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 2021-02-01 to 2025-02-01.)
ArticleCitations
Molecular Cytogenetic Characterization of Rare but Repeatedly Observed Inversions in German Population18
Runs of Homozygosity Decipher Genetic Diversity in Cattle Breed Dwelling in the Colder Regions of the World9
The Parental Centromere Sizes Remain Unaltered in Allopolyploid Wheat-Rye Hybrids7
Epigenetic Clocks: In Aging-Related and Complex Diseases6
International Comparison Exercise for Biological Dosimetry after Exposures with Neutrons Performed at Two Irradiation Facilities as Part of the BALANCE Project6
Front & Back Matter6
Meiotic Segregation of an Isodicentric Derived from Chromosome 15 in Sperm of a Patient with Mosaic Karyotype: Case Report and Review of the Literature5
Downregulation of lncRNA FOXD2-AS1 Confers Radiosensitivity to Gastric Cancer Cells via miR-1913/SETD1A Axis5
Whole-Exome Sequencing Targeting a Gene Panel for Sensorineural Hearing Loss: The First Portuguese Cohort Study4
scRepli-Seq: A Powerful Tool to Study Replication Timing and Genome Instability3
A Paternal "Balanced" Chromosome 2 and 4 Translocation with Chromosome 21q Insertion Leading to Duplication of 2q22.1q24.1 in Two Siblings3
Genotype-Phenotype Correlation of Distal 2q37 Deletions3
Somatic Variants and Exon-Level Copy Number Changes in Five Hyperplastic Oral Leukoplakias3
Germline-Restricted Chromosomes and Autosomal Variants Revealed by Pachytene Karyotyping of 17 Avian Species3
Diversity and Evolution of Highly Repetitive DNA Sequences Constituting Chromosome Site-Specific Heterochromatin in Two Gerbillinae Species2
Low-Level Germline 48,XYY,+21 Mosaicism Associated with Transient Abnormal Myelopoiesis in a Phenotypically Normal Neonate2
Candidate Gene Expression in Regional Population and Its Relevance for Radiation Triage2
Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions2
Applicability of Scoring Calyculin A-Induced Premature Chromosome Condensation Objects for Dose Assessment Including for Radiotherapy Patients2
Cytogenetic Mapping of Cattle BAC Probes for the Hypothetical Ancestral Karyotype of the Family Cervidae2
Acknowledgement to Reviewers2
Fourth Report on Chicken Genes and Chromosomes 20222
Front & Back Matter2
Identification of Key Genes from the Visceral Adipose Tissues of Overweight/Obese Adults with Hypertension through Transcriptome Sequencing2
Recurrent Mutations in Refractory/Relapsed Diffuse Large B-Cell Lymphoma by Targeted Gene Sequencing2
B-Cell Acute Lymphoblastic Leukemia with iAMP21 in a Patient with Constitutional Ring Chromosome 212
Xp22.33p22.13 Duplication in a Male Patient Carrying a Recombinant X Chromosome Derived from an Inherited Intrachromosomal Insertion1
Tracking Chromosomal Origins in the Northern Italy System of Metacentric Races of the House Mouse1
Tandem Triplication 11p15.5-ICR1 (H19/IGF2) Detected by Microarray and Optical Genome Mapping in a Prenatal Beckwith-Wiedemann Case1
Nucleotide Sequence and Chromosome Mapping of 5S Ribosomal DNA from the Dojo Loach, Misgurnus anguillicaudatus1
Front & Back Matter1
Comparative Cytogenetic Analysis of Diploid and Triploid Pacific Abalone, <i>Haliotis discus hannai</i>1
Interstitial 2q24.2q24.3 Microdeletion: Two New Cases with Similar Clinical Features with the Exception of Profound Deafness1
Epileptic Encephalopathy with Variants in the PHACTR1 and AFF2 Genes: A Case Report1
Improved Basic Cytogenetics Challenges Holocentricity of Butterfly Chromosomes1
Interaction between m6A and ncRNAs and Its Association with Diseases1
Confirmation of Natural Hybridization between Kengyilia (StStYYPP) and Campeiostachys (StStYYHH) (Triticeae: Poaceae) Based on Morphological and Molecular Cytogenetic Analyses1
Repetitive DNA Mapping in Five Genera of Tree Frogs (Amphibia: Anura) from the Atlantic Forest: New Highlights on Genomic Organization in Hylidae1
Cytogenomic Analysis of Long-Term Epilepsy-Associated Tumors Using an Array-Based CGH Strategy1
Identification of Centromere-Specific Repeats in the Zebra Finch Genome1
Molecular Analysis of Parthenogenetic Chimerism in a 46,XX/46,XY Patient with Idiopathic Oligoasthenoteratozoospermia1
Shugoshin Regulates Cohesin, Kinetochore-Microtubule Attachments, and Chromosomal Instability1
Molecular Cytogenetic Characterization of C-Band-Positive Heterochromatin of the Greater Long-Tailed Hamster (Tscherskia triton, Cricetinae)1
