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Guy Rouleau

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Valdmanis Paul N; Belzil Veronique V; Lee James; Dion Patrick A; St-Onge Judith; Hince Pascale; Funalot Benoit; Couratier Philippe; Clavelou Pierre; Camu William; Rouleau Guy A
A mutation that creates a pseudoexon in SOD1 causes familial ALS.
Dion Patrick A; Daoud Hussein; Rouleau Guy A
Genetics of motor neuron disorders: new insights into pathogenic mechanisms.
Rivière Jean-Baptiste; Xiong Lan; Levchenko Anastasia; St-Onge Judith; Gaspar Claudia; Dion Yves; Lespérance Paul; Tellier Geneviève; Richer François; Chouinard Sylvain; Rouleau Guy A;
Association of intronic variants of the BTBD9 gene with Tourette syndrome.

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All Publications

2009: Valdmanis Paul N; Belzil Veronique V; Lee James; Dion Patrick A; St-Onge Judith; Hince Pascale; Funalot Benoit; Couratier Philippe; Clavelou Pierre; Camu William; Rouleau Guy A
A mutation that creates a pseudoexon in SOD1 causes familial ALS.
Annals of human genetics 2009;73(Pt 6):652-7.
2009: Dion Patrick A; Daoud Hussein; Rouleau Guy A
Genetics of motor neuron disorders: new insights into pathogenic mechanisms.
Nature reviews. Genetics 2009;10(11):769-82.
2009: Rivière Jean-Baptiste; Xiong Lan; Levchenko Anastasia; St-Onge Judith; Gaspar Claudia; Dion Yves; Lespérance Paul; Tellier Geneviève; Richer François; Chouinard Sylvain; Rouleau Guy A;
Association of intronic variants of the BTBD9 gene with Tourette syndrome.
Archives of neurology 2009;66(10):1267-72.
2009: Belzil V V; Valdmanis P N; Dion P A; Daoud H; Kabashi E; Noreau A; Gauthier J; Hince P; Desjarlais A; Bouchard J-P; Lacomblez L; Salachas F; Pradat P-F; Camu W; Meininger V; Dupré N; Rouleau G A
Mutations in FUS cause FALS and SALS in French and French Canadian populations.
Neurology 2009;73(15):1176-9.
2009: Srour M; Philibert M; Dion M-H; Duquette A; Richer F; Rouleau G A; Chouinard S
Familial congenital mirror movements: report of a large 4-generation family.
Neurology 2009;73(9):729-31.
2009: Hamdan Fadi F; Piton Amélie; Gauthier Julie; Lortie Anne; Dubeau François; Dobrzeniecka Sylvia; Spiegelman Dan; Noreau Anne; Pellerin Stéphanie; Côté Mélanie; Henrion Edouard; Fombonne Eric; Mottron Laurent; Marineau Claude; Drapeau Pierre; Lafrenière Ronald G; Lacaille Jean Claude; Rouleau Guy A; Michaud Jacques L
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.
Annals of neurology 2009;65(6):748-53.
2009: Messaed C; Rouleau G A
Molecular mechanisms underlying polyalanine diseases.
Neurobiology of disease 2009;34(3):397-405.
2009: Valdmanis Paul N; Daoud Hussein; Dion Patrick A; Rouleau Guy A
Recent advances in the genetics of amyotrophic lateral sclerosis.
Current neurology and neuroscience reports 2009;9(3):198-205.
2009: Duan Qing Ling; Binkley Karen; Rouleau Guy A
Genetic analysis of Factor XII and bradykinin catabolic enzymes in a family with estrogen-dependent inherited angioedema.
The Journal of allergy and clinical immunology 2009;123(4):906-10.
2009: McCaffery Jeanne M; Duan Qing Ling; Frasure-Smith Nancy; Barhdadi Amina; Lespérance Francois; Théroux Pierre; Rouleau Guy A; Dubé Marie-Pierre
Genetic predictors of depressive symptoms in cardiac patients.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(3):381-8.
2009: Gauthier Julie; Spiegelman Dan; Piton Amélie; Lafrenière Ronald G; Laurent Sandra; St-Onge Judith; Lapointe Line; Hamdan Fadi F; Cossette Patrick; Mottron Laurent; Fombonne Eric; Joober Ridha; Marineau Claude; Drapeau Pierre; Rouleau Guy A
Novel de novo SHANK3 mutation in autistic patients.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(3):421-4.
2009: Rivière Jean-Baptiste; Dion Patrick; Shekarabi Masoud; Girard Nathalie; Faivre Laurence; Lafrenière Ronald G; Samuels Mark; Rouleau Guy A
[Mutations in the HSN2 exon of WNK1 cause hereditary sensory neuropathy type II]
Médecine sciences : M/S 2009;25(3):235-8.
2009: Valdmanis Paul N; Verlaan Dominique J; Rouleau Guy A
The proportion of mutations predicted to have a deleterious effect differs between gain and loss of function genes in neurodegenerative disease.
Human mutation 2009;30(3):E481-9.
2009: Kabashi Edor; Daoud Hussein; Rivière Jean-Baptiste; Valdmanis Paul N; Bourgouin Patrick; Provencher Pierre; Pourcher Emmanuelle; Dion Patrick; Dupré Nicolas; Rouleau Guy A
No TARDBP mutations in a French Canadian population of patients with Parkinson disease.
Archives of neurology 2009;66(2):281-2.
2009: Hamdan Fadi F; Gauthier Julie; Spiegelman Dan; Noreau Anne; Yang Yan; Pellerin Stéphanie; Dobrzeniecka Sylvia; Côté Mélanie; Perreau-Linck Elizabeth; Carmant Lionel; D'Anjou Guy; Fombonne Eric; Addington Anjene M; Rapoport Judith L; Delisi Lynn E; Krebs Marie-Odile; Mouaffak Faycal; Joober Ridha; Mottron Laurent; Drapeau Pierre; Marineau Claude; Lafrenière Ronald G; Lacaille Jean Claude; Rouleau Guy A; Michaud Jacques L;
Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation.
The New England journal of medicine 2009;360(6):599-605.
2009: Daoud H; Valdmanis P N; Kabashi E; Dion P; Dupré N; Camu W; Meininger V; Rouleau G A
Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.
Journal of medical genetics 2009;46(2):112-4.
2009: Sequeira Adolfo; Mamdani Firoza; Ernst Carl; Vawter Marquis P; Bunney William E; Lebel Veronique; Rehal Sonia; Klempan Tim; Gratton Alain; Benkelfat Chawki; Rouleau Guy A; Mechawar Naguib; Turecki Gustavo
Global brain gene expression analysis links glutamatergic and GABAergic alterations to suicide and major depression.
PloS one 2009;4(8):e6585.
2008: Piton Amélie; Michaud Jacques L; Peng Huashan; Aradhya Swaroop; Gauthier Julie; Mottron Laurent; Champagne Nathalie; Lafrenière Ronald G; Hamdan Fadi F; Joober Ridha; Fombonne Eric; Marineau Claude; Cossette Patrick; Dubé Marie-Pierre; Haghighi Pejmun; Drapeau Pierre; Barker Philip A; Carbonetto Salvatore; Rouleau Guy A
Mutations in the calcium-related gene IL1RAPL1 are associated with autism.
Human molecular genetics 2008;17(24):3965-74.
2008: Meijer Inge A; Simoes-Lopes Ana A; Laurent Sandra; Katz Tanya; St-Onge Judith; Verlaan Dominique J; Dupré Nicolas; Thibault Manon; Mathurin Johanne; Bouchard Jean-Pierre; Rouleau Guy A
A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophy.
Archives of neurology 2008;65(11):1496-501.
2008: Salin-Cantegrel Adèle; Shekarabi Masoud; Holbert Sébastien; Dion Patrick; Rochefort Daniel; Laganière Janet; Dacal Sandra; Hince Pascale; Karemera Liliane; Gaspar Claudia; Lapointe Jean-Yves; Rouleau Guy A
HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl- co-transporter 3.
Human molecular genetics 2008;17(17):2703-11.
2008: Gros-Louis Francois; Kriz Jasna; Kabashi Edor; McDearmid Jonathan; Millecamps Stéphanie; Urushitani Makoto; Lin Li; Dion Patrick; Zhu Qinzhang; Drapeau Pierre; Julien Jean-Pierre; Rouleau Guy A
Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish.
Human molecular genetics 2008;17(17):2691-702.
2008: Moeller Jeremy J; Macaulay Robert J B; Valdmanis Paul N; Weston Lyle E; Rouleau Guy A; Dupré Nicolas
Autosomal dominant sensory ataxia: a neuroaxonal dystrophy.
Acta neuropathologica 2008;116(3):331-6.
2008: Valdmanis P N; Kabashi E; Dyck A; Hince P; Lee J; Dion P; D'Amour M; Souchon F; Bouchard J-P; Salachas F; Meininger V; Andersen P M; Camu W; Dupré N; Rouleau G A
Association of paraoxonase gene cluster polymorphisms with ALS in France, Quebec, and Sweden.
Neurology 2008;71(7):514-20.
2008: Khoury Samar; Rouleau Guy A; Rompré Pierre H; Mayer Pierre; Montplaisir Jacques Y; Lavigne Gilles J
A significant increase in breathing amplitude precedes sleep bruxism.
Chest 2008;134(2):332-7.
2008: Shekarabi Masoud; Girard Nathalie; Rivière Jean-Baptiste; Dion Patrick; Houle Martin; Toulouse André; Lafrenière Ronald G; Vercauteren Freya; Hince Pascale; Laganiere Janet; Rochefort Daniel; Faivre Laurence; Samuels Mark; Rouleau Guy A
Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II.
The Journal of clinical investigation 2008;118(7):2496-505.
2008: Catoire Hélène; Pasco Matthieu Y; Abu-Baker Aida; Holbert Sébastien; Tourette Cendrine; Brais Bernard; Rouleau Guy A; Parker J Alex; Néri Christian
Sirtuin inhibition protects from the polyalanine muscular dystrophy protein PABPN1.
Human molecular genetics 2008;17(14):2108-17.
2008: Kabashi Edor; Valdmanis Paul N; Dion Patrick; Spiegelman Dan; McConkey Brendan J; Vande Velde Christine; Bouchard Jean-Pierre; Lacomblez Lucette; Pochigaeva Ksenia; Salachas Francois; Pradat Pierre-Francois; Camu William; Meininger Vincent; Dupre Nicolas; Rouleau Guy A
TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.
Nature genetics 2008;40(5):572-4.
2008: Klein Arnaud F; Ebihara Mitsuru; Alexander Christine; Dicaire Marie-Josée; Sasseville A Marie-Josée; Langelier Yves; Rouleau Guy A; Brais Bernard
PABPN1 polyalanine tract deletion and long expansions modify its aggregation pattern and expression.
Experimental cell research 2008;314(8):1652-66.
2008: Valdmanis Paul N; Dupré Nicolas; Rouleau Guy A
A locus for primary lateral sclerosis on chromosome 4ptel-4p16.1.
Archives of neurology 2008;65(3):383-6.
2008: Kinirons Peter; Verlaan Dominique J; Dubé Marie-Pierre; Poirier Josée; Deacon Charles; Lortie Anne; Clément Jean-François; Desbiens Richard; Carmant Lionel; Cieuta-Walti Cecile; Shevell Michael; Rouleau Guy A; Cossette Patrick
A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11.
American journal of medical genetics. Part A 2008;146A(5):578-84.
