Adeline Bonnard

SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype

Marialetizia Motta, Giulia Fasano, Sina Gredy et al. · The American Journal of Human Genetics · 2021 · 80 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients

Clémence Jacquin, Emilie Landais, Céline Poirsier et al. · American Journal of Medical Genetics Part A · 2022 · 37 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Oligo-astrocytoma in LZTR1-related Noonan syndrome

Adeline Jacquinet, Adeline Bonnard, Yline Capri et al. · European Journal of Medical Genetics · 2019 · 27 citations · Full text

Medicine, Neurology, Neurogenetics +5

Expanding the molecular spectrum of pathogenic<i>SHOC2</i>variants underlying Mazzanti syndrome

Marialetizia Motta, Maja Šolman, Adeline Bonnard et al. · Human Molecular Genetics · 2022 · 20 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Growth charts in Kabuki syndrome 1

Valentin Ruault, Carole Corsini, Claire Duflos et al. · American Journal of Medical Genetics Part A · 2019 · 16 citations · Full text

Medicine, Endocrinology, Pediatrics +17