| Year |
Citation |
Score |
| 2019 |
Harutyunyan AS, Krug B, Chen H, Papillon-Cavanagh S, Zeinieh M, De Jay N, Deshmukh S, Chen CCL, Belle J, Mikael LG, Marchione DM, Li R, Nikbakht H, Hu B, Cagnone G, ... ... Montpetit A, et al. H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis. Nature Communications. 10: 1262. PMID 30890717 DOI: 10.1038/S41467-019-09140-X |
0.343 |
|
| 2016 |
Torchia J, Golbourn B, Feng S, Ho KC, Sin-Chan P, Vasiljevic A, Norman JD, Guilhamon P, Garzia L, Agamez NR, Lu M, Chan TS, Picard D, de Antonellis P, Khuong-Quang DA, ... ... Montpetit A, et al. Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors. Cancer Cell. 30: 891-908. PMID 27960086 DOI: 10.1016/J.Ccell.2016.11.003 |
0.361 |
|
| 2016 |
Morin A, Kwan T, Ge B, Letourneau L, Ban M, Tandre K, Caron M, Sandling JK, Carlsson J, Bourque G, Laprise C, Montpetit A, Syvanen AC, Ronnblom L, Sawcer SJ, et al. Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells. Bmc Medical Genomics. 9: 59. PMID 27624058 DOI: 10.1186/S12920-016-0220-7 |
0.406 |
|
| 2016 |
Panichnantakul P, Bourgey M, Montpetit A, Bourque G, Riazalhosseini Y. RNA-Seq as a Tool to Study the Tumor Microenvironment. Methods in Molecular Biology (Clifton, N.J.). 1458: 311-37. PMID 27581031 DOI: 10.1007/978-1-4939-3801-8_22 |
0.313 |
|
| 2015 |
Fontebasso AM, Shirinian M, Khuong-Quang DA, Bechet D, Gayden T, Kool M, De Jay N, Jacob K, Gerges N, Hutter B, Ş Eker-Cin H, Witt H, Montpetit A, Brunet S, Lepage P, et al. Non-random aneuploidy specifies subgroups of pilocytic astrocytoma and correlates with older age. Oncotarget. PMID 26378811 DOI: 10.18632/Oncotarget.5571 |
0.329 |
|
| 2015 |
Nicolas G, Wallon D, Charbonnier C, Quenez O, Rousseau S, Richard AC, Rovelet-Lecrux A, Coutant S, Le Guennec K, Bacq D, Garnier JG, Olaso R, Boland A, Meyer V, Deleuze JF, ... ... Montpetit A, et al. Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons. European Journal of Human Genetics : Ejhg. PMID 26242991 DOI: 10.1038/Ejhg.2015.173 |
0.319 |
|
| 2015 |
Torchia J, Picard D, Lafay-Cousin L, Hawkins CE, Kim SK, Letourneau L, Ra YS, Ho KC, Chan TS, Sin-Chan P, Dunham CP, Yip S, Ng HK, Lu JQ, Albrecht S, ... ... Montpetit A, et al. Molecular subgroups of atypical teratoid rhabdoid tumours in children: an integrated genomic and clinicopathological analysis. The Lancet. Oncology. 16: 569-82. PMID 25882982 DOI: 10.1016/S1470-2045(15)70114-2 |
0.309 |
|
| 2014 |
Wang J, Pritchard JR, Kreitmann L, Montpetit A, Behr MA. Disruption of Mycobacterium avium subsp. paratuberculosis-specific genes impairs in vivo fitness. Bmc Genomics. 15: 415. PMID 24885784 DOI: 10.1186/1471-2164-15-415 |
0.373 |
|
| 2014 |
Buczkowicz P, Hoeman C, Rakopoulos P, Pajovic S, Letourneau L, Dzamba M, Morrison A, Lewis P, Bouffet E, Bartels U, Zuccaro J, Agnihotri S, Ryall S, Barszczyk M, Chornenkyy Y, ... ... Montpetit A, et al. Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations. Nature Genetics. 46: 451-6. PMID 24705254 DOI: 10.1038/Ng.2936 |
0.375 |
|
| 2014 |
Witola WH, Liu SR, Montpetit A, Welti R, Hypolite M, Roth M, Zhou Y, Mui E, Cesbron-Delauw MF, Fournie GJ, Cavailles P, Bisanz C, Boyer K, Withers S, Noble AG, et al. ALOX12 in human toxoplasmosis. Infection and Immunity. 82: 2670-9. PMID 24686056 DOI: 10.1128/Iai.01505-13 |