2008: Xiong Lan; Levchenko Anastasia; Montplaisir Jacques; Rivière Jean-Baptiste; Thibodeau Pascale; St-Onge Judith; Gaspar Claudia; Desautels Alex; Lespérance Paul; Chouinard Sylvain; Turecki Gustavo; Rouleau Guy A
Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians.
Sleep medicine 2008;9(3):273-82.
2008: Valdmanis Paul N; Kabashi Edor; Dion Patrick A; Rouleau Guy A
ALS predisposition modifiers: knock NOX, who's there? SOD1 mice still are.
European journal of human genetics : EJHG 2008;16(2):140-2.
2008: Valdmanis Paul N; Rouleau Guy A
Genetics of familial amyotrophic lateral sclerosis.
Neurology 2008;70(2):144-52.
2008: Fathalli Ferid; Rouleau Guy A; Xiong Lan; Tabbane Karim; Benkelfat Chawki; Deguzman Rosherrie; Zoltan Danics; Lal Samarthji; D'cruz Sarogini; Joober Ridha
No association between the DRD3 Ser9Gly polymorphism and schizophrenia.
Schizophrenia research 2008;98(1-3):98-104.
2007: Kabashi Edor; Valdmanis Paul N; Dion Patrick; Rouleau Guy A
Oxidized/misfolded superoxide dismutase-1: the cause of all amyotrophic lateral sclerosis?
Annals of neurology 2007;62(6):553-9.
2007: Zouk Hana; McGirr Alexander; Lebel Véronique; Benkelfat Chawky; Rouleau Guy; Turecki Gustavo
The effect of genetic variation of the serotonin 1B receptor gene on impulsive aggressive behavior and suicide.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(8):996-1002.
2007: Martins Sandra; Calafell Francesc; Gaspar Claudia; Wong Virginia C N; Silveira Isabel; Nicholson Garth A; Brunt Ewout R; Tranebjaerg Lisbeth; Stevanin Giovanni; Hsieh Mingli; Soong Bing-Wen; Loureiro Leal; Dürr Alexandra; Tsuji Shoji; Watanabe Mitsunori; Jardim Laura B; Giunti Paola; Riess Olaf; Ranum Laura P W; Brice Alexis; Rouleau Guy A; Coutinho Paula; Amorim António; Sequeiros Jorge
Asian origin for the worldwide-spread mutational event in Machado-Joseph disease.
Archives of neurology 2007;64(10):1502-8.
2007: Xiong Lan; Dion Patrick; Montplaisir Jacques; Levchenko Anastasia; Thibodeau Pascale; Karemera Liliane; Rivière Jean-Baptiste; St-Onge Judith; Gaspar Claudia; Dubé Marie-Pierre; Desautels Alex; Turecki Gustavo; Rouleau Guy A
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 2007;144B(7):911-7.
2007: Salin-Cantegrel A; Rivière J-B; Dupré N; Charron F M; Shekarabi M; Karéméra L; Gaspar C; Horst J; Tekin M; Deda G; Krause A; Lippert M M; Willemsen M A A P; Jarrar R; Lapointe J-Y; Rouleau G A
Distal truncation of KCC3 in non-French Canadian HMSN/ACC families.
Neurology 2007;69(13):1350-5.
2007: Ahmad Sultan; Dahllund Leif; Eriksson Anders B; Hellgren Dennis; Karlsson Urban; Lund Per-Eric; Meijer Inge A; Meury Luc; Mills Tracy; Moody Adrian; Morinville Anne; Morten John; O'donnell Dajan; Raynoschek Carina; Salter Hugh; Rouleau Guy A; Krupp Johannes J
A stop codon mutation in SCN9A causes lack of pain sensation.
Human molecular genetics 2007;16(17):2114-21.
2007: Dupré Nicolas; Rivière Jean-Baptiste; Myers Richard H; Provencher Pierre; Pourcher Emmanuelle; Emond François; Rouleau Guy A
LRRK2 is not a significant cause of Parkinson's disease in French-Canadians.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2007;34(3):333-5.
2007: Dupré Nicolas; Gros-Louis François; Chrestian Nicolas; Verreault Steve; Brunet Denis; de Verteuil Danielle; Brais Bernard; Bouchard Jean-Pierre; Rouleau Guy A
Clinical and genetic study of autosomal recessive cerebellar ataxia type 1.
Annals of neurology 2007;62(1):93-8.
2007: Sequeira A; Klempan T; Canetti L; ffrench-Mullen J; Benkelfat C; Rouleau G A; Turecki G
Patterns of gene expression in the limbic system of suicides with and without major depression.
Molecular psychiatry 2007;12(7):640-55.
2007: Beetz Christian; Zuchner Stephan; Ashley-Koch Allison; Auer-Grumbach Michaela; Byrne Paula; Chinnery Patrick F; Hutchinson Michael; McDermott Christopher J; Meijer Inge A; Nygren Anders O H; Pericak-Vance Margaret; Pyle Angela; Rouleau Guy A; Schickel Jörg; Shaw Pamela J; Deufel Thomas
Linkage to a known gene but no mutation identified: comprehensive reanalysis of SPG4 HSP pedigrees reveals large deletions as the sole cause.
Human mutation 2007;28(7):739-40.
2007: Lopez de Lara Catalina; Brezo Jelena; Rouleau Guy; Lesage Alain; Dumont Mimi; Alda Martin; Benkelfat Chawki; Turecki Gustavo
Effect of tryptophan hydroxylase-2 gene variants on suicide risk in major depression.
Biological psychiatry 2007;62(1):72-80.
2007: Meijer Inge A; Dion Patrick; Laurent Sandra; Dupré Nicolas; Brais Bernard; Levert Annie; Puymirat Jacques; Rioux Marie France; Sylvain Michel; Zhu Peng-Peng; Soderblom Cynthia; Stadler Julia; Blackstone Craig; Rouleau Guy A
Characterization of a novel SPG3A deletion in a French-Canadian family.
Annals of neurology 2007;61(6):599-603.
2007: Messaed Christiane; Dion Patrick A; Abu-Baker Aida; Rochefort Daniel; Laganiere Janet; Brais Bernard; Rouleau Guy A
Soluble expanded PABPN1 promotes cell death in oculopharyngeal muscular dystrophy.
Neurobiology of disease 2007;26(3):546-57.
2007: Duan Qing Ling; Dubé Marie-Pierre; Frasure-Smith Nancy; Barhdadi Amina; Lesperance François; Théroux Pierre; St-Onge Judith; Rouleau Guy A; McCaffery Jeanne M
Additive effects of obesity and TCF7L2 variants on risk for type 2 diabetes among cardiac patients.
Diabetes care 2007;30(6):1621-3.
2007: Meijer Inge A; Dupré Nicolas; Brais Bernard; Cossette Patrick; St-Onge Judith; Rioux Marie-France; Benard Melanie; Rouleau Guy A
SPG4 founder effect in French Canadians with hereditary spastic paraplegia.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2007;34(2):211-4.
2007: Xiong L; Jang K; Montplaisir J; Levchenko A; Thibodeau P; Gaspar C; Turecki G; Rouleau G A
Canadian restless legs syndrome twin study.
Neurology 2007;68(19):1631-3.
2007: Lemay M; Termoz N; Lesperance P; Chouinard S; Rouleau G A; Richer F
Postural control anomalies in children with Tourette syndrome.
Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale 2007;179(3):525-30.
2007: Dupré Nicolas; Valdmanis Paul N; Bouchard Jean-Pierre; Rouleau Guy A
Autosomal dominant primary lateral sclerosis.
Neurology 2007;68(14):1156-7.
2007: Dupré Nicolas; Bouchard Jean-Pierre; Gros-Louis François; Rouleau Guy A
[Mutations in SYNE-1 lead to a newly discovered form of autosomal recessive cerebellar ataxia]
Médecine sciences : M/S 2007;23(3):261-2.
2007: Valdmanis Paul N; Dupre Nicolas; Bouchard Jean-Pierre; Camu William; Salachas François; Meininger Vincent; Strong Michael; Rouleau Guy A
Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p.
Archives of neurology 2007;64(2):240-5.
2007: Abu-Baker Aida; Rouleau Guy A
Oculopharyngeal muscular dystrophy: recent advances in the understanding of the molecular pathogenic mechanisms and treatment strategies.
Biochimica et biophysica acta 2007;1772(2):173-85.
2007: Valdmanis Paul N; Meijer Inge A; Reynolds Annie; Lei Adrienne; MacLeod Patrick; Schlesinger David; Zatz Mayana; Reid Evan; Dion Patrick A; Drapeau Pierre; Rouleau Guy A
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia.
American journal of human genetics 2007;80(1):152-61.
2007: Gros-Louis François; Dupré Nicolas; Dion Patrick; Fox Michael A; Laurent Sandra; Verreault Steve; Sanes Joshua R; Bouchard Jean-Pierre; Rouleau Guy A
Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
Nature genetics 2007;39(1):80-5.
2007: Rouleau Guy; Meijer Inge
CSCI/RCPSC Henry Friesen lecture: the past and the future of neurogenetics.
Clinical and investigative medicine. Médecine clinique et experimentale 2007;30(6):E269-73.
2007: Mamdani Firoza; Sequeira Adolfo; Alda Martin; Grof Paul; Rouleau Guy; Turecki Gustavo
No association between the PREP gene and lithium responsive bipolar disorder.
BMC psychiatry 2007;7():9.
2006: Valdmanis P N; Brunet D; St-Onge J; Weston L; Rouleau G A; Dupré N
A founder haplotype for autosomal dominant sensory ataxia in Eastern Canada.
Neurology 2006;67(12):2239-42.
2006: Jindal Hitesh K; Yoshinaga Kazumi; Seo Pil-Soo; Lutchman Mohini; Dion Patrick A; Rouleau Guy A; Hanada Toshihiko; Chishti Athar H
Purification of the NF2 tumor suppressor protein from human erythrocytes.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2006;33(4):394-402.
2006: Molinaro G; Duan Q L; Chagnon M; Moreau M E; Simon P; Clavel P; Lavaud S; Boileau G; Rouleau G A; Lepage Y; Adam A; Chanard J
Kinin-dependent hypersensitivity reactions in hemodialysis: metabolic and genetic factors.
Kidney international 2006;70(10):1823-31.
2006: Torkamanzehi Adam; Boksa Patricia; Ayoubi Mouhssine; Fortier Marie-Eve; Ng Ying Kin N M K; Skamene Emile; Rouleau Guy; Joober Ridha
Identification of informative strains and provisional QTL mapping of amphetamine (AMPH)-induced locomotion in recombinant congenic strains (RCS) of mice.
Behavior genetics 2006;36(6):903-13.
2006: Gros-Louis Francois; Gaspar Claudia; Rouleau Guy A
Genetics of familial and sporadic amyotrophic lateral sclerosis.
Biochimica et biophysica acta 2006;1762(11-12):956-72.
2006: Levchenko A; Provost S; Montplaisir J Y; Xiong L; St-Onge J; Thibodeau P; Rivière J B; Desautels A; Turecki G; Dubé M P; Rouleau G A
A novel autosomal dominant restless legs syndrome locus maps to chromosome 20p13.
Neurology 2006;67(5):900-1.
2006: Marie-Josée Sasseville A; Caron Antoine W; Bourget Lucie; Klein Arnaud F; Dicaire Marie-Josée; Rouleau Guy A; Massie Bernard; Langelier Yves; Brais Bernard
The dynamism of PABPN1 nuclear inclusions during the cell cycle.
Neurobiology of disease 2006;23(3):621-9.
