Elise Boudry‐Labis

A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features

Elise Boudry‐Labis, Bénédicte Demeer, Cédric Le Caignec et al. · European Journal of Medical Genetics · 2012 · 73 citations

Medicine, Genetics, Molecular Genetics +17

<i>Neurofibromatosis‐1</i> gene deletions and mutations in de novo adult acute myeloid leukemia

Elise Boudry‐Labis, Catherine Roche‐Lestienne, Olivier Nibourel et al. · American Journal of Hematology · 2013 · 49 citations · Full text

Life Sciences, Genetics, Oncology +16

MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype

Thomas Smol, Florence Petit, Amélie Piton et al. · Neurogenetics · 2018 · 44 citations

Life Sciences, Genetics, Molecular Genetics +14

SNP-array lesions in core binding factor acute myeloid leukemia

Nicolas Duployez, Elise Boudry‐Labis, Christophe Roumier et al. · Oncotarget · 2018 · 18 citations · Full text

Medicine, Hematology, Molecular Genetics +15

A heterozygous microdeletion of 20q13.13 encompassing ADNP gene in a child with Helsmoortel–van der Aa syndrome

Minh‐Tuan Huynh, Elise Boudry‐Labis, Alfred Massard et al. · European Journal of Human Genetics · 2018 · 18 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9