| Year |
Citation |
Score |
| 2020 |
Caron M, St-Onge P, Sontag T, Wang YC, Richer C, Ragoussis I, Sinnett D, Bourque G. Single-cell analysis of childhood leukemia reveals a link between developmental states and ribosomal protein expression as a source of intra-individual heterogeneity. Scientific Reports. 10: 8079. PMID 32415257 DOI: 10.1038/S41598-020-64929-X |
0.325 |
|
| 2020 |
Gagné V, St-Onge P, Beaulieu P, Laverdière C, Leclerc JM, Tran TH, Sallan SE, Neuberg D, Silverman LB, Sinnett D, Krajinovic M. HLA alleles associated with asparaginase hypersensitivity in childhood ALL: a report from the DFCI Consortium. Pharmacogenomics. PMID 32372697 DOI: 10.2217/Pgs-2019-0195 |
0.335 |
|
| 2020 |
Caru M, Petrykey K, Samoilenko M, Drouin S, Lemay V, Kern L, Romo L, Beaulieu P, St-Onge P, Bertout L, Lefebvre G, Andelfinger G, Krajinovic M, Laverdière C, Sinnett D, et al. Abstract B62: The need to improve exercise prescriptions to support care in pediatric oncology Cancer Research. 80. DOI: 10.1158/1538-7445.Pedca19-B62 |
0.319 |
|
| 2020 |
Benmoussa A, Bélanger V, Levy E, Laverdière C, Stintzi A, Sinnett D, Marcil V. Abstract A56: Effect of chemotherapy on gut microbiota and microbiota-derived metabolites in children with cancer Cancer Research. 80. DOI: 10.1158/1538-7445.Pedca19-A56 |
0.303 |
|
| 2019 |
Ansari M, Petrykey K, Rezgui MA, Vecchio VD, Cortyl J, Ralph RO, Nava T, Beaulieu P, St-Onge P, Mlakar SJ, Curtis PH, Uppugunduri CRS, Lesne L, Théoret Y, Chalandon Y, ... ... Sinnett D, et al. Genetic susceptibility to hepatic sinusoidal obstruction syndrome in pediatric patients undergoing HSCT. Biology of Blood and Marrow Transplantation : Journal of the American Society For Blood and Marrow Transplantation. PMID 31790828 DOI: 10.1016/J.Bbmt.2019.11.026 |
0.348 |
|
| 2019 |
Cardin S, Bilodeau M, Roussy M, Aubert L, Milan T, Jouan L, Rouette A, Laramée L, Gendron P, Duchaine J, Decaluwe H, Spinella JF, Mourad S, Couture F, Sinnett D, et al. Human models of NUP98-KDM5A megakaryocytic leukemia in mice contribute to uncovering new biomarkers and therapeutic vulnerabilities. Blood Advances. 3: 3307-3321. PMID 31698461 DOI: 10.1182/Bloodadvances.2019030981 |
0.322 |
|
| 2019 |
Gagné V, Aubry-Morin A, Plesa M, Abaji R, Petrykey K, St-Onge P, Beaulieu P, Laverdière C, Alos N, Leclerc JM, Sallan SE, Neuberg D, Kutok JL, Silverman LB, Sinnett D, et al. Genes identified through genome-wide association studies of osteonecrosis in childhood acute lymphoblastic leukemia patients. Pharmacogenomics. PMID 31686588 DOI: 10.2217/Pgs-2019-0087 |
0.358 |
|
| 2019 |
Brown AL, de Smith AJ, Gant VU, Yang W, Scheurer ME, Walsh KM, Chernus JM, Kallsen NA, Peyton SA, Davies GE, Ehli EA, Winick N, Heerema NA, Carroll AJ, Borowitz MJ, ... ... Sinnett D, et al. Inherited genetic susceptibility of acute lymphoblastic leukemia in Down syndrome. Blood. PMID 31350265 DOI: 10.1182/Blood.2018890764 |
0.354 |
|
| 2019 |
de Smith AJ, Walsh KM, Morimoto LM, Francis SS, Hansen HM, Jeon S, Gonseth S, Chen M, Sun H, Luna-Fineman S, Antillón F, Girón V, Kang AY, Smirnov I, Shao X, ... ... Sinnett D, et al. Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome. Leukemia. PMID 31296947 DOI: 10.1038/S41375-019-0514-9 |
0.331 |
|
| 2019 |
Petrykey K, Lippé S, Robaey P, Sultan S, Laniel J, Drouin S, Bertout L, Beaulieu P, St-Onge P, Boulet-Craig A, Rezgui A, Yasui Y, Sapkota Y, Krull KR, Hudson MM, ... ... Sinnett D, et al. Influence of genetic factors on long-term treatment related neurocognitive complications, and on anxiety and depression in survivors of childhood acute lymphoblastic leukemia: The Petale study. Plos One. 14: e0217314. PMID 31181069 DOI: 10.1371/Journal.Pone.0217314 |
0.302 |
|
| 2019 |
Nadeau G, Ouimet-Grennan E, Aaron M, Drouin S, Bertout L, Shalmiev A, Beaulieu P, St-Onge P, Veilleux LN, Rauch F, Petrykey K, Laverdière C, Sinnett D, Alos N, Krajinovic M. Identification of genetic variants associated with skeletal muscle function deficit in childhood acute lymphoblastic leukemia survivors. Pharmacogenomics and Personalized Medicine. 12: 33-45. PMID 31114288 DOI: 10.2147/Pgpm.S192924 |
0.322 |
|
| 2019 |
Caru M, Petrykey K, Drouin S, Beaulieu P, St-Onge P, Lemay V, Bertout L, Laverdiere C, Andelfinger G, Krajinovic M, Sinnett D, Curnier D. Identification of genetic association between cardiorespiratory fitness and the trainability genes in childhood acute lymphoblastic leukemia survivors. Bmc Cancer. 19: 443. PMID 31088516 DOI: 10.1186/S12885-019-5651-Z |
0.333 |
|
| 2019 |
Aaron M, Nadeau G, Ouimet-Grennan E, Drouin S, Bertout L, Beaulieu P, St-Onge P, Shalmiev A, Veilleux LN, Rauch F, Petrykey K, Laverdière C, Sinnett D, Alos N, Krajinovic M. Identification of a single nucleotide polymorphism within CDH2 gene associated with bone morbidity in childhood acute lymphoblastic leukemia survivors. Pharmacogenomics. PMID 30983502 DOI: 10.2217/Pgs-2018-0169 |