2006: Thiffault I; Rioux M F; Tetreault M; Jarry J; Loiselle L; Poirier J; Gros-Louis F; Mathieu J; Vanasse M; Rouleau G A; Bouchard J P; Lesage J; Brais B
A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.
Brain : a journal of neurology 2006;129(Pt 9):2332-40.
2006: Verlaan D J; Dubé M-P; St-Onge J; Noreau A; Roussel J; Satgé N; Wallace M C; Rouleau G A
A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2-14.3.
Journal of medical genetics 2006;43(6):e31.
2006: Brinkman Ryan R; Dubé Marie-Pierre; Rouleau Guy A; Orr Andrew C; Samuels Mark E
Human monogenic disorders - a source of novel drug targets.
Nature reviews. Genetics 2006;7(4):249-60.
2006: McCaffery Jeanne M; Frasure-Smith Nancy; Dubé Marie-Pierre; Théroux Pierre; Rouleau Guy A; Duan Qingling; Lespérance Francois
Common genetic vulnerability to depressive symptoms and coronary artery disease: a review and development of candidate genes related to inflammation and serotonin.
Psychosomatic medicine 2006;68(2):187-200.
2006: Murdoch Sharlene; Djuric Ugljesa; Mazhar Batool; Seoud Muheiddine; Khan Rabia; Kuick Rork; Bagga Rashmi; Kircheisen Renate; Ao Asangla; Ratti Bhawna; Hanash Samir; Rouleau Guy A; Slim Rima
Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
Nature genetics 2006;38(3):300-2.
2006: Gauthier J; Joober R; Dubé M-P; St-Onge J; Bonnel A; Gariépy D; Laurent S; Najafee R; Lacasse H; St-Charles L; Fombonne E; Mottron L; Rouleau G A
Autism spectrum disorders associated with X chromosome markers in French-Canadian males.
Molecular psychiatry 2006;11(2):206-13.
2006: Sequeira Adolfo; Gwadry Fuad G; Ffrench-Mullen Jarlath M H; Canetti Lilian; Gingras Yves; Casero Robert A; Rouleau Guy; Benkelfat Chawki; Turecki Gustavo
Implication of SSAT by gene expression and genetic variation in suicide and major depression.
Archives of general psychiatry 2006;63(1):35-48.
2006: Lopez de Lara Catalina; Dumais Alexandre; Rouleau Guy; Lesage Alain; Dumont Mimi; Chawky Nadia; Alda Martin; Benkelfat Chawki; Turecki Gustavo
STin2 variant and family history of suicide as significant predictors of suicide completion in major depression.
Biological psychiatry 2006;59(2):114-20.
2006: Sengupta Sarojini; Xiong Lan; Fathalli Ferid; Benkelfat Chawki; Tabbane Karim; Danics Zoltan; Labelle Alain; Lal Samarthji; Krebs Marie-Odile; Rouleau Guy; Joober Ridha
Association study of the trinucleotide repeat polymorphism within SMARCA2 and schizophrenia.
BMC genetics 2006;7():34.
2005: Verlaan D J; Roussel J; Laurent S B; Elger C E; Siegel A M; Rouleau G A
CCM3 mutations are uncommon in cerebral cavernous malformations.
Neurology 2005;65(12):1982-3.
2005: Dumais A; Lesage A D; Alda M; Rouleau G; Dumont M; Chawky N; Roy M; Mann J J; Benkelfat C; Turecki Gustavo
Risk factors for suicide completion in major depression: a case-control study of impulsive and aggressive behaviors in men.
The American journal of psychiatry 2005;162(11):2116-24.
2005: Duan Qing Ling; Nikpoor Borzoo; Dube Marie-Pierre; Molinaro Giuseppe; Meijer Inge A; Dion Patrick; Rochefort Daniel; Saint-Onge Judith; Flury Leah; Brown Nancy J; Gainer James V; Rouleau Jean L; Agostoni Angelo; Cugno Massimo; Simon Pierre; Clavel Pierre; Potier Jacky; Wehbe Bassem; Benarbia Seddik; Marc-Aurele Julien; Chanard Jacques; Foroud Tatiana; Adam Albert; Rouleau Guy A
A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors.
American journal of human genetics 2005;77(4):617-26.
2005: Díaz-Anzaldúa Adriana; Rivière Jean-Baptiste; Dubé Marie-Pierre; Joober Ridha; Saint-Onge Judith; Dion Yves; Lespérance Paul; Richer Francois; Chouinard Sylvain; Rouleau Guy Armand;
Chromosome 11-q24 region in Tourette syndrome: association and linkage disequilibrium study in the French Canadian population.
American journal of medical genetics. Part A 2005;138A(3):225-8.
2005: Nikpoor Borzoo; Duan Qing Ling; Rouleau Guy A
Acute adverse reactions associated with angiotensin-converting enzyme inhibitors: genetic factors and therapeutic implications.
Expert opinion on pharmacotherapy 2005;6(11):1851-6.
2005: Abu-Baker Aida; Laganiere Simon; Fan Xueping; Laganiere Janet; Brais Bernard; Rouleau Guy A
Cytoplasmic targeting of mutant poly(A)-binding protein nuclear 1 suppresses protein aggregation and toxicity in oculopharyngeal muscular dystrophy.
Traffic (Copenhagen, Denmark) 2005;6(9):766-79.
2005: Toulouse André; Au-Yeung Faith; Gaspar Claudia; Roussel Julie; Dion Patrick; Rouleau Guy A
Ribosomal frameshifting on MJD-1 transcripts with long CAG tracts.
Human molecular genetics 2005;14(18):2649-60.
2005: Joober Ridha; Rouleau Guy A; Lal Samarthji; Bloom David; Lalonde Pierre; Labelle Alain; Benkelfat Chawki
Increased prevalence of schizophrenia spectrum disorders in relatives of neuroleptic-nonresponsive schizophrenic patients.
Schizophrenia research 2005;77(1):35-41.
2005: Gauthier Julie; de Amorim Giovana; Mnatzakanian Gevork N; Saunders Carol; Vincent John B; Toupin Sylvie; Kauffman David; St-Onge Judith; Laurent Sandra; Macleod Patrick M; Minassian Berge A; Rouleau Guy A
Clinical stringency greatly improves mutation detection in Rett syndrome.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2005;32(3):321-6.
2005: Millecamps Stéphanie; Gentil Benoît J; Gros-Louis François; Rouleau Guy; Julien Jean-Pierre
Alsin is partially associated with centrosome in human cells.
Biochimica et biophysica acta 2005;1745(1):84-100.
2005: Baser M E; Kuramoto L; Woods R; Joe H; Friedman J M; Wallace A J; Ramsden R T; Olschwang S; Bijlsma E; Kalamarides M; Papi L; Kato R; Carroll J; Lázaro C; Joncourt F; Parry D M; Rouleau G A; Evans D G R
The location of constitutional neurofibromatosis 2 (NF2) splice site mutations is associated with the severity of NF2.
Journal of medical genetics 2005;42(7):540-6.
2005: Alda Martin; Grof Paul; Rouleau Guy A; Turecki Gustavo; Young L Trevor
Investigating responders to lithium prophylaxis as a strategy for mapping susceptibility genes for bipolar disorder.
Progress in neuro-psychopharmacology & biological psychiatry 2005;29(6):1038-45.
2005: Roddier K; Thomas T; Marleau G; Gagnon A M; Dicaire M J; St-Denis A; Gosselin I; Sarrazin A M; Larbrisseau A; Lambert M; Vanasse M; Gaudet D; Rouleau G A; Brais B
Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians.
Neurology 2005;64(10):1762-7.
2005: Desautels Alex; Turecki Gustavo; Montplaisir Jacques; Xiong Lan; Walters Arthur S; Ehrenberg Bruce L; Brisebois Kateri; Desautels Amelie K; Gingras Yves; Johnson William G; Lugaresi Elio; Coccagna Giorgio; Picchietti Daniel L; Lazzarini Alice; Rouleau Guy A
Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity.
Archives of neurology 2005;62(4):591-6.
2005: Corbeil-Girard Louis-Philippe; Klein Arnaud F; Sasseville A Marie-Josée; Lavoie Hugo; Dicaire Marie-Josée; Saint-Denis Anik; Pagé Martin; Duranceau André; Codère François; Bouchard Jean-Pierre; Karpati George; Rouleau Guy A; Massie Bernard; Langelier Yves; Brais Bernard
PABPN1 overexpression leads to upregulation of genes encoding nuclear proteins that are sequestered in oculopharyngeal muscular dystrophy nuclear inclusions.
Neurobiology of disease 2005;18(3):551-67.
2005: Dion Patrick; Shanmugam Vijayalakshmi; Gaspar Claudia; Messaed Christiane; Meijer Inge; Toulouse André; Laganiere Janet; Roussel Julie; Rochefort Daniel; Laganiere Simon; Allen Carol; Karpati George; Bouchard Jean-Pierre; Brais Bernard; Rouleau Guy A
Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice.
Neurobiology of disease 2005;18(3):528-36.
2005: El-Maarri Osman; Seoud Muhieddine; Rivière Jean-Baptiste; Oldenburg Johannes; Walter Jörn; Rouleau Guy; Slim Rima
Patients with familial biparental hydatidiform moles have normal methylation at imprinted genes.
European journal of human genetics : EJHG 2005;13(4):486-90.
2005: Devon Rebecca S; Schwab Claudia; Topp Justin D; Orban Paul C; Yang Yu-Zhou; Pape Terry D; Helm Jeffrey R; Davidson Tara-Lynne; Rogers Daniel A; Gros-Louis Francois; Rouleau Guy; Horazdovsky Bruce F; Leavitt Blair R; Hayden Michael R
Cross-species characterization of the ALS2 gene and analysis of its pattern of expression in development and adulthood.
Neurobiology of disease 2005;18(2):243-57.
2005: Siegel A M; Bertalanffy H; Dichgans J J; Elger C E; Hopf H; Hopf N; Keidel M; Kleider A; Nowak G; Pfeiffer R A; Schramm J; Spuck S; Stefan H; Sure U; Baumann C R; Rouleau G A; Verlaan D J; Andermann E; Andermann F
[Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families]
Der Nervenarzt 2005;76(2):175-80.
2005: Xiong Lan; Rouleau Guy A; Delisi Lynn E; St-Onge Judith; Najafee Robert; Rivière Jean-Baptiste; Benkelfat Chawki; Tabbane Karim; Fathalli Ferid; Danics Zoltan; Labelle Alain; Lal Samarthji; Joober Ridha
CAA insertion polymorphism in the 3'UTR of Nogo gene on 2p14 is not associated with schizophrenia.
Brain research. Molecular brain research 2005;133(1):153-6.
2005: Gauthier Julie; Bonnel Anna; St-Onge Judith; Karemera Liliane; Laurent Sandra; Mottron Laurent; Fombonne Eric; Joober Ridha; Rouleau Guy A
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;132B(1):74-5.
2005: Cossette Patrick; Lortie Anne; Vanasse Michel; Saint-Hilaire Jean-Marc; Rouleau Guy A
Autosomal dominant juvenile myoclonic epilepsy and GABRA1.
Advances in neurology 2005;95():255-63.
2004: Grewal K K; Stefanelli M G; Meijer I A; Hand C K; Rouleau G A; Ives E J
A founder effect in three large Newfoundland families with a novel clinically variable spastic ataxia and supranuclear gaze palsy.
American journal of medical genetics. Part A 2004;131(3):249-54.
2004: Verlaan D J; Laurent S B; Rouleau G A; Siegel A M
No CCM2 mutations in a cohort of 31 sporadic cases.
Neurology 2004;63(10):1979.
