Cytogenetic and Genome Research

Article	Citations
Germline-Restricted Chromosomes and Autosomal Variants Revealed by Pachytene Karyotyping of 17 Avian Species	26
Epigenetic Clocks: In Aging-Related and Complex Diseases	17
International Comparison Exercise for Biological Dosimetry after Exposures with Neutrons Performed at Two Irradiation Facilities as Part of the BALANCE Project	11
Nucleotide Sequence and Chromosome Mapping of 5S Ribosomal DNA from the Dojo Loach, Misgurnus anguillicaudatus	10
Putative Condition-Dependent Viability Selection in Wild-Type Stocks of <b><i>Drosophila pseudoobscura</i></b>	9
Interaction between m6A and ncRNAs and Its Association with Diseases	9
Retraction Statement	6
The NIAID/RNCP Biodosimetry Program: An Overview	5
Acknowledgement to Reviewers	5
The Neo-X Does Not Form a Barr Body but Shows a Slightly Condensed Structure in the Okinawa Spiny Rat (Tokudaia muenninki)	5
Comparative Cytogenetic Analysis of Diploid and Triploid Pacific Abalone, <i>Haliotis discus hannai</i>	5
Biomarkers for Biodosimetry and Their Role in Predicting Radiation Injury	4
The New Mitogenome of Erpornis zantholeuca (Aves: Passeriformes): Sequence, Structure, and Phylogenetic Analyses	4
The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems	4
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	4
Simultaneous EYFP-CENH3/H2B-DsRed Expression Is Impaired Differentially in Meristematic and Differentiated Nuclei of Arabidopsis Double Transformants	3
Y Chromosome Genomic Variations and Biological Significance in Human Diseases and Health	3
Applicability of Scoring Calyculin A-Induced Premature Chromosome Condensation Objects for Dose Assessment Including for Radiotherapy Patients	3
Genomic Features of Interstitial Deletions of Chromosome 9q in Acute Myeloid Leukemia	3
Retrospective Evaluation of Cytogenetic Effects Induced by Internal Radioiodine Exposure: A 27-Year Follow-Up Study	3
Loss of One X and the Y Chromosome Changes the Configuration of the X Inactivation Center in the Genus <i>Tokudaia</i>	3
The Association between Short Telomere Length and Cardiovascular Disease	3
B-Cell Acute Lymphoblastic Leukemia with iAMP21 in a Patient with Constitutional Ring Chromosome 21	3
Recurrent Mutations in Refractory/Relapsed Diffuse Large B-Cell Lymphoma by Targeted Gene Sequencing	3
Karyotype Evolution of Talking Thorny Catfishes Anadoras (Doradidae, Astrodoradinae): A Process Mediated by Structural Rearrangements and Intense Reorganization of Repetitive DNAs	3

Exploring the Role of Extrachromosomal Circular DNA in Human Diseases	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
Cytogenetic Mapping of Cattle BAC Probes for the Hypothetical Ancestral Karyotype of the Family Cervidae	3
Confirmation of Natural Hybridization between Kengyilia (StStYYPP) and Campeiostachys (StStYYHH) (Triticeae: Poaceae) Based on Morphological and Molecular Cytogenetic Analyses	3
The Molecular Mechanism of Aurora-B Regulating Kinetochore-Microtubule Attachment in Mitosis and Oocyte Meiosis	3
Comparative Somatic Variant Analysis of a Rare Case with Concurrent Oral Leukoplakia and Oral Submucosal Fibrosis	3
Isodicentric Y Chromosome with Multiple Breakpoints in the Pseudoautosomal Region 1	2
Chromosomal Evolution of Suboscines: Karyotype Diversity and Evolutionary Trends in Ovenbirds (Passeriformes, Furnariidae)	2
Erratum	2
Improved Basic Cytogenetics Challenges Holocentricity of Butterfly Chromosomes	2
Frequency of Sex Chromosome Involvement in a Large Cohort of Subjects with Two Copy Number Variants	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
Xp22.33p22.13 Duplication in a Male Patient Carrying a Recombinant X Chromosome Derived from an Inherited Intrachromosomal Insertion	2
