- Characterization of additive gene–environment interactions for colorectal cancer risk
- Investigating Undiagnosed Fabry Disease in Young Adults with Ischemic Stroke: A Multicenter Cohort Study
- Comparison of Nucleotide MALDI-TOF MS with Xpert MTB/RIF for Rifampicin Susceptibility Identification and Associated Risk Factors of Rifampicin Resistance Among Drug Resistant Mycobacterium tuberculosis
- Association of PPARGC1A gene polymorphism and mtDNA methylation with coal-burning fluorosis: a case–control study
- DPYD Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, American College of Medical Genetics and Genomics, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, Pharmacogenomics Knowledgebase, and Pharmacogene Variation Consortium
- Genotype-phenotype correlation and founder effect analysis in southeast Chinese patients with sialidosis type I
- Blood-based HYAL2 methylation as a potential marker for the preclinical detection of coronary heart disease and stroke
- Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns
- Genetic influences on non-syndromic cleft lip palate: The impact of BMP4, RUNX2, PAX7, and TGFB3 allelic variations
- Association between genetic polymorphisms in chromosome region 9q21 and pelvic organ prolapse in Northwestern Chinese women
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