Adriana Ochoa

Mutations in EFHC1 cause juvenile myoclonic epilepsy

Toshimitsu Suzuki, Antonio V. Delgado‐Escueta, Kripamoy Aguan et al. · Nature Genetics · 2004 · 373 citations

Medicine, Genetics, Molecular Genetics +12

Hyperglycosylation and Reduced GABA Currents of Mutated GABRB3 Polypeptide in Remitting Childhood Absence Epilepsy

Miyabi Tanaka, Richard W. Olsen, Marco T. Medina et al. · The American Journal of Human Genetics · 2008 · 193 citations · Full text

Medicine, Neurology, Neuroscience +16

Assessment of the nutrition status of patients with Huntington's disease

Araceli Trejo, Rosa Marı́a Tarrats, Ma. Elisa Alonso et al. · Nutrition · 2004 · 157 citations

Agriculture, Nutrition, Nutritional Sciences +10

Clinical and genetic analysis of 4 Mexican families with spinocerebellar ataxia type 10

Astrid Rasmussen, Tohru Matsuura, Luís Ruano et al. · Annals of Neurology · 2001 · 143 citations

Life Sciences, Genetics, Neurology +17

Huntington Disease in Children: Genotype-Phenotype Correlation

Astrid Rasmussen, Rosario Márquez Macías, Petra Yescas et al. · Neuropediatrics · 2000 · 88 citations

Life Sciences, Genetics, Molecular Genetics +17