0.342 |
|
| 2019 |
Hamdi Y, Leclerc M, Dumont M, Dubois S, Tranchant M, Reimnitz G, Soucy P, Cassart P, Ouimet M, Sinnett D, Chaieb MLL, Simard J. Functional Analysis of Promoter Variants in Genes Involved in Sex Steroid Action, DNA Repair and Cell Cycle Control. Genes. 10. PMID 30823486 DOI: 10.3390/Genes10030186 |
0.38 |
|
| 2019 |
Caru M, Petrykey K, Samoilenko M, Drouin S, Lemay V, Kern L, Romo L, Beaulieu P, St-Onge P, Bertout L, Lefebvre G, Leverdiere C, Andelfinger G, Krajinovic M, Sinnett D, et al. Trainability Genes Provide Answers To The Cardiorespiratory Fitness Deficit In Childhood Acute Lymphoblastic Leukemia Survivors. Medicine & Science in Sports & Exercise. 51: 157. DOI: 10.1249/01.Mss.0000560975.70132.F3 |
0.318 |
|
| 2018 |
Caron M, St-Onge P, Drouin S, Richer C, Sontag T, Busche S, Bourque G, Pastinen T, Sinnett D. Very long intergenic non-coding RNA transcripts and expression profiles are associated to specific childhood acute lymphoblastic leukemia subtypes. Plos One. 13: e0207250. PMID 30440012 DOI: 10.1371/Journal.Pone.0207250 |
0.341 |
|
| 2018 |
Neveu B, Caron M, Lagacé K, Richer C, Sinnett D. Genome wide mapping of ETV6 binding sites in pre-B leukemic cells. Scientific Reports. 8: 15526. PMID 30341373 DOI: 10.1038/S41598-018-33947-1 |
0.358 |
|
| 2018 |
Spinella JF, Richer C, Cassart P, Ouimet M, Healy J, Sinnett D. Mutational dynamics of early and late relapsed childhood ALL: rapid clonal expansion and long-term dormancy. Blood Advances. 2: 177-188. PMID 29365312 DOI: 10.1182/Bloodadvances.2017011510 |
0.315 |
|
| 2018 |
Brown AL, Smith AJd, Scheurer ME, Kallsen NA, Peyton SA, Davies GE, Ehli EA, Zwick ME, Winick N, Maloney K, Angiolillo AL, Schore R, Burke MM, Salzer WL, Heerema NA, ... ... Sinnett D, et al. Abstract 222: Genome-wide association study of acute lymphoblastic leukemia in children with Down syndrome Cancer Research. 78: 222-222. DOI: 10.1158/1538-7445.Am2018-222 |
0.332 |
|
| 2018 |
Costa EMD, Armaos G, Beaudry A, Richer C, Caron M, St-Onge P, Johnson J, Krogan N, Sai Y, Downey M, Sinnett D, McGraw S, Raynal NJ. Abstract 1381: Targeting histone acetyltransferases to reprogram high C-MYC expressing cancers Cancer Research. 78: 1381-1381. DOI: 10.1158/1538-7445.Am2018-1381 |
0.335 |
|
| 2017 |
Plesa M, Gagné V, Glisovic S, Younan M, Sharif-Askari B, Laverdière C, Alos N, Leclerc JM, Sallan SE, Neuberg D, Kutok JL, Silverman LB, Sinnett D, Krajinovic M. Influence of BCL2L11 polymorphism on osteonecrosis during treatment of childhood acute lymphoblastic leukemia. The Pharmacogenomics Journal. PMID 29282361 DOI: 10.1038/S41397-017-0002-4 |
0.34 |
|
| 2017 |
Gioia R, Drouin S, Ouimet M, Caron M, St-Onge P, Richer C, Sinnett D. LncRNAs downregulated in childhood acute lymphoblastic leukemia modulate apoptosis, cell migration, and DNA damage response. Oncotarget. 8: 80645-80650. PMID 29113332 DOI: 10.18632/Oncotarget.20817 |
0.323 |
|
| 2017 |
Mehanna P, Gagné V, Lajoie M, Spinella JF, St-Onge P, Sinnett D, Brukner I, Krajinovic M. Characterization of the microDNA through the response to chemotherapeutics in lymphoblastoid cell lines. Plos One. 12: e0184365. PMID 28877255 DOI: 10.1371/Journal.Pone.0184365 |
0.314 |
|
| 2017 |
Abaji R, Gagné V, Xu CJ, Spinella JF, Ceppi F, Laverdière C, Leclerc JM, Sallan SE, Neuberg D, Kutok JL, Silverman LB, Sinnett D, Krajinovic M. Whole-exome sequencing identified genetic risk factors for asparaginase-related complications in childhood all patients. Oncotarget. PMID 28574850 DOI: 10.18632/Oncotarget.17959 |
0.345 |
|
| 2017 |
Luca A, Hankard R, Borys JM, Sinnett D, Marcil V, Levy E. Nutriepigenomics and malnutrition. Epigenomics. PMID 28571478 DOI: 10.2217/Epi-2016-0168 |
0.333 |
|
| 2017 |
Glisovic SJ, Pastore YD, Gagne V, Plesa M, Laverdière C, Leclerc JM, Sinnett D, Krajinovic M. Impact of genetic polymorphisms determining leukocyte/neutrophil count on chemotherapy toxicity. The Pharmacogenomics Journal. PMID 28534526 DOI: 10.1038/Tpj.2017.16 |
0.34 |
|
| 2017 |
Lajoie M, Drouin S, Caron M, St-Onge P, Ouimet M, Gioia R, Lafond MH, Vidal R, Richer C, Oualkacha K, Droit A, Sinnett D. Specific expression of novel long non-coding RNAs in high-hyperdiploid childhood acute lymphoblastic leukemia. Plos One. 12: e0174124. PMID 28346506 DOI: 10.1371/Journal.Pone.0174124 |
0.335 |
|
| 2017 |
Khater F, Vairy S, Langlois S, Healy J, Dumoucel S, Lajoie M, Sontag T, St-Onge P, Bittencourt H, Soglio DD, Carret A, Cellot S, Champagne J, Duval M, Krajinovic M, ... ... Sinnett D, et al. Abstract 4885: Identification of actionable targets for refractory/relapsed childhood cancer leading to personalized targeted therapy (TRICEPS Study) Cancer Research. 77: 4885-4885. DOI: 10.1158/1538-7445.Am2017-4885 |
0.332 |
|
| 2016 |