2004: Rivière Jean-Baptiste; Verlaan Dominique J; Shekarabi Masoud; Lafrenière Ronald G; Bénard Mélanie; Der Kaloustian Vazken M; Shbaklo Zuhayr; Rouleau Guy A
A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family.
Annals of neurology 2004;56(4):572-5.
2004: Meijer Inge A; Cossette Patrick; Roussel Julie; Benard Melanie; Toupin Sylvie; Rouleau Guy A
A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1.
Annals of neurology 2004;56(4):579-82.
2004: Gros-Louis François; Larivière Roxanne; Gowing Geneviève; Laurent Sandra; Camu William; Bouchard Jean-Pierre; Meininger Vincent; Rouleau Guy A; Julien Jean-Pierre
A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis.
The Journal of biological chemistry 2004;279(44):45951-6.
2004: Lespérance P; Djerroud N; Diaz Anzaldua A; Rouleau G A; Chouinard S; Richer F;
Restless legs in Tourette syndrome.
Movement disorders : official journal of the Movement Disorder Society 2004;19(9):1084-7.
2004: Levchenko Anastasia; Robitaille Yves; Strong Michael J; Rouleau Guy A
TAU mutations are not a predominant cause of frontotemporal dementia in Canadian patients.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2004;31(3):363-7.
2004: Valdmanis P N; Simões Lopes A A; Gros-Louis F; Stewart J D; Rouleau G A; Dupré N
A novel neurodegenerative disease characterised by posterior column ataxia and pyramidal tract involvement maps to chromosome 8p12-8q12.1.
Journal of medical genetics 2004;41(8):634-9.
2004: Levchenko Anastasia; Montplaisir Jacques-Yves; Dubé Marie-Pierre; Riviere Jean-Baptiste; St-Onge Judith; Turecki Gustavo; Xiong Lan; Thibodeau Pascale; Desautels Alex; Verlaan Dominique J; Rouleau Guy A
The 14q restless legs syndrome locus in the French Canadian population.
Annals of neurology 2004;55(6):887-91.
2004: Verlaan Dominique J; Laurent Sandra B; Rochefort Daniel L; Liquori Christina L; Marchuk Douglas A; Siegel Adrian M; Rouleau Guy A
CCM2 mutations account for 13% of cases in a large collection of kindreds with hereditary cavernous malformations.
Annals of neurology 2004;55(5):757-8.
2004: Díaz-Anzaldúa Adriana; Joober Ridha; Rivière Jean-Baptiste; Dion Yves; Lespérance Paul; Chouinard Sylvain; Richer Francois; Rouleau Guy Armand
Association between 7q31 markers and Tourette syndrome.
American journal of medical genetics. Part A 2004;127A(1):17-20.
2004: Lafreniere Ronald G; MacDonald Marcia L E; Dube Marie-Pierre; MacFarlane Julie; O'Driscoll Mary; Brais Bernard; Meilleur Sebastien; Brinkman Ryan R; Dadivas Owen; Pape Terry; Platon Christele; Radomski Chris; Risler Jenni; Thompson Jay; Guerra-Escobio Ana-Maria; Davar Gudarz; Breakefield Xandra O; Pimstone Simon N; Green Roger; Pryse-Phillips William; Goldberg Y Paul; Younghusband H Banfield; Hayden Michael R; Sherrington Robin; Rouleau Guy A; Samuels Mark E;
Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates.
American journal of human genetics 2004;74(5):1064-73.
2004: Verlaan D J; Laurent S B; Sure U; Bertalanffy H; Andermann E; Andermann F; Rouleau G A; Siegel A M
CCM1 mutation screen of sporadic cases with cerebral cavernous malformations.
Neurology 2004;62(7):1213-5.
2004: Díaz-Anzaldúa A; Joober R; Rivière J-B; Dion Y; Lespérance P; Richer F; Chouinard S; Rouleau G A;
Tourette syndrome and dopaminergic genes: a family-based association study in the French Canadian founder population.
Molecular psychiatry 2004;9(3):272-7.
2004: Jafari-Schluep H F; Khoris J; Mayeux-Portas V; Hand C; Rouleau G; Camu W;
[Superoxyde dismutase 1 gene abnormalities in familial amyotrophic lateral sclerosis: phenotype/genotype correlations. The French experience and review of the literature]
Revue neurologique 2004;160(1):44-50.
2004: Desautels Alex; Turecki Gustavo; Xiong Lan; Rochefort Daniel; Montplaisir Jacques; Rouleau Guy A
Mutational analysis of neurotensin in familial restless legs syndrome.
Movement disorders : official journal of the Movement Disorder Society 2004;19(1):90-4.
2003: Forget-Dubois Nadine; Pérusse Daniel; Turecki Gustavo; Girard Alain; Billette Jean-Michel; Rouleau Guy; Boivin Michel; Malo Jocelyn; Tremblay Richard E
Diagnosing zygosity in infant twins: physical similarity, genotyping, and chorionicity.
Twin research : the official journal of the International Society for Twin Studies 2003;6(6):479-85.
2003: Desautels Alex; Turecki Gustavo; Montplaisir Jacques; Brisebois Katéri; Desautels Amélie K; Adam Benoît; Rouleau Guy A
Analysis of CAG repeat expansions in restless legs syndrome.
Sleep 2003;26(8):1055-7.
2003: Hand Collette K; Devon Rebecca S; Gros-Louis Francois; Rochefort Daniel; Khoris Jawad; Meininger Vincent; Bouchard Jean-Pierre; Camu William; Hayden Michael R; Rouleau Guy A
Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis.
Archives of neurology 2003;60(12):1768-71.
2003: Gros-Louis Francois; Laurent Sandra; Lopes Ana Amelia Simões; Khoris Jawad; Meininger Vincent; Camu William; Rouleau Guy A
Absence of mutations in the hypoxia response element of VEGF in ALS.
Muscle & nerve 2003;28(6):774-5.
2003: Liquori Christina L; Berg Michel J; Siegel Adrian M; Huang Elizabeth; Zawistowski Jon S; Stoffer T'Prien; Verlaan Dominique; Balogun Fiyinfolu; Hughes Lori; Leedom Tracey P; Plummer Nicholas W; Cannella Milena; Maglione Vittorio; Squitieri Ferdinando; Johnson Eric W; Rouleau Guy A; Ptacek Louis; Marchuk Douglas A
Mutations in a gene encoding a novel protein containing a phosphotyrosine-binding domain cause type 2 cerebral cavernous malformations.
American journal of human genetics 2003;73(6):1459-64.
2003: Lavoie Hugo; Debeane Francois; Trinh Quoc-Dien; Turcotte Jean-Francois; Corbeil-Girard Louis-Philippe; Dicaire Marie-Josée; Saint-Denis Anik; Pagé Martin; Rouleau Guy A; Brais Bernard
Polymorphism, shared functions and convergent evolution of genes with sequences coding for polyalanine domains.
Human molecular genetics 2003;12(22):2967-79.
2003: Koenekoop Robert K; Loyer Magali; Hand Collette K; Al Mahdi Huda; Dembinska Olga; Beneish Raquel; Racine Julie; Rouleau Guy A
Novel RPGR mutations with distinct retinitis pigmentosa phenotypes in French-Canadian families.
American journal of ophthalmology 2003;136(4):678-87.
2003: Abu-Baker Aida; Messaed Christiane; Laganiere Janet; Gaspar Claudia; Brais Bernard; Rouleau Guy A
Involvement of the ubiquitin-proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophy.
Human molecular genetics 2003;12(20):2609-23.
2003: Devon R S; Helm J R; Rouleau G A; Leitner Y; Lerman-Sagie T; Lev D; Hayden M R
The first nonsense mutation in alsin results in a homogeneous phenotype of infantile-onset ascending spastic paralysis with bulbar involvement in two siblings.
Clinical genetics 2003;64(3):210-5.
2003: Fan Xueping; Messaed Christiane; Dion Patrick; Laganiere Janet; Brais Bernard; Karpati George; Rouleau Guy A
HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2003;30(3):244-51.
2003: Toulouse André; Rochefort Daniel; Roussel Julie; Joober Ridha; Rouleau Guy A
Molecular cloning and characterization of human RAI1, a gene associated with schizophrenia.
Genomics 2003;82(2):162-71.
2003: Laurans Maxwell S H; DiLuna Michael L; Shin Dana; Niazi Faheem; Voorhees Jennifer R; Nelson-Williams Carol; Johnson Eric W; Siegel Adrian M; Steinberg Gary K; Berg Michel J; Scott R Michael; Tedeschi Gioacchino; Enevoldson T Peter; Anson John; Rouleau Guy A; Ogilvy Christopher; Awad Issam A; Lifton Richard P; Gunel Murat
Mutational analysis of 206 families with cavernous malformations.
Journal of neurosurgery 2003;99(1):38-43.
2003: Dupré Nicolas; Howard Heidi C; Mathieu Jean; Karpati George; Vanasse Michel; Bouchard Jean-Pierre; Carpenter Stirling; Rouleau Guy A
Hereditary motor and sensory neuropathy with agenesis of the corpus callosum.
Annals of neurology 2003;54(1):9-18.
2003: El-Maarri Osman; Seoud Muhieddine; Coullin Philippe; Herbiniaux Ursula; Oldenburg Johannes; Rouleau Guy; Slim Rima
Maternal alleles acquiring paternal methylation patterns in biparental complete hydatidiform moles.
Human molecular genetics 2003;12(12):1405-13.
2003: Dupré Nicolas; Verlaan Dominique J; Hand Collette K; Laurent Sandra B; Turecki Gustavo; Davenport W Jeptha; Acciarri Nicola; Dichgans Johannes; Ohkuma Akio; Siegel Adrian M; Rouleau Guy A
Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2003;30(2):122-8.
2003: Sequeira Adolfo; Kim Caroline; Seguin Monique; Lesage Alain; Chawky Nadia; Desautels Alex; Tousignant Michel; Vanier Claude; Lipp Olivier; Benkelfat Chawki; Rouleau Guy; Turecki Gustavo
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 2003;119B(1):108-13.
2003: Howard Heidi C; Dupré Nicolas; Mathieu Jean; Bouchard Jean-Pierre; Rouleau Guy A
[Severe neuropathy with agenesis of the corpus callosum]
Médecine sciences : M/S 2003;19(4):414-6.
2003: Gauthier Julie; Joober Ridha; Mottron Laurent; Laurent Sandra; Fuchs Marketa; De Kimpe Violaine; Rouleau Guy A
Mutation screening of FOXP2 in individuals diagnosed with autistic disorder.
American journal of medical genetics. Part A 2003;118A(2):172-5.
2003: Turecki G; Sequeira A; Gingras Y; Séguin M; Lesage A; Tousignant M; Chawky N; Vanier C; Lipp O; Benkelfat C; Rouleau G A
Suicide and serotonin: study of variation at seven serotonin receptor genes in suicide completers.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;118B(1):36-40.
2003: Fan Xueping; Rouleau Guy A
Progress in understanding the pathogenesis of oculopharyngeal muscular dystrophy.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2003;30(1):8-14.
2003: Cossette Patrick; Loukas Andrew; Lafrenière Ronald G; Rochefort Daniel; Harvey-Girard Eric; Ragsdale David S; Dunn Robert J; Rouleau Guy A
Functional characterization of the D188V mutation in neuronal voltage-gated sodium channel causing generalized epilepsy with febrile seizures plus (GEFS).
Epilepsy research 2003;53(1-2):107-17.
