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Items: 1 to 50 of 113

1.

Compromised Neurocircuitry in Chronic Blast-Related Mild Traumatic Brain Injury.

Yeh PH, Guan Koay C, Wang B, Morissette J, Sham E, Senseney J, Joy D, Kubli A, Yeh CH, Eskay V, Liu W, French LM, Oakes TR, Riedy G, Ollinger J.

Hum Brain Mapp. 2017 Jan;38(1):352-369. doi: 10.1002/hbm.23365. Epub 2016 Sep 15.

PMID:
27629984
2.

Development of a molecular test of Paget's disease of bone.

Guay-Bélanger S, Simonyan D, Bureau A, Gagnon E, Albert C, Morissette J, Siris ES, Orcel P, Brown JP, Michou L.

Bone. 2016 Mar;84:213-221. doi: 10.1016/j.bone.2016.01.007. Epub 2016 Jan 6.

3.

Findings from Structural MR Imaging in Military Traumatic Brain Injury.

Riedy G, Senseney JS, Liu W, Ollinger J, Sham E, Krapiva P, Patel JB, Smith A, Yeh PH, Graner J, Nathan D, Caban J, French LM, Harper J, Eskay V, Morissette J, Oakes TR.

Radiology. 2016 Apr;279(1):207-15. doi: 10.1148/radiol.2015150438. Epub 2015 Dec 15.

PMID:
26669604
4.

Radiographic predictors of lead conductor fracture.

Krahn AD, Morissette J, Lahm R, Haddad T, Baxter WW, McVenes R, Crystal E, Ayala-Paredes F, Cameron D, Verma A, Simpson CS, Exner DV, Birnie DH.

Circ Arrhythm Electrophysiol. 2014 Dec;7(6):1070-7. doi: 10.1161/CIRCEP.114.001612. Epub 2014 Sep 27.

PMID:
25262117
5.

Detection of SQSTM1/P392L post-zygotic mutations in Paget's disease of bone.

Guay-Bélanger S, Picard S, Gagnon E, Morissette J, Siris ES, Orcel P, Brown JP, Michou L.

Hum Genet. 2015 Jan;134(1):53-65. doi: 10.1007/s00439-014-1488-3. Epub 2014 Sep 21.

6.

Identification of rare genetic variants in novel loci associated with Paget's disease of bone.

Beauregard M, Gagnon E, Guay-Bélanger S, Morissette J, Brown JP, Michou L.

Hum Genet. 2014 Jun;133(6):755-68. doi: 10.1007/s00439-013-1409-x. Epub 2013 Dec 27.

PMID:
24370779
7.

Fire regime zonation under current and future climate over eastern Canada.

Boulanger Y, Gauthier S, Gray DR, Le Goff H, Lefort P, Morissette J.

Ecol Appl. 2013 Jun;23(4):904-23.

PMID:
23865239
8.

Genetic association study of Dickkopf-1 and sclerostin genes with paget disease of bone.

Beauregard M, Gagnon E, Guay-Bélanger S, Siris ES, Morissette J, Brown JP, Michou L.

Calcif Tissue Int. 2013 Nov;93(5):405-12. doi: 10.1007/s00223-013-9762-2. Epub 2013 Jul 9.

PMID:
23836157
9.

Genetic association study of UCMA/GRP and OPTN genes (PDB6 locus) with Paget's disease of bone.

Michou L, Conceição N, Morissette J, Gagnon E, Miltenberger-Miltenyi G, Siris ES, Brown JP, Cancela ML.

Bone. 2012 Oct;51(4):720-8. doi: 10.1016/j.bone.2012.06.028. Epub 2012 Jul 14.

10.

Epidemiogenetic study of French families with Paget's disease of bone.

Michou L, Collet C, Morissette J, Audran M, Thomas T, Gagnon E, Launay JM, Laplanche JL, Brown JP, Orcel P.

Joint Bone Spine. 2012 Jul;79(4):393-8. doi: 10.1016/j.jbspin.2011.07.005. Epub 2011 Oct 1.

PMID:
21962384
11.

Contributions of the measles virus nucleocapsid gene and the SQSTM1/p62(P392L) mutation to Paget's disease.

