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「"Nalls MA "[Author]」の検索結果

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Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke.

Large-scale pathway specific polygenic risk and transcriptomic community network analysis identifies novel functional pathways in Parkinson disease.

Sequential screening nominates the Parkinson's disease associated kinase LRRK2 as a regulator of Clathrin-mediated endocytosis.

Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose.

Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci.

Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study.

Comprehensive assessment of PINK1 variants in Parkinson's disease.

Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information.

Fine-mapping of SNCA in REM sleep behavior disorder and overt synucleinopathies.

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

Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis.

Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson's disease.

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

Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with Metabolic Syndrome.

Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.

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

Associations of autozygosity with a broad range of human phenotypes.

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.

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.

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