Perdry H - Search Results

1

Moment estimators of relatedness from low-depth whole-genome sequencing data.

Herzig AF, Ciullo M; FranceGenRef Consortium; Leutenegger AL, Perdry H. Herzig AF, et al. Among authors: perdry h. BMC Bioinformatics. 2022 Jun 24;23(1):254. doi: 10.1186/s12859-022-04795-8. BMC Bioinformatics. 2022. PMID: 35751014 Free PMC article.

2

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

3

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.

4

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.

5

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.

6

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.

7

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

8

First genome-wide association study of non-severe malaria in two birth cohorts in Benin.

Milet J, Boland A, Luisi P, Sabbagh A, Sadissou I, Sonon P, Domingo N, Palstra F, Gineau L, Courtin D, Massougbodji A, Garcia A, Deleuze JF, Perdry H. Milet J, et al. Among authors: perdry h. Hum Genet. 2019 Dec;138(11-12):1341-1357. doi: 10.1007/s00439-019-02079-5. Epub 2019 Oct 30. Hum Genet. 2019. PMID: 31667592

9

Mixed logistic regression in genome-wide association studies.

Milet J, Courtin D, Garcia A, Perdry H. Milet J, et al. Among authors: perdry h. BMC Bioinformatics. 2020 Nov 23;21(1):536. doi: 10.1186/s12859-020-03862-2. BMC Bioinformatics. 2020. PMID: 33228527 Free PMC article.

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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