2003: Yamamoto Kenji; Cubells Joseph F; Gelernter Joel; Benkelfat Chawki; Lalonde Pierre; Bloom David; Lal Samarthji; Labelle Alain; Turecki Gustavo; Rouleau Guy A; Joober Ridha
Dopamine beta-hydroxylase (DBH) gene and schizophrenia phenotypic variability: a genetic association study.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;117B(1):33-8.
2003: Gros-Louis François; Meijer Inge A; Hand Collette K; Dubé Marie-Pierre; MacGregor Daune L; Seni Marie-Hélène; Devon Rebecca S; Hayden Michael R; Andermann Frederick; Andermann Eva; Rouleau Guy A
An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred.
Annals of neurology 2003;53(1):144-5.
2002: Desautels A; Michaud M; Montplaisir J; Turecki G; Rouleau G A
[Restless leg syndrome: clinical aspects, etiology and genetic factors]
Revue neurologique 2002;158(12 Pt 1):1225-31.
2002: Howard Heidi C; Mount David B; Rochefort Daniel; Byun Nellie; Dupré Nicolas; Lu Jianming; Fan Xuemo; Song Luyan; Rivière Jean-Baptiste; Prévost Claude; Horst Jürgen; Simonati Alessandro; Lemcke Beate; Welch Rick; England Roger; Zhan Frank Q; Mercado Adriana; Siesser William B; George Alfred L; McDonald Michael P; Bouchard Jean-Pierre; Mathieu Jean; Delpire Eric; Rouleau Guy A
The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum.
Nature genetics 2002;32(3):384-92.
2002: Zhao Y; Kumar R A; Baser M E; Evans D G R; Wallace A; Kluwe L; Mautner V F; Parry D M; Rouleau G A; Joe H; Friedman J M
Intrafamilial correlation of clinical manifestations in neurofibromatosis 2 (NF2).
Genetic epidemiology 2002;23(3):245-59.
2002: Joober Ridha; Boksa Patricia; Benkelfat Chawki; Rouleau Guy
Genetics of schizophrenia: from animal models to clinical studies.
Journal of psychiatry & neuroscience : JPN 2002;27(5):336-47.
2002: Desautels A; Turecki G; Montplaisir J; Brisebois K; Sequeira A; Adam B; Rouleau G A
Evidence for a genetic association between monoamine oxidase A and restless legs syndrome.
Neurology 2002;59(2):215-9.
2002: Howard Heidi C; Dubé Marie-Pierre; Prévost Claude; Bouchard Jean-Pierre; Mathieu Jean; Rouleau Guy A
Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population.
European journal of human genetics : EJHG 2002;10(7):406-12.
2002: Joober Ridha; Gauthier Julie; Lal Samarthji; Bloom David; Lalonde Pierre; Rouleau Guy; Benkelfat Chawki; Labelle Alain
Catechol-O-methyltransferase Val-108/158-Met gene variants associated with performance on the Wisconsin Card Sorting Test.
Archives of general psychiatry 2002;59(7):662-3.
2002: Cossette Patrick; Liu Lidong; Brisebois Katéri; Dong Haiheng; Lortie Anne; Vanasse Michel; Saint-Hilaire Jean-Marc; Carmant Lionel; Verner Andrei; Lu Wei-Yang; Wang Yu Tian; Rouleau Guy A
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.
Nature genetics 2002;31(2):184-9.
2002: Verlaan Dominique J; Siegel Adrian M; Rouleau Guy A
Krit1 missense mutations lead to splicing errors in cerebral cavernous malformation.
American journal of human genetics 2002;70(6):1564-7.
2002: Verlaan D J; Davenport W J; Stefan H; Sure U; Siegel A M; Rouleau G A
Cerebral cavernous malformations: mutations in Krit1.
Neurology 2002;58(6):853-7.
2002: Meijer I A; Hand C K; Grewal K K; Stefanelli M G; Ives E J; Rouleau G A
A locus for autosomal dominant hereditary spastic ataxia, SAX1, maps to chromosome 12p13.
American journal of human genetics 2002;70(3):763-9.
2002: Hand Collette K; Rouleau Guy A
Familial amyotrophic lateral sclerosis.
Muscle & nerve 2002;25(2):135-59.
2002: Meijer Inge A; Hand Collette K; Cossette P; Figlewicz Denise A; Rouleau Guy A
Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia.
Archives of neurology 2002;59(2):281-6.
2002: Joober Ridha; Rouleau Guy A; Lal Samarthji; Dixon Michael; O'Driscoll Gillian; Palmour Roberta; Annable Lawrence; Bloom David; Lalonde Pierre; Labelle Alain; Benkelfat Chawki
Neuropsychological impairments in neuroleptic-responder vs. -nonresponder schizophrenic patients and healthy volunteers.
Schizophrenia research 2002;53(3):229-38.
2002: Hand Collette K; Khoris Jawad; Salachas François; Gros-Louis François; Lopes Ana Amélia Simões; Mayeux-Portas Veronique; Brewer Carl G; Brown Robert H; Meininger Vincent; Camu William; Rouleau Guy A
A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q.
American journal of human genetics 2002;70(1):251-6.
2001: Desautels A; Turecki G; Montplaisir J; Sequeira A; Verner A; Rouleau G A
Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q.
American journal of human genetics 2001;69(6):1266-70.
2001: Maciel P; Costa M C; Ferro A; Rousseau M; Santos C S; Gaspar C; Barros J; Rouleau G A; Coutinho P; Sequeiros J
Improvement in the molecular diagnosis of Machado-Joseph disease.
Archives of neurology 2001;58(11):1821-7.
2001: Fan X; Dion P; Laganiere J; Brais B; Rouleau G A
Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell death.
Human molecular genetics 2001;10(21):2341-51.
2001: Desautels A; Turecki G; Montplaisir J; Ftouhi-Paquin N; Michaud M; Chouinard V A; Rouleau G A
Dopaminergic neurotransmission and restless legs syndrome: a genetic association analysis.
Neurology 2001;57(7):1304-6.
2001: Hadano S; Hand C K; Osuga H; Yanagisawa Y; Otomo A; Devon R S; Miyamoto N; Showguchi-Miyata J; Okada Y; Singaraja R; Figlewicz D A; Kwiatkowski T; Hosler B A; Sagie T; Skaug J; Nasir J; Brown R H; Scherer S W; Rouleau G A; Hayden M R; Ikeda J E
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.
Nature genetics 2001;29(2):166-73.
2001: Turecki G; Grof P; Grof E; D'Souza V; Lebuis L; Marineau C; Cavazzoni P; Duffy A; Bétard C; Zvolský P; Robertson C; Brewer C; Hudson T J; Rouleau G A; Alda M
Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithium.
Molecular psychiatry 2001;6(5):570-8.
2001: Nikpoor B; Turecki G; Fournier C; Théroux P; Rouleau G A
A functional myeloperoxidase polymorphic variant is associated with coronary artery disease in French-Canadians.
American heart journal 2001;142(2):336-9.
2001: Jannatipour M; Dion P; Khan S; Jindal H; Fan X; Laganière J; Chishti A H; Rouleau G A
Schwannomin isoform-1 interacts with syntenin via PDZ domains.
The Journal of biological chemistry 2001;276(35):33093-100.
2001: Alda M; Keller D; Grof E; Turecki G; Cavazzoni P; Duffy A; Rouleau G A; Grof P; Young L T
Is lithium response related to G(s)alpha levels in transformed lymphoblasts from subjects with bipolar disorder?
Journal of affective disorders 2001;65(2):117-22.
2001: Fortin A; Diez E; Rochefort D; Laroche L; Malo D; Rouleau G A; Gros P; Skamene E
Recombinant congenic strains derived from A/J and C57BL/6J: a tool for genetic dissection of complex traits.
Genomics 2001;74(1):21-35.
2001: Pramatarova A; Laganière J; Roussel J; Brisebois K; Rouleau G A
Neuron-specific expression of mutant superoxide dismutase 1 in transgenic mice does not lead to motor impairment.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2001;21(10):3369-74.
2001: Ftouhi-Paquin N; Alda M; Grof P; Chretien N; Rouleau G; Turecki G
Identification of three polymorphisms in the translated region of PLC-gamma1 and their investigation in lithium responsive bipolar disorder.
American journal of medical genetics 2001;105(3):301-5.
2001: Yamamoto K; Bloom D; La S; Turecki G; Joober R; Benkelfat C; Lalonde P; Labelle A; Rouleau G A
Polymorphism in the cell division cycle 45 like gene and schizophrenia.
American journal of medical genetics 2001;105(2):214-5.
2001: Dupré N; Cossette L; Hand C K; Bouchard J P; Rouleau G A; Puymirat J
A founder mutation in French-Canadian families with X-linked hereditary neuropathy.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2001;28(1):51-5.
2001: Davenport W J; Siegel A M; Dichgans J; Drigo P; Mammi I; Pereda P; Wood N W; Rouleau G A
CCM1 gene mutations in families segregating cerebral cavernous malformations.
Neurology 2001;56(4):540-3.
2001: Hand C K; Mayeux-Portas V; Khoris J; Briolotti V; Clavelou P; Camu W; Rouleau G A
Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family.
Annals of neurology 2001;49(2):267-71.
2001: Gaspar C; Lopes-Cendes I; Hayes S; Goto J; Arvidsson K; Dias A; Silveira I; Maciel P; Coutinho P; Lima M; Zhou Y X; Soong B W; Watanabe M; Giunti P; Stevanin G; Riess O; Sasaki H; Hsieh M; Nicholson G A; Brunt E; Higgins J J; Lauritzen M; Tranebjaerg L; Volpini V; Wood N; Ranum L; Tsuji S; Brice A; Sequeiros J; Rouleau G A
Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study.
American journal of human genetics 2001;68(2):523-8.
2001: Turecki G; Zhu Z; Tzenova J; Lesage A; Séguin M; Tousignant M; Chawky N; Vanier C; Lipp O; Alda M; Joober R; Benkelfat C; Rouleau G A
TPH and suicidal behavior: a study in suicide completers.
Molecular psychiatry 2001;6(1):98-102.
2001: Hadano S; Yanagisawa Y; Skaug J; Fichter K; Nasir J; Martindale D; Koop B F; Scherer S W; Nicholson D W; Rouleau G A; Ikeda J; Hayden M R
Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2.
Genomics 2001;71(2):200-13.
2001: Ichikawa Y; Goto J; Hattori M; Toyoda A; Ishii K; Jeong S Y; Hashida H; Masuda N; Ogata K; Kasai F; Hirai M; Maciel P; Rouleau G A; Sakaki Y; Kanazawa I
The genomic structure and expression of MJD, the Machado-Joseph disease gene.
Journal of human genetics 2001;46(7):413-22.
2000: Blumen S C; Korczyn A D; Lavoie H; Medynski S; Chapman J; Asherov A; Nisipeanu P; Inzelberg R; Carasso R L; Bouchard J P; Tomé F M; Rouleau G A; Brais B
Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene.
Neurology 2000;55(9):1267-70.
2000: Shanmugam V; Dion P; Rochefort D; Laganière J; Brais B; Rouleau G A
PABP2 polyalanine tract expansion causes intranuclear inclusions in oculopharyngeal muscular dystrophy.
Annals of neurology 2000;48(5):798-802.
2000: Lamartine J; Munhoz Essenfelder G; Kibar Z; Lanneluc I; Callouet E; Laoudj D; Lemaître G; Hand C; Hayflick S J; Zonana J; Antonarakis S; Radhakrishna U; Kelsell D P; Christianson A L; Pitaval A; Der Kaloustian V; Fraser C; Blanchet-Bardon C; Rouleau G A; Waksman G
Mutations in GJB6 cause hidrotic ectodermal dysplasia.
