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Alexandre Desautels - Publications

Affiliations: 
Université de Montréal, Montréal, Canada 
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40 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Mufti K, Yu E, Rudakou U, Krohn L, Ruskey JA, Asayesh F, Laurent SB, Spiegelman D, Arnulf I, Hu MTM, Montplaisir JY, Gagnon JF, Desautels A, Dauvilliers Y, Gigli GL, et al. Novel Associations of and with Rapid Eye Movement Sleep Behavior Disorder. Neurology. PMID 33397775 DOI: 10.1212/WNL.0000000000011464  0.422
2020 Mufti K, Rudakou U, Yu E, Krohn L, Ruskey JA, Asayesh F, Laurent SB, Spiegelman D, Arnulf I, Hu MTM, Montplaisir JY, Gagnon JF, Desautels A, Dauvilliers Y, Gigli GL, et al. Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 33001463 DOI: 10.1002/mds.28318  0.424
2020 Krohn L, Ruskey JA, Rudakou U, Leveille E, Asayesh F, Hu MTM, Arnulf I, Dauvilliers Y, Högl B, Stefani A, Monaca CC, Beatriz A, Plazzi G, Antelmi E, Ferini-Strambi L, ... ... Desautels A, et al. variants in REM sleep behavior disorder: a multicenter study. Neurology. PMID 32591474 DOI: 10.1212/Wnl.0000000000010042  0.41
2020 Rudakou U, Futhey NC, Krohn L, Ruskey JA, Heilbron K, Cannon P, Alam A, Arnulf I, Hu MTM, Montplaisir JY, Gagnon JF, Desautels A, Dauvilliers Y, Toffoli M, et al. SMPD1 variants do not have a major role in rapid eye movement sleep behavior disorder. Neurobiology of Aging. PMID 32409254 DOI: 10.1016/J.Neurobiolaging.2020.04.005  0.448
2020 Rudakou U, Ruskey JA, Krohn L, Laurent SB, Spiegelman D, Greenbaum L, Yahalom G, Desautels A, Montplaisir JY, Fahn S, Waters CH, Levy O, Kehoe CM, Narayan S, Dauvilliers Y, et al. Analysis of common and rare variants in late-onset Parkinson disease. Neurology. Genetics. 6: 385. PMID 32042909 DOI: 10.1212/Nxg.0000000000000385  0.341
2020 Krohn L, Wu RY, Heilbron K, Ruskey JA, Laurent SB, Blauwendraat C, Alam A, Arnulf I, Hu MTM, Dauvilliers Y, Högl B, Toft M, Bjørnarå KA, Stefani A, Holzknecht E, ... ... Desautels A, et al. Fine-mapping of SNCA in REM sleep behavior disorder and overt synucleinopathies. Annals of Neurology. PMID 31976583 DOI: 10.1002/Ana.25687  0.416
2019 Gan-Or Z, Rao T, Leveille E, Degroot C, Chouinard S, Cicchetti F, Dagher A, Das S, Desautels A, Drouin-Ouellet J, Durcan T, Gagnon JF, Genge A, Karamchandani J, Lafontaine AL, et al. The Quebec Parkinson Network: A Researcher-Patient Matching Platform and Multimodal Biorepository. Journal of Parkinson's Disease. PMID 31868683 DOI: 10.3233/Jpd-191775  0.342
2019 Krohn L, Öztürk TN, Vanderperre B, Ouled Amar Bencheikh B, Ruskey JA, Laurent SB, Spiegelman D, Postuma RB, Arnulf I, Hu MTM, Dauvilliers Y, Högl B, Stefani A, Monaca CC, Plazzi G, ... ... Desautels A, et al. Genetic, structural and functional evidence link TMEM175 to synucleinopathies. Annals of Neurology. PMID 31658403 DOI: 10.1002/Ana.25629  0.405
2018 El Gewely M, Welman M, Xiong L, Yin S, Catoire H, Rouleau G, Montplaisir JY, Desautels A, Warby SC. Reassessing GWAS findings for the shared genetic basis of insomnia and restless legs syndrome. Sleep. PMID 30215811 DOI: 10.1093/Sleep/Zsy164  0.516
