Clerget-Darpoux F - Search Results

1

Consanguinity and the sib-pair method: an approach using identity by descent between and within individuals.

Génin E, Clerget-Darpoux F. Génin E, et al. Am J Hum Genet. 1996 Nov;59(5):1149-62. Am J Hum Genet. 1996. PMID: 8900245 Free PMC article.

2

Comparison of family based haplotype methods using intragenic SNPs in candidate genes.

Bourgain C, Genin E, Clerget-Darpoux F. Bourgain C, et al. Eur J Hum Genet. 2002 May;10(5):313-9. doi: 10.1038/sj.ejhg.5200808. Eur J Hum Genet. 2002. PMID: 12082506

3

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

4

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.

5

Posterior probability of linkage and maximal lod score.

Génin E, Martinez M, Clerget-Darpoux F. Génin E, et al. Ann Hum Genet. 1995 Jan;59(1):123-32. doi: 10.1111/j.1469-1809.1995.tb01610.x. Ann Hum Genet. 1995. PMID: 7762980

6

Association studies in consanguineous populations.

Génin E, Clerget-Darpoux F. Génin E, et al. Am J Hum Genet. 1996 Apr;58(4):861-6. Am J Hum Genet. 1996. PMID: 8644750 Free PMC article.

7

Information provided by pairs of distantly affected relatives to search for genes involved in rare autosomal dominant diseases.

Génin E, Bellis G, Clerget-Darpoux F. Génin E, et al. Ann Hum Genet. 1997 Jan;61(Pt 1):25-36. doi: 10.1046/j.1469-1809.1997.6110025.x. Ann Hum Genet. 1997. PMID: 9066925

8

Heterogeneity of marker allele frequencies hinders interpretation of linkage analysis: illustration on chromosome 18 markers.

Margaritte-Jeannin P, Babron MC, Génin E, Eichenbaum-Voline S, Clerget-Darpoux F. Margaritte-Jeannin P, et al. Genet Epidemiol. 1997;14(6):669-74. doi: 10.1002/(SICI)1098-2272(1997)14:6<669::AID-GEPI20>3.0.CO;2-N. Genet Epidemiol. 1997. PMID: 9433561

9

A gene for Meckel syndrome maps to chromosome 11q13.

Roume J, Genin E, Cormier-Daire V, Ma HW, Mehaye B, Attie T, Razavi-Encha F, Fallet-Bianco C, Buenerd A, Clerget-Darpoux F, Munnich A, Le Merrer M. Roume J, et al. Am J Hum Genet. 1998 Oct;63(4):1095-101. doi: 10.1086/302062. Am J Hum Genet. 1998. PMID: 9758620 Free PMC article.

10

Optimization of genome search strategies for homozygosity mapping: influence of marker spacing on power and threshold criteria for identification of candidate regions.

Génin E, Todorov AA, Clerget-Darpoux F. Génin E, et al. Ann Hum Genet. 1998 Sep;62(Pt 5):419-29. doi: 10.1046/j.1469-1809.1998.6250419.x. Ann Hum Genet. 1998. PMID: 10088039

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

187 results

Search Page

Filters