Nature genetics 2000;26(2):142-4.
2000: Duffy A; Turecki G; Grof P; Cavazzoni P; Grof E; Joober R; Ahrens B; Berghöfer A; Müller-Oerlinghausen B; Dvoráková M; Libigerová E; Vojtechovský M; Zvolský P; Nilsson A; Licht R W; Rasmussen N A; Schou M; Vestergaard P; Holzinger A; Schumann C; Thau K; Robertson C; Rouleau G A; Alda M
Association and linkage studies of candidate genes involved in GABAergic neurotransmission in lithium-responsive bipolar disorder.
Journal of psychiatry & neuroscience : JPN 2000;25(4):353-8.
2000: Gaspar C; Jannatipour M; Dion P; Laganière J; Sequeiros J; Brais B; Rouleau G A
CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulation.
Human molecular genetics 2000;9(13):1957-66.
2000: Joober R; Toulouse A; Benkelfat C; Lal S; Bloom D; Labelle A; Lalonde P; Turecki G; Rouleau G A
DRD3 and DAT1 genes in schizophrenia: an association study.
Journal of psychiatric research 2000;34(4-5):285-91.
2000: Hayes S; Turecki G; Brisebois K; Lopes-Cendes I; Gaspar C; Riess O; Ranum L P; Pulst S M; Rouleau G A
CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2).
Human molecular genetics 2000;9(12):1753-8.
2000: Lamartine J; Pitaval A; Soularue P; Lanneluc I; Lemaître G; Kibar Z; Rouleau G A; Waksman G
A 1.5-Mb physical map of the hidrotic ectodermal dysplasia (Clouston syndrome) gene region on human chromosome 13q11.
Genomics 2000;67(2):232-6.
2000: Joober R; Benkelfat C; Lal S; Bloom D; Labelle A; Lalonde P; Turecki G; Rozen R; Rouleau G A
Association between the methylenetetrahydrofolate reductase 677C-->T missense mutation and schizophrenia.
Molecular psychiatry 2000;5(3):323-6.
2000: Kibar Z; Dubé M P; Powell J; McCuaïg C; Hayflick S J; Zonana J; Hovnanian A; Radhakrishna U; Antonarakis S E; Benohanian A; Sheeran A D; Stephan M L; Gosselin R; Kelsell D P; Christianson A L; Fraser F C; Der Kaloustian V M; Rouleau G A
Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping.
European journal of human genetics : EJHG 2000;8(5):372-80.
2000: Alda M; Turecki G; Grof P; Cavazzoni P; Duffy A; Grof E; Ahrens B; Berghöfer A; Müller-Oerlinghausen B; Dvoráková M; Libigerová E; Vojtechovský M; Zvolský P; Joober R; Nilsson A; Prochazka H; Licht R W; Rasmussen N A; Schou M; Vestergaard P; Holzinger A; Schumann C; Thau K; Rouleau G A
Association and linkage studies of CRH and PENK genes in bipolar disorder: a collaborative IGSLI study.
American journal of medical genetics 2000;96(2):178-81.
2000: Turecki G; Alda M; Grof P; Joober R; Lafrenière R; Cavazzoni P; Duffy A; Grof E; Ahrens B; Berghöfer A; Müller-Oerlinghausen B; Dvoráková M; Libigerová E; Vojtechovský M; Zvolský P; Nilsson A; Prochazka H; Licht R W; Rasmussen N A; Schou M; Vestergaard P; Holzinger A; Schumann C; Thau K; Rouleau G A
Polyglutamine coding genes in bipolar disorder: lack of association with selected candidate loci.
Journal of affective disorders 2000;58(1):63-8.
2000: Lamartine J; Laoudj D; Blanchet-Bardon C; Kibar Z; Soularue P; Ridoux V; Dubertret L; Rouleau G A; Waksman G
Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French family.
The British journal of dermatology 2000;142(2):248-52.
2000: Lopes-Cendes I; Scheffer I E; Berkovic S F; Rousseau M; Andermann E; Rouleau G A
A new locus for generalized epilepsy with febrile seizures plus maps to chromosome 2.
American journal of human genetics 2000;66(2):698-701.
1999: Joober R; Benkelfat C; Toulouse A; Lafrenière R G; Lal S; Ajroud S; Turecki G; Bloom D; Labelle A; Lalonde P; Alda M; Morgan K; Palmour R; Rouleau G A
Analysis of 14 CAG repeat-containing genes in schizophrenia.
American journal of medical genetics 1999;88(6):694-9.
1999: Turecki G; Brière R; Dewar K; Antonetti T; Lesage A D; Séguin M; Chawky N; Vanier C; Alda M; Joober R; Benkelfat C; Rouleau G A
Prediction of level of serotonin 2A receptor binding by serotonin receptor 2A genetic variation in postmortem brain samples from subjects who did or did not commit suicide.
The American journal of psychiatry 1999;156(9):1456-8.
1999: Turecki G; Grof P; Cavazzoni P; Duffy A; Grof E; Martin R; Joober R; Rouleau G A; Alda M
Lithium responsive bipolar disorder, unilineality, and chromosome 18: A linkage study.
American journal of medical genetics 1999;88(4):411-5.
1999: Blumen S C; Brais B; Korczyn A D; Medinsky S; Chapman J; Asherov A; Nisipeanu P; Codère F; Bouchard J P; Fardeau M; Tomé F M; Rouleau G A
Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease.
Annals of neurology 1999;46(1):115-8.
1999: Camu W; Khoris J; Moulard B; Salachas F; Briolotti V; Rouleau G A; Meininger V
Genetics of familial ALS and consequences for diagnosis. French ALS Research Group.
Journal of the neurological sciences 1999;165 Suppl 1():S21-6.
1999: Parboosingh J S; Meininger V; McKenna-Yasek D; Brown R H; Rouleau G A
Deletions causing spinal muscular atrophy do not predispose to amyotrophic lateral sclerosis.
Archives of neurology 1999;56(6):710-2.
1999: Turecki G; Alda M; Grof P; Joober R; Cavazzoni P; Duffy A; Grof E; Ahrens B; Berghöfer A; Müller-Oerlinghausen B; Dvoráková M; Libigerová E; Vojtechovský M; Zvolský P; Nilsson A; Prochazka H; Licht R W; Rasmussen N A; Schou M; Vestergaard P; Holzinger A; Schumann C; Thau K; Rouleau G A
Polyglutamine tracts: no evidence of a major role in bipolar disorder.
Molecular psychiatry 1999;4(3):220-1.
1999: Joober R; Benkelfat C; Brisebois K; Toulouse A; Lafrenière R G; Turecki G; Lal S; Bloom D; Labelle A; Lalonde P; Fortin D; Alda M; Palmour R; Rouleau G A
Lack of association between the hSKCa3 channel gene CAG polymorphism and schizophrenia.
American journal of medical genetics 1999;88(2):154-7.
1999: Turecki G; Grof P; Cavazzoni P; Duffy A; Grof E; Ahrens B; Berghöfer A; Müller-Oerlinghausen B; Dvoráková M; Libigerová E; Vojtechovsky M; Zvolsky P; Joober R; Nilsson A; Prochazka H; Licht R W; Rasmussen N A; Schou M; Vestergaard P; Holzinger A; Schumann C; Thau K; Rouleau G A; Alda M
MAOA: association and linkage studies with lithium responsive bipolar disorder.
Psychiatric genetics 1999;9(1):13-6.
1999: Joober R; Benkelfat C; Brisebois K; Toulouse A; Turecki G; Lal S; Bloom D; Labelle A; Lalonde P; Fortin D; Alda M; Palmour R; Rouleau G A
T102C polymorphism in the 5HT2A gene and schizophrenia: relation to phenotype and drug response variability.
Journal of psychiatry & neuroscience : JPN 1999;24(2):141-6.
1999: Maciel P; Gaspar C; Guimarães L; Goto J; Lopes-Cendes I; Hayes S; Arvidsson K; Dias A; Sequeiros J; Sousa A; Rouleau G A
Study of three intragenic polymorphisms in the Machado-Joseph disease gene (MJD1) in relation to genetic instability of the (CAG)n tract.
European journal of human genetics : EJHG 1999;7(2):147-56.
1999: Kibar Z; Lafrenière R G; Chakravarti A; Wang J C; Chevrette M; Der Kaloustian V M; Rouleau G A
A radiation hybrid map of 48 loci including the clouston hidrotic ectodermal dysplasia locus in the pericentromeric region of chromosome 13q.
Genomics 1999;56(1):127-30.
1999: Mezei M M; Mankodi A; Brais B; Marineau C; Thornton C A; Rouleau G A; Karpati G
Minimal expansion of the GCG repeat in the PABP2 gene does not predispose to sporadic inclusion body myositis.
Neurology 1999;52(3):669-70.
1999: Joober R; Benkelfat C; Jannatipour M; Turecki G; Lal S; Mandel J L; Bloom D; Lalonde P; Lopes-Cendes I; Fortin D; Rouleau G
Polyglutamine-containing proteins in schizophrenia.
Molecular psychiatry 1999;4(1):53-7.
1999: Turecki G; Rouleau G A; Alda M
Family density of alcoholism and linkage information in the analysis of the COGA data.
Genetic epidemiology 1999;17 Suppl 1():S361-6.
1998: Siegel A M; Andermann F; Badhwar A; Rouleau G A; Dam M; Hopf H C; Dichgans J; Sturzenegger M; Hopf N J; Yasui N; Stepper F; Killer M; Vanneste J A; Acciarri N; Drigo P; Christensen J; Braun V; Könü D; Andermann E
Anticipation in familial cavernous angioma: ascertainment bias or genetic cause.
Acta neurologica Scandinavica 1998;98(6):372-6.
1998: Turecki G; Grof P; Cavazzoni P; Duffy A; Grof E; Ahrens B; Berghöfer A; Müller-Oerlinghausen B; Dvoráková M; Libigerová E; Vojtechovský M; Zvolský P; Joober R; Nilsson A; Prochazka H; Licht R W; Rasmussen N A; Schou M; Vestergaard P; Holzinger A; Schumann C; Thau K; Rouleau G A; Alda M
Evidence for a role of phospholipase C-gamma1 in the pathogenesis of bipolar disorder.
Molecular psychiatry 1998;3(6):534-8.
1998: Siegel A M; Andermann E; Badhwar A; Rouleau G A; Wolford G L; Andermann F; Hess K
Anticipation in familial cavernous angioma: a study of 52 families from International Familial Cavernous Angioma Study. IFCAS Group.
Lancet 1998;352(9141):1676-7.
1998: Xie Y G; Rochefort D; Brais B; Howard H; Han F Y; Gou L P; Maciel P; The B T; Larsson C; Rouleau G A
Restriction map of a YAC and cosmid contig encompassing the oculopharyngeal muscular dystrophy candidate region on chromosome 14q11.2-q13.
Genomics 1998;52(2):201-4.
1998: Boukaftane Y; Khoris J; Moulard B; Salachas F; Meininger V; Malafosse A; Camu W; Rouleau G A
Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosis.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 1998;25(3):192-6.
1998: Silveira I; Coutinho P; Maciel P; Gaspar C; Hayes S; Dias A; Guimarães J; Loureiro L; Sequeiros J; Rouleau G A
Analysis of SCA1, DRPLA, MJD, SCA2, and SCA6 CAG repeats in 48 Portuguese ataxia families.
American journal of medical genetics 1998;81(2):134-8.
