2002/2003 Publications Page |
2002/2003 Publications Page |
Ah Mew N, Hamel N, Galvez M, Al-Saffar M and Foulkes
WD: Haplotype analysis of a BRCA1:185delAG mutation in a Chilean family
supports its Ashkenazi origins. Clin Genet 62:151-156, 2002.
Al-Saffar M and Foulkes WD: Hereditary ovarian cancer resulting from a
non-ovarian cancer cluster region (OCCR) BRCA2 mutation: is the OCCR useful clinically? J
Med Genet. 39:e68, 2002.
Arbour L, Christensen B, Delormier T, Platt R, Gilfix B, Forbes P,
Kovitch I, Morel J and Rozen R: Spina bifida, folate metabolism, and dietary folate intake
in a Northern Canadian aboriginal population. Int J Circumpolar Health.
61:341-51, 2002.
Brisson D, Ledoux K, Bossé Y, St-Pierre J, Julien P, Perron P, Hudson TJ,
Vohl MC and Gaudet D : Effect of apolipoprotein E, peroxisome proliferator-activated
receptor alpha and lipoprotein lipase gene mutations on the ability of fenofibrate to
improve lipid profiles and reach clinical guideline targets among hypertriglyceridemic
patients. Pharmacogenetics 12: 313-320, 2002.
Bull SB, Greenwood CMT, Mirea L and K. Morgan: Regression models for
allele sharing: analysis of accumulating data in affected sib pair studies. (Statistics
and Health, Edmonton Statistics Conference 2000, Edmonton, 11-13 June 2000) Statistics
in Medicine 21:431-444, 2002.
Caron J, Loredo-Osti JC, Laroche L, Skamene E, Morgan K and Malo D:
Identification of genetic loci controlling bacterial clearance in experimental Salmonella
enteriditis infection: an unexpected role of Nramp1 (Slc11a1) in
the persistence of infection in mice. Genes and Immunity 3:196-204, 2002.
de la Casa-Esperón E, Loredo-Osti JC, E., Pardo-Manuel de Villena F, Briscoe TL, Malette
JM, Rosa M, Vaughan JE, Morgan K and Sapienza C: X chromosome effect on
maternal recombination and meiotic drive in the mouse. Genetics 161:1651-1659,
2002.
Chagnon P, Michaud J, Mitchell G, Mercier J, Marion JF, Drouin E, Rasquin-Weber A, Hudson
TJ and Richter A: A missense mutation (R565W) in cirhin (FLJ14728) in North
American Indian childhood cirrhosis. Am J Hum Genet 71:1443-14439, 2002.
Chen Z, Ge B, Hudson TJ and Rozen R: Microarray analysis of brain RNA in
mice with methylenetetrahydrofolate reductase deficiency and hyperhomocysteinemia. Gene
Expression Patterns 1:89-93, 2002.
Chappuis PO, Goffin J, Perret C, Wong N, Ghadirian P, Tonin PN and Foulkes
WD: A significant response to neoadjuvant chemotherapy in BRCA1/2-related breast
cancer. J Med Genet 39:608-610, 2002.
Chiu C-H, Amemiya C, Dewar K, Kim C-B, Ruddle F and Wagner G: Molecular evolution of the
HoxA cluster in the three major gnthostome lineages. Proc Natl Acad Sci USA 99:
5492-5497, 2002.
Cossette P, Liu L, Brisebois K, Dong H, Lortie A, Vanasse M, Saint?Hilaire JM, Carmant L,
Verner A, Lu WY, Tian Wang Y and Rouleau GA: Mutation of GABRA1 in an
autosomal dominant form of juvenile myoclonic epilepsy. Nat Genet 31:184-9, 2002.
Croteau S, Andrade MF, Huang F, Greenwood CMT, Morgan K and Naumova AK:
Inheritance patterns of maternal alleles in imprinted regions of the mouse genome at
different stages of development. Mammalian Genome 13:24-29, 2002.
Desautels A, Michaud M, Montplaisir J, Turecki G and Rouleau GA: Restless
leg syndrome arousal: clinic, etiology and genetic perspectives. Rev Neurol (Paris)
158:1225?31, 2002.
