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 2020-04-01 to 2024-04-01.)
ArticleCitations
One Hundred Years of Gene Balance: How Stoichiometric Issues Affect Gene Expression, Genome Evolution, and Quantitative Traits28
International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts18
Cytogenetic Analysis of the Products of Conception After Spontaneous Abortion in the First Trimester12
Fourth Report on Chicken Genes and Chromosomes 202211
G-Quadruplex Assembly by Ribosomal DNA: Emerging Roles in Disease Pathogenesis and Cancer Biology11
Re: International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts, by T. Liehr11
Destabilizing Effects of Ionizing Radiation on Chromosomes: Sizing up the Damage9
Human RecQL4 as a Novel Molecular Target for Cancer Therapy9
Downregulation of lncRNA FOXD2-AS1 Confers Radiosensitivity to Gastric Cancer Cells via miR-1913/SETD1A Axis8
Circ_ROBO2/miR-149 Axis Promotes the Proliferation and Migration of Human Aortic Smooth Muscle Cells by Activating NF-κB Signaling7
Deciphering the Mechanism of Glyphosate Resistance in <b><i>Amaranthus palmeri</i></b> by Cytogenomics7
Characterization of Nucleotide Binding ­Site-Encoding Genes in Sweetpotato, <b><i>Ipomoea batatas</i></b>(L.) Lam., and Their Response to Biotic and Abiotic Stresses7
Cytogenetic Damage of Human Lymphocytes in Humanized Mice Exposed to Neutrons and X Rays 24 h After Exposure6
Crosstalk among DNA Damage, Mitochondrial Dysfunction, Impaired Mitophagy, Stem Cell Attrition, and Senescence in the Accelerated Ageing Disorder Werner Syndrome6
Differential DNA Methylation of the IMMP2L Gene in Families with Maternally Inherited 7q31.1 Microdeletions is Associated with Intellectual Disability and Developmental Delay6
Camptothecin-Induced Replication Stress Affects DNA Replication Profiling by E/L Repli-Seq5
Cytogenetic Analysis of <b><i>Panaqolus tankei</i></b> Cramer &amp; Sousa, 2016 (Siluriformes, Loricariidae), an Ornamental Fish Endemic to Xingu River, Brazil5
Chromosomal Analysis of <b><i>Ctenolucius hujeta</i></b> Valenciennes, 1850 (Characiformes): A New Piece in the Chromosomal Evolution of the Ctenoluciidae5
Characterization of Each St and Y Genome Chromosome of Roegneria grandis Based on Newly Developed FISH Markers5
<b><i>RAP1GAP</i></b> Functions as a Tumor Suppressor Gene and Is Regulated by DNA Methylation in Differentiated Thyroid Cancer4
Uterine Leiomyomas with an Apparently Normal Karyotype Comprise Minor Heteroploid Subpopulations Differently Represented in vivo and in vitro4
Analysis of Genetic Alterations Related to DNA Methylation in Testicular Germ Cell Tumors Based on Data Mining4
Interaction between m6A and ncRNAs and Its Association with Diseases4
The microRNA-210/Casp8ap2 Axis Alleviates Hypoxia-Induced Myocardial Injury by Regulating Apoptosis and Autophagy4
FISH Identifies Chromosome Differentiation Between Contemporary Genomes of Wild Types and the Ancestral Genome of Unisexual Clones of Dojo Loach, <b><i>Misgurnus anguillicaudatus</i>4
Evolution of Sex Chromosome Heteromorphy in Geographic Populations of the Japanese Tago’s Brown Frog Complex4
Comparative Cytogenetics in Four <b><i>Leptodactylus</i></b> Species (Amphibia, Anura, Leptodactylidae): Evidence of Inner Chromosomal Diversification in Highly Conserved Karyo4
Evolutionary Mechanisms of Cancer Suggest Rational Therapeutic Approaches4
A New Variant B Chromosome in Auchenipteridae: The Role of (GATA)<sub>n</sub> and (TTAGGG)<sub>n</sub> Sequences in Understanding the Evolution of Supernumeraries in <b>&4
Comparative Cytogenetic Analysis of Three Eumeninae Species (Hymenoptera, Vespidae)3
Epigenetic Clocks: In Aging-Related and Complex Diseases3
PinX1 Depletion Improves Liver Injury in a Mouse Model of Nonalcoholic Fatty Liver Disease via Increasing Telomerase Activity and Inhibiting Apoptosis3
Evolution of Tandemly Arranged Repetitive DNAs in Three Species of Cyprinoidei with Different Ploidy Levels3
