Cytogenetic and Genome Research

Article	Citations
International Comparison Exercise for Biological Dosimetry after Exposures with Neutrons Performed at Two Irradiation Facilities as Part of the BALANCE Project	26
Germline-Restricted Chromosomes and Autosomal Variants Revealed by Pachytene Karyotyping of 17 Avian Species	19
Epigenetic Clocks: In Aging-Related and Complex Diseases	13
Nucleotide Sequence and Chromosome Mapping of 5S Ribosomal DNA from the Dojo Loach, Misgurnus anguillicaudatus	11
Retraction Statement	10
Comparative Cytogenetic Analysis of Diploid and Triploid Pacific Abalone, <i>Haliotis discus hannai</i>	9
Acknowledgement to Reviewers	7
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 Analyses	5
Erratum	5
Interaction between m6A and ncRNAs and Its Association with Diseases	5
Biomarkers for Biodosimetry and Their Role in Predicting Radiation Injury	5
The NIAID/RNCP Biodosimetry Program: An Overview	5
The Neo-X Does Not Form a Barr Body but Shows a Slightly Condensed Structure in the Okinawa Spiny Rat (Tokudaia muenninki)	5
The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems	4
Exploring the Role of Extrachromosomal Circular DNA in Human Diseases	4
Simultaneous EYFP-CENH3/H2B-DsRed Expression Is Impaired Differentially in Meristematic and Differentiated Nuclei of Arabidopsis Double Transformants	4
The Association between Short Telomere Length and Cardiovascular Disease	3
Karyotype Evolution of Talking Thorny Catfishes Anadoras (Doradidae, Astrodoradinae): A Process Mediated by Structural Rearrangements and Intense Reorganization of Repetitive DNAs	3
Jumping translocation of 3q in a patient with Mantle Cell Lymphoma: A case report and review of the literature	3
Genomic Features of Interstitial Deletions of Chromosome 9q in Acute Myeloid Leukemia	3
B-Cell Acute Lymphoblastic Leukemia with iAMP21 in a Patient with Constitutional Ring Chromosome 21	3
The Molecular Mechanism of Aurora-B Regulating Kinetochore-Microtubule Attachment in Mitosis and Oocyte Meiosis	3
Retrospective Evaluation of Cytogenetic Effects Induced by Internal Radioiodine Exposure: A 27-Year Follow-Up Study	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
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
Loss of One X and the Y Chromosome Changes the Configuration of the X Inactivation Center in the Genus <i>Tokudaia</i>	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
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
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
Epileptic Encephalopathy with Variants in the PHACTR1 and AFF2 Genes: A Case Report	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
Improved Basic Cytogenetics Challenges Holocentricity of Butterfly Chromosomes	2
Erratum	2
Xp22.33p22.13 Duplication in a Male Patient Carrying a Recombinant X Chromosome Derived from an Inherited Intrachromosomal Insertion	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
Association of Leukocyte Telomere Length and the Risk of Disease Severity and Metabolic Comorbidities in Arab Patients with Psoriasis	1
Meiosis in hybrids: looking for the order in disorder	1
Acknowledgement to Reviewers	1
Prelims	1
Prelims	1
Diversity of telomeric sequences in true bugs (Heteroptera): new data on the infraorders Pentatomomorpha and Cimicomorpha	1
Fertility cost (or sometimes a lack of it) in relation to heterozygosity for Robertsonian rearrangements in mammals: a review	1
Fourth Report on Chicken Genes and Chromosomes 2022	1
Contents Vol. 162, 2022	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
New Karyotype Information for Ctenomys (Rodentia: Ctenomyidae) from Midwest and Northern Brazil	1
Hidden Y Chromosome Material and Congenital Cardiovascular Malformations in a Cohort of Turner Syndrome Patients with 45,X Blood Karyotype	1
Sex as a Factor in Murine Radiation Research: Implications for Countermeasure Development	1
Front & Back Matter	1
Tandem Triplication 11p15.5-ICR1 (H19/IGF2) Detected by Microarray and Optical Genome Mapping in a Prenatal Beckwith-Wiedemann Case	1
Low-Level Germline 48,XYY,+21 Mosaicism Associated with Transient Abnormal Myelopoiesis in a Phenotypically Normal Neonate	1
