Cytogenetic and Genome Research

Article	Citations
Clustered structural variants involving PHEX at Xp22 in a female patient with X-linked hypophosphatemia	29
International Comparison Exercise for Biological Dosimetry after Exposures with Neutrons Performed at Two Irradiation Facilities as Part of the BALANCE Project	27
Germline-Restricted Chromosomes and Autosomal Variants Revealed by Pachytene Karyotyping of 17 Avian Species	14
Epigenetic Clocks: In Aging-Related and Complex Diseases	12
Nucleotide Sequence and Chromosome Mapping of 5S Ribosomal DNA from the Dojo Loach, Misgurnus anguillicaudatus	11
Comparative Cytogenetic Analysis of Diploid and Triploid Pacific Abalone, <i>Haliotis discus hannai</i>	10
Acknowledgement to Reviewers	9
Retraction Statement	7
The New Mitogenome of Erpornis zantholeuca (Aves: Passeriformes): Sequence, Structure, and Phylogenetic Analyses	6
Putative Condition-Dependent Viability Selection in Wild-Type Stocks of <b><i>Drosophila pseudoobscura</i></b>	6
Biomarkers for Biodosimetry and Their Role in Predicting Radiation Injury	6
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 Diseases	6
Erratum	5
The NIAID/RNCP Biodosimetry Program: An Overview	5
Localization of rDNA-associated retrotransposons refines the heterochromatin map of the X chromosome in Drosophila melanogaster	5
Retrospective Evaluation of Cytogenetic Effects Induced by Internal Radioiodine Exposure: A 27-Year Follow-Up Study	4
The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems	4
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 literature	4
Exploring the Role of Extrachromosomal Circular DNA in Human Diseases	4
Erratum	4
Simultaneous EYFP-CENH3/H2B-DsRed Expression Is Impaired Differentially in Meristematic and Differentiated Nuclei of Arabidopsis Double Transformants	4
B-Cell Acute Lymphoblastic Leukemia with iAMP21 in a Patient with Constitutional Ring Chromosome 21	3
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 Process	3

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, China	3
The Association between Short Telomere Length and Cardiovascular Disease	3
Applicability of Scoring Calyculin A-Induced Premature Chromosome Condensation Objects for Dose Assessment Including for Radiotherapy Patients	3
Cytogenetic Mapping of Cattle BAC Probes for the Hypothetical Ancestral Karyotype of the Family Cervidae	3
The Molecular Mechanism of Aurora-B Regulating Kinetochore-Microtubule Attachment in Mitosis and Oocyte Meiosis	3
Meiotic segregation analysis in sperm of a pericentric inversion of chromosome 19 heterozygous carrier: assessment of recombination frequency and genetic risk	3
Karyotype Evolution of Talking Thorny Catfishes Anadoras (Doradidae, Astrodoradinae): A Process Mediated by Structural Rearrangements and Intense Reorganization of Repetitive DNAs	3
Recurrent Mutations in Refractory/Relapsed Diffuse Large B-Cell Lymphoma by Targeted Gene Sequencing	3
Confirmation of Natural Hybridization between Kengyilia (StStYYPP) and Campeiostachys (StStYYHH) (Triticeae: Poaceae) Based on Morphological and Molecular Cytogenetic Analyses	3
Comparative Somatic Variant Analysis of a Rare Case with Concurrent Oral Leukoplakia and Oral Submucosal Fibrosis	3
Y Chromosome Genomic Variations and Biological Significance in Human Diseases and Health	3
Genomic Features of Interstitial Deletions of Chromosome 9q in Acute Myeloid Leukemia	3
Epileptic Encephalopathy with Variants in the PHACTR1 and AFF2 Genes: A Case Report	2
Improved Basic Cytogenetics Challenges Holocentricity of Butterfly Chromosomes	2
Chromosomal Evolution of Suboscines: Karyotype Diversity and Evolutionary Trends in Ovenbirds (Passeriformes, Furnariidae)	2
Isodicentric Y Chromosome with Multiple Breakpoints in the Pseudoautosomal Region 1	2
Frequency of Sex Chromosome Involvement in a Large Cohort of Subjects with Two Copy Number Variants	2
Xp22.33p22.13 Duplication in a Male Patient Carrying a Recombinant X Chromosome Derived from an Inherited Intrachromosomal Insertion	2
Biased Clonal Evolution in Acute Promyelocytic Leukemia through Imbalances Affecting the der(17) but Not the der(15) Chromosome: Report of Two Cases	2
Erratum	2
Front & Back Matter	1
Front & Back Matter	1
