These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
195 related articles for article (PubMed ID: 21234765)
1. Genomic and genealogical investigation of the French Canadian founder population structure. Roy-Gagnon MH; Moreau C; Bherer C; St-Onge P; Sinnett D; Laprise C; Vézina H; Labuda D Hum Genet; 2011 May; 129(5):521-31. PubMed ID: 21234765 [TBL] [Abstract][Full Text] [Related]
2. Genome-wide patterns of identity-by-descent sharing in the French Canadian founder population. Gauvin H; Moreau C; Lefebvre JF; Laprise C; Vézina H; Labuda D; Roy-Gagnon MH Eur J Hum Genet; 2014 Jun; 22(6):814-21. PubMed ID: 24129432 [TBL] [Abstract][Full Text] [Related]
3. GENLIB: an R package for the analysis of genealogical data. Gauvin H; Lefebvre JF; Moreau C; Lavoie EM; Labuda D; Vézina H; Roy-Gagnon MH BMC Bioinformatics; 2015 May; 16():160. PubMed ID: 25971991 [TBL] [Abstract][Full Text] [Related]
4. Admixed ancestry and stratification of Quebec regional populations. Bherer C; Labuda D; Roy-Gagnon MH; Houde L; Tremblay M; Vézina H Am J Phys Anthropol; 2011 Mar; 144(3):432-41. PubMed ID: 21302269 [TBL] [Abstract][Full Text] [Related]
5. Correspondence Between Genomic- and Genealogical/Coalescent-Based Inference of Homozygosity by Descent in Large French-Canadian Genealogies. Burkett KM; Rakesh M; Morris P; Vézina H; Laprise C; Freeman EE; Roy-Gagnon MH Front Genet; 2021; 12():808829. PubMed ID: 35126470 [TBL] [Abstract][Full Text] [Related]
6. Native American admixture in the Quebec founder population. Moreau C; Lefebvre JF; Jomphe M; Bhérer C; Ruiz-Linares A; Vézina H; Roy-Gagnon MH; Labuda D PLoS One; 2013; 8(6):e65507. PubMed ID: 23776491 [TBL] [Abstract][Full Text] [Related]
7. Human genetics: lessons from Quebec populations. Scriver CR Annu Rev Genomics Hum Genet; 2001; 2():69-101. PubMed ID: 11701644 [TBL] [Abstract][Full Text] [Related]
8. [The limited spectrum of pathogenic BRCA1 and BRCA2 mutations in the French Canadian breast and breast-ovarian cancer families, a founder population of Quebec, Canada]. Tonin PN Bull Cancer; 2006 Sep; 93(9):841-6. PubMed ID: 16980226 [TBL] [Abstract][Full Text] [Related]
9. Fragmentation of the Québec population genetic pool (Canada): evidence from the genetic contribution of founders per region in the 17th and 18th centuries. Gagnon A; Heyer E Am J Phys Anthropol; 2001 Jan; 114(1):30-41. PubMed ID: 11150050 [TBL] [Abstract][Full Text] [Related]
10. The interval of linkage disequilibrium (LD) detected with microsatellite and SNP markers in chromosomes of Finnish populations with different histories. Varilo T; Paunio T; Parker A; Perola M; Meyer J; Terwilliger JD; Peltonen L Hum Mol Genet; 2003 Jan; 12(1):51-9. PubMed ID: 12490532 [TBL] [Abstract][Full Text] [Related]
11. Deafblindness in French Canadians from Quebec: a predominant founder mutation in the USH1C gene provides the first genetic link with the Acadian population. Ebermann I; Lopez I; Bitner-Glindzicz M; Brown C; Koenekoop RK; Bolz HJ Genome Biol; 2007; 8(4):R47. PubMed ID: 17407589 [TBL] [Abstract][Full Text] [Related]
12. Linkage disequilibrium analysis in young populations: pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians. Labuda M; Labuda D; Korab-Laskowska M; Cole DE; Zietkiewicz E; Weissenbach J; Popowska E; Pronicka E; Root AW; Glorieux FH Am J Hum Genet; 1996 Sep; 59(3):633-43. PubMed ID: 8751865 [TBL] [Abstract][Full Text] [Related]
13. Mucolipidosis II: a single causal mutation in the N-acetylglucosamine-1-phosphotransferase gene (GNPTAB) in a French Canadian founder population. Plante M; Claveau S; Lepage P; Lavoie EM; Brunet S; Roquis D; Morin C; Vézina H; Laprise C Clin Genet; 2008 Mar; 73(3):236-44. PubMed ID: 18190596 [TBL] [Abstract][Full Text] [Related]
14. Molecular and genealogical characterization of the R1443X BRCA1 mutation in high-risk French-Canadian breast/ovarian cancer families. Vézina H; Durocher F; Dumont M; Houde L; Szabo C; Tranchant M; Chiquette J; Plante M; Laframboise R; Lépine J; Nevanlinna H; Stoppa-Lyonnet D; Goldgar D; Bridge P; Simard J Hum Genet; 2005 Jul; 117(2-3):119-32. PubMed ID: 15883839 [TBL] [Abstract][Full Text] [Related]
15. [Genealogical study of oculopharyngeal dystrophy at Saguenay-Lac-St-Jean, Quebec, Canada]. Tremblay-Tymczuk S; Mathieu J; Morgan K; Bouchard JP; De Braekeleer M Rev Neurol (Paris); 1992; 148(10):601-4. PubMed ID: 1295054 [TBL] [Abstract][Full Text] [Related]
16. Evidence of a founder effect for the protein C gene 3363 inserted C mutation in thrombophilic pedigrees of French origin. Couture P; Bovill EG; Demers C; Simard J; Delage R; Scott BT; Valliere JE; Callas PW; Jomphe M; Rosendaal FR; Aiach M; Long GL Thromb Haemost; 2001 Oct; 86(4):1000-6. PubMed ID: 11686315 [TBL] [Abstract][Full Text] [Related]
17. On the genes, genealogies, and geographies of Quebec. Anderson-Trocmé L; Nelson D; Zabad S; Diaz-Papkovich A; Kryukov I; Baya N; Touvier M; Jeffery B; Dina C; Vézina H; Kelleher J; Gravel S Science; 2023 May; 380(6647):849-855. PubMed ID: 37228217 [TBL] [Abstract][Full Text] [Related]
18. Deciphering the genetic structure of the Quebec founder population using genealogies. Gagnon L; Moreau C; Laprise C; Vézina H; Girard SL Eur J Hum Genet; 2024 Jan; 32(1):91-97. PubMed ID: 37016017 [TBL] [Abstract][Full Text] [Related]
19. Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping. Kibar Z; Dubé MP; Powell J; McCuaïg C; Hayflick SJ; Zonana J; Hovnanian A; Radhakrishna U; Antonarakis SE; Benohanian A; Sheeran AD; Stephan ML; Gosselin R; Kelsell DP; Christianson AL; Fraser FC; Der Kaloustian VM; Rouleau GA Eur J Hum Genet; 2000 May; 8(5):372-80. PubMed ID: 10854098 [TBL] [Abstract][Full Text] [Related]
20. The contribution of founder mutations to early-onset breast cancer in French-Canadian women. Ghadirian P; Robidoux A; Zhang P; Royer R; Akbari M; Zhang S; Fafard E; Costa M; Martin G; Potvin C; Patocskai E; Larouche N; Younan R; Nassif E; Giroux S; Narod SA; Rousseau F; Foulkes WD Clin Genet; 2009 Nov; 76(5):421-6. PubMed ID: 19863560 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]