Ouimet M, Drouin S, Lajoie M, Caron M, St-Onge P, Gioia R, Richer C, Sinnett D. A childhood acute lymphoblastic leukemia-specific lncRNA implicated in prednisolone resistance, cell proliferation, and migration. Oncotarget. PMID 27980230 DOI: 10.18632/Oncotarget.13936 |
0.329 |
|
| 2016 |
Teppo S, Laukkanen S, Liuksiala T, Nordlund J, Oittinen M, Teittinen KJ, Grönroos T, St-Onge P, Sinnett D, Syvänen AC, Nykter M, Viiri K, Heinäniemi M, Lohi O. Genome-wide repression of eRNA and target gene loci by the ETV6-RUNX1 fusion in acute leukemia. Genome Research. PMID 27620872 DOI: 10.1101/Gr.193649.115 |
0.336 |
|
| 2016 |
Spinella JF, Cassart P, Richer C, Saillour V, Ouimet M, Langlois S, St-Onge P, Sontag T, Healy J, Minden MD, Sinnett D. Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutations. Oncotarget. PMID 27602765 DOI: 10.18632/Oncotarget.11796 |
0.308 |
|
| 2016 |
Wahlberg P, Lundmark A, Nordlund J, Busche S, Raine A, Tandre K, Rönnblom L, Sinnett D, Forestier E, Pastinen T, Lönnerholm G, Syvänen AC. DNA methylome analysis of acute lymphoblastic leukemia cells reveals stochastic de novo DNA methylation in CpG islands. Epigenomics. PMID 27552300 DOI: 10.2217/Epi-2016-0052 |
0.302 |
|
| 2016 |
Neveu B, Spinella JF, Richer C, Lagace' K, Cassart P, Lajoie M, Jananji S, Drouin S, Healy J, Hickson GR, Sinnett D. CLIC5: a novel ETV6 target gene in childhood acute lymphoblastic leukemia. Haematologica. PMID 27540136 DOI: 10.3324/Haematol.2016.149740 |
0.363 |
|
| 2016 |
Langlois S, Healy J, Lajoie M, Dumoucel S, Khater F, Sontag T, St-Onge P, Beaulieu P, Bittencourt H, Soglio DD, Carret A, Cellot S, Champagne J, Duval M, Krajinovic M, ... ... Sinnett D, et al. Abstract A41: TRICEPS: A feasibility study of personalized targeted therapy in relapsed/refractory childhood cancers Cancer Research. 76. DOI: 10.1158/1538-7445.Pedca15-A41 |
0.313 |
|
| 2015 |
Krajinovic M, Elbared J, Drouin S, Bertout L, Rezgui A, Ansari M, Raboisson MJ, Lipshultz SE, Silverman LB, Sallan SE, Neuberg DS, Kutok JL, Laverdière C, Sinnett D, Andelfinger G. Polymorphisms of ABCC5 and NOS3 genes influence doxorubicin cardiotoxicity in survivors of childhood acute lymphoblastic leukemia. The Pharmacogenomics Journal. PMID 26345518 DOI: 10.1038/Tpj.2015.63 |
0.337 |
|
| 2015 |
Spinella JF, Cassart P, Garnier N, Rousseau P, Drullion C, Richer C, Ouimet M, Saillour V, Healy J, Autexier C, Sinnett D. A novel somatic mutation in ACD induces telomere lengthening and apoptosis resistance in leukemia cells. Bmc Cancer. 15: 621. PMID 26345285 DOI: 10.1186/S12885-015-1639-5 |
0.308 |
|
| 2015 |
Spinella JF, Healy J, Saillour V, Richer C, Cassart P, Ouimet M, Sinnett D. Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes. Bmc Cancer. 15: 539. PMID 26201965 DOI: 10.1186/S12885-015-1549-6 |
0.378 |
|
| 2015 |
Sun J, Zheng J, Tang L, Healy J, Sinnett D, Dai YE. Association between CEBPE Variant and Childhood Acute Leukemia Risk: Evidence from a Meta-Analysis of 22 Studies. Plos One. 10: e0125657. PMID 25938438 DOI: 10.1371/Journal.Pone.0125657 |
0.322 |
|
| 2015 |
Ben Tanfous M, Sharif-Askari B, Ceppi F, Laaribi H, Gagné V, Rousseau J, Labuda M, Silverman LB, Sallan SE, Neuberg D, Kutok JL, Sinnett D, Laverdière C, Krajinovic M. Polymorphisms of asparaginase pathway and asparaginase-related complications in children with acute lymphoblastic leukemia. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 21: 329-34. PMID 24907114 DOI: 10.1158/1078-0432.Ccr-14-0508 |
0.368 |
|
| 2015 |
Dumoucel S, Duval M, Marzouki M, Bittencourt H, Samson Y, Cellot S, Rivard G, Teira P, Carret A, Healy J, Dal Soglio D, Patey N, Piche N, Sontag T, Langlois S, ... ... Sinnett D, et al. TR-16 * PERSONALIZED TARGETED THERAPY IN REFRACTORY OR RELAPSED CANCER IN CHILDHOOD (TRICEPS STUDY) Neuro-Oncology. 17: iii40-iii40. DOI: 10.1093/Neuonc/Nov061.161 |
0.301 |
|
| 2014 |
Dai YE, Tang L, Healy J, Sinnett D. Contribution of polymorphisms in IKZF1 gene to childhood acute leukemia: a meta-analysis of 33 case-control studies. Plos One. 9: e113748. PMID 25423013 DOI: 10.1371/Journal.Pone.0113748 |
0.328 |
|
| 2014 |
Ceppi F, Langlois-Pelletier C, Gagné V, Rousseau J, Ciolino C, De Lorenzo S, Kevin KM, Cijov D, Sallan SE, Silverman LB, Neuberg D, Kutok JL, Sinnett D, Laverdière C, Krajinovic M. Polymorphisms of the vincristine pathway and response to treatment in children with childhood acute lymphoblastic leukemia. Pharmacogenomics. 15: 1105-16. PMID 25084203 DOI: 10.2217/Pgs.14.68 |
0.36 |
|
| 2014 |
Sanchez R, St-Cyr J, Lalonde ME, Healy J, Richer C, Gagné V, Laverdière C, Silverman LB, Sallan SE, Neuberg D, Kutok JL, Kritikou EA, Krajinovic M, Sinnett D. Impact of promoter polymorphisms in key regulators of the intrinsic apoptosis pathway on the outcome of childhood acute lymphoblastic leukemia. Haematologica. 99: 314-21. PMID 24038028 DOI: 10.3324/Haematol.2013.085340 |
0.366 |
|
| 2014 |