Intragenic Deletion of the <b><i>ZMYND11</i></b> Gene in 10p15.3 is Associated with Developmental Delay Phenotype: A Case Report3
Female Reproductive Ageing and Chromosomal Abnormalities in a Large Series of Women Undergoing IVF3
SINE-B1 Distribution and Chromosome Rearrangements in the South American <b><i>Proechimys</i></b> gr. <b><i>goeldii</i></b> (Echimyidae, Rodentia)2
Methylation Status of the miR-141-3p Promoter Regulates miR-141-3p Expression, Inflammasome Formation, and the Invasiveness of HTR-8/SVneo Cells2
Telomerase-Positive Somatic Tissues of Honeybee Queens <b><i>(Apis mellifera)</i></b> Display No DNA Replication2
Effect of Age and Sex on Gene Expression-Based Radiation Biodosimetry Using Mouse Peripheral Blood2
Anti-Proliferative Effects of E2F1 Suppression in Glioblastoma Cells2
Multicolor-FISH Characterization of a Prenatal Mosaicism for a Chromosomal Rearrangement Undetected by Molecular Cytogenetics2
Skewed X-Chromosome Inactivation as a Possible Marker of X-Linked CNV in Women with Pregnancy Loss2
Molecular Cytogenetic Classification of Down Syndrome and Screening of Somatic Aneuploidy in Mothers2
Robertsonian Fusion Site in Rineloricaria pentamaculata (Siluriformes: Loricariidae): Involvement of 5S Ribosomal DNA and Satellite Sequences2
Novel <b><i>SNX13</i></b> Frameshift Variant in an Individual with Developmental Delay2
Silencing of miR-1246 Induces Cell Cycle Arrest and Apoptosis in Cisplatin-Resistant Ovarian Cancer Cells by Promoting <b><i>ZNF23</i></b> Transcription2
Cytogenetic Mapping of Cattle BAC Probes for the Hypothetical Ancestral Karyotype of the Family Cervidae2
Chromosome Mapping of U2 snDNA in Species of <b><i>Leptodactylus</i></b> (Anura, Leptodactylidae)2
Ionizing Radiation-Induced DNA Damage Response in Primary Melanocytes and Keratinocytes of Human Skin2
Comparative Somatic Variant Analysis of a Rare Case with Concurrent Oral Leukoplakia and Oral Submucosal Fibrosis2
Cohesin <b><i>RAD21</i></b> Gene Promoter Methylation Correlated with Better Prognosis in Breast Cancer Patients2
Comparative Studies of Karyotypes in the Cervidae Family2
Germline-Restricted Chromosomes and Autosomal Variants Revealed by Pachytene Karyotyping of 17 Avian Species2
Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions1
Identification of Key Genes from the Visceral Adipose Tissues of Overweight/Obese Adults with Hypertension through Transcriptome Sequencing1
Chromosome Painting in Lonchorhina aurita Sheds Light onto the Controversial Phylogenetic Position of Sword-Nosed Bats (Chiroptera, Phyllostomidae)1
A Heterozygous Variant of FGF13 Caused X-Linked Developmental and Epileptic Encephalopathy 90 in a Chinese Family1
Sex as a Factor in Murine Radiation Research: Implications for Countermeasure Development1
Cleft Lip Palate in a Patient with 5q14.3 Deletion Syndrome: A Possible Unreported Feature?1
Higher Intercellular Variation in Genome-Wide Recombination Rate in Female Mice1
Epileptic Encephalopathy with Variants in the PHACTR1 and AFF2 Genes: A Case Report1
miR-3929 Inhibits Proliferation and Promotes Apoptosis by Downregulating Cripto-1 Expression in Cervical Cancer Cells1
An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.31
International Comparison Exercise for Biological Dosimetry after Exposures with Neutrons Performed at Two Irradiation Facilities as Part of the BALANCE Project1
Identification of Chromosome 17 Trisomy in a Cynomolgus Monkey (<b><i>Macaca fascicularis</i></b>) by Multicolor FISH Techniques1
Erratum1
Genome Mapping Nomenclature1
Chromosomal Instability and Origin of B Chromosomes in the Amazonian Glass Tetra <b><i>Moenkhausia oligolepis</i></b> (Günther, 1864) (Characiformes, Characidae)1
Addenda to ISCN 20201
Molecular Cytogenetic Characterization of C-Band-Positive Heterochromatin of the Greater Long-Tailed Hamster (Tscherskia triton, Cricetinae)1
Nucleotide Sequence and Chromosome Mapping of 5S Ribosomal DNA from the Dojo Loach, Misgurnus anguillicaudatus1
