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Items: 12

1.

Relaxed Selection During a Recent Human Expansion.

Peischl S, Dupanloup I, Foucal A, Jomphe M, Bruat V, Grenier JC, Gouy A, Gilbert KJ, Gbeha E, Bosshard L, Hip-Ki E, Agbessi M, Hodgkinson A, Vézina H, Awadalla P, Excoffier L.

Genetics. 2018 Feb;208(2):763-777. doi: 10.1534/genetics.117.300551. Epub 2017 Nov 29.

2.

Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm.

Chetaille P, Preuss C, Burkhard S, Côté JM, Houde C, Castilloux J, Piché J, Gosset N, Leclerc S, Wünnemann F, Thibeault M, Gagnon C, Galli A, Tuck E, Hickson GR, El Amine N, Boufaied I, Lemyre E, de Santa Barbara P, Faure S, Jonzon A, Cameron M, Dietz HC, Gallo-McFarlane E, Benson DW, Moreau C, Labuda D; FORGE Canada Consortium, Zhan SH, Shen Y, Jomphe M, Jones SJ, Bakkers J, Andelfinger G.

Nat Genet. 2014 Nov;46(11):1245-9. doi: 10.1038/ng.3113. Epub 2014 Oct 5.

PMID:
25282101
3.

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 Jun 12;8(6):e65507. doi: 10.1371/journal.pone.0065507. Print 2013.

4.

Deep human genealogies reveal a selective advantage to be on an expanding wave front.

Moreau C, Bhérer C, Vézina H, Jomphe M, Labuda D, Excoffier L.

Science. 2011 Nov 25;334(6059):1148-50. doi: 10.1126/science.1212880. Epub 2011 Nov 3.

5.

When genetics and genealogies tell different stories-maternal lineages in Gaspesia.

Moreau C, Vézina H, Jomphe M, Lavoie EM, Roy-Gagnon MH, Labuda D.

Ann Hum Genet. 2011 Mar;75(2):247-54. doi: 10.1111/j.1469-1809.2010.00617.x. Epub 2010 Nov 8.

6.

Geography and genealogy of the human host harbouring a distinctive drug-resistant strain of tuberculosis.

Brassard P, Henry KA, Schwartzman K, Jomphe M, Olson SH.

Infect Genet Evol. 2008 May;8(3):247-57. doi: 10.1016/j.meegid.2007.11.008. Epub 2007 Dec 7.

PMID:
18316250
7.

Genome-wide scan for linkage to obesity-associated hypertension in French Canadians.

Pausova Z, Gaudet D, Gossard F, Bernard M, Kaldunski ML, Jomphe M, Tremblay J, Hudson TJ, Bouchard G, Kotchen TA, Cowley AW, Hamet P.

Hypertension. 2005 Dec;46(6):1280-5. Epub 2005 Oct 10.

PMID:
16216983
8.

A "Fille du Roy" introduced the T14484C Leber hereditary optic neuropathy mutation in French Canadians.

Laberge AM, Jomphe M, Houde L, Vezina H, Tremblay M, Desjardins B, Labuda D, St-Hilaire M, Macmillan C, Shoubridge EA, Brais B.

Am J Hum Genet. 2005 Aug;77(2):313-7. Epub 2005 Jun 13.

9.

Quantitative founder-effect analysis of French Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension.

Hamet P, Merlo E, Seda O, Broeckel U, Tremblay J, Kaldunski M, Gaudet D, Bouchard G, Deslauriers B, Gagnon F, Antoniol G, Pausová Z, Labuda M, Jomphe M, Gossard F, Tremblay G, Kirova R, Tonellato P, Orlov SN, Pintos J, Platko J, Hudson TJ, Rioux JD, Kotchen TA, Cowley AW Jr.

Am J Hum Genet. 2005 May;76(5):815-32. Epub 2005 Mar 30.

10.

A genealogical study of essential hypertension with and without obesity in French Canadians.

Pausova Z, Jomphe M, Houde L, Vezina H, Orlov SN, Gossard F, Gaudet D, Tremblay J, Kotchen TA, Cowley AW, Bouchard G, Hamet P.

Obes Res. 2002 Jun;10(6):463-70.

11.

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.

PMID:
11686315
12.

Type I protein C deficiency in French Canadians: evidence of a founder effect and association of specific protein C gene mutations with plasma protein C levels.

Couture P, Demers C, Morissette J, Delage R, Jomphe M, Couture L, Simard J.

Thromb Haemost. 1998 Oct;80(4):551-6.

PMID:
9798967

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