Hassawi M, Shestakova EA, Fournier M, Lebert-Ghali CÉ, Vaisson G, Frison H, Sinnett D, Vidal R, Thompson A, Bijl JJ. Hoxa9 collaborates with E2A-PBX1 in mouse B cell leukemia in association with Flt3 activation and decrease of B cell gene expression. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 243: 145-58. PMID 23996689 DOI: 10.1002/Dvdy.24056 |
0.322 |
|
| 2013 |
Nordlund J, Bäcklin CL, Wahlberg P, Busche S, Berglund EC, Eloranta ML, Flaegstad T, Forestier E, Frost BM, Harila-Saari A, Heyman M, Jónsson OG, Larsson R, Palle J, Rönnblom L, ... ... Sinnett D, et al. Genome-wide signatures of differential DNA methylation in pediatric acute lymphoblastic leukemia. Genome Biology. 14: r105. PMID 24063430 DOI: 10.1186/Gb-2013-14-9-R105 |
0.318 |
|
| 2013 |
Gagné V, Rousseau J, Labuda M, Sharif-Askari B, Brukner I, Laverdière C, Ceppi F, Sallan SE, Silverman LB, Neuberg D, Kutok JL, Sinnett D, Krajinovic M. Bim polymorphisms: influence on function and response to treatment in children with acute lymphoblastic leukemia. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 19: 5240-9. PMID 23908358 DOI: 10.1158/1078-0432.Ccr-13-1215 |
0.366 |
|
| 2013 |
Bareke E, Saillour V, Spinella JF, Vidal R, Healy J, Sinnett D, Csűrös M. Joint genotype inference with germline and somatic mutations. Bmc Bioinformatics. 14: S3. PMID 23734724 DOI: 10.1186/1471-2105-14-S5-S3 |
0.326 |
|
| 2013 |
Busche S, Ge B, Vidal R, Spinella JF, Saillour V, Richer C, Healy J, Chen SH, Droit A, Sinnett D, Pastinen T. Integration of high-resolution methylome and transcriptome analyses to dissect epigenomic changes in childhood acute lymphoblastic leukemia. Cancer Research. 73: 4323-36. PMID 23722552 DOI: 10.1158/0008-5472.Can-12-4367 |
0.374 |
|
| 2013 |
Metayer C, Milne E, Clavel J, Infante-Rivard C, Petridou E, Taylor M, Schüz J, Spector LG, Dockerty JD, Magnani C, Pombo-de-Oliveira MS, Sinnett D, Murphy M, Roman E, Monge P, et al. The Childhood Leukemia International Consortium. Cancer Epidemiology. 37: 336-47. PMID 23403126 DOI: 10.1016/J.Canep.2012.12.011 |
0.354 |
|
| 2013 |
Hussin J, Sinnett D, Casals F, Idaghdour Y, Bruat V, Saillour V, Healy J, Grenier JC, de Malliard T, Busche S, Spinella JF, Larivière M, Gibson G, Andersson A, Holmfeldt L, et al. Rare allelic forms of PRDM9 associated with childhood leukemogenesis. Genome Research. 23: 419-30. PMID 23222848 DOI: 10.1101/Gr.144188.112 |
0.36 |
|
| 2012 |
Lalonde ME, Ouimet M, Larivière M, Kritikou EA, Sinnett D. Identification of functional DNA variants in the constitutive promoter region of MDM2. Human Genomics. 6: 15. PMID 23244604 DOI: 10.1186/1479-7364-6-15 |
0.357 |
|
| 2012 |
Marcil V, Sinnett D, Seidman E, Boudreau F, Gendron FP, Beaulieu JF, Menard D, Lambert M, Bitton A, Sanchez R, Amre D, Levy E. Association between genetic variants in the HNF4A gene and childhood-onset Crohn's disease. Genes and Immunity. 13: 556-65. PMID 22914433 DOI: 10.1038/Gene.2012.37 |
0.313 |
|
| 2012 |
Ouimet M, Cassart P, Larivière M, Kritikou EA, Simard J, Sinnett D. Functional analysis of promoter variants in KU70 and their role in cancer susceptibility. Genes, Chromosomes & Cancer. 51: 1007-13. PMID 22833453 DOI: 10.1002/Gcc.21983 |
0.364 |
|
| 2012 |
Berlivet S, Moussette S, Ouimet M, Verlaan DJ, Koka V, Al Tuwaijri A, Kwan T, Sinnett D, Pastinen T, Naumova AK. Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines. Human Genetics. 131: 1161-71. PMID 22271045 DOI: 10.1007/S00439-012-1142-X |
0.38 |
|
| 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 |
0.641 |
|
| 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 |
0.633 |
|
| 2011 |
Rousseau J, Gagné V, Labuda M, Beaubois C, Sinnett D, Laverdière C, Moghrabi A, Sallan SE, Silverman LB, Neuberg D, Kutok JL, Krajinovic M. ATF5 polymorphisms influence ATF function and response to treatment in children with childhood acute lymphoblastic leukemia. Blood. 118: 5883-90. PMID 21972289 DOI: 10.1182/Blood-2011-05-355560 |
0.387 |
|
| 2011 |
Cox DG, Simard J, Sinnett D, Hamdi Y, Soucy P, Ouimet M, Barjhoux L, Verny-Pierre C, McGuffog L, Healey S, Szabo C, Greene MH, Mai PL, Andrulis IL, et al. Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers. Human Molecular Genetics. 20: 4732-47. PMID 21890493 DOI: 10.1093/Hmg/Ddr388 |
0.321 |
|
| 2011 |
Bourgey M, Healy J, Saint-Onge P, Massé H, Sinnett D, Roy-Gagnon MH. Genome-wide detection and characterization of mating asymmetry in human populations. Genetic Epidemiology. 35: 526-35. PMID 21769930 DOI: 10.1002/Gepi.20602 |
0.324 |
|
| 2011 |
Almalte Z, Samarani S, Iannello A, Debbeche O, Duval M, Infante-Rivard C, Amre DK, Sinnett D, Ahmad A. Novel associations between activating killer-cell immunoglobulin-like receptor genes and childhood leukemia. Blood. 118: 1323-8. PMID 21613255 DOI: 10.1182/Blood-2010-10-313791 |
0.359 |
|
| 2011 |
