2001/2002 Publications Page



  1. Alda M, Keller D, Grof E, Turecki G, Cavazzoni P, Duffy A, Rouleau GA, Grof P, and Young T: Is lithium response related to Gs? Levels in transformed lymphoblasts from subjects with bipolar disorder? J Affect Disord.; 65:117-22, 2001.

  2. Bevan S, Pal T, Greenberg CR, Green H, Wixey J, Bignell G, Narod SA, Foulkes WD, Stratton MR and Houlston RS: A comprehensive analysis of MNG1, TCO1, Fptc, PTEN, RET, TSHR and TRKA in familial non-medullary thyroid cancer: confirmation of linkage to TCO1. J Clin Endocrinol Metab 86:3701-4, 2001.

  3. Bodamer OAF, Rosenblatt DS, Appel SH, and Beaudet AL: Adult-onset combined methylmalonic aciduria and homocystinuria. Neurology 56:1113-1114, 2001.

  4. Bourgault C, Elstein E, Baltzan MA, Le Lorier J and Suissa S: Antihypertensives and myocardial infarction risk: The modifying effect of history of drug use, Pharmacoepidemiol Drug Safety; 10:287-294, 2001.

  5. Brisson D, Vohl M-C, St-Pierre J, Hudson TJ and Gaudet D: Glycerol: A neglected variable in metabolic processes? BioEssays 23:534-542, 2001.

  6. Bruder CE, Hirvela C, Tapia-Paez I, Fransson I, Segraves R, Hamilton G, Zhang X, Evans E, Baser M, Zucman-Rossi J, Hergersberg M, Boltshauser E, Papi L, Rouleau GA, Poptodorov G, Jordanova A, Kluwe L, Mautner V, Saino M, Hung G, Mathiesen T, Moller C, Pulst S, Harder H, Heilber A, Hondo M, Sahlen S, Blennow E, Albertson D, Pinkel D and Dumanski J: High resolution deletion analysis of constitutional DNA from Neurofibromatosis type 2 (NF2) patients using microarray-CGH. Hum Mol Genet 10:271-282, 2001.

  7. Bull SB, Darlington GA, Shin J and Greenwood CMT. Efficiency of association studies of candidate genes in families. Genet Epidemiol 20:149-174, 2001

  8. Chambers DM, Rouleau GA and Abbott CM: Comparative genomic analysis of genes encoding translation elongation factor 1ba in human and mouse shows eef1b1 to be a retrotransposition event. Genomics 77:145-148, 2001.

  9. Chappuis PO, Hamel N, Paradis A-J, Deschenes J, Robidoux A, Potvin C, Cantin J, Tonin PN, Ghadirian P and Foulkes WD: Prevalence of founder BRCA1 and BRCA2 mutations in unselected French Canadian women with breast cancer. Clin Genet 59: 418-423, 2001.

  10. Chappius PO, Hamel N, Paradis A-J, Deschenes J, Tonin PN, Ghadirian P, Foulkes WD: Re: Population-based study of BRCA1 and BRCA2 mutations in 1305 unselected Finnish breast cancer patients. J Natl Cancer Inst 93:152-153, 2001. Letter to the editor (Peer Review)

  11. Clee SM, Zwinderman AH, Engert JC, Zwarts KY, Molhuizen HOF, Roomp K, Jukema JW, van Wijland M, van Dam M, Hudson TJ, Brooks-Wilson A, GenestJr. J, Kastelein JJP and Hayden MR: Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease. Circulation. 103:1198-1205, 2001.

  12. Codere F, Brais B, Rouleau G and Lafontaine E: Oculopharyngeal muscular dystrophy: What's new? Orbit.; 20(4):259-266, 2001.

  13. Daly MJ, Rioux JD, Schaffner JD, Hudson TJ, and Lander ES: High-resolution haplotype structure in the human genome. Nat Genet 29: 229-232, 2001.

  14. Davenport WJ, Siegel AM, Dichgans J, Drigo P, Mammi I, Pereda P, Wood NW and Rouleau GA: CCM1 mutations in families segregating cerebral cavernous malformations. Neurol 56:540-543, 2001.

  15. Deal C, Ma J, Wilkin F, Paquette J, Rozen F, Ge B, Hudson TJ, Stampfer M and Pollak M: Novel promoter polymorphism in insulin-like growth factor-binding protein-3: correlation with serum levels and interaction with known regulators. J Clin Endocrinol Metab 86:1274-1280, 2001.

