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Alexandre Montpetit

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Genes & Molecular Sequences

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Quebec

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Adam M Fontebasso; Miklós Garami; Noha Gerges; Djihad Hadjadj; Peter Hauser; Nada Jabado; David T W Jones; Dong-Anh Khuong-Quang; Almos Klekner; Marcel Kool; Andrey Korshunov; Pierre Lepage; Pawel P Liberski; Xiao-Yang Liu; Alexandre Montpetit; Stefan M Pfister; Jeremy Schwartzentruber; Alfredo Staffa; Dominik Sturm; Hendrik Witt; Gelareh Zadeh; Magdalena Zakrzewska; Krzystof Zakrzewski; Steffen Albrecht; Laszlo Bognar; Stephan Busche; Damien Faury; Adam Fleming; Jacek Majewski
Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas.
Diego Martinelli; Alexandre Montpetit; Stefania Petrini; Teresa Rizza; Giuliano Torre; Lorena Travaglini; Enrico Bertini; Rosalba Carrozzo; Irene Ceballos-Picot; Pascale de Lonlay; Christian A Drouin; Maya El Hachem; Laurence Hubert; Carlo Dionisi Vici
MEDNIK syndrome: a novel defect of copper metabolism treatable by zinc acetate therapy.
Marc Hitz; Pamela A Hoodless; Paul Khairy; Sabine Klaassen; Louis-Philippe Lemieux-Perreault; Emmanuelle Lemyre; Anath Christopher Lionel; Christian Marshall; Alexandre Montpetit; Mona Nemer; Bert Overduin; Andrea Richter; Stephen W Scherer; Alexandre Stewart; Maryse Thibeault; Shi Wei Yang; Philip Awadalla; Julie Hussin; Youssef Idaghdour; Jean-Luc Bigras; Cornelius Boerkoel; Philippe Chetaille; Rebecca Cullum; Guylaine D'Amours; Robbie Davies; Marie-Pierre Dubé; Yassamin Feroz-Zada; Gregor Andelfinger
Rare copy number variants contribute to congenital left-sided heart disease.

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All Publications

2013: Adam M Fontebasso; Miklós Garami; Noha Gerges; Djihad Hadjadj; Peter Hauser; Nada Jabado; David T W Jones; Dong-Anh Khuong-Quang; Almos Klekner; Marcel Kool; Andrey Korshunov; Pierre Lepage; Pawel P Liberski; Xiao-Yang Liu; Alexandre Montpetit; Stefan M Pfister; Jeremy Schwartzentruber; Alfredo Staffa; Dominik Sturm; Hendrik Witt; Gelareh Zadeh; Magdalena Zakrzewska; Krzystof Zakrzewski; Steffen Albrecht; Laszlo Bognar; Stephan Busche; Damien Faury; Adam Fleming; Jacek Majewski
Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas.
Acta neuropathologica 2013;125(5):659-69.
2013: Diego Martinelli; Alexandre Montpetit; Stefania Petrini; Teresa Rizza; Giuliano Torre; Lorena Travaglini; Enrico Bertini; Rosalba Carrozzo; Irene Ceballos-Picot; Pascale de Lonlay; Christian A Drouin; Maya El Hachem; Laurence Hubert; Carlo Dionisi Vici
MEDNIK syndrome: a novel defect of copper metabolism treatable by zinc acetate therapy.
Brain : a journal of neurology 2013;136(Pt 3):872-81.
2012: Marc Hitz; Pamela A Hoodless; Paul Khairy; Sabine Klaassen; Louis-Philippe Lemieux-Perreault; Emmanuelle Lemyre; Anath Christopher Lionel; Christian Marshall; Alexandre Montpetit; Mona Nemer; Bert Overduin; Andrea Richter; Stephen W Scherer; Alexandre Stewart; Maryse Thibeault; Shi Wei Yang; Philip Awadalla; Julie Hussin; Youssef Idaghdour; Jean-Luc Bigras; Cornelius Boerkoel; Philippe Chetaille; Rebecca Cullum; Guylaine D'Amours; Robbie Davies; Marie-Pierre Dubé; Yassamin Feroz-Zada; Gregor Andelfinger
Rare copy number variants contribute to congenital left-sided heart disease.
