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    1. Hand, CK; Khoris, J; Salachas, F; Gros-Louis, F; Lopes, AAS; Mayeux-Portas, V; Brown, RH; Meininger, V; Camu, W; Rouleau, GA
      A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Ichikawa, Y; Goto, J; Hattori, M; Toyoda, A; Ishii, K; Jeong, SY; Hashida, H; Masuda, N; Ogata, K; Kasai, F; Hirai, M; Maciel, P; Rouleau, GA; Sakaki, Y; Kanazawa, I
      The genomic structure and expression of MJD, the Machado-Joseph disease gene

      JOURNAL OF HUMAN GENETICS
    3. Kotorii, S; Takahashi, K; Kamimura, K; Nishio, T; Arima, K; Yamada, H; Uyama, E; Uchino, M; Suenaga, A; Matsumoto, M; Kuchel, G; Rouleau, GA; Tabira, T
      Mutations of the Notch3 gene in non-caucasian patients with suspected CADASIL syndrome

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    4. Turecki, G; Grof, P; Grof, E; D'Souza, V; Lebuis, L; Marineau, C; Cavazzoni, P; Duffy, A; Betard, C; Zvolsky, P; Robertson, C; Brewer, C; Hudson, TJ; Rouleau, GA; Alda, M
      Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithium

      MOLECULAR PSYCHIATRY
    5. Turecki, G; Zhu, Z; Tzenova, J; Lesage, A; Seguin, M; Tousignant, M; Chawky, N; Vanier, C; Lipp, O; Alda, M; Joober, R; Benkelfat, C; Rouleau, GA
      TPH and suicidal behavior: a study in suicide completers

      MOLECULAR PSYCHIATRY
    6. Hadano, S; Hand, CK; Osuga, H; Yanagisawa, Y; Otomo, A; Devon, RS; Miyamoto, N; Showguchi-Miyata, J; Okada, Y; Singaraja, R; Figlewicz, DA; Kwiatkowski, T; Hosler, BA; Sagie, T; Skaug, J; Nasir, J; Brown, RH; Scherer, SW; Rouleau, GA; Hayden, MR; Ikeda, JE
      A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2 (vol 29, pg 166, 2001)

      NATURE GENETICS
    7. Hadano, S; Hand, CK; Osuga, H; Yanagisawa, Y; Otomo, A; Devon, RS; Miyamoto, N; Showguchi-Miyata, J; Okada, Y; Singaraja, R; Figlewicz, DA; Kwiatkowski, T; Hosler, BA; Sagie, T; Skaug, J; Nasir, J; Brown, RH; Scherer, SW; Rouleau, GA; Hayden, MR; Ikeda, JE
      A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

      NATURE GENETICS
    8. Bruder, CEG; Hirvela, C; Tapia-Paez, I; Fransson, I; Segraves, R; Hamilton, G; Zhang, XX; Evans, DG; Wallace, AJ; Baser, ME; Zucman-Rossi, J; Hergersberg, M; Boltshauser, E; Papi, L; Rouleau, GA; Poptodorov, G; Jordanova, A; Rask-Andersen, H; Kluwe, L; Mautner, V; Sainio, M; Hung, G; Mathiesen, T; Moller, C; Pulst, SM; Harder, H; Heiberg, A; Honda, M; Miimura, M; Sahlen, S; Blennow, E; Albertson, DG; Pinkel, D; Dumanski, JP
      High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH

      HUMAN MOLECULAR GENETICS
    9. Fan, XP; Dion, P; Laganiere, J; Brais, B; Rouleau, GA
      Oligomerization of polyalanine expanded PABPN1 facilitates nuclear proteinaggregation that is associated with cell death

      HUMAN MOLECULAR GENETICS
    10. Chambers, DM; Rouleau, GA; Abbott, CM
      Comparative genomic analysis of genes encoding translation elongation factor 1B alpha in human and mouse shows EEF1B1 to be a recent retrotransposition event

      GENOMICS
    11. Fortin, A; Diez, E; Rochefort, D; Laroche, L; Malo, D; Rouleau, GA; Gros, P; Skamene, E
      Recombinant congenic strains derived from A/J and C57BL/6J: A tool for genetic dissection of complex traits

