Bruno Moulard
Publications by Year
Research Areas
Epilepsy research and treatment, Ion channel regulation and function, Amyotrophic Lateral Sclerosis Research, Neuroscience and Neuropharmacology Research, Metabolism and Genetic Disorders
Most-Cited Works
- → Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2(2000)985 cited
- → Identification of a New Locus for Generalized Epilepsy with Febrile Seizures Plus (GEFS+) on Chromosome 2q24-q33(1999)136 cited
- → Apolipoprotein E genotyping in sporadic amyotrophic lateral sclerosis: evidence for a major influence on the clinical presentation and prognosis(1996)90 cited
- → Genetics of familial ALS and consequences for diagnosis(1999)88 cited
- → Association between centromeric deletions of the SMN gene and sporadic adult‐onset lower motor neuron disease(1998)78 cited
- → Ion channel variation causes epilepsies(2001)78 cited
- → Identification of Six Novel SOD1 Gene Mutations in Familial Amyotrophic Lateral Sclerosis(1998)68 cited
- → A nonsense mutation in the α4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI)(1994)45 cited
- → Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country(2000)34 cited
- → Polymorphism analysis of JRK/JH8, the human homologue of mouse jerky, and description of a rare mutation in a case of CAE evolving to JME(2001)34 cited