Sherborne AL, Hemminki K, Kumar R, Bartram CR, Stanulla M, Schrappe M, Petridou E, Semsei AF, Szalai C, Sinnett D, Krajinovic M, Healy J, Lanciotti M, Dufour C, Indaco S, et al. Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia. Haematologica. 96: 1049-54. PMID 21459794 DOI: 10.3324/Haematol.2011.040121 |
0.354 |
|
| 2011 |
Marcil V, Levy E, Mack DR, Kumar V, Israel DM, Deslandres C, Faure C, Sinnett D, Seidman EG, Amre DK. The PTPN2 Gene and Pediatric Crohn's Disease. Associations With Multiple Markers and Enhanced Expression in Intestinal Inflammation Gastroenterology. 140: S-269-S-270. DOI: 10.1016/S0016-5085(11)61079-2 |
0.31 |
|
| 2010 |
Gravel S, Malouf C, Boulais PE, Berchiche YA, Oishi S, Fujii N, Leduc R, Sinnett D, Heveker N. The peptidomimetic CXCR4 antagonist TC14012 recruits beta-arrestin to CXCR7: roles of receptor domains. The Journal of Biological Chemistry. 285: 37939-43. PMID 20956518 DOI: 10.1074/Jbc.C110.147470 |
0.714 |
|
| 2010 |
Healy J, Bourgey M, Richer C, Sinnett D, Roy-Gagnon MH. Detection of fetomaternal genotype associations in early-onset disorders: evaluation of different methods and their application to childhood leukemia. Journal of Biomedicine & Biotechnology. 2010: 369534. PMID 20617153 DOI: 10.1155/2010/369534 |
0.331 |
|
| 2010 |
Healy J, Richer C, Bourgey M, Kritikou EA, Sinnett D. Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia. Haematologica. 95: 1608-11. PMID 20460642 DOI: 10.3324/Haematol.2010.022459 |
0.333 |
|
| 2010 |
Sherborne AL, Hosking FJ, Prasad RB, Kumar R, Koehler R, Vijayakrishnan J, Papaemmanuil E, Bartram CR, Stanulla M, Schrappe M, Gast A, Dobbins SE, Ma Y, Sheridan E, Taylor M, ... ... Sinnett D, et al. Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk. Nature Genetics. 42: 492-4. PMID 20453839 DOI: 10.1038/Ng.585 |
0.328 |
|
| 2010 |
Labuda M, Gahier A, Gagné V, Moghrabi A, Sinnett D, Krajinovic M. Polymorphisms in glucocorticoid receptor gene and the outcome of childhood acute lymphoblastic leukemia (ALL). Leukemia Research. 34: 492-7. PMID 19758697 DOI: 10.1016/J.Leukres.2009.08.007 |
0.329 |
|
| 2009 |
Al-Shakfa F, Dulucq S, Brukner I, Milacic I, Ansari M, Beaulieu P, Moghrabi A, Laverdière C, Sallan SE, Silverman LB, Neuberg D, Kutok JL, Sinnett D, Krajinovic M. DNA variants in region for noncoding interfering transcript of dihydrofolate reductase gene and outcome in childhood acute lymphoblastic leukemia. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 15: 6931-8. PMID 19861437 DOI: 10.1158/1078-0432.Ccr-09-0641 |
0.371 |
|
| 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, ... Sinnett D, 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 |
0.622 |
|
| 2009 |
Verlaan DJ, Berlivet S, Hunninghake GM, Madore AM, Larivière M, Moussette S, Grundberg E, Kwan T, Ouimet M, Ge B, Hoberman R, Swiatek M, Dias J, Lam KC, Koka V, ... ... Sinnett D, et al. Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease. American Journal of Human Genetics. 85: 377-93. PMID 19732864 DOI: 10.1016/J.Ajhg.2009.08.007 |
0.367 |
|
| 2009 |
Sinilnikova OM, Antoniou AC, Simard J, Healey S, Léoné M, Sinnett D, Spurdle AB, Beesley J, Chen X, Greene MH, Loud JT, Lejbkowicz F, Rennert G, Dishon S, et al. The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. British Journal of Cancer. 101: 1456-60. PMID 19707196 DOI: 10.1038/Sj.Bjc.6605279 |
0.305 |
|
| 2009 |
Grundberg E, Kwan T, Ge B, Lam KC, Koka V, Kindmark A, Mallmin H, Dias J, Verlaan DJ, Ouimet M, Sinnett D, Rivadeneira F, Estrada K, Hofman A, van Meurs JM, et al. Population genomics in a disease targeted primary cell model. Genome Research. 19: 1942-52. PMID 19654370 DOI: 10.1101/Gr.095224.109 |
0.371 |
|
| 2009 |
Healy J, Dionne J, Bélanger H, Larivière M, Beaulieu P, Labuda D, Sinnett D. Functional impact of sequence variation in the promoter region of TGFB1. International Journal of Cancer. Journal International Du Cancer. 125: 1483-9. PMID 19536820 DOI: 10.1002/Ijc.24526 |
0.375 |
|
| 2009 |
Ansari M, Sauty G, Labuda M, Gagné V, Laverdière C, Moghrabi A, Sinnett D, Krajinovic M. Polymorphisms in multidrug resistance-associated protein gene 4 is associated with outcome in childhood acute lymphoblastic leukemia. Blood. 114: 1383-6. PMID 19515727 DOI: 10.1182/Blood-2008-11-191098 |
0.36 |
|
| 2009 |
Healy J, Roy-Gagnon MH, Sinnett D. No evidence for association between TGFB1 promoter SNPs and the risk of childhood pre-B acute lymphoblastic leukemia among French Canadians. Haematologica. 94: 1034-5. PMID 19491338 DOI: 10.3324/Haematol.2009.005991 |
0.359 |
|
| 2009 |
Krajinovic M, Ansari M, Sinnett D. Response: MRP4 gene polymorphisms and treatment response in adult ALL Blood. 114: 5401-5402. DOI: 10.1182/Blood-2009-10-245175 |
0.333 |
|
| 2008 |
Boily G, Beaulieu P, Healy J, Sinnett D. Connections between ETV6-modulated genes: identification of shared features. Cancer Informatics. 6: 183-201. PMID 19259410 DOI: 10.4137/Cin.S556 |
0.351 |
|
| 2008 |