0.369 |
|
| 2014 |
Bailey SD, Xie C, Paré G, Montpetit A, Mohan V, Yusuf S, Gerstein H, Engert JC, Anand SS. Variation at the DPP4 locus influences apolipoprotein B levels in South Asians and exhibits heterogeneity in Europeans related to BMI. Diabetologia. 57: 738-45. PMID 24362726 DOI: 10.1007/S00125-013-3142-3 |
0.303 |
|
| 2014 |
Li R, Montpetit A, Rousseau M, Wu SY, Greenwood CM, Spector TD, Pollak M, Polychronakos C, Richards JB. Somatic point mutations occurring early in development: a monozygotic twin study. Journal of Medical Genetics. 51: 28-34. PMID 24123875 DOI: 10.1136/Jmedgenet-2013-101712 |
0.357 |
|
| 2013 |
Anand SS, Meyre D, Pare G, Bailey SD, Xie C, Zhang X, Montpetit A, Desai D, Bosch J, Mohan V, Diaz R, McQueen MJ, Cordell HJ, Keavney B, Yusuf S, et al. Genetic information and the prediction of incident type 2 diabetes in a high-risk multiethnic population: the EpiDREAM genetic study. Diabetes Care. 36: 2836-42. PMID 23603917 DOI: 10.2337/Dc12-2553 |
0.314 |
|
| 2013 |
Lowe R, Gemma C, Beyan H, Hawa MI, Bazeos A, Leslie RD, Montpetit A, Rakyan VK, Ramagopalan SV. Buccals are likely to be a more informative surrogate tissue than blood for epigenome-wide association studies. Epigenetics : Official Journal of the Dna Methylation Society. 8: 445-54. PMID 23538714 DOI: 10.4161/Epi.24362 |
0.362 |
|
| 2013 |
Fontebasso AM, Schwartzentruber J, Khuong-Quang DA, Liu XY, Sturm D, Korshunov A, Jones DT, Witt H, Kool M, Albrecht S, Fleming A, Hadjadj D, Busche S, Lepage P, Montpetit A, et al. Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas. Acta Neuropathologica. 125: 659-69. PMID 23417712 DOI: 10.1007/S00401-013-1095-8 |
0.306 |
|
| 2013 |
Yauk CL, Lucas Argueso J, Auerbach SS, Awadalla P, Davis SR, Demarini DM, Douglas GR, Dubrova YE, Elespuru RK, Glover TW, Hales BF, Hurles ME, Klein CB, Lupski JR, Manchester DK, ... ... Montpetit A, et al. Harnessing genomics to identify environmental determinants of heritable disease. Mutation Research. 752: 6-9. PMID 22935230 DOI: 10.1016/J.Mrrev.2012.08.002 |
0.328 |
|
| 2012 |
Hitz MP, Lemieux-Perreault LP, Marshall C, Feroz-Zada Y, Davies R, Yang SW, Lionel AC, D'Amours G, Lemyre E, Cullum R, Bigras JL, Thibeault M, Chetaille P, Montpetit A, Khairy P, et al. Rare copy number variants contribute to congenital left-sided heart disease. Plos Genetics. 8: e1002903. PMID 22969434 DOI: 10.1371/Journal.Pgen.1002903 |
0.365 |
|
| 2012 |
Dyment DA, Cader MZ, Chao MJ, Lincoln MR, Morrison KM, Disanto G, Morahan JM, De Luca GC, Sadovnick AD, Lepage P, Montpetit A, Ebers GC, Ramagopalan SV. Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene. Neurology. 79: 406-11. PMID 22744673 DOI: 10.1212/Wnl.0B013E3182616Fc4 |
0.392 |
|
| 2012 |
Schwartzentruber J, Korshunov A, Liu XY, Jones DT, Pfaff E, Jacob K, Sturm D, Fontebasso AM, Quang DA, Tönjes M, Hovestadt V, Albrecht S, Kool M, Nantel A, Konermann C, ... ... Montpetit A, et al. Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma. Nature. 482: 226-31. PMID 22286061 DOI: 10.1038/Nature10833 |
0.329 |
|
| 2012 |
