Virginie Saillour

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

Ferrán Casals, Alan Hodgkinson, Julie Hussin et al. · PLoS Genetics · 2013 · 92 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

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

Jean-François Spinella, Pamela Mehanna, Ramón Vidal et al. · BMC Genomics · 2016 · 70 citations · Full text

Medicine, Genetics, Oncology +17

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

Jean-François Spinella, Pauline Cassart, Chantal Richer et al. · Oncotarget · 2016 · 65 citations · Full text

Medicine, Genetics, Oncology +17

Integration of High-Resolution Methylome and Transcriptome Analyses to Dissect Epigenomic Changes in Childhood Acute Lymphoblastic Leukemia

Stephan Busche, Bing Ge, Ramón Vidal et al. · Cancer Research · 2013 · 59 citations

Life Sciences, Molecular Biology, Oncology +17

Rare allelic forms of <i>PRDM9</i> associated with childhood leukemogenesis

Julie Hussin, Daniel Sinnett, Ferrán Casals et al. · Genome Research · 2012 · 50 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15