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Identification of genetic loci jointly influencing COVID-19 and coronary heart diseases.
- Published in:
- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00547-8
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- Article
Smoking-related dysregulation of plasma circulating microRNAs: the Rotterdam study.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00504-5
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- Article
What is the functional reach of wastewater surveillance for respiratory viruses, pathogenic viruses of concern, and bacterial antibiotic resistance genes of interest?
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00563-8
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- Article
SPP1 is associated with adverse prognosis and predicts immunotherapy efficacy in penile cancer.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00558-5
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- Publication type:
- Article
Mitochondrial DNA copy number variation across three generations: a possible biomarker for assessing perinatal outcomes.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00567-4
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- Article
Mitochondrial DNA copy number variation across three generations: a possible biomarker for assessing perinatal outcomes.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00567-4
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- Publication type:
- Article
LINE-1 global DNA methylation, iron homeostasis genes, sex and age in sudden sensorineural hearing loss (SSNHL).
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00562-9
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- Publication type:
- Article
Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00559-4
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- Publication type:
- Article
Mendelian randomization analysis reveals fresh fruit intake as a protective factor for urolithiasis.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00523-2
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- Article
Triangulating nutrigenomics, metabolomics and microbiomics toward personalized nutrition and healthy living.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00561-w
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- Publication type:
- Article
Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families.
- Published in:
- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00559-4
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- Publication type:
- Article
Whole mitogenome sequencing uncovers a relation between mitochondrial heteroplasmy and leprosy severity.
- Published in:
- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00555-8
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- Publication type:
- Article
Targeted sequencing of high-density SNPs provides an enhanced tool for forensic applications and genetic landscape exploration in Chinese Korean ethnic group.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00541-0
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- Publication type:
- Article
A case–control comparison of acute-phase peripheral blood gene expression in participants diagnosed with minor ischaemic stroke or stroke mimics.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00551-y
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- Publication type:
- Article
Dispersed DNA variants underlie hearing loss in South Florida's minority population.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00556-7
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- Article
Emerging trends in pharmacogenomics: from common variant associations toward comprehensive genomic profiling.
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- 2023
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- Publication type:
- Editorial
Phenome-wide association study on miRNA-related sequence variants: the UK Biobank.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00553-w
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- Publication type:
- Article
The hospital Israelita Albert Einstein standards for constitutional sequence variants classification: version 2023.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00549-6
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- Publication type:
- Article
Genetic evidence for the causal association between type 1 diabetes and the risk of polycystic ovary syndrome.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00550-z
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- Publication type:
- Article
The burden of rare variants in DPYS gene is a novel predictor of the risk of developing severe fluoropyrimidine-related toxicity.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00546-9
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- Publication type:
- Article
Multidimensional fragmentomic profiling of cell-free DNA released from patient-derived organoids.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00533-0
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- Publication type:
- Article
The attitude and behaviors of the different spheres of the community of the United Arab Emirates toward the clinical utility and bioethics of secondary genetic findings: a cross-sectional study.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00548-7
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- Publication type:
- Article
Comprehensive analysis of alternative splicing across multiple transcriptomic cohorts reveals prognostic signatures in prostate cancer.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00545-w
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- Publication type:
- Article
The complex impact of cancer-related missense mutations on the stability and on the biophysical and biochemical properties of MAPK1 and MAPK3 somatic variants.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00544-x
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- Publication type:
- Article
Transcriptome driven discovery of novel candidate genes for human neurological disorders in the telomer-to-telomer genome assembly era.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00543-y
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- Publication type:
- Article
FGFR1 variants contributed to families with tooth agenesis.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00539-8
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- Publication type:
- Article
Epigenomic signature of major congenital heart defects in newborns with Down syndrome.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00540-1
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- Article
Decoding cell-type contributions to the cfRNA transcriptomic landscape of liver cancer.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00537-w
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- Article
Revealing parental mosaicism: the hidden answer to the recurrence of apparent de novo variants.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00535-y
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- Publication type:
- Article
Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00538-9
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- Publication type:
- Article
The causal relationship between COVID-19 and seventeen common digestive diseases: a two-sample, multivariable Mendelian randomization study.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00536-x
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- Publication type:
- Article
ANXA1 is identified as a key gene associated with high risk and T cell infiltration in primary sclerosing cholangitis.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00534-z
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- Publication type:
- Article
Identification of molecular signatures and pathways involved in Rett syndrome using a multi-omics approach.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00532-1
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- Publication type:
- Article
Generation and characterization of a zebrafish knockout model of abcb4, a homolog of the human multidrug efflux transporter P-glycoprotein.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00530-3
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- Article
RUN(X) out of blood: emerging RUNX1 functions beyond hematopoiesis and links to Down syndrome.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00531-2
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- Article
Genetics in ophthalmology: molecular blueprints of retinoblastoma.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00529-w
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- Publication type:
- Article
A genome-wide cross-trait analysis identifies genomic correlation, pleiotropic loci, and causal relationship between sex hormone-binding globulin and rheumatoid arthritis.
- Published in:
- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00528-x
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- Publication type:
- Article
Correction: Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes.
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- 2023
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- Publication type:
- Correction Notice
The RNA m6A modification might participate in microglial activation during hypoxic–ischemic brain damage in neonatal mice.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00527-y
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- Publication type:
- Article
Developing neural network diagnostic models and potential drugs based on novel identified immune-related biomarkers for celiac disease.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00526-z
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- Publication type:
- Article
Next-generation sequencing analysis of the molecular spectrum of thalassemia in Southern Jiangxi, China.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00520-5
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- Publication type:
- Article
Determining the utility of diagnostic genomics: a conceptual framework.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00524-1
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- Publication type:
- Article
Correction: Landscape of germline pathogenic variants in patients with dual primary breast and lung cancer.
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- 2023
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- Publication type:
- Correction Notice
The application of long-read sequencing in clinical settings.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00522-3
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- Publication type:
- Article
Total RNA sequencing reveals gene expression and microbial alterations shared by oral pre-malignant lesions and cancer.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00519-y
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- Publication type:
- Article
Transcriptome and proteome analysis reveals the anti-cancer properties of Hypnea musciformis marine macroalga extract in liver and intestinal cancer cells.
- Published in:
- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00517-0
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- Publication type:
- Article
Mitochondrial genome study in blood of maternally inherited ALS cases.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00516-1
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- Publication type:
- Article
CVD-associated SNPs with regulatory potential reveal novel non-coding disease genes.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00513-4
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- Publication type:
- Article
COVID-19 annual update: a narrative review.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00515-2
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- Publication type:
- Article
Characterizing the polygenic architecture of complex traits in populations of East Asian and European descent.
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- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00514-3
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- Publication type:
- Article