Babron MC - Search Results

1

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: babron mc. Hum Hered. 2012;74(3-4):142-52. doi: 10.1159/000346790. Epub 2013 Apr 11. Hum Hered. 2012. PMID: 23594492 Free article.

2

High level of inbreeding in final phase of 1000 Genomes Project.

Gazal S, Sahbatou M, Babron MC, Génin E, Leutenegger AL. Gazal S, et al. Among authors: babron mc. Sci Rep. 2015 Dec 2;5:17453. doi: 10.1038/srep17453. Sci Rep. 2015. PMID: 26625947 Free PMC article.

3

Detection of susceptibility loci by genome-wide linkage analysis.

Babron MC, Bourgain C, Leutenegger AL, Clerget-Darpoux F. Babron MC, et al. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S18. doi: 10.1186/1471-2156-6-S1-S18. BMC Genet. 2005. PMID: 16451626 Free PMC article.

4

A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.

Hanein S, Dürr A, Ribai P, Forlani S, Leutenegger AL, Nelson I, Babron MC, Elleuch N, Depienne C, Charon C, Brice A, Stevanin G. Hanein S, et al. Among authors: babron mc. Hum Genet. 2007 Nov;122(3-4):261-73. doi: 10.1007/s00439-007-0396-1. Epub 2007 Jun 28. Hum Genet. 2007. PMID: 17605047

5

Genetic association and gene-environment interaction: a new method for overcoming the lack of exposure information in controls.

Kazma R, Babron MC, Génin E. Kazma R, et al. Among authors: babron mc. Am J Epidemiol. 2011 Jan 15;173(2):225-35. doi: 10.1093/aje/kwq352. Epub 2010 Nov 17. Am J Epidemiol. 2011. PMID: 21084555

6

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. 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.

7

Comparative power of family-based association strategies to detect disease-causing variants under two-locus models.

Babron MC, Guilloud-Bataille M, Sahbatou M, Demenais F, Génin E, Dizier MH. Babron MC, et al. Genet Epidemiol. 2012 Dec;36(8):848-55. doi: 10.1002/gepi.21672. Epub 2012 Aug 9. Genet Epidemiol. 2012. PMID: 22887021

8

FSuite: exploiting inbreeding in dense SNP chip and exome data.

Gazal S, Sahbatou M, Babron MC, Génin E, Leutenegger AL. Gazal S, et al. Among authors: babron mc. Bioinformatics. 2014 Jul 1;30(13):1940-1. doi: 10.1093/bioinformatics/btu149. Epub 2014 Mar 14. Bioinformatics. 2014. PMID: 24632498 Free article.

9

The ordered transmission disequilibrium test: detection of modifier genes.

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

10

Can whole-exome sequencing data be used for linkage analysis?

Gazal S, Gosset S, Verdura E, Bergametti F, Guey S, Babron MC, Tournier-Lasserve E. Gazal S, et al. Among authors: babron mc. Eur J Hum Genet. 2016 Apr;24(4):581-6. doi: 10.1038/ejhg.2015.143. Epub 2015 Jul 15. Eur J Hum Genet. 2016. PMID: 26173971 Free PMC article.

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