EDP Sciences logo
Subscriber Authentication Point
Search
Menu
Home All issues Volume 23 / No 11 (Novembre 2007) Med Sci (Paris), 23 11 (2007) 1008-1013 References
Free Access
Issue
Med Sci (Paris)
Volume 23, Number 11, Novembre 2007
Page(s) 1008 - 1013
Section M/S revues
DOI https://doi.org/10.1051/medsci/200723111008
Published online 15 November 2007
  1. Laberge AM, Michaud J, Richter A, et al. Population history and its impact on medical genetics in Quebec. Clin Genet 2005; 68 : 287–301. [Google Scholar]
  2. Scriver CR. Human genetics: lessons from Quebec populations. Annu Rev Genomics Hum Genet 2001; 2: 69–101. [Google Scholar]
  3. Yotova V, Labuda D, Zietkiewicz E, et al. Anatomy of a founder effect: myotonic dystrophy in Northeastern Quebec. Hum Genet 2005; 117 : 177–87. [Google Scholar]
  4. Charbonneau H, Desjardins B, Légaré J, Denis H. The population of the St-Lawrence Valley, 1608-1760. In : Haines MR, Steckel RH, eds. A population history of North America. New York : Cambridge University Press, 2000 : 99–142. [Google Scholar]
  5. Henripin J, Péron Y. La transition démographique de la province de Québec. In : Charbonneau H, ed. La population du Québec: études rétrospectives. Trois-Rivières: Éditions du Boréal Express, 1973 : 23–44. [Google Scholar]
  6. Pouyez C, Lavoie Y. Les Saguenayens. Introduction à l’histoire des populations du Saguenay. Québec : Presses de l’Université du Québec, 1983. [Google Scholar]
  7. Institut de la statistique du Québec. Gouvernement du Québec. http://www.stat.gouv.qc.ca/regions/profils/region_02_00.htm, 2006. [Google Scholar]
  8. Desjardins M, Frenette Y, Bélanger J, Hétu B. Histoire de la Gaspésie. Québec : Les presses de l’Université Laval, 1999 : 796 p. [Google Scholar]
  9. Statistique Canada. Gouvernement du Canada. http://www12.statcan.ca/francais/census01/home/Index.cfm, 2006. [Google Scholar]
  10. Mayr E. Animal species and evolution. Cambridge: Harvard University Press, 1963 : 812 p. [Google Scholar]
  11. Fix AG. Migration and colonization in human microevolution. Cambridge, UK : Cambridge University Press, 1999 : 254 p. [Google Scholar]
  12. Bouchard G. Information génétique et risque de stigmatisation collective. L’exemple du Saguenay-Lac-St-Jean. Med Sci (Paris) 2004; 20 : 933–4. [Google Scholar]
  13. Jetté R, Gauvreau D, Guérin M. Aux origines d’une région: le peuplement fondateur de Charlevoix avant 1850. In : Bouchard G, de Braekeleer M, eds. Histoire d’un génome. Population et génétique dans l’est du Québec. Québec : Presses de l’Université du Québec, 1991 : 75–106. [Google Scholar]
  14. Gagnon A, Heyer E. Fragmentation of the Quebec population genetic pool (Canada): evidence from the genetic contribution of founders per region in the 17th and 18th centuries. Am J Phys Anthropol 2001; 114 : 30–41. [Google Scholar]
  15. Gauvreau D, Guérin M, Hamel M. De Charlevoix au Saguenay : mesure et caractéristiques du mouvement migratoire avant 1911. In : Bouchard G, de Braekeleer M, eds. Histoire d’un génome. Population et génétique dans l’est du Québec. Sillery (Québec) : Presses de l’Université du Québec, 1991 : 145–59. [Google Scholar]
  16. Lavoie EM, Tremblay M, Houde L, Vezina H. Demogenetic study of three populations within a region with strong founder effects. Community Genet 2005; 8 : 152–60. [Google Scholar]
  17. Austerlitz F, Heyer E. Social transmission of reproductive behavior increases frequency of inherited disorders in a young-expanding population. Proc Natl Acad Sci USA 1998; 95 : 15140–4. [Google Scholar]