Dobson CM, Wai T, Leclerc D, Wilson A, Wu X, Dore C, Hudson TJ, Rosenblatt DS and Gravel
RA: Identification of the gene responsible for the cblA complementation group of vitamin
B12-responsive methylmalonic acidemia based on the analysis of prokaryotic gene
arrangements. Proc Natl Acad.Sci USA 99:15554-15559, 2002.
Dobson CM, Wai T, Leclerc D, Kadir H, Narang M, Lerner-Ellis JP, Hudson TJ, Rosenblatt
DS and Gravel RA: Identification of the gene responsible for the cblB
complementation group of vitamin B12-dependent methylmalonic aciduria. Hum Molec Genet.
11:3361-3369, 2002.
Dobson-Stone C, Danek A, Rampoldi L, Hardie RJ, Chalmers RM, Wood NW, Bohlega S, Dotti MT,
Federico A, Shizuka M, Tanaka M, Watanabe M, Ikeda Y, Brin M, Goldfarb LG, Karp BI,
Mohiddin S, Fananapazir L, Storch A, Fryer AE, Maddison P, Sibon I, Trevisol-Bittencourt
PC, Singer C, Caballero IR, Aasly JO, Schmierer K, Dengler R, Hiersemenzel LP, Zeviani M,
Meiner V, Lossos A, Johnson S, Mercado FC, Sorrentino G, Dupre N, Rouleau GA,
Volkmann J, Arpa J, Lees A, Geraud G, Chouinard S, Nemeth A and Monaco AP: Mutational
spectrum of the CHAC gene in patients with chorea-acanthocytosis. Eur J Hum Genet 10:
773?81, 2002.
Dombrowski C, Lévesque S, Morel ML, Rouillard P, Morgan K and Rousseau
F: Premutation and intermediate-size FMR1 alleles in 10572 males from the general
population: loss of an AGG interruption is a late event in the generation of fragile X
syndrome alleles. Hum Molec Genet 11:371-378, 2002.
Elstein J, Gilfix BM and Elstein E: Predicting
atherosclerotic risk in type II diabetic patients: Is there a role for hsCRP? Diabetes
Quarterly Fall:5-9, 2002.
Engert JC, Vohl MC, Williams SM, Lepage P, Loredo-Osti JC, Faith J, Doré C, Renaud Y,
Burtt NP, Villeneuve A, Hirschhorn JN, Altshuler D, Groop LC, Despré JP, Gaudet D and Hudson
TJ: 5’ Flanking variants of Resistin are associated with obesity. Diabetes
51: 1629-34, 2002.
Ernest S, Christensen B, Gilfix BM, Mamer OA, Hosack A, Rodier M,
Colmenares C, McGrath J, Bale A, Balling R, Sankoff D, Rosenblatt DS and
Nadeau JH: Genetic and molecular control of folate-homocysteine metabolism in mutant mice.
Mammalian Genome 13:259-267, 2002.
Fan JB, Gehl D, Hsie L, Shen N, Lindblad-Toh K, Laviolette JP, Robinson E, Lipshutz R,
Wang D, Hudson TJ and Labuda D: Assessing DNA sequence variations in
human ESTs in a phylogenetic context using high-density oligonucleotide arrays. Genomics
80:1-10, 2002.
Foulkes WD, Brunet J-S, Wong N, Goffin J and Chappuis PO: Change in the
penetrance of founder BRCA1/2 mutations? A retrospective cohort study. J Med Genet
39:407-409, 2002.
Foulkes WD, Thiffault I, Gruber SB, Horwitz M, Hamel N, Lee C, Shia J,
Markowitz A, Figer A, Friedman E, Farber D, Greenwood CM, Bonner JD, Nafa K, Walsh T,
Marcus V, Tomsho L, Gebert J, Macrae FA, Gaff CL, Paillerets BB, Gregersen PK, Weitzel J,
Gordon PH, MacNamara E, King MC, Hampel H, de la Chapelle A, Boyd J, Offit K, Rennert G,
Chong G and Ellis NA: The founder mutation MSH2*1906G>C is an important cause of
Hereditary Non-Polyposis Colorectal Cancer in the Ashkenazi Jewish population. Am J
Hum Genet 71:1395-412, 2002.
