Brain-Derived Neurotrophic Factor Gene Variants and Alzheimer Disease: An Association Study in an Alzheimer Disease Italian Population
Chiara Boiocchi(Fondazione Istituto Neurologico Nazionale Casimiro Mondino), Mariaclara Cuccia(University of Pavia), Elena Sinforiani(Fondazione Istituto Neurologico Nazionale Casimiro Mondino), Elisa Maggioli(University of Pavia), Giovanni Ricevuti, Michele Zorzetto(University of Pavia), Cristina Cereda(University of Milan)
Cited by 17
Related Papers
Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>
|American Journal of Medical Genetics Part A|2015|617
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
|Nature Genetics|2021|567
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study
|The Lancet Neurology|2013|441