Associations between microRNA (miR-25, miR-32, miR-125, and miR-222) polymorphisms and recurrent implantation failure in Korean women
Authors (first, second and last of 9)
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Volume 13, issue 1, December 2019
60 articles in this issue
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Downregulation of miR-542-3p promotes osteogenic transition of vascular smooth muscle cells in the aging rat by targeting BMP7
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Investigating RNA expression profiles altered by nicotinamide mononucleotide therapy in a chronic model of alcoholic liver disease
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Human genetics and genomics research in Ecuador: historical survey, current state, and future directions
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EFTUD2 gene deficiency disrupts osteoblast maturation and inhibits chondrocyte differentiation via activation of the p53 signaling pathway
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Factors affecting cell-free DNA fetal fraction: statistical analysis of 13,661 maternal plasmas for non-invasive prenatal screening
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Genetics and functions of the retinoic acid pathway, with special emphasis on the eye
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Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 42,910 single pregnancies with different clinical features
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Association between polymorphism in CDKN2B-AS1 gene and its interaction with smoking on the risk of lung cancer in a Chinese population
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Common polymorphic inversions at 17q21.31 and 8p23.1 associate with cancer prognosis
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Genetic variants of VEGFR-1 gene promoter in acute myocardial infarction
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Identification and functional characterization of two novel mutations in KCNJ10 and PI4KB in SeSAME syndrome without electrolyte imbalance
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RETRACTED ARTICLE: lncRNA TUG1 modulates proliferation, apoptosis, invasion, and angiogenesis via targeting miR-29b in trophoblast cells
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Novel analytical methods to interpret large sequencing data from small sample sizes
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Translating pharmacogenomics into clinical decisions: do not let the perfect be the enemy of the good
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Diversity of ATM gene variants: a population-based genome data analysis for precision medicine
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Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes
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Identification and potential mechanisms of a 4-lncRNA signature that predicts prognosis in patients with laryngeal cancer
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Meeting report: the Human Genome Meeting (HGM) 2019 in Seoul, Korea
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Next-generation sequencing in liquid biopsy: cancer screening and early detection
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Helicobacter pylori infection, serum pepsinogens as markers of atrophic gastritis, and leukocyte telomere length: a population-based study
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Essential genetic findings in neurodevelopmental disorders
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A novel knowledge-derived data potentizing method revealed unique liver cancer-associated genetic variants
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Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study
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IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patients
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Statement on bioinformatics and capturing the benefits of genome sequencing for society
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What influences public views on forensic DNA testing in the criminal field? A scoping review of quantitative evidence
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Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans
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Studies of liver tissue identify functional gene regulatory elements associated to gene expression, type 2 diabetes, and other metabolic diseases
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Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion
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The significance of trisomy 7 mosaicism in noninvasive prenatal screening
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Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases
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Correction to: The evolutionary genetics of lactase persistence in seven ethnic groups across the Iranian plateau
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Transcriptome-wide analysis of differentially expressed chemokine receptors, SNPs, and SSRs in the age-related macular degeneration
Authors (first, second and last of 6)
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Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 8141 single pregnancies
Authors (first, second and last of 9)
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Association of HTRA1 and ARMS2 gene polymorphisms with response to intravitreal ranibizumab among neovascular age-related macular degenerative subjects
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Association of genetic ancestry with colorectal tumor location in Puerto Rican Latinos
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Update on the human and mouse lipocalin (LCN) gene family, including evidence the mouse Mup cluster is result of an “evolutionary bloom”
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