M. Martinez

发表

The −2 bp deletion in exon 6 of the ‘alpha 7-like’ nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficit

D. Campion, T. Frebourg, S. Louchart, 2002, Molecular Psychiatry.

Genetic overlap between Alzheimer’s disease and Parkinson’s disease at the MAPT locus

A Smith, M A Pericak-Vance, L A Farrer, 2015, Molecular Psychiatry.

No major role for the dopamine D2 receptor Ser → Cys311 mutation in schizophrenia

T. d'Amato, J. Mallet, D. Campion, 1994, Psychiatric genetics.

The Washington Heights-Inwood Genetic Study of Essential Tremor: methodologic issues in essential-tremor research.

E D Louis, S Fahn, R Ottman, 1997, Neuroepidemiology.

Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer disease.

Y. Agid, B. Dubois, D. Campion, 1998, Archives of neurology.

Homozygosity at the dopamine D3 receptor locus is not associated with schizophrenia.

J. Mallet, D. Campion, D. Samolyk, 1994, Journal of medical genetics.

Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex.

Y. Agid, B. Dubois, F. Pasquier, 1997, American journal of human genetics.

De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.

Miguel Ángel Martínez, Y. Agid, D. Campion, 1998, Journal of medical genetics.

A rare allele of a microsatellite located in the tyrosine hydroxylase gene found in schizophrenic patients.

D. Campion, D. Samolyk, S. Dollfus, 1995, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

Detection of two new polymorphic sites in the human interleukin‐1β gene: lack of association with schizophrenia in a French population

J. Mallet, D. Campion, D. Samolyk, 1997, Psychiatric genetics.

Evidence of a cohort effect for age at onset of schizophrenia.

F. Thibaut, J. Ménard, M. Petit, 2001, The American journal of psychiatry.

Linkage disequilibrium on the COMT gene in French schizophrenics and controls.

J. Mallet, D. Campion, D. Samolyk, 1999, American journal of medical genetics.

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

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

Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk

Sonja W. Scholz, D. Hernandez, M. Nalls, 2018 .

Anticipation in schizophrenia: no evidence of expanded CAG/CTG repeat sequences in French families and sporadic cases.

H. Cann, J. Mallet, D. Campion, 1998, American journal of medical genetics.

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

Miguel Ángel Martínez, M. Farrer, M. Breteler, 2004, Journal of Medical Genetics.

Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex.

Miguel Ángel Martínez, Y Agid, Y. Agid, 1997, American journal of human genetics.

No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.

Miguel Ángel Martínez, Y. Agid, B. Dubois, 1996, Journal of medical genetics.

Identifying genetic risk factors for idiopathic Parkinson's disease by combining genome-wide copy number variation data and published data from genome-wide sib-pair linkage studies

Aj Lees, Patrick M. Abou-Sleiman, Nicholas W. Wood, 2006 .

A large pedigree with early-onset Alzheimer's disease

Y. Agid, B. Dubois, J. Mallet, 1995, Neurology.

schizophrenia-759 C > T Polymorphism of the HTR 2 C Gene is Associated with Second Generation Antipsychotic-Induced Weight Gain in Female Patients with Schizophrenia

M. Martinez, R. Rothlin, F. Daray, 2017 .

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

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

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

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

A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 years.

Y. Agid, M. Baulac, C. Duyckaerts, 1996, Neuroreport.

No eVect of the á1-antichymotrypsin A allele in Alzheimer’s disease

Y. Agid, F. Pasquier, D. Campion, 1998 .

Characteristics of familial aggregation in early-onset Alzheimer's disease: evidence of subgroups.

B. Dubois, D. Campion, D. Hannequin, 1995, American journal of medical 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.

No e V ect of the á 1-antichymotrypsin A allele in Alzheimer ’ s disease

Y. Agid, B. Dubois, F. Pasquier, 1998 .

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.

Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset

D. Hernandez, M. Nalls, J. Hoenicka, 2019, npj Parkinson's Disease.

Serotonin transporter gene polymorphism and schizophrenia: An association study

J. Mallet, D. Campion, C. Laurent, 1998, Schizophrenia Research.