Cytogenetic and Genome Research

Papers
(The median citation count of Cytogenetic and Genome Research is 1. 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 2022-06-01 to 2026-06-01.)
ArticleCitations
Clustered structural variants involving PHEX at Xp22 in a female patient with X-linked hypophosphatemia52
International Comparison Exercise for Biological Dosimetry after Exposures with Neutrons Performed at Two Irradiation Facilities as Part of the BALANCE Project44
Epigenetic Clocks: In Aging-Related and Complex Diseases19
Acknowledgement to Reviewers19
Comparative Cytogenetic Analysis of Diploid and Triploid Pacific Abalone, <i>Haliotis discus hannai</i>12
Localization of Ribosomal DNA-Associated Retrotransposons Refines the Heterochromatin Map of the X Chromosome in Drosophila melanogaster11
The NIAID/RNCP Biodosimetry Program: An Overview11
Erratum9
Biomarkers for Biodosimetry and Their Role in Predicting Radiation Injury9
Simultaneous EYFP-CENH3/H2B-DsRed Expression Is Impaired Differentially in Meristematic and Differentiated Nuclei of Arabidopsis Double Transformants8
Exploring the Role of Extrachromosomal Circular DNA in Human Diseases8
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, China7
Jumping Translocation of 3q in a Patient with Mantle Cell Lymphoma: A Case Report and Review of the Literature7
Retrospective Evaluation of Cytogenetic Effects Induced by Internal Radioiodine Exposure: A 27-Year Follow-Up Study6
Loss of One X and the Y Chromosome Changes the Configuration of the X Inactivation Center in the Genus <i>Tokudaia</i>6
The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems6
The Association between Short Telomere Length and Cardiovascular Disease5
Meiotic Segregation Analysis in Sperm of a Pericentric Inversion of Chromosome 19 Heterozygous Carrier: Assessment of Recombination Frequency and Genetic Risk5
Y Chromosome Genomic Variations and Biological Significance in Human Diseases and Health5
Isodicentric Y Chromosome with Multiple Breakpoints in the Pseudoautosomal Region 14
Functional Divergence between the Z and W Alleles of the UBAP2 Gene Revealed by Differences in Their Expression Patterns in Japanese Quail4
Erratum4
Recurrent Mutations in Refractory/Relapsed Diffuse Large B-Cell Lymphoma by Targeted Gene Sequencing4
The Molecular Mechanism of Aurora-B Regulating Kinetochore-Microtubule Attachment in Mitosis and Oocyte Meiosis4
Xp22.33p22.13 Duplication in a Male Patient Carrying a Recombinant X Chromosome Derived from an Inherited Intrachromosomal Insertion4
Applicability of Scoring Calyculin A-Induced Premature Chromosome Condensation Objects for Dose Assessment Including for Radiotherapy Patients4
New Karyotype Information for Ctenomys (Rodentia: Ctenomyidae) from Midwest and Northern Brazil3
Association of Leukocyte Telomere Length and the Risk of Disease Severity and Metabolic Comorbidities in Arab Patients with Psoriasis3
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024)3
Sex as a Factor in Murine Radiation Research: Implications for Countermeasure Development3
Meiosis in Hybrids: Looking for the Order in Disorder3
Fluorescence in situ Hybridization Analysis of Oligonucleotide 5S Ribosomal DNA, 45S Ribosomal DNA, and (TTTAGGG)3 Locations in Gloriosa superba L.3
Prenatal Diagnosis of Fetuses with 4q35 Deletion: Case Series and Review of the Literature3
Acknowledgement to Reviewers3
Detection and Genetic Analysis of Small Supernumerary Marker Chromosomes in Prenatal Diagnosis3
Prelims3
A Detailed Karyological Investigation of three Endemic Cobitis Linnaeus, 1758 Species (Teleostei, Cobitidae) in Anatolia, Türkiye3
Coexistence of Mosaic Marker Chromosome and Isodisomy 1 in Reproductive Failure: A Cytogenomic Case Report and Review of the Literature3
Hidden Y Chromosome Material and Congenital Cardiovascular Malformations in a Cohort of Turner Syndrome Patients with 45,X Blood Karyotype3
High Amplification of CLA-SAT-149 Satellite DNA in Bighead Catfish: Insights into Satellite DNA Evolution in Clariid Lineages2