2018 Li J, Ruskey JA, Arnulf I, Dauvilliers Y, Hu MTM, Högl B, Leblond CS, Zhou S, Ambalavanan A, Ross JP, Bourassa CV, Spiegelman D, Laurent SB, Stefani A, Charley Monaca C, ... ... Desautels A, et al. Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 29756641 DOI: 10.1002/Mds.27385  0.41
2018 El Gewely M, Melanie W, Lan X, Sophie Y, Rouleau G, Montplaisir J, Desautels A, Warby S. 0690 The Association Of Meis1 Gene In Restless Leg Syndrome And Rls Related Phenotypes But Not With Chronic Insomnia Disorder Sleep. 41: A255-A256. DOI: 10.1093/Sleep/Zsy061.689  0.428
2016 Gan-Or Z, Zhou S, Johnson A, Montplaisir JY, Allen RP, Earley CJ, Desautels A, Dion PA, Xiong L, Rouleau GA. Case-Control and Family-Based Association Study of Specific Variants in Restless Legs Syndrome. Movement Disorders Clinical Practice. 3: 460-464. PMID 30363591 DOI: 10.1002/Mdc3.12306  0.453
2016 Gan-Or Z, Montplaisir JY, Ross JP, Poirier J, Warby SC, Arnulf I, Strong S, Dauvilliers Y, Leblond CS, Hu MT, Högl B, Stefani A, Monaca CC, De Cock VC, Boivin M, ... ... Desautels A, et al. The dementia-associated APOE ε4 allele is not associated with rapid eye movement sleep behavior disorder. Neurobiology of Aging. PMID 27814994 DOI: 10.1016/J.Neurobiolaging.2016.10.002  0.459
2016 Gan-Or Z, Mohsin N, Girard SL, Montplaisir JY, Ambalavanan A, Strong S, Mallett V, Laurent SB, Bourassa CV, Boivin M, Langlois M, Arnulf I, Högl B, Frauscher B, Monaca C, ... Desautels A, et al. The role of the melanoma gene MC1R in Parkinson disease and REM sleep behavior disorder. Neurobiology of Aging. PMID 27131830 DOI: 10.1016/J.Neurobiolaging.2016.03.029  0.43
2015 Gan-Or Z, Mirelman A, Postuma RB, Arnulf I, Bar-Shira A, Dauvilliers Y, Desautels A, Gagnon JF, Leblond CS, Frauscher B, Alcalay RN, Saunders-Pullman R, Bressman SB, Marder K, Monaca C, et al. GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder. Annals of Clinical and Translational Neurology. 2: 941-5. PMID 26401515 DOI: 10.1002/Acn3.228  0.422
2015 Gan-Or Z, Zhou S, Ambalavanan A, Leblond CS, Xie P, Johnson A, Spiegelman D, Allen RP, Earley CJ, Desautels A, Montplaisir JY, Dion PA, Xiong L, Rouleau GA. Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndrome. Sleep Medicine. 16: 1151-5. PMID 26298793 DOI: 10.1016/J.Sleep.2015.06.002  0.456
2015 Gan-Or Z, Girard SL, Noreau A, Leblond CS, Gagnon JF, Arnulf I, Mirarchi C, Dauvilliers Y, Desautels A, Mitterling T, Cochen De Cock V, Frauscher B, Monaca C, Hogl B, Dion PA, et al. Parkinson's Disease Genetic Loci in Rapid Eye Movement Sleep Behavior Disorder. Journal of Molecular Neuroscience : Mn. 56: 617-22. PMID 25929833 DOI: 10.1007/S12031-015-0569-7  0.469
2014 Daoud H, Postuma RB, Bourassa CV, Rochefort D, Gauthier MT, Montplaisir J, Gagnon JF, Arnulf I, Dauvilliers Y, Charley CM, Inoue Y, Sasai T, Högl B, Desautels A, Frauscher B, et al. C9orf72 repeat expansions in rapid eye movement sleep behaviour disorder. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 41: 759-62. PMID 25377888 DOI: 10.1017/Cjn.2014.39  0.421
