| Associations between microRNA (miR-25, miR-32, miR-125, and miR-222) polymorphisms and recurrent implantation failure in Korean women |
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✓ |
Korean women |
| Downregulation of miR-542-3p promotes osteogenic transition of vascular smooth muscle cells in the aging rat by targeting BMP7 |
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| Human genetics and genomics research in Ecuador: historical survey, current state, and future directions |
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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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| The multi-faceted functioning portrait of LRF/ZBTB7A |
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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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| EFTUD2 gene deficiency disrupts osteoblast maturation and inhibits chondrocyte differentiation via activation of the p53 signaling pathway |
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✓ |
Chinese |
| 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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| Transcriptomic analysis of monocytes from HIV-positive men on antiretroviral therapy reveals effects of tobacco smoking on interferon and stress response systems associated with depressive symptoms |
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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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| Copy number of 8q24.3 drives HSF1 expression and patient outcome in cancer: an individual patient data meta-analysis |
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| Identification of key candidate genes and molecular pathways in white fat browning: an anti-obesity drug discovery based on computational biology |
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| Size matters: how sample size affects the reproducibility and specificity of gene set analysis |
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| Using Apache Spark on genome assembly for scalable overlap-graph reduction |
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| A semi-supervised machine learning framework for microRNA classification |
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| HMNPPID—human malignant neoplasm protein–protein interaction database |
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| Prediction of microbial communities for urban metagenomics using neural network approach |
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| An embedded method for gene identification problems involving unwanted data heterogeneity |
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| Robust hypergraph regularized non-negative matrix factorization for sample clustering and feature selection in multi-view gene expression data |
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| Human mitochondrial genome compression using machine learning techniques |
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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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| Genomics of rare genetic diseases—experiences from India |
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| SLC39A8 gene encoding a metal ion transporter: discovery and bench to bedside |
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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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| Three miRNAs cooperate with host genes involved in human cardiovascular disease |
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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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| Identification of a novel long non-coding RNA within RUNX1 intron 5 |
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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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| Correction to: Evidence that DNA repair genes, a family of tumor suppressor genes, are associated with evolution rate and size of genomes |
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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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| Interplay Between the Host, the Human Microbiome, and Drug Metabolism |
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| Evidence that DNA repair genes, a family of tumor suppressor genes, are associated with evolution rate and size of genomes |
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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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| Genetics of heart rate in heart failure patients (GenHRate) |
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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 |
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| Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 8141 single pregnancies |
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| vi-HMM: a novel HMM-based method for sequence variant identification in short-read data |
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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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✓ |
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Puerto Rican Latinos |
| 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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| Considerations for the use of Cre recombinase for conditional gene deletion in the mouse lens |
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| Toward a clinical diagnostic pipeline for SPINK1 intronic variants |
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| The evolutionary genetics of lactase persistence in seven ethnic groups across the Iranian plateau |
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| A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts |
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| The association of functional polymorphisms in genes expressed in endothelial cells and smooth muscle cells with the myocardial infarction |
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| Population and breast cancer patients’ analysis reveals the diversity of genomic variation of the BRCA genes in the Mexican population |
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| Germline TP53 and MSH6 mutations implicated in sporadic triple-negative breast cancer (TNBC): a preliminary study |
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| The X chromosome and sex-specific effects in infectious disease susceptibility |
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| Preimplantation genetic diagnosis and screening (PGD/S) using a semiconductor sequencing platform |
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