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Genome instability and crosstalk with the immune response
Genome instability, tumour-promoting inflammation, and immune escape are three distinct hallmarks of cancer. However, accu...
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Single-cell multi-omics analysis revealed the expansion of age-associated B cells in the pancreas of type 1 autoimmune pancreatitis patients
Type 1 autoimmune pancreatitis (AIP) is pancreatic manifestation of IgG4-related disease (IgG4-RD), characterized by pancr...
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Mendelian randomization analyses suggest a causal role for circulating GIP and IL-1RA levels in homeostatic model assessment-derived measures of β-cell function and insulin sensitivity in Africans without type 2 diabetes
In vitro and in vivo studies have shown that certain cytokines and hormones may play a role in the development and progres...
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Evaluating the association of biallelic OGDHL variants with significant phenotypic heterogeneity
Biallelic variants in OGDHL, encoding part of the α-ketoglutarate dehydrogenase complex, have been associated with hi...
Genome Medicine
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Genome-wide prediction of pathogenic gain- and loss-of-function variants from ensemble learning of a diverse feature set
Gain-of-function (GOF) variants give rise to increased/novel protein functions whereas loss-of-function (LOF) variants lea...
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Mobilizable plasmids drive the spread of antimicrobial resistance genes and virulence genes in Klebsiella pneumoniae
Klebsiella pneumoniae is a notorious clinical pathogen and frequently carries various plasmids, which are the main carrier...
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Personalized tumor combination therapy optimization using the single-cell transcriptome
The precise characterization of individual tumors and immune microenvironments using transcriptome sequencing has provided...
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A phenome-wide scan reveals convergence of common and rare variant associations
Common and rare variants contribute to the etiology of complex traits. However, the extent to which the phenotypic effects...
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GITR and TIGIT immunotherapy provokes divergent multicellular responses in the tumor microenvironment of gastrointestinal cancers
Understanding the mechanistic effects of novel immunotherapy agents is critical to improving their successful clinical tra...
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Massive underrepresentation of Arabs in genomic studies of common disease
Arabs represent 5% of the world population and have a high prevalence of common disease, yet remain greatly underrepresent...
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Loss of p53-DREAM-mediated repression of cell cycle genes as a driver of lymph node metastasis in head and neck cancer
The prognosis for patients with head and neck cancer (HNC) is poor and has improved little in recent decades, partially du...
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The role of admixture in the rare variant contribution to inflammatory bowel disease
Identification of rare variants involved in complex, polygenic diseases like Crohn’s disease (CD) has accelerated wi...
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Building blocks for better biorepositories in Africa
Biorepositories archive and distribute well-characterized biospecimens for research to support the development of medical ...
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Early detection of hepatocellular carcinoma via no end-repair enzymatic methylation sequencing of cell-free DNA and pre-trained neural network
Early detection of hepatocellular carcinoma (HCC) is important in order to improve patient prognosis and survival rate. Me...
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Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases
Whole genome sequencing is increasingly being used for the diagnosis of patients with rare diseases. However, the diagnost...
Genome Medicine
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Rapid profiling of Plasmodium parasites from genome sequences to assist malaria control
Malaria continues to be a major threat to global public health. Whole genome sequencing (WGS) of the underlying Plasmodium...
Genome Medicine
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Skeletal muscle regeneration failure in ischemic-damaged limbs is associated with pro-inflammatory macrophages and premature differentiation of satellite cells
Chronic limb-threatening ischemia (CLTI), a severe manifestation of peripheral arterial disease (PAD), is associated with ...
Genome Medicine
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Analysis of transcriptomic features reveals molecular endotypes of SLE with clinical implications
Systemic lupus erythematosus (SLE) is known to be clinically heterogeneous. Previous efforts to characterize subsets of SL...
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Single-cell RNA sequencing distinctly characterizes the wide heterogeneity in pediatric mixed phenotype acute leukemia
Mixed phenotype acute leukemia (MPAL), a rare subgroup of leukemia characterized by blast cells with myeloid and lymphoid ...
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Recommendations for the classification of germline variants in the exonuclease domain of POLE and POLD1
Germline variants affecting the proofreading activity of polymerases epsilon and delta cause a hereditary cancer and adeno...
Genome Medicine
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Cancer origin tracing and timing in two high-risk prostate cancers using multisample whole genome analysis: prospects for personalized medicine
Prostate cancer (PrCa) genomic heterogeneity causes resistance to therapies such as androgen deprivation. Such heterogenei...
Genome Medicine
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Small extrachromosomal circular DNA harboring targeted tumor suppressor gene mutations supports intratumor heterogeneity in mouse liver cancer induced by multiplexed CRISPR/Cas9
Primary liver cancer has significant intratumor genetic heterogeneity (IGH), which drives cancer evolution and prevents ef...
Genome Medicine
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Global analysis of suppressor mutations that rescue human genetic defects
Genetic suppression occurs when the deleterious effects of a primary “query” mutation, such as a disease-causi...
Genome Medicine
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Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study
Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by impaired social and communication skills...
Genome Medicine
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Meiotic and mitotic aneuploidies drive arrest of in vitro fertilized human preimplantation embryos
The high incidence of aneuploidy in early human development, arising either from errors in meiosis or postzygotic mitosis,...
Genome Medicine
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Integrated study of systemic and local airway transcriptomes in asthma reveals causal mediation of systemic effects by airway key drivers
Systemic and local profiles have each been associated with asthma, but parsing causal relationships between system-wide an...
Genome Medicine
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Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human
Dilated cardiomyopathy (DCM) is a life-threatening heart disease and a common cause of heart failure due to systolic dysfu...
Genome Medicine
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Long-read sequencing reveals the landscape of aberrant alternative splicing and novel therapeutic target in colorectal cancer
Alternative splicing complexity plays a vital role in carcinogenesis and cancer progression. Improved understanding of nov...
Genome Medicine
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Spatial transcriptomics analysis of neoadjuvant cabozantinib and nivolumab in advanced hepatocellular carcinoma identifies independent mechanisms of resistance and recurrence
Novel immunotherapy combination therapies have improved outcomes for patients with hepatocellular carcinoma (HCC), but res...
Genome Medicine
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Identification of novel protein biomarkers and drug targets for colorectal cancer by integrating human plasma proteome with genome
The proteome is a major source of therapeutic targets. We conducted a proteome-wide Mendelian randomization (MR) study to ...
Genome Medicine
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