      GENOMICS
    12. Hadano, S; Yanagisawa, Y; Skaug, J; Fichter, K; Nasir, J; Martindale, D; Koop, BF; Scherer, SW; Nicholson, DW; Rouleau, GA; Ikeda, JE; Hayden, MR
      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
    13. Hand, CK; Mayeux-Portas, V; Khoris, J; Briolotti, V; Clavelou, P; Camu, W; Rouleau, GA
      Compound heterozygosity and variable penetrance in SOD1 amyotrophic lateral sclerosis pedigrees - Reply

      ANNALS OF NEUROLOGY
    14. Hand, CK; Mayeux-Portas, V; Khoris, J; Briolotti, V; Clavelou, P; Camu, W; Rouleau, GA
      Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family

      ANNALS OF NEUROLOGY
    15. Dupre, N; Cossette, L; Hand, CK; Bouchard, JP; Rouleau, GA; Puymirat, J
      A founder mutation in French-Canadian families with X-linked hereditary neuropathy

      CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
    16. Pramatarova, A; Laganiere, J; Roussel, J; Brisebois, K; Rouleau, GA
      Neuron-specific expression of mutant superoxide dismutase 1 in transgenic mice does not lead to motor impairment

      JOURNAL OF NEUROSCIENCE
    17. Alda, M; Keller, D; Grof, E; Turecki, G; Cavazzoni, P; Duffy, A; Rouleau, GA; Grof, P; Young, LT
      Is lithium response related to G(s)alpha levels in transformed lymphoblasts from subjects with bipolar disorder?

      JOURNAL OF AFFECTIVE DISORDERS
    18. Yamamoto, K; Bloom, D; La, S; Turecki, G; Joober, R; Yamamoto, K; Benkelfat, C; Joober, R; Lalonde, P; Labelle, A; Turecki, G; Rouleau, GA; Joober, R
      Polymorphism in the cell division cycle 45 like gene and schizophrenia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    19. 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
    20. Davenport, WJ; Siegel, AM; Dichgans, J; Drigo, P; Mammi, I; Pereda, P; Wood, NW; Rouleau, GA
      CCM1 gene mutations in families segregating cerebral cavernous malformations

      NEUROLOGY
    21. Jannatipour, M; Dion, P; Khan, S; Jindal, H; Fan, XP; Laganiere, J; Chishti, AH; Rouleau, GA
      Schwannomin isoform-1 interacts with syntenin via PDZ domains

      JOURNAL OF BIOLOGICAL CHEMISTRY
    22. Maciel, P; Costa, MDC; Ferro, A; Rousseau, M; Santos, CS; Gaspar, C; Barros, J; Rouleau, GA; Coutinho, P; Sequeiros, J
      Improvement in the molecular diagnosis of Machado-Joseph disease

      ARCHIVES OF NEUROLOGY
    23. Turecki, G; Briere, R; Dewar, K; Lesage, AD; Seguin, M; Chawky, N; Vanier, C; Alda, M; Joober, R; Benkelfat, C; Rouleau, GA
      Levels of serotonin receptor 2A higher in suicide victims? - Dr. Turecki and colleagues reply

      AMERICAN JOURNAL OF PSYCHIATRY
    24. 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
    25. Gaspar, C; Lopes-Cendes, I; Hayes, S; Goto, J; Arvidsson, K; Dias, A; Silveira, I; Maciel, P; Coutinho, P; Lima, M; Zhou, YX; Soong, BW; Watanabe, M; Giunti, P; Stevanin, G; Riess, O; Sasaki, H; Hsieh, M; Nicholson, GA; Brunt, E; Higgins, JJ; Lauritzen, M; Tranebjaerg, L; Volpini, V; Wood, N; Ranum, L; Tsuji, S; Brice, A; Sequeiros, J; Rouleau, GA
      Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study

      AMERICAN JOURNAL OF HUMAN GENETICS
    26. Nikpoor, B; Turecki, G; Fournier, C; Theroux, P; Rouleau, GA
      A functional myeloperoxidase polymorphic variant is associated with coronary artery disease in French-Canadians

      AMERICAN HEART JOURNAL
    27. Denghien, I; Joober, R; Rouleau, GA; Neri, C
      Polyglutamine tracts in schizophrenia: gaining new insights

      MOLECULAR PSYCHIATRY
    28. Joober, R; Benkelfat, C; Lal, S; Bloom, D; Labelle, A; Lalonde, P; Turecki, G; Rozen, R; Rouleau, GA
      Association between the methylenetetrahydrofolate reductase 677C -> T missense mutation and schizophrenia