Spinella J, Saillour V, Richer C, Ouimet M, Cassart P, Healy J, Bareke E, Larivière M, St-Onge P, Busche S, Ge B, Montpetit A, Pastinen T, Sinnett D. Abstract 4335: The genomic landscape of childhood pre-B acute lymphoblastic leukemia Cancer Research. 72: 4335-4335. DOI: 10.1158/1538-7445.Am2012-4335 |
0.572 |
|
| 2012 |
Healy J, Saillour V, Spinella J, Vidal R, Bareke E, Richer C, Larivière M, Busche S, Ge B, Montpetit A, Pastinen T, Sinnett D. Abstract 2484: Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia Cancer Research. 72: 2484-2484. DOI: 10.1158/1538-7445.Am2012-2484 |
0.568 |
|
| 2012 |
Schwartzentruber J, Korshunov A, Liu X, Jones DTW, Pfaff E, Jacob K, Sturm D, Fontebasso AM, Quang DK, Tönjes M, Hovestadt V, Albrecht S, Kool M, Nantel A, Konermann C, ... ... Montpetit A, et al. Erratum: Corrigendum: Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma Nature. 484: 130-130. DOI: 10.1038/Nature11026 |
0.336 |
|
| 2012 |
Lanktree M, Guo Y, Murtaza M, Glessner J, Bailey S, Onland-Moret N, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson C, Klopp N, Baumert J, Padmanabhan S, ... ... Montpetit A, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height The American Journal of Human Genetics. 90: 1116-1117. DOI: 10.1016/J.Ajhg.2012.05.017 |
0.335 |
|
| 2011 |
Ramagopalan SV, Dyment DA, Cader MZ, Morrison KM, Disanto G, Morahan JM, Berlanga-Taylor AJ, Handel A, De Luca GC, Sadovnick AD, Lepage P, Montpetit A, Ebers GC. Rare variants in the CYP27B1 gene are associated with multiple sclerosis. Annals of Neurology. 70: 881-6. PMID 22190362 DOI: 10.1136/Jnnp-2012-304200A.128 |
0.374 |
|
| 2011 |
Rousseau J, Chapdelaine P, Boisvert S, Almeida LP, Corbeil J, Montpetit A, Tremblay JP. Endonucleases: tools to correct the dystrophin gene. The Journal of Gene Medicine. 13: 522-37. PMID 21954090 DOI: 10.1002/Jgm.1611 |
0.334 |
|
| 2011 |
Majewski J, Schwartzentruber J, Lalonde E, Montpetit A, Jabado N. What can exome sequencing do for you? Journal of Medical Genetics. 48: 580-9. PMID 21730106 DOI: 10.1136/Jmedgenet-2011-100223 |
0.372 |
|
| 2011 |
Tucker T, Montpetit A, Chai D, Chan S, Chénier S, Coe BP, Delaney A, Eydoux P, Lam WL, Langlois S, Lemyre E, Marra M, Qian H, Rouleau GA, Vincent D, et al. Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation. Bmc Medical Genomics. 4: 25. PMID 21439053 DOI: 10.1186/1755-8794-4-25 |
0.342 |
|
| 2011 |
Morcos L, Ge B, Koka V, Lam KC, Pokholok DK, Gunderson KL, Montpetit A, Verlaan DJ, Pastinen T. Genome-wide assessment of imprinted expression in human cells. Genome Biology. 12: R25. PMID 21418647 DOI: 10.1186/Gb-2011-12-3-R25 |
0.391 |
|
| 2011 |
Lanktree MB, Guo Y, Murtaza M, Glessner JT, Bailey SD, Onland-Moret NC, Lettre G, Ongen H, Rajagopalan R, Johnson T, Shen H, Nelson CP, Klopp N, Baumert J, Padmanabhan S, ... ... Montpetit A, et al. Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height. American Journal of Human Genetics. 88: 6-18. PMID 21194676 DOI: 10.1016/J.Ajhg.2010.11.007 |
0.44 |
|
| 2011 |
Tremblay N, Yang SW, Hitz MP, Asselin G, Ginns J, Riopel K, Gendron R, Montpetit A, Duhig E, Dubé MP, Radford D, Andelfinger G. Familial ventricular aneurysms and septal defects map to chromosome 10p15. European Heart Journal. 32: 568-73. PMID 21169613 DOI: 10.1093/Eurheartj/Ehq447 |