  18. Labuda M, Labuda D, Korab-Laskowska M, et al. Linkage disequilibrium analysis in young populations: pseudo-vitamin D- deficiency rickets and the founder effect in French Canadians. Am J Hum Genet 1996; 59 : 633–43. [Google Scholar]
  19. Labuda D, Zietkiewicz E, Labuda M. The genetic clock and the age of the founder effect in growing populations: a lesson from French Canadians and Ashkenazim. Am J Hum Genet 1997; 61 : 768–71. [Google Scholar]
  20. Brais B, Bouchard JP, Xie YG, et al. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy. Nat Genet 1998; 18 : 164–7. [Google Scholar]
  21. Roddier K, Thomas T, Marleau G, et al. Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians. Neurology 2005; 64 : 1762–7. [Google Scholar]
  22. Hechtman P, Kaplan F, Bayleran J, et al. More than one mutant allele causes infantile Tay-Sachs disease in French-Canadians. Am J Hum Genet 1990; 47 : 815–22. [Google Scholar]
  23. Kere J. Human population genetics: lessons from Finland. Annu Rev Genomics Hum Genet 2001; 2 : 103–28. [Google Scholar]
  24. Jobling MA, Hurles ME, Tyler-Smith C. Human evolutionary genetics: origins, peoples and disease. Garland Science Publishing, 2003 : 458 p. [Google Scholar]
  25. Gerbault P. Régionalisation de l’effet fondateur au Québec. Mémoire de maîtrise, Université de Montréal, 2006. [Google Scholar]
  26. Yotova V, Lefebvre JF, Kohany O, et al. Complex structure of the ancestral human population or earlier Speciation of Modern Humans. Am J Hum Genet 2007 (sous presse). [Google Scholar]
  27. Zietkiewicz E, Yotova V, Gehl D, et al. Haplotypes in the dystrophin DNA segment point to a mosaic origin of modern humans’ diversity. Am J Hum Genet 2003; 73 : 994–1015. [Google Scholar]
  28. Chakraborty R. Mitochondrial DNA polymorphism reveals hidden heterogeneity within some Asian populations. Am J Hum Genet 1990; 47 : 87–94. [Google Scholar]
  29. Excoffier L, Laval G, Schneider S. Arlequin ver. 3.0: an integrated software package for population genetics data analysis. Evolutionary Bioinformatics Online 2005; 1 : 47-50. http://cmpg.unibe.ch/software/arlequin3/. [Google Scholar]
  30. Wright S. The genetical structure of populations. Ann Eugen 1951; 15 : 323–54. [Google Scholar]
  31. Piercy R, Sullivan KM, Benson N, Gill P. The application of mitochondrial DNA typing to the study of white Caucasian genetic identification. Int J Legal Med 1993; 106 : 85–90. [Google Scholar]
  32. Richards M, Côrte-Real H, Forster P, et al. Paleolithic and neolithic lineages in the European mitochondrial gene pool. Am J Hum Genet 1996; 59 : 185–203. [Google Scholar]
  33. Rousselet F, Mangin P. Mitochondrial DNA polymorphisms: a study of 50 French Caucasian individuals and application to forensic casework. Int J Legal Med 1998; 111: 292–8. [Google Scholar]
  34. Helgason A, Hickey E, Goodacre S, et al. mtDna and the islands of the North Atlantic: estimating the proportions of Norse and Gaelic ancestry. Am J Hum Genet 2001; 68 : 723–37. [Google Scholar]
  35. Dubut V, Chollet L, Murail P, et al. mtDNA polymorphisms in five French groups: importance of regional sampling. Eur J Hum Genet 2004; 12 : 293–300. [Google Scholar]
  36. Roewer L, Croucher P J, Willuweit S, et al. Signature of recent historical events in the European Y-chromosomal STR haplotype distribution. Hum Genet 2005; 116 : 279–91. [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.