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 2021-09-01 to 2025-09-01.)
ArticleCitations
Clustered structural variants involving PHEX at Xp22 in a female patient with X-linked hypophosphatemia31
International Comparison Exercise for Biological Dosimetry after Exposures with Neutrons Performed at Two Irradiation Facilities as Part of the BALANCE Project29
Germline-Restricted Chromosomes and Autosomal Variants Revealed by Pachytene Karyotyping of 17 Avian Species15
Epigenetic Clocks: In Aging-Related and Complex Diseases14
Nucleotide Sequence and Chromosome Mapping of 5S Ribosomal DNA from the Dojo Loach, Misgurnus anguillicaudatus11
Comparative Cytogenetic Analysis of Diploid and Triploid Pacific Abalone, <i>Haliotis discus hannai</i>10
Acknowledgement to Reviewers9
Retraction Statement7
The Neo-X Does Not Form a Barr Body but Shows a Slightly Condensed Structure in the Okinawa Spiny Rat (Tokudaia muenninki)6
Putative Condition-Dependent Viability Selection in Wild-Type Stocks of <b><i>Drosophila pseudoobscura</i></b>6
The New Mitogenome of Erpornis zantholeuca (Aves: Passeriformes): Sequence, Structure, and Phylogenetic Analyses6
Erratum6
Interaction between m6A and ncRNAs and Its Association with Diseases6
The NIAID/RNCP Biodosimetry Program: An Overview5
The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems5
Localization of rDNA-associated retrotransposons refines the heterochromatin map of the X chromosome in Drosophila melanogaster5
Exploring the Role of Extrachromosomal Circular DNA in Human Diseases5
Biomarkers for Biodosimetry and Their Role in Predicting Radiation Injury5
Erratum4
Loss of One X and the Y Chromosome Changes the Configuration of the X Inactivation Center in the Genus <i>Tokudaia</i>4
Retrospective Evaluation of Cytogenetic Effects Induced by Internal Radioiodine Exposure: A 27-Year Follow-Up Study4
Jumping Translocation of 3q in a Patient with Mantle Cell Lymphoma: A Case Report and Review of the Literature4
Simultaneous EYFP-CENH3/H2B-DsRed Expression Is Impaired Differentially in Meristematic and Differentiated Nuclei of Arabidopsis Double Transformants4
Confirmation of Natural Hybridization between Kengyilia (StStYYPP) and Campeiostachys (StStYYHH) (Triticeae: Poaceae) Based on Morphological and Molecular Cytogenetic Analyses3
Molecular and Chromosomal Evolution of DsTc1_5 and DsPogo_8 Elements (Tc1-Mariner) in Species of the Dichotomius Genus (Coleoptera: Scarabaeidae): Contributions to the Speciation Process3
Comparative Somatic Variant Analysis of a Rare Case with Concurrent Oral Leukoplakia and Oral Submucosal Fibrosis3
Karyotype Evolution of Talking Thorny Catfishes Anadoras (Doradidae, Astrodoradinae): A Process Mediated by Structural Rearrangements and Intense Reorganization of Repetitive DNAs3
Meiotic Segregation Analysis in Sperm of a Pericentric Inversion of Chromosome 19 Heterozygous Carrier: Assessment of Recombination Frequency and Genetic Risk3
Recurrent Mutations in Refractory/Relapsed Diffuse Large B-Cell Lymphoma by Targeted Gene Sequencing3
Xp22.33p22.13 Duplication in a Male Patient Carrying a Recombinant X Chromosome Derived from an Inherited Intrachromosomal Insertion3
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, China3
The Molecular Mechanism of Aurora-B Regulating Kinetochore-Microtubule Attachment in Mitosis and Oocyte Meiosis3
Cytogenetic Mapping of Cattle BAC Probes for the Hypothetical Ancestral Karyotype of the Family Cervidae3
B-Cell Acute Lymphoblastic Leukemia with iAMP21 in a Patient with Constitutional Ring Chromosome 213
Epileptic Encephalopathy with Variants in the PHACTR1 and AFF2 Genes: A Case Report3
Genomic Features of Interstitial Deletions of Chromosome 9q in Acute Myeloid Leukemia3
Y Chromosome Genomic Variations and Biological Significance in Human Diseases and Health3
The Association between Short Telomere Length and Cardiovascular Disease3
Applicability of Scoring Calyculin A-Induced Premature Chromosome Condensation Objects for Dose Assessment Including for Radiotherapy Patients3
Isodicentric Y Chromosome with Multiple Breakpoints in the Pseudoautosomal Region 12
Erratum2
Frequency of Sex Chromosome Involvement in a Large Cohort of Subjects with Two Copy Number Variants2
Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia2
Improved Basic Cytogenetics Challenges Holocentricity of Butterfly Chromosomes2
Sex as a Factor in Murine Radiation Research: Implications for Countermeasure Development2
New Karyotype Information for Ctenomys (Rodentia: Ctenomyidae) from Midwest and Northern Brazil2