0.357 |
|
| 2010 |
Do R, Bailey SD, Paré G, Montpetit A, Desbiens K, Hudson TJ, Yusuf S, Bouchard C, Gaudet D, Pérusse L, Anand S, Vohl MC, Pastinen T, Engert JC. Fine mapping of the insulin-induced gene 2 identifies a variant associated with LDL cholesterol and total apolipoprotein B levels. Circulation. Cardiovascular Genetics. 3: 454-61. PMID 20858904 DOI: 10.1161/Circgenetics.109.917039 |
0.367 |
|
| 2010 |
El Kares R, Manolescu DC, Lakhal-Chaieb L, Montpetit A, Zhang Z, Bhat PV, Goodyer P. A human ALDH1A2 gene variant is associated with increased newborn kidney size and serum retinoic acid. Kidney International. 78: 96-102. PMID 20375987 DOI: 10.1038/Ki.2010.101 |
0.347 |
|
| 2010 |
Manolescu DC, El-Kares R, Lakhal-Chaieb L, Montpetit A, Bhat PV, Goodyer P. Newborn serum retinoic acid level is associated with variants of genes in the retinol metabolism pathway. Pediatric Research. 67: 598-602. PMID 20308937 DOI: 10.1203/Pdr.0B013E3181Dcf18A |
0.307 |
|
| 2010 |
Qu HQ, Jacob K, Fatet S, Ge B, Barnett D, Delattre O, Faury D, Montpetit A, Solomon L, Hauser P, Garami M, Bognar L, Hansely Z, Mio R, Farmer JP, et al. Genome-wide profiling using single-nucleotide polymorphism arrays identifies novel chromosomal imbalances in pediatric glioblastomas. Neuro-Oncology. 12: 153-63. PMID 20150382 DOI: 10.1093/Neuonc/Nop001 |
0.433 |
|
| 2009 |
Ge B, Pokholok DK, Kwan T, Grundberg E, Morcos L, Verlaan DJ, Le J, Koka V, Lam KC, Gagné V, Dias J, Hoberman R, Montpetit A, Joly MM, Harvey EJ, et al. Global patterns of cis variation in human cells revealed by high-density allelic expression analysis. Nature Genetics. 41: 1216-22. PMID 19838192 DOI: 10.1038/Ng.473 |
0.55 |
|
| 2009 |
Rung J, Cauchi S, Albrechtsen A, Shen L, Rocheleau G, Cavalcanti-Proença C, Bacot F, Balkau B, Belisle A, Borch-Johnsen K, Charpentier G, Dina C, Durand E, Elliott P, Hadjadj S, ... ... Montpetit A, et al. Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia. Nature Genetics. 41: 1110-5. PMID 19734900 DOI: 10.1038/Ng.443 |
0.394 |
|
| 2009 |
Jacob K, Albrecht S, Sollier C, Faury D, Sader E, Montpetit A, Serre D, Hauser P, Garami M, Bognar L, Hanzely Z, Montes JL, Atkinson J, Farmer JP, Bouffet E, et al. Duplication of 7q34 is specific to juvenile pilocytic astrocytomas and a hallmark of cerebellar and optic pathway tumours. British Journal of Cancer. 101: 722-33. PMID 19603027 DOI: 10.1038/Sj.Bjc.6605179 |
0.345 |
|
| 2009 |
Bouron-Dal Soglio D, Rougemont AL, Absi R, Barrette S, Montpetit A, Fetni R, Fournet JC. SNP genotyping of a sclerosing rhabdomyosarcoma: reveals highly aneuploid profile and a specific MDM2/HMGA2 amplification. Human Pathology. 40: 1347-52. PMID 19454362 DOI: 10.1016/j.humpath.2009.01.021 |
0.305 |
|
| 2009 |
Warby SC, Montpetit A, Hayden AR, Carroll JB, Butland SL, Visscher H, Collins JA, Semaka A, Hudson TJ, Hayden MR. CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup. American Journal of Human Genetics. 84: 351-66. PMID 19249009 DOI: 10.1016/J.Ajhg.2009.02.003 |
0.388 |
|
| 2009 |