Frosk PT, Weiler E. Nylen T. Sudha CR, Greenberg, Morgan K, Fujiwara TM
and Wrogemann K: Limb-girdle muscular dystrophy type 2H associated with mutation in
TRIM32, a putative E3-ubiquitin-ligase gene. Am J Hum Genet 70:663-672, 2002.
Ghadirian P, Liu G, Gallinger S, Schmocker B, Paradis A-J, Lal G, Brunet J-S, Foulkes
WD and Narod SA: Family history is a risk factor for pancreatic cancer. Int J
Cancer 97:807-810, 2002.
Hand CK, Khoris J, Salachas F, Gros-Louis F, Simoes Lopes AA, Mayeux-Portas V, Brown RH,
Meininger V, Camu W and Rouleau GA: A novel locus for familial
amyotrophic lateral sclerosis, on chromosome 18q. Am J Hum Genet 70:251-256,
2002.
Hand CK, and Rouleau GA: Familial Amyotrophic Lateral Sclerosis. Muscle
Nerve 25:135-159, 2002.
Hébert-Blouin M-H, Koufogianis V, Gillett P and Foulkes WD: Fallopian
tube cancer in a BRCA1 mutation carrier: rapid development and failure of screening. Am
J Obstet Gynecol 186:53-54, 2002.
Howard HC, Dubé, M-P, Prévost C, Bouchard J-P, Mathieu J and Rouleau GA:
Fine mapping the candidate region for peripheral neuropathy with or without agenesis of
the corpus callosum in the French Canadian population. Eur J Hum Gen 10:406-12,
2002.
Howard HC, Mount DB, Rochefort D, Byun N, Dupre N, Lu J, Fan X, Song L, Riviere JB,
Prevost C, Horst J, Simonati A, Lemcke B, Welch R, England R, Zhan FQ, Mercado A, Siesser
WB, George AL, McDonald MP, Bouchard JP, Mathieu J, Delpire E and Rouleau GA:
The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with
agenesis of the corpus callosum. Nat Genet 32: 384-92, 2002.
Hutter P, Wijnen J, Rey-Berthod C, Thiffault I, Verkuijlen P, Farber D,Hamel N, Bapat B,
Thibodeau SN, Burn J, Wu J, MacNamara E, Heinimann K, Chong G and Foulkes WD:
An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing
mutation in MLH1. J Med Genet 39:323-327, 2002.
Joober R, Boksa P, Benkelfat C and Rouleau GA: Genetics of schizophrenia:
From animal models to clinical studies. J Psych Neurosc 27:336-47, 2002.
Joober R, Gauthier J, Lal S, Bloom D, Lalonde P, Rouleau GA, Benkelfat C
and Labelle A: Catechol-o-methyltransferase val-108/158-met gene variants associated with
performance on the Wisconsin card sorting test. Arch Gen Psychiatry 59:662-3,
2002.
Joober R, Rouleau GA, Lal S, Dixon M, O'Driscoll G, Palmour R, Annable L,
Bloom D, Lalonde P, Labelle A and Benkelfat C: Neuropsychological impairments in
neuroleptic-responder vs. -nonresponder schizophrenic patients and healthy volunteers. Schizophr
Res 53:229?238, 2002.
Joober R, Zarate JM, Rouleau GA, Skamene E and Boksa P: Provisional
mapping of quantitative trait loci modulating the acoustic startle response and prepulse
inhibition of acoustic startle. Neuropsychopharmacology 27:765-81, 2002.
Koumanis DJ, Christou NV, Wang XL and Gilfix BM: Pilot study examining
the frequency of several gene polymorphisms in a morbidly obese population. Obes Surg 12:759-64,
2002.
Laazsir K, Sutton M, Ghadirian P, Scott A, Paradis A-J, Tonin PN and Foulkes
WD: Is there a correlation between the structure of hair and breast cancer or
BRCA1/2 mutations? Phys Med Biol 47:1623-1632, 2002.
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, 2002.
