Review
Published on 18 Nov 2022
Paternal epigenetic influences on placental health and their impacts on offspring development and disease
Frontiers in Genetics
doi 10.3389/fgene.2022.1068408
- 49,134 views
- 38 citations
3,801 Publications
volumes
Original Research
Published on 18 Nov 2022
Abnormal expression of TSG-6 disturbs extracellular matrix homeostasis in chondrocytes from endemic osteoarthritis
Frontiers in Genetics
doi 10.3389/fgene.2022.1064565
- 5,605 views
- 16 citations
Original Research
Published on 18 Nov 2022
Challenges of genetic diagnosis of inborn errors of metabolism in a major tertiary care center in Lebanon
Frontiers in Genetics
doi 10.3389/fgene.2022.1029947
- 6,839 views
- 7 citations
Original Research
Published on 18 Nov 2022
Bioinformatics-based study reveals that AP2M1 is regulated by the circRNA-miRNA-mRNA interaction network and affects Alzheimer’s disease
Frontiers in Genetics
doi 10.3389/fgene.2022.1049786
- 6,737 views
- 29 citations
Review
Published on 18 Nov 2022
Multilevel view on chromatin architecture alterations in cancer
Frontiers in Genetics
doi 10.3389/fgene.2022.1059617
- 6,307 views
- 21 citations
Original Research
Published on 18 Nov 2022
Temporal transcriptome of tomato elucidates the signaling pathways of induced systemic resistance and systemic acquired resistance activated by Chaetomium globosum
Frontiers in Genetics
doi 10.3389/fgene.2022.1048578
- 4,596 views
- 5 citations
Original Research
Published on 18 Nov 2022
GOLM1 is related to the inflammatory/immune nature of uveal melanoma and acts as a promising indicator for prognosis and immunotherapy response
Frontiers in Genetics
doi 10.3389/fgene.2022.1051168
- 3,095 views
- 4 citations
![Case report: Mild phenotype of a patient with vascular Ehlers–Danlos syndrome and COL3A1 duplication mutation without alteration in the [Gly-X-Y] repeat sequence](https://www.frontiersin.org/files/myhome article library/1017446/1017446_Thumb_400.jpg)
Case Report
Published on 18 Nov 2022
Case report: Mild phenotype of a patient with vascular Ehlers–Danlos syndrome and COL3A1 duplication mutation without alteration in the [Gly-X-Y] repeat sequence
Frontiers in Genetics
doi 10.3389/fgene.2022.1017446
- 15,175 views
- 3 citations
Editorial
Published on 18 Nov 2022
Editorial: Computational tools in inferring cancer tissue-of-origin and molecular classification towards personalized cancer therapy, volume III
Frontiers in Genetics
doi 10.3389/fgene.2022.1078871
- 1,727 views
Original Research
Published on 18 Nov 2022
Immune mechanism of low bone mineral density caused by ankylosing spondylitis based on bioinformatics and machine learning
Frontiers in Genetics
doi 10.3389/fgene.2022.1054035
- 4,050 views
- 2 citations
Case Report
Published on 18 Nov 2022
Case report and a brief review: Analysis and challenges of prenatal imaging phenotypes and genotypes in Joubert syndrome
Frontiers in Genetics
doi 10.3389/fgene.2022.1038274
- 4,199 views
- 12 citations
Original Research
Published on 17 Nov 2022
miRNA–mRNA–protein dysregulated network in COPD in women
Frontiers in Genetics
doi 10.3389/fgene.2022.1010048
- 4,109 views
- 3 citations
Original Research
Published on 17 Nov 2022
Simultaneous detection of novel genes and SNPs by adaptive p-value combination
Frontiers in Genetics
doi 10.3389/fgene.2022.1009428
- 3,639 views
- 1 citation
Original Research
Published on 17 Nov 2022
Comprehensive analysis of cuproptosis-related lncRNAs to predict prognosis and immune infiltration characteristics in colorectal cancer
Frontiers in Genetics
doi 10.3389/fgene.2022.984743
- 4,556 views
- 9 citations
Original Research
Published on 17 Nov 2022
RNA interference analysis of potential functions of cyclin A in the reproductive development of male oriental river prawns (Macrobrachium nipponense)
Frontiers in Genetics
doi 10.3389/fgene.2022.1053826
- 2,669 views
- 10 citations
Original Research
Published on 17 Nov 2022
Identification of RNA N6-methyladenosine regulation in epilepsy: Significance of the cell death mode, glycometabolism, and drug reactivity
Frontiers in Genetics
doi 10.3389/fgene.2022.1042543
- 7,626 views
- 13 citations
Original Research
Published on 17 Nov 2022
Integration of small RNAs from plasma and cerebrospinal fluid for classification of multiple sclerosis
Frontiers in Genetics
doi 10.3389/fgene.2022.1042483
- 3,481 views
- 2 citations
Original Research
Published on 17 Nov 2022
Benefit sharing in genomic and biobanking research in Uganda: Perceptions of researchers and research ethics committee members
Frontiers in Genetics
doi 10.3389/fgene.2022.1037401
- 5,855 views
- 10 citations
Mini Review
Published on 17 Nov 2022
Understanding the genetics of peripartum depression: Research challenges, strategies, and opportunities
Frontiers in Genetics
doi 10.3389/fgene.2022.1022188
- 5,164 views
- 4 citations
Original Research
Published on 17 Nov 2022
Antimicrobial Peptides Prediction method based on sequence multidimensional feature embedding
Frontiers in Genetics
doi 10.3389/fgene.2022.1069558
- 5,273 views
- 8 citations
Original Research
Published on 17 Nov 2022
Construction of an immune-related ceRNA network to screen for potential diagnostic markers for autism spectrum disorder
Frontiers in Genetics
doi 10.3389/fgene.2022.1025813
- 3,869 views
- 8 citations
Review
Published on 17 Nov 2022
Fragile sites, chromosomal lesions, tandem repeats, and disease
Frontiers in Genetics
doi 10.3389/fgene.2022.985975
- 16,011 views
- 31 citations
Original Research
Published on 17 Nov 2022
Identification of four novel variants in the CDH23 gene from four affected families with hearing loss
Frontiers in Genetics
doi 10.3389/fgene.2022.1027396
- 3,493 views
- 8 citations
Original Research
Published on 17 Nov 2022
Genome-wide analysis of MADS-box gene family in kiwifruit (Actinidia chinensis var. chinensis) and their potential role in floral sex differentiation
Frontiers in Genetics
doi 10.3389/fgene.2022.1043178
- 4,936 views
- 13 citations