Cytogenetic and Genome Research

Papers
(The median citation count of Cytogenetic and Genome Research is 0. 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 2021-05-01 to 2025-05-01.)
ArticleCitations
Germline-Restricted Chromosomes and Autosomal Variants Revealed by Pachytene Karyotyping of 17 Avian Species26
Epigenetic Clocks: In Aging-Related and Complex Diseases17
International Comparison Exercise for Biological Dosimetry after Exposures with Neutrons Performed at Two Irradiation Facilities as Part of the BALANCE Project11
Nucleotide Sequence and Chromosome Mapping of 5S Ribosomal DNA from the Dojo Loach, Misgurnus anguillicaudatus10
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 Diseases9
Retraction Statement6
The NIAID/RNCP Biodosimetry Program: An Overview5
Acknowledgement to Reviewers5
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 Injury4
The New Mitogenome of Erpornis zantholeuca (Aves: Passeriformes): Sequence, Structure, and Phylogenetic Analyses4
The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems4
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, China4
Simultaneous EYFP-CENH3/H2B-DsRed Expression Is Impaired Differentially in Meristematic and Differentiated Nuclei of Arabidopsis Double Transformants3
Y Chromosome Genomic Variations and Biological Significance in Human Diseases and Health3
Applicability of Scoring Calyculin A-Induced Premature Chromosome Condensation Objects for Dose Assessment Including for Radiotherapy Patients3
Genomic Features of Interstitial Deletions of Chromosome 9q in Acute Myeloid Leukemia3
Retrospective Evaluation of Cytogenetic Effects Induced by Internal Radioiodine Exposure: A 27-Year Follow-Up Study3
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 Disease3
B-Cell Acute Lymphoblastic Leukemia with iAMP21 in a Patient with Constitutional Ring Chromosome 213
Recurrent Mutations in Refractory/Relapsed Diffuse Large B-Cell Lymphoma by Targeted Gene Sequencing3
Karyotype Evolution of Talking Thorny Catfishes Anadoras (Doradidae, Astrodoradinae): A Process Mediated by Structural Rearrangements and Intense Reorganization of Repetitive DNAs3
Exploring the Role of Extrachromosomal Circular DNA in Human Diseases3
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
Cytogenetic Mapping of Cattle BAC Probes for the Hypothetical Ancestral Karyotype of the Family Cervidae3
Confirmation of Natural Hybridization between Kengyilia (StStYYPP) and Campeiostachys (StStYYHH) (Triticeae: Poaceae) Based on Morphological and Molecular Cytogenetic Analyses3
The Molecular Mechanism of Aurora-B Regulating Kinetochore-Microtubule Attachment in Mitosis and Oocyte Meiosis3
Comparative Somatic Variant Analysis of a Rare Case with Concurrent Oral Leukoplakia and Oral Submucosal Fibrosis3
Isodicentric Y Chromosome with Multiple Breakpoints in the Pseudoautosomal Region 12
Chromosomal Evolution of Suboscines: Karyotype Diversity and Evolutionary Trends in Ovenbirds (Passeriformes, Furnariidae)2
Erratum2
Improved Basic Cytogenetics Challenges Holocentricity of Butterfly Chromosomes2
Frequency of Sex Chromosome Involvement in a Large Cohort of Subjects with Two Copy Number Variants2
Biased Clonal Evolution in Acute Promyelocytic Leukemia through Imbalances Affecting the der(17) but Not the der(15) Chromosome: Report of Two Cases2
Xp22.33p22.13 Duplication in a Male Patient Carrying a Recombinant X Chromosome Derived from an Inherited Intrachromosomal Insertion2
Epileptic Encephalopathy with Variants in the PHACTR1 and AFF2 Genes: A Case Report2
Sex as a Factor in Murine Radiation Research: Implications for Countermeasure Development2
Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia1
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024)1
Contents Vol. 162, 20221
Diversity of telomeric sequences in true bugs (Heteroptera): new data on the infraorders Pentatomomorpha and Cimicomorpha1
Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions1
Prelims1
Prelims1
Prenatal Diagnosis of Fetuses with 4q35 Deletion: Case Series and Review of the Literature1
Fluorescence in situ Hybridization Analysis of Oligonucleotide 5S Ribosomal DNA, 45S Ribosomal DNA, and (TTTAGGG)3 Locations in Gloriosa superba L.1
Prelims1
Association of Leukocyte Telomere Length and the Risk of Disease Severity and Metabolic Comorbidities in Arab Patients with Psoriasis1
Whole-Genome Sequencing Reveals a Novel Pathogenic GRIN2B Variant in a Patient with Neurodevelopmental Disorder and an inv(6)(p24p11.2)pat1
A Paternal &quot;Balanced&quot; Chromosome 2 and 4 Translocation with Chromosome 21q Insertion Leading to Duplication of 2q22.1q24.1 in Two Siblings1
Diversity and Evolution of Highly Repetitive DNA Sequences Constituting Chromosome Site-Specific Heterochromatin in Two Gerbillinae Species1
