Clerget-Darpoux F - Search Results

1

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. Science. 2011 Apr 8;332(6026):240-3. doi: 10.1126/science.1202205. Science. 2011. PMID: 21474761

2

New disease gene location and high genetic heterogeneity in idiopathic scoliosis.

Edery P, Margaritte-Jeannin P, Biot B, Labalme A, Bernard JC, Chastang J, Kassai B, Plais MH, Moldovan F, Clerget-Darpoux F. Edery P, et al. Eur J Hum Genet. 2011 Aug;19(8):865-9. doi: 10.1038/ejhg.2011.31. Epub 2011 Mar 16. Eur J Hum Genet. 2011. PMID: 21407261 Free PMC article.

3

[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. 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.

4

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.

5

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.

6

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

7

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. 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.

8

Functional variants of POC5 identified in patients with idiopathic scoliosis.

Patten SA, Margaritte-Jeannin P, Bernard JC, Alix E, Labalme A, Besson A, Girard SL, Fendri K, Fraisse N, Biot B, Poizat C, Campan-Fournier A, Abelin-Genevois K, Cunin V, Zaouter C, Liao M, Lamy R, Lesca G, Menassa R, Marcaillou C, Letexier M, Sanlaville D, Berard J, Rouleau GA, Clerget-Darpoux F, Drapeau P, Moldovan F, Edery P. Patten SA, et al. Among authors: clerget darpoux f. J Clin Invest. 2015 Mar 2;125(3):1124-8. doi: 10.1172/JCI77262. Epub 2015 Feb 2. J Clin Invest. 2015. PMID: 25642776 Free PMC article.

9

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.

10

Chromosome 21 scan in Down syndrome reveals DSCAM as a predisposing locus in Hirschsprung disease.

Jannot AS, Pelet A, Henrion-Caude A, Chaoui A, Masse-Morel M, Arnold S, Sanlaville D, Ceccherini I, Borrego S, Hofstra RM, Munnich A, Bondurand N, Chakravarti A, Clerget-Darpoux F, Amiel J, Lyonnet S. Jannot AS, et al. Among authors: clerget darpoux f. PLoS One. 2013 May 6;8(5):e62519. doi: 10.1371/journal.pone.0062519. Print 2013. PLoS One. 2013. PMID: 23671607 Free PMC article.

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