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

Gérard Lucotte

Institute of Molecular Anthropology

44 rue Monge




Name/email consistency: high



  • Institute of Molecular Anthropology, 44 rue Monge, Paris, France. 2001 - 2010
  • Centre de Neurogénétique Moléculaire, 44 rue Monge, 75005 Paris, France. 2003 - 2005


  1. A decreasing gradient of 374F allele frequencies in the skin pigmentation gene SLC45A2, from the north of West Europe to North Africa. Lucotte, G., Mercier, G., Diéterlen, F., Yuasa, I. Biochem. Genet. (2010) [Pubmed]
  2. A rare variant of the mtDNA HVS1 sequence in the hairs of Napoléon's family. Lucotte, G. Investig. Genet (2010) [Pubmed]
  3. Mutations of the noggin (NOG) and of the activin A type I receptor (ACVR1) genes in a series of twenty-seven French fibrodysplasia ossificans progressiva (FOP) patients. Lucotte, G., Houzet, A., Hubans, C., Lagarde, J.P., Lenoir, G. Genet. Couns. (2009) [Pubmed]
  4. High prevalences of carriers of the 35delG mutation of connexin 26 in the Mediterranean area. Lucotte, G. Int. J. Pediatr. Otorhinolaryngol. (2007) [Pubmed]
  5. The population distribution of the Met allele at the PRNP129 polymorphism (a high risk factor for Creutzfeldt-Jakob disease) in various regions of France and in West Europe. Lucotte, G., Mercier, G. Infect. Genet. Evol. (2005) [Pubmed]
  6. The 35delG mutation in the connexin 26 gene (GJB2) associated with congenital deafness: European carrier frequencies and evidence for its origin in ancient Greece. Lucotte, G., Diéterlen, F. Genet. Test. (2005) [Pubmed]
  7. Brief communication: Y-chromosome haplotypes in Egypt. Lucotte, G., Mercier, G. Am. J. Phys. Anthropol. (2003) [Pubmed]
  8. Paternal European ancestry in French Polynesia detected by Y-chromosome haplotypes. Lucotte, G. Hum. Biol. (2003) [Pubmed]
  9. Y-chromosome DNA haplotypes in Jews: comparisons with Lebanese and Palestinians. Lucotte, G., Mercier, G. Genet. Test. (2003) [Pubmed]
  10. A European allele map of the C282Y mutation of hemochromatosis: Celtic versus Viking origin of the mutation?. Lucotte, G., Dieterlen, F. Blood Cells Mol. Dis. (2003) [Pubmed]
  11. Duplex PCR-RFLP for simultaneous detection of factor V Leiden and prothrombin G20210A. Lucotte, G., Champenois, T. Mol. Cell. Probes (2003) [Pubmed]
  12. More about the Viking hypothesis of origin of the delta32 mutation in the CCR5 gene conferring resistance to HIV-1 infection. Lucotte, G., Dieterlen, F. Infect. Genet. Evol. (2003) [Pubmed]
  13. CCR5-Delta32 allele frequencies in Ashkenazi Jews. Lucotte, G., Smets, P. Genet. Test. (2003) [Pubmed]
  14. Frequencies of 32 base pair deletion of the (Delta 32) allele of the CCR5 HIV-1 co-receptor gene in Caucasians: a comparative analysis. Lucotte, G. Infect. Genet. Evol. (2002) [Pubmed]
  15. North African genes in Iberia studied by Y-chromosome DNA haplotype V. Lucotte, G., Gérard, N., Mercier, G. Hum. Immunol. (2001) [Pubmed]
  16. Distribution of the CCR5 gene 32-basepair deletion in West Europe. A hypothesis about the possible dispersion of the mutation by the Vikings in historical times. Lucotte, G. Hum. Immunol. (2001) [Pubmed]
  17. Meta-analysis of GJB2 mutation 35delG frequencies in Europe. Lucotte, G., Mercier, G. Genet. Test. (2001) [Pubmed]
  18. A rare case of a patient heterozygous for the hemochromatosis mutation C282Y and homozygous for H63D. Lucotte, G., Champenois, T., Sémonin, O. Blood Cells Mol. Dis. (2001) [Pubmed]
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