Leutenegger AL - Search Results

1

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

2

The importance of connections: joining components of the Hutterite pedigree.

Chapman NH, Leutenegger AL, Badzioch MD, Bogdan M, Conlon EM, Daw EW, Gagnon F, Li N, Maia JM, Wijsman EM, Thompson EA. Chapman NH, et al. Among authors: leutenegger al. Genet Epidemiol. 2001;21 Suppl 1:S230-5. doi: 10.1002/gepi.2001.21.s1.s230. Genet Epidemiol. 2001. PMID: 11793674

3

Estimation of the inbreeding coefficient through use of genomic data.

Leutenegger AL, Prum B, Génin E, Verny C, Lemainque A, Clerget-Darpoux F, Thompson EA. Leutenegger AL, et al. Am J Hum Genet. 2003 Sep;73(3):516-23. doi: 10.1086/378207. Epub 2003 Jul 29. Am J Hum Genet. 2003. PMID: 12900793 Free PMC article.

4

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.

5

Modeling the effect of a genetic factor for a complex trait in a simulated population.

Bourgey M, Leutenegger AL, Cousin E, Bourgain C, Babron MC, Clerget-Darpoux F. Bourgey M, et al. Among authors: leutenegger al. BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S87. doi: 10.1186/1471-2156-6-S1-S87. BMC Genet. 2005. PMID: 16451702 Free PMC article.

6

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.

7

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.

8

Association of TALS developmental disorder with defect in minor splicing component U4atac snRNA.

Edery P, Marcaillou C, Sahbatou M, Labalme A, Chastang J, Touraine R, Tubacher E, Senni F, Bober MB, Nampoothiri S, Jouk PS, Steichen E, Berland S, Toutain A, Wise CA, Sanlaville D, Rousseau F, Clerget-Darpoux F, Leutenegger AL. Edery P, et al. Among authors: leutenegger al. Science. 2011 Apr 8;332(6026):240-3. doi: 10.1126/science.1202205. Science. 2011. PMID: 21474761

9

[Extreme microcephaly and growth retardation caused by mutations in a non-coding RNA component of the minor spliceosome].

Edery P, Alix E, Clerget-Darpoux F, Leutenegger AL. Edery P, et al. Among authors: leutenegger al. Med Sci (Paris). 2012 Feb;28(2):130-3. doi: 10.1051/medsci/2012282004. Epub 2012 Feb 27. Med Sci (Paris). 2012. PMID: 22377294 Free article. French. No abstract available.

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: 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.

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