PLoS genetics 2012;8(9):e1002903.
2012: Dong-Anh Khuong-Quang; Marcel Kool; Andrey Korshunov; Pierre Lepage; Louis Letourneau; Peter Lichter; Xiao-Yang Liu; Jacek Majewski; Alexandre Montpetit; Stefan M Pfister; Patricia Rakopoulos; Jeremy Schwartzentruber; Dominik Sturm; Andreas von Deimling; Steffen Albrecht; Ute Bartels; Eric Bouffet; Mathieu Bourgey; Guillaume Bourque; Genevieve Bourret; Pawel Buczkowicz; Damien Faury; Adam Fleming; Adam M Fontebasso; Nada Jabado; David T Jones; Cynthia Hawkins
K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas.
Acta neuropathologica 2012;124(3):439-47.
2011: Jacek Majewski; Alexandre Montpetit; Jeremy Schwartzentruber; Emilie Lalonde; Nada Jabado
What can exome sequencing do for you?
Journal of medical genetics 2011;48(9):580-9.
2011: Nicolas Tremblay; Shi Wei Yang; Marc-Phillip Hitz; Géraldine Asselin; Jonathan Ginns; Kathleen Riopel; Roxanne Gendron; Alexandre Montpetit; Edwina Duhig; Marie-Pierre Dubé; Dorothy Radford; Gregor Andelfinger
Familial ventricular aneurysms and septal defects map to chromosome 10p15.
European heart journal 2011;32(5):568-73.
2011: Lisanne Morcos; Dmitry K Pokholok; Dominique J Verlaan; Bing Ge; Kevin L Gunderson; Vonda Koka; Kevin C L Lam; Alexandre Montpetit; Tomi Pastinen
Genome-wide assessment of imprinted expression in human cells.
Genome biology 2011;12(3):R25.
2010: Swneke D Bailey; Changchun Xie; Ron Do; Alexandre Montpetit; Rafael Diaz; Viswanathan Mohan; Bernard Keavney; Salim Yusuf; Hertzel C Gerstein; James C Engert; Sonia Anand
Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care 2010;33(10):2250-3.
2010: Hui-Qi Qu; Karine Jacob; Sarah Fatet; Bing Ge; David Barnett; Olivier Delattre; Damien Faury; Alexandre Montpetit; Lauren Solomon; Peter Hauser; Miklos Garami; Laszlo Bognar; Zoltan Hansely; Robert Mio; Jean-Pierre Farmer; Steffen Albrecht; Constantin Polychronakos; Cynthia Hawkins; Nada Jabado
Genome-wide profiling using single-nucleotide polymorphism arrays identifies novel chromosomal imbalances in pediatric glioblastomas.
Neuro-oncology 2010;12(2):153-63.
2009: Bing Ge; Dmitry K Pokholok; Tony Kwan; Elin Grundberg; Lisanne Morcos; Dominique J Verlaan; Jennie Le; Vonda Koka; Kevin C L Lam; Vincent Gagné; Joana Dias; Rose Hoberman; Alexandre Montpetit; Marie-Michele Joly; Edward Harvey; Daniel Sinnett; Patrick Beaulieu; Robert Hamon; Alexandru Graziani; Ken Dewar; Eef Harmsen; Jacek Majewski; Harald HH Goring; Anna K Naumova; Mathieu Blanchette; Kevin L Gunderson; Tomi Pastinen
Global patterns of cis variation in human cells revealed by high-density allelic expression analysis.
Nature genetics 2009;41(11):1216-22.
2009: K Jacob; Steffen Albrecht; C Sollier; Damien Faury; E Sader; Alexandre Montpetit; david serre; Péter Hauser; Miklós Garami; L Bognar; Z Hanzely; J L Montes; J Atkinson; J-P Farmer; Eric Bouffet; Cynthia Hawkins; Uri Tabori; Nada Jabado
Duplication of 7q34 is specific to juvenile pilocytic astrocytomas and a hallmark of cerebellar and optic pathway tumours.
British journal of cancer 2009;101(4):722-33.
