Cytogenetic and Genome Research

Papers
(The TQCC 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 2021-08-01 to 2025-08-01.)
ArticleCitations
Clustered structural variants involving PHEX at Xp22 in a female patient with X-linked hypophosphatemia29
International Comparison Exercise for Biological Dosimetry after Exposures with Neutrons Performed at Two Irradiation Facilities as Part of the BALANCE Project27
Germline-Restricted Chromosomes and Autosomal Variants Revealed by Pachytene Karyotyping of 17 Avian Species14
Epigenetic Clocks: In Aging-Related and Complex Diseases12
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
Biomarkers for Biodosimetry and Their Role in Predicting Radiation Injury6
The Neo-X Does Not Form a Barr Body but Shows a Slightly Condensed Structure in the Okinawa Spiny Rat (Tokudaia muenninki)6
Interaction between m6A and ncRNAs and Its Association with Diseases6
The New Mitogenome of Erpornis zantholeuca (Aves: Passeriformes): Sequence, Structure, and Phylogenetic Analyses6
Putative Condition-Dependent Viability Selection in Wild-Type Stocks of <b><i>Drosophila pseudoobscura</i></b>6
Localization of rDNA-associated retrotransposons refines the heterochromatin map of the X chromosome in Drosophila melanogaster5
Erratum5
The NIAID/RNCP Biodosimetry Program: An Overview5
Erratum4
Simultaneous EYFP-CENH3/H2B-DsRed Expression Is Impaired Differentially in Meristematic and Differentiated Nuclei of Arabidopsis Double Transformants4
Retrospective Evaluation of Cytogenetic Effects Induced by Internal Radioiodine Exposure: A 27-Year Follow-Up Study4
The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems4
Loss of One X and the Y Chromosome Changes the Configuration of the X Inactivation Center in the Genus <i>Tokudaia</i>4
Jumping translocation of 3q in a patient with Mantle Cell Lymphoma: A case report and review of the literature4
Exploring the Role of Extrachromosomal Circular DNA in Human Diseases4
The Molecular Mechanism of Aurora-B Regulating Kinetochore-Microtubule Attachment in Mitosis and Oocyte Meiosis3
Meiotic segregation analysis in sperm of a pericentric inversion of chromosome 19 heterozygous carrier: assessment of recombination frequency and genetic risk3
Karyotype Evolution of Talking Thorny Catfishes Anadoras (Doradidae, Astrodoradinae): A Process Mediated by Structural Rearrangements and Intense Reorganization of Repetitive DNAs3
Recurrent Mutations in Refractory/Relapsed Diffuse Large B-Cell Lymphoma by Targeted Gene Sequencing3
Confirmation of Natural Hybridization between Kengyilia (StStYYPP) and Campeiostachys (StStYYHH) (Triticeae: Poaceae) Based on Morphological and Molecular Cytogenetic Analyses3
Comparative Somatic Variant Analysis of a Rare Case with Concurrent Oral Leukoplakia and Oral Submucosal Fibrosis3
Y Chromosome Genomic Variations and Biological Significance in Human Diseases and Health3
Genomic Features of Interstitial Deletions of Chromosome 9q in Acute Myeloid Leukemia3
B-Cell Acute Lymphoblastic Leukemia with iAMP21 in a Patient with Constitutional Ring Chromosome 213
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
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 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
Cytogenetic Mapping of Cattle BAC Probes for the Hypothetical Ancestral Karyotype of the Family Cervidae3
Isodicentric Y Chromosome with Multiple Breakpoints in the Pseudoautosomal Region 12
Frequency of Sex Chromosome Involvement in a Large Cohort of Subjects with Two Copy Number Variants2
Xp22.33p22.13 Duplication in a Male Patient Carrying a Recombinant X Chromosome Derived from an Inherited Intrachromosomal Insertion2
Biased Clonal Evolution in Acute Promyelocytic Leukemia through Imbalances Affecting the der(17) but Not the der(15) Chromosome: Report of Two Cases2
Erratum2
Epileptic Encephalopathy with Variants in the PHACTR1 and AFF2 Genes: A Case Report2
Improved Basic Cytogenetics Challenges Holocentricity of Butterfly Chromosomes2
Chromosomal Evolution of Suboscines: Karyotype Diversity and Evolutionary Trends in Ovenbirds (Passeriformes, Furnariidae)2
Sex as a Factor in Murine Radiation Research: Implications for Countermeasure Development1
Prelims1
Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia1
Hidden Y Chromosome Material and Congenital Cardiovascular Malformations in a Cohort of Turner Syndrome Patients with 45,X Blood Karyotype1
Meiosis in hybrids: looking for the order in disorder1
Girl-Boy Twins with Developmental Delay from 16p11.2 Triplication due to Biparental Inheritance from Two Parents with 16p11.2 Duplication1
Comparative Studies of Karyotypes in the Cervidae Family1
Prelims1
A Paternal &quot;Balanced&quot; Chromosome 2 and 4 Translocation with Chromosome 21q Insertion Leading to Duplication of 2q22.1q24.1 in Two Siblings1
Fertility cost (or sometimes a lack of it) in relation to heterozygosity for Robertsonian rearrangements in mammals: a review1
A Detailed Karyological Investigation of three Endemic Cobitis Linnaeus, 1758 Species (Teleostei, Cobitidae) in Anatolia, Türkiye1
Cytogenetic Analysis of the Fungus-Farming Ant Cyphomyrmex rimosus (Spinola, 1851) (Formicidae: Myrmicinae: Attini) Highlights Karyotypic Variation1
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024)1
Fluorescence in situ Hybridization Analysis of Oligonucleotide 5S Ribosomal DNA, 45S Ribosomal DNA, and (TTTAGGG)3 Locations in Gloriosa superba L.1
Detection and genetic analysis of small supernumerary marker chromosomes in prenatal diagnosis1
Front & Back Matter1
Front & Back Matter1
Front & Back Matter1
Fourth Report on Chicken Genes and Chromosomes 20221
Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions1
Erratum1
Prenatal Diagnosis of Fetuses with 4q35 Deletion: Case Series and Review of the Literature1
Prelims1
Acknowledgement to Reviewers1
New Karyotype Information for Ctenomys (Rodentia: Ctenomyidae) from Midwest and Northern Brazil1
Whole-Genome Sequencing Reveals a Novel Pathogenic GRIN2B Variant in a Patient with Neurodevelopmental Disorder and an inv(6)(p24p11.2)pat1
Diversity of telomeric sequences in true bugs (Heteroptera): new data on the infraorders Pentatomomorpha and Cimicomorpha1
Addenda to ISCN 20201
Tandem Triplication 11p15.5-ICR1 (H19/IGF2) Detected by Microarray and Optical Genome Mapping in a Prenatal Beckwith-Wiedemann Case1
Contents Vol. 162, 20221
Diversity and Evolution of Highly Repetitive DNA Sequences Constituting Chromosome Site-Specific Heterochromatin in Two Gerbillinae Species1
Low-Level Germline 48,XYY,+21 Mosaicism Associated with Transient Abnormal Myelopoiesis in a Phenotypically Normal Neonate1
Association of Leukocyte Telomere Length and the Risk of Disease Severity and Metabolic Comorbidities in Arab Patients with Psoriasis1
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