Kurihara N, Hiruma Y, Yamana K, Michou L, Rousseau C, Morissette J, Galson DL, Teramachi J, Zhou H, Dempster DW, Windle JJ, Brown JP, Roodman GD.

Cell Metab. 2011 Jan 5;13(1):23-34. doi: 10.1016/j.cmet.2010.12.002.

12.

Novel SQSTM1 mutations in patients with Paget's disease of bone in an unrelated multiethnic American population.

Michou L, Morissette J, Gagnon ER, Marquis A, Dellabadia M, Brown JP, Siris ES.

Bone. 2011 Mar 1;48(3):456-60. doi: 10.1016/j.bone.2010.11.004. Epub 2010 Nov 10.

PMID:
21073987
13.

Effects of postfire salvage logging on deadwood-associated beetles.

Cobb TP, Morissette JL, Jacobs JM, Koivula MJ, Spence JR, Langor DW.

Conserv Biol. 2011 Feb;25(1):94-104. doi: 10.1111/j.1523-1739.2010.01566.x. Epub 2010 Aug 23.

PMID:
20735453
14.

Gene expression profile in osteoclasts from patients with Paget's disease of bone.

Michou L, Chamoux E, Couture J, Morissette J, Brown JP, Roux S.

Bone. 2010 Mar;46(3):598-603. doi: 10.1016/j.bone.2009.11.012. Epub 2009 Nov 17. Erratum in: Bone. 2010 Jun;46(6):1668-9.

15.

The p62 P392L mutation linked to Paget's disease induces activation of human osteoclasts.

Chamoux E, Couture J, Bisson M, Morissette J, Brown JP, Roux S.

Mol Endocrinol. 2009 Oct;23(10):1668-80. doi: 10.1210/me.2009-0066. Epub 2009 Jul 9.

16.

Pangenomic changes induced by DHEA in the skin of postmenopausal women.

Calvo E, Luu-The V, Morissette J, Martel C, Labrie C, Bernard B, Bernerd F, Deloche C, Chaussade V, Leclaire J, Labrie F.

J Steroid Biochem Mol Biol. 2008 Dec;112(4-5):186-93. doi: 10.1016/j.jsbmb.2008.10.008. Epub 2008 Nov 1.

PMID:
19013239
17.

Fine temporal analysis of DHT transcriptional modulation of the ATM/Gadd45g signaling pathways in the mouse uterus.

Ivanga M, Labrie Y, Calvo E, Belleau P, Martel C, Pelletier G, Morissette J, Labrie F, Durocher F.

Mol Reprod Dev. 2009 Mar;76(3):278-88. doi: 10.1002/mrd.20949.

PMID:
18671277
18.

Bio2RDF: towards a mashup to build bioinformatics knowledge systems.

Belleau F, Nolin MA, Tourigny N, Rigault P, Morissette J.

J Biomed Inform. 2008 Oct;41(5):706-16. doi: 10.1016/j.jbi.2008.03.004. Epub 2008 Mar 21.

19.

Temporal analysis of E2 transcriptional induction of PTP and MKP and downregulation of IGF-I pathway key components in the mouse uterus.

Ivanga M, Labrie Y, Calvo E, Belleau P, Martel C, Luu-The V, Morissette J, Labrie F, Durocher F.

Physiol Genomics. 2007 Mar 14;29(1):13-23.

20.

Sequestosome 1: mutation frequencies, haplotypes, and phenotypes in familial Paget's disease of bone.

Morissette J, Laurin N, Brown JP.

J Bone Miner Res. 2006 Dec;21 Suppl 2:P38-44.

21.

Dehydroepiandrosterone (DHEA) is an anabolic steroid like dihydrotestosterone (DHT), the most potent natural androgen, and tetrahydrogestrinone (THG).

Labrie F, Luu-The V, Martel C, Chernomoretz A, Calvo E, Morissette J, Labrie C.

J Steroid Biochem Mol Biol. 2006 Jul;100(1-3):52-8. Epub 2006 Jun 21.

PMID:
16797178
22.

Clinical nurse specialist as leader of a bariatric program.

Morissette J.

Nurs Leadersh Forum. 2004 Winter;9(2):75-9.

PMID:
16033047
23.

Mechanisms underlying reorganization of fractured tactile cerebellar maps after deafferentation in developing and adult rats.

