Réda Ouazzani

Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1).

Maria D. Lalioti, Maria Mirotsou, Catherine Burési et al. · PubMed · 1997 · 148 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Sleep quality and mental health in the context of COVID-19 pandemic and lockdown in Morocco

Abdelkrim Janati Idrissi, Abdelaziz Lamkaddem, Abdelilah Benouajjit et al. · Sleep Medicine · 2020 · 137 citations · Full text

Medicine, Health Sciences, Psychiatry +14

Loss of Function of GALNT2 Lowers High-Density Lipoproteins in Humans, Nonhuman Primates, and Rodents

Sumeet A. Khetarpal, Katrine T. Schjoldager, Christina Christoffersen et al. · Cell Metabolism · 2016 · 128 citations · Full text

Life Sciences, Biochemistry, Physiology +13

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Ziv Gan‐Or, Naïma Bouslam, Nazha Birouk et al. · The American Journal of Human Genetics · 2016 · 114 citations · Full text

Life Sciences, Genetics, Neurology +8

Role of the phosphoinositide phosphatase <i>FIG4</i> gene in familial epilepsy with polymicrogyria

Stéphanie Baulac, Guy M. Lenk, Béatrice Dufresnois et al. · Neurology · 2014 · 108 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17