Adeline Vigouroux

Novel<i>FOXF1</i>Mutations in Sporadic and Familial Cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins Imply a Role for its DNA Binding Domain

Partha Sen, Yaping Yang, Iris A. L. Silva et al. · Human Mutation · 2013 · 127 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Molecular findings and clinical data in a cohort of 150 patients with anophthalmia/microphthalmia

Nicolas Chassaing, Alexandre Causse, Adeline Vigouroux et al. · Clinical Genetics · 2013 · 119 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Phenotypic spectrum of<i>STRA6</i>mutations: from Matthew-Wood syndrome to non-lethal anophthalmia

Nicolas Chassaing, Christelle Golzio, Sylvie Odent et al. · Human Mutation · 2009 · 98 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements

Lila Allou, Laëtitia Lambert, Daniel Amsallem et al. · European Journal of Human Genetics · 2012 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

<i>OTX2</i> mutations contribute to the otocephaly-dysgnathia complex

Nicolas Chassaing, Susanna Sorrentino, Erica E. Davis et al. · Journal of Medical Genetics · 2012 · 63 citations

Life Sciences, Genetics, Molecular Genetics +17