| Alu retrotransposons and COVID-19 susceptibility and morbidity |
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| Network machine learning maps phytochemically rich “Hyperfoods” to fight COVID-19 |
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| Correction to: Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility |
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| Detection of low-level parental somatic mosaicism for clinically relevant SNVs and indels identified in a large exome sequencing dataset |
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| Identification of a novel signature based on unfolded protein response-related gene for predicting prognosis in bladder cancer |
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| Driving mosaicism: somatic variants in reference population databases and effect on variant interpretation in rare genetic disease |
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| Estimating prevalence of human traits among populations from polygenic risk scores |
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| A regulatory miRNA–mRNA network is associated with transplantation response in acute kidney injury |
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| Single-cell transcriptome identifies molecular subtype of autism spectrum disorder impacted by de novo loss-of-function variants regulating glial cells |
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| RNA-seq driven expression and enrichment analysis to investigate CVD genes with associated phenotypes among high-risk heart failure patients |
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| A robust and stable gene selection algorithm based on graph theory and machine learning |
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| Genetic polymorphisms of Vascular Endothelial Growth Factor (VEGF) associated with endometriosis in Nigerian women |
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| Breast cancer in West Africa: molecular analysis of BRCA genes in early-onset breast cancer patients in Burkina Faso |
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African ancestry; Burkinabe |
| Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene |
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| Development of the pharmacogenomics and genomics literacy framework for pharmacists |
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| Seven novel glucose-6-phosphate dehydrogenase (G6PD) deficiency variants identified in the Qatari population |
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| Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci |
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| Correction to: Update on human genetic susceptibility to COVID-19: susceptibility to virus and response |
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| Evaluation of low-pass genome sequencing in polygenic risk score calculation for Parkinson’s disease |
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| Update on human genetic susceptibility to COVID-19: susceptibility to virus and response |
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| Correction to: The evolutionary genetics of lactase persistence in seven ethnic groups across the Iranian plateau |
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| Abnormal expression profile of plasma-derived exosomal microRNAs in patients with treatment-resistant depression |
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| Perception of personalized medicine, pharmacogenomics, and genetic testing among undergraduates in Hong Kong |
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| Identification of subgroups along the glycolysis-cholesterol synthesis axis and the development of an associated prognostic risk model |
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| Established and candidate transthyretin amyloidosis variants identified in the Saudi population by data mining |
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| A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants |
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| LncRNA-TUG1 promotes the progression of infantile hemangioma by regulating miR-137/IGFBP5 axis |
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| The limits of clinical findings in similar phenotypes, from Carpenter to ATRX syndrome using a whole exome sequencing approach: a case review |
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| A comprehensive analysis of copy number variation in a Turkish dementia cohort |
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| Altered splicing associated with the pathology of inflammatory bowel disease |
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| Implementation and implications for polygenic risk scores in healthcare |
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| ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variants |
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| Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism |
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| High-throughput screening of circRNAs reveals novel mechanisms of tuberous sclerosis complex-related renal angiomyolipoma |
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| TMEM263: a novel candidate gene implicated in human autosomal recessive severe lethal skeletal dysplasia |
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| Performances of NIPT for copy number variations at different sequencing depths using the semiconductor sequencing platform |
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| Single-cell chromatin accessibility landscape of human umbilical cord blood in trisomy 18 syndrome |
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| HCP5, as the sponge of miR-1291, facilitates AML cell proliferation and restrains apoptosis via increasing PIK3R5 expression |
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| Identification of hub genes associated with prognosis, diagnosis, immune infiltration and therapeutic drug in liver cancer by integrated analysis |
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| Advancing clinical genomics and precision medicine with GVViZ: FAIR bioinformatics platform for variable gene-disease annotation, visualization, and expression analysis |
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| Regulatory VCAN polymorphism is associated with shoulder pain and disability in breast cancer survivors |
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| Correction to: Self-reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparities |
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| Genome-based therapeutic interventions for β-type hemoglobinopathies |
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| Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences |
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Finnish |
| Predicting anticancer hyperfoods with graph convolutional networks |
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| Correction to: An application of slow feature analysis to the genetic sequences of coronaviruses and influenza viruses |
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| Epigenetics and microRNAs in UGT1As |
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| Initial study on TMPRSS2 p.Val160Met genetic variant in COVID-19 patients |
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| Whole genome sequencing reveals a frameshift mutation and a large deletion in YY1AP1 in a girl with a panvascular artery disease |
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| COVID-19 one year into the pandemic: from genetics and genomics to therapy, vaccination, and policy |
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| An application of slow feature analysis to the genetic sequences of coronaviruses and influenza viruses |
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| The transcriptome profile of human trisomy 21 blood cells |
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| Cathelicidin antimicrobial peptide (CAMP) gene promoter methylation induces chondrocyte apoptosis |
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| An ensemble of the iCluster method to analyze longitudinal lncRNA expression data for psoriasis patients |
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| Identification of differentially expressed genes and signaling pathways in human conjunctiva and reproductive tract infected with Chlamydia trachomatis |
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| Targeted exome sequencing identifies mutational landscape in a cohort of 1500 Chinese patients with non-small cell lung carcinoma (NSCLC) |
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| How to design a national genomic project—a systematic review of active projects |
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| Genetic-variant hotspots and hotspot clusters in the human genome facilitating adaptation while increasing instability |
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| Exploration and validation of related hub gene expression during SARS-CoV-2 infection of human bronchial organoids |
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| Ethical issues in genomics research on neurodevelopmental disorders: a critical interpretive review |
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| Genetic and molecular biology of autism spectrum disorder among Middle East population: a review |
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Middle East population; Middle East countries |
| C-X-C motif chemokine 16, modulated by microRNA-545, aggravates myocardial damage and affects the inflammatory responses in myocardial infarction |
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| cfDNA deconvolution via NIPT of a pregnant woman after bone marrow transplant and donor egg IVF |
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| Standardized nomenclature and open science in Human Genomics |
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| The Human Genome Organisation (HUGO) and the 2020 COVID-19 pandemic |
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| Pathogenic convergence of CNVs in genes functionally associated to a severe neuromotor developmental delay syndrome |
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| Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data |
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white British ancestry; some ethnic groups |
| Convergent lines of evidence support BIN1 as a risk gene of Alzheimer’s disease |
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| High heterogeneity undermines generalization of differential expression results in RNA-Seq analysis |
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| Genetic risk factors for autoimmune hepatitis: implications for phenotypic heterogeneity and biomarkers for drug response |
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European AIH; Europeans; Latin Americans; Japanese |
| ACE2 Nascence, trafficking, and SARS-CoV-2 pathogenesis: the saga continues |
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| Screening of disease-related biomarkers related to neuropathic pain (NP) after spinal cord injury (SCI) |
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| Correction to: Hyperinsulinism associated with GLUD1 mutation: allosteric regulation and functional characterization of p.G446V glutamate dehydrogenase |
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| Comprehensive assessments of germline deletion structural variants reveal the association between prognostic MUC4 and CEP72 deletions and immune response gene expression in colorectal cancer patients |
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