  16. Desautels A, Turecki G, Montplaisir J, Ftouhi-Paquin N, Michaud M, Chouinard V-A and Rouleau GA: Dopaminergic neurotransmission and restless legs syndrome: A genetic association analysis. Neurol 57:1304-1306, 2001.

  17. Desautels A, Turecki G, Montplaisir J, Sequeira A, Verner A and Rouleau GA: Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q. Am J Hum Genet; 69:1266-1270, 2001.

  18. Dupré N, Cossette L, Hand CK, Bouchard J-P, Rouleau GA and Puymirat J: A founder mutation in French-Canadian families with X-linked hereditary neuropathy. Can. J. Neuroscience 38:51-55, 2001.

  19. Elhaji YA, Gottleib B, Lumbroso R, Beitel LK, Foulkes WD, Pinsky L and Trifiro M: The polymorphic CAG repeat of the androgen receptor gene: A potential role in breast cancer in women over 40. Breast Can Res Treatment 70:109-16, 2001.

  20. Fan X, Dion P, Laganiere J, Brais B and Rouleau GA: Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell death. Hum Molec Genet 10:2341-2351, 2001.

  21. Fitch D, Lesage A, Seguin M, Trousignant M, Bankelfat C, Rouleau GA and Turecki G: Suicide and the serotonin transporter gene. Mol Psychiatry 6:127-8, 2001.

  22. Forghani R, Garofalo L, Foran DR, Farhadi HF, Lepage P, Hudson TJ, Tretjakoff I, Valera P and Peterson A: A distal upstream enhancer from the myelin basic protein gene regulates expression in myelin forming Schwann cells. J. Neurosc 21 (11):3780-3787, 2001.

  23. Fortin A, Diez E, Rochefort D, Laroche L, Malo D, Rouleau GA, Gros P, and Skamene E: Recombinant congenic strains derived from A/J and C57BL/6J: A tool for genetic dissection of complex traits. Genomics; 74:21-35, 2001.

  24. Ftouhi-Paquin N, Alda M, Grof P, Chretien N, Rouleau G, and Turecki G: Identification of three polymorphisms in the translated region of PLC-gamma1 and their investigation in lithium responsive bipolar disorder. Am J Med Genet 105:301-5, 2001.

  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, and Rouleau GA: Ancestral origins of the Machado-Josheph disease mutation: A worldwide haplotype study. Am J Hum Genet 68:523-528, 2001.

  26. Goobie S, Popovic M, Morrison J, Ellis L, Ginzberg H, Boocock GRB, Ethesham N, Bétard C, Brewer CG, Roslin NM, Hudson TJ, Morgan K, Fujiwara TM, Durie PR and Rommens JM: Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7. Am J Hum Genet 68:1048-1054, 2001.

  27. Greenblatt MS, Chappuis PO, Bond JP, Hamel N and Foulkes WD: TP53 mutations in BRCA1/2-related breast cancer: distinctive spectrum and structural distribution. Can Res 61:4092-97, 2001.

  28. Greenwood CMT, Bureau A, Loredo-Osti JC, Roslin NM, Crumley MJ, Brewer CG, Fujiwara TM, Goldstein DR, and Morgan K: Pedigree selection and tests of linkage in a Hutterite asthma pedigree. (Proceedings of the Genetic Analysis Workshop 12, 23-26 October 2000, San Antonio: Analysis of complex genetic traits: Applications to asthma and simulated data, edited by Wijsman EM, Almasy L, Amos CI, Borecki I, Falk CT, King TM, Martinez MM, Meyers D, Neuman R , Olson JM, Rich S, Spence MA, Thomas DC, Vieland VJ, Witte JS, and MacCluer JW). Genet Epidemiol 21(Suppl 1):S244-251, 2001.

  29. 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 and Ikeda J-E: A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2. Nat Genet 29:166-173. 2001.

  30. Hadano S, Yanagisawa Y, Skaug J, Fichter K, Nasir J, Martindale D, Koop BF, Scherer SW, Nicholson DW, Rouleau GA, Ikeda JE and 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 71:200-213, 2001.

  31. Hand C, Mayeux-Portas V, Khoris J, Briolotti V, Clavelou P, Camu W and Rouleau GA. Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family. Ann Neurol 49:267-271, 2001.

  32. Harvey M, Cerone R, Schiaffino MC, Fantasia AR, Minniti G, Caruso U, Lorini R, Watkins D, Matiaszuk N, Rosenblatt DS, Schwahn B, Rozen R, LeGros L, Kotb M, Capdevila A, Luka Z, Finkelstein JD, Stabler SP, Allen RH, and Wagner C: Glycine N-methyltransferase deficiency : a novel inborn error causing persistent isolated hypermethioninaemia. J Inherit Metab Dis 24(4):448-464, 2001.