Hidden Y Chromosome Material and Congenital Cardiovascular Malformations in a Cohort of Turner Syndrome Patients with 45,X Blood Karyotype2
Biased Clonal Evolution in Acute Promyelocytic Leukemia through Imbalances Affecting the der(17) but Not the der(15) Chromosome: Report of Two Cases2
Chromosomal Evolution of Suboscines: Karyotype Diversity and Evolutionary Trends in Ovenbirds (Passeriformes, Furnariidae)2
Acknowledgement to Reviewers2
FISH analysis can reveal subtle chromosomal rearrangements in pericentromeric regions of acrocentric chromosomes in patients with reproductive failure1
Diversity and Evolution of Highly Repetitive DNA Sequences Constituting Chromosome Site-Specific Heterochromatin in Two Gerbillinae Species1
Addenda to ISCN 20201
Girl-Boy Twins with Developmental Delay from 16p11.2 Triplication due to Biparental Inheritance from Two Parents with 16p11.2 Duplication1
Whole-Genome Sequencing Reveals a Novel Pathogenic GRIN2B Variant in a Patient with Neurodevelopmental Disorder and an inv(6)(p24p11.2)pat1
In silico Characterization of Satellitomes and Cross-Amplification of Putative satDNAs in Two Species of the Hypostomus ancistroides Complex (Siluriformes, Loricariidae)1
Prenatal Diagnosis of Fetuses with 4q35 Deletion: Case Series and Review of the Literature1
Cytogenetic Analysis of the Fungus-Farming Ant Cyphomyrmex rimosus (Spinola, 1851) (Formicidae: Myrmicinae: Attini) Highlights Karyotypic Variation1
Detection and Genetic Analysis of Small Supernumerary Marker Chromosomes in Prenatal Diagnosis1
Prelims1
Tandem Triplication 11p15.5-ICR1 (H19/IGF2) Detected by Microarray and Optical Genome Mapping in a Prenatal Beckwith-Wiedemann Case1
Intersexual Twins due to Tetragametic Chimerism1
First Karyotypic Insights into <i>Potamotrygon schroederi</i> Fernández-Yépez, 1958: Association of Different Classes of Repetitive DNA1
Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy Loss1
A Paternal &quot;Balanced&quot; Chromosome 2 and 4 Translocation with Chromosome 21q Insertion Leading to Duplication of 2q22.1q24.1 in Two Siblings1
SHOX Whole Gene Duplications Are Overrepresented in SHOX Haploinsufficiency Phenotype Cohorts1
Diversity of telomeric sequences in true bugs (Heteroptera): new data on the infraorders Pentatomomorpha and Cimicomorpha1
Contents Vol. 162, 20221
Chromosomal and Cellular Insights into Sexual Reproduction and Evolution: A Special Issue Honoring Professor Oxana L. Kolomiets1
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024)1
Front & Back Matter1
A Detailed Karyological Investigation of three Endemic Cobitis Linnaeus, 1758 Species (Teleostei, Cobitidae) in Anatolia, Türkiye1
Fluorescence in situ Hybridization Analysis of Oligonucleotide 5S Ribosomal DNA, 45S Ribosomal DNA, and (TTTAGGG)3 Locations in Gloriosa superba L.1
Fertility cost (or sometimes a lack of it) in relation to heterozygosity for Robertsonian rearrangements in mammals: a review1
Study on DNA Damage Gene in Spermatogonial Stem Cells from Idiopathic Nonobstructive Azoospermia: A Bioinformatics Investigation Based on scRNA-seq Data1
Patient with Mosaic Turner Syndrome and a Derivative X Chromosome with a Variant Triple X Diagnosis in Fetus: A Case Report1
Front & Back Matter1
Genetic and epigenetic insights into Werner Syndrome1
Low-Level Germline 48,XYY,+21 Mosaicism Associated with Transient Abnormal Myelopoiesis in a Phenotypically Normal Neonate1
Novel 10q21.1-q22.1 Duplication in a Boy with Minor Facial Dysmorphism, Mild Intellectual Disability, Autism Spectrum Disorder-Like Phenotype, and Short Stature1
Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions1
Genome Mapping Nomenclature1
Erratum1
Front & Back Matter1
Comparative Studies of Karyotypes in the Cervidae Family1
Prelims1
Analysis of Chromosome Test Results of 24,175 Miscarried Fetuses in Japan from 2000 to 20211
Association of Leukocyte Telomere Length and the Risk of Disease Severity and Metabolic Comorbidities in Arab Patients with Psoriasis1
Meiosis in hybrids: looking for the order in disorder1
Prelims1
Front & Back Matter1
Comparative Cytogenetics in Tyrannidae (Aves, Passeriformes): High Genetic Diversity despite Conserved Karyotype Organization1
Delineating the W Sex Chromosome in the Clam Shrimp, Eulimnadia texana1
Complex Congenital Cardiac Defect Associated with the Combination of 5p Deletion and 4q Duplication in a Newborn: A Case Report1
Fourth Report on Chicken Genes and Chromosomes 20221
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