Ève Lalancette

ÈL

Publications

Citations

H-Index

2020

Active since

Affiliations

Centre Hospitalier Universitaire Sainte-Justine(Current)

Université de Montréal

Cégep Marie-Victorin

Ève Lalancette is an author at Centre Hospitalier Universitaire Sainte-Justine specializing in molecular genetics, developmental delay, and fragile x premutation.

ORCID

Top concepts

GeneticsMedicineDown SyndromeFragile X SpectrumMolecular GeneticsDevelopmental DelayDevelopmental BiologyFragile X Premutation

Publications per year

2020–2024

Publications

Distinct patterns of repetition suppression in Fragile X syndrome, down syndrome, tuberous sclerosis complex and mutations in SYNGAP1

Valérie Côté, Ève Lalancette, Inga Sophia Knoth et al. · Brain Research · 2020 · 32 citations

Down Syndrome, Tuberous Sclerosis Complex, Developmental Biology +12

Steady-state visual evoked potentials in children with neurofibromatosis type 1: associations with behavioral rating scales and impact of psychostimulant medication

Ève Lalancette, Audrey-Rose Charlebois-Poirier, Kristian Agbogba et al. · Journal of Neurodevelopmental Disorders · 2022 · 13 citations · Full text

Impact of trametinib on the neuropsychological profile of NF1 patients

Ève Lalancette, Édith Cantin, Marie-Ève Routhier et al. · Journal of Neuro-Oncology · 2024 · 12 citations

Rows per page

1–3 of 3