Perdry H - Search Results

1

Accuracy of heritability estimations in presence of hidden population stratification.

Dandine-Roulland C, Bellenguez C, Debette S, Amouyel P, Génin E, Perdry H. Dandine-Roulland C, et al. Among authors: perdry h. Sci Rep. 2016 May 25;6:26471. doi: 10.1038/srep26471. Sci Rep. 2016. PMID: 27220488 Free PMC article.

2

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

3

Impaired performance of FDR-based strategies in whole-genome association studies when SNPs are excluded prior to the analysis.

Marenne G, Dalmasso C, Perdry H, Génin E, Broët P. Marenne G, et al. Among authors: perdry h. Genet Epidemiol. 2009 Jan;33(1):45-53. doi: 10.1002/gepi.20355. Genet Epidemiol. 2009. PMID: 18618761

4

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.

5

Inbreeding coefficient estimation with dense SNP data: comparison of strategies and application to HapMap III.

Gazal S, Sahbatou M, Perdry H, Letort S, Génin E, Leutenegger AL. Gazal S, et al. Among authors: perdry h. Hum Hered. 2014;77(1-4):49-62. doi: 10.1159/000358224. Epub 2014 Jul 29. Hum Hered. 2014. PMID: 25060269 Free article.

6

Where is the causal variant? On the advantage of the family design over the case-control design in genetic association studies.

Dandine-Roulland C, Perdry H. Dandine-Roulland C, et al. Among authors: perdry h. Eur J Hum Genet. 2015 Oct;23(10):1357-63. doi: 10.1038/ejhg.2014.284. Epub 2015 Jan 14. Eur J Hum Genet. 2015. PMID: 25585700 Free PMC article.

7

The Use of the Linear Mixed Model in Human Genetics.

Dandine-Roulland C, Perdry H. Dandine-Roulland C, et al. Among authors: perdry h. Hum Hered. 2015;80(4):196-206. doi: 10.1159/000447634. Epub 2016 Sep 1. Hum Hered. 2015. PMID: 27576760 Review.

8

Detecting the dominance component of heritability in isolated and outbred human populations.

Herzig AF, Nutile T, Ruggiero D, Ciullo M, Perdry H, Leutenegger AL. Herzig AF, et al. Among authors: perdry h. Sci Rep. 2018 Dec 21;8(1):18048. doi: 10.1038/s41598-018-36050-7. Sci Rep. 2018. PMID: 30575761 Free PMC article.

9

Rare variant association testing for multicategory phenotype.

Bocher O, Marenne G, Saint Pierre A, Ludwig TE, Guey S, Tournier-Lasserve E, Perdry H, Génin E. Bocher O, et al. Among authors: perdry h. Genet Epidemiol. 2019 Sep;43(6):646-656. doi: 10.1002/gepi.22210. Epub 2019 May 13. Genet Epidemiol. 2019. PMID: 31087445

10

Extension of SKAT to multi-category phenotypes through a geometrical interpretation.

Bocher O, Marenne G, Tournier-Lasserve E; FREX Consortium,; Génin E, Perdry H. Bocher O, et al. Among authors: perdry h. Eur J Hum Genet. 2021 May;29(5):736-744. doi: 10.1038/s41431-020-00792-8. Epub 2021 Jan 14. Eur J Hum Genet. 2021. PMID: 33446828 Free PMC article.

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