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UnknownDesign and evaluation of bi-functional iron chelators for protection of dopaminergic neurons from toxicants.
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S-EPMC7415766 | biostudies-literature
UnknownRefining a Multifaceted Model of Perceived Utility of Genomic Sequencing Results.
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S-EPMC10614499 | biostudies-literature
UnknownReturning integrated genomic risk and clinical recommendations: The eMERGE study.
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UnknownGenetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson's disease.
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S-EPMC8474559 | biostudies-literature
UnknownIdentification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.
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S-EPMC8422160 | biostudies-literature
UnknownThe clinical and cost-effectiveness of total versus partial knee replacement in patients with medial compartment osteoarthritis (TOPKAT): 5-year outcomes of a randomised controlled trial.
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S-EPMC6727069 | biostudies-literature
UnknownAssessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study.
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S-EPMC6113773 | biostudies-literature
UnknownAssociation of Whole-Genome and NETRIN1 Signaling Pathway-Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank.
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S-EPMC6374980 | biostudies-literature
UnknownThe Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study.
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S-EPMC8482304 | biostudies-literature
UnknownIdentification of common genetic risk variants for autism spectrum disorder.
Not available
S-EPMC6454898 | biostudies-literature
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