Morissette J - Search Results

1

A common gene for juvenile and adult-onset primary open-angle glaucomas confined on chromosome 1q.

Morissette J, Côté G, Anctil JL, Plante M, Amyot M, Héon E, Trope GE, Weissenbach J, Raymond V. Morissette J, et al. Am J Hum Genet. 1995 Jun;56(6):1431-42. Am J Hum Genet. 1995. PMID: 7762566 Free PMC article.

2

Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone.

Laurin N, Brown JP, Morissette J, Raymond V. Laurin N, et al. Among authors: morissette j. Am J Hum Genet. 2002 Jun;70(6):1582-8. doi: 10.1086/340731. Epub 2002 Apr 30. Am J Hum Genet. 2002. PMID: 11992264 Free PMC article.

3

Founder TIGR/myocilin mutations for glaucoma in the Québec population.

Faucher M, Anctil JL, Rodrigue MA, Duchesne A, Bergeron D, Blondeau P, Côté G, Dubois S, Bergeron J, Arseneault R, Morissette J, Raymond V; Québec Glaucoma Network. Faucher M, et al. Among authors: morissette j. Hum Mol Genet. 2002 Sep 1;11(18):2077-90. doi: 10.1093/hmg/11.18.2077. Hum Mol Genet. 2002. PMID: 12189160

4

Genome-wide search for linkage of bipolar affective disorders in a very large pedigree derived from a homogeneous population in quebec points to a locus of major effect on chromosome 12q23-q24.

Morissette J, Villeneuve A, Bordeleau L, Rochette D, Laberge C, Gagné B, Laprise C, Bouchard G, Plante M, Gobeil L, Shink E, Weissenbach J, Barden N. Morissette J, et al. Am J Med Genet. 1999 Oct 15;88(5):567-87. doi: 10.1002/(sici)1096-8628(19991015)88:5<567::aid-ajmg24>3.0.co;2-8. Am J Med Genet. 1999. PMID: 10490718

5

Paget disease of bone: mapping of two loci at 5q35-qter and 5q31.

Laurin N, Brown JP, Lemainque A, Duchesne A, Huot D, Lacourcière Y, Drapeau G, Verreault J, Raymond V, Morissette J. Laurin N, et al. Among authors: morissette j. Am J Hum Genet. 2001 Sep;69(3):528-43. doi: 10.1086/322975. Epub 2001 Jul 25. Am J Hum Genet. 2001. PMID: 11473345 Free PMC article.

6

A 10-cM YAC contig spanning GLC1A, the primary open-angle glaucoma locus at 1q23-q25.

Clépet C, Dauwerse HJ, Desmaze C, van Ommen GJ, Weissenbach J, Morissette J. Clépet C, et al. Among authors: morissette j. Eur J Hum Genet. 1996;4(5):250-9. doi: 10.1159/000472211. Eur J Hum Genet. 1996. PMID: 8946170

7

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.

Mears AJ, Jordan T, Mirzayans F, Dubois S, Kume T, Parlee M, Ritch R, Koop B, Kuo WL, Collins C, Marshall J, Gould DB, Pearce W, Carlsson P, Enerbäck S, Morissette J, Bhattacharya S, Hogan B, Raymond V, Walter MA. Mears AJ, et al. Among authors: morissette j. Am J Hum Genet. 1998 Nov;63(5):1316-28. doi: 10.1086/302109. Am J Hum Genet. 1998. PMID: 9792859 Free PMC article.

8

Evidence for association and linkage between atopy, airway hyper-responsiveness, and the beta subunit Glu237Gly variant of the high-affinity receptor for immunoglobulin E in the French-Canadian population.

Laprise C, Boulet LP, Morissette J, Winstall E, Raymond V. Laprise C, et al. Among authors: morissette j. Immunogenetics. 2000 Jul;51(8-9):695-702. doi: 10.1007/s002510000185. Immunogenetics. 2000. PMID: 10941841

9

Homozygotes carrying an autosomal dominant TIGR mutation do not manifest glaucoma.

Morissette J, Clépet C, Moisan S, Dubois S, Winstall E, Vermeeren D, Nguyen TD, Polansky JR, Côté G, Anctil JL, Amyot M, Plante M, Falardeau P, Raymond V. Morissette J, et al. Nat Genet. 1998 Aug;19(4):319-21. doi: 10.1038/1203. Nat Genet. 1998. PMID: 9697688 No abstract available.

10

Support for the presence of bipolar disorder susceptibility loci on chromosome 5: heterogeneity in a homogeneous population in Quebec.

Shink E, Morissette J, Villeneuve A, Bordeleau L, Rochette D, Gagné B, Laprise C, Plante M, Barden N. Shink E, et al. Among authors: morissette j. Prog Neuropsychopharmacol Biol Psychiatry. 2002 Dec;26(7-8):1273-7. doi: 10.1016/s0278-5846(02)00266-x. Prog Neuropsychopharmacol Biol Psychiatry. 2002. PMID: 12502013

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