Perdry H - Search Results

1

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

2

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.

3

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.

4

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.

5

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.

6

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.

7

Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score.

Bocher O, Ludwig TE, Oglobinsky MS, Marenne G, Deleuze JF, Suryakant S, Odeberg J, Morange PE, Trégouët DA, Perdry H, Génin E. Bocher O, et al. Among authors: perdry h. PLoS Genet. 2022 Sep 16;18(9):e1009923. doi: 10.1371/journal.pgen.1009923. eCollection 2022 Sep. PLoS Genet. 2022. PMID: 36112662 Free PMC article.

8

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

9

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.

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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