Neurodegenerative DiseasesGenetic LociGenetic Predisposition to DiseaseDisease SusceptibilityGenome-Wide Association StudyPolymorphism, Single NucleotideGenotypeAllelesCase-Control StudiesChromosome MappingLinkage DisequilibriumHaplotypesGene FrequencyNerve DegenerationQuantitative Trait LociGenetic LinkageAlzheimer DiseaseGenetic VariationBrainPolymorphism, GeneticAmyotrophic Lateral SclerosisNeuronsInterleukin-18 Receptor beta SubunitPhenotypeMutationGenome, HumanGenetic MarkersHuntington Diseasetau ProteinsParkinson DiseaseDisease Models, Animalalpha-SynucleinChromosomes, Human, Pair 6Genetic Association StudiesEuropean Continental Ancestry GroupNerve Tissue ProteinsPrionsMice, TransgenicMolecular Sequence DataTauopathiesRisk FactorsNeuroprotective AgentsPrion DiseasesCrohn DiseaseChromosomes, Human, Pair 2Chromosomes, Human, Pair 8Mice, Inbred C57BLChromosomes, Human, Pair 5Inclusion BodiesHeredodegenerative Disorders, Nervous SystemProteostasis DeficienciesChromosomes, Human, Pair 9Genotyping TechniquesMicrogliaMicrobial Sensitivity TestsModels, GeneticAsian Continental Ancestry GroupSynucleinsCell DeathOxidative StressAmyloid beta-PeptidesCells, CulturedSpinocerebellar AtaxiasPedigreeGene Expression RegulationFrontotemporal Lobar DegenerationMicrosatellite RepeatsBase SequenceAmino Acid SequenceAgingTrinucleotide Repeat ExpansionChromosomes, Human, Pair 12MitochondriaHLA-DQ AntigensSignal TransductionOligonucleotide Array Sequence AnalysisArthritis, RheumatoidImmunity, InnateFrontotemporal DementiaFriedreich AtaxiaRiskCrosses, GeneticModels, BiologicalNod2 Signaling Adaptor ProteinHLA-DRB1 ChainsEpistasis, GeneticAutophagyHLA-DQ beta-ChainsMice, KnockoutHLA-DR3 AntigenCohort StudiesHLA-DR AntigensGuamComplement C4aNeuronal Ceroid-LipofuscinosesAmyloidPolymerase Chain ReactionSequence Analysis, DNAPlant DiseasesMeta-Analysis as Topic