Alfredo Ramı́rez

Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease

Valentina Escott‐Price, Céline Bellenguez, Li‐San Wang et al. · PLoS ONE · 2014 · 1.4K citations · Full text

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

Alfredo Ramı́rez, André Heimbach, Jan Gründemann et al. · Nature Genetics · 2006 · 1.2K citations

Alzheimer's Disease, P-type Atpase, Hereditary Parkinsonism +10

TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis

Gernot Kleinberger, Yoshinori Yamanishi, Marc Suárez‐Calvet et al. · Science Translational Medicine · 2014 · 805 citations

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

Hanno J. Bolz, Benigna von Brederlow, Alfredo Ramı́rez et al. · Nature Genetics · 2001 · 493 citations

Genetic Disorder, Genetics, Pathogenesis +6

G protein–coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

Sandra M. Pasternack, Ivar von Kügelgen, Khalid Al Aboud et al. · Nature Genetics · 2008 · 406 citations

Molecular Pharmacology, Protein Function, Signal Transduction +12