2013 Faraco J, Lin L, Kornum BR, Kenny EE, Trynka G, Einen M, Rico TJ, Lichtner P, Dauvilliers Y, Arnulf I, Lecendreux M, Javidi S, Geisler P, Mayer G, Pizza F, ... ... Desautels A, et al. ImmunoChip study implicates antigen presentation to T cells in narcolepsy. Plos Genetics. 9: e1003270. PMID 23459209 DOI: 10.1371/Journal.Pgen.1003270  0.448
2011 Kornum BR, Kawashima M, Faraco J, Lin L, Rico TJ, Hesselson S, Axtell RC, Kuipers H, Weiner K, Hamacher A, Kassack MU, Han F, Knudsen S, Li J, Dong X, ... ... Desautels A, et al. Common variants in P2RY11 are associated with narcolepsy. Nature Genetics. 43: 66-71. PMID 21170044 DOI: 10.1038/Ng.734  0.579
2011 Kornum BR, Kawashima M, Faraco J, Lin L, Rico TJ, Hesselson S, Axtell RC, Kuipers H, Weiner K, Hamacher A, Kassack MU, Han F, Knudsen S, Li J, Dong X, ... ... Desautels A, et al. Erratum: Common variants in P2RY11 are associated with narcolepsy Nature Genetics. 43: 1040-1040. DOI: 10.1038/Ng1011-1040B  0.532
2010 Xiong L, Montplaisir J, Desautels A, Barhdadi A, Turecki G, Levchenko A, Thibodeau P, Dubé MP, Gaspar C, Rouleau GA. Family study of restless legs syndrome in Quebec, Canada: clinical characterization of 671 familial cases. Archives of Neurology. 67: 617-22. PMID 20457962 DOI: 10.1001/Archneurol.2010.67  0.513
2009 Hallmayer J, Faraco J, Lin L, Hesselson S, Winkelmann J, Kawashima M, Mayer G, Plazzi G, Nevsimalova S, Bourgin P, Hong SC, Hong SS, Honda Y, Honda M, Högl B, ... ... Desautels A, et al. Narcolepsy is strongly associated with the T-cell receptor alpha locus. Nature Genetics. 41: 708-11. PMID 19412176 DOI: 10.1038/Ng.372  0.614
2009 Levchenko A, Montplaisir JY, Asselin G, Provost S, Girard SL, Xiong L, Lemyre E, St-Onge J, Thibodeau P, Desautels A, Turecki G, Gaspar C, Dubé MP, Rouleau GA. Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 40-50. PMID 18946881 DOI: 10.1002/Mds.22263  0.583
2009 Hallmayer J, Faraco J, Lin L, Hesselson S, Winkelmann J, Kawashima M, Mayer G, Plazzi G, Nevsimalova S, Bourgin P, Hong SS, Honda Y, Honda M, Högl B, Longstreth WT, ... ... Desautels A, et al. Erratum: Narcolepsy is strongly associated with the T-cell receptor alpha locus Nature Genetics. 41: 859-859. DOI: 10.1038/Ng0709-859B  0.535
2008 Xiong L, Levchenko A, Montplaisir J, Rivière JB, Thibodeau P, St-Onge J, Gaspar C, Desautels A, Lespérance P, Chouinard S, Turecki G, Rouleau GA. Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians. Sleep Medicine. 9: 273-82. PMID 17644423 DOI: 10.1016/J.Sleep.2007.03.020  0.602
2007 Xiong L, Dion P, Montplaisir J, Levchenko A, Thibodeau P, Karemera L, Rivière JB, St-Onge J, Gaspar C, Dubé MP, Desautels A, Turecki G, Rouleau GA. Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 144: 911-7. PMID 17510944 DOI: 10.1002/Ajmg.B.30528  0.57
2006 Levchenko A, Provost S, Montplaisir JY, Xiong L, St-Onge J, Thibodeau P, Rivière JB, Desautels A, Turecki G, Dubé MP, Rouleau GA. A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13. Neurology. 67: 900-1. PMID 16966564 DOI: 10.1212/01.Wnl.0000233991.20410.B6  0.565