Daley D, Lemire M, Akhabir L, Chan-Yeung M, He JQ, McDonald T, Sandford A, Stefanowicz D, Tripp B, Zamar D, Bosse Y, Ferretti V, Montpetit A, Tessier MC, Becker A, et al. Analyses of associations with asthma in four asthma population samples from Canada and Australia. Human Genetics. 125: 445-59. PMID 19247692 DOI: 10.1007/S00439-009-0643-8 |
0.382 |
|
| 2009 |
Bossé Y, Bacot F, Montpetit A, Rung J, Qu HQ, Engert JC, Polychronakos C, Hudson TJ, Froguel P, Sladek R, Desrosiers M. Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans. Human Genetics. 125: 305-18. PMID 19184112 DOI: 10.1007/S00439-009-0626-9 |
0.405 |
|
| 2009 |
Meyre D, Delplanque J, Chèvre JC, Lecoeur C, Lobbens S, Gallina S, Durand E, Vatin V, Degraeve F, Proença C, Gaget S, Körner A, Kovacs P, Kiess W, Tichet J, ... ... Montpetit A, et al. Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. Nature Genetics. 41: 157-9. PMID 19151714 DOI: 10.1038/Ng.301 |
0.353 |
|
| 2008 |
Houlston RS, Webb E, Broderick P, Pittman AM, Di Bernardo MC, Lubbe S, Chandler I, Vijayakrishnan J, Sullivan K, Penegar S, Carvajal-Carmona L, Howarth K, Jaeger E, ... ... Montpetit A, et al. Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. Nature Genetics. 40: 1426-35. PMID 19011631 DOI: 10.1038/Ng.262 |
0.405 |
|
| 2008 |
McKay JD, Hung RJ, Gaborieau V, Boffetta P, Chabrier A, Byrnes G, Zaridze D, Mukeria A, Szeszenia-Dabrowska N, Lissowska J, Rudnai P, Fabianova E, Mates D, Bencko V, Foretova L, ... ... Montpetit A, et al. Lung cancer susceptibility locus at 5p15.33. Nature Genetics. 40: 1404-6. PMID 18978790 DOI: 10.1038/Ng.254 |
0.348 |
|
| 2008 |
Keating BJ, Tischfield S, Murray SS, Bhangale T, Price TS, Glessner JT, Galver L, Barrett JC, Grant SF, Farlow DN, Chandrupatla HR, Hansen M, Ajmal S, Papanicolaou GJ, Guo Y, ... ... Montpetit A, et al. Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies. Plos One. 3: e3583. PMID 18974833 DOI: 10.1371/Journal.Pone.0003583 |
0.437 |
|
| 2008 |
Tremblay K, Daley D, Chamberland A, Lemire M, Montpetit A, Laviolette M, Musk AW, James AL, Chan-Yeung M, Becker A, Kozyrskyj AL, Sandford AJ, Hudson TJ, Paré PD, Laprise C. Genetic variation in immune signaling genes differentially expressed in asthmatic lung tissues. The Journal of Allergy and Clinical Immunology. 122: 529-36.e17. PMID 18774388 DOI: 10.1016/J.Jaci.2008.05.049 |
0.357 |
|
| 2008 |
Chao MJ, Barnardo MC, Lincoln MR, Ramagopalan SV, Herrera BM, Dyment DA, Montpetit A, Sadovnick AD, Knight JC, Ebers GC. HLA class I alleles tag HLA-DRB1*1501 haplotypes for differential risk in multiple sclerosis susceptibility. Proceedings of the National Academy of Sciences of the United States of America. 105: 13069-74. PMID 18765817 DOI: 10.1073/Pnas.0801042105 |
0.317 |
|
| 2008 |
Zogopoulos G, Jorgensen C, Bacani J, Montpetit A, Lepage P, Ferretti V, Chad L, Selvarajah S, Zanke B, Hudson TJ, Pawson T, Gallinger S. Germline EPHB2 receptor variants in familial colorectal cancer. Plos One. 3: e2885. PMID 18682749 DOI: 10.1371/Journal.Pone.0002885 |
0.349 |
|
| 2008 |
Tenesa A, Farrington SM, Prendergast JG, Porteous ME, Walker M, Haq N, Barnetson RA, Theodoratou E, Cetnarskyj R, Cartwright N, Semple C, Clark AJ, Reid FJ, Smith LA, Kavoussanakis K, ... ... Montpetit A, et al. Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. Nature Genetics. 40: 631-7. PMID 18372901 DOI: 10.1038/Ng.133 |