Putative Condition-Dependent Viability Selection in Wild-Type Stocks of <b><i>Drosophila pseudoobscura</i></b>1
Isodicentric Y Chromosome with Multiple Breakpoints in the Pseudoautosomal Region 11
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<1
Cytogenetic Abnormalities in Multiple Myeloma: Incidence, Prognostic Significance, and Geographic Heterogeneity in Indian and Western Populations0
Sex as a Factor in Murine Radiation Research: Implications for Countermeasure Development0
Minimal Critical Region and Genes for a Typical Presentation of Langer-Giedion Syndrome0
The Molecular Mechanism of Aurora-B Regulating Kinetochore-Microtubule Attachment in Mitosis and Oocyte Meiosis0
Front & Back Matter0
Erratum0
Contents Vol. 162, 20220
The association between short telomere length and cardiovascular disease0
Optical Genome Mapping for a Patient with a Congenital Disorder and Chromosomal Translocation0
Transcriptional Analysis of Microsatellites in Velvetbean Caterpillar Anticarsia gemmatalis Hübner, 18180
Comparative Cytogenetics in Tyrannidae (Aves, Passeriformes): High Genetic Diversity despite Conserved Karyotype Organization0
Multiple Aneuploidy: First Report of a Patient Presenting with a Karyotype 45,X/48,XXX,+210
Simultaneous EYFP-CENH3/H2B-DsRed Expression Is Impaired Differentially in Meristematic and Differentiated Nuclei of Arabidopsis Double Transformants0
Biomarkers for Biodosimetry and Their Role in Predicting Radiation Injury0
Radiation Biodosimetry: Current Status and Future Initiatives0
Acknowledgement to Reviewers0
Frequency of Sex Chromosome Involvement in a Large Cohort of Subjects with Two Copy Number Variants0
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
Biased Clonal Evolution in Acute Promyelocytic Leukemia through Imbalances Affecting the der(17) but Not the der(15) Chromosome: Report of Two Cases0
Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy Loss0
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, China0
Revealing the Satellite DNA Content in <i>Ancistrus</i> sp. (Siluriformes: Loricariidae) by Genomic and Bioinformatic Analysis0
Front & Back Matter0
Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia0
Intersexual Twins due to Tetragametic Chimerism0
Prelims0
Identification of key genes and drug recommendations in diffuse large B-cell lymphoma based on analysis of glutathione-related genes0
Comparison of Isolated Lymphocyte and Whole Blood-Based CBMN Assays for Radiation Triage0
Effect of Age and Sex on Gene Expression-Based Radiation Biodosimetry Using Mouse Peripheral Blood0
Front & Back Matter0
Comparative Studies of Karyotypes in the Cervidae Family0
A detailed karyological investigation of three endemic Cobitis L. 1758 species (Teleostei, Cobitidae) in Anatolia, Türkiye0
Karyotypic Reshuffling in the Genus Rhipidomys (Rodentia: Cricetidae: Sigmodontinae) Revealed by Zoo-FISH0
The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems0
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
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 Process0
Prenatal Diagnosis of Fetuses with 4q35 Deletion: Case Series and Review of the Literature0
Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders0
Cohesin <b><i>RAD21</i></b> Gene Promoter Methylation Correlated with Better Prognosis in Breast Cancer Patients0
Contents Vol.163, 20230
Association of Leukocyte Telomere Length and the Risk of Disease Severity and Metabolic Comorbidities in Arab Patients with Psoriasis0
A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family0
The Neo-X Does Not Form a Barr Body but Shows a Slightly Condensed Structure in the Okinawa Spiny Rat (Tokudaia muenninki)0
Spaghetti Connections: Synaptonemal Complexes as a Tool to Explore Chromosome Structure, Evolution, and Meiotic Behavior in Fish0
Whole-Genome Sequencing Reveals a Novel Pathogenic GRIN2B Variant in a Patient with Neurodevelopmental Disorder and an inv(6)(p24p11.2)pat0
Hidden Y Chromosome Material and Congenital Cardiovascular Malformations in a Cohort of Turner Syndrome Patients with 45,X Blood Karyotype0
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
Assessment of Micronuclei Frequency in the Peripheral Blood of Adult and Pediatric Patients Receiving Fractionated Total Body Irradiation0
Karyotype Evolution of Talking Thorny Catfishes Anadoras (Doradidae, Astrodoradinae): A Process Mediated by Structural Rearrangements and Intense Reorganization of Repetitive DNAs0
