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  • Bérénice A. Benayoun, Adrien Georges, +7 authors Reiner A. Veitia
  • Biology, Medicine
  • Human molecular genetics
  • 2011 (First Publication: 1 May 2011)
  • FOXL2 is a transcription factor that is essential for ovarian function and maintenance, the germline mutations of which are responsible for the Blepharophimosis Ptosis Epicanthus-inversus SyndromeContinue Reading
  • Sandrine Caburet, Alice Demarez, Lara Moumné, Marc Mardoche Fellous, Elfride De Baere, Reiner A. Veitia
  • Biology, Medicine
  • Journal of medical genetics
  • 2004 (First Publication: 1 December 2004)
  • Blepharophimosis syndrome is an autosomal dominant disease characterised by eyelid malformations, associated or not with premature ovarian failure. It is caused by mutations in the FOXL2 gene, whichContinue Reading
  • Adrien Georges, Bérénice A. Benayoun, Sandrine Caburet, Reiner A. Veitia
  • Medicine, Biology
  • FASEB journal : official publication of the…
  • 2010 (First Publication: 1 February 2010)
  • A transcription reaction relies on the specific recognition of cis-regulatory regions containing short DNA motifs. Such sequences are bound by transcription factors (TFs) involved in the recruitment,Continue Reading
  • Bérénice A. Benayoun, Sandrine Caburet, +5 authors Reiner A. Veitia
  • Biology, Medicine
  • Human molecular genetics
  • 2008 (First Publication: 15 October 2008)
  • The Forkhead transcription factor FOXL2 plays a crucial role in ovarian development and maintenance. In humans, its mutations lead to craniofacial abnormalities, isolated or associated with ovarianContinue Reading