ORIGINAL
ARTICLES
- 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.
- 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.
- Bodamer OAF, Rosenblatt DS, Appel SH, and Beaudet
AL: Adult-onset combined methylmalonic aciduria and homocystinuria. Neurology
56:1113-1114, 2001.
- 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.
- 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.
- 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.
- Bull SB, Darlington GA, Shin J and Greenwood CMT.
Efficiency of association studies of candidate genes in families. Genet Epidemiol
20:149-174, 2001
- 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.
- 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.
- 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)
- 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.
- Codere F, Brais B, Rouleau G and Lafontaine E:
Oculopharyngeal muscular dystrophy: What's new? Orbit.; 20(4):259-266, 2001.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- Naumova A, Greenwood CMT, and Morgan K: Imprinting
and deviation from Mendelian transmission ratios. Genome 44:311-320, 2001.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- Rosenblatt DS: Methylenetetrahydrofolate reductase. Clin
Invest Med 24 (1):56-59, (Clinically Important Genes), 2001.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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
- 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.
- 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.
- 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.
- 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.
- 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
- Watkins D, and Rosenblatt DS: Cobalamin and inborn
errors of cobalamin absorption and metabolism. Endocrinologist 11:98-104, 2001.
- 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.
BOOK CHAPTERS
- 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.
- 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.
- 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.
- 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.
ABSTRACTS
- 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.
- 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.
- 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.
- 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.
- 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
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- Hudson TJ: The Human Genome Project. Breakfast at
Parliament Hill. Ottawa, Ontario, April 5, 2001.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- 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.
- Rosenblatt DS: Molecular bases of
hyperhomocysteinemia due to inborn errors of folate and cobalamin metabolism. Pteridines
12(2):73, 2001.
- 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.
- 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.
- 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.
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