Perdry H - Search Results

1

Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis.

Babron MC, Perdry H, Handel AE, Ramagopalan SV, Damotte V, Fontaine B, Müller-Myhsok B, Ebers GC, Clerget-Darpoux F. Babron MC, et al. Among authors: perdry h. Eur J Hum Genet. 2012 Mar;20(3):321-5. doi: 10.1038/ejhg.2011.197. Epub 2011 Nov 16. Eur J Hum Genet. 2012. PMID: 22085902 Free PMC article.

2

Estimating cancer risk in HNPCC by the GRL method.

Alarcon F, Lasset C, Carayol J, Bonadona V, Perdry H, Desseigne F, Wang Q, Bonaïti-Pellié C. Alarcon F, et al. Among authors: perdry h. Eur J Hum Genet. 2007 Aug;15(8):831-6. doi: 10.1038/sj.ejhg.5201843. Epub 2007 May 2. Eur J Hum Genet. 2007. PMID: 17473834

3

Modeling the effect of PTPN22 in rheumatoid arthritis.

Bourgey M, Perdry H, Clerget-Darpoux F. Bourgey M, et al. Among authors: perdry h. BMC Proc. 2007;1 Suppl 1(Suppl 1):S37. doi: 10.1186/1753-6561-1-s1-s37. Epub 2007 Dec 18. BMC Proc. 2007. PMID: 18466535 Free PMC article.

4

An ordered subset approach to including covariates in the transmission disequilibrium test.

Perdry H, Maher BS, Babron MC, McHenry T, Clerget-Darpoux F, Marazita ML. Perdry H, et al. BMC Proc. 2007;1 Suppl 1(Suppl 1):S77. doi: 10.1186/1753-6561-1-s1-s77. Epub 2007 Dec 18. BMC Proc. 2007. PMID: 18466579 Free PMC article.

5

HLA-DRB1*15 allele influences the later course of relapsing remitting multiple sclerosis.

Cournu-Rebeix I, Génin E, Leray E, Babron MC, Cohen J, Gout C, Alizadeh M, Perdry H, Semana G, Brassat D, Clerget-Darpoux F, Yaouanq J, Edan G, Rosenheim M, Fontaine B. Cournu-Rebeix I, et al. Among authors: perdry h. Genes Immun. 2008 Sep;9(6):570-4. doi: 10.1038/gene.2008.52. Epub 2008 Jul 10. Genes Immun. 2008. PMID: 18615093

6

The ordered transmission disequilibrium test: detection of modifier genes.

Perdry H, Babron MC, Clerget-Darpoux F. Perdry H, et al. Genet Epidemiol. 2009 Jan;33(1):1-5. doi: 10.1002/gepi.20348. Genet Epidemiol. 2009. PMID: 19548341

7

Estimating penetrance from multiple case families with predisposing mutations: extension of the 'genotype-restricted likelihood' (GRL) method.

Bonaïti B, Bonadona V, Perdry H, Andrieu N, Bonaïti-Pellié C. Bonaïti B, et al. Among authors: perdry h. Eur J Hum Genet. 2011 Feb;19(2):173-9. doi: 10.1038/ejhg.2010.158. Epub 2010 Oct 6. Eur J Hum Genet. 2011. PMID: 20924409 Free PMC article.

8

Modeling the effect of susceptibility factors (HLA and PTPN22) in rheumatoid arthritis.

Perdry H, Clerget-Darpoux F. Perdry H, et al. Methods Mol Biol. 2011;713:201-14. doi: 10.1007/978-1-60327-416-6_15. Methods Mol Biol. 2011. PMID: 21153621

9

Using affected sib-pairs to uncover rare disease variants.

Perdry H, Müller-Myhsok B, Clerget-Darpoux F. Perdry H, et al. Hum Hered. 2012;74(3-4):129-41. doi: 10.1159/000346788. Epub 2013 Apr 11. Hum Hered. 2012. PMID: 23594491 Free article.

10

Could inbred cases identified in GWAS data succeed in detecting rare recessive variants where affected sib-pairs have failed?

Génin E, Sahbatou M, Gazal S, Babron MC, Perdry H, Leutenegger AL. Génin E, et al. Among authors: perdry h. Hum Hered. 2012;74(3-4):142-52. doi: 10.1159/000346790. Epub 2013 Apr 11. Hum Hered. 2012. PMID: 23594492 Free article.

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