  33. Héon E, Paterson AD, Fraser M, Billingsley G, Priston M, Balmer A, Schorderet DF, Verner A, Hudson TJ and Munier FL: A progressive autosomal recessive cataract locus maps to chromosome 9q13 - q22. Am J Hum Genet 68:772-777, 2001.

  34. Hirschhorn JN, Lindgren CM, Daly MJ, Kirby A, Schaffner F, Burtt NP, Altshuler D, Parker A, Rioux JD, Platko J, Gaudet D, Hudson TJ, Groop LC and Lander ES: Genome-wide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height. Am J Hum Genet 69(1):106-16, 2001.

  35. Hudson TJ, Church DM, Greenaway S, Nguyen H, Cook A, Steen RG, Van Etten WJ, Strivens MA, Trickett P, Heuston C, Davison C, Southwell A, Hardisty R, Varela-Carver A, Haynes AR, Rodriguez-Tome P, Doi H , Ko MSH, Pontius J, Schriml L, Wagner L, Maglott D, Brown SDM, Lander ES, Schuler G and Denny P: A radiation hybrid map of mouse genes. Nat Genet 29: 201-205, 2001.

  36. Ichikawa Y, Goto J, Hattori M, Toyoda A, Ishii K, Jeong S-Y, Hashida H, Masuda N, Ogata K, Kasai F, Hirai M, Macial P, Rouleau GA, Sakaki Y and Kanazawa I : The genomic structure and expression of MJD, the Machado-Joseph disease gene. J Hum Genet 46:413-422, 2001.

  37. Jannatipour M, Dion P, Khan S, Jindal H, Fan X, Laganière J, Chishti AH and Rouleau GA: Schwannomin isofirm-1 interacts with syntenin via PDZ domians. J Biol Chem 276:33,093-33,100. 2001.

  38. Jefferies S, Edwards SM, Hamoudi R, A'Hern R, Foulkes W, Goldgar D, MPT collaborators and Eeles R. No germline mutations in mCDKN2A (p16) in patients with squamous cell cancer of the head and neck and second primary tumours. Br J Can 85:1383-6, 2001.

  39. Jernstrom H, Deal C, Wilkin F, Chu W, TaoY, Majeed N, Hudson TJ, Narod SA and Pollak M: Genetic and nongenetic factors associated with variation of plasma levels of insulin-like growth factor-i and insulin-like growth factor-binding protein-3 in healthy premenopausal women. Cancer Epidemiology, Biomarkers Prevention 10(4):377-84, 2001.

  40. Jiralerspong S, Ge B, Hudson TJ and Pandolfo M: Manganese superoxide dismutase induction by iron is impaired in Friedreich Ataxia cells. FEBS Letters 509:101-105, 2001.

  41. Jones AO, Tzenova J, Frappier D, Crumley MJ, Roslin NM, Kos CH, Tieder M, Langman CB, Proesmans W, Carpenter TO, Rice A, Anderson D, Morgan K, Fujiwara TM and Tenenhouse HS: Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene. J Am Soc Nephrol 12:507-514, 2001.

  42. Julian-Reynier C, Bouchard L, Evans DGR, Eisinger F, Foulkes WD, Kerr B, Blanquaert, Moatti J-P and Sobol H: Women's attitudes towards preventive strategies for Hereditary Breast/Ovarian cancer risk differ from one country to another: differences between Manchester (UK), Marseilles (F) and Montreal (Ca). Cancer 92:959-68, 2001.

  43. Kauppi P, Lindblad-Toh K, Sevon P, Toivonen HTT, Rioux JD, Villapakkam A, Laitinen LA, Hudson TJ, Kere J and Laitinen T: A second generation association study on the 5q31 cytokine gene cluster and IL4RA gene in asthma. Genomics 77:35-42, 2001.

  44. Khittoo G, Manning AP, Mustun H, Appadoo J, Venkatasamy S, Fagoonee I, Ghadirian P and Tonin PN: Mutation analysis of a Mauritian hereditary breast cancer family reveals the BRCA2 6503delTT mutation previously found to recur in different ethnic populations. Hum Hered 52:55-58, 2001.

  45. Kotorii S, Takahashi K, Kamimura K, Nishio T, Arima K, Yamada H, Uyama E, Uchino M, Suenaga A, Matsumoto M, Kuchel G, Rouleau GA and Tabira T: Mutations of the notch3 gene in non-caucasian patients with suspected CADASIL syndrome. Dement Geriatr Cogn Disord; 12:185-193. 2001.

