Riadh Gouider

Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma

Hamid Azzedine, Alessandra Bolino, T. Taïeb et al. · The American Journal of Human Genetics · 2003 · 302 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Reducing the Risk of Cognitive Decline and Dementia: WHO Recommendations

Neerja Chowdhary, Corrado Barbui, Kaarin J. Anstey et al. · Frontiers in Neurology · 2022 · 201 citations · Full text

Medicine, Geriatric Medicine, Health Policy +17

Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion

Philippe Mouton, Sandrine Tardieu, Riadh Gouider et al. · Neurology · 1999 · 185 citations

Medicine, Neurology, Neuroscience +15

The evolving SARS-CoV-2 epidemic in Africa: Insights from rapidly expanding genomic surveillance

Houriiyah Tegally, James Emmanuel San, Matthew Cotten et al. · Science · 2022 · 179 citations · Full text

Life Sciences, Health Sciences, Infectious Diseases +14

X-linked Charcot-Marie-Tooth disease with connexin 32 mutations

Nazha Birouk, Éric Leguern, Thierry Maisonobe et al. · Neurology · 1998 · 170 citations

Life Sciences, Genetics, Neurology +16