Original Research
Published on 03 Feb 2023
Gene expression signature of human neuropathic pain identified through transcriptome analysis
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2023.1127167
- 3,645 views
- 5 citations
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12,856 articles
Editorial
Published on 03 Feb 2023
Editorial: Machine learning for biological sequence analysis
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1150688
- 2,638 views
- 9 citations
Original Research
Published on 03 Feb 2023
Characterization of the microenvironment in different immune-metabolism subtypes of cervical cancer with prognostic significance
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1067666
- 4,666 views
- 6 citations
Perspective
Published on 03 Feb 2023
piRNA pathway evolution beyond gonad context: Perspectives from apicomplexa and trypanosomatids
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2023.1129194
- 3,421 views
- 2 citations
Original Research
Published on 03 Feb 2023
Rare copy number variation analysis identifies disease-related variants in atrioventricular septal defect patients
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1075349
- 4,406 views
- 3 citations
Original Research
Published on 03 Feb 2023
Strategies to improve healthcare services for patients with sickle cell disease in Nigeria: The perspectives of stakeholders
in ELSI in Science and Genetics
Frontiers in Genetics
doi 10.3389/fgene.2023.1052444
- 9,195 views
- 4 citations
Original Research
Published on 03 Feb 2023
Identification and verification of m7G-Related genes as biomarkers for prognosis of sarcoma
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1101683
- 4,432 views
- 7 citations
Original Research
Published on 03 Feb 2023
Smoking, alcohol consumption, and frailty: A Mendelian randomization study
in Behavioral and Psychiatric Genetics
Frontiers in Genetics
doi 10.3389/fgene.2023.1092410
- 11,687 views
- 20 citations
Original Research
Published on 03 Feb 2023
Identification of a basement membrane-based risk scoring system for prognosis prediction and individualized therapy in clear cell renal cell carcinoma
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1038924
- 2,362 views
Original Research
Published on 02 Feb 2023
Instrumental variable-based high-dimensional mediation analysis with unmeasured confounders for survival data in the observational epigenetic study
in Statistical Genetics and Methodology
Frontiers in Genetics
doi 10.3389/fgene.2023.1092489
- 3,769 views
- 7 citations
Original Research
Published on 02 Feb 2023
Genomic epidemiology of Mycobacterium avium subsp. paratuberculosis isolates from Canadian dairy herds provides evidence for multiple infection events
in Livestock Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1043598
- 6,339 views
- 12 citations
Case Report
Published on 02 Feb 2023
Identification of two near-identical novel HIV-1 unique recombinant forms (CRF01_AE/B) among men who have sex with men in baoding, hebei, China
in Evolutionary and Genomic Microbiology
Frontiers in Genetics
doi 10.3389/fgene.2023.1105739
- 1,862 views
- 3 citations
Original Research
Published on 02 Feb 2023
Prognosis and personalized medicine prediction by integrated whole exome and transcriptome sequencing of hepatocellular carcinoma
in Cancer Genetics and Oncogenomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1075347
- 2,727 views
Original Research
Published on 02 Feb 2023
Differential expression profiling of tRNA-Derived small RNAs and their potential roles in methamphetamine self-administered rats
in RNA
Frontiers in Genetics
doi 10.3389/fgene.2023.1088498
- 3,007 views
- 4 citations
Case Report
Published on 02 Feb 2023
Case Report: A novel mutation in WFS1 gene (c.1756G>A p.A586T) is responsible for early clinical features of cognitive impairment and recurrent ischemic stroke
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1072978
- 3,636 views
- 3 citations
Original Research
Published on 02 Feb 2023
Diversity of clinical phenotypes in a cohort of Han Chinese patients with PAX6 variants
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2023.1011060
- 2,605 views
- 1 citation