  46. Laitinen T, Daly MJ, Rioux JD, Kauppi P, Laprise C, Petäys T, Green T, Cargill M, Haahtela T, Lander ES, Laitinen LA, Hudson TJ and Kere J: A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population. Nat Genet 28:87-91, 2001.

  47. Lalonde L, Clarke AE, Joseph L, Mackenzie T, Grover SA, (Canadian Cardiac Assessment Group) Cassidy LE, Green L, Larochelle D, Motchula R, McCans J, McLeod PJ, Fortier RR, Stewart JA, Balnk DW, Charbonneau F, Gilfix BM, Sami M, Sherman MH, and Smilovitch M: Health related quality of life with coronary heart disease prevention and treatment. J Clin Epidemiol 54(10):1011-1018, 2001.

  48. LaRow JA, Mysliborski J, Rappaport IP, Rouleau GA and Carlson, JA: Alopecia areata universalis in an infant. J Cutan Med Surg; 5:131-134, 2001.

  49. Lee N, Daly MJ, Delmonte T, Lander ES, Xu F, Hudson TJ, Mitchell GA, Morin CC, Robinson BH and Rioux JD: A genome-wide linkage disequilibrium scan localizes the Saguenay-Lac-Saint-Jean COX oxidase deficiency to 2p16. Am J Hum Genet 68:397-409, 2001.

  50. Lee SH, Gitas J, Zafer A, Lepage P, Hudson TJ, Belouchi A and Vidal SM: Haplotype mapping indicates two independent origins for the Cmv1s susceptibility allele to cytomegalovirus infection and refines its localization within the Ly49 cluster. Immunogenetics 53(6):501-5, 2001.

  51. Lee PD, Sladek R, Greenwood CMT and Hudson TJ: Control genes and variability: absence of ubiquitous reference transcripts in diverse mammalian expression studies. Genome Res (12) 292-297, 2001.

  52. Maciel P, Costa MC, Ferro A, Rousseau M, Santos CS, Gaspar C, Barros J, Rouleau GA, Coutinho P, and Sequeiros J: Improvement in the molecular diagnosis of Machado-Joseph disease. Arch Neurol 58:1821-1827, 2001.

  53. Manning AP, Abelovich D, Ghadirian P, Lambert JA, Frappier D, Provencher D, Robidoux A, Peretz T, Narod SA, Mes-Masson A-M, Foulkes WD, Wang T, Morgan K, Fujiwara TM, and Tonin PN: Haplotype analysis of BRCA2 8765delAG Mutation Carriers in French Canadian and Yeminite Jewish Hereditary Breast Cancer Families. Hum Hered 52:116-120, 2001.

  54. McLeod RS, Geerts WH, Sniderman KW, Greenwood C, Gregoire RC, Taylor BM, Silverman RE, Atkinson KG, Burnstein M, Marshall JC, Burul CJ, Anderson DR, Ross T, Wilson SR, Barton P. Subcutaneous heparin versus low-molecular-weight heparin as thromboprophylaxis in patients undergoing colorectal surgery: results of the Canadian colorectal DVT prophylaxis trial: a randomized double-blind trial. Ann Surg 233(3): 438-444, 2001.

  55. Narod SA, Sun P, Ghadirian P, Lynch H, Isaacs C, Garver J, Weber B, Karlan B, Fishman D, Rosen B, Tung N, and Heuhausen SL, Hereditary Ovarian Cancer Clinical Study Group*: Tubal ligation and risk of ovarian cancer in carriers of BRCA1 and BRCA2 mutations: a case control study. Lancet 357:1467-1470, 2001. *Member contributing data.

  56. Naumova A, Greenwood CMT, and Morgan K: Imprinting and deviation from Mendelian transmission ratios. Genome 44:311-320, 2001.

  57. Nikpoor B, Turecki G, Fournier C, Theroux P, and Rouleau GA: A Functional Myeloperoxidase Polymorphic Variant is associated with coronary artery disease in French Canadians. Am Heart J; 142:336-339, 2001.

  58. Pal T, Hamel N, Vesprini D, Sanders K, Mitchell M, Quercia N, Ng Cheong N, Murray A, Foulkes WD and Narod SA: Double primary cancers of the breast and thyroid in women: molecular analysis and genetic implications. Familial Cancer 1: 17-24, 2001.