Fourth Report on Chicken Genes and Chromosomes 2022	1
Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions	1
Erratum	1
Prenatal Diagnosis of Fetuses with 4q35 Deletion: Case Series and Review of the Literature	1
Prelims	1
Acknowledgement to Reviewers	1
New Karyotype Information for Ctenomys (Rodentia: Ctenomyidae) from Midwest and Northern Brazil	1
Whole-Genome Sequencing Reveals a Novel Pathogenic GRIN2B Variant in a Patient with Neurodevelopmental Disorder and an inv(6)(p24p11.2)pat	1
Diversity of telomeric sequences in true bugs (Heteroptera): new data on the infraorders Pentatomomorpha and Cimicomorpha	1
Addenda to ISCN 2020	1
Tandem Triplication 11p15.5-ICR1 (H19/IGF2) Detected by Microarray and Optical Genome Mapping in a Prenatal Beckwith-Wiedemann Case	1
Contents Vol. 162, 2022	1
Diversity and Evolution of Highly Repetitive DNA Sequences Constituting Chromosome Site-Specific Heterochromatin in Two Gerbillinae Species	1
Low-Level Germline 48,XYY,+21 Mosaicism Associated with Transient Abnormal Myelopoiesis in a Phenotypically Normal Neonate	1
Association of Leukocyte Telomere Length and the Risk of Disease Severity and Metabolic Comorbidities in Arab Patients with Psoriasis	1
Sex as a Factor in Murine Radiation Research: Implications for Countermeasure Development	1
Prelims	1
Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia	1
Hidden Y Chromosome Material and Congenital Cardiovascular Malformations in a Cohort of Turner Syndrome Patients with 45,X Blood Karyotype	1
Meiosis in hybrids: looking for the order in disorder	1
Girl-Boy Twins with Developmental Delay from 16p11.2 Triplication due to Biparental Inheritance from Two Parents with 16p11.2 Duplication	1
Comparative Studies of Karyotypes in the Cervidae Family	1
Prelims	1
A Paternal "Balanced" Chromosome 2 and 4 Translocation with Chromosome 21q Insertion Leading to Duplication of 2q22.1q24.1 in Two Siblings	1
Fertility cost (or sometimes a lack of it) in relation to heterozygosity for Robertsonian rearrangements in mammals: a review	1
A Detailed Karyological Investigation of three Endemic Cobitis Linnaeus, 1758 Species (Teleostei, Cobitidae) in Anatolia, Türkiye	1
Cytogenetic Analysis of the Fungus-Farming Ant Cyphomyrmex rimosus (Spinola, 1851) (Formicidae: Myrmicinae: Attini) Highlights Karyotypic Variation	1
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 diagnosis	1
Front & Back Matter	1
Dosage Effect of the Ph1 Locus on Homologous Crossovers in a Segment of Chromosome 1B of Bread Wheat (Triticum aestivum L.)	0
Spaghetti Connections: Synaptonemal Complexes as a Tool to Explore Chromosome Structure, Evolution, and Meiotic Behavior in Fish	0
Robertsonian Fusion Site in Rineloricaria pentamaculata (Siluriformes: Loricariidae): Involvement of 5S Ribosomal DNA and Satellite Sequences	0
Karyotype and Repetitive DNA Analysis in Turcichondrostoma fahirae (Cypriniformes, Leuciscidae): A Step toward the Use of Molecular Cytogenetics in Taxonomy of Freshwater Fishes in Türkiye	0
Multiple Aneuploidy: First Report of a Patient Presenting with a Karyotype 45,X/48,XXX,+21	0
Content 2024, Vol. 164	0
Molecular Cytogenetic Characterization of C-Band-Positive Heterochromatin of the Greater Long-Tailed Hamster (Tscherskia triton, Cricetinae)	0
Some peculiarities of MLH1 foci distribution in common degu (Octodon degus, Rodentia: Octodontidae) chromosomes: presence in pericentromeric regions and absence in XY	0
Comparative Cytogenetics in Tyrannidae (Aves, Passeriformes): High Genetic Diversity despite Conserved Karyotype Organization	0
Identification of Centromere-Specific Repeats in the Zebra Finch Genome	0
Front & Back Matter	0
Front & Back Matter	0
Meiotic Arrest and Synaptonemal Complex failure in Infertile Men with Y Chromosome Microdeletions	0
A Familial Case of 1q31.2q32.2 Deletion with No Phenotypic Presentation	0
Genotype-Phenotype Correlation of Distal 2q37 Deletions	0
Insights on the Radiation-Induced Adaptive Response at the Cellular Level and Its Implications in Cancer Therapy	0
The Legacy of George M. Martin: From Segmental Progeroid Syndromes to Antigeroid Syndromes	0
Atypical Presence of Interstitial Telomeric Sequences in Thamnophilus Species (Passeriformes: Thamnophilidae)	0