0.387 |
|
| 2008 |
Do R, Paré G, Montpetit A, Hudson TJ, Gaudet D, Engert JC. K45R variant of squalene synthase increases total cholesterol levels in two study samples from a French Canadian population. Human Mutation. 29: 689-94. PMID 18350552 DOI: 10.1002/Humu.20702 |
0.32 |
|
| 2008 |
Do R, Bailey SD, Desbiens K, Belisle A, Montpetit A, Bouchard C, Pérusse L, Vohl MC, Engert JC. Genetic variants of FTO influence adiposity, insulin sensitivity, leptin levels, and resting metabolic rate in the Quebec Family Study. Diabetes. 57: 1147-50. PMID 18316358 DOI: 10.2337/Db07-1267 |
0.338 |
|
| 2008 |
Cunninghame Graham DS, Vyse TJ, Fortin PR, Montpetit A, Cai YC, Lim S, McKenzie T, Farwell L, Rhodes B, Chad L, Hudson TJ, Sharpe A, Terhorst C, Greenwood CM, Wither J, et al. Association of LY9 in UK and Canadian SLE families. Genes and Immunity. 9: 93-102. PMID 18216865 DOI: 10.1038/Sj.Gene.6364453 |
0.376 |
|
| 2008 |
Serre D, Montpetit A, Paré G, Engert JC, Yusuf S, Keavney B, Hudson TJ, Anand S. Correction of population stratification in large multi-ethnic association studies. Plos One. 3: e1382. PMID 18196181 DOI: 10.1371/Journal.Pone.0001382 |
0.333 |
|
| 2008 |
Engert JC, Lemire M, Faith J, Brisson D, Fujiwara TM, Roslin NM, Brewer CG, Montpetit A, Darmond-Zwaig C, Renaud Y, Doré C, Bailey SD, Verner A, Tremblay G, St-Pierre J, et al. Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population. European Journal of Human Genetics : Ejhg. 16: 105-14. PMID 17805225 DOI: 10.1038/Sj.Ejhg.5201920 |
0.425 |
|
| 2007 |
DeLuca GC, Ramagopalan SV, Herrera BM, Dyment DA, Lincoln MR, Montpetit A, Pugliatti M, Barnardo MC, Risch NJ, Sadovnick AD, Chao M, Sotgiu S, Hudson TJ, Ebers GC. An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus. Proceedings of the National Academy of Sciences of the United States of America. 104: 20896-901. PMID 18087043 DOI: 10.1073/Pnas.0707731105 |
0.312 |
|
| 2007 |
Sabeti PC, Varilly P, Fry B, Lohmueller J, Hostetter E, Cotsapas C, Xie X, Byrne EH, McCarroll SA, Gaudet R, Schaffner SF, Lander ES, Frazer KA, Ballinger DG, ... ... Montpetit A, et al. Genome-wide detection and characterization of positive selection in human populations. Nature. 449: 913-8. PMID 17943131 DOI: 10.1038/Nature06250 |
0.386 |
|
| 2007 |
Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, Gibbs RA, Belmont JW, Boudreau A, Hardenbol P, Leal SM, Pasternak S, Wheeler DA, Willis TD, Yu F, ... ... Montpetit A, et al. A second generation human haplotype map of over 3.1 million SNPs. Nature. 449: 851-61. PMID 17943122 DOI: 10.1038/Nature06258 |
0.396 |
|
| 2007 |
Zogopoulos G, Ha KC, Naqib F, Moore S, Kim H, Montpetit A, Robidoux F, Laflamme P, Cotterchio M, Greenwood C, Scherer SW, Zanke B, Hudson TJ, Bader GD, Gallinger S. Germ-line DNA copy number variation frequencies in a large North American population. Human Genetics. 122: 345-53. PMID 17638019 DOI: 10.1007/S00439-007-0404-5 |
0.416 |
|
| 2007 |
Zanke BW, Greenwood CM, Rangrej J, Kustra R, Tenesa A, Farrington SM, Prendergast J, Olschwang S, Chiang T, Crowdy E, Ferretti V, Laflamme P, Sundararajan S, Roumy S, Olivier JF, ... ... Montpetit A, et al. Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. Nature Genetics. 39: 989-94. PMID 17618283 DOI: 10.1038/Ng2089 |
