Serge Jaumà

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

Sandy Hsu, Renee Sears, Roberta R. Lemos et al. · Neurogenetics · 2013 · 145 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +8

Frontal and associative visual areas related to visual hallucinations in dementia with Lewy bodies and Parkinson's disease with dementia

Cristina Sánchez‐Castañeda, Ramón Reñé, Blanca Ramı́rez-Ruiz et al. · Movement Disorders · 2010 · 130 citations

Neuropsychology, Brain Function, Corticobasal Degeneration +18

Sleep Disorders in Parkinsonian and Nonparkinsonian LRRK2 Mutation Carriers

Claustre Pont‐Sunyer, Álex Iranzo, Carles Gaig et al. · PLoS ONE · 2015 · 90 citations · Full text

Correlations between gray matter reductions and cognitive deficits in dementia with Lewy Bodies and Parkinson's disease with dementia

Cristina Sánchez‐Castañeda, Ramón Reñé, Blanca Ramı́rez-Ruiz et al. · Movement Disorders · 2009 · 74 citations

Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson’s disease study

Ana Westenberger, Volha Skrahina, Tatiana Usnich et al. · Brain · 2024 · 73 citations · Full text

Genetic Testing, Genetics, Genetic Epidemiology +19