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- 2023
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Mark
The genetic regulation of protein expression in cerebrospinal fluid
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- Contribution to journal › Article
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Manganese efflux transporter SLC30A10 missense polymorphism T95I associated with liver injury retains manganese efflux activity
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- Contribution to journal › Article
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Type 2 diabetes candidate genes, including PAX5, cause impaired insulin secretion in human pancreatic islets
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- Contribution to journal › Article
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Mark
Liver saturated fat content associates with hepatic DNA methylation in obese individuals
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- Contribution to journal › Article
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Mark
Associations of genetically determined lipid traits and lipid-modifying agents with the risk of diabetic retinopathy : A Mendelian randomization study
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- Contribution to journal › Article
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Mark
A novel scatterplot-based method to detect copy number variation (CNV)
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- Contribution to journal › Article
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HNF1B variant without hyperglycaemia as a cause of isolated profound hypomagnesaemia
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- Contribution to journal › Article
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Mosaic Loss of Chromosome Y Is Associated With Functional Outcome After Ischemic Stroke
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- Contribution to journal › Article
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Mark
Rare-variant collapsing and bioinformatic analyses for amyloidosis, dementia and Parkinson’s disease in the UK biobank reveal novel susceptibility loci
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- Contribution to journal › Letter
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Mark
Causality assessment of circulating Vitamin D level on venous thromboembolism : A Mendelian randomization study
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- Contribution to journal › Article