Chromosome Evolution in the Genus Partamona (Apidae: Meliponini), with Comments on B Chromosome Origin1
Clinical Features of de novo Pure 16q21q24.1 Chromosome Duplication1
<b><i>Mus musculus</i></b> Barrier-To-Autointegration Factor 2 (<b><i>Banf2</i></b>) is Not Essential for Spermatogenesis or Fertility1
Coexistence of a Homozygous Chromosome 4q35.2 Deletion and Hidden <b><i>IQSEC2</i></b> Pathogenic Variant in a Child with Intellectual Disability1
Homogeneously Staining Regions (HSR) in Chromosome 1 of the House Mouse: Synapsis and Recombination at Meiosis1
FISH-Based Karyotype Analyses of Four <b><i>Dracaena</i></b> Species1
MDS/MPN-Unclassifiable with t(X;17)(q28;q21) and <b><i>KANSL1-MTCP1/CMC4</i></b> Fusion Gene1
Confirmation of Natural Hybridization between Kengyilia (StStYYPP) and Campeiostachys (StStYYHH) (Triticeae: Poaceae) Based on Morphological and Molecular Cytogenetic Analyses1
Improved Basic Cytogenetics Challenges Holocentricity of Butterfly Chromosomes1
Front & Back Matter0
Novel Centromeric and Subtelomeric Repetitive DNA Sequences for Karyotyping the Bambara Groundnut (<b><i>Vigna subterranea</i></b> L. Verdc.)0
New Karyotype Information for Ctenomys (Rodentia: Ctenomyidae) from Midwest and Northern Brazil0
Preface0
Front & Back Matter0
Low-Level Germline 48,XYY,+21 Mosaicism Associated with Transient Abnormal Myelopoiesis in a Phenotypically Normal Neonate0
Front & Back Matter0
Application of Restriction Site-Associated DNA Sequencing (RAD-Seq) for Copy Number Variation and Triploidy Detection in Human0
Preface0
Repetitive DNA Mapping in Five Genera of Tree Frogs (Amphibia: Anura) from the Atlantic Forest: New Highlights on Genomic Organization in Hylidae0
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
Optical Genome Mapping for a Patient with a Congenital Disorder and Chromosomal Translocation0
Tandem Triplication 11p15.5-ICR1 (H19/IGF2) Detected by Microarray and Optical Genome Mapping in a Prenatal Beckwith-Wiedemann Case0
Accurate Identification of Breakpoints in a Cryptic Reciprocal Translocation by Whole-Genome Sequencing0
SHOX Whole Gene Duplications Are Overrepresented in SHOX Haploinsufficiency Phenotype Cohorts0
Cytogenomic Analysis of Long-Term Epilepsy-Associated Tumors Using an Array-Based CGH Strategy0
The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems0
Tracking Chromosomal Origins in the Northern Italy System of Metacentric Races of the House Mouse0
Patient with Mosaic Turner Syndrome and a Derivative X Chromosome with a Variant Triple X Diagnosis in Fetus: A Case Report0
Hidden Y Chromosome Material and Congenital Cardiovascular Malformations in a Cohort of Turner Syndrome Patients with 45,X Blood Karyotype0
Interstitial 2q24.2q24.3 Microdeletion: Two New Cases with Similar Clinical Features with the Exception of Profound Deafness0
Intersexual Twins due to Tetragametic Chimerism0
Incidence and Types of Fetal Chromosomal Abnormalities in First Trimester of Thai Pregnant Women between Miscarriages and Intrauterine Survivals0
Genomic Chaos (Multiple Copy Number Variations and Structural Reorganization) Detected in Two Prenatal Cases0
Comparative cytogenetics in Tyrannidae (Aves, Passeriformes): High genetic diversity despite conserved karyotype organization0
Author Index0
Front & Back Matter0
Diversity and Evolution of Highly Repetitive DNA Sequences Constituting Chromosome Site-Specific Heterochromatin in Two Gerbillinae Species0
Assessment of Micronuclei Frequency in the Peripheral Blood of Adult and Pediatric Patients Receiving Fractionated Total Body Irradiation0
Prelims0
Whole-Exome Sequencing Targeting a Gene Panel for Sensorineural Hearing Loss: The First Portuguese Cohort Study0
Spaghetti connections: synaptonemal complexes as a tool to explore chromosome structure, evolution, and meiotic behavior in fish0
Front & Back Matter0
The Neo-X Does Not Form a Barr Body but Shows a Slightly Condensed Structure in the Okinawa Spiny Rat (Tokudaia muenninki)0