0.365 |
|
| 2007 |
Mägi R, Pfeufer A, Nelis M, Montpetit A, Metspalu A, Remm M. Evaluating the performance of commercial whole-genome marker sets for capturing common genetic variation. Bmc Genomics. 8: 159. PMID 17562002 DOI: 10.1186/1471-2164-8-159 |
0.385 |
|
| 2007 |
Bégin P, Tremblay K, Daley D, Lemire M, Claveau S, Salesse C, Kacel S, Montpetit A, Becker A, Chan-Yeung M, Kozyrskyj AL, Hudson TJ, Laprise C. Association of urokinase-type plasminogen activator with asthma and atopy. American Journal of Respiratory and Critical Care Medicine. 175: 1109-16. PMID 17363771 DOI: 10.1164/Rccm.200607-1012Oc |
0.336 |
|
| 2007 |
Pare G, Serre D, Brisson D, Anand SS, Montpetit A, Tremblay G, Engert JC, Hudson TJ, Gaudet D. 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. 80: 673-82. PMID 17357073 DOI: 10.1086/513286 |
0.391 |
|
| 2007 |
Sladek R, Rocheleau G, Rung J, Dina C, Shen L, Serre D, Boutin P, Vincent D, Belisle A, Hadjadj S, Balkau B, Heude B, Charpentier G, Hudson TJ, Montpetit A, et al. A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature. 445: 881-5. PMID 17293876 DOI: 10.1038/Nature05616 |
0.409 |
|
| 2007 |
Qu HQ, Lu Y, Marchand L, Bacot F, Fréchette R, Tessier MC, Montpetit A, Polychronakos C. Genetic control of alternative splicing in the TAP2 gene: possible implication in the genetics of type 1 diabetes. Diabetes. 56: 270-5. PMID 17192492 DOI: 10.2337/Db06-0865 |
0.363 |
|
| 2006 |
Montpetit A, Chagnon F. [The Haplotype Map of the human genome: a revolution in the genetics of complex diseases]. MéDecine Sciences : M/S. 22: 1061-7. PMID 17156727 DOI: 10.1051/Medsci/200622121061 |
0.405 |
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| 2006 |
Saarela J, Kallio SP, Chen D, Montpetit A, Jokiaho A, Choi E, Asselta R, Bronnikov D, Lincoln MR, Sadovnick AD, Tienari PJ, Koivisto K, Palotie A, Ebers GC, Hudson TJ, et al. PRKCA and multiple sclerosis: association in two independent populations. Plos Genetics. 2: e42. PMID 16596167 DOI: 10.1371/Journal.Pgen.0020042 |
0.398 |
|
| 2006 |
Montpetit A, Nelis M, Laflamme P, Magi R, Ke X, Remm M, Cardon L, Hudson TJ, Metspalu A. An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population. Plos Genetics. 2: e27. PMID 16532062 DOI: 10.1371/Journal.Pgen.0020027 |
0.346 |
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| 2006 |
Lerner-Ellis JP, Gradinger AB, Watkins D, Tirone JC, Villeneuve A, Dobson CM, Montpetit A, Lepage P, Gravel RA, Rosenblatt DS. Mutation and biochemical analysis of patients belonging to the cblB complementation class of vitamin B12-dependent methylmalonic aciduria. Molecular Genetics and Metabolism. 87: 219-25. PMID 16410054 DOI: 10.1016/J.Ymgme.2005.11.011 |
0.318 |
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| 2005 |
Lincoln MR, Montpetit A, Cader MZ, Saarela J, Dyment DA, Tiislar M, Ferretti V, Tienari PJ, Sadovnick AD, Peltonen L, Ebers GC, Hudson TJ. A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis. Nature Genetics. 37: 1108-12. PMID 16186814 DOI: 10.1038/Ng1647 |
0.369 |
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| 2005 |