2005 Desautels A, Turecki G, Montplaisir J, Xiong L, Walters AS, Ehrenberg BL, Brisebois K, Desautels AK, Gingras Y, Johnson WG, Lugaresi E, Coccagna G, Picchietti DL, Lazzarini A, Rouleau GA. Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity. Archives of Neurology. 62: 591-6. PMID 15824258 DOI: 10.1001/Archneur.62.4.591  0.574
2004 Levchenko A, Montplaisir JY, Dubé MP, Riviere JB, St-Onge J, Turecki G, Xiong L, Thibodeau P, Desautels A, Verlaan DJ, Rouleau GA. The 14q restless legs syndrome locus in the French Canadian population. Annals of Neurology. 55: 887-91. PMID 15174026 DOI: 10.1002/Ana.20140  0.569
2004 Sequeira A, Mamdani F, Lalovic A, Anguelova M, Lesage A, Seguin M, Chawky N, Desautels A, Turecki G. Alpha 2A adrenergic receptor gene and suicide. Psychiatry Research. 125: 87-93. PMID 15006432 DOI: 10.1016/J.Psychres.2003.12.002  0.65
2004 Desautels A, Turecki G, Xiong L, Rochefort D, Montplaisir J, Rouleau GA. Mutational analysis of neurotensin in familial restless legs syndrome. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 90-4. PMID 14743366 DOI: 10.1002/Mds.10617  0.579
2003 Desautels A, Turecki G, Montplaisir J, Brisebois K, Desautels AK, Adam B, Rouleau GA. Analysis of CAG repeat expansions in restless legs syndrome. Sleep. 26: 1055-7. PMID 14746390 DOI: 10.1093/Sleep/26.8.1055  0.559
2003 Sequeira A, Kim C, Seguin M, Lesage A, Chawky N, Desautels A, Tousignant M, Vanier C, Lipp O, Benkelfat C, Rouleau G, Turecki G. Wolfram syndrome and suicide: Evidence for a role of WFS1 in suicidal and impulsive behavior. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 119: 108-13. PMID 12707947 DOI: 10.1002/Ajmg.B.20011  0.74
2002 Desautels A, Michaud M, Montplaisir J, Turecki G, Rouleau GA. [Restless leg syndrome: clinical aspects, etiology and genetic factors]. Revue Neurologique. 158: 1225-31. PMID 12690746  0.426
2002 Desautels A, Michaud M, Montplaisir J, Turecki G, Rouleau GA. [Restless leg syndrome arousal: clinic, etiology and genetic perspectives] Revue Neurologique. 158: 1225-31. PMID 12500149  0.428
2002 Desautels A, Turecki G, Montplaisir J, Brisebois K, Sequeira A, Adam B, Rouleau GA. Evidence for a genetic association between monoamine oxidase A and restless legs syndrome. Neurology. 59: 215-9. PMID 12136060 DOI: 10.1212/Wnl.59.2.215  0.739
2002 Desautels A, Turecki G, Montplaisir J, Rouleau G. Reply to Kock et al. The American Journal of Human Genetics. 71: 208. DOI: 10.1086/341098  0.55
2001 Desautels A, Turecki G, Montplaisir J, Sequeira A, Verner A, Rouleau GA. Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q. American Journal of Human Genetics. 69: 1266-70. PMID 11704926 DOI: 10.1086/324649  0.735
2001 Desautels A, Turecki G, Montplaisir J, Ftouhi-Paquin N, Michaud M, Chouinard VA, Rouleau GA. Dopaminergic neurotransmission and restless legs syndrome: a genetic association analysis. Neurology. 57: 1304-6. PMID 11591853 DOI: 10.1212/Wnl.57.7.1304  0.592
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