Connections Between ETV6-Modulated Genes: Identification of Shared Features

por Boily, Gino, Beaulieu, Patrick, Healy, Jasmine, Sinnett, Daniel
Publicado 2008

Contribution of Polymorphisms in IKZF1 Gene to Childhood Acute Leukemia: A Meta-Analysis of 33 Case-Control Studies

por Dai, Yue-e, Tang, Linjun, Healy, Jasmine, Sinnett, Daniel
Publicado 2014

Detection of Fetomaternal Genotype Associations in Early-Onset Disorders: Evaluation of Different Methods and Their Application to Childhood Leukemia

por Healy, Jasmine, Bourgey, Mathieu, Richer, Chantal, Sinnett, Daniel, Roy-Gagnon, Marie-Helene
Publicado 2010

Association between CEBPE Variant and Childhood Acute Leukemia Risk: Evidence from a Meta-Analysis of 22 Studies

por Sun, Jian, Zheng, Jinyu, Tang, Linjun, Healy, Jasmine, Sinnett, Daniel, Dai, Yue-e
Publicado 2015

Joint genotype inference with germline and somatic mutations

por Bareke, Eric, Saillour, Virginie, Spinella, Jean-François, Vidal, Ramon, Healy, Jasmine, Sinnett, Daniel, Csűrös, Miklós
Publicado 2013

Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes

por Spinella, Jean-François, Healy, Jasmine, Saillour, Virginie, Richer, Chantal, Cassart, Pauline, Ouimet, Manon, Sinnett, Daniel
Publicado 2015

SNooPer: a machine learning-based method for somatic variant identification from low-pass next-generation sequencing

por Spinella, Jean-François, Mehanna, Pamela, Vidal, Ramon, Saillour, Virginie, Cassart, Pauline, Richer, Chantal, Ouimet, Manon, Healy, Jasmine, Sinnett, Daniel
Publicado 2016

A novel somatic mutation in ACD induces telomere lengthening and apoptosis resistance in leukemia cells

por Spinella, Jean-François, Cassart, Pauline, Garnier, Nicolas, Rousseau, Philippe, Drullion, Claire, Richer, Chantal, Ouimet, Manon, Saillour, Virginie, Healy, Jasmine, Autexier, Chantal, Sinnett, Daniel
Publicado 2015

Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutations

por Spinella, Jean-François, Cassart, Pauline, Richer, Chantal, Saillour, Virginie, Ouimet, Manon, Langlois, Sylvie, St-Onge, Pascal, Sontag, Thomas, Healy, Jasmine, Minden, Mark D., Sinnett, Daniel
Publicado 2016

Recurrent somatic BRAF insertion (p.V504_R506dup): a tumor marker and a potential therapeutic target in pilocytic astrocytoma

por Khater, Fida, Langlois, Sylvie, Cassart, Pauline, Roy, Anne-Marie, Lajoie, Mathieu, Healy, Jasmine, Richer, Chantal, St-Onge, Pascal, Piché, Nelson, Perreault, Sebastien, Cellot, Sonia, Marzouki, Monia, Jabado, Nada, Sinnett, Daniel
Publicado 2018

Patient, Family Member and Physician Perspectives and Experiences with AML Treatment Decision-Making

por LeBlanc, Thomas W., Russell, Nigel H., Hernandez-Aldama, Loriana, Panter, Charlotte, Bell, Timothy J., Welch, Verna, Vega, Diana Merino, O’Hara, Louise, Stein, Julia, Barclay, Melissa, Peloquin, Francois, Brown, Andrew, Healy, Jasmine, Morgan, Lucy, Gater, Adam, Hohman, Ryan, Amer, Karim, Maze, Dawn, Walter, Roland B.
Publicado 2022

Rare allelic forms of PRDM9 associated with childhood leukemogenesis

por Hussin, Julie, Sinnett, Daniel, Casals, Ferran, Idaghdour, Youssef, Bruat, Vanessa, Saillour, Virginie, Healy, Jasmine, Grenier, Jean-Christophe, de Malliard, Thibault, Busche, Stephan, Spinella, Jean-François, Larivière, Mathieu, Gibson, Greg, Andersson, Anna, Holmfeldt, Linda, Ma, Jing, Wei, Lei, Zhang, Jinghui, Andelfinger, Gregor, Downing, James R., Mullighan, Charles G., Awadalla, Philip
Publicado 2013

Whole-Exome Sequencing Reveals a Rapid Change in the Frequency of Rare Functional Variants in a Founding Population of Humans

por Casals, Ferran, Hodgkinson, Alan, Hussin, Julie, Idaghdour, Youssef, Bruat, Vanessa, de Maillard, Thibault, Grenier, Jean-Cristophe, Gbeha, Elias, Hamdan, Fadi F., Girard, Simon, Spinella, Jean-François, Larivière, Mathieu, Saillour, Virginie, Healy, Jasmine, Fernández, Isabel, Sinnett, Daniel, Michaud, Jacques L., Rouleau, Guy A., Haddad, Elie, Le Deist, Françoise, Awadalla, Philip
Publicado 2013

Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome

por de Smith, Adam J., Walsh, Kyle M., Morimoto, Libby M., Francis, Stephen S., Hansen, Helen M., Jeon, Soyoung, Gonseth, Semira, Chen, Minhui, Sun, Hanxiao, Luna-Fineman, Sandra, Antillón, Federico, Girón, Verónica, Kang, Alice Y., Smirnov, Ivan, Shao, Xiaorong, Whitehead, Todd P., Barcellos, Lisa F., Jolly, Kent W., Healy, Jasmine, Laverdière, Caroline, Sinnett, Daniel, Taub, Jeffrey W., Birch, Jillian M., Thompson, Pamela D., Pombo-de-Oliveira, Maria S., Spector, Logan G., DeWan, Andrew T., Mueller, Beth A., Chiang, Charleston, Metayer, Catherine, Ma, Xiaomei, Wiemels, Joseph L.
Publicado 2019