Leboyer M - Search Results

1

No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects.

Delorme R, Durand CM, Betancur C, Wagner M, Ruhrmann S, Grabe HJ, Nygren G, Gillberg C, Leboyer M, Bourgeron T, Courtet P, Jollant F, Buresi C, Aubry JM, Baud P, Bondolfi G, Bertschy G, Perroud N, Malafosse A. Delorme R, et al. Among authors: leboyer m. Biol Psychiatry. 2006 Jul 15;60(2):202-3. doi: 10.1016/j.biopsych.2005.12.014. Epub 2006 Apr 11. Biol Psychiatry. 2006. PMID: 16581035

2

Failure to replicate linkage between chromosome 5q11-q13 markers and schizophrenia in 28 families.

Campion D, d'Amato T, Laklou H, Sabate O, Jay M, Leboyer M, Malafosse A, Gorwood P, Babron MC, Hillaire D, et al. Campion D, et al. Among authors: leboyer m. Psychiatry Res. 1992 Dec;44(3):171-9. doi: 10.1016/0165-1781(92)90021-t. Psychiatry Res. 1992. PMID: 1363250

3

Absence of linkage between chromosome 11p15 markers and manic-depressive illness in a Belgian pedigree.

Mendlewicz J, Leboyer M, De Bruyn A, Malafosse A, Sevy S, Hirsch D, Van Broeckhoven C, Mallet J. Mendlewicz J, et al. Among authors: leboyer m. Am J Psychiatry. 1991 Dec;148(12):1683-7. doi: 10.1176/ajp.148.12.1683. Am J Psychiatry. 1991. PMID: 1683520

4

Two TaqI dimorphic sites at the human beta-hydroxylase locus.

D'Amato T, Leboyer M, Malafosse A, Samolyk D, Lamouroux A, Junien C, Mallet J. D'Amato T, et al. Among authors: leboyer m. Nucleic Acids Res. 1989 Jul 25;17(14):5871. doi: 10.1093/nar/17.14.5871. Nucleic Acids Res. 1989. PMID: 2569723 Free PMC article. No abstract available.

5

Association between the tryptophan hydroxylase gene and manic-depressive illness.

Bellivier F, Leboyer M, Courtet P, Buresi C, Beaufils B, Samolyk D, Allilaire JF, Feingold J, Mallet J, Malafosse A. Bellivier F, et al. Among authors: leboyer m. Arch Gen Psychiatry. 1998 Jan;55(1):33-7. doi: 10.1001/archpsyc.55.1.33. Arch Gen Psychiatry. 1998. PMID: 9435758

6

Manic depressive illness and tyrosine hydroxylase gene: linkage heterogeneity and association.

Malafosse A, Leboyer M, d'Amato T, Amadéo S, Abbar M, Campion D, Canseil O, Castelnau D, Gheysen F, Granger B, Henrikson B, Poirier MF, Sabaté O, Samolyk D, Feingold J, Mallet J. Malafosse A, et al. Among authors: leboyer m. Neurobiol Dis. 1997;4(5):337-49. doi: 10.1006/nbdi.1997.0149. Neurobiol Dis. 1997. PMID: 9440122

7

Whole blood serotonin and plasma beta-endorphin in autistic probands and their first-degree relatives.

Leboyer M, Philippe A, Bouvard M, Guilloud-Bataille M, Bondoux D, Tabuteau F, Feingold J, Mouren-Simeoni MC, Launay JM. Leboyer M, et al. Biol Psychiatry. 1999 Jan 15;45(2):158-63. doi: 10.1016/s0006-3223(97)00532-5. Biol Psychiatry. 1999. PMID: 9951562

8

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: leboyer m. Hum Mol Genet. 1999 May;8(5):805-12. doi: 10.1093/hmg/8.5.805. Hum Mol Genet. 1999. PMID: 10196369

9

Association between bipolar disorder and monoamine oxidase A gene polymorphisms: results of a multicenter study.

Preisig M, Bellivier F, Fenton BT, Baud P, Berney A, Courtet P, Hardy P, Golaz J, Leboyer M, Mallet J, Matthey ML, Mouthon D, Neidhart E, Nosten-Bertrand M, Stadelmann-Dubuis E, Guimon J, Ferrero F, Buresi C, Malafosse A. Preisig M, et al. Among authors: leboyer m. Am J Psychiatry. 2000 Jun;157(6):948-55. doi: 10.1176/appi.ajp.157.6.948. Am J Psychiatry. 2000. PMID: 10831475

10

Possible association between serotonin transporter gene polymorphism and violent suicidal behavior in mood disorders.

Bellivier F, Szöke A, Henry C, Lacoste J, Bottos C, Nosten-Bertrand M, Hardy P, Rouillon F, Launay JM, Laplanche JL, Leboyer M. Bellivier F, et al. Among authors: leboyer m. Biol Psychiatry. 2000 Aug 15;48(4):319-22. doi: 10.1016/s0006-3223(00)00891-x. Biol Psychiatry. 2000. PMID: 10960164

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