Martinez M - Search Results

1

Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families.

Dorkins H, Junien C, Mandel JL, Wrogemann K, Moison JP, Martinez M, Old JM, Bundey S, Schwartz M, Carpenter N, et al. Dorkins H, et al. Among authors: martinez m. Hum Genet. 1985;71(2):103-7. doi: 10.1007/BF00283362. Hum Genet. 1985. PMID: 2995231

2

A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32.

Varret M, Rabès JP, Saint-Jore B, Cenarro A, Marinoni JC, Civeira F, Devillers M, Krempf M, Coulon M, Thiart R, Kotze MJ, Schmidt H, Buzzi JC, Kostner GM, Bertolini S, Pocovi M, Rosa A, Farnier M, Martinez M, Junien C, Boileau C. Varret M, et al. Among authors: martinez m. Am J Hum Genet. 1999 May;64(5):1378-87. doi: 10.1086/302370. Am J Hum Genet. 1999. PMID: 10205269 Free PMC article.

3

Detection of linkage for heterogeneous disorders by using multipoint linkage analysis.

Martinez M, Goldin LR. Martinez M, et al. Am J Hum Genet. 1991 Dec;49(6):1300-5. Am J Hum Genet. 1991. PMID: 1684087 Free PMC article.

4

Detection of marker associations with a dominant disease gene in genetically complex and heterogeneous diseases.

Gershon ES, Martinez M, Goldin L, Gelernter J, Silver J. Gershon ES, et al. Among authors: martinez m. Am J Hum Genet. 1989 Oct;45(4):578-85. Am J Hum Genet. 1989. PMID: 2491015 Free PMC article.

5

Can a susceptibility locus for schizophrenia be excluded from chromosome 5q11-13?

Amos CI, Martinez M, Bale SJ. Amos CI, et al. Among authors: martinez m. Am J Hum Genet. 1991 Jun;48(6):1206-9. Am J Hum Genet. 1991. PMID: 2035539 Free PMC article. No abstract available.

6

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.

Philippe A, Martinez M, Guilloud-Bataille M, Gillberg C, Råstam M, Sponheim E, Coleman M, Zappella M, Aschauer H, Van Maldergem L, Penet C, Feingold J, Brice A, Leboyer M. Philippe A, et al. Among authors: martinez m. Hum Mol Genet. 1999 May;8(5):805-12. doi: 10.1093/hmg/8.5.805. Hum Mol Genet. 1999. PMID: 10196369

7

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

8

Complex segregation analysis accounting for GxE of bone mineral density in European pedigrees selected through a male proband with low BMD.

Pelat C, Van Pottelbergh I, Cohen-Solal M, Ostertag A, Kaufman JM, Martinez M, de Vernejoul MC. Pelat C, et al. Among authors: martinez m. Ann Hum Genet. 2007 Jan;71(Pt 1):29-42. doi: 10.1111/j.1469-1809.2006.00295.x. Ann Hum Genet. 2007. PMID: 17227475

9

The transmission probability model is useful to prevent false inference.

Demenais F, Martinez M, Andrieu N. Demenais F, et al. Among authors: martinez m. Am J Hum Genet. 1993 Feb;52(2):441-2. Am J Hum Genet. 1993. PMID: 8430705 Free PMC article. No abstract available.

10

Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease.

Martinez M, Brice A, Vaughan JR, Zimprich A, Breteler MM, Meco G, Filla A, Farrer MJ, Bétard C, Hardy J, De Michele G, Bonifati V, Oostra B, Gasser T, Wood NW, Dürr A; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Martinez M, et al. J Med Genet. 2004 Dec;41(12):900-7. doi: 10.1136/jmg.2004.022632. J Med Genet. 2004. PMID: 15591275 Free PMC article.

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