      MOLECULAR PSYCHIATRY
    29. Khoris, J; Moulard, B; Briolotti, V; Hayer, M; Durieux, A; Clavelou, P; Malafosse, A; Rouleau, GA; Camu, W
      Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country

      EUROPEAN JOURNAL OF NEUROLOGY
    30. Duffy, A; Turecki, G; Grof, P; Cavazzoni, P; Grof, E; Joober, R; Ahrens, B; Berghofer, A; Muller-Oerlinghausen, B; Dvorakova, M; Libigerova, E; Vojtechovsky, M; Zvolsky, P; Nilsson, A; Licht, RW; Rasmussen, NA; Schou, M; Vestergaard, P; Holzinger, A; Schumann, C; Thau, K; Robertson, C; Rouleau, GA; Alda, M
      Association and linkage studies of candidate genes involved in GABAergic neurotransmission in lithium-responsive bipolar disorder

      JOURNAL OF PSYCHIATRY & NEUROSCIENCE
    31. Lamartine, J; Essenfelder, GM; Kibar, Z; Lanneluc, I; Callouet, E; Laoudj, D; Lemaitre, G; Hand, C; Hayflick, SJ; Zonana, J; Antonarakis, S; Radhakrishna, U; Kelsell, DP; Christianson, AL; Pitaval, A; Der Kaloustian, V; Fraser, C; Blanchet-Bardon, C; Rouleau, GA; Waksman, G
      Mutations in GJB6 cause hidrotic ectodermal dysplasia

      NATURE GENETICS
    32. Kibar, Z; Dube, MP; Powell, J; McCuaig, C; Hayflick, SJ; Zonana, J; Hovnanian, A; Radhakrishna, U; Antonarakis, SE; Benohanian, A; Sheeran, AD; Stephan, ML; Gosselin, R; Kelsell, DP; Christianson, AL; Fraser, FC; Kaloustian, VMD; Rouleau, GA
      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
    33. Gaspar, C; Jannatipour, M; Dion, P; Laganiere, J; Sequeiros, J; Brais, B; Rouleau, GA
      CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulation

      HUMAN MOLECULAR GENETICS
    34. Hayes, S; Turecki, G; Brisebois, K; Lopes-Cendes, I; Gaspar, C; Riess, O; Ranum, LPW; Pulst, SM; Rouleau, GA
      CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)

      HUMAN MOLECULAR GENETICS
    35. Lamartine, J; Pitaval, A; Soularue, P; Lanneluc, I; Lemaitre, G; Kibar, Z; Rouleau, GA; Waksman, G
      A 1.5-mb physical map of the hidrotic ectodermal dysplasia (Clouston syndrome) gene region on human chromosome 13q11

      GENOMICS
    36. Legoix, P; Sarkissian, HD; Cazes, L; Giraud, S; Sor, F; Rouleau, GA; Lenoir, G; Thomas, G; Zucman-Rossi, J
      Molecular characterization of germline NF2 gene rearrangements

      GENOMICS
    37. Shanmugam, V; Dion, P; Rochefort, D; Laganiere, J; Brais, B; Rouleau, GA
      PABP2 polyalanine tract expansion causes intranuclear inclusions in oculopharyngeal muscular dystrophy

      ANNALS OF NEUROLOGY
    38. Furukawa, Y; Guttman, M; Sparagana, SP; Trugman, JM; Hyland, K; Wyatt, P; Lang, AE; Rouleau, GA; Shimadzu, M; Kish, SJ
      Dopa-responsive dystonia due to a large deletion in the GTP cyclohydrolaseI gene

      ANNALS OF NEUROLOGY
    39. Turecki, G; Alda, M; Grof, P; Joober, R; Lafreniere, R; Cavazzoni, P; Duffy, A; Grof, E; Ahrens, B; Berghofer, A; Muller-Oerlinghausen, B; Dvorkova, M; Libigerova, E; Vojtechovsky, M; Zvolsky, P; Nilsson, A; Prochazka, H; Licht, RW; Rasmussen, NA; Schou, M; Vestergaard, P; Holzinger, A; Schumann, C; Thau, K; Rouleau, GA
      Polyglutamine coding genes in bipolar disorder: lack of association with selected candidate loci

