M. Martinez

发表

Sib‐pair linkage analysis of alcohol dependence taking into account covariates and age‐of‐onset variability: Evaluation of the residual approach

F. Demenais, Z. Uhry, F. Tores, 1999, Genetic epidemiology.

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

Y. Agid, J. Mallet, D. Campion, 1996, American journal of medical genetics.

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

B. Dubois, D. Campion, D. Hannequin, 1999, American journal of human genetics.

New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study.

G. Gyapay, J. Weissenbach, J. Prud'homme, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Detection of quantitative trait loci associated with alcohol‐dependence: Use of model‐free sib‐pair method and combined segregation‐linkage analysis based on regressive models

J. O’Connell, G. Durrieu, F. Demenais, 1999, Genetic epidemiology.

Allelic association at the D14S43 locus in early onset Alzheimer's disease. French Alzheimer's Disease Collaborative Study Group.

B. Dubois, J. Mallet, D. Campion, 1995, American journal of medical genetics.

Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q.

N. Andreasen, D. Levinson, E. Gershon, 1999, American journal of medical genetics.

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

M. Leboyer, F. Clerget-Darpoux, M. Khlat, 1989, Genetic epidemiology.

Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees.

E. Gershon, J. Badner, A. Cravchik, 1997, Genomics.

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

C. Gillberg, M. Leboyer, A. Brice, 1999, Human molecular genetics.

Different familial transmission patterns in bipolar I disorder with onset before and after age 25.

M. Nöthen, P. Propping, M. Grigoroiu-Serbanescu, 2001, American journal of medical genetics.

New Strategies in Linkage Research in Psychiatry

E. Gershon, P. Gejman, M. Martinez, 1989 .

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

C. Junien, M. Krempf, C. Boileau, 1999, American journal of human genetics.

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

Y. Agid, A. Delacourte, D. Campion, 1995, American journal of medical genetics.

Patterns of parental transmission and familial aggregation models in bipolar affective disorder.

M. Nöthen, P. Propping, M. Grigoroiu-Serbanescu, 1998, American journal of medical genetics.

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

L. Goldin, M. Martinez, 1991, American journal of human genetics.

A systematic search for a bipolar predisposing locus on chromosome 5.

S. Detera-Wadleigh, D. Muniec, W. Berrettini, 1992, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology.

The detection of linkage and heterogeneity in nuclear families for complex disorders: one versus two marker loci.

L. Goldin, M. Martinez, Maria M. Martinez, 1989, American journal of human genetics.

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

E. Gershon, J. Gelernter, L. Goldin, 1989, American journal of human genetics.

Gene-covariate interaction between dysplastic nevi and the CDKN2A gene in American melanoma-prone families.

M. Tucker, A. Goldstein, F. Demenais, 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

How can maximum likelihood methods reveal candidate gene effects on a quantitative trait?

L. Abel, F. Demenais, M. Martinez, 1995, Genetic epidemiology.

Genetic mapping of adrenergic receptor genes in humans

M. Leppert, J. Lalouel, J. Holik, 1995, Journal of Molecular Medicine.

Genetic mapping of the Gs-alpha subunit gene (GNAS1) to the distal long arm of chromosome 20 using a polymorphism detected by denaturing gradient gel electrophoresis.

E. Gershon, P. Gejman, L. Weinstein, 1991, Genomics.

Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia

J. Duan, A. Sanders, P. Gejman, 2005, Molecular Psychiatry.

Genetic mapping of common diseases: the challenges of manic-depressive illness and schizophrenia.

E. Gershon, P. Gejman, L. Goldin, 1990, Trends in genetics : TIG.

Genetic and physical mapping of the human cannabinoid receptor gene to chromosome 6q14-q15.

T. Bonner, E. Gershon, W. Modi, 1991, The New biologist.

Manic depressive illness not linked to factor IX region in an independent series of pedigrees.

E. Gershon, S. Detera-Wadleigh, J. Gelernter, 1990, Genomics.

Genetic linkage mapping of the m4 human muscarinic receptor (CHRM4).

T. Bonner, E. Gershon, S. Detera-Wadleigh, 1992, Genomics.

[Genetic markers and risk factors in diseases with complex etiology: psychiatric diseases].

M. Martinez, 1993, Revue d'epidemiologie et de sante publique.