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Catherine Bourgain

Journal articles12 documents

  • Claire Beaudevin, Ashveen Peerbaye, Catherine Bourgain. ‘It has to become true genetics’: tumour genetics and the division of diagnostic labour in the clinic. Sociology of Health and Illness, Wiley, 2019, 41 (4), pp.643-657. ⟨10.1111/1467-9566.12844⟩. ⟨halshs-02167532⟩
  • Alexandre Disser, Philippe Dillmann, Marc Leroy, Maxime l'Héritier, Philippe Fluzin, et al.. Iron supply for the building of Metz cathedral: new methodological development for provenance studies and historical considerations. Archaeometry, Wiley, 2017, 59, ⟨10.1111/arcm.12265⟩. ⟨hal-01465722⟩
  • Jacqueline Milet, Gérald Le Gac, Virginie Scotet, Isabelle Gourlaouen, Corine Thèze, et al.. A common SNP near BMP2 is associated with severity of the iron burden in HFE p.C282Y homozygous patients: a follow-up study.. Blood Cells, Molecules and Diseases, Elsevier, 2010, 44 (1), pp.34-7. ⟨10.1016/j.bcmd.2009.10.001⟩. ⟨inserm-00434960⟩
  • Jérôme Abadie, Benoît Hédan, Edouard Cadieu, Clotilde de Brito, Patrick Devauchelle, et al.. Epidemiology, pathology, and genetics of histiocytic sarcoma in the Bernese mountain dog breed.. The Journal of Heredity, 2009, 100 Suppl 1, pp.S19-27. ⟨10.1093/jhered/esp039⟩. ⟨inserm-00405708⟩
  • Flora Alarcon, Catherine Bourgain, Marion Gauthier-Villars, Violaine Planté-Bordeneuve, Dominique Stoppa-Lyonnet, et al.. PEL: an unbiased method for estimating age-dependent genetic disease risk from pedigree data unselected for family history.. Genetic Epidemiology, Wiley, 2009, 33 (5), pp.379-85. ⟨10.1002/gepi.20390⟩. ⟨inserm-00358140⟩
  • Thierry Vilboux, Gilles Chaudieu, Patricia Jeannin, Delphine Delattre, Benoît Hédan, et al.. Progressive retinal atrophy in the Border Collie: a new XLPRA.. BMC Veterinary Research, BioMed Central, 2008, 4, pp.10. ⟨10.1186/1746-6148-4-10⟩. ⟨hal-00277538⟩
  • Yves Deugnier, Catherine Bourgain, Jean Mosser. Facteurs acquis et génétiques de modulation de la pénétrance de l'hémochromatose HFE [Acquired and genetic factors influencing the penetrance of HFE haemochromatosis]. Bulletin de l'Académie Nationale de Médecine, Elsevier Masson, 2008, 192 (5), pp.873-81; discussion 881. ⟨inserm-00372137⟩
  • Catherine Bourgain, Emmanuelle Génin, Nancy Cox, Françoise Clerget-Darpoux. Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?. European Journal of Human Genetics, Nature Publishing Group, 2007, 15 (3), pp.260-263. ⟨10.1038/sj.ejhg.5201753⟩. ⟨inserm-00119120⟩
  • Joseph Pickrell, Françoise Clerget-Darpoux, Catherine Bourgain. Power of genome-wide association studies in the presence of interacting loci.. Genetic Epidemiology, Wiley, 2007, 31 (7), pp.748-62. ⟨10.1002/gepi.20238⟩. ⟨inserm-00148316⟩
  • Marie-Claude Babron, Catherine Bourgain, Anne-Louise Leutenegger, Françoise Clerget-Darpoux. Detection of susceptibility loci by genome-wide linkage analysis.. BMC Genetics, BioMed Central, 2005, 6 Suppl 1, pp.S18. ⟨10.1186/1471-2156-6-S1-S18⟩. ⟨inserm-00089254⟩
  • Catherine Bourgain. Comparing strategies for association mapping in samples with related individuals.. BMC Genetics, BioMed Central, 2005, 6 Suppl 1, pp.S98. ⟨10.1186/1471-2156-6-S1-S98⟩. ⟨inserm-00089271⟩
  • Mathieu Bourgey, Anne-Louise Leutenegger, Emmanuelle Cousin, Catherine Bourgain, Marie-Claude Babron, et al.. Modeling the effect of a genetic factor for a complex trait in a simulated population.. BMC Genetics, BioMed Central, 2005, 6 Suppl 1, pp.S87. ⟨10.1186/1471-2156-6-S1-S87⟩. ⟨inserm-00089272⟩

Conference papers1 document

  • Ashveen Peerbaye, Catherine Bourgain, Claire Beaudevin. Genomic Platforms at Work: a French Case Study. Genomics as a health care strategy: persons, practices, policies, SIRIC Workshop (CNRS, Inserm, Université Paris Descartes, EHESS, INCa), Apr 2016, Paris, France. ⟨hal-01399965⟩