Original Research
Accepted on 10 Feb 2026
Low-dose X-Ray induced genetic damage in human peripheral blood lymphocytes
in Cytogenomics
Frontiers in Genetics
- 184 views
- Frontiers in Genetics
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37 articles
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Case Report
Published on 10 Feb 2026
Pediatric-onset spinocerebellar ataxia type 3 with dual ATXN3 and HTT gene mutations: a case report and literature-informed hypothesis
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2026.1723599
- 563 views
Original Research
Published on 09 Jan 2026
The value of quantitative fluorescence polymerase chain reaction for the products of conception in the era of copy number variation sequencing
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1750362
- 646 views
Original Research
Published on 29 Oct 2025
LDLRAD4 is a potential diagnostic and prognostic biomarker correlated with immune infiltration in myelodysplastic syndromes
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1540161
- 1,710 views
Original Research
Published on 22 Oct 2025
S100A10 knockdown exacerbates phenylephrine-induced cardiomyocyte hypertrophy via modulating mitochondrial oxidative phosphorylation
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1610008
- 1,882 views
- 1 citation
Original Research
Published on 20 Oct 2025
DLL1 haploinsufficiency in prenatal brain anomalies: a retrospective analysis of 6q terminal deletions
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1640775
- 1,839 views
Original Research
Published on 25 Aug 2025
Analysis of complex chromosomal structural variants through optical genome mapping integrated with karyotyping
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1605461
- 4,300 views
- 1 citation
Original Research
Published on 23 Jul 2025
Identification of key genes associated with infertile endometriosis based on bioinformatic analysis
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1615268
- 3,761 views
Original Research
Published on 25 Jun 2025
Application of chromosome microarray analysis and karyotyping in fetal cardiac abnormalities
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1611388
- 3,493 views
Original Research
Published on 23 Jun 2025
Directional genomic hybridization (dGH™) identifies small inverted duplications in situ
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1604822
- 3,118 views
Original Research
Published on 23 Jun 2025
Uncovering genetic contributors to developmental delay and intellectual disability: a focus on CNVs in pediatric patients
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1539902
- 3,022 views
- 1 citation
Systematic Review
Published on 11 Jun 2025
Exome sequencing and prenatal skeletal abnormalities: comprehensive review and meta-analysis and way forward
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1502538
- 2,774 views
Original Research
Published on 30 May 2025
Hapten-labeled DNA probes can be stored and used in fluorescence in situ hybridization for decades
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1569308
- 2,637 views
Case Report
Published on 22 May 2025
Case Report: Optical genome mapping enables identification of complex balanced chromosomal rearrangements
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1555485
- 2,970 views
- 1 citation
Case Report
Published on 06 May 2025
Case Report: A prenatal case with sex discordance between non-invasive prenatal testing and fetal genetic testings due to maternal rare chromosome karyotype
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1546579
- 3,218 views
- 1 citation
Original Research
Published on 25 Mar 2025
Karyotype and genome size analyses for two spiders of the lycosidae family
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1544087
- 3,159 views
Case Report
Published on 05 Mar 2025
Lessons from a phenotypically normal infant with uniparental isodisomy of chromosome 21: a Case Report and review
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2025.1544565
- 2,381 views
- 1 citation
Original Research
Published on 13 Jan 2025
Improving prenatal diagnosis with combined karyotyping, CNV-seq and QF-PCR: a comprehensive analysis of chromosomal abnormalities in high-risk pregnancies
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1517270
- 3,994 views
- 4 citations
Original Research
Published on 15 Oct 2024
Prenatal diagnosis and postnatal follow-up of 15 fetuses with 16p13.11 microduplication syndrome
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1486974
- 4,496 views
- 5 citations
Case Report
Published on 19 Sep 2024
Case report: A novel FBXW7 gene variant causes global developmental delay
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1436462
- 2,828 views
- 2 citations
Original Research
Published on 29 Aug 2024
Prenatal diagnosis of the recurrent 1q21.1 microdeletions in fetuses with ultrasound anomalies and review of the literature
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1448341
- 3,640 views
- 2 citations
Case Report
Published on 18 Jul 2024
Prenatal diagnosis of dicentric chromosome X mosaicism: a case report and review
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1436469
- 2,271 views
Original Research
Published on 04 Jul 2024
Unraveling chromosomal and genotoxic damage in individuals occupationally exposed to coal from underground mining
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1422938
- 2,972 views
- 1 citation
Editorial
Published on 17 Apr 2024
Editorial: Co-occurrence of numerical and structural aberration—small supernumerary marker chromosomes and B-chromosomes
in Cytogenomics
Frontiers in Genetics
doi 10.3389/fgene.2024.1408674
- 1,638 views