  59. Pal T, Vogl FD, Chappuis PO, Tsang R, Brierley J, Renard H, Sanders K, Kantemiroff T, Bagha S, Goldgar DE, Narod SA and Foulkes WD. Increased risk for non-medullary thyroid cancer (NMTC) in the first-degree relatives of prevalent cases of NMTC: a hospital-based study. J Clin Endocrinol Metab 86:5307-5312, 2001.

  60. Powers JM, Rosenblatt DS, Schmidt RE, Cross AH, Black JT, Moser AB, Moser HW and Morgan DJ: Neurological and Neuropathology heterogeneity in two brothers with cobalamin C deficiency (cblC). Ann Neurol 49:396-400, 2001.

  61. Pramatarova A, Laganière L, Roussel J, Brisebois K, and Rouleau GA: Neuron specific expression of mutant SOD1 in transgenic mice does not lead to motor impairment. J Neuroscience; 21:3369-74, 2001.

  62. Rioux JD, Daly MJ, Lindblad K, Silverberg MS, Delmonte T, Kocher K, Miller K, Guschwan S, Kulbokas EJ, O'Leary S, Winchester E, Dewar K, Cohen A, Langelier D, Lapointe G, Gaudet D, Faith J, Branco N, McLeod RS, Griffiths AM, Bull SB,Bitton A, Greenberg GR, Steinhart H, Cohen Z, Lander ES. Siminovitch KA and Hudson TJ: Genetic variation in 5q31 cytokine gene cluster confers susceptibility to Crohn disease. Nat Genet 29:223-228, 2001.

  63. Rosenblatt DS: Methylenetetrahydrofolate reductase. Clin Invest Med 24 (1):56-59, (Clinically Important Genes), 2001.

  64. Routy J-P, Smith GHR, Blank DW, and Gilfix BM: Plasmapheresis in the treatment of an acute pancreatitis due to protease inhibitor-induced hypertriglyceridemia. J Clin Apheresis; 16:157-159, 2001.

  65. Runnebaum IB, Wang-Gohrke S, Vesprini D, Kreienberg R, Lynch H, Moslehi R, Ghadirian P, Weber B, Godwin AK, Risch H, Garber J, Lerman C, Olapade OI, Foulkes WD, Karlan B, Warner E, Rosen B, Rebbeck T, Tonin P, Dubé M-P, Kieback DG, Narod SA: Progesterone receptor variant increases ovarian cancer risk in BRCA1 and BRCA. mutation carriers who were never exposed to oral contraceptives. Pharmacogenet 11:1-4, 2001.

  66. Satagopan JM, Offit K, Foulkes WD, Robson ME, Wacholder S, Eng CM, Karp SE, and Begg CB: The lifetime risk of breast cancer in Ashkenazi Jewish carriers of BRCA1 and BRCA2 mutations. Can Epidemiol Biomarkers Prevention 10:467-73, 2001.

  67. Seyda A, Newbold RB, Hudson TJ, Verner A, MacKay N, Winter S, Feigenbaum A,Malaney S, Gonzalez-Halphen D, Cuthbert AP & Robinson BH: A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13. Am J Hum Genet 68:386-396, 2001.

  68. Silverberg MS, Moskovitz DN, Daly MJ, Rioux JD, McLeod RS, Cohen Z, Greenberg GR, Hudson TJ, Siminovitch KA & Steinhart H: Diagnostic misclassification reduces the ability to detect linkage in inflammatory bowel disease genetic studies. Gut 49:(6)773-6, 2001.

  69. St. Pierre J, Vohl MC, Brisson D, Perron P, Després JP, Hudson TJ and Gaudet D: A sequence variation in the mitochondrial glycerol-3-phosphate dehydrogenase gene Is associated with increased plasma glycerol and free fatty acid concentrations among French Canadians. Molecular Gen Metab 72:209-217, 2001.

  70. Thompson D, Easton D, and the Breast Cancer Linkage Consortium*: Variation in cancer risks by mutation position in BRCA2 mutation carriers. Am J Hum Genet. 68:410-419, 2001. *Member contributing data

  71. Tonin PN, Hudson TJ, Rodier F, Bossolasco M, Lee P, Novak J, Manderson EN, Provencher D, Mes-Masson A-M: Microarray analysis of gene expression mirrors the biology of an ovarian cancer model. Oncogene 20:6617-6626, 2001.

  72. Tonin PN, Perret C, Lambert JA, Paradis A-J, Kantemiroff T, Benoit M-H, Martin G, Foulkes WD, Ghadirian P: Founder BRCA1 and BRCA2 mutations in early-onset French Canadian breast cancer cases unselected for family history. Int J Cancer (Pred. Oncol.) 95:189-193, 2001.

