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Hélène Bruyère

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Physiology

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Yasser R Abou Mourad; Michael J Barnett; Rahul Bhargava; Hélène Bruyère; Donna L Forrest; Tanya Gillian; Stephen H Nantel; Thomas J Nevill; Cynthia L Toze; John D Shepherd
Normal Karyotype CALLA-Positive Adult Pre-B ALL: Dismal Outcome With Chemotherapy for Patients With Loss/Gain of ABL1 and/or BCR FISH Signals.
Kamilla Schlade-Bartusiak; Lindsay Brown; Hélène Bruyère; Tanya Gillan; Sara Hamilton; Brenda Lomax; Barbara C McGillivray; Patrice Eydoux
BPES with atypical premature ovarian insufficiency, and evidence of mitotic recombination, in a woman with trisomy X and a translocation t(3;11)(q22.3;q14.1).
Hélène Bruyère; Heather J Sutherland; Katherine Chipperfield; Monika Hudoba
Concomitant and successive amplifications of MYC in APL-like leukemia.

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2013: Yasser R Abou Mourad; Michael J Barnett; Rahul Bhargava; Hélène Bruyère; Donna L Forrest; Tanya Gillian; Stephen H Nantel; Thomas J Nevill; Cynthia L Toze; John D Shepherd
Normal Karyotype CALLA-Positive Adult Pre-B ALL: Dismal Outcome With Chemotherapy for Patients With Loss/Gain of ABL1 and/or BCR FISH Signals.
Clinical lymphoma, myeloma & leukemia 2013;13(3):281-6.
2012: Kamilla Schlade-Bartusiak; Lindsay Brown; Hélène Bruyère; Tanya Gillan; Sara Hamilton; Brenda Lomax; Barbara C McGillivray; Patrice Eydoux
BPES with atypical premature ovarian insufficiency, and evidence of mitotic recombination, in a woman with trisomy X and a translocation t(3;11)(q22.3;q14.1).
American journal of medical genetics. Part A 2012;158A(9):2322-7.
2010: Hélène Bruyère; Heather J Sutherland; Katherine Chipperfield; Monika Hudoba
Concomitant and successive amplifications of MYC in APL-like leukemia.
Cancer genetics and cytogenetics 2010;197(1):75-80.
2006: Yulia Lin; Hélène Bruyère; Douglas E Horsman; Tapio Pantzar; Michael J Barnett; Donna E Hogge; Thomas J Nevill; Stephen H Nantel; Heather J Sutherland; Cynthia L Toze; John D Shepherd; Julye C Lavoie; Kevin W Song; Clayton A Smith; Donna L Forrest
Philadelphia-negative clonal hematopoiesis following imatinib therapy in patients with chronic myeloid leukemia: a report of nine cases and analysis of predictive factors.
Cancer genetics and cytogenetics 2006;170(1):16-23.
2006: Meaghan Hysert; Hélène Bruyère; Gilbert B. Côté; Angelika J Dawson; Jo-Anna Dolling; raouf fetni; Monica Hrynchak; Josée Lavoie; Jean McGowan-Jordan; Frédérique Tihy; Alessandra M V Duncan
Prenatal cytogenetic assessment and inv(2)(p11.2q13).
Prenatal diagnosis 2006;26(9):810-3.
2006: Hélène Bruyère; Marsha Speevak; Elizabeth J T Winsor; B de Fréminville; Sandra A Farrell; Jean McGowan-Jordan; Barbara C McGillivray; David Chitayat; Deborah McFadden; V Adouard; D Terespolsky; F Prieur; Tapio Pantzar; Monica Hrynchak
Isodicentric Yp: prenatal diagnosis and outcome in 12 cases.
Prenatal diagnosis 2006;26(4):324-9.
2005: JL Gair; Laura Arbour; Rosemarie Rupps; R Jiang; Hélène Bruyère; Wendy P Robinson
Recurrent trisomy 21: four cases in three generations.
Clinical genetics 2005;68(5):430-5.
2004: Hélène Bruyère; R Douglas Wilson; Sylvie Langlois
Risk of mosaicism and uniparental disomy associated with the prenatal diagnosis of a non-homologous Robertsonian translocation carrier.
Fetal diagnosis and therapy 2004;19(5):399-403.
2002: Wendy P Robinson; Deborah E McFadden; Irene Barrett; Brian Kuchinka; Maria S Peñaherrera; Hélène Bruyère; Robert G Best; Denise Araújo Lapa Pedreira; Sylvie Langlois; Dagmar K Kalousek
Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism.
Prenatal diagnosis 2002;22(12):1076-85.
2002: Hélène Bruyère; Evica Rajcan-Separovic; Dagmar K Kalousek
Molecular cytogenetics in reproductive pathology.
Methods in molecular biology (Clifton, N.J.) 2002;204():299-307.
2000: Maria S Peñaherrera; Irene Barrett; Carolyn J Brown; Sylvie Langlois; Siu Li Yong; S Lewis; Hélène Bruyère; P N Howard-Peebles; Dagmar K Kalousek; Wendy P Robinson
An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta.
Clinical genetics 2000;58(6):436-46.
2000: Hélène Bruyère; Rosemarie Rupps; Brian Kuchinka; Jan M Friedman; Wendy P Robinson
Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line.
American journal of medical genetics 2000;94(1):35-41.
1999: Hélène Bruyère; M E Lewis; S Wood; Patrick M MacLeod; Sylvie Langlois
Increasing evidence for a new X-linked mental retardation/epilepsy gene localized to Xp21.3-Xp22.1.
American journal of medical genetics 1999;86(4):401.