PINK1-linked parkinsonism is associated with Lewy body pathology

Lluı́s Samaranch, Oswaldo Lorenzo‐Betancor, José Matías Arbelo, +8

Brain

Automated <scp>N</scp>euromelanin <scp>I</scp>maging as a <scp>D</scp>iagnostic <scp>B</scp>iomarker for <scp>P</scp>arkinson's <scp>D</scp>isease

Gabriel Castellanos, María A. Fernández‐Seara, Oswaldo Lorenzo‐Betancor, +10

Movement Disorders

TREM2 is associated with the risk of Alzheimer's disease in Spanish population

Bruno A. Benítez, Breanna Cooper, Pau Pástor, +4

Neurobiology of Aging

Neurodegenerative DiseasesAlzheimer's DiseaseSpanish PopulationDementiaVascular Dementia +7

Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia

Oriol Dols‐Icardo, María J. Bullido, Pau Pástor, +25

Neurobiology of Aging

Alzheimer's DiseaseDementiaPathologyRisk FactorVascular Dementia +8

Heterozygous <i>STUB1</i> mutation causes familial ataxia with cognitive affective syndrome (SCA48)

Sara Ortega‐Cubero, Héctor San Nicolás, Jordi Corral, +16

Neurology

Genetic variation in APOE cluster region and Alzheimer's disease risk

Sebastián Cervantes, Lluı́s Samaranch, José Vidal, +14

Neurobiology of Aging

Alzheimer's DiseaseMedicineDementiaGeneticsGenetic Epidemiology +9

Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes

Mathias Thelen, Cristina Razquín, Isabel Hernández, +44

Neurobiology of Aging

Alzheimer's DiseaseCorticobasal DegenerationGeneticsDementiaDegenerative Disease +9

Frontobasal gray matter loss is associated with the TREM2 p.R47H variant

Elkin O. Luís, Sara Ortega‐Cubero, Isabel Lamet, +7

Neurobiology of Aging

PhysicsDark MatterRadiologyTrem2 P.r47h Variant

Cortical Atrophy and Language Network Reorganization Associated with a Novel Progranulin Mutation

Carlos Cruchaga, María A. Fernández‐Seara, Manuel Seijo‐Martínez, +10

Cerebral Cortex

NeuropsychologyFamily MembersGeneticsNeurolinguisticsProgressive Nonfluent Aphasia +20

No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population

Laura Fachal, Ana Mosquera‐Miguel, Pau Pástor, +10

American Journal of Medical Genetics Part B Neuropsychiatric Genetics

Systemic DiseasesGeneticsMtdna VariationGenetic EpidemiologyNeurochemical Biomarkers +19