Dulucq S, St-Onge G, Gagné V, Ansari M, Sinnett D, Labuda D, Moghrabi A, Krajinovic M. DNA variants in the dihydrofolate reductase gene and outcome in childhood ALL. Blood. 111: 3692-700. PMID 18096764 DOI: 10.1182/Blood-2007-09-110593 |
0.359 |
|
| 2007 |
Sinnett D, N'Diaye N, St-Onge P, Healy J. [Childhood leukemia: a genetic disease!]. MéDecine Sciences : M/S. 23: 968-74. PMID 18021709 DOI: 10.1051/Medsci/20072311968 |
0.363 |
|
| 2007 |
Boily G, Ouellet S, Langlois S, Larivière M, Drouin R, Sinnett D. In vivo footprinting analysis of the Glypican 3 (GPC3) promoter region in neuroblastoma cells. Biochimica Et Biophysica Acta. 1769: 182-93. PMID 17350117 DOI: 10.1016/J.Bbaexp.2007.01.014 |
0.335 |
|
| 2007 |
Labuda D, Labbé C, Langlois S, Lefebvre JF, Freytag V, Moreau C, Sawicki J, Beaulieu P, Pastinen T, Hudson TJ, Sinnett D. Patterns of variation in DNA segments upstream of transcription start sites. Human Mutation. 28: 441-50. PMID 17274005 DOI: 10.1002/Humu.20463 |
0.308 |
|
| 2007 |
Boily G, Larose J, Langlois S, Sinnett D. Identification of transcripts modulated by ETV6 expression. British Journal of Haematology. 136: 48-62. PMID 17069581 DOI: 10.1111/J.1365-2141.2006.06377.X |
0.363 |
|
| 2007 |
Healy J, Bélanger H, Beaulieu P, Larivière M, Labuda D, Sinnett D. Promoter SNPs in G1/S checkpoint regulators and their impact on the susceptibility to childhood leukemia. Blood. 109: 683-92. PMID 17008550 DOI: 10.1182/Blood-2006-02-003236 |
0.393 |
|
| 2006 |
Tremblay E, Auclair J, Delvin E, Levy E, Ménard D, Pshezhetsky AV, Rivard N, Seidman EG, Sinnett D, Vachon PH, Beaulieu JF. Gene expression profiles of normal proliferating and differentiating human intestinal epithelial cells: a comparison with the Caco-2 cell model. Journal of Cellular Biochemistry. 99: 1175-86. PMID 16795037 DOI: 10.1002/Jcb.21015 |
0.316 |
|
| 2006 |
Sinnett D, Labuda D, Krajinovic M. Challenges identifying genetic determinants of pediatric cancers--the childhood leukemia experience. Familial Cancer. 5: 35-47. PMID 16528607 DOI: 10.1007/S10689-005-2574-4 |
0.375 |
|
| 2006 |
Sinnett D, Beaulieu P, Bélanger H, Lefebvre JF, Langlois S, Théberge MC, Drouin S, Zotti C, Hudson TJ, Labuda D. Detection and characterization of DNA variants in the promoter regions of hundreds of human disease candidate genes. Genomics. 87: 704-10. PMID 16500075 DOI: 10.1016/J.Ygeno.2006.01.001 |
0.379 |
|
| 2005 |
Bélanger H, Beaulieu P, Moreau C, Labuda D, Hudson TJ, Sinnett D. Functional promoter SNPs in cell cycle checkpoint genes. Human Molecular Genetics. 14: 2641-8. PMID 16081466 DOI: 10.1093/Hmg/Ddi298 |
0.386 |
|
| 2004 |
Fleury I, Primeau M, Doreau A, Costea I, Moghrabi A, Sinnett D, Krajinovic M. Polymorphisms in genes involved in the corticosteroid response and the outcome of childhood acute lymphoblastic leukemia. American Journal of Pharmacogenomics : Genomics-Related Research in Drug Development and Clinical Practice. 4: 331-41. PMID 15462611 DOI: 10.2165/00129785-200404050-00006 |
0.341 |
|
| 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 |
0.659 |
|
| 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 |
0.575 |
|
| 2004 |
Boily G, Saikali Z, Sinnett D. Methylation analysis of the glypican 3 gene in embryonal tumours. British Journal of Cancer. 90: 1606-11. PMID 15083193 DOI: 10.1038/Sj.Bjc.6601716 |
0.748 |
|
| 2004 |
Le Jossec M, Wambach T, Labuda D, Sinnett D, Levy E. Genetic diversity patterns in the SR-BI/II locus can be explained by a recent selective sweep. Molecular Biology and Evolution. 21: 760-9. PMID 14963100 DOI: 10.1093/Molbev/Msh074 |
0.323 |
|
| 2004 |
Pastinen T, Sladek R, Gurd S, Sammak A, Ge B, Lepage P, Lavergne K, Villeneuve A, Gaudin T, Brändström H, Beck A, Verner A, Kingsley J, Harmsen E, Labuda D, ... ... Sinnett D, et al. A survey of genetic and epigenetic variation affecting human gene expression Physiological Genomics. 16: 184-193. PMID 14583597 DOI: 10.1152/Physiolgenomics.00163.2003 |
0.349 |
|
| 2004 |
Krajinovic M, Lamothe S, Labuda D, Lemieux-Blanchard E, Theoret Y, Moghrabi A, Sinnett D. Role of MTHFR genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia. Blood. 103: 252-7. PMID 12958073 DOI: 10.1182/Blood-2003-06-1794 |
0.359 |
|
| 2003 |
Mathonnet G, Labuda D, Meloche C, Wambach T, Krajinovic M, Sinnett D. Variable continental distribution of polymorphisms in the coding regions of DNA-repair genes. Journal of Human Genetics. 48: 659-64. PMID 14625810 DOI: 10.1007/S10038-003-0097-0 |
0.348 |
|
| 2003 |
Mathonnet G, Krajinovic M, Labuda D, Sinnett D. Role of DNA mismatch repair genetic polymorphisms in the risk of childhood acute lymphoblastic leukaemia. British Journal of Haematology. 123: 45-8. PMID 14510941 DOI: 10.1046/J.1365-2141.2003.04551.X |
0.363 |
|
| 2003 |
Fleury I, Beaulieu P, Primeau M, Labuda D, Sinnett D, Krajinovic M. Characterization of the BclI polymorphism in the glucocorticoid receptor gene. Clinical Chemistry. 49: 1528-31. PMID 12928238 DOI: 10.1373/49.9.1528 |