Front & Back Matter	0
Transcriptional Analysis of Microsatellites in Velvetbean Caterpillar Anticarsia gemmatalis Hübner, 1818	0
Concerted Evolution of Genus-Specific Centromeric Satellite DNA in Eremias (Lacertidae, Reptilia)	0
Zea mays meiotic spindle ultrastructure reveals kinetochore-microtubule interface and embedded membrane components	0
Post-translational modifications of the Werner syndrome protein WRN	0
Dynamics of RTEL1 helicase in meiotic cells: spatiotemporal distribution during prophase I in the rat Rattus norvegicus	0
Radiation-Induced Gene Expression Changes Used for Biodosimetry and Clinical Outcome Prediction: Challenges and Promises	0
Molecular Cytogenetic Characterization of Rare but Repeatedly Observed Inversions in German Population	0
Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders	0
Erratum	0
scRepli-Seq: A Powerful Tool to Study Replication Timing and Genome Instability	0
ACAN Repeat Number Polymorphism in Patients with Idiopathic Short Stature	0
Effect of Age and Sex on Gene Expression-Based Radiation Biodosimetry Using Mouse Peripheral Blood	0
Genome Mapping Nomenclature	0
A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family	0
First Karyotypic Insights into <i>Potamotrygon schroederi</i> Fernández-Yépez, 1958: Association of Different Classes of Repetitive DNA	0
Toward a Comprehensive Overview of Cytogenomics in the Galliformes: a Focus on Western Capercaillie and Hazel Grouse Karyotypes	0
Complex Congenital Cardiac Defect Associated with the Combination of 5p Deletion and 4q Duplication in a Newborn: A Case Report	0
Identification of a New Enhancer That Promotes <i>Sox9</i> Expression by a Comparative Analysis of Mouse and <i>Sry</i>-Deficient Amami Spiny Rat	0
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<	0
Optical Genome Mapping for a Patient with a Congenital Disorder and Chromosomal Translocation	0
Delineating the W Sex Chromosome in the Clam Shrimp, Eulimnadia texana	0
Accurate Identification of Breakpoints in a Cryptic Reciprocal Translocation by Whole-Genome Sequencing	0
Revealing the Satellite DNA Content in <i>Ancistrus</i> sp. (Siluriformes: Loricariidae) by Genomic and Bioinformatic Analysis	0
Incidence and Types of Fetal Chromosomal Abnormalities in First Trimester of Thai Pregnant Women between Miscarriages and Intrauterine Survivals	0
Front & Back Matter	0
Novel 10q21.1-q22.1 Duplication in a Boy with Minor Facial Dysmorphism, Mild Intellectual Disability, Autism Spectrum Disorder-Like Phenotype, and Short Stature	0
Genomic Imprinting: Insights into diverse epigenetic regulatory mechanisms	0
In situ and in silico localization of major satellite DNAs in the genome of the red-eared slider (Trachemys scripta elegans, Emydidae, Testudines)	0
Somatic Variants and Exon-Level Copy Number Changes in Five Hyperplastic Oral Leukoplakias	0
New insights into chromosomal regions 15p11.2 to 15q11.2 by studying submicroscopic variations using molecular cytogenetics	0
ISCN 2024: Summary of Revisions and New Nomenclature	0
Runs of Homozygosity Decipher Genetic Diversity in Cattle Breed Dwelling in the Colder Regions of the World	0
Karyotypes and Chromosomal Mapping of Some Repetitive DNAs in Two Stingless Bee Species (Apidae: Meliponini), with the Description of a B Chromosome in Plebeia Genus	0
Contents Vol.163, 2023	0
Erratum	0
Repetitive DNA Mapping in Five Genera of Tree Frogs (Amphibia: Anura) from the Atlantic Forest: New Highlights on Genomic Organization in Hylidae	0
Paper-Based Vertical Flow Immunoassay for the Point-of-Care Multiplex Detection of Radiation Dosimetry Genes	0
Interstitial 2q24.2q24.3 Microdeletion: Two New Cases with Similar Clinical Features with the Exception of Profound Deafness	0
The Parental Centromere Sizes Remain Unaltered in Allopolyploid Wheat-Rye Hybrids	0
Identification of Key Genes and Drug Recommendations in Diffuse Large B-Cell Lymphoma Based on Analysis of Glutathione-Related Genes	0
Whole-arm chromosome rearrangements and telomeric signal displays: current cytogenetic updates on the examples of mammalian karyotype integrative variation	0
Front & Back Matter	0
A Novel Partial Deletion of the TBL1XR1 Gene Detected Using SNP Array in a Patient with Motor Delay, Growth Failure, and Klinefelter Syndrome	0