Epileptic Encephalopathy with Variants in the PHACTR1 and AFF2 Genes: A Case Report	2
Sex as a Factor in Murine Radiation Research: Implications for Countermeasure Development	2
Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia	1
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024)	1
Contents Vol. 162, 2022	1
Diversity of telomeric sequences in true bugs (Heteroptera): new data on the infraorders Pentatomomorpha and Cimicomorpha	1
Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions	1
Prelims	1
Prelims	1
Prenatal Diagnosis of Fetuses with 4q35 Deletion: Case Series and Review of the Literature	1
Fluorescence in situ Hybridization Analysis of Oligonucleotide 5S Ribosomal DNA, 45S Ribosomal DNA, and (TTTAGGG)3 Locations in Gloriosa superba L.	1
Prelims	1
Association of Leukocyte Telomere Length and the Risk of Disease Severity and Metabolic Comorbidities in Arab Patients with Psoriasis	1
Whole-Genome Sequencing Reveals a Novel Pathogenic GRIN2B Variant in a Patient with Neurodevelopmental Disorder and an inv(6)(p24p11.2)pat	1
A Paternal "Balanced" Chromosome 2 and 4 Translocation with Chromosome 21q Insertion Leading to Duplication of 2q22.1q24.1 in Two Siblings	1
Diversity and Evolution of Highly Repetitive DNA Sequences Constituting Chromosome Site-Specific Heterochromatin in Two Gerbillinae Species	1
Girl-Boy Twins with Developmental Delay from 16p11.2 Triplication due to Biparental Inheritance from Two Parents with 16p11.2 Duplication	1
A Detailed Karyological Investigation of three Endemic Cobitis Linnaeus, 1758 Species (Teleostei, Cobitidae) in Anatolia, Türkiye	1
Detection and genetic analysis of small supernumerary marker chromosomes in prenatal diagnosis	1
Acknowledgement to Reviewers	1
Hidden Y Chromosome Material and Congenital Cardiovascular Malformations in a Cohort of Turner Syndrome Patients with 45,X Blood Karyotype	1
Front & Back Matter	1
Erratum	1
Fourth Report on Chicken Genes and Chromosomes 2022	1
Low-Level Germline 48,XYY,+21 Mosaicism Associated with Transient Abnormal Myelopoiesis in a Phenotypically Normal Neonate	1
Cytogenetic Analysis of the Fungus-Farming Ant Cyphomyrmex rimosus (Spinola, 1851) (Formicidae: Myrmicinae: Attini) Highlights Karyotypic Variation	1
New Karyotype Information for Ctenomys (Rodentia: Ctenomyidae) from Midwest and Northern Brazil	1
Front & Back Matter	0
Front & Back Matter	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
Cytogenomic Analysis of Long-Term Epilepsy-Associated Tumors Using an Array-Based CGH Strategy	0
Paper-Based Vertical Flow Immunoassay for the Point-of-Care Multiplex Detection of Radiation Dosimetry Genes	0
Comparative Studies of Karyotypes in the Cervidae Family	0
A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family	0
Concerted Evolution of Genus-Specific Centromeric Satellite DNA in Eremias (Lacertidae, Reptilia)	0
In silico Characterization of Satellitomes and Cross-Amplification of Putative satDNAs in Two Species of the Hypostomus ancistroides Complex (Siluriformes, Loricariidae)	0
Spaghetti Connections: Synaptonemal Complexes as a Tool to Explore Chromosome Structure, Evolution, and Meiotic Behavior in Fish	0

Heterozygous Deletion of Long Noncoding RNA AK127244 Is a Susceptibility Factor for Neurodevelopmental Delay	0
Assessment of Micronuclei Frequency in the Peripheral Blood of Adult and Pediatric Patients Receiving Fractionated Total Body Irradiation	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
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
First Karyotypic Insights into <i>Potamotrygon schroederi</i> Fernández-Yépez, 1958: Association of Different Classes of Repetitive DNA	0
