Methods
Published on 21 Nov 2022
A depth-first search algorithm for oligonucleotide design in gene assembly
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1023092
- 1,044 views
- 1 citation
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14,452 articles
Articles
Original Research
Published on 21 Nov 2022
Identification of a novel AIFM1 variant from a Chinese family with auditory neuropathy
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1064823
- 1,178 views
Mini Review
Published on 21 Nov 2022
Keeping the balance: Trade-offs between human brain evolution, autism, and schizophrenia
in Epigenomics and Epigenetics
Frontiers in Genetics
doi 10.3389/fgene.2022.1009390
- 2,559 views
Case Report
Published on 18 Nov 2022
Case Report: Precision genetic diagnosis in a case of Dyggve-Melchior-Clausen syndrome reveals paternal isodisomy and heterodisomy of chromosome 18 with imprinting clinical implications
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1005573
- 1,395 views
- 1 citation
Editorial
Published on 18 Nov 2022
Editorial: Cancer systems biology
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1083902
- 1,357 views
Original Research
Published on 18 Nov 2022
Identification of susceptibility modules and hub genes of osteoarthritis by WGCNA analysis
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1036156
- 4,805 views
- 3 citations
Review
Published on 18 Nov 2022
Paternal epigenetic influences on placental health and their impacts on offspring development and disease
in Toxicogenomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1068408
- 5,665 views
- 6 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
in Stem Cell Research
Frontiers in Genetics
doi 10.3389/fgene.2022.1049786
- 3,659 views
- 3 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
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.1029947
- 2,377 views
- 2 citations
Review
Published on 18 Nov 2022
Multilevel view on chromatin architecture alterations in cancer
in Epigenomics and Epigenetics
Frontiers in Genetics
doi 10.3389/fgene.2022.1059617
- 2,316 views
- 5 citations
Original Research
Published on 18 Nov 2022
Abnormal expression of TSG-6 disturbs extracellular matrix homeostasis in chondrocytes from endemic osteoarthritis
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1064565
- 1,725 views
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
in Genomics of Plants and the Phytoecosystem
Frontiers in Genetics
doi 10.3389/fgene.2022.1048578
- 1,728 views
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
in Epigenomics and Epigenetics
Frontiers in Genetics
doi 10.3389/fgene.2022.1051168
- 1,427 views
- 1 citation
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
in Genetics of Common and Rare Diseases
![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)
Frontiers in Genetics
doi 10.3389/fgene.2022.1017446
- 2,807 views
- 1 citation
Original Research
Published on 18 Nov 2022
Immune mechanism of low bone mineral density caused by ankylosing spondylitis based on bioinformatics and machine learning
in Computational Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1054035
- 2,114 views
- 1 citation
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
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2022.1038274
- 1,618 views
- 1 citation