      JOURNAL OF AFFECTIVE DISORDERS
    40. Alda, M; Turecki, G; Grof, P; Cavazzoni, P; Duffy, A; Grof, E; Ahrens, B; Berghofer, A; Muller-Oerlinghausen, B; Dvorakova, M; Libigerova, E; Vojtechovsky, M; Zvolsky, P; Joober, R; Nilsson, A; Prochazka, H; Licht, RW; Rasmussen, NA; Schou, M; Vestergaard, P; Holzinger, A; Schumann, C; Thau, K; Rouleau, GA
      Association and linkage studies of CRH and PENK genes in bipolar disorder:A collaborative IGSLI study

      AMERICAN JOURNAL OF MEDICAL GENETICS
    41. Blumen, SC; Korczyn, AD; Lavoie, H; Medynski, S; Chapman, J; Asherov, A; Nisipeanu, P; Inzelberg, R; Carasso, RL; Bouchard, JP; Tome, FMS; Rouleau, GA; Brais, B
      Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene

      NEUROLOGY
    42. Minassian, BA; Ianzano, L; Meloche, M; Andermann, E; Rouleau, GA; Delgado-Escueta, AV; Scherer, SW
      Mutation spectrum and predicted function of laforin in Lafora's progressive myoclonus epilepsy

      NEUROLOGY
    43. Joober, R; Toulouse, A; Benkelfat, C; Lal, S; Bloom, D; Labelle, A; Lalonde, P; Turecki, G; Rouleau, GA
      DRD3 and DAT1 genes in schizophrenia: an association study

      JOURNAL OF PSYCHIATRIC RESEARCH
    44. Lamartine, J; Laoudj, D; Blanchet-Bardon, C; Kibar, Z; Soularue, P; Ridoux, V; Dubertret, L; Rouleau, GA; Waksman, G
      Refined localization of the gene for Clouston syndrome (hidrotic ectodermal dysplasia) in a large French family

      BRITISH JOURNAL OF DERMATOLOGY
    45. Turecki, G; Briere, R; Dewar, K; Lesage, A; Seguin, M; Chawky, N; Vanier, C; Alda, M; Joober, R; Benkelfat, C; Rouleau, GA
      Serotonin 2A receptor polymorphisms and [H-3]ketanserin binding - Dr. Turecki and colleagues reply

      AMERICAN JOURNAL OF PSYCHIATRY
    46. Lopes-Cendes, I; Scheffer, IE; Berkovic, SF; Rousseau, M; Andermann, E; Rouleau, GA
      A new locus for generalized epilepsy with febrile seizures plus maps to chromosome 2

      AMERICAN JOURNAL OF HUMAN GENETICS
    47. Turecki, G; Alda, M; Grof, P; Joober, R; Cavazzoni, P; Duffy, A; Grof, E; Ahrens, B; Berghofer, A; Muller-Oerlinghausen, B; Dvorakova, M; Libigerova, E; Vojtechovsky, M; Zvolsky, P; Nilsson, A; Prochazka, H; Licht, RW; Rasmussen, NA; Schou, M; Vestergaard, P; Holzinger, A; Schumann, C; Thau, K; Rouleau, GA
      Polyglutamine tracts: no evidence of a major role in bipolar disorder

      MOLECULAR PSYCHIATRY
    48. 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, GA
      T102C polymorphism in the 5HT(2A) gene and schizophrenia: relation to phenotype and drug response variability

      JOURNAL OF PSYCHIATRY & NEUROSCIENCE
    49. Maciel, P; Gasper, C; Guimaraes, L; Goto, J; Lopez-Cendes, I; Hayes, S; Arvidsson, K; Dias, A; Sequeiros, J; Sousa, A; Rouleau, GA
      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
    50. Larson, GP; Ding, SF; Lafreniere, RG; Rouleau, GA; Krontiris, TG
      Instability of the EPM1 minisatellite

      HUMAN MOLECULAR GENETICS
    51. Kibar, Z; Lafreniere, RG; Chakravarti, A; Wang, JC; Chevrette, M; Der Kaloustian, VM; Rouleau, GA
      A radiation hybrid map of 48 loci including the Clouston hidrotic ectodermal dysplasia locus in the pericentromeric region of chromosome 13q

      GENOMICS
    52. Turecki, G; Rouleau, GA; Alda, M
      Family density of alcoholism and linkage information in the analysis of the COGA data

