Génin E - Search Results

1

Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?

Bourgain C, Génin E, Cox N, Clerget-Darpoux F. Bourgain C, et al. Among authors: genin e. Eur J Hum Genet. 2007 Mar;15(3):260-3. doi: 10.1038/sj.ejhg.5201753. Epub 2006 Dec 13. Eur J Hum Genet. 2007. PMID: 17164797

2

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

3

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.

4

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.

5

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

6

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. Among authors: genin e. 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

7

Caution in the interpretation of MLS.

Eichenbaum-Voline S, Génin E, Babron MC, Margaritte-Jeannin P, Prum B, Clerget-Darpoux F. Eichenbaum-Voline S, et al. Among authors: genin e. Genet Epidemiol. 1997;14(6):1079-83. doi: 10.1002/(SICI)1098-2272(1997)14:6<1079::AID-GEPI86>3.0.CO;2-E. Genet Epidemiol. 1997. PMID: 9433627

8

On the probability of identity states in permutable populations: reply to Cannings.

Génin E, Quesneville H, Clerget-Darpoux F. Génin E, et al. Am J Hum Genet. 1998 Mar;62(3):726-7. doi: 10.1086/301771. Am J Hum Genet. 1998. PMID: 9497268 Free PMC article. No abstract available.

9

Modelling the major histocompatibility complex susceptibility to RA using the MASC method.

Génin E, Babron MC, McDermott MF, Mulcahy B, Waldron-Lynch F, Adams C, Clegg DO, Ward RH, Shanahan F, Molloy MG, O'Gara F, Clerget-Darpoux F. Génin E, et al. Genet Epidemiol. 1998;15(4):419-30. doi: 10.1002/(SICI)1098-2272(1998)15:4<419::AID-GEPI7>3.0.CO;2-X. Genet Epidemiol. 1998. PMID: 9671990

10

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. Among authors: genin e. Am J Hum Genet. 1998 Oct;63(4):1095-101. doi: 10.1086/302062. Am J Hum Genet. 1998. PMID: 9758620 Free PMC article.

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