Girl-Boy Twins with Developmental Delay from 16p11.2 Triplication due to Biparental Inheritance from Two Parents with 16p11.2 Duplication1
A Detailed Karyological Investigation of three Endemic Cobitis Linnaeus, 1758 Species (Teleostei, Cobitidae) in Anatolia, Türkiye1
Detection and genetic analysis of small supernumerary marker chromosomes in prenatal diagnosis1
Acknowledgement to Reviewers1
Hidden Y Chromosome Material and Congenital Cardiovascular Malformations in a Cohort of Turner Syndrome Patients with 45,X Blood Karyotype1
Front & Back Matter1
Erratum1
Fourth Report on Chicken Genes and Chromosomes 20221
Low-Level Germline 48,XYY,+21 Mosaicism Associated with Transient Abnormal Myelopoiesis in a Phenotypically Normal Neonate1
Cytogenetic Analysis of the Fungus-Farming Ant Cyphomyrmex rimosus (Spinola, 1851) (Formicidae: Myrmicinae: Attini) Highlights Karyotypic Variation1
New Karyotype Information for Ctenomys (Rodentia: Ctenomyidae) from Midwest and Northern Brazil1
Front & Back Matter0
Front & Back Matter0
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 Strategy0
Paper-Based Vertical Flow Immunoassay for the Point-of-Care Multiplex Detection of Radiation Dosimetry Genes0
Comparative Studies of Karyotypes in the Cervidae Family0
A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family0
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 Fish0
Heterozygous Deletion of Long Noncoding RNA AK127244 Is a Susceptibility Factor for Neurodevelopmental Delay0
Assessment of Micronuclei Frequency in the Peripheral Blood of Adult and Pediatric Patients Receiving Fractionated Total Body Irradiation0
A Novel Partial Deletion of the TBL1XR1 Gene Detected Using SNP Array in a Patient with Motor Delay, Growth Failure, and Klinefelter Syndrome0
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 DNA0
Multiple Aneuploidy: First Report of a Patient Presenting with a Karyotype 45,X/48,XXX,+210
Ionizing Radiation-Induced DNA Damage Response in Primary Melanocytes and Keratinocytes of Human Skin0
Shugoshin Regulates Cohesin, Kinetochore-Microtubule Attachments, and Chromosomal Instability0
Complex congenital cardiac defect associated with the combination of 5p deletion and 4q duplication in a newborn: A case report0
Front & Back Matter0
Contents Vol.163, 20230
Robertsonian Fusion Site in Rineloricaria pentamaculata (Siluriformes: Loricariidae): Involvement of 5S Ribosomal DNA and Satellite Sequences0
Comparative Cytogenetics in Tyrannidae (Aves, Passeriformes): High Genetic Diversity despite Conserved Karyotype Organization0
Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China0
Cytogenomic Characterization of Murine Osteosarcoma Cell Line SEWA0
Front & Back Matter0
Radiation-Induced Gene Expression Changes Used for Biodosimetry and Clinical Outcome Prediction: Challenges and Promises0
Front & Back Matter0
Minimal Critical Region and Genes for a Typical Presentation of Langer-Giedion Syndrome0
Intersexual Twins due to Tetragametic Chimerism0
Atypical Presence of Interstitial Telomeric Sequences in Thamnophilus Species (Passeriformes: Thamnophilidae)0
Molecular Cytogenetic Characterization of Rare but Repeatedly Observed Inversions in German Population0
Candidate Gene Expression in Regional Population and Its Relevance for Radiation Triage0
Whole-Exome Sequencing Targeting a Gene Panel for Sensorineural Hearing Loss: The First Portuguese Cohort Study0
Cytogenetic Abnormalities in Multiple Myeloma: Incidence, Prognostic Significance, and Geographic Heterogeneity in Indian and Western Populations0
Tandem Triplication 11p15.5-ICR1 (H19/IGF2) Detected by Microarray and Optical Genome Mapping in a Prenatal Beckwith-Wiedemann Case0
Effect of Age and Sex on Gene Expression-Based Radiation Biodosimetry Using Mouse Peripheral Blood0
Karyotypic Reshuffling in the Genus Rhipidomys (Rodentia: Cricetidae: Sigmodontinae) Revealed by Zoo-FISH0
Addenda to ISCN 20200
The Parental Centromere Sizes Remain Unaltered in Allopolyploid Wheat-Rye Hybrids0
Dynamics of RTEL1 helicase in meiotic cells: spatiotemporal distribution during prophase I in the rat Rattus norvegicus0
Genome Mapping Nomenclature0
Accurate Identification of Breakpoints in a Cryptic Reciprocal Translocation by Whole-Genome Sequencing0
Front & Back Matter0
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 Initiatives0
Large Chromosome 2p Duplication-Associated Mechanisms and Clinical Presentations0
Identification of Centromere-Specific Repeats in the Zebra Finch Genome0
Analysis of Chromosome Test Results of 24,175 Miscarried Fetuses in Japan from 2000 to 20210
Application of the Cytokinesis-Block Micronucleus Assay for High-Dose Exposures Using Imaging Flow Cytometry0