      GENETIC EPIDEMIOLOGY
    53. Blumen, SC; Brais, B; Korczyn, AD; Medinsky, S; Chapman, J; Asherov, A; Nisipeanu, P; Codere, F; Bouchard, JP; Fardeau, M; Tome, FMS; Rouleau, GA
      Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease

      ANNALS OF NEUROLOGY
    54. Brais, B; Rouleau, GA; Bouchard, JP; Fardeau, M; Tome, FMS
      Oculopharyngeal muscular dystrophy

      SEMINARS IN NEUROLOGY
    55. Joober, R; Benkelfat, C; Toulouse, A; Lafreniere, RGA; Lal, S; Ajroud, S; Turecki, G; Bloom, D; Labelle, A; Lalonde, P; Alda, M; Morgan, K; Palmour, R; Rouleau, GA
      Analysis of 14 CAG repeat-containing genes in schizophrenia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    56. Turecki, G; Grof, P; Cavazzoni, P; Duffy, A; Grof, E; Martin, R; Joober, R; Rouleau, GA; Alda, M
      Lithium responsive bipolar disorder, unilineality, and chromosome 18: A linkage study

      AMERICAN JOURNAL OF MEDICAL GENETICS
    57. Joober, R; Benkelfat, C; Brisebois, K; Toulouse, A; Lafreniere, RG; Turecki, G; Lal, S; Bloom, D; Labelle, A; Lalonde, P; Fortin, D; Alda, M; Palmour, R; Rouleau, GA
      Lack of association between the hSKCa3 channel gene CAG polymorphism and schizophrenia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    58. Mezei, MM; Mankodi, A; Brais, B; Marineau, C; Thornton, CA; Rouleau, GA; Karpati, G
      Minimal expansion of the GCG repeat in the PABP2 gene does not predispose to sporadic inclusion body myositis

      NEUROLOGY
    59. Camu, W; Khoris, J; Moulard, B; Salachas, F; Briolotti, V; Rouleau, GA; Meininger, V
      Genetics of familial ALS and consequences for diagnosis

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    60. Parboosingh, JS; Meininger, V; McKenna-Yasek, D; Brown, RH; Rouleau, GA
      Deletions causing spinal muscular atrophy do not predispose to amyotrophiclateral sclerosis

      ARCHIVES OF NEUROLOGY
    61. Turecki, G; Briere, R; Dewar, K; Antonetti, T; Lesage, AD; Seguin, M; Chawky, N; Vanier, C; Alda, M; Joober, R; Benkelfat, C; Rouleau, GA
      Prediction of level of serotonin 2A receptor binding by serotonin receptor2A genetic variation in postmortem brain samples from subjects who did or did not commit suicide

      AMERICAN JOURNAL OF PSYCHIATRY
    62. TURECKI G; GROF P; CAVAZZONI P; DUFFY A; GROF E; AHRENS B; BERGHOFER A; MULLEROERLINGHAUSEN B; DVORAKOVA M; LIBIGEROVA E; VOJTECHOVSKY M; ZVOLSKY P; JOOBER R; NILSSON A; PROCHAZKA H; LICHT RW; RASMUSSEN NA; SCHOU M; VESTERGAARD P; HOLZINGER A; SCHUMANN C; THAU K; ROULEAU GA; ALDA M
      EVIDENCE FOR A ROLE OF PHOSPHOLIPASE C-GAMMA-1 IN THE PATHOGENESIS OFBIPOLAR DISORDER

      Molecular psychiatry
    63. MINASSIAN BA; LEE JR; HERBRICK JA; HUIZENGA J; SODER S; MUNGALL AJ; DUNHAM I; GARDNER R; FONG CG; CARPENTER S; JARDIM L; SATISHCHANDRA P; ANDERMANN E; SNEAD OC; LOPESCENDES I; TSUI LC; DELGADOESCUETA AV; ROULEAU GA; SCHERER SW
      MUTATIONS IN A GENE ENCODING A NOVEL PROTEIN-TYROSINE-PHOSPHATASE CAUSE PROGRESSIVE MYOCLONUS EPILEPSY