2008: Alexandre Montpetit; Stéphanie Côté; Edna Brustein; Christian A Drouin; Line Lapointe; Michèle Boudreau; Caroline Meloche; Régen Drouin; Thomas J Hudson; Pierre Drapeau; Patrick Cossette
Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cord.
PLoS genetics 2008;4(12):e1000296.
2008: Ron Do; Guillaume Paré; Alexandre Montpetit; Thomas J Hudson; Daniel Gaudet; James C Engert
K45R variant of squalene synthase increases total cholesterol levels in two study samples from a French Canadian population.
Human mutation 2008;29(5):689-94.
2008: Ron Do; Swneke D Bailey; Katia Desbiens; Alexandre Belisle; Alexandre Montpetit; Claude Bouchard; Louis Pérusse; Marie-Claude Vohl; James C Engert
Genetic variants of FTO influence adiposity, insulin sensitivity, leptin levels, and resting metabolic rate in the Quebec Family Study.
Diabetes 2008;57(4):1147-50.
2008: david serre; Alexandre Montpetit; Guillaume Paré; James C Engert; Salim Yusuf; Bernard Keavney; Thomas J Hudson; Sonia Anand
Correction of population stratification in large multi-ethnic association studies.
PloS one 2008;3(1):e1382.
2008: James C Engert; Mathieu Lemire; Janet Faith; Diane Brisson; T Mary Fujiwara; Nicole M Roslin; Carl G Brewer; Alexandre Montpetit; Corinne Darmond-Zwaig; Yannick Renaud; Carole Doré; Swneke D Bailey; Andrei Verner; Gérald Tremblay; Julie St-Pierre; Christine Bétard; Jill Platko; John D Rioux; Kenneth Morgan; Thomas J Hudson; Daniel Gaudet
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.
European journal of human genetics : EJHG 2008;16(1):105-14.
2007: George Zogopoulos; Kevin C H Ha; Faisal Naqib; Sara Moore; Hyeja Kim; Alexandre Montpetit; Frederick Robidoux; Philippe Laflamme; Michelle Cotterchio; Celia Greenwood; Stephen W Scherer; Brent Zanke; Thomas J Hudson; Gary Bader; Steven Gallinger
Germ-line DNA copy number variation frequencies in a large North American population.
Human genetics 2007;122(3-4):345-53.
2007: Philippe Bégin; Karine Tremblay; Denise Daley; Mathieu Lemire; Sébastien Claveau; Charleen Salesse; Sabine Kacel; Alexandre Montpetit; Allan Becker; Moira Chan-Yeung; Anita L Kozyrskyj; Thomas J Hudson; Catherine Laprise
Association of urokinase-type plasminogen activator with asthma and atopy.
American journal of respiratory and critical care medicine 2007;175(11):1109-16.
2007: Hui-Qi Qu; Alexandre Montpetit; Bing Ge; Thomas J Hudson; Constantin Polychronakos
Toward further mapping of the association between the IL2RA locus and type 1 diabetes.
Diabetes 2007;56(4):1174-6.
2007: Guillaume Pare; david serre; Diane Brisson; Sonia S Anand; Alexandre Montpetit; Gérald Tremblay; James C Engert; Thomas J Hudson; Daniel Gaudet
Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol.
American journal of human genetics 2007;80(4):673-82.
2007: Robert Sladek; Ghislain Rocheleau; Johan Rung; Christian Dina; Lishuang Shen; david serre; Philippe Boutin; Daniel Vincent; Alexandre Belisle; Samy HADJADJ; Beverley Balkau; Barbara Heude; Guillaume Charpentier; Thomas J Hudson; Alexandre Montpetit; Alexey V Pshezhetsky; Marc Prentki; Barry Posner; David J Balding; David Meyre; Constantin Polychronakos; philippe froguel
A genome-wide association study identifies novel risk loci for type 2 diabetes.
Nature 2007;445(7130):881-5.
2007: Reedik Mägi; Arne Pfeufer; Mari Nelis; Alexandre Montpetit; Andres Metspalu; Maido Remm
Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation.
BMC genomics 2007;8():159.