Levy HL, Vargas JE, Waisbren SE, Kurczynski TW, Roeder E, Schwartz R, Rosengren S, Prasad
C, Greenberg CR, Gilfix BM, MacGregor D, Shin VE, Bao L and Kraus JP:
Reproductive fitness in maternal homocystinuria due to cystathionine ß-synthase
deficiency. J Inherit Metab Dis 25:299-314, 2002.
Lin R, Nagai Y, Sladek R, Bastien Y, Ho J, Petrecca K, Sotiropoulou G, Diamandis E,
Hudson TJ and White J: Expression profiling in squamous carcinoma cells reveals
pleiotropic effects of vitamin D3 analog EB1089 signaling on cell proliferation,
differentiation and immune system regulation. Molecular Endocrinology 16:1243-1256,
2002.
Liu S, Lu W, Obara T, Kuida S, Lehoczky J, Dewar K, Drummond IA and Beier
DR : A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and
in zebrafish. Development 129:5839-5846, 2002.
Manderson EN, Mes-Masson A-M, Novak J, Lee PD, Provencher D, Hudson TJ
and Tonin PN: Expression profiles of 290 ESTs mapped to chromosome 3 in
human epithelial ovarian cancer cell lines using DNA expression oligonucleotide
microarrays. Genome Res 12:112-121, 2002.
Manderson EN, Presneau N, Provencher D, Mes-Masson A-M and Tonin PN:
Comparative analysis of loss of heterozygosity of specific chromosome 3, 13, 17 and X loci
and TP53 mutations in human epithelial ovarian cancer. Molec Carcinogen 34:78-90,
2002.
Meijer I, Hand CK, Cossette P, Figlewicz DA and Rouleau GA: Spectrum of
SPG4 mutations in a large collection on North American families with Hereditary Spastic
Paraplegia. Arch Neurol 59:281-286, 2002.
Meijer I, Hand CK, Grewal KK, Stefanelli MG, Ives EJ and Rouleau GA: A
locus for autosomal dominant hereditary spastic ataxia, SAX1, maps to Chromosome 12p13.
Am J Hum Genet 70:763-769, 2002.
Moustafa A-E, Alaoui-Jamali MA, Batist G, Hernadez-Perez M, Serruya C, Alpert L, Black MJ,
Sladek R and Foulkes WD: Identification of genes associated with head and
neck carcinogenesis by cDNA microarray comparison between matched normal and squamous cell
carcinoma cells. Oncogene 21:2634-2640, 2002.
Narod SA, Dubé M-P, Klijn J, Lubinski J, Lynch HT, Ghadirian P, Provencher D, Heimdal K,
Moller P, Robson M, Offit K, Isaacs C, Weber B, Friedman E, Gershoni-Baruch R, Rennert G,
Pasini B, Wagner T, Daly M, Garber JE, Neuhausen S, Ainsworth P, Olsson H, Evans G,
Osborne M, Couch F, Foulkes WD, Warner E, Kim-Sing C, Olopade O, Tung N,
Saal HM, Weitzel J, Merajver S, Gauthier-Villars M, Jernstrom H, Sun P and Brunet JS. Oral
contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers. J
Natl Cancer Inst 94:1773-9, 2002.
Novak JP, Sladek R and Hudson TJ: Characterization of variability in
large scale gene expression data: Implications for study design. Genomics 79:104-113,
2003.
Park S-S, Stankiewicz P, Bi W, Shaw C, Lehoczky J, Dewar K, Birren B and
Lupski JR: Structure and evolution of the Smith-Magenis syndrome repeat gene clusters,
SMS-REPs. Genome Res 12: 729-738, 2002.
Raby BA, Klimecki WT, Laprise C, Renaud Y, Faith J, Lemire M, Greenwood C, Weiland KM,
Lange C, Palmer LJ, Lazarus R, Vercelli D, Kwiatkowski DJ, Silverman EK, Martinez F, Hudson
TJ and Weiss S: Polymophisms in Toll-like Receptor 4 are not associated with
asthma or atopy-related phenotypes. Am J Respir Crit Care Med 166:1449-1456,
2002.
Roslin NM, Loredo-Osti JC, Greenwood CMT and Morgan K: Genetic analysis
of the role of the HLA region in inflammatory bowel disease. Can J Stat 30:158-167,
2002.
