Rousseau F - Search Results

1

Transcriptomic characterization of prurigo nodularis and the therapeutic response to nemolizumab.

Tsoi LC, Hacini-Rachinel F, Fogel P, Rousseau F, Xing X, Patrick MT, Billi AC, Berthier CC, Kahlenberg JM, Lazzari A, Wiegmann H, Ständer S, Piketty C, Julia V, Krishnaswamy JK, Gudjonsson JE. Tsoi LC, et al. Among authors: rousseau f. J Allergy Clin Immunol. 2022 Apr;149(4):1329-1339. doi: 10.1016/j.jaci.2021.10.004. Epub 2021 Nov 29. J Allergy Clin Immunol. 2022. PMID: 34857395 Free PMC article.

2

Filaggrin gene mutation associations with peanut allergy persist despite variations in peanut allergy diagnostic criteria or asthma status.

Asai Y, Greenwood C, Hull PR, Alizadehfar R, Ben-Shoshan M, Brown SJ, Campbell L, Michel DL, Bussières J, Rousseau F, Fujiwara TM, Morgan K, Irvine AD, McLean WH, Clarke A. Asai Y, et al. Among authors: rousseau f. J Allergy Clin Immunol. 2013 Jul;132(1):239-42. doi: 10.1016/j.jaci.2013.03.043. Epub 2013 May 16. J Allergy Clin Immunol. 2013. PMID: 23684069 Free PMC article. No abstract available.

3

The fragile x mental retardation syndrome 20 years after the FMR1 gene discovery: an expanding universe of knowledge.

Rousseau F, Labelle Y, Bussières J, Lindsay C. Rousseau F, et al. Clin Biochem Rev. 2011 Aug;32(3):135-62. Clin Biochem Rev. 2011. PMID: 21912443 Free PMC article.

4

Screening and instability of FMR1 alleles in a prospective sample of 24,449 mother-newborn pairs from the general population.

Lévesque S, Dombrowski C, Morel ML, Rehel R, Côté JS, Bussières J, Morgan K, Rousseau F. Lévesque S, et al. Among authors: rousseau f. Clin Genet. 2009 Dec;76(6):511-23. doi: 10.1111/j.1399-0004.2009.01237.x. Epub 2009 Oct 23. Clin Genet. 2009. PMID: 19863547

5

UGT2B17 gene deletion associated with an increase in bone mineral density similar to the effect of hormone replacement in postmenopausal women.

Giroux S, Bussières J, Bureau A, Rousseau F. Giroux S, et al. Among authors: rousseau f. Osteoporos Int. 2012 Mar;23(3):1163-70. doi: 10.1007/s00198-011-1662-6. Epub 2011 May 26. Osteoporos Int. 2012. PMID: 21614655

6

High-density polymorphisms analysis of 23 candidate genes for association with bone mineral density.

Giroux S, Elfassihi L, Clément V, Bussières J, Bureau A, Cole DE, Rousseau F. Giroux S, et al. Among authors: rousseau f. Bone. 2010 Nov;47(5):975-81. doi: 10.1016/j.bone.2010.06.030. Epub 2010 Jul 30. Bone. 2010. PMID: 20654748

7

Risk of Misdiagnosis Due to Allele Dropout and False-Positive PCR Artifacts in Molecular Diagnostics: Analysis of 30,769 Genotypes.

Blais J, Lavoie SB, Giroux S, Bussières J, Lindsay C, Dionne J, Laroche M, Giguère Y, Rousseau F. Blais J, et al. Among authors: rousseau f. J Mol Diagn. 2015 Sep;17(5):505-14. doi: 10.1016/j.jmoldx.2015.04.004. Epub 2015 Jul 3. J Mol Diagn. 2015. PMID: 26146130 Free article.

8

The association between heel ultrasound and hormone replacement therapy is modulated by a two-locus vitamin D and estrogen receptor genotype.

Giguère Y, Dodin S, Blanchet C, Morgan K, Rousseau F. Giguère Y, et al. Among authors: rousseau f. J Bone Miner Res. 2000 Jun;15(6):1076-84. doi: 10.1359/jbmr.2000.15.6.1076. J Bone Miner Res. 2000. PMID: 10841176 Free article.

9

Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

Rousseau F, Rouillard P, Morel ML, Khandjian EW, Morgan K. Rousseau F, et al. Am J Hum Genet. 1995 Nov;57(5):1006-18. Am J Hum Genet. 1995. PMID: 7485149 Free PMC article.

10

A frequent regulatory variant of the estrogen-related receptor alpha gene associated with BMD in French-Canadian premenopausal women.

Laflamme N, Giroux S, Loredo-Osti JC, Elfassihi L, Dodin S, Blanchet C, Morgan K, Giguère V, Rousseau F. Laflamme N, et al. Among authors: rousseau f. J Bone Miner Res. 2005 Jun;20(6):938-44. doi: 10.1359/JBMR.050203. Epub 2005 Feb 7. J Bone Miner Res. 2005. PMID: 15883633 Free article.

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