2007: Hui-Qi Qu; Yang Lu; Luc Marchand; François Bacot; Rosalie Fréchette; Marie-Catherine Tessier; Alexandre Montpetit; Constantin Polychronakos
Genetic control of alternative splicing in the TAP2 gene: possible implication in the genetics of type 1 diabetes.
Diabetes 2007;56(1):270-5.
2006: Alexandre Montpetit; Michael S Phillips; Ian Mongrain; Réal Lemieux; Maryse St-Louis
High-throughput molecular profiling of blood donors for minor red blood cell and platelet antigens.
Transfusion 2006;46(5):841-8.
2006: Alexandre Montpetit; Mari Nelis; Philippe Laflamme; Reedik Magi; Xiayi Ke; Maido Remm; Lon Cardon; Thomas J Hudson; Andres Metspalu
An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population.
PLoS genetics 2006;2(3):e27.
2006: Jordan P Lerner-Ellis; Abigail B Gradinger; David Watkins; Jamie C Tirone; Amélie Villeneuve; C Melissa Dobson; Alexandre Montpetit; Pierre Lepage; Roy A Gravel; David S Rosenblatt
Mutation and biochemical analysis of patients belonging to the cblB complementation class of vitamin B12-dependent methylmalonic aciduria.
Molecular genetics and metabolism 2006;87(3):219-25.
2005: Thomas G Saba; Alexandre Montpetit; Andrei Verner; Pierre Rioux; Thomas J Hudson; Régen Drouin; Christian A Drouin
An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22.
Human genetics 2005;116(3):167-71.
2004: Audrey H Poon; Catherine Laprise; Mathieu Lemire; Alexandre Montpetit; Daniel Sinnett; Erwin Schurr; Thomas J Hudson
Association of vitamin D receptor genetic variants with susceptibility to asthma and atopy.
American journal of respiratory and critical care medicine 2004;170(9):967-73.
2004: Alexandre Montpetit; J Larose; Gino Boily; Sylvie Langlois; N Trudel; Daniel Sinnett
Mutational and expression analysis of the chromosome 12p candidate tumor suppressor genes in pre-B acute lymphoblastic leukemia.
Leukemia 2004;18(9):1499-504.
2004: Marcelo T Mira; Alexandre Alcaïs; Van Thuc Nguyen; Milton O Moraes; Celestino Di Flumeri; Hong Thai Vu; Chi Phuong Mai; Thu Huong Nguyen; Ngoc Ba Nguyen; Xuan Khoa Pham; Euzenir N Sarno; Andrea Alter; Alexandre Montpetit; Maria Moraes; José R Moraes; Carole Doré; Caroline J Gallant; Pierre Lepage; Andrei Verner; Esther van de Vosse; Thomas J Hudson; Laurent Abel; Erwin Schurr
Susceptibility to leprosy is associated with PARK2 and PACRG.
Nature 2004;427(6975):636-40.
2003: Alexandre Montpetit; Michael D Wilson; Mario Chevrette; Ben F Koop; Daniel Sinnett
Analysis of the conservation of synteny between Fugu and human chromosome 12.
BMC genomics 2003;4(1):30.
2003: Daniel Sinnett; Alexandre Montpetit
Isolation of cosmid and BAC DNA from E. coli.
Methods in molecular biology (Clifton, N.J.) 2003;235():99-102.
2002: Alexandre Montpetit; Gino Boily; Daniel Sinnett
A detailed transcriptional map of the chromosome 12p12 tumour suppressor locus.
European journal of human genetics : EJHG 2002;10(1):62-71.
2001: Alexandre Montpetit; Daniel Sinnett
Comparative analysis of the ETV6 gene in vertebrate genomes from pufferfish to human.
Oncogene 2001;20(26):3437-42.
1999: Alexandre Montpetit; Daniel Sinnett
Physical mapping of the G-protein coupled receptor 19 (GPR19) in the chromosome 12p12.3 region frequently rearranged in cancer cells.
Human genetics 1999;105(1-2):162-4.
1998: Alexandre Montpetit; C Payant; James Nolan; Léa Brakier-Gingras
Analysis of the conformation of the 3' major domain of Escherichia coli16S ribosomal RNA using site-directed photoaffinity crosslinking.
RNA (New York, N.Y.) 1998;4(11):1455-66.