Martinez M - Search Results

1

Is a single mutation at the same locus responsible for all affected cases in a large Alzheimer pedigree (FAD4)?

Martinez M, Campion D, Babron MC, Clerget-Darpoux F. Martinez M, et al. Genet Epidemiol. 1993;10(6):431-5. doi: 10.1002/gepi.1370100617. Genet Epidemiol. 1993. PMID: 8314039

2

Performance of linkage analysis under misclassification error when the genetic model is unknown.

Martinez M, Khlat M, Leboyer M, Clerget-Darpoux F. Martinez M, et al. Genet Epidemiol. 1989;6(1):253-8. doi: 10.1002/gepi.1370060144. Genet Epidemiol. 1989. PMID: 2731714

3

Linkage detection by the Affected-Pedigree-Member method: what is really tested?

Babron MC, Martinez M, Bonaïti-Pellié C, Clerget-Darpoux F. Babron MC, et al. Among authors: martinez m. Genet Epidemiol. 1993;10(6):389-94. doi: 10.1002/gepi.1370100610. Genet Epidemiol. 1993. PMID: 8314032

4

Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group.

Martinez M, Campion D, Babron MC, Hannequin D, Agid Y, Bellis M, Brice A, Mallet J, Michon A, Thomas-Anterion C, Clerget-Darpoux F. Martinez M, et al. Am J Med Genet. 1996 Feb 16;67(1):9-12. doi: 10.1002/ajmg.1320670102. Am J Med Genet. 1996. PMID: 8678122

5

Evidence for apolipoprotein E epsilon 4 association in early-onset Alzheimer's patients with late-onset relatives.

Pérez-Tur J, Campion D, Martinez M, Brice A, Tardieu S, Hannequin D, Agid Y, Delacourte A, Clerget-Darpoux F, Chartier-Harlin MC. Pérez-Tur J, et al. Among authors: martinez m. Am J Med Genet. 1995 Dec 18;60(6):550-3. doi: 10.1002/ajmg.1320600613. Am J Med Genet. 1995. PMID: 8825894

6

Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.

Campion D, Dumanchin C, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Anterion C, Michon A, Martin C, Charbonnier F, Raux G, Camuzat A, Penet C, Mesnage V, Martinez M, Clerget-Darpoux F, Brice A, Frebourg T. Campion D, et al. Among authors: martinez m. Am J Hum Genet. 1999 Sep;65(3):664-70. doi: 10.1086/302553. Am J Hum Genet. 1999. PMID: 10441572 Free PMC article.

7

Multilocus linkage analysis of markers located on short arm of chromosome 11.

Bonaïti-Pellié C, Martinez M, Clerget-Darpoux F. Bonaïti-Pellié C, et al. Among authors: martinez m. Genet Epidemiol Suppl. 1986;1:129-34. doi: 10.1002/gepi.1370030720. Genet Epidemiol Suppl. 1986. PMID: 3471655 No abstract available.

8

Discrimination between genetic models for insulin dependent diabetes mellitus.

Clerget-Darpoux F, Dizier MH, Bonaïti-Pellié C, Babron MC, Hochez J, Martinez M. Clerget-Darpoux F, et al. Among authors: martinez m. Genet Epidemiol Suppl. 1986;1:313-8. doi: 10.1002/gepi.1370030747. Genet Epidemiol Suppl. 1986. PMID: 3471664 No abstract available.

9

Segregation analysis of the Jacobsen data.

Demenais F, Martinez M, Bonaïti-Pellié C, Clerget-Darpoux F, Feingold N. Demenais F, et al. Among authors: martinez m. Genet Epidemiol Suppl. 1986;1:49-54. doi: 10.1002/gepi.1370030708. Genet Epidemiol Suppl. 1986. PMID: 3569870 No abstract available.

10

Posterior probability of linkage and maximal lod score.

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

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