Mallet J - Search Results

1

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

Brice A, Tardieu S, Campion D, Le Guern E, Martinez M, Carpentier A, Penet C, Dubois B, Bellis M, Mallet J, et al. Brice A, et al. Among authors: mallet j. Am J Med Genet. 1995 Apr 24;60(2):91-3. doi: 10.1002/ajmg.1320600202. Am J Med Genet. 1995. PMID: 7485257

2

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. Among authors: mallet j. Am J Med Genet. 1996 Feb 16;67(1):9-12. doi: 10.1002/ajmg.1320670102. Am J Med Genet. 1996. PMID: 8678122

3

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

de Chaldée M, Laurent C, Thibaut F, Martinez M, Samolyk D, Petit M, Campion D, Mallet J. de Chaldée M, et al. Among authors: mallet j. Am J Med Genet. 1999 Oct 15;88(5):452-7. doi: 10.1002/(sici)1096-8628(19991015)88:5<452::aid-ajmg2>3.3.co;2-s. Am J Med Genet. 1999. PMID: 10490696

4

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

Laurent C, Savoye C, Samolyk D, Meloni R, Mallet J, Campion D, Martinez M, D'Amato T, Bastard C, Dollfus S. Laurent C, et al. Among authors: mallet j. J Med Genet. 1994 Mar;31(3):260. doi: 10.1136/jmg.31.3.260-a. J Med Genet. 1994. PMID: 8014983 Free PMC article. No abstract available.

5

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

Laurent C, Thibaut F, Ravassard P, Campion D, Samolyk D, Lafargue C, Petit M, Martinez M, Mallet J. Laurent C, et al. Among authors: mallet j. Psychiatr Genet. 1997 Autumn;7(3):103-5. doi: 10.1097/00041444-199723000-00002. Psychiatr Genet. 1997. PMID: 9323321

6

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

Laurent C, Zander C, Thibaut F, Bonnet-Brilhault F, Chavand O, Jay M, Samolyk D, Petit M, Martinez M, Campion D, Néri C, Mallet J, Cann H. Laurent C, et al. Among authors: mallet j. Am J Med Genet. 1998 Jul 10;81(4):342-6. doi: 10.1002/(sici)1096-8628(19980710)81:4<342::aid-ajmg12>3.0.co;2-l. Am J Med Genet. 1998. PMID: 9674982

7

[Molecular genetics: a new approach of clinical neurosciences].

Brice A, Mallet J. Brice A, et al. Among authors: mallet j. Rev Neurol (Paris). 1991;147(1):1-16. Rev Neurol (Paris). 1991. PMID: 2014378 Review. French.

8

No mutation in codon 713 of the amyloid precursor gene in schizophrenic patients.

Carter D, Campion D, d'Amato T, Jay M, Brice A, Bellis M, Mallet J, Agid Y. Carter D, et al. Among authors: mallet j. Hum Mol Genet. 1993 Mar;2(3):321. doi: 10.1093/hmg/2.3.321. Hum Mol Genet. 1993. PMID: 8499923 No abstract available.

9

No evidence for linkage between COMT and schizophrenia in a French population.

de Chaldée M, Corbex M, Campion D, Jay M, Samolyk D, Petit M, Thibaut F, Laurent C, Mallet J. de Chaldée M, et al. Among authors: mallet j. Psychiatry Res. 2001 May 10;102(1):87-90. doi: 10.1016/s0165-1781(01)00237-2. Psychiatry Res. 2001. PMID: 11368843

10

Serotonin transporter gene polymorphism and schizophrenia: an association study.

Bonnet-Brilhault F, Laurent C, Thibaut F, Campion D, Chavand O, Samolyk D, Martinez M, Petit M, Mallet J. Bonnet-Brilhault F, et al. Among authors: mallet j. Biol Psychiatry. 1997 Oct 1;42(7):634-6. doi: 10.1016/S0006-3223(97)00320-X. Biol Psychiatry. 1997. PMID: 9376461 Clinical Trial. No abstract available.

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