Clinical Findings in a Series of Thirty Eight Patients with Williams-Beuren Syndrome0
Incidence and Types of Fetal Chromosomal Abnormalities in First Trimester of Thai Pregnant Women between Miscarriages and Intrauterine Survivals0
Genetic and epigenetic insights into Werner Syndrome0
Somatic Variants and Exon-Level Copy Number Changes in Five Hyperplastic Oral Leukoplakias0
New insights into chromosomal regions 15p11.2 to 15q11.2 by studying submicroscopic variations using molecular cytogenetics0
Optical Genome Mapping for a Patient with a Congenital Disorder and Chromosomal Translocation0
Study on DNA damage gene in spermatogonial stem cells from idiopathic non-obstructive azoospermia(NOA) : an bioinformatics investigation based on scRNA-seq data0
The Legacy of George M. Martin: From Segmental Progeroid Syndromes to Antigeroid Syndromes0
Some peculiarities of MLH1 foci distribution in common degu (Octodon degus, Rodentia: Octodontidae) chromosomes: presence in pericentromeric regions and absence in XY0
Novel 10q21.1-q22.1 Duplication in a Boy with Minor Facial Dysmorphism, Mild Intellectual Disability, Autism Spectrum Disorder-Like Phenotype, and Short Stature0
A Familial Case of 1q31.2q32.2 Deletion with No Phenotypic Presentation0
Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy Loss0
Variation and morphological manifestation of germline restricted chromosomes in three species of leaf warblers of genus Phylloscopus0
Molecular Analysis of Parthenogenetic Chimerism in a 46,XX/46,XY Patient with Idiopathic Oligoasthenoteratozoospermia0
Interstitial 2q24.2q24.3 Microdeletion: Two New Cases with Similar Clinical Features with the Exception of Profound Deafness0
scRepli-Seq: A Powerful Tool to Study Replication Timing and Genome Instability0
Runs of Homozygosity Decipher Genetic Diversity in Cattle Breed Dwelling in the Colder Regions of the World0
Tracking Chromosomal Origins in the Northern Italy System of Metacentric Races of the House Mouse0
Karyotypes and Chromosomal Mapping of Some Repetitive DNAs in Two Stingless Bee Species (Apidae: Meliponini), with the Description of a B Chromosome in Plebeia Genus0
Front & Back Matter0
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 a0
Transcriptional Analysis of Microsatellites in Velvetbean Caterpillar Anticarsia gemmatalis Hübner, 18180
Front & Back Matter0
Front & Back Matter0
Identification of Key Genes from the Visceral Adipose Tissues of Overweight/Obese Adults with Hypertension through Transcriptome Sequencing0
Toward a Comprehensive Overview of Cytogenomics in the Galliformes: a Focus on Western Capercaillie and Hazel Grouse Karyotypes0
Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders0
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 Cohorts0
Identification of a New Enhancer That Promotes <i>Sox9</i> Expression by a Comparative Analysis of Mouse and <i>Sry</i>-Deficient Amami Spiny Rat0
Identification of Key Genes and Drug Recommendations in Diffuse Large B-Cell Lymphoma Based on Analysis of Glutathione-Related Genes0
Karyotype and repetitive DNA analysis in Turcichondrostoma fahirae (Cypriniformes, Leuciscidae): A step towards the use of molecular cytogenetics in taxonomy of freshwater fishes in Türkiye0
Meiotic Segregation of an Isodicentric Derived from Chromosome 15 in Sperm of a Patient with Mosaic Karyotype: Case Report and Review of the Literature0
Repetitive DNA Mapping in Five Genera of Tree Frogs (Amphibia: Anura) from the Atlantic Forest: New Highlights on Genomic Organization in Hylidae0
Content 2024, Vol. 1640
Cohesin <b><i>RAD21</i></b> Gene Promoter Methylation Correlated with Better Prognosis in Breast Cancer Patients0
Patient with Mosaic Turner Syndrome and a Derivative X Chromosome with a Variant Triple X Diagnosis in Fetus: A Case Report0
Downregulation of lncRNA FOXD2-AS1 Confers Radiosensitivity to Gastric Cancer Cells via miR-1913/SETD1A Axis0
Insights on the Radiation-Induced Adaptive Response at the Cellular Level and Its Implications in Cancer Therapy0
Comparison of Isolated Lymphocyte and Whole Blood-Based CBMN Assays for Radiation Triage0
Delineating the W Sex Chromosome in the Clam Shrimp, Eulimnadia texana0
Revealing the Satellite DNA Content in <i>Ancistrus</i> sp. (Siluriformes: Loricariidae) by Genomic and Bioinformatic Analysis0
Oxana L. Kolomiets: 42 Years at the Forefront of Meiotic Chromosome Study0
Genotype-Phenotype Correlation of Distal 2q37 Deletions0
ISCN 2024: Summary of revisions and new nomenclature0
Whole-arm chromosome rearrangements and telomeric signal displays: current cytogenetic updates on the examples of mammalian karyotype integrative variation0
Erratum0
Kallmann syndrome due to balanced X chromosomal pericentric inversion disrupting ANOS10
0.074420928955078