Diversity and Evolution of Highly Repetitive DNA Sequences Constituting Chromosome Site-Specific Heterochromatin in Two Gerbillinae Species	1
Erratum	1
Prenatal Diagnosis of Fetuses with 4q35 Deletion: Case Series and Review of the Literature	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
Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia	1
Whole-Genome Sequencing Reveals a Novel Pathogenic GRIN2B Variant in a Patient with Neurodevelopmental Disorder and an inv(6)(p24p11.2)pat	1
Prelims	1
A Paternal &quot;Balanced&quot; Chromosome 2 and 4 Translocation with Chromosome 21q Insertion Leading to Duplication of 2q22.1q24.1 in Two Siblings	1
Girl-Boy Twins with Developmental Delay from 16p11.2 Triplication due to Biparental Inheritance from Two Parents with 16p11.2 Duplication	1
Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions	1
Identification of Centromere-Specific Repeats in the Zebra Finch Genome	0
Runs of Homozygosity Decipher Genetic Diversity in Cattle Breed Dwelling in the Colder Regions of the World	0
Revealing the Satellite DNA Content in <i>Ancistrus</i> sp. (Siluriformes: Loricariidae) by Genomic and Bioinformatic Analysis	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
Robertsonian Fusion Site in Rineloricaria pentamaculata (Siluriformes: Loricariidae): Involvement of 5S Ribosomal DNA and Satellite Sequences	0

Front & Back Matter	0
Molecular Analysis of Parthenogenetic Chimerism in a 46,XX/46,XY Patient with Idiopathic Oligoasthenoteratozoospermia	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
Identification of Key Genes from the Visceral Adipose Tissues of Overweight/Obese Adults with Hypertension through Transcriptome Sequencing	0
Some peculiarities of MLH1 foci distribution in common degu (Octodon degus, Rodentia: Octodontidae) chromosomes: presence in pericentromeric regions and absence in XY	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
Transcriptional Analysis of Microsatellites in Velvetbean Caterpillar Anticarsia gemmatalis Hübner, 1818	0
Radiation-Induced Gene Expression Changes Used for Biodosimetry and Clinical Outcome Prediction: Challenges and Promises	0
Repetitive DNA Mapping in Five Genera of Tree Frogs (Amphibia: Anura) from the Atlantic Forest: New Highlights on Genomic Organization in Hylidae	0
Variation and morphological manifestation of germline restricted chromosomes in three species of leaf warblers of genus Phylloscopus	0
scRepli-Seq: A Powerful Tool to Study Replication Timing and Genome Instability	0
Atypical Presence of Interstitial Telomeric Sequences in Thamnophilus Species (Passeriformes: Thamnophilidae)	0
Concerted Evolution of Genus-Specific Centromeric Satellite DNA in Eremias (Lacertidae, Reptilia)	0
Whole-Exome Sequencing Targeting a Gene Panel for Sensorineural Hearing Loss: The First Portuguese Cohort Study	0
Oxana L. Kolomiets: 42 Years at the Forefront of Meiotic Chromosome Study	0
Front & Back Matter	0
Genotype-Phenotype Correlation of Distal 2q37 Deletions	0
Large Chromosome 2p Duplication-Associated Mechanisms and Clinical Presentations	0
Tracking Chromosomal Origins in the Northern Italy System of Metacentric Races of the House Mouse	0
Addenda to ISCN 2020	0
Ionizing Radiation-Induced DNA Damage Response in Primary Melanocytes and Keratinocytes of Human Skin	0
A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family	0
In silico Characterization of Satellitomes and Cross-Amplification of Putative satDNAs in Two Species of the Hypostomus ancistroides Complex (Siluriformes, Loricariidae)	0
The Legacy of George M. Martin: From Segmental Progeroid Syndromes to Antigeroid Syndromes	0
Application of the Cytokinesis-Block Micronucleus Assay for High-Dose Exposures Using Imaging Flow Cytometry	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
Contents Vol.163, 2023	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
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
Optical Genome Mapping for a Patient with a Congenital Disorder and Chromosomal Translocation	0
Intersexual Twins due to Tetragametic Chimerism	0
Front & Back Matter	0
Patient with Mosaic Turner Syndrome and a Derivative X Chromosome with a Variant Triple X Diagnosis in Fetus: A Case Report	0
Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China	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
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
Paper-Based Vertical Flow Immunoassay for the Point-of-Care Multiplex Detection of Radiation Dosimetry Genes	0
A Familial Case of 1q31.2q32.2 Deletion with No Phenotypic Presentation	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
Minimal Critical Region and Genes for a Typical Presentation of Langer-Giedion Syndrome	0
Front & Back Matter	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
Whole-arm chromosome rearrangements and telomeric signal displays: current cytogenetic updates on the examples of mammalian karyotype integrative variation	0
Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders	0
Somatic Variants and Exon-Level Copy Number Changes in Five Hyperplastic Oral Leukoplakias	0
Front & Back Matter	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
Front & Back Matter	0
New insights into chromosomal regions 15p11.2 to 15q11.2 by studying submicroscopic variations using molecular cytogenetics	0
Molecular Cytogenetic Characterization of Rare but Repeatedly Observed Inversions in German Population	0
Assessment of Micronuclei Frequency in the Peripheral Blood of Adult and Pediatric Patients Receiving Fractionated Total Body Irradiation	0
SHOX Whole Gene Duplications Are Overrepresented in SHOX Haploinsufficiency Phenotype Cohorts	0
Insights on the Radiation-Induced Adaptive Response at the Cellular Level and Its Implications in Cancer Therapy	0
Toward a Comprehensive Overview of Cytogenomics in the Galliformes: a Focus on Western Capercaillie and Hazel Grouse Karyotypes	0
Molecular Cytogenetic Characterization of C-Band-Positive Heterochromatin of the Greater Long-Tailed Hamster (Tscherskia triton, Cricetinae)	0
Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy Loss	0
Cytogenetic Abnormalities in Multiple Myeloma: Incidence, Prognostic Significance, and Geographic Heterogeneity in Indian and Western Populations	0
Dosage Effect of the Ph1 Locus on Homologous Crossovers in a Segment of Chromosome 1B of Bread Wheat (Triticum aestivum L.)	0
Incidence and Types of Fetal Chromosomal Abnormalities in First Trimester of Thai Pregnant Women between Miscarriages and Intrauterine Survivals	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
Comparison of Isolated Lymphocyte and Whole Blood-Based CBMN Assays for Radiation Triage	0
Comparative Cytogenetics in Tyrannidae (Aves, Passeriformes): High Genetic Diversity despite Conserved Karyotype Organization	0
Kallmann syndrome due to balanced X chromosomal pericentric inversion disrupting ANOS1	0
Front & Back Matter	0
Karyotypic Reshuffling in the Genus Rhipidomys (Rodentia: Cricetidae: Sigmodontinae) Revealed by Zoo-FISH	0
Front & Back Matter	0
Genetic and epigenetic insights into Werner Syndrome	0
ISCN 2024: Summary of revisions and new nomenclature	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
Erratum	0
Downregulation of lncRNA FOXD2-AS1 Confers Radiosensitivity to Gastric Cancer Cells via miR-1913/SETD1A Axis	0
Candidate Gene Expression in Regional Population and Its Relevance for Radiation Triage	0
Identification of Key Genes and Drug Recommendations in Diffuse Large B-Cell Lymphoma Based on Analysis of Glutathione-Related Genes	0
Cytogenomic Characterization of Murine Osteosarcoma Cell Line SEWA	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
Cytogenomic Analysis of Long-Term Epilepsy-Associated Tumors Using an Array-Based CGH Strategy	0
Comparative Studies of Karyotypes in the Cervidae Family	0
Dynamics of RTEL1 helicase in meiotic cells: spatiotemporal distribution during prophase I in the rat Rattus norvegicus	0
Effect of Age and Sex on Gene Expression-Based Radiation Biodosimetry Using Mouse Peripheral Blood	0
Genome Mapping Nomenclature	0
Clinical Findings in a Series of Thirty Eight Patients with Williams-Beuren Syndrome	0
Front & Back Matter	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
Analysis of Chromosome Test Results of 24,175 Miscarried Fetuses in Japan from 2000 to 2021	0
Content 2024, Vol. 164	0
Spaghetti Connections: Synaptonemal Complexes as a Tool to Explore Chromosome Structure, Evolution, and Meiotic Behavior in Fish	0