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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Cédric Le Caignec

Service de Génétique Médicale

Centre Hospitalo-Universitaire




Name/email consistency: high



  • Service de Génétique Médicale, Centre Hospitalo-Universitaire, Nantes, France. 2003 - 2005
  • Centre for Human Genetics, University Hospital Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium. 2005
  • Laboratoire d'Etude du Polymorphisme de l'ADN, Faculté de Médecine, Nantes, France. 2002


  1. Subtelomeric 6p deletion: clinical, FISH, and array CGH characterization of two cases. Le Caignec, C., De Mas, P., Vincent, M.C., Bocéno, M., Bourrouillou, G., Rival, J.M., David, A. Am. J. Med. Genet. A (2005) [Pubmed]
  2. Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations. Le Caignec, C., Boceno, M., Saugier-Veber, P., Jacquemont, S., Joubert, M., David, A., Frebourg, T., Rival, J.M. J. Med. Genet. (2005) [Pubmed]
  3. Interstitial 6q deletion: clinical and array CGH characterisation of a new patient. Le Caignec, C., Swillen, A., Van Asche, E., Fryns, J.P., Vermeesch, J.R. Eur. J. Med. Genet (2005) [Pubmed]
  4. Sonographic findings in Beckwith-Wiedemann syndrome related to H19 hypermethylation. Le Caignec, C., Gicquel, C., Gubler, M.C., Guyot, C., You, M.C., Laurent, A., Joubert, M., Winer, N., David, A., Rival, J.M. Prenat. Diagn. (2004) [Pubmed]
  5. Inherited ring chromosome 8 without loss of subtelomeric sequences. Le Caignec, C., Boceno, M., Jacquemont, S., Nguyen The Tich, S., Rival, J.M., David, A. Ann. Genet. (2004) [Pubmed]
  6. 46,XY gonadal dysgenesis: evidence for autosomal dominant transmission in a large kindred. Le Caignec, C., Baron, S., McElreavey, K., Joubert, M., Rival, J.M., Mechinaud, F., David, A. Am. J. Med. Genet. A (2003) [Pubmed]
  7. Prenatal diagnosis of a small supernumerary, XIST-negative, mosaic ring X chromosome identified by fluorescence in situ hybridization in an abnormal male fetus. Le Caignec, C., Boceno, M., Joubert, M., Winer, N., Aubron, F., Fallet-Bianco, C., Rival, J.M. Prenat. Diagn. (2003) [Pubmed]
  8. Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p. Le Caignec, C., Winer, N., Boceno, M., Delnatte, C., Podevin, G., Liet, J.M., Quere, M.P., Joubert, M., Rival, J.M. Prenat. Diagn. (2003) [Pubmed]
  9. Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1. Le Caignec, C., Lefevre, M., Schott, J.J., Chaventre, A., Gayet, M., Calais, C., Moisan, J.P. Am. J. Hum. Genet. (2002) [Pubmed]
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