Solenn Legallic

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey et al. · Nature · 2011 · 480 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease

Cyril Pottier, Didier Hannequin, Sophie Coutant et al. · Molecular Psychiatry · 2012 · 318 citations

Life Sciences, Genetics, Neurology +15

<i>TARDBP</i> mutations in motoneuron disease with frontotemporal lobar degeneration

Lina Benajiba, Isabelle Le Ber, Agnès Camuzat et al. · Annals of Neurology · 2009 · 302 citations

Life Sciences, Neurology, Neuroscience +17

Mutation of the <i>PDGFRB</i> gene as a cause of idiopathic basal ganglia calcification

Gaël Nicolas, Cyril Pottier, David Maltête et al. · Neurology · 2012 · 277 citations

Life Sciences, Genetics, Molecular Genetics +17

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome

Grégory Raux, Emilie Bumsel, B. Hecketsweiler et al. · Human Molecular Genetics · 2006 · 171 citations

Life Sciences, Genetics, Molecular Genetics +15