Didier Hannequin

<i>SOD1</i>, <i>ANG</i>, <i>VAPB</i>, <i>TARDBP</i>, and <i>FUS</i> mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

Stéphanie Millecamps, François Salachas, C. Cazeneuve et al. · Journal of Medical Genetics · 2010 · 296 citations · Full text

Life Sciences, Genetics, Neurology +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

No association of apolipoprotein epsilon 4 allele with schizophrenia even in cognitively impaired patients

Florence Thibaut, Beatrice Coron, Didier Hannequin et al. · Schizophrenia Research · 1998 · 25 citations

Medicine, Genetics, Psychiatry +12

Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencing

Stéphanie David, Joana Ferreira, Olivier Quenez et al. · European Journal of Human Genetics · 2016 · 24 citations · Full text

Life Sciences, Molecular Genetics, Neuroscience +16

Angiographic cerebral vasospasm and delayed ischemic deficit on anterior part of the circle of Willis. Usefulness of transcranial Doppler.

F. Proust, Bertrand Debono, Emmanuel Gérardin et al. · PubMed · 2002 · 21 citations

Medicine, Neurology, Neuroscience +17