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

2

Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us?

Leutenegger AL, Sahbatou M, Gazal S, Cann H, Génin E. Leutenegger AL, et al. Eur J Hum Genet. 2011 May;19(5):583-7. doi: 10.1038/ejhg.2010.205. Epub 2011 Mar 2. Eur J Hum Genet. 2011. PMID: 21364699 Free PMC article.

3

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: leutenegger al. Hum Hered. 2014;77(1-4):49-62. doi: 10.1159/000358224. Epub 2014 Jul 29. Hum Hered. 2014. PMID: 25060269 Free article.

4

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: leutenegger al. Sci Rep. 2015 Dec 2;5:17453. doi: 10.1038/srep17453. Sci Rep. 2015. PMID: 26625947 Free PMC article.

5

Impact of parental relationships in maximum lod score affected sib-pair method.

Leutenegger AL, Génin E, Thompson EA, Clerget-Darpoux F. Leutenegger AL, et al. Genet Epidemiol. 2002 Nov;23(4):413-25. doi: 10.1002/gepi.10190. Genet Epidemiol. 2002. PMID: 12432507

6

Detection of susceptibility loci by genome-wide linkage analysis.

Babron MC, Bourgain C, Leutenegger AL, Clerget-Darpoux F. Babron MC, et al. Among authors: leutenegger 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.

7

Using genomic inbreeding coefficient estimates for homozygosity mapping of rare recessive traits: application to Taybi-Linder syndrome.

Leutenegger AL, Labalme A, Genin E, Toutain A, Steichen E, Clerget-Darpoux F, Edery P. Leutenegger AL, et al. Am J Hum Genet. 2006 Jul;79(1):62-6. doi: 10.1086/504640. Epub 2006 Apr 28. Am J Hum Genet. 2006. PMID: 16773566 Free PMC article.

8

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: leutenegger al. 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

9

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: leutenegger al. Bioinformatics. 2014 Jul 1;30(13):1940-1. doi: 10.1093/bioinformatics/btu149. Epub 2014 Mar 14. Bioinformatics. 2014. PMID: 24632498 Free article.

10

Relationship inference from the genetic data on parents or offspring: A comparative study.

Gazal S, Génin E, Leutenegger AL. Gazal S, et al. Among authors: leutenegger al. Theor Popul Biol. 2016 Feb;107:31-8. doi: 10.1016/j.tpb.2015.09.002. Epub 2015 Sep 30. Theor Popul Biol. 2016. PMID: 26431644 Free article.

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