Cytogenetic and Genome Research

Papers
(The TQCC of Cytogenetic and Genome Research is 3. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2022-08-01 to 2026-08-01.)
ArticleCitations
Clustered structural variants involving PHEX at Xp22 in a female patient with X-linked hypophosphatemia58
International Comparison Exercise for Biological Dosimetry after Exposures with Neutrons Performed at Two Irradiation Facilities as Part of the BALANCE Project48
Epigenetic Clocks: In Aging-Related and Complex Diseases21
Acknowledgement to Reviewers19
The NIAID/RNCP Biodosimetry Program: An Overview13
Comparative Cytogenetic Analysis of Diploid and Triploid Pacific Abalone, <i>Haliotis discus hannai</i>13
Localization of Ribosomal DNA-Associated Retrotransposons Refines the Heterochromatin Map of the X Chromosome in Drosophila melanogaster11
Biomarkers for Biodosimetry and Their Role in Predicting Radiation Injury10
Erratum10
Exploring the Role of Extrachromosomal Circular DNA in Human Diseases10
Simultaneous EYFP-CENH3/H2B-DsRed Expression Is Impaired Differentially in Meristematic and Differentiated Nuclei of Arabidopsis Double Transformants10
Jumping Translocation of 3q in a Patient with Mantle Cell Lymphoma: A Case Report and Review of the Literature9
Loss of One X and the Y Chromosome Changes the Configuration of the X Inactivation Center in the Genus <i>Tokudaia</i>8
Exploration of Multi-Gene DNA Barcode Markers to Reveal the Broad Genetic Diversity of Field Ticks (Acari: Ixodidae) in a Tropical Environment of Hainan Island, China6
Meiotic Segregation Analysis in Sperm of a Pericentric Inversion of Chromosome 19 Heterozygous Carrier: Assessment of Recombination Frequency and Genetic Risk6
The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems6
The Association between Short Telomere Length and Cardiovascular Disease6
Retrospective Evaluation of Cytogenetic Effects Induced by Internal Radioiodine Exposure: A 27-Year Follow-Up Study6
Functional Divergence between the Z and W Alleles of the UBAP2 Gene Revealed by Differences in Their Expression Patterns in Japanese Quail5
Recurrent Mutations in Refractory/Relapsed Diffuse Large B-Cell Lymphoma by Targeted Gene Sequencing5
Y Chromosome Genomic Variations and Biological Significance in Human Diseases and Health5
The Molecular Mechanism of Aurora-B Regulating Kinetochore-Microtubule Attachment in Mitosis and Oocyte Meiosis5
Isodicentric Y Chromosome with Multiple Breakpoints in the Pseudoautosomal Region 14
Coexistence of Mosaic Marker Chromosome and Isodisomy 1 in Reproductive Failure: A Cytogenomic Case Report and Review of the Literature4
Detection and Genetic Analysis of Small Supernumerary Marker Chromosomes in Prenatal Diagnosis4
Xp22.33p22.13 Duplication in a Male Patient Carrying a Recombinant X Chromosome Derived from an Inherited Intrachromosomal Insertion4
Hidden Y Chromosome Material and Congenital Cardiovascular Malformations in a Cohort of Turner Syndrome Patients with 45,X Blood Karyotype4
Fluorescence in situ Hybridization Analysis of Oligonucleotide 5S Ribosomal DNA, 45S Ribosomal DNA, and (TTTAGGG)3 Locations in Gloriosa superba L.4
Applicability of Scoring Calyculin A-Induced Premature Chromosome Condensation Objects for Dose Assessment Including for Radiotherapy Patients4
Erratum4
Acknowledgement to Reviewers4
Sex as a Factor in Murine Radiation Research: Implications for Countermeasure Development4
Molecular Characterization of MECOM Rearrangements in Two Cases with Myelodysplastic Syndrome and t(2;3)(p23;q26.2)3
Prelims3
Association of Leukocyte Telomere Length and the Risk of Disease Severity and Metabolic Comorbidities in Arab Patients with Psoriasis3
Molecular Mechanisms of Proliferative Senescence and Genomic Instability in Werner Syndrome and the WRN Gene Network3
Prenatal Diagnosis of Fetuses with 4q35 Deletion: Case Series and Review of the Literature3
Meiosis in Hybrids: Looking for the Order in Disorder3
New Karyotype Information for Ctenomys (Rodentia: Ctenomyidae) from Midwest and Northern Brazil3
A Detailed Karyological Investigation of three Endemic Cobitis Linnaeus, 1758 Species (Teleostei, Cobitidae) in Anatolia, Türkiye3
Diversity of Telomeric Sequences in True Bugs (Heteroptera): New Data on the Infraorders Pentatomomorpha and Cimicomorpha3
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024)3
High Amplification of CLA-SAT-149 Satellite DNA in Bighead Catfish: Insights into Satellite DNA Evolution in Clariid Lineages3
Whole-Genome Sequencing Reveals a Novel Pathogenic GRIN2B Variant in a Patient with Neurodevelopmental Disorder and an inv(6)(p24p11.2)pat3
Diversity and Evolution of Highly Repetitive DNA Sequences Constituting Chromosome Site-Specific Heterochromatin in Two Gerbillinae Species3
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