Stojanovic N, Chang JL, Lehoczky J, Zody MC and Dewar K: Identification
of mixups among DNA sequencing plates. Bioinformatics 18: 1418-1426, 2002.
Straume O, Chappuis PO, Salvesen HB, Halvorsen OJ, Haukaas SA, Goffin JR, Bégin LR,
Foulkes WD and Akslen LA: Prognostic importance of glomeruloid microvascular
proliferation indicates an aggressive angiogenic phenotype in human cancers. Cancer
Res 62:6808-6811, 2002.
Verlaan DJ, Davenport WJ, Stefan H, Sure U, Siegel AM and Rouleau GA:
Cerebral cavernous
malformations:
Mutations in Krit1. Neurol 58:853-7, 2002.
Verlaan DJ, Siegel AM and Rouleau GA: Krit1 missense mutations lead to
splicing errors in cerebral cavernous malformation (CCM). Am J Hum Genet
70:1564-7, 2002.
Watkins D, Ru M, Hwang H-Y, Kim CD, Murray A, Phillip NS, Kim W, Legakis
H, Wai T, Hilton JF, Ge B, Doré C, Hosack A, Wilson A, Gravel RA, Shane B, Hudson TJ and Rosenblatt
DS: Hyperhomocysteinemia due to a methionine synthase deficiency, cblG: structure
of the MTR gene, genotype diversity, and recognition of a common mutation,
P1173L. Am J Hum Genet 71:143-153, 2002.
Weiner MP and Hudson TJ: Introduction to SNPs: Discovery of markers for
disease. BioTechniques 32:S4-S13, 2002.
Zhao Y, Kumar RA, Baser ME, Evans DG, Wallace A, Kluwe L, Mautner VF, Parry DM, Rouleau
GA, Joe H and Friedman JM: Intrafamilial correlation of clinical manifestations
in neurofibromatosis 2 (NF2). Genet Epidemiol 23: 245-59, 2002.
Zwarts KY, Clee SM, Zwinderman AH, Engert JC, Singaraja R, Loubser O, James E, Roomp K, Hudson
TJ, Jukema JW, Kastelein JJP and Hayden MR: ABCA1 regulatory variants influence
coronary artery disease independent of effects on plasma lipid levels. Clin Genet
61:115-125, 2002.
Chappuis PO and Foulkes WD: Risk
assessment and genetic testing. In: Ovarian Cancer, M.S. Stack D. Fishman (eds) D. (Cancer
Treatment and Research series, Rosen S, series editor) Kluwer Academic, Boston. 2002, pp.
29-59.
Chappuis PO and Foulkes WD: Overview of clinical genetics of ovarian
cancer, in Familial Breast And Ovarian Cancer, P. Morrison, S.V. Hodgson, and N. Haites
(eds). Cambridge University Press, 2002, pp. 43-72.
Chappuis PO and Foulkes WD: Management of Hereditary Breast Cancer, in
Familial Breast and Ovarian Cancer, P. Morrison, S.V. Hodgson, and N. Haites (eds).
Cambridge University Press, 2002, pp. 237-274.
Chappuis PO, Stoppa-Lyonnet D, Asselin B and Foulkes WD: Natural history
of hereditary breast cancer, in Familial Breast and Ovarian Cancer, P. Morrison, S.V.
Hodgson, and N. Haites (eds). Cambridge University Press, 2002, pp. 81-107.
Hudson TJ: Genomics: A Question of Scale, in Inno’va-tion, J. Downey
and L. Claxton (eds). Key Porter Books, 2002, pp. 229-235.
Weiner MP and Hudson TJ: Introduction to SNPs: Discovery of markers for
disease, in BioTechniques. 2002, pp. S4-S13.
Rosenblatt DS: Molecular bases of hyperhomocysteinemia due to inborn
errors of folate and cobalamin metabolism, in Chemistry and Biology of Pteridines and
Folates, S. Milstein, G. Kapatos, R.A. Levine, and B. Shane, (eds). Kluwer Academic
Publishers. 2002, pp. 587-591.