1998: Brais B; Bouchard J P; Xie Y G; Rochefort D L; Chrétien N; Tomé F M; Lafrenière R G; Rommens J M; Uyama E; Nohira O; Blumen S; Korczyn A D; Heutink P; Mathieu J; Duranceau A; Codère F; Fardeau M; Rouleau G A;
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.
Nature genetics 1998;18(2):164-7.
1997: Brais B; Bouchard J P; Gosselin F; Xie Y G; Fardeau M; Tomé F M; Rouleau G A
Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy gene.
Neuromuscular disorders : NMD 1997;7 Suppl 1():S70-4.
1997: Bouchard J P; Brais B; Brunet D; Gould P V; Rouleau G A
Recent studies on oculopharyngeal muscular dystrophy in Québec.
Neuromuscular disorders : NMD 1997;7 Suppl 1():S22-9.
1997: Lafrenière R G; Kibar Z; Rochefort D L; Han F Y; Fon E A; Dubé M P; Kang X; Baird S; Korneluk R G; Rommens J M; Rouleau G A
Genomic structure of the human GT334 (EHOC-1) gene mapping to 21q22.3.
Gene 1997;198(1-2):313-21.
1997: Shinotoh H; Thiessen B; Snow B J; Hashimoto S; MacLeod P; Silveira I; Rouleau G A; Schulzer M; Calne D B
Fluorodopa and raclopride PET analysis of patients with Machado-Joseph disease.
Neurology 1997;49(4):1133-6.
1997: Lopes-Cendes I; Teive H G; Calcagnotto M E; Da Costa J C; Cardoso F; Viana E; Maciel J A; Radvany J; Arruda W O; Trevisol-Bittencourt P C; Rosa Neto P; Silveira I; Steiner C E; Pinto Júnior W; Santos A S; Correa Neto Y; Werneck L C; Araújo A Q; Carakushansky G; Mello L R; Jardim L B; Rouleau G A
Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients.
Arquivos de neuro-psiquiatria 1997;55(3B):519-29.
1997: Goto J; Watanabe M; Ichikawa Y; Yee S B; Ihara N; Endo K; Igarashi S; Takiyama Y; Gaspar C; Maciel P; Tsuji S; Rouleau G A; Kanazawa I
Machado-Joseph disease gene products carrying different carboxyl termini.
Neuroscience research 1997;28(4):373-7.
1997: Parboosingh J S; Figlewicz D A; Krizus A; Meininger V; Azad N A; Newman D S; Rouleau G A
Spinobulbar muscular atrophy can mimic ALS: the importance of genetic testing in male patients with atypical ALS.
Neurology 1997;49(2):568-72.
1997: Turecki G; Rouleau G A; Mari J; Joober R; Morgan K
Lack of association between bipolar disorder and tyrosine hydroxylase: a meta-analysis.
American journal of medical genetics 1997;74(4):348-52.
1997: Robitaille Y; Lopes-Cendes I; Becher M; Rouleau G; Clark A W
The neuropathology of CAG repeat diseases: review and update of genetic and molecular features.
Brain pathology (Zurich, Switzerland) 1997;7(3):901-26.
1997: Claudio J O; Veneziale R W; Menko A S; Rouleau G A
Expression of schwannomin in lens and Schwann cells.
Neuroreport 1997;8(8):2025-30.
1997: Turecki G; Rouleau G A; Joober R; Mari J; Morgan K
Schizophrenia and chromosome 6p.
American journal of medical genetics 1997;74(2):195-8.
1997: Lafrenière R G; Rochefort D L; Chrétien N; Rommens J M; Cochius J I; Kälviäinen R; Nousiainen U; Patry G; Farrell K; Söderfeldt B; Federico A; Hale B R; Cossio O H; Sørensen T; Pouliot M A; Kmiec T; Uldall P; Janszky J; Pranzatelli M R; Andermann F; Andermann E; Rouleau G A
Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1.
Nature genetics 1997;15(3):298-302.
1997: Dubé M P; Mlodzienski M A; Kibar Z; Farlow M R; Ebers G; Harper P; Kolodny E H; Rouleau G A; Figlewicz D A
Hereditary spastic paraplegia: LOD-score considerations for confirmation of linkage in a heterogeneous trait.
American journal of human genetics 1997;60(3):625-9.
1997: Turecki G; Rouleau G; Morgan K
Modeling the phenotype in parametric linkage analysis of bipolar disorder.
Genetic epidemiology 1997;14(6):687-91.
1996: Lafrenière R G; Rochefort D L; Kibar Z; Fon E A; Han F; Cochius J; Kang X; Baird S; Korneluk R G; Andermann E; Rommens J M; Rouleau G A
Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3.
Genomics 1996;38(3):264-72.
1996: Lafrenière R G; Rochefort D L; Chrétien N; Neville C E; Korneluk R G; Zuo L; Wei Y; Lichter J; Rouleau G A
Isolation and genomic structure of a human homolog of the yeast periodic tryptophan protein 2 (PWP2) gene mapping to 21q22.3.
Genome research 1996;6(12):1216-26.
1996: Watkins D; Ruttledge M H; Sarrazin J; Rangaratnam S; Poisson M; Delattre J Y; Rouleau G A
Loss of heterozygosity on chromosome 22 in human gliomas does not inactivate the neurofibromatosis type 2 gene.
Cancer genetics and cytogenetics 1996;92(1):73-8.
1996: Lopes-Cendes I; Silveira I; Maciel P; Gaspar C; Radvany J; Chitayat D; Babul R; Stewart J; Dolliver M; Robitaille Y; Rouleau G A; Sequeiros J
Limits of clinical assessment in the accurate diagnosis of Machado-Joseph disease.
Archives of neurology 1996;53(11):1168-74.
1996: Gaspar C; Lopes-Cendes I; DeStefano A L; Maciel P; Silveira I; Coutinho P; MacLeod P; Sequeiros J; Farrer L A; Rouleau G A
Linkage disequilibrium analysis in Machado-Joseph disease patients of different ethnic origins.
Human genetics 1996;98(5):620-4.
1996: Lopes-Cendes I; Steiner C E; Silveira I; Pinto Júnior W; Maciel J A; Rouleau G A
Clinical and molecular characteristics of a Brazilian family with spinocerebellar ataxia type 1.
Arquivos de neuro-psiquiatria 1996;54(3):412-8.
1996: Cavazzoni P; Alda M; Turecki G; Rouleau G; Grof E; Martin R; Duffy A; Grof P
Lithium-responsive affective disorders: no association with the tyrosine hydroxylase gene.
Psychiatry research 1996;64(2):91-6.
1996: Lutchman M; Rouleau G A
Neurofibromatosis type 2: a new mechanism of tumor suppression.
Trends in neurosciences 1996;19(9):373-7.
1996: Turecki G; Grand'Maison F; Lemieux B; Rouleau G
Hyperekplexia and the alpha1 subunit glycine receptor gene (GLRA1)
Archives of neurology 1996;53(9):836-7.
1996: Lopes-Cendes I; Maciel P; Kish S; Gaspar C; Robitaille Y; Clark H B; Koeppen A H; Nance M; Schut L; Silveira I; Coutinho P; Sequeiros J; Rouleau G A
Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and Machado-Joseph disease.
Annals of neurology 1996;40(2):199-206.
1996: Melanson M; Chalk C; Georgevich L; Fett K; Lapierre Y; Duong H; Richardson J; Marineau C; Rouleau G A
Varicella-zoster virus DNA in CSF and arteries in delayed contralateral hemiplegia: evidence for viral invasion of cerebral arteries.
Neurology 1996;47(2):569-70.
1996: Ruttledge M H; Andermann A A; Phelan C M; Claudio J O; Han F Y; Chretien N; Rangaratnam S; MacCollin M; Short P; Parry D; Michels V; Riccardi V M; Weksberg R; Kitamura K; Bradburn J M; Hall B D; Propping P; Rouleau G A
Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease.
American journal of human genetics 1996;59(2):331-42.
1996: Turecki G; Alda M; Grof P; Martin R; Cavazzoni P A; Duffy A; Maciel P; Rouleau G A
No association between chromosome-18 markers and lithium-responsive affective disorders.
Psychiatry research 1996;63(1):17-23.
1996: Fink J K; Heiman-Patterson T; Bird T; Cambi F; Dubé M P; Figlewicz D A; Fink J K; Haines J L; Heiman-Patterson T; Hentati A; Pericak-Vance M A; Raskind W; Rouleau G A; Siddique T
Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.
Neurology 1996;46(6):1507-14.
1996: Turecki G; Rouleau G A; Mari J J; Morgan K
A systematic evaluation of linkage studies in bipolar disorder.
Acta psychiatrica Scandinavica 1996;93(5):317-26.
1996: Kibar Z; Der Kaloustian V M; Brais B; Hani V; Fraser F C; Rouleau G A
The gene responsible for Clouston hidrotic ectodermal dysplasia maps to the pericentromeric region of chromosome 13q.
Human molecular genetics 1996;5(4):543-7.
1996: Joober R; Rouleau G; Fon E; Lal S; Palmour R; Bloom D; Labelle A; Benkelfat C
Apolipoprotein E genotype in schizophrenia.
American journal of medical genetics 1996;67(2):235.
1996: Rooke K; Figlewicz D A; Han F Y; Rouleau G A
Analysis of the KSP repeat of the neurofilament heavy subunit in familiar amyotrophic lateral sclerosis.
Neurology 1996;46(3):789-90.
1996: Rouleau G A; Clark A W; Rooke K; Pramatarova A; Krizus A; Suchowersky O; Julien J P; Figlewicz D
SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis.
Annals of neurology 1996;39(1):128-31.
1996: Silveira I; Lopes-Cendes I; Kish S; Maciel P; Gaspar C; Coutinho P; Botez M I; Teive H; Arruda W; Steiner C E; Pinto-Júnior W; Maciel J A; Jerin S; Sack G; Andermann E; Sudarsky L; Rosenberg R; MacLeod P; Chitayat D; Babul R; Sequeiros J; Rouleau G A
Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients.
Neurology 1996;46(1):214-8.
1996: Casaubon L K; Melanson M; Lopes-Cendes I; Marineau C; Andermann E; Andermann F; Weissenbach J; Prévost C; Bouchard J P; Mathieu J; Rouleau G A
The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q.
American journal of human genetics 1996;58(1):28-34.
1995: Fon E A; Sarrazin J; Meunier C; Alarcia J; Shevell M I; Philippe A; Leboyer M; Rouleau G A
Adenylosuccinate lyase (ADSL) and infantile autism: absence of previously reported point mutation.
American journal of medical genetics 1995;60(6):554-7.
1995: Claudio J O; Lutchman M; Rouleau G A
Widespread but cell type-specific expression of the mouse neurofibromatosis type 2 gene.
Neuroreport 1995;6(14):1942-6.
1995: DeStefano A L; Farrer L A; Maciel P; Gaspar C; Rouleau G A; Coutinho P; Sequeiros J
Gender equality in Machado-Joseph disease.
Nature genetics 1995;11(2):118-9.
1995: Belliveau M J; Lutchman M; Claudio J O; Marineau C; Rouleau G A
Schwannomin: new insights into this member of the band 4.1 superfamily.
Biochemistry and cell biology = Biochimie et biologie cellulaire 1995;73(9-10):733-7.
1995: Lafrenière R G; de Jong P J; Rouleau G A
A 405-kb cosmid contig and HindIII restriction map of the progressive myoclonus epilepsy type 1 (EPM1) candidate region in 21q22.3.
Genomics 1995;29(1):288-90.
