Works matching IS 14739542 AND DT 2021 AND VI 15
Results: 77
A regulatory miRNA–mRNA network is associated with transplantation response in acute kidney injury.
- Published in:
- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00363-y
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- Publication type:
- Article
Correction to: Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility.
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- 2021
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- Publication type:
- Correction Notice
Detection of low-level parental somatic mosaicism for clinically relevant SNVs and indels identified in a large exome sequencing dataset.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00369-6
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- Article
A robust and stable gene selection algorithm based on graph theory and machine learning.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00366-9
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- Article
Estimating prevalence of human traits among populations from polygenic risk scores.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00370-z
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- Article
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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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00362-z
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- Article
Identification of a novel signature based on unfolded protein response-related gene for predicting prognosis in bladder cancer.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00372-x
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- Publication type:
- Article
RNA-seq driven expression and enrichment analysis to investigate CVD genes with associated phenotypes among high-risk heart failure patients.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00367-8
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- Publication type:
- Article
Driving mosaicism: somatic variants in reference population databases and effect on variant interpretation in rare genetic disease.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00371-y
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- Publication type:
- Article
Breast cancer in West Africa: molecular analysis of BRCA genes in early-onset breast cancer patients in Burkina Faso.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00365-w
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- Article
Genetic polymorphisms of Vascular Endothelial Growth Factor (VEGF) associated with endometriosis in Nigerian women.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00364-x
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- Publication type:
- Article
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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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00368-7
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- Article
Development of the pharmacogenomics and genomics literacy framework for pharmacists.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00361-0
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- Publication type:
- Article
Seven novel glucose-6-phosphate dehydrogenase (G6PD) deficiency variants identified in the Qatari population.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00358-9
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- Publication type:
- Article
Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00359-8
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- Publication type:
- Article
Correction to: Update on human genetic susceptibility to COVID-19: susceptibility to virus and response.
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- 2021
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- Correction Notice
Update on human genetic susceptibility to COVID-19: susceptibility to virus and response.
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- 2021
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- Publication type:
- Editorial
Evaluation of low-pass genome sequencing in polygenic risk score calculation for Parkinson's disease.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00357-w
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- Article
Update on human genetic susceptibility to COVID-19: susceptibility to virus and response.
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- 2021
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- Publication type:
- Editorial
Correction to: The evolutionary genetics of lactase persistence in seven ethnic groups across the Iranian plateau.
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- 2021
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- Publication type:
- Correction Notice
Abnormal expression profile of plasma-derived exosomal microRNAs in patients with treatment-resistant depression.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00354-z
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- Article
Perception of personalized medicine, pharmacogenomics, and genetic testing among undergraduates in Hong Kong.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00353-0
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- Article
Identification of subgroups along the glycolysis-cholesterol synthesis axis and the development of an associated prognostic risk model.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00350-3
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- Article
Established and candidate transthyretin amyloidosis variants identified in the Saudi population by data mining.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00351-2
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- Article
A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00352-1
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- Article
Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00342-3
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- Article
LncRNA-TUG1 promotes the progression of infantile hemangioma by regulating miR-137/IGFBP5 axis.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00349-w
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- Article
A comprehensive analysis of copy number variation in a Turkish dementia cohort.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00346-z
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- Article
Altered splicing associated with the pathology of inflammatory bowel disease.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00347-y
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- Article
Implementation and implications for polygenic risk scores in healthcare.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00339-y
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- Publication type:
- Article
ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variants.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00345-0
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- Article
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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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00348-x
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- Publication type:
- Article
High-throughput screening of circRNAs reveals novel mechanisms of tuberous sclerosis complex-related renal angiomyolipoma.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00344-1
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- Article
TMEM263: a novel candidate gene implicated in human autosomal recessive severe lethal skeletal dysplasia.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00343-2
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- Article
Performances of NIPT for copy number variations at different sequencing depths using the semiconductor sequencing platform.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00332-5
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- Article
Single-cell chromatin accessibility landscape of human umbilical cord blood in trisomy 18 syndrome.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00338-z
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- Article
Identification of hub genes associated with prognosis, diagnosis, immune infiltration and therapeutic drug in liver cancer by integrated analysis.
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- Human Genomics, 2021, v. 15, p. 1, doi. 10.1186/s40246-021-00341-4
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- Article
Predicting anticancer hyperfoods with graph convolutional networks.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00333-4
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- Article
HCP5, as the sponge of miR-1291, facilitates AML cell proliferation and restrains apoptosis via increasing PIK3R5 expression.
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- Human Genomics, 2021, v. 15, p. 1, doi. 10.1186/s40246-021-00340-5
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- Publication type:
- Article
Regulatory VCAN polymorphism is associated with shoulder pain and disability in breast cancer survivors.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00337-0
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- Publication type:
- Article
Correction to: Self-reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparities.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00322-7
- Publication type:
- Article
Correction to: Self-reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparities.
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- 2021
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- Publication type:
- Correction Notice
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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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00335-2
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- Publication type:
- Article
Advancing clinical genomics and precision medicine with GVViZ: FAIR bioinformatics platform for variable gene-disease annotation, visualization, and expression analysis.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00336-1
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- Publication type:
- Article
Genome-based therapeutic interventions for β-type hemoglobinopathies.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00329-0
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- Article
Correction to: An application of slow feature analysis to the genetic sequences of coronaviruses and influenza viruses.
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- 2021
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- Publication type:
- Correction Notice
Epigenetics and microRNAs in UGT1As.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00331-6
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- Publication type:
- Article
Initial study on TMPRSS2 p.Val160Met genetic variant in COVID-19 patients.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00330-7
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- Publication type:
- Article
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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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00328-1
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- Publication type:
- Article
Identification of differentially expressed genes and signaling pathways in human conjunctiva and reproductive tract infected with Chlamydia trachomatis.
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- Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00313-8
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- Publication type:
- Article