Life Sciences, Developmental Biology, Endocrinology +13

NADPH Oxidase NOX4 Is a Critical Mediator of BRAF ^V600E -Induced Downregulation of the Sodium/Iodide Symporter in Papillary Thyroid Carcinomas

Naïma Azouzi, Jérémy Cailloux, Juliana Cazarin et al. · Antioxidants and Redox Signaling · 2016 · 91 citations

Medicine, Molecular Genetics, Oncology +17

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

Life Sciences, Genetics, Molecular Genetics +11