Analysis of the conservation of synteny between Fugu and human chromosome 12

Por Montpetit, Alexandre, Wilson, Michael D, Chevrette, Mario, Koop, Ben F, Sinnett, Daniel
Publicado em 2003

Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation

Por Mägi, Reedik, Pfeufer, Arne, Nelis, Mari, Montpetit, Alexandre, Metspalu, Andres, Remm, Maido
Publicado em 2007

Disruption of Mycobacterium avium subsp. paratuberculosis-specific genes impairs in vivo fitness

Por Wang, Joyce, Pritchard, Justin R, Kreitmann, Louis, Montpetit, Alexandre, Behr, Marcel A
Publicado em 2014

Correction of Population Stratification in Large Multi-Ethnic Association Studies

Por Serre, David, Montpetit, Alexandre, Paré, Guillaume, Engert, James C., Yusuf, Salim, Keavney, Bernard, Hudson, Thomas J., Anand, Sonia
Publicado em 2008

An Evaluation of the Performance of Tag SNPs Derived from HapMap in a Caucasian Population

Por Montpetit, Alexandre, Nelis, Mari, Laflamme, Philippe, Magi, Reedik, Ke, Xiayi, Remm, Maido, Cardon, Lon, Hudson, Thomas J, Metspalu, Andres
Publicado em 2006

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-Densit...

Por Paré, Guillaume , Serre, David , Brisson, Diane , Anand, Sonia S. , Montpetit, Alexandre , Tremblay, Gérald , Engert, James C. , Hudson, Thomas J. , Gaudet, Daniel 
Publicado em 2007

Genome-wide assessment of imprinted expression in human cells

Por Morcos, Lisanne, Ge, Bing, Koka, Vonda, Lam, Kevin CL, Pokholok, Dmitry K, Gunderson, Kevin L, Montpetit, Alexandre, Verlaan, Dominique J, Pastinen, Tomi
Publicado em 2011

Buccals are likely to be a more informative surrogate tissue than blood for epigenome-wide association studies

Por Lowe, Robert, Gemma, Carolina, Beyan, Huriya, Hawa, Mohammed I., Bazeos, Alexandra, Leslie, R. David, Montpetit, Alexandre, Rakyan, Vardhman K., Ramagopalan, Sreeram V.
Publicado em 2013

Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord

Por Montpetit, Alexandre, Côté, Stéphanie, Brustein, Edna, Drouin, Christian A., Lapointe, Line, Boudreau, Michèle, Meloche, Caroline, Drouin, Régen, Hudson, Thomas J., Drapeau, Pierre, Cossette, Patrick
Publicado em 2008

Germline EPHB2 Receptor Variants in Familial Colorectal Cancer

Por Zogopoulos, George, Jorgensen, Claus, Bacani, Julinor, Montpetit, Alexandre, Lepage, Pierre, Ferretti, Vincent, Chad, Lauren, Selvarajah, Subani, Zanke, Brent, Hudson, Thomas J., Pawson, Tony, Gallinger, Steven
Publicado em 2008

Variation at the NFATC2 Locus Increases the Risk of Thiazolidinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study

Por Bailey, Swneke D., Xie, Changchun, Do, Ron, Montpetit, Alexandre, Diaz, Rafael, Mohan, Viswanathan, Keavney, Bernard, Yusuf, Salim, Gerstein, Hertzel C., Engert, James C., Anand, Sonia
Publicado em 2010

Impaired Innate Immunity in Mice Deficient in Interleukin-1 Receptor-Associated Kinase 4 Leads to Defective Type 1 T Cell Responses, B Cell Expansion, and Enhanced Susceptibility t...

Por Béla, Samantha R., Dutra, Míriam S., Mui, Ernest, Montpetit, Alexandre, Oliveira, Fernanda S., Oliveira, Sérgio C., Arantes, Rosa M. E., Antonelli, Lis R., McLeod, Rima, Gazzinelli, Ricardo T.
Publicado em 2012

CAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup

Por Warby, Simon C., Montpetit, Alexandre, Hayden, Anna R., Carroll, Jeffrey B., Butland, Stefanie L., Visscher, Henk, Collins, Jennifer A., Semaka, Alicia, Hudson, Thomas J., Hayden, Michael R.
Publicado em 2009

Identification of T. gondii epitopes, adjuvants, & host genetic factors that influence protection of mice & humans

Por Tan, Tze Guan, Mui, Ernest, Cong, Hua, Witola, William, Montpetit, Alexandre, Muench, Stephen P., Sidney, John, Alexander, Jeff, Sette, Alessandro, Grigg, Michael, Maewal, Ajesh, McLeod, Rima
Publicado em 2010

NALP1 Influences Susceptibility to Human Congenital Toxoplasmosis, Proinflammatory Cytokine Response, and Fate of Toxoplasma gondii-Infected Monocytic Cells

Por Witola, William H., Mui, Ernest, Hargrave, Aubrey, Liu, Susan, Hypolite, Magali, Montpetit, Alexandre, Cavailles, Pierre, Bisanz, Cordelia, Cesbron-Delauw, Marie-France, Fournié, Gilbert J., McLeod, Rima
Publicado em 2011

HLA class I alleles tag HLA-DRB1*1501 haplotypes for differential risk in multiple sclerosis susceptibility

Por Chao, Michael J., Barnardo, Martin C. N. M., Lincoln, Matthew R., Ramagopalan, Sreeram V., Herrera, Blanca M., Dyment, David A., Montpetit, Alexandre, Sadovnick, A. Dessa, Knight, Julian C., Ebers, George C.
Publicado em 2008

Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene

Por Dyment, David A., Cader, M. Zameel, Chao, Michael J., Lincoln, Matthew R., Morrison, Katie M., Disanto, Giulio, Morahan, Julia M., De Luca, Gabriele C., Sadovnick, A. Dessa, Lepage, Pierre, Montpetit, Alexandre, Ebers, George C., Ramagopalan, Sreeram V.
Publicado em 2012

PRKCA and Multiple Sclerosis: Association in Two Independent Populations

Por Saarela, Janna, Kallio, Suvi P, Chen, Daniel, Montpetit, Alexandre, Jokiaho, Anne, Choi, Eva, Asselta, Rosanna, Bronnikov, Denis, Lincoln, Matthew R, Sadovnick, A. Dessa, Tienari, Pentti J, Koivisto, Keijo, Palotie, Aarno, Ebers, George C, Hudson, Thomas J, Peltonen, Leena
Publicado em 2006

Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells

Por Morin, Andréanne, Kwan, Tony, Ge, Bing, Letourneau, Louis, Ban, Maria, Tandre, Karolina, Caron, Maxime, Sandling, Johanna K., Carlsson, Jonas, Bourque, Guillaume, Laprise, Catherine, Montpetit, Alexandre, Syvanen, Ann-Christine, Ronnblom, Lars, Sawcer, Stephen J., Lathrop, Mark G., Pastinen, Tomi
Publicado no BMC Med Genomics (2016)

Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation

Por Tucker, Tracy, Montpetit, Alexandre, Chai, David, Chan, Susanna, Chénier, Sébastien, Coe, Bradley P, Delaney, Allen, Eydoux, Patrice, Lam, Wan L, Langlois, Sylvie, Lemyre, Emmanuelle, Marra, Marco, Qian, Hong, Rouleau, Guy A, Vincent, David, Michaud, Jacques L, Friedman, Jan M
Publicado em 2011