Genotype-Phenotype Correlation of Distal 2q37 Deletions0
Erratum0
Y Chromosome Genomic Variations and Biological Significance in Human Diseases and Health0
The NIAID/RNCP Biodosimetry Program: An Overview0
Front & Back Matter0
Front & Back Matter0
Subject Index Vol. 161, No. 6-7, 20210
Front & Back Matter0
Meiotic Segregation of an Isodicentric Derived from Chromosome 15 in Sperm of a Patient with Mosaic Karyotype: Case Report and Review of the Literature0
The New Mitogenome of Erpornis zantholeuca (Aves: Passeriformes): Sequence, Structure, and Phylogenetic Analyses0
A Novel Partial Deletion of the TBL1XR1 Gene Detected Using SNP Array in a Patient with Motor Delay, Growth Failure, and Klinefelter Syndrome0
Prelims0
Candidate Gene Expression in Regional Population and Its Relevance for Radiation Triage0
Insights on the Radiation-Induced Adaptive Response at the Cellular Level and Its Implications in Cancer Therapy0
Expanding the Clinical and Molecular Spectrum of FOXG1- and ZBTB18-Associated Neurodevelopmental Disorders0
Front & Back Matter0
Cytogenetic Abnormalities in Multiple Myeloma: Incidence, Prognostic Significance, and Geographic Heterogeneity in Indian and Western Populations0
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
Retraction Statement0
Retrospective Evaluation of Cytogenetic Effects Induced by Internal Radioiodine Exposure: A 27-Year Follow-Up Study0
Putative Condition-Dependent Viability Selection in Wild-Type Stocks of <b><i>Drosophila pseudoobscura</i></b>0
Contents Vol. 162, 20220
Author Index Vol. 161, No. 6-7, 20210
Front & Back Matter0
Tandem Repeat-Based Probes Support the Loop Model of Pericentromere Packing0
Expression of Concern0
Front & Back Matter0
The Legacy of George M. Martin: From Segmental Progeroid Syndromes to Antigeroid Syndromes0
Prelims0
Erratum0
Somatic Variants and Exon-Level Copy Number Changes in Five Hyperplastic Oral Leukoplakias0
Radiation Biodosimetry: Current Status and Future Initiatives0
Cytogenetic Analysis of the Fungus-Farming Ant Cyphomyrmex rimosus (Spinola, 1851) (Formicidae: Myrmicinae: Attini) Highlights Karyotypic Variation0
Retraction Statement0
Prenatal Genetic Diagnosis of Fetal Cystic Hygroma: A Retrospective Single-Center Study from China0
Front & Back Matter0
Frequency of Sex Chromosome Involvement in a Large Cohort of Subjects with Two Copy Number Variants0
Applicability of Scoring Calyculin A-Induced Premature Chromosome Condensation Objects for Dose Assessment Including for Radiotherapy Patients0
Minimal Critical Region and Genes for a Typical Presentation of Langer-Giedion Syndrome0
Genomic Features of Interstitial Deletions of Chromosome 9q in Acute Myeloid Leukemia0
Paper-Based Vertical Flow Immunoassay for the Point-of-Care Multiplex Detection of Radiation Dosimetry Genes0
Front & Back Matter0
A Paternal &quot;Balanced&quot; Chromosome 2 and 4 Translocation with Chromosome 21q Insertion Leading to Duplication of 2q22.1q24.1 in Two Siblings0
Chromosomal Evolution of Suboscines: Karyotype Diversity and Evolutionary Trends in Ovenbirds (Passeriformes, Furnariidae)0
Large Chromosome 2p Duplication-Associated Mechanisms and Clinical Presentations0
scRepli-Seq: A Powerful Tool to Study Replication Timing and Genome Instability0
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
Karyotype Evolution of Talking Thorny Catfishes Anadoras (Doradidae, Astrodoradinae): A Process Mediated by Structural Rearrangements and Intense Reorganization of Repetitive DNAs0
Contents Col. 161, 20210
Xp22.33p22.13 Duplication in a Male Patient Carrying a Recombinant X Chromosome Derived from an Inherited Intrachromosomal Insertion0
Front & Back Matter0
Simultaneous EYFP-CENH3/H2B-DsRed Expression Is Impaired Differentially in Meristematic and Differentiated Nuclei of Arabidopsis Double Transformants0
Shugoshin Regulates Cohesin, Kinetochore-Microtubule Attachments, and Chromosomal Instability0
Heterozygous Deletion of Long Noncoding RNA AK127244 