Chromosomal Evolution of Suboscines: Karyotype Diversity and Evolutionary Trends in Ovenbirds (Passeriformes, Furnariidae)0
Insights on the Radiation-Induced Adaptive Response at the Cellular Level and Its Implications in Cancer Therapy0
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024)0
Erratum0
Heterozygous Deletion of Long Noncoding RNA AK127244 Is a Susceptibility Factor for Neurodevelopmental Delay0
Clinical Findings in a Series of Thirty Eight Patients with Williams-Beuren Syndrome0
Delineating the W Sex Chromosome in the Clam Shrimp, Eulimnadia texana0
SHOX Whole Gene Duplications Are Overrepresented in SHOX Haploinsufficiency Phenotype Cohorts0
Patient with Mosaic Turner Syndrome and a Derivative X Chromosome with a Variant Triple X Diagnosis in Fetus: A Case Report0
First Karyotypic Insights into <i>Potamotrygon schroederi</i> Fernández-Yépez, 1958: Association of Different Classes of Repetitive DNA0
Loss of One X and the Y Chromosome Changes the Configuration of the X Inactivation Center in the Genus <i>Tokudaia</i>0
Y Chromosome Genomic Variations and Biological Significance in Human Diseases and Health0
Incidence and Types of Fetal Chromosomal Abnormalities in First Trimester of Thai Pregnant Women between Miscarriages and Intrauterine Survivals0
Front & Back Matter0
Prelims0
In silico Characterization of Satellitomes and Cross-Amplification of Putative satDNAs in Two Species of the Hypostomus ancistroides Complex (Siluriformes, Loricariidae)0
Girl-Boy Twins with Developmental Delay from 16p11.2 Triplication due to Biparental Inheritance from Two Parents with 16p11.2 Duplication0
Prelims0
Retrospective Evaluation of Cytogenetic Effects Induced by Internal Radioiodine Exposure: A 27-Year Follow-Up Study0
Genome Mapping Nomenclature0
Accurate Identification of Breakpoints in a Cryptic Reciprocal Translocation by Whole-Genome Sequencing0
Ionizing Radiation-Induced DNA Damage Response in Primary Melanocytes and Keratinocytes of Human Skin0
New Karyotype Information for Ctenomys (Rodentia: Ctenomyidae) from Midwest and Northern Brazil0
The New Mitogenome of Erpornis zantholeuca (Aves: Passeriformes): Sequence, Structure, and Phylogenetic Analyses0
Application of the Cytokinesis-Block Micronucleus Assay for High-Dose Exposures Using Imaging Flow Cytometry0
Complex congenital cardiac defect associated with the combination of 5p deletion and 4q duplication in a newborn: A case report0
Large Chromosome 2p Duplication-Associated Mechanisms and Clinical Presentations0
Addenda to ISCN 20200
Radiation-Induced Gene Expression Changes Used for Biodosimetry and Clinical Outcome Prediction: Challenges and Promises0
Analysis of Chromosome Test Results of 24,175 Miscarried Fetuses in Japan from 2000 to 20210
Front & Back Matter0
Paper-Based Vertical Flow Immunoassay for the Point-of-Care Multiplex Detection of Radiation Dosimetry Genes0
Front & Back Matter0
Robertsonian Fusion Site in Rineloricaria pentamaculata (Siluriformes: Loricariidae): Involvement of 5S Ribosomal DNA and Satellite Sequences0
The NIAID/RNCP Biodosimetry Program: An Overview0
The Legacy of George M. Martin: From Segmental Progeroid Syndromes to Antigeroid Syndromes0
Exploring the Role of Extrachromosomal Circular DNA in Human Diseases0
Novel 10q21.1-q22.1 Duplication in a Boy with Minor Facial Dysmorphism, Mild Intellectual Disability, Autism Spectrum Disorder-Like Phenotype, and Short Stature0
Comparative Somatic Variant Analysis of a Rare Case with Concurrent Oral Leukoplakia and Oral Submucosal Fibrosis0
Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China0
Dosage Effect of the Ph1 Locus on Homologous Crossovers in a Segment of Chromosome 1B of Bread Wheat (Triticum aestivum L.)0
A Novel Partial Deletion of the TBL1XR1 Gene Detected Using SNP Array in a Patient with Motor Delay, Growth Failure, and Klinefelter Syndrome0
Cytogenetic Analysis of the Fungus-Farming Ant Cyphomyrmex rimosus (Spinola, 1851) (Formicidae: Myrmicinae: Attini) Highlights Karyotypic Variation0
Fluorescence in situ Hybridization Analysis of Oligonucleotide 5S Ribosomal DNA, 45S Ribosomal DNA, and (TTTAGGG)3 Locations in Gloriosa superba L.0
Front & Back Matter0
Cytogenomic characterization of murine osteosarcoma cell line SEWA0
Genomic Features of Interstitial Deletions of Chromosome 9q in Acute Myeloid Leukemia0
Retraction Statement0
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