Search Results - "Healy, Jasmine"
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Contribution of polymorphisms in IKZF1 gene to childhood acute leukemia: a meta-analysis of 33 case-control studies
Published in PloS one (25-11-2014)“…Two common polymorphisms in the IKZF1 gene (rs4132601 and rs11978267 variants) have been reported to be associated with childhood acute leukemia (AL) risk,…”
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Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia
Published in Haematologica (Roma) (01-09-2010)“…Although childhood acute lymphoblastic leukemia is the most common pediatric cancer, its etiology remains poorly understood. In an attempt to replicate the…”
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3
CLIC5: a novel ETV6 target gene in childhood acute lymphoblastic leukemia
Published in Haematologica (Roma) (01-12-2016)“…The most common rearrangement in childhood precursor B-cell acute lymphoblastic leukemia is the t(12;21)(p13;q22) translocation resulting in the ETV6-AML1…”
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Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans
Published in PLoS genetics (01-09-2013)“…Whole-exome or gene targeted resequencing in hundreds to thousands of individuals has shown that the majority of genetic variants are at low frequency in human…”
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Association between CEBPE Variant and Childhood Acute Leukemia Risk: Evidence from a Meta-Analysis of 22 Studies
Published in PloS one (04-05-2015)“…The CCAAT/enhancer binding proteins (CEBPs) have been involved in the etiology of acute leukemia (AL) and investigated in numerous genetic association studies,…”
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Mutational dynamics of early and late relapsed childhood ALL: rapid clonal expansion and long-term dormancy
Published in Blood advances (13-02-2018)“…Childhood acute lymphoblastic leukemia (cALL) is the most frequent pediatric cancer. Refractory/relapsed cALL presents a survival rate of ∼45% and is still one…”
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Impact of promoter polymorphisms in key regulators of the intrinsic apoptosis pathway on the outcome of childhood acute lymphoblastic leukemia
Published in Haematologica (Roma) (01-02-2014)“…The introduction of multiagent treatment protocols has led to a remarkable increase in survival rates for children diagnosed with acute lymphoblastic leukemia,…”
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Patient mutations alter ATRX targeting to PML nuclear bodies
Published in European journal of human genetics : EJHG (01-02-2008)“…ATRX is a SWI/SNF-like chromatin remodeling protein mutated in several X-linked mental retardation syndromes. Gene inactivation studies in mice demonstrate…”
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No evidence for association between TGFB1 promoter SNPs and the risk of childhood pre-B acute lymphoblastic leukemia among French Canadians
Published in Haematologica (Roma) (01-07-2009)Get full text
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10
Connections Between ETV6-Modulated Genes: Identification of Shared Features
Published in Cancer informatics (01-01-2008)“…Gino Boily1, Patrick Beaulieu1, Jasmine Healy1 and Daniel Sinnett1,2 1Division of Hematology-Oncology, Charles-Bruneau Cancer Center, Research Center, CHU…”
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SNooPer: a machine learning-based method for somatic variant identification from low-pass next-generation sequencing
Published in BMC genomics (14-11-2016)“…Next-generation sequencing (NGS) allows unbiased, in-depth interrogation of cancer genomes. Many somatic variant callers have been developed yet accurate…”
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Recurrent somatic BRAF insertion (p.V504_R506dup): a tumor marker and a potential therapeutic target in pilocytic astrocytoma
Published in Oncogene (01-04-2019)“…Pilocytic astrocytoma (PA) is emerging as a tumor entity with dysregulated RAS/RAF/MEK/ERK signaling. In this study, we report the identification of a novel…”
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Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutations
Published in Oncotarget (04-10-2016)“…T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematologic malignancy with variable prognosis. It represents 15% of diagnosed pediatric ALL cases…”
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Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome
Published in Blood (10-10-2019)“…Children with Down syndrome (DS) have a 20-fold increased risk of acute lymphoblastic leukemia (ALL) and distinct somatic features, including CRLF2…”
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Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk
Published in Nature genetics (01-06-2010)“…Using data from a genome-wide association study of 907 individuals with childhood acute lymphoblastic leukemia (cases) and 2,398 controls and with validation…”
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A fork in the road: A mixed methods study exploring why older adults with acute myeloid leukemia choose different treatment paths
Published in Journal of clinical oncology (20-05-2020)“…Abstract only 7520 Background: Current treatment options for acute myeloid leukemia (AML) are diverse, including intensive chemotherapy (IC), low intensity…”
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A mixed methods study exploring the role of perceived side effects on treatment decision-making in older adults with acute myeloid leukemia (AML)
Published in Journal of clinical oncology (20-05-2021)“…Abstract only 7016 Background: AML patients may be treated with intensive chemotherapy (IC), or non-intensive chemotherapy (NIC) or they may receive best…”
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Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes
Published in BMC cancer (23-07-2015)“…Acute lymphoblastic leukemia (ALL) is the most common pediatric cancer. While the multi-step model of pediatric leukemogenesis suggests interplay between…”
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Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome
Published in Leukemia (01-11-2019)Get full text
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Integration of High-Resolution Methylome and Transcriptome Analyses to Dissect Epigenomic Changes in Childhood Acute Lymphoblastic Leukemia
Published in Cancer research (Chicago, Ill.) (15-07-2013)“…B-cell precursor acute lymphoblastic leukemia (pre-B ALL) is the most common pediatric cancer. Although the genetic determinants underlying disease onset…”
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