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| Open AccessAffective response to physical activity as a deep phenotype in a non-randomized pilot study
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| Open AccessGene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes
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| Open AccessControlling for background genetic effects using polygenic scores improves the power of genome-wide association studies
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| Open AccessA comprehensive meta-analysis and a case–control study give insights into genetic susceptibility of lung cancer and subgroups
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| Open AccessThe effect of diabetes and the common diabetogenic TBC1D4 p.Arg684Ter variant on cardiovascular risk in Inuit in Greenland
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| Open AccessA large deletion on CFA28 omitting ACSL5 gene is associated with intestinal lipid malabsorption in the Australian Kelpie dog breed
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| Open AccessThe effects of common variants in MDM2 and GNRH2 genes on the risk and survival of osteosarcoma in Han populations from Northwest China
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| Open AccessCommon BACE2 Polymorphisms are Associated with Altered Risk for Alzheimer’s Disease and CSF Amyloid Biomarkers in APOE ε4 Non-Carriers
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| Open AccessNovel, rare and common pathogenic variants in the CFTR gene screened by high-throughput sequencing technology and predicted by in silico tools
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| Open AccessAssociations between SLC16A11 variants and diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)
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