  73. Turecki G, Brière R, Dewar K, Lesage A, Séguin M, Chawky N, Vanier C, Alda M; Joober R, Benkelfat C, Rouleau GA: Reply to Harrison. Am J Psychiatry; 158:148. 2001.

  74. Turecki G, Grof P, Grof E, D'Souza V, Lebuis L, Marineau C, Cavazzoni P, Duffy A,Bétard 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. Molec Psychiat 6(5):570-578, 2001.

  75. 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 GA: TPH and suicidal behavior: A study in suicide completers. Mol Psychiat; 6:98-102, 2001

  76. Watkins D, and Rosenblatt DS: Cobalamin and inborn errors of cobalamin absorption and metabolism. Endocrinologist 11:98-104, 2001.

  77. Yamamoto K, Bloom D, La S, Turecki G, Joober R, Benkelfat C, Lalonde P, Labelle A, Rouleau GA: Polymorphism in the cell division cycle 45 like gene and schizophrenia. Am J Med Genet; 105:214-5, 2001.



  1. Fenton WA, Gravel RA, and Rosenblatt DS: Disorders of propionate and methylmalonate metabolism, in The Metabolic and Molecular Bases of Inherited Metabolic Disease (eighth edition). CR Scriver, AL Beaudet, WS Sly, D Valle (eds), B Childs, KW Kinzler, B Vogelstein (co-eds): McGraw-Hill, New York. 2001, pp 2165-2193.

  2. Hudson TJ: Le génome humain: un jeu de mots cachés à peine entamé. Michel Venne (Ed.): La révolution génétique. Les Presses de l'Université Laval, Canada 2001, pp 17-23.

  3. Rosenblatt DS, Fenton WA: Inherited disorders of folate and cobalamin transport and metabolism, in The Metabolic and Molecular Bases of Inherited Metabolic Disease (eighth edition). CR Scriver, AL Beaudet, WS Sly, D Valle (eds), B Childs, KW Kinzler, B Vogelstein (co-eds): McGraw-Hill, New York. 2001, pp 3897-3933.

  4. Rosenblatt DS: Inborn errors of folate and cobalamin metabolism, in Homocysteine in Health and Disease, Ralph Carmel and Donald W. Jacobsen (eds.) Cambridge University Press. 2001, pp 244-258.



  1. Arcand S, Mes-Masson AM, Wang J, Novak J, Provencher D, Hudson TJ & Tonin P. Characterization of a novel chromosome 22 HSR in human epithelial ovarian cancer using high density oligonucleotide array technology, Graduate Student Research Days, Dept of Human Genetics. McGill University, April 25, 2001.

  2. Brisson D, Vohl MC, Perron P, Hudson TJ & Gaudet D. Association entre la mutation L162V du gène PPARa et les concentrations de cholestérol et triglycérides des fractions lipoprotéiques. Oral presentation: 9e Réunion Scientifique Annuelle de La Société Québécoise d'Hypertension Artérielle, Québec, January 11-13, Médecine/Sciences. 2001.

  3. Brisson D, Vohl M-C, Perron P, Després JP, Hudson TJ & Gaudet D. Association of the PPARa L162V missense mutation with cholesterol and tryglyceride contents of lipoproteins subfractions. First International Symposium on PPARs: from Basic Science to Clinical Applications. Florence, Italy, April 4 -7, 2001.

  4. Brisson D, Vohl MC, Perron P, and Hudson TJ and Gaudet D: Comparaison des effets de la mutation PPAR a- L162V et d'autres génotypes dyslipidémiants sur les concentrations de cholestérol et triglycérides des fractions lipoprotéiques. a). Deuxième Réunion Annuelle de la Société Québécoise de Lipidologie, Nutrition et Métabolisme. Lac Delage, April 27-29, Médecine/Sciences. 2001.

  5. Bull S, Greenwood C. Mirea L, Biernacka, and K. Morgan: Analysis of accumulating data in genomewide studies of affected sib pairs. Genet Epidemiolo 21:145, 2001. Oral presentation

  6. Caron J, Laroche L, Skamene E, Loredo-Osti JC, Morgan K, and Malo D: Identification of genetic loci controlling Salmonella enteritidis clearance: an unexpected role of Nramp1 in the persistence of infection. Poster at the 15th International Mouse Genome Conference, Final Programme and Book of Abstracts, p. 63, 2001.

  7. Cartier L, Khalife S, Desilets V, Beaumier L, Flageole H, Laberge J-M: Prenatal detection and perinatal management of a giant cervical teratoma. Am J Hum Genet 69 (Suppl 4): 662 (2825), 2001.