      Nature genetics
    64. BRAIS B; BOUCHARD JP; XIE YG; ROCHEFORT DL; CHRETIEN N; TOME FMS; LAFRENIERE RG; ROMMENS JM; UYAMA E; NOHIRA O; BLUMEN S; KORCYN AD; HEUTINK P; MATHIEU J; DURANCEAU A; CODERE F; FARDEAU M; ROULEAU GA
      SHORT GCG EXPANSIONS IN THE PABP2 GENE CAUSE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Nature genetics
    65. HOWARD HC; DUBE MP; PREVOST C; LOPESCENDES I; CASAUBON LK; MELANSON M; ANDERMANN E; ANDERMANN F; BOUCHARD JP; MATHIEU J; ROULEAU GA
      THE CANDIDATE INTERVAL FOR PERIPHERAL NEUROPATHY WITH OR WITHOUT AGENESIS OF THE CORPUS-CALLOSUM MAPS TO A 1 CM REGION ON CHROMOSOME 15Q

      European journal of human genetics
    66. SILVEIRA I; COUTINHO P; MACIEL P; HAYES S; DIAS A; GUIMARAES J; LOUREIRO LL; BARROS J; CHORAO R; RIBEIRO P; BETTENCOURT M; SERRANO P; SILVA C; ROULEAU GA; SEQUEIROS J
      FREQUENCY OF SCA1, DRPLA, MJD, SCA2 AND SCA6 MUTATIONS IN A LARGE GROUP OF PORTUGUESE FAMILIES WITH SPINOCEREBELLAR ATAXIA

      European journal of human genetics
    67. PRAMATAROVA A; ROUSSEL J; BRISEBOIS K; ROULEAU GA
      TRANSGENIC MICE EXPRESSING A MUTANT HUMAN CU ZN SUPEROXIDE-DISMUTASE GENE DRIVEN BY A NFL PROMOTER/

      European journal of human genetics
    68. CHISHTI AH; KIM AC; MARFATIA SM; LUTCHMAN M; HANSPAL M; JINDAL H; LIU SC; LOW PS; ROULEAU GA; MOHANDAS N; CHASIS JA; CONBOY JG; GASCARD P; TAKAKUWA Y; HUANG SC; BENZ EJ; BRETSCHER A; FEHON RG; GUSELLA AF; RAMESH V; SOLOMON F; MARCHESI VT; TSUKITA S; TSUKITA S; ARPIN M; LOUVARD D; TONKS NK; ANDERSON JM; FANNING AS; BRYANT PJ; WOODS DF; HOOVER KB
      THE FERM DOMAIN - A UNIQUE MODULE INVOLVED IN THE LINKAGE OF CYTOPLASMIC PROTEINS TO THE MEMBRANE

      Trends in biochemical sciences
    69. XIE YG; ROCHEFORT D; BRAIS B; HOWARD H; HAN FY; GOU LP; MACIEL P; THE BT; LARSSON C; ROULEAU GA
      RESTRICTION MAP OF A YAC AND COSMID CONTIG ENCOMPASSING THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY CANDIDATE REGION ON CHROMOSOME 14Q11.2-Q13

      Genomics (San Diego, Calif.)
    70. SIEGEL AM; BADHWAR A; ANDERMANN F; ROULEAU GA; HESS K; ANDERMANN E
      ANTICIPATION IN FAMILIAR CAVERNOUS ANGIOMAS

      Annals of neurology
    71. BRAIS B; BOUCHARD JP; TOME FMS; FARDEAU M; CODERE F; DURANCEAU A; ROULEAU GA
      GENETIC-EVIDENCE FOR THE INVOLVEMENT OF OTHER GENES IN MODULATING THESEVERITY OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Annals of neurology
    72. UYAMA E; BRAIS B; NOHIRA O; TOKUNAGA M; CHATEAU D; TOME FMS; ROULEAU GA; UCHINO M
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY - PHENOTYPE GENOTYPE DIFFERENCE IN2 UNRELATED JAPANESE FAMILIES/

      Annals of neurology
    73. BOUKAFTANE Y; KHORIS J; MOULARD B; SALACHAS F; MEININGER V; MALAFOSSE A; CAMU W; ROULEAU GA
      IDENTIFICATION OF 6 NOVEL SOD1 GENE-MUTATIONS IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS

      Canadian journal of neurological sciences
    74. SEQUEIROS J; MACIEL P; TABORDA F; LEDO S; ROCHA JC; LOPES A; RETO F; FORTUNA AM; ROUSSEAU M; FLEMING M; COUTINHO P; ROULEAU GA; JORGE CS
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/10/19 alle ore 04:11:11