Shumway C, Morissette J, Bower JM.

J Neurophysiol. 2005 Oct;94(4):2630-43. Epub 2005 Jun 29.

24.

Tetrahydrogestrinone induces a genomic signature typical of a potent anabolic steroid.

Labrie F, Luu-The V, Calvo E, Martel C, Cloutier J, Gauthier S, Belleau P, Morissette J, Lévesque MH, Labrie C.

J Endocrinol. 2005 Feb;184(2):427-33.

PMID:
15684350
25.

Effects of dihydrotestosterone on adipose tissue measured by serial analysis of gene expression.

Bolduc C, Larose M, Yoshioka M, Ye P, Belleau P, Labrie C, Morissette J, Raymond V, Labrie F, St-Amand J.

J Mol Endocrinol. 2004 Oct;33(2):429-44.

PMID:
15525599
26.

No evidence of maternal cell colonization in reverted liver nodules of tyrosinemia type I patients.

Bergeron A, Lettre F, Russo P, Morissette J, Tanguay RM.

Gastroenterology. 2004 Nov;127(5):1381-5.

PMID:
15521007
27.

A genome-wide scan points to a susceptibility locus for bipolar disorder on chromosome 12.

Shink E, Morissette J, Sherrington R, Barden N.

Mol Psychiatry. 2005 Jun;10(6):545-52.

PMID:
15494705
28.

Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation family.

Mortemousque B, Amati-Bonneau P, Couture F, Graffan R, Dubois S, Colin J, Bonneau D, Morissette J, Lacombe D, Raymond V.

Arch Ophthalmol. 2004 Oct;122(10):1527-33.

PMID:
15477465
29.

Intracellular sequestration of hetero-oligomers formed by wild-type and glaucoma-causing myocilin mutants.

Gobeil S, Rodrigue MA, Moisan S, Nguyen TD, Polansky JR, Morissette J, Raymond V.

Invest Ophthalmol Vis Sci. 2004 Oct;45(10):3560-7.

PMID:
15452063
30.

Adipose tissue transcriptome by serial analysis of gene expression.

Bolduc C, Larose M, Lafond N, Yoshioka M, Rodrigue MA, Morissette J, Labrie C, Raymond V, St-Amand J.

Obes Res. 2004 May;12(5):750-7.

31.

Transcriptome of mouse uterus by serial analysis of gene expression (SAGE): comparison with skeletal muscle.

Larose M, St-Amand J, Yoshioka M, Belleau P, Morissette J, Labrie C, Raymond V, Labrie F.

Mol Reprod Dev. 2004 Jun;68(2):142-8.

PMID:
15095334
32.

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.

Segurado R, Detera-Wadleigh SD, Levinson DF, Lewis CM, Gill M, Nurnberger JI Jr, Craddock N, DePaulo JR, Baron M, Gershon ES, Ekholm J, Cichon S, Turecki G, Claes S, Kelsoe JR, Schofield PR, Badenhop RF, Morissette J, Coon H, Blackwood D, McInnes LA, Foroud T, Edenberg HJ, Reich T, Rice JP, Goate A, McInnis MG, McMahon FJ, Badner JA, Goldin LR, Bennett P, Willour VL, Zandi PP, Liu J, Gilliam C, Juo SH, Berrettini WH, Yoshikawa T, Peltonen L, Lönnqvist J, Nöthen MM, Schumacher J, Windemuth C, Rietschel M, Propping P, Maier W, Alda M, Grof P, Rouleau GA, Del-Favero J, Van Broeckhoven C, Mendlewicz J, Adolfsson R, Spence MA, Luebbert H, Adams LJ, Donald JA, Mitchell PB, Barden N, Shink E, Byerley W, Muir W, Visscher PM, Macgregor S, Gurling H, Kalsi G, McQuillin A, Escamilla MA, Reus VI, Leon P, Freimer NB, Ewald H, Kruse TA, Mors O, Radhakrishna U, Blouin JL, Antonarakis SE, Akarsu N.

Am J Hum Genet. 2003 Jul;73(1):49-62. Epub 2003 Jun 11.

33.

Genetic heterogeneity in a very large bipolar affective disorder pedigree from Quebec.

Shink E, Morissette J, Barden N.

Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):65-8.

PMID:
12707941
34.

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.

Prog Neuropsychopharmacol Biol Psychiatry. 2002 Dec;26(7-8):1273-7.

PMID:
12502013
35.

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.

Hum Mol Genet. 2002 Sep 1;11(18):2077-90.

PMID:
12189160
36.

Osteogenesis imperfecta type VII maps to the short arm of chromosome 3.

Labuda M, Morissette J, Ward LM, Rauch F, Lalic L, Roughley PJ, Glorieux FH.

Bone. 2002 Jul;31(1):19-25.

PMID:
12110407
37.

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

Laurin N, Brown JP, Morissette J, Raymond V.

Am J Hum Genet. 2002 Jun;70(6):1582-8. Epub 2002 Apr 30.

38.

Criterion validity study of lumbar goniometers BROM II and EDI-320 for range of motion of lumbar flexion of low back pain patients.

Tousignant M, Morissette J, Murphy M.

J Back Musculoskelet Rehabil. 2002 Jan 1;16(4):159-67.

PMID:
22387441
39.

A radiation hybrid transcript map of the mouse genome.

Avner P, Bruls T, Poras I, Eley L, Gas S, Ruiz P, Wiles MV, Sousa-Nunes R, Kettleborough R, Rana A, Morissette J, Bentley L, Goldsworthy M, Haynes A, Herbert E, Southam L, Lehrach H, Weissenbach J, Manenti G, Rodriguez-Tome P, Beddington R, Dunwoodie S, Cox RD.

Nat Genet. 2001 Oct;29(2):194-200.

PMID:
11586301
40.

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.

Am J Hum Genet. 2001 Sep;69(3):528-43. Epub 2001 Jul 25.

41.

Isolated four-chamber working swine heart model.

Chinchoy E, Soule CL, Houlton AJ, Gallagher WJ, Hjelle MA, Laske TG, Morissette J, Iaizzo PA.

Ann Thorac Surg. 2000 Nov;70(5):1607-14.

PMID:
11093495
43.

Plasticity in cerebellar tactile maps in the adult rat.

Shumway CA, Morissette J, Gruen P, Bower JM.

J Comp Neurol. 1999 Nov 1;413(4):583-92.

PMID:
10495444
44.

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.

Am J Med Genet. 1999 Oct 15;88(5):567-87.

PMID:
10490718
45.

Chromosome 13 workshop report.

Barden N, Morissette J.

Am J Med Genet. 1999 Jun 18;88(3):260-2.

PMID:
10374741
46.
47.

Type I protein C deficiency in French Canadians: evidence of a founder effect and association of specific protein C gene mutations with plasma protein C levels.

Couture P, Demers C, Morissette J, Delage R, Jomphe M, Couture L, Simard J.

Thromb Haemost. 1998 Oct;80(4):551-6.

PMID:
9798967
48.

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.

Am J Hum Genet. 1998 Nov;63(5):1316-28.

49.

A physical map of 30,000 human genes.

Deloukas P, Schuler GD, Gyapay G, Beasley EM, Soderlund C, Rodriguez-Tomé P, Hui L, Matise TC, McKusick KB, Beckmann JS, Bentolila S, Bihoreau M, Birren BB, Browne J, Butler A, Castle AB, Chiannilkulchai N, Clee C, Day PJ, Dehejia A, Dibling T, Drouot N, Duprat S, Fizames C, Fox S, Gelling S, Green L, Harrison P, Hocking R, Holloway E, Hunt S, Keil S, Lijnzaad P, Louis-Dit-Sully C, Ma J, Mendis A, Miller J, Morissette J, Muselet D, Nusbaum HC, Peck A, Rozen S, Simon D, Slonim DK, Staples R, Stein LD, Stewart EA, Suchard MA, Thangarajah T, Vega-Czarny N, Webber C, Wu X, Hudson J, Auffray C, Nomura N, Sikela JM, Polymeropoulos MH, James MR, Lander ES, Hudson TJ, Myers RM, Cox DR, Weissenbach J, Boguski MS, Bentley DR.

Science. 1998 Oct 23;282(5389):744-6.

50.

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.

Nat Genet. 1998 Aug;19(4):319-21. No abstract available.

PMID:
9697688

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