Saba TG, Montpetit A, Verner A, Rioux P, Hudson TJ, Drouin R, Drouin CA. An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22. Human Genetics. 116: 167-71. PMID 15668823 DOI: 10.1007/S00439-004-1193-8 |
0.416 |
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| 2005 |
Belmont JW, Boudreau A, Leal SM, Hardenbol P, Pasternak S, Wheeler DA, Willis TD, Yu F, Yang H, Gao Y, Hu H, Hu W, Li C, Lin W, Liu S, ... ... Montpetit A, et al. A haplotype map of the human genome Nature. 437: 1299-1320. DOI: 10.1038/Nature04226 |
0.419 |
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| 2004 |
Montpetit A, Larose J, Boily G, Langlois S, Trudel N, Sinnett D. Mutational and expression analysis of the chromosome 12p candidate tumor suppressor genes in pre-B acute lymphoblastic leukemia. Leukemia. 18: 1499-504. PMID 15284860 DOI: 10.1038/Sj.Leu.2403441 |
0.532 |
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| 2004 |
Poon AH, Laprise C, Lemire M, Montpetit A, Sinnett D, Schurr E, Hudson TJ. Association of vitamin D receptor genetic variants with susceptibility to asthma and atopy. American Journal of Respiratory and Critical Care Medicine. 170: 967-73. PMID 15282199 DOI: 10.1164/Rccm.200403-412Oc |
0.548 |
|
| 2004 |
Mira MT, Alcaïs A, Nguyen VT, Moraes MO, Di Flumeri C, Vu HT, Mai CP, Nguyen TH, Nguyen NB, Pham XK, Sarno EN, Alter A, Montpetit A, Moraes ME, Moraes JR, et al. Susceptibility to leprosy is associated with PARK2 and PACRG. Nature. 427: 636-40. PMID 14737177 DOI: 10.1038/Nature02326 |
0.435 |
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| 2003 |
Sinnett D, Montpetit A. Isolation of cosmid and BAC DNA from E. coli. Methods in Molecular Biology (Clifton, N.J.). 235: 99-102. PMID 12904652 DOI: 10.1385/1-59259-409-3:99 |
0.426 |
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| 2003 |
Montpetit A, Wilson MD, Chevrette M, Koop BF, Sinnett D. Analysis of the conservation of synteny between Fugu and human chromosome 12. Bmc Genomics. 4: 30. PMID 12877756 DOI: 10.1186/1471-2164-4-30 |
0.519 |
|
| 2003 |
Belmont JW, Hardenbol P, Willis TD, Yu F, Yang H, Ch'Ang LY, Huang W, Liu B, Shen Y, Tam PKH, Tsui LC, Waye MMY, Wong JTF, Zeng C, Zhang Q, ... ... Montpetit A, et al. The international HapMap project Nature. 426: 789-796. DOI: 10.1038/Nature02168 |
0.366 |
|
| 2002 |
Montpetit A, Boily G, Sinnett D. A detailed transcriptional map of the chromosome 12p12 tumour suppressor locus. European Journal of Human Genetics : Ejhg. 10: 62-71. PMID 11896457 DOI: 10.1038/Sj.Ejhg.5200766 |
0.526 |
|
| 2001 |
Montpetit A, Sinnett D. Comparative analysis of the ETV6 gene in vertebrate genomes from pufferfish to human. Oncogene. 20: 3437-42. PMID 11423994 DOI: 10.1038/Sj.Onc.1204444 |
0.512 |
|
| 2001 |
Montpetit A, Trudel N, Sinnett D. A detailed transcript map of the human chromosome 12p12.3 tumor suppressor locus: the usefulness of an integrative approach Nature Genetics. 27: 86-87. DOI: 10.1038/87218 |
0.507 |
|
| 1999 |
Montpetit A, Sinnett D. Physical mapping of the G-protein coupled receptor 19 (GPR19) in the chromosome 12p12.3 region frequently rearranged in cancer cells. Human Genetics. 105: 162-4. PMID 10480372 DOI: 10.1007/S004399900083 |
0.555 |
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