Multiple Aneuploidy: First Report of a Patient Presenting with a Karyotype 45,X/48,XXX,+21	0
Ionizing Radiation-Induced DNA Damage Response in Primary Melanocytes and Keratinocytes of Human Skin	0
Shugoshin Regulates Cohesin, Kinetochore-Microtubule Attachments, and Chromosomal Instability	0
Complex congenital cardiac defect associated with the combination of 5p deletion and 4q duplication in a newborn: A case report	0
Front & Back Matter	0
Contents Vol.163, 2023	0
Robertsonian Fusion Site in Rineloricaria pentamaculata (Siluriformes: Loricariidae): Involvement of 5S Ribosomal DNA and Satellite Sequences	0
Comparative Cytogenetics in Tyrannidae (Aves, Passeriformes): High Genetic Diversity despite Conserved Karyotype Organization	0
Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China	0
Cytogenomic Characterization of Murine Osteosarcoma Cell Line SEWA	0
Front & Back Matter	0
Radiation-Induced Gene Expression Changes Used for Biodosimetry and Clinical Outcome Prediction: Challenges and Promises	0
Front & Back Matter	0
Minimal Critical Region and Genes for a Typical Presentation of Langer-Giedion Syndrome	0
Intersexual Twins due to Tetragametic Chimerism	0
Atypical Presence of Interstitial Telomeric Sequences in Thamnophilus Species (Passeriformes: Thamnophilidae)	0
Molecular Cytogenetic Characterization of Rare but Repeatedly Observed Inversions in German Population	0
Candidate Gene Expression in Regional Population and Its Relevance for Radiation Triage	0
Whole-Exome Sequencing Targeting a Gene Panel for Sensorineural Hearing Loss: The First Portuguese Cohort Study	0
Cytogenetic Abnormalities in Multiple Myeloma: Incidence, Prognostic Significance, and Geographic Heterogeneity in Indian and Western Populations	0
Tandem Triplication 11p15.5-ICR1 (H19/IGF2) Detected by Microarray and Optical Genome Mapping in a Prenatal Beckwith-Wiedemann Case	0
Effect of Age and Sex on Gene Expression-Based Radiation Biodosimetry Using Mouse Peripheral Blood	0
Karyotypic Reshuffling in the Genus Rhipidomys (Rodentia: Cricetidae: Sigmodontinae) Revealed by Zoo-FISH	0
Addenda to ISCN 2020	0
The Parental Centromere Sizes Remain Unaltered in Allopolyploid Wheat-Rye Hybrids	0
Dynamics of RTEL1 helicase in meiotic cells: spatiotemporal distribution during prophase I in the rat Rattus norvegicus	0
Genome Mapping Nomenclature	0
Accurate Identification of Breakpoints in a Cryptic Reciprocal Translocation by Whole-Genome Sequencing	0
Front & Back Matter	0
Dosage Effect of the Ph1 Locus on Homologous Crossovers in a Segment of Chromosome 1B of Bread Wheat (Triticum aestivum L.)	0
Radiation Biodosimetry: Current Status and Future Initiatives	0
Large Chromosome 2p Duplication-Associated Mechanisms and Clinical Presentations	0
Identification of Centromere-Specific Repeats in the Zebra Finch Genome	0
Analysis of Chromosome Test Results of 24,175 Miscarried Fetuses in Japan from 2000 to 2021	0
Application of the Cytokinesis-Block Micronucleus Assay for High-Dose Exposures Using Imaging Flow Cytometry	0
Clinical Findings in a Series of Thirty Eight Patients with Williams-Beuren Syndrome	0
Incidence and Types of Fetal Chromosomal Abnormalities in First Trimester of Thai Pregnant Women between Miscarriages and Intrauterine Survivals	0
Genetic and epigenetic insights into Werner Syndrome	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
Optical Genome Mapping for a Patient with a Congenital Disorder and Chromosomal Translocation	0
Study on DNA damage gene in spermatogonial stem cells from idiopathic non-obstructive azoospermia（NOA） : an bioinformatics investigation based on scRNA-seq data	0
The Legacy of George M. Martin: From Segmental Progeroid Syndromes to Antigeroid Syndromes	0