Molecular Mechanisms of Proliferative Senescence and Genomic Instability in Werner Syndrome and the WRN Gene Network2
Prelims2
Chromosomal and Cellular Insights into Sexual Reproduction and Evolution: A Special Issue Honoring Professor Oxana L. Kolomiets2
In silico Characterization of Satellitomes and Cross-Amplification of Putative satDNAs in Two Species of the Hypostomus ancistroides Complex (Siluriformes, Loricariidae)2
Complex Congenital Cardiac Defect Associated with the Combination of 5p Deletion and 4q Duplication in a Newborn: A Case Report2
Molecular Characterization of MECOM Rearrangements in Two Cases with Myelodysplastic Syndrome and t(2;3)(p23;q26.2)2
Diversity of Telomeric Sequences in True Bugs (Heteroptera): New Data on the Infraorders Pentatomomorpha and Cimicomorpha2
Tandem Triplication 11p15.5-ICR1 (H19/IGF2) Detected by Microarray and Optical Genome Mapping in a Prenatal Beckwith-Wiedemann Case2
Addenda to ISCN 20202
Fluorescence in situ Hybridization Analysis Can Reveal Subtle Chromosomal Rearrangements in Pericentromeric Regions of Acrocentric Chromosomes in Patients with Reproductive Failure2
Erratum2
Whole-Genome Sequencing Reveals a Novel Pathogenic GRIN2B Variant in a Patient with Neurodevelopmental Disorder and an inv(6)(p24p11.2)pat2
Diversity and Evolution of Highly Repetitive DNA Sequences Constituting Chromosome Site-Specific Heterochromatin in Two Gerbillinae Species2
Fertility Cost (or Sometimes a Lack of It) in Relation to Heterozygosity for Robertsonian Rearrangements in Mammals: A Review2
Genome Mapping Nomenclature2
A 30-Year Cytogenetic Follow-Up Study on a Thyroid Cancer Patient after Internal Radioiodine Therapy2
Karyotype and Repetitive DNA Analysis in Turcichondrostoma fahirae (Cypriniformes, Leuciscidae): A Step toward the Use of Molecular Cytogenetics in Taxonomy of Freshwater Fishes in Türkiye1
Comparison of Isolated Lymphocyte and Whole Blood-Based CBMN Assays for Radiation Triage1
Establishment of cell cultures from the cavefish Astyanax mexicanus: a resource for in vitro studies of supernumerary B chromosome biology1
Analysis of Chromosome Test Results of 24,175 Miscarried Fetuses in Japan from 2000 to 20211
Delineating the W Sex Chromosome in the Clam Shrimp, Eulimnadia texana1
Novel 10q21.1-q22.1 Duplication in a Boy with Minor Facial Dysmorphism, Mild Intellectual Disability, Autism Spectrum Disorder-Like Phenotype, and Short Stature1
In situ and in silico Localization of Major Satellite DNAs in the Genome of the Red-Eared Slider (Trachemys scripta elegans, Emydidae, Testudines)1
Diagnostic Utility of Chromosomal Microarray Analysis in a Turkish Pediatric Cohort: Insights from 1,022 Patients with Neurodevelopmental Disorders and Congenital Anomalies1
Cytogenomic Characterization of Murine Osteosarcoma Cell Line SEWA1
Runs of Homozygosity Decipher Genetic Diversity in Cattle Breed Dwelling in the Colder Regions of the World1
Genetic and epigenetic insights into Werner Syndrome1
Comparative Cytogenetics in Tyrannidae (Aves, Passeriformes): High Genetic Diversity despite Conserved Karyotype Organization1
Erratum1
Oxana L. Kolomiets: 42 Years at the Forefront of Meiotic Chromosome Study1
Robertsonian Translocation Rob(13;19) Identified in Guinea Pig (Cavia porcellus, Rodentia)1
Supernumerary B Chromosomes of <i>Tetragonisca fiebrigi</i> Share Repeat Content with Standard Chromosome Set of both <i>T. fiebrigi</i> and <i>Tetragonisca angustula<1
First Karyotypic Insights into <i>Potamotrygon schroederi</i> Fernández-Yépez, 1958: Association of Different Classes of Repetitive DNA1
Fork Stalling and Template Switching in a Complex der(6)dn with Duplication of 6q24.3qter and 6p25.3: A Case Report1
Study on DNA Damage Gene in Spermatogonial Stem Cells from Idiopathic Nonobstructive Azoospermia: A Bioinformatics Investigation Based on scRNA-seq Data1
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