A. Laquérrière

Phenotype associated with APP duplication in five families

L. Cabrejo, Lucie Guyant‐Maréchal, A. Laquérrière et al. · Brain · 2006 · 335 citations · Full text

Medicine, Neurology, Neuroscience +17

Valosin-containing protein gene mutations

Lucie Guyant‐Maréchal, A. Laquérrière, Charles Duyckaerts et al. · Neurology · 2006 · 149 citations

Life Sciences, Genetics, Neurology +17

Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization

Jorge A. Bevilacqua, Nicole Monnier, Marc Bitoun et al. · Neuropathology and Applied Neurobiology · 2010 · 116 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Integrated multi-omics analysis of oligodendroglial tumours identifies three subgroups of 1p/19q co-deleted gliomas

Aurélie Kamoun, Ahmed Idbaïh, Caroline Dehais et al. · Nature Communications · 2016 · 113 citations · Full text

Medicine, Molecular Genetics, Oncology +17

Differential transcript usage unravels gene expression alterations in Alzheimer’s disease human brains

Diego Marques‐Coelho, Lukas da Cruz Carvalho Iohan, Ana Raquel Melo de Farias et al. · npj Aging and Mechanisms of Disease · 2021 · 106 citations · Full text

Life Sciences, Molecular Biology, Neuroscience +17