The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Joris Andrieux

Laboratoires de Génétique Médicale

Hôpital Jeanne de Flandre

CHRU de Lille

France

[email]@chru-lille.fr

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Laboratoires de Génétique Médicale, Hôpital Jeanne de Flandre, CHRU de Lille, France. 2002 - 2009
  • Medical Genetics Laboratory, Jeanne de Flandre Hospital, CHRU, 2 Avenue Oscar Lambret, 59037 Lille, France. 2007
  • INSERM Unité 524, Institut de Recherche sur le Cancer de Lille, Lille, France. 2004

References

  1. Genotype-phenotype correlation in four 15q24 deleted patients identified by array-CGH. Andrieux, J., Dubourg, C., Rio, M., Attie-Bitach, T., Delaby, E., Mathieu, M., Journel, H., Copin, H., Blondeel, E., Doco-Fenzy, M., Landais, E., Delobel, B., Odent, S., Manouvrier-Hanu, S., Holder-Espinasse, M. Am. J. Med. Genet. A (2009) [Pubmed]
  2. Deletion 18q21.2q21.32 involving TCF4 in a boy diagnosed by CGH-array. Andrieux, J., Lepretre, F., Cuisset, J.M., Goldenberg, A., Delobel, B., Manouvrier-Hanu, S., Holder-Espinasse, M. Eur. J. Med. Genet (2008) [Pubmed]
  3. Characterization by array-CGH of an interstitial de novo tandem 6p21.2p22.1 duplication in a boy with epilepsy and developmental delay. Andrieux, J., Richebourg, S., Duban-Bedu, B., Petit, F., Leprêtre, F., Sukno, S., Dehouck, M.B., Delobel, B. Eur. J. Med. Genet (2008) [Pubmed]
  4. Bone morphogenetic protein antagonist gene NOG is involved in myeloproliferative disease associated with myelofibrosis. Andrieux, J., Roche-Lestienne, C., Geffroy, S., Desterke, C., Grardel, N., Plantier, I., Selleslag, D., Demory, J.L., Laï, J.L., Leleu, X., Le Bousse-Kerdiles, C., Vandenberghe, P. Cancer Genet. Cytogenet. (2007) [Pubmed]
  5. Cryptic 6p21.3 duplications and triplication involving HMGA1 partially masked by add 6p in four cases of myelodysplasia. Andrieux, J., Geffroy, S., Bilhou-Nabera, C., Dupriez, B., Demory, J.L., Bauters, F., Laï, J.L., Dastugue, N. Cancer Genet. Cytogenet. (2006) [Pubmed]
  6. Prenatal diagnosis of ring chromosome 6 in a fetus with cerebellar hypoplasia and partial agenesis of corpus callosum: case report and review of the literature. Andrieux, J., Devisme, L., Valat, A.S., Robert, Y., Frnka, C., Savary, J.B. Eur. J. Med. Genet (2005) [Pubmed]
  7. Dysregulation and overexpression of HMGA2 in myelofibrosis with myeloid metaplasia. Andrieux, J., Demory, J.L., Dupriez, B., Quief, S., Plantier, I., Roumier, C., Bauters, F., Laï, J.L., Kerckaert, J.P. Genes. Chromosomes. Cancer (2004) [Pubmed]
  8. Karyotypic abnormalities in myelofibrosis following polycythemia vera. Andrieux, J., Demory, J.L., Caulier, M.T., Agape, P., Wetterwald, M., Bauters, F., Laï, J.L. Cancer Genet. Cytogenet. (2003) [Pubmed]
  9. Frequency of structural abnormalities of the long arm of chromosome 12 in myelofibrosis with myeloid metaplasia. Andrieux, J., Demory, J.L., Morel, P., Plantier, I., Dupriez, B., Caulier, M.T., Bauters, F., Laï, J.L. Cancer Genet. Cytogenet. (2002) [Pubmed]
 
WikiGenes - Universities