  8. Chapman NH, Crumley J, Fujiwara TM, Morgan K, and Thompson EA: Estimation of small map distances using chromosome data from an isolated population. Am J Hum Genet 69 (Suppl 4):410, (1336), 2001.

  9. Chappuis PO, Goffin J, Hamel N, Wong N, Paradis A-J, Roberge D, Brunet JS, Yee C, Tonin P, Boyd J, Ghadirian P, Begin LR, and Foulkes WD: Good response to chemotherapy (CT) and hormonotherapy (HT) in patients with BRCA1-BC). Am J Hum Genet 60 (Suppl 4):249 (383), 2001.

  10. Daly MJ, Rioux JD, Schaffner SF, Hudson TJ and Lander ES: Fine structure LD map of 5q31 and implications for gene mapping.Genome Sequencing & Biology, Cold Springs Harbor, NY, p.212-213. 2001.

  11. Daly MJ, Rioux JD, Schaffner SF, Hudson TJ, Lander ES: Fine-Structure haplotype map of 5q31: implications for gene-based association studies and genomic LD mapping. Am J Hum Genet 69: (Suppl. 4): 181(28), 2001.

  12. Désilets VA, Tan SL, Ao A,: Limitations of preimplantation genetic diagnosis for a paternal carrier of a t(9;15) chromosome. Am J Hum Genet 69 (Suppl 4): 665 (2846), 2001.

  13. Desautels A, Montplaisir J, Paquin N, Sequeira A, Hudson TJ, Rouleau G and Turecki G. A molecular genetics study of restless legs syndrome. Graduate Student Research Days, Dep't of Human Genetics. McGill University, March 21, 2001.

  14. Engert JC, Vohl M-C, Fujiwara TM, Roslin N, Brewer C, Verner A, Platko J, Rioux J, Gaudet D, Morgan K and Hudson TJ: A genome-wide scan for CHD susceptibility in the Saugenay-Lac-Staint-Jean region of Quebec. Poster at the Canadian Genetic Diseases Network Annual Scientific Meeting 2001, Poster Abstracts, p. 18, 2001.

  15. Forgetta V, Verner A, Laroche L, Hudson TJ and Malo D. Systematic search for Salmonella-susceptibility quantitative trait loci (QTL) in chickens using a whole genome scan approach, Graduate Student Research Days, Dep't of Human Genetics. McGill University, April 25, 2001.

  16. Greenwood CMT, Lemire M, and Morgan K: Regression trees to select maximally-linked phenotypes in relative-pair linkage analysis of multivariate traits. Am J Hum Genet 69:(Suppl. 4):396, (1250), 2001.

  17. Greenwood CMT, Loredo-Osti JC, Roslin NM, Fujiwara TM, and Morgan K: Pedigree selection and tests of linkage for asthma and IgE in an extended Hutterite pedigree. Presentation by C. Greenwood and poster at the Canadian Genetic Diseases Network Annual Scientific Meeting 2001, Poster Abstracts, p. 19, 2001.

  18. Hudson TJ: The Human Genome Project. Breakfast at Parliament Hill. Ottawa, Ontario, April 5, 2001.

  19. Hudson TJ, Church DM, Greenaway S, Nguyen H, Cook A, Steen RG, Van Etten WJ, Strivens MJ, Trickett P, Heuston C, Davison C, Southwell A, Hardisty R, Varela-Carver A, Haynes AR, Rodriguez-Tome P, Doi H, Ko MSH, Pontius J, Schriml L, Wagner L, Maglott D, Brown SDM, Lander ES, Schuler G and Denny P: A Gene Map of the mouse genome. Genome Sequencing & Biology, Cold Springs Harbor, NY, p129, 2001.

  20. Jaykar P, Vasconsellos E, and Rosenblatt DS: Early retinal and MRI changes in a neonate with homocystinuria and methylmalonic aciduria (cblC). Am J Hum Genet 69:(Suppl. 4):487, 2001.

  21. Kaplan F, Comber J, MacRae T, Sladek R, Hudson TJ, Sweezey NB: Developmental patterns of altered gene expression in the lungs of a glucocorticoid receptor knock-out mouse: Altered expression of the retinoic acid responsive growth facture midkine. Am J Hum Genet 69:(Suppl. 4):344 (944), 2001.

  22. Laflamme N, Laroche J, Dodin S, Giguère Y, Morgan K, and Rousseau F: Two genes involved in bone response to hormone replacement therapy in postmenopausal women. Genet Epidemiol 21:162, 2001.