Some peculiarities of MLH1 foci distribution in common degu (Octodon degus, Rodentia: Octodontidae) chromosomes: presence in pericentromeric regions and absence in XY	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
A Familial Case of 1q31.2q32.2 Deletion with No Phenotypic Presentation	0
Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy Loss	0
Variation and morphological manifestation of germline restricted chromosomes in three species of leaf warblers of genus Phylloscopus	0
Molecular Analysis of Parthenogenetic Chimerism in a 46,XX/46,XY Patient with Idiopathic Oligoasthenoteratozoospermia	0
Interstitial 2q24.2q24.3 Microdeletion: Two New Cases with Similar Clinical Features with the Exception of Profound Deafness	0
scRepli-Seq: A Powerful Tool to Study Replication Timing and Genome Instability	0
Runs of Homozygosity Decipher Genetic Diversity in Cattle Breed Dwelling in the Colder Regions of the World	0
Tracking Chromosomal Origins in the Northern Italy System of Metacentric Races of the House Mouse	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
Front & Back Matter	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
Transcriptional Analysis of Microsatellites in Velvetbean Caterpillar Anticarsia gemmatalis Hübner, 1818	0
Front & Back Matter	0
Front & Back Matter	0
Identification of Key Genes from the Visceral Adipose Tissues of Overweight/Obese Adults with Hypertension through Transcriptome Sequencing	0
Toward a Comprehensive Overview of Cytogenomics in the Galliformes: a Focus on Western Capercaillie and Hazel Grouse Karyotypes	0
Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders	0
Molecular Cytogenetic Characterization of C-Band-Positive Heterochromatin of the Greater Long-Tailed Hamster (Tscherskia triton, Cricetinae)	0
SHOX Whole Gene Duplications Are Overrepresented in SHOX Haploinsufficiency Phenotype Cohorts	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
Identification of Key Genes and Drug Recommendations in Diffuse Large B-Cell Lymphoma Based on Analysis of Glutathione-Related Genes	0
Karyotype and repetitive DNA analysis in Turcichondrostoma fahirae (Cypriniformes, Leuciscidae): A step towards the use of molecular cytogenetics in taxonomy of freshwater fishes in Türkiye	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
Repetitive DNA Mapping in Five Genera of Tree Frogs (Amphibia: Anura) from the Atlantic Forest: New Highlights on Genomic Organization in Hylidae	0
Content 2024, Vol. 164	0
Cohesin <b><i>RAD21</i></b> Gene Promoter Methylation Correlated with Better Prognosis in Breast Cancer Patients	0
Patient with Mosaic Turner Syndrome and a Derivative X Chromosome with a Variant Triple X Diagnosis in Fetus: A Case Report	0
Downregulation of lncRNA FOXD2-AS1 Confers Radiosensitivity to Gastric Cancer Cells via miR-1913/SETD1A Axis	0
Insights on the Radiation-Induced Adaptive Response at the Cellular Level and Its Implications in Cancer Therapy	0
Comparison of Isolated Lymphocyte and Whole Blood-Based CBMN Assays for Radiation Triage	0

Delineating the W Sex Chromosome in the Clam Shrimp, Eulimnadia texana	0
Revealing the Satellite DNA Content in <i>Ancistrus</i> sp. (Siluriformes: Loricariidae) by Genomic and Bioinformatic Analysis	0
Oxana L. Kolomiets: 42 Years at the Forefront of Meiotic Chromosome Study	0
Genotype-Phenotype Correlation of Distal 2q37 Deletions	0
ISCN 2024: Summary of revisions and new nomenclature	0
Whole-arm chromosome rearrangements and telomeric signal displays: current cytogenetic updates on the examples of mammalian karyotype integrative variation	0
Erratum	0
Kallmann syndrome due to balanced X chromosomal pericentric inversion disrupting ANOS1	0