In silico Characterization of Satellitomes and Cross-Amplification of Putative satDNAs in Two Species of the Hypostomus ancistroides Complex (Siluriformes, Loricariidae)	0
Cytogenomic Analysis of Long-Term Epilepsy-Associated Tumors Using an Array-Based CGH Strategy	0
Heterozygous Deletion of Long Noncoding RNA AK127244 Is a Susceptibility Factor for Neurodevelopmental Delay	0
Differences in Variants in the Structural Domain of <b><i>BCR-ABL1</i></b> Kinase between Chinese Han and Minority Patients with Chronic Myeloid Leukemia by Sanger Sequencing a	0
SHOX Whole Gene Duplications Are Overrepresented in SHOX Haploinsufficiency Phenotype Cohorts	0
Front & Back Matter	0
Analysis of Chromosome Test Results of 24,175 Miscarried Fetuses in Japan from 2000 to 2021	0
Radiation Biodosimetry: Current Status and Future Initiatives	0
Cohesin <b><i>RAD21</i></b> Gene Promoter Methylation Correlated with Better Prognosis in Breast Cancer Patients	0
Genetic and epigenetic insights into Werner Syndrome	0
Assessment of Micronuclei Frequency in the Peripheral Blood of Adult and Pediatric Patients Receiving Fractionated Total Body Irradiation	0
Cytogenomic Characterization of Murine Osteosarcoma Cell Line SEWA	0
Comparison of Isolated Lymphocyte and Whole Blood-Based CBMN Assays for Radiation Triage	0
Study on DNA Damage Gene in Spermatogonial Stem Cells from Idiopathic Nonobstructive Azoospermia: A Bioinformatics Investigation Based on scRNA-seq Data	0
Molecular Analysis of Parthenogenetic Chimerism in a 46,XX/46,XY Patient with Idiopathic Oligoasthenoteratozoospermia	0

Ionizing Radiation-Induced DNA Damage Response in Primary Melanocytes and Keratinocytes of Human Skin	0
Oxana L. Kolomiets: 42 Years at the Forefront of Meiotic Chromosome Study	0
Patient with Mosaic Turner Syndrome and a Derivative X Chromosome with a Variant Triple X Diagnosis in Fetus: A Case Report	0
Variation and morphological manifestation of germline restricted chromosomes in three species of leaf warblers of genus Phylloscopus	0
Meiotic Segregation of an Isodicentric Derived from Chromosome 15 in Sperm of a Patient with Mosaic Karyotype: Case Report and Review of the Literature	0
Whole-Exome Sequencing Targeting a Gene Panel for Sensorineural Hearing Loss: The First Portuguese Cohort Study	0
Clinical Findings in a Series of Thirty Eight Patients with Williams-Beuren Syndrome	0
Minimal Critical Region and Genes for a Typical Presentation of Langer-Giedion Syndrome	0
Establishment of cell cultures from the cavefish Astyanax mexicanus: a resource for in vitro studies of supernumerary B chromosome biology	0
Karyotypic Reshuffling in the Genus Rhipidomys (Rodentia: Cricetidae: Sigmodontinae) Revealed by Zoo-FISH	0
Cytogenetic Abnormalities in Multiple Myeloma: Incidence, Prognostic Significance, and Geographic Heterogeneity in Indian and Western Populations	0
Retraction Statement	0
Intersexual Twins due to Tetragametic Chimerism	0
Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China	0
Candidate Gene Expression in Regional Population and Its Relevance for Radiation Triage	0
Kallmann syndrome due to balanced X chromosomal pericentric inversion disrupting ANOS1	0
Front & Back Matter	0
Shugoshin Regulates Cohesin, Kinetochore-Microtubule Attachments, and Chromosomal Instability	0
Downregulation of lncRNA FOXD2-AS1 Confers Radiosensitivity to Gastric Cancer Cells via miR-1913/SETD1A Axis	0
Large Chromosome 2p Duplication-Associated Mechanisms and Clinical Presentations	0
Chromosomal and Cellular Insights into Sexual Reproduction and Evolution: A Special Issue Honoring Professor Oxana L. Kolomiets	0
Tracking Chromosomal Origins in the Northern Italy System of Metacentric Races of the House Mouse	0
Identification of Key Genes from the Visceral Adipose Tissues of Overweight/Obese Adults with Hypertension through Transcriptome Sequencing	0
FISH analysis can reveal subtle chromosomal rearrangements in pericentromeric regions of acrocentric chromosomes in patients with reproductive failure	0
Application of the Cytokinesis-Block Micronucleus Assay for High-Dose Exposures Using Imaging Flow Cytometry	0
Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy Loss	0