Genetic and Genomic Medicine
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Statistical examination of shared loci in neuropsychiatric diseases using genome-wide association study summary statistics
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Maternal smoking DNA methylation risk score associated with health outcomes in offspring of European and South Asian ancestry
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Genotype-specific differences in infertile men due to loss-of-function variants inM1APorZZSgenes
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Genomic landscape of endometrial, ovarian and cervical cancers in Japan from database in the Center for Cancer Genomics and Advanced Therapeutics
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Ethnic and region-specific genetic risk variants of stroke and its comorbid conditions may better define the variations in the burden of stroke and its phenotypic traits
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Risk factors affecting polygenic score performance across diverse cohorts
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Heterozygous variants inPLCG1affect hearing, vision, cardiac, and immune function
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Discovery of runs-of-homozygosity diplotype clusters and their associations with diseases in UK Biobank
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Explaining the counter-intuitive effectiveness of trophectoderm biopsy for PGT-A using computational modelling
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Allelic strengths of encephalopathy-associatedUBA5variants correlate betweenin vivoandin vitroassays
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