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新型ウイルス対応医師ら職場で“バイ菌”扱い 学会が抗議声明

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「"Gibbs JR "[Author]」の検索結果

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Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score.

Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.

Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.

The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.

The Parkinson's Disease Mendelian Randomization Research Portal.

Conversion of Sox2-dependent Merkel cell carcinoma to a differentiated neuron-like phenotype by T antigen inhibition.

Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts.

Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset.

Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms.

The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease.

A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease.

Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease.

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3.

Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes.

Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease.

Transcriptomic profiling of the human brain reveals that altered synaptic gene expression is associated with chronological aging.

Establishing the role of rare coding variants in known Parkinson's disease risk loci.

NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases.

Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases.

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