0.368 |
|
| 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 |
0.553 |
|
| 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 |
0.622 |
|
| 2003 |
Simard J, Dumont M, Labuda D, Sinnett D, Meloche C, El-Alfy M, Berger L, Lees E, Labrie F, Tavtigian SV. Prostate cancer susceptibility genes: lessons learned and challenges posed. Endocrine-Related Cancer. 10: 225-59. PMID 12790786 DOI: 10.1677/Erc.0.0100225 |
0.337 |
|
| 2002 |
Krajinovic M, Labuda D, Sinnett D. Glutathione S-transferase P1 genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukaemia. Pharmacogenetics. 12: 655-8. PMID 12439226 DOI: 10.1097/00008571-200211000-00010 |
0.336 |
|
| 2002 |
Labuda D, Krajinovic M, Sabbagh A, Infante-Rivard C, Sinnett D. Parental genotypes in the risk of a complex disease. American Journal of Human Genetics. 71: 193-7. PMID 12058344 DOI: 10.1086/341345 |
0.304 |
|
| 2002 |
Infante-Rivard C, Amre D, Sinnett D. GSTT1 and CYP2E1 polymorphisms and trihalomethanes in drinking water: effect on childhood leukemia. Environmental Health Perspectives. 110: 591-3. PMID 12055050 DOI: 10.1289/Ehp.02110591 |
0.302 |
|
| 2002 |
Brockstedt U, Krajinovic M, Richer C, Mathonnet G, Sinnett D, Pfau W, Labuda D. Analyses of bulky DNA adduct levels in human breast tissue and genetic polymorphisms of cytochromes P450 (CYPs), myeloperoxidase (MPO), quinone oxidoreductase (NQO1), and glutathione S-transferases (GSTs). Mutation Research. 516: 41-7. PMID 11943609 DOI: 10.1016/S1383-5718(02)00019-0 |
0.324 |
|
| 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 |
0.645 |
|
| 2002 |
Krajinovic M, Sinnett H, Richer C, Labuda D, Sinnett D. Role of NQO1, MPO and CYP2E1 genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia. International Journal of Cancer. 97: 230-6. PMID 11774269 DOI: 10.1002/Ijc.1589 |
0.362 |
|
| 2002 |
Labuda D, Krajinovic M, Sabbagh A, Infante-Rivard C, Sinnett D. Reply to Comments by Kraft and Wilson and by Weinberg and Mitchell on “Parental Genotypes in the Risk of a Complex Disease” American Journal of Human Genetics. 71: 1240-1242. DOI: 10.1086/344144 |
0.311 |
|
| 2001 |
Krajinovic M, Labuda D, Sinnett D. Childhood acute lymphoblastic leukemia: genetic determinants of susceptibility and disease outcome. Reviews On Environmental Health. 16: 263-280. PMID 12041882 DOI: 10.1515/Reveh.2001.16.4.263 |
0.327 |
|
| 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 |
0.625 |
|
| 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 |
0.595 |
|
| 2000 |
Saikali Z, Sinnett D. Expression of glypican 3 (GPC3) in embryonal tumors. International Journal of Cancer. 89: 418-22. PMID 11008203 DOI: 10.1002/1097-0215(20000920)89:5<418::Aid-Ijc4>3.0.Co;2-I |
0.751 |
|
| 2000 |
Sinnett D, Krajinovic M, Labuda D. Genetic susceptibility to childhood acute lymphoblastic leukemia. Leukemia & Lymphoma. 38: 447-462. PMID 10953966 DOI: 10.3109/10428190009059264 |
0.365 |
|
| 2000 |
Infante-Rivard C, Mathonnet G, Sinnett D. Risk of childhood leukemia associated with diagnostic irradiation and polymorphisms in DNA repair genes. Environmental Health Perspectives. 108: 495-8. PMID 10856021 DOI: 10.1289/Ehp.00108495 |
0.315 |
|
| 1999 |
Aı̈ssani B, Sinnett D. Fine physical and transcript mapping of a 1.8 Mb region spanning the locus for childhood acute lymphoblastic leukemia on chromosome 12p12. 3. Gene. 240: 297-305. PMID 10580149 DOI: 10.1016/S0378-1119(99)00449-7 |
0.366 |
|
| 1999 |
Labuda D, Krajinovic M, Richer C, Skoll A, Sinnett H, Yotova V, Sinnett D. Rapid detection of CYP1A1, CYP2D6, and NAT variants by multiplex polymerase chain reaction and allele-specific oligonucleotide assay. Analytical Biochemistry. 275: 84-92. PMID 10542112 DOI: 10.1006/Abio.1999.4293 |
0.314 |
|
| 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 |
0.642 |
|
| 1999 |
Bovenzi V, Lê NLO, Côté S, Sinnett D, Momparler LF, Momparler RL. DNA methylation of retinoic acid receptor beta in breast cancer and possible therapeutic role of 5-aza-2'-deoxycytidine. Anti-Cancer Drugs. 10: 471-476. PMID 10477167 DOI: 10.1097/00001813-199906000-00007 |
0.326 |
|
| 1999 |
Aïssani B, Bonan C, Baccichet A, Sinnett D. Childhood acute lymphoblastic leukemia: is there a tumor suppressor gene in chromosome 12p12.3? Leukemia & Lymphoma. 34: 231-9. PMID 10439360 DOI: 10.3109/10428199909050948 |
0.392 |
|
| 1999 |
Benachenhou N, Guiral S, Gorska-Flipot I, Labuda D, Sinnett D. Frequent loss of heterozygosity at the DNA mismatch-repair loci hMLH1 and hMSH3 in sporadic breast cancer. British Journal of Cancer. 79: 1012-7. PMID 10098729 DOI: 10.1038/Sj.Bjc.6690162 |
0.313 |
|
| 1999 |
Krajinovic M, Labuda D, Richer C, Karimi S, Sinnett D. Susceptibility to Childhood Acute Lymphoblastic Leukemia: Influence of CYP1A1, CYP2D6, GSTM1, and GSTT1 Genetic Polymorphisms Blood. 93: 1496-1501. DOI: 10.1182/Blood.V93.5.1496.405A36_1496_1501 |