Arthus M-F, Lonergan M, Robertson G, Goodyer P, Morgan
K, Fujiwara TM and Bichet DG: Thirteen large deletions/rearrangements of the
AVPR2 gene causing X-linked nephrogenic diabetes insipidus. Poster presentation at the NDI
Foundation 2002 Global Conference, Heemskerk, The Netherlands, 26-28 April 2002.
Caron J, Loredo-Osti JC, Skamene E, Morgan K and Malo D: Identification
of genetic loci controlling bacterial clearance in experimental Salmonella enteritidis
infection: an unexpected role of Nramp1 (Slc11a1) in the persistence of infection
in mice. Poster at the Annual General Meeting of the Canadian Bacterial Diseases
Network/Canadian Microbiology Consortium Inc, Saskatoon, 20-23 June 2002, Poster
Abstracts and oral presentation by Danielle Malo at the 2002
Meeting of International Research Scholars, Palm Cove, Australia, 25-28 June 2002, Program
and Abstracts, p. 36.
Cartier L, Duncan A and Désilets VA: Prenatal diagnosis for mosaicism
for structurally abnormal Y and 45,X variants. Am J Hum Genet 71:A564, 2002.
Désilets VA, Fitzpatrick J and Rochon L: First trimester identification
of a severe form of Pallister-Hall syndrome. Am J Hum Genet 71:A567, 2002.
Dobson CM, Wai T, Leclerc D, Wilson A, Wu X, Dore C, Hudson T, Rosenblatt DS
and Gravel R: Identification of the gene responsible for the cblA complementation group of
disorders of human vitamin B12 metabolism based on analysis of prokaryotic gene
arrangements. Am J Hum Genet 71:173 (46), 2002.
Frosk PD, Hoke A, Morgan K, Fujiwara TM, Greenberg CR and Wrogemann K:
Phenotypic and genetic heterogeneity of autosomal recessive limb girdle muscular dystrophy
(LGMD) in the Hutterite population. Amer J Hum Genet 71 (Suppl):537, 2002.(Poster
presentation)
Frosk P, Lamont R, Brunham L, Weiler T, Nylen E, Greenberg CR, Hoke A, Frappier D, Roslin
N, Hudson TJ, Morgan K, Fujiwara TM and Wrogemann K: Genetic
heterogeneity of limb girdle muscular dystrophy in Hutterites. J Neurological Sci
199 (Suppl 1):S58, 2002. (Poster)
Frosk P, Weiler T, Nylen E, Sudha T, Morgan K, Fujiwara TM, Greenberg CR
and Wrogemann K: Limb girdle muscular dystrophy type 2H (LGMD2H) is associated with
mutation in TRIM32. J Neurological Sci 199 (Suppl 1):S90, 2002.(Oral
presentation)
Laflamme N, Giroux S, Cardinal G, Dodin S, Blanchette C, Morgan K and
Rousseau F: Negative effect of smoking on bone density is modulated by estrogen receptor
beta gene in postmenopausal French Canadian women. Genet Epidemiol 23:291, 2002.
(Oral presentation)
Loredo-Osti JC, Lemire M, Roslin NM, Fujiwara TM, Greenwood CMT and Morgan
K: Genetic Analysis Group. Poster at the Canadian Genetic Diseases Network Annual
Scientific Meeting, Saint-Sauveur-des-Monts, 4-7 April 2002, Poster Abstracts, p.
25.
Maharaj S, Morin L and Désilets VA: Prenatal identification of
phenotypic features suggestive of Simpsons-Golabi syndrome. Ultrasound Obstet Gynecol
20(s1), 2002.
Loredo-Osti JC, Smith BR and Morgan K: Likelihood for quantitative and
threshold traits under a mixed model of inheritance revisited. Genetic Epidemiology
23:293, 2002. (Poster presentation)
Pastinen T, Sladek R, Beck A, Sammak A, Ge B, Gurd S, Verner A, Kingsley J, Dewar
K, Greenwood C, Harmsen E, Labuda D, Lepage P, Meloche C, Morgan K,
Peterson A, Sinnett D, Vohl M-C, Long AD and Hudson TJ: Regulatory
polymorphism discovery using allelic imbalance detection. Genome Sequencing and
Biology, p. 214, 2002. (Poster)
Presneau N, Mes-Masson A-M, Bing G, Provencher D, Hudson TJ and Tonin
P: 2002. Comparison des profiles d’expression des gènes localisés sur le
chromosome 17 entre 12 cultures primaries d’épithélium normal de surface de
l’ovaire et 4 lignées cellularies tumorales ovariennes. Qui fait quoi?