  23. Ledoux K, Brisson D, St-Pierre J, Julien P, Peron P, Hudson TJ, Vohl MC and Gaudet D: Effet de mutations dans les gènes de la LPL, de PPAR a et de PPAR ? sur la réponse à un traitement hypolipidémiant au fénofibrate (un agoniste PPAR a). Deuxième Réunion Annuelle de la Société Québécoise de Lipidologie, Nutrition et Métabolisme. Médecine/Sciences. 2001.

  24. Lee PD, Sladek R, Novak J and Hudson TJ: Control genes and microarray gene expression data. Genome Sequencing & Biology, Cold Springs Harbor, NY, 156, 2001.

  25. Lepage P, Farhadi HF, Forghani R, Miller W, Hudson TJ and Peterson AC. Identification of modules controlling myelination by cross-species sequence comparisons and conrolled transgenesis. Genome Sequencing & Biology, Cold Springs Harbor, NY, 298, 2001.

  26. Naumova AK, Croteau S, Greenwood CMT, and Morgan K: Inheritance patterns of alleles in imprinted regions of the mouse genome at different stages of development. Am J Hum Genet 69(Suppl. 4): 571 (2290), 2001.

  27. Pastinen T, Long AD and Hudson TJ: Cost-efficient analysis of SNPS using allele-specific extension coupled with TAG-arrays. Genome Sequencing & Biology, Cold Springs Harbor, NY, 189, 2001.

  28. Provencher D, Tonin P, Perret C, Foulkes W, Nolet S, Mes-Masson A-M, Narod S, Ghadirian P: Oncologic features of our first 200 women carrying a mutation in the BRCA genes. Society for Oncologists and Gynecologists of Canada- 57th Annual Clinical Meeting, 2001.

  29. Raby BA, Laprise C, Fortin J, Renaud Y, Murphy J, Sinnett D, Greenwood C, Morgan K, Gagné D, Bégin P, and Hudson TJ: Asthma and atopy susceptibility polymorphisms in a founder population from Saguenay-Lac-St-Jean, Québec. Clin Invest Med 24(4):225, 2001.

  30. Rioux JD, Daly MJ, Lindblad-Toh K, Silverberg MS, Delmonte T, Kocher K, Kulbokas EJ, Miller K, O'Leary S, Winchester E, Bitton A, Steinhart H, Cohen Z, Siminovitch K, Hudson TJ & Lander ES. A nested hierarchical approach to linkage disequilibrium mapping of complex traits: identification of a common risk haplotype conferring susceptibility to Chron's disease (CD). Genome Sequencing & Biology, Cold Springs Harbor, NY, 219, 2001.

  31. Rioux JD, Daily MJ, Silverberg M, Lindblad K, Steinhart H, Cohen Z, Delmonte T, Kocher K, Miller K, Guschwan S, McLeod R, Cohen A, Langelier D, Lapointe G, Griffiths A, Bitton A, Greenberg G, Lander E, Simminovitch K, Hudson TJ: Hierarchical linkage disequilibrium lapping of a susceptibility gene for Crohn`s disease (CD) to the cytokine cluster on chromosome 5. Am J Hum Genet 69:(Suppl. 4):225 (247), 2001.

  32. Rosenblatt DS: Molecular bases of hyperhomocysteinemia due to inborn errors of folate and cobalamin metabolism. Pteridines 12(2):73, 2001.

  33. Sladek R, Brewer J, Comber J, Kaplan F, Sweezey NB, Muglia LJ and Hudson TJ A Genomic study of tissue-specific responses following glucocorticoid treatment. Genome Sequencing & Biology, Cold Springs Harbor, NY, 237, 2001.

  34. Verner A, Darmond-Zwaig C, Frappier D, Fortin Y, Renaud Y, Sammak A, Brewer C, Roslin N, Fujiwara M, Engert J, Morgan K, and Hudson TJ: CGDN genotyping core facility. Poster at the Canadian Genetic Diseases Network Annual Scientific Meeting 14, 2001.

  35. Yotova V, Zikiewicz E, Lemieux-blanchard E, Labuda M, Bourgeois S, Labuda D, Fortin J, Lepage P, Hudson TJ, Lescault A, and Laberge C: Founder effect in North-Estern Quebec and the extent of the genetic signature associated with the myotonic dystrophy mutation. Am J Hum Genet 69:(Suppl. 4):421 (1401), 2001.


Members | Report | Meetings
Publications | Funds | Financials

| Top | Home | McGill |

© 2002 Finestone Laboratory