1995: Demczuk S; Lévy A; Aubry M; Croquette M F; Philip N; Prieur M; Sauer U; Bouvagnet P; Rouleau G A; Thomas G
Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature.
Human genetics 1995;96(1):9-13.
1995: Lutchman M; Rouleau G A
The neurofibromatosis type 2 gene product, schwannomin, suppresses growth of NIH 3T3 cells.
Cancer research 1995;55(11):2270-4.
1995: Garofalo O; Figlewicz D A; Thomas S M; Butler R; Lebuis L; Rouleau G; Meininger V; Leigh P N
Superoxide dismutase activity in lymphoblastoid cells from motor neurone disease/amyotrophic lateral sclerosis (MND/ALS) patients.
Journal of the neurological sciences 1995;129 Suppl():90-2.
1995: Demczuk S; Aledo R; Zucman J; Delattre O; Desmaze C; Dauphinot L; Jalbert P; Rouleau G A; Thomas G; Aurias A
Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity.
Human molecular genetics 1995;4(4):551-8.
1995: Pramatarova A; Figlewicz D A; Krizus A; Han F Y; Ceballos-Picot I; Nicole A; Dib M; Meininger V; Brown R H; Rouleau G A
Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis.
American journal of human genetics 1995;56(3):592-6.
1995: Mérel P; Hoang-Xuan K; Sanson M; Bijlsma E; Rouleau G; Laurent-Puig P; Pulst S; Baser M; Lenoir G; Sterkers J M
Screening for germ-line mutations in the NF2 gene.
Genes, chromosomes & cancer 1995;12(2):117-27.
1995: Twist E C; Casaubon L K; Ruttledge M H; Rao V S; Macleod P M; Radvany J; Zhao Z; Rosenberg R N; Farrer L A; Rouleau G A
Machado Joseph disease maps to the same region of chromosome 14 as the spinocerebellar ataxia type 3 locus.
Journal of medical genetics 1995;32(1):25-31.
1995: Parboosingh J S; Rouleau G A; Meninger V; McKenna-Yasek D; Brown R H; Figlewicz D A
Absence of mutations in the Mn superoxide dismutase or catalase genes in familial amyotrophic lateral sclerosis.
Neuromuscular disorders : NMD 1995;5(1):7-10.
1994: Cochius J; Carpenter S; Andermann E; Rouleau G; Nousiainen U; Kalviainen R; Farrell K; Andermann F
Sweat gland vacuoles in Unverricht-Lundborg disease: a clue to diagnosis?
Neurology 1994;44(12):2372-5.
1994: Pramatarova A; Goto J; Nanba E; Nakashima K; Takahashi K; Takagi A; Kanazawa I; Figlewicz D A; Rouleau G A
A two basepair deletion in the SOD 1 gene causes familial amyotrophic lateral sclerosis.
Human molecular genetics 1994;3(11):2061-2.
1994: Figlewicz D A; Krizus A; Martinoli M G; Meininger V; Dib M; Rouleau G A; Julien J P
Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis.
Human molecular genetics 1994;3(10):1757-61.
1994: Lopes-Cendes I; Andermann E; Attig E; Cendes F; Bosch S; Wagner M; Gerstenbrand F; Andermann F; Rouleau G A
Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region.
American journal of human genetics 1994;54(5):774-81.
1994: Claudio J O; Malo D; Rouleau G A
The mouse neurofibromatosis type 2 gene maps to chromosome 11.
Genomics 1994;21(2):437-9.
1994: Lopes-Cendes I; Andermann E; Rouleau G A
Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locus.
Genomics 1994;21(1):270-4.
1994: Twist E C; Farrer L A; Macleod P M; Radvany J; Chamberlain S; Rosenberg R N; Rouleau G A
Machado Joseph disease is not an allele of the spinocerebellar ataxia 2 locus.
Human genetics 1994;93(3):335-8.
1994: Watkins D; Dion F; Poisson M; Delattre J Y; Rouleau G A
Analysis of oncogene expression in primary human gliomas: evidence for increased expression of the ros oncogene.
Cancer genetics and cytogenetics 1994;72(2):130-6.
1994: Claudio J O; Marineau C; Rouleau G A
The mouse homologue of the neurofibromatosis type 2 gene is highly conserved.
Human molecular genetics 1994;3(1):185-90.
1994: Twist E C; Ruttledge M H; Rousseau M; Sanson M; Papi L; Merel P; Delattre O; Thomas G; Rouleau G A
The neurofibromatosis type 2 gene is inactivated in schwannomas.
Human molecular genetics 1994;3(1):147-51.
1994: Figlewicz D A; Garruto R M; Krizus A; Yanagihara R; Rouleau G A
The Cu/Zn superoxide dismutase gene in ALS and parkinsonism-dementia of Guam.
Neuroreport 1994;5(5):557-60.
1994: Watkins D; Rouleau G A
Genetics, prognosis and therapy of central nervous system tumors.
Cancer detection and prevention 1994;18(2):139-44.
1994: Demczuk S; Desmaze C; Aikem M; Prieur M; Ledeist F; Sanson M; Rouleau G; Thomas G; Aurias A
Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization.
Annales de génétique 1994;37(2):60-5.
1993: Aubry M; Demczuk S; Desmaze C; Aikem M; Aurias A; Julien J P; Rouleau G A
Isolation of a zinc finger gene consistently deleted in DiGeorge syndrome.
Human molecular genetics 1993;2(10):1583-7.
1993: Figlewicz D A; Rouleau G A; Krizus A; Julien J P
Polymorphism in the multi-phosphorylation domain of the human neurofilament heavy-subunit-encoding gene.
Gene 1993;132(2):297-300.
1993: Sanson M; Zhang F; Demczuk S; Delattre O; DeJong P; Aurias A; Thomas G; Rouleau G A
Isolation and mapping of 45 NotI linking clones to chromosome 22.
Genomics 1993;17(3):776-9.
1993: Figlewicz D A; Delattre O; Guellaen G; Krizus A; Thomas G; Zucman J; Rouleau G A
Mapping of human gamma-glutamyl transpeptidase genes on chromosome 22 and other human autosomes.
Genomics 1993;17(2):299-305.
1993: Rouleau G A; Merel P; Lutchman M; Sanson M; Zucman J; Marineau C; Hoang-Xuan K; Demczuk S; Desmaze C; Plougastel B
Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2.
Nature 1993;363(6429):515-21.
1993: Goto J; Gnirke A; Khodr N; Kaufer E; Krizus A; Figlewicz D A; Rouleau G A
Dinucleotide repeat polymorphism at the D21S370 locus which flanks the PRGS (GARS)-PAIS (AIRS)-PGFT (GART) gene.
Human molecular genetics 1993;2(5):616.
1993: Garofalo O; Figlewicz D A; Leigh P N; Powell J F; Meininger V; Dib M; Rouleau G A
Androgen receptor gene polymorphisms in amyotrophic lateral sclerosis.
Neuromuscular disorders : NMD 1993;3(3):195-9.
1993: Marineau C; Baron C; Delattre O; Zucman J; Thomas G; Rouleau G A
Dinucleotide repeat polymorphism at the D22S268 locus.
Human molecular genetics 1993;2(3):336.
1993: Goto J; Figlewicz D A; Haines J L; Brown R H; Khodr N; Rouleau G A
The glycinamide ribonucleotide transformylase (GART) gene is not responsible for familial amyotrophic lateral sclerosis.
Neuromuscular disorders : NMD 1993;3(2):157-60.
1993: Fon E A; Demczuk S; Delattre O; Thomas G; Rouleau G A
Mapping of the human adenylosuccinate lyase (ADSL) gene to chromosome 22q13.1-->q13.2.
Cytogenetics and cell genetics 1993;64(3-4):201-3.
1992: Goto J; Figlewicz D A; Gnirke A; Khodr N; Krizus A; Rouleau G A
Dinucleotide repeat polymorphism at the D21S219 locus which flanks the GARS-AIRS-GART gene.
Human molecular genetics 1992;1(9):782.
1992: Zucman J; Delattre O; Desmaze C; Plougastel B; Joubert I; Melot T; Peter M; De Jong P; Rouleau G; Aurias A
Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints.
Genes, chromosomes & cancer 1992;5(4):271-7.
1992: Delattre O; Zucman J; Plougastel B; Desmaze C; Melot T; Peter M; Kovar H; Joubert I; de Jong P; Rouleau G
Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours.
Nature 1992;359(6391):162-5.
1992: Goto J; Tassone F; Demczuk S; Gardiner K; Figlewicz D A; Khodr N; Rouleau G A
Dinucleotide repeat polymorphism at the D21S65 locus.
Human molecular genetics 1992;1(5):350.
1992: Carson W J; Radvany J; Farrer L A; Vincent D; Rosenberg R N; MacLeod P M; Rouleau G A
The Machado-Joseph disease locus is different from the spinocerebellar ataxia locus (SCA1).
Genomics 1992;13(3):852-5.
1992: Aubry M; Marineau C; Zhang F R; Zahed L; Figlewicz D; Delattre O; Thomas G; de Jong P J; Julien J P; Rouleau G A
Cloning of six new genes with zinc finger motifs mapping to short and long arms of human acrocentric chromosome 22 (p and q11.2).
Genomics 1992;13(3):641-8.
1992: Zucman J; Delattre O; Desmaze C; Azambuja C; Rouleau G; De Jong P; Aurias A; Thomas G
Rapid isolation of cosmids from defined subregions by differential Alu-PCR hybridization on chromosome 22-specific library.
Genomics 1992;13(2):395-401.
1992: Marineau C; Aubry M; Julien J P; Rouleau G A
Dinucleotide repeat polymorphism at the D22S264 locus.
Nucleic acids research 1992;20(6):1430.
1992: Marineau C; Rouleau G A
Dinucleotide repeat polymorphism at the human CRYB2 gene locus (22q11.2).
Nucleic acids research 1992;20(6):1430.
1992: Goto J; Figlewicz D A; Marineau C; Khodr N; Rouleau G A
Dinucleotide repeat polymorphism at the IGF2R locus.
Nucleic acids research 1992;20(4):923.
1992: Watkins D; Rouleau G A
Oncogenes and glial tumors.
Revue neurologique 1992;148(6-7):402-7.
1991: Goto J; Figlewicz D A; Lutchman M; Ruddle F; Rouleau G A
A PvuII RFLP at the HOX 1.4 homeobox locus (HOX1D).
Nucleic acids research 1991;19(13):3755.
1991: Delattre O; Azambuja C J; Aurias A; Zucman J; Peter M; Zhang F; Hors-Cayla M C; Rouleau G; Thomas G
Mapping of human chromosome 22 with a panel of somatic cell hybrids.
Genomics 1991;9(4):721-7.
1990: Sanson M; Delattre O; Couturier J; Philippon J; Cophignon J; Derome P; Rouleau G A; Thomas G
Parental origin of chromosome 22 alleles lost in meningioma.
American journal of human genetics 1990;47(5):877-80.
1990: Zhang F R; Aurias A; Delattre O; Stern M H; Benitez J; Rouleau G; Thomas G
Mapping of human chromosome 22 by in situ hybridization.
Genomics 1990;7(3):319-24.
1990: Couturier J; Delattre O; Kujas M; Philippon J; Peter M; Rouleau G; Aurias A; Thomas G
Assessment of chromosome 22 anomalies in neurinomas by combined karyotype and RFLP analyses.
Cancer genetics and cytogenetics 1990;45(1):55-62.
1990: Zhang F R; Delattre O; Rouleau G; Couturier J; Lefrançois; Thomas G; Aurias A
The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus.
Genomics 1990;6(1):174-7.

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