Original Research
Published on 09 Jan 2023
Identification of COL4A4 variants in Chinese patients with familial hematuria
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1064491
- 1,314 views
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1,597 articles
Articles
Case Report
Published on 09 Jan 2023
Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay—Does both possibly act to modulate a candidate gene region for the patient’s phenotype?
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1061539
- 1,222 views
Original Research
Published on 09 Jan 2023
A novel frameshift mutation in TRPV6 is associated with hereditary pancreatitis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1058057
- 1,784 views
Brief Research Report
Published on 09 Jan 2023
Clinical impact of exome sequencing in the setting of a general pediatric ward for hospitalized children with suspected genetic disorders
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1018062
- 1,916 views
Brief Research Report
Published on 09 Jan 2023
Novel candidate genes for cholesteatoma in chronic otitis media
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1033965
- 1,072 views
Original Research
Published on 06 Jan 2023
Identification of two rare NPRL3 variants in two Chinese families with familial focal epilepsy with variable foci 3: NGS analysis with literature review
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1054567
- 1,442 views
- 3 citations
Original Research
Published on 06 Jan 2023
Positive regulation of innate immune response by miRNA-let-7a-5p
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1025539
- 2,103 views
- 3 citations
Original Research
Published on 06 Jan 2023
Transcriptomic analysis of the upper lip and primary palate development in mice
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1039850
- 1,733 views
- 1 citation
Case Report
Published on 06 Jan 2023
Case report: LAMC3-associated cortical malformations: Case report of a novel stop-gain variant and literature review
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.990350
- 1,880 views
- 2 citations
Original Research
Published on 06 Jan 2023
A potential three-gene-based diagnostic signature for idiopathic pulmonary fibrosis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.985217
- 2,127 views
Original Research
Published on 06 Jan 2023
Diagnostic application of exome sequencing in Chinese children with suspected inherited kidney diseases
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.933636
- 883 views
- 2 citations
Original Research
Published on 04 Jan 2023
Identification of rare thalassemia variants using third-generation sequencing
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1076035
- 1,486 views
- 3 citations
Brief Research Report
Published on 04 Jan 2023
Differential methylation of microRNA encoding genes may contribute to high myopia
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1089784
- 2,927 views
- 1 citation
Original Research
Published on 04 Jan 2023
Identification of oxidative stress-related genes and potential mechanisms in atherosclerosis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.998954
- 2,199 views
- 1 citation
Review
Published on 04 Jan 2023
Clinical, genetic, and experimental research of hyperphenylalaninemia
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1051153
- 3,699 views
- 3 citations
Original Research
Published on 04 Jan 2023
An integrative analysis of an lncRNA–mRNA competing endogenous RNA network to identify functional lncRNAs in uterine leiomyomas with RNA sequencing
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1053845
- 872 views