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Joëlle Michaud

Walter and Eliza Hall Institute of Medical Research

17

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1912

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RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML.

2020 Blood Advances
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Economic evaluation of a novel genetic screening test for risk of venous thromboembolism compared with standard of care in women considering combined hormonal contraception in Switzerland.

2019 BMJ Open
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Expanded Phenotypic and Genetic Heterogeneity in the Clinical Spectrum of FPD-AML: Lymphoid Malignancies and Skin Disorders Are Common Features in Carriers of Germline RUNX1 Mutations

2016 Blood
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Person and place in perinatal outcomes: how the interaction between rural residence and Aboriginal heritage alters birth outcomes

2015
- Joëlle Michaud
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HCFC1 is a common component of active human CpG-island promoters and coincides with ZNF143, THAP11, YY1, and GABP transcription factor occupancy

2013 Genome Research
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implications for mechanisms of pathogenesis familial platelet disorder with predisposition to acute myelogenous leukemia: In vitro analyses of known and novel RUNX1/AML1 mutations in dominant

2013
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Genomic Study of RNA Polymerase II and III SNAPc-Bound Promoters Reveals a Gene Transcribed by Both Enzymes and a Broad Use of Common Activators

2012 PLOS Genetics
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Integrative analysis of RUNX1 downstream pathways and target genes

2008 BMC Genomics
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Genetic mechanisms and heterogeneity in familial myeloid leukemia

2007 Clinical Cancer Research
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A pedigree with autosomal dominant thrombocytopenia, red cell macrocytosis, and an occurrence of t(12:21) positive pre-B acute lymphoblastic leukemia

2007 Blood Cells Molecules and Diseases
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Citations (2)