0.369 |
|
| 1998 |
Benachenhou N, Guiral S, Gorska-Flipot I, Michalski R, Labuda D, Sinnett D. Allelic losses and DNA methylation at DNA mismatch repair loci in sporadic colorectal cancer. Carcinogenesis. 19: 1925-9. PMID 9855004 DOI: 10.1093/Carcin/19.11.1925 |
0.328 |
|
| 1998 |
Côté S, Sinnett D, Momparler RL. Demethylation by 5-aza-2'-deoxycytidine of specific 5-methylcytosine sites in the promoter region of the retinoic acid receptor beta gene in human colon carcinoma cells. Anti-Cancer Drugs. 9: 743-750. PMID 9840718 DOI: 10.1097/00001813-199810000-00001 |
0.35 |
|
| 1998 |
Krajinovic M, Richer C, Gorska-Flipot I, Gaboury L, Novakovic I, Labuda D, Sinnett D. Genomic loci susceptible to replication errors in cancer cells. British Journal of Cancer. 78: 981-5. PMID 9792139 DOI: 10.1038/Bjc.1998.616 |
0.315 |
|
| 1998 |
Krajinovic M, Richer C, Lukovic L, Labuda D, Sinnett D. Chromosomal assignment of loci susceptible to replication errors by radiation hybrid mapping. Mutation Research/Mutation Research Genomics. 382: 81-83. PMID 9691987 DOI: 10.1016/S1383-5726(97)00015-0 |
0.311 |
|
| 1998 |
Benachenhou N, Guiral S, Gorska-Flipot I, Labuda D, Sinnett D. High resolution deletion mapping reveals frequent allelic losses at the DNA mismatch repair loci hMLH1 and hMSH3 in non-small cell lung cancer. International Journal of Cancer. 77: 173-80. PMID 9650548 DOI: 10.1002/(Sici)1097-0215(19980717)77:2<173::Aid-Ijc1>3.0.Co;2-N |
0.344 |
|
| 1998 |
Baccichet A, Qualman SK, Sinnett D. Allelic loss in childhood acute lymphoblastic leukemia. Leukemia Research. 21: 817-23. PMID 9393596 DOI: 10.1016/S0145-2126(97)00075-1 |
0.323 |
|
| 1997 |
Baccichet A, Sinnett D. Frequent deletion of chromosome 12p12.3 in children with acute lymphoblastic leukaemia British Journal of Haematology. 99: 107-114. PMID 9359510 DOI: 10.1046/J.1365-2141.1997.3663180.X |
0.399 |
|
| 1997 |
Kim Y, Glatt H, Xie W, Sinnett D, Lalande M. Human gamma-aminobutyric acid-type A receptor alpha5 subunit gene (GABRA5): characterization and structural organization of the 5' flanking region. Genomics. 42: 378-87. PMID 9205108 DOI: 10.1006/Geno.1997.4770 |
0.317 |
|
| 1997 |
Baccichet A, Benachenhou N, Couture F, Leclerc J-, Sinnett D. Microsatellite instability in childhood T cell acute lymphoblastic leukemia. Leukemia. 11: 797-802. PMID 9177430 DOI: 10.1038/Sj.Leu.2400650 |
0.392 |
|
| 1997 |
Jarnik M, Tang JQ, Korab-Laskowska M, Zietkiewicz E, Cardinal G, Gorska-Flipot I, Sinnett D, Labuda D. Overall informativity, OI, in DNA polymorphisms revealed by inter-Alu PCR: detection of genomic rearrangements. Genomics. 36: 388-98. PMID 8884261 DOI: 10.1006/Geno.1996.0483 |
0.337 |
|
| 1996 |
Sinnett D, Woolf E, Xie W, Glatt K, Kirkness EF, Nielsen TO, Zannis-Hadjopoulos M, Price GB, Lalande M. Identification of a putative DNA replication origin in the gamma-aminobutyric acid receptor subunit beta3 and alpha5 gene cluster on human chromosome 15q11-q13, a region associated with parental imprinting and allele-specific replication timing. Gene. 173: 171-7. PMID 8964494 DOI: 10.1016/0378-1119(96)00106-0 |
0.322 |
|
| 1994 |
Glatt K, Sinnett D, Lalande M. The human gamma-aminobutyric acid receptor subunit beta 3 and alpha 5 gene cluster in chromosome 15q11-q13 is rich in highly polymorphic (CA)n repeats. Genomics. 19: 157-60. PMID 8188218 DOI: 10.1006/Geno.1994.1027 |
0.302 |
|
| 1992 |
Zietkiewicz E, Sinnett D, Richer C, Mitchell G, Vanasse M, Labuda D. Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus. Human Genetics. 89: 453-6. PMID 1618495 DOI: 10.1007/Bf00194322 |
0.32 |
|
| 1992 |
Zietkiewicz E, Labuda M, Sinnett D, Glorieux FH, Labuda D. Linkage mapping by simultaneous screening of multiple polymorphic loci using Alu oligonucleotide-directed PCR. Proceedings of the National Academy of Sciences of the United States of America. 89: 8448-8451. PMID 1528850 DOI: 10.1073/Pnas.89.18.8448 |
0.336 |
|
| 1990 |
Sinnett D, Deragon J, Simard LR, Labuda D. Alumorphs--human DNA polymorphisms detected by polymerase chain reaction using Alu-specific primers. Genomics. 7: 331-334. PMID 1973138 DOI: 10.1016/0888-7543(90)90166-R |
0.311 |
|
| 1989 |
Sinnett D, Lavergne L, Melançon SB, Dallaire L, Potier M, Labuda D. Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe. Human Genetics. 81: 4-8. PMID 2904404 DOI: 10.1007/Bf00283719 |
0.318 |
|
| 1989 |
Sefiani A, Abel L, Heuertz S, Sinnett D, Lavergne L, Labuda D, Hors-Cayla MC. The gene for incontinentia pigmenti is assigned to Xq28. Genomics. 4: 427-9. PMID 2714798 DOI: 10.1016/0888-7543(89)90350-9 |
0.302 |
|
| 1987 |
Sinnett D, Mitchell G, Lavergne L, Melanqon SB, Dallaire L, Pocicr M, Labuda D. INCONTINENTIA PIGMENTI (IP): LINKAGE ANALYSIS OF A KINDRED USING MULTIPLE Xp CENOMIC MARKERS Pediatric Research. 21. DOI: 10.1203/00006450-198704010-00385 |
0.322 |
|
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