Quatrièmes Journées de Génétiques, Montréal, Québec, May 22-24, 2002.
Ren F, Maugard C, Provencher D, Ouellet V, Ge B, Hudson TJ and Tonin
P, Mes-Masson A-M: Selection and validation of target genes reflecting
histological features of ovarian cancer. Canadian Conference on Ovarian Cancer Research,
Ottawa, Ontario, 2002.
Rosenblatt DS, Hilton JF, Christensen K, Hudson TJ, Raby
BA, Estivill X, de la Luna S and MacKenzie RE: Mutations in the FTCD gene on chromosome 21
are the cause of glutamate formiminotransferase deficiency. Qui fait quoi? Quatrièmes
Journées de Génétiques, Montréal, Québec, May 22-24, 2002.
Rousseau F, Laflamme N, Giroux S, Cardinal G, Dodin S, Blanchette C, Laroche J, Fournier
H, Chrétien P, Giguère Y and Morgan K: Génétique moléculare et des
populations: du syndrome de l’Xfragile aux maladies complexes. Qui fait quoi?
Quatrièmes Journées de Génétiques, Montreal, Québec, May 22-24, 2002. (Oral
presentation)
Su Z, Good MF, Sher A, Morgan K, Loredo-Osti JC and Stevenson MM:
Nematode infection suppresses dendritic cell function leading to impaired immunity to
concurrent blood-stage malaria in mice. Late Breakers in Molecular Biology, at the 51st
Annual Meeting of American Society of Tropical Medicine and Hygiene, Denver, 10-14
November 2002. (Poster presentation)
Verner A, Darmond-Zwaig C, Fortin Y, Frappier D, Lei M, Renaud Y, Sammak A, Roslin N, Fujiwara
TM, Engert J, Morgan K and Hudson TJ: CGDN
genotyping core facility. Poster at the Canadian Genetic Diseases Network Annual
Scientific Meeting, Saint-Sauveur-des-Monts, 4-7 April 2002, p. 36. (Poster)
Wai T, Dobson CM, Leclerc D, Wilson A, Wu X, Dore C, Hudson TJ, Rosenblatt DS,
and Gravel R: Identification of the gene responsible for the cblA form of vitamin
B12-responsive methylmalonic aciduria, based on the analysis of prokaryotic gene
arrangements. Qui fait quoi? May 22-24, 2002.
Watkins D, Ru M, Hwang H-Y, Kim CD, Murray A, Philip NS, Kim W, Legakis
H, Wai T, Hilton JF, Ge B, Doré C, Hosack A, Wilson A, Graval RA, Shane B, Hudson TJ and Rosenblatt
DS: Hyperhomocysteinemia due to methionine synthase deficiency (cblG): structure
of the MTR gene, genotype diversity and recognition of a common mutation, P1173L. Qui
fait quoi? Quatrièmes Journées de Génétiques, Montreal, Québec, May 22-24, 2002.
Wrogemann K, Frosk P, Lamont R, Brunham L, Hoke A, Weiler T, Nylen E, Frappier D, Roslin
N, Hudson TJ, Morgan K, Fujiwara TM and Greenberg CR: TRIM32, another new
gene in limb girdle muscular dystrophy, codes for a putative E3 ubiquitin ligase. (K.
Wrogemann, keynote speaker at the 7th International Congress of the World Muscle Society,
Rotterdam, 2-5 October 2002) Neuromuscular Disorders 12:718, 2002.
OTHERS
Gilfix BM: Troponin assays for coronary syndrome diagnosis. CMAJ
166(1):13-14,2002. [letter to the editor]
Tonin PN: BRCA1 and BRCA2 and inherited predisposition to breast and
ovarian cancers. McGill Med J 6:130-142, 2002.
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