文章名稱引用次數(shù)

• Integrating rare genetic variants into pharmacogenetic drug response predictions30
• Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 910 single pregnancies with different clinical features13
• Update on the human and mouse lipocalin (LCN) gene family, including evidence the mouse Mup cluster is result of an evolutionary bloom9
• Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 8141 single pregnancies9
• Beyond genomics: understanding exposotypes through metabolomics7
• Better governance, better access: practising responsible data sharing in the METADAC governance infrastructure6
• Including all voices in international data-sharing governance6
• Transcriptome-wide analysis of differentially expressed chemokine receptors, SNPs, and SSRs in the age-related macular degeneration5
• Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi community5
• What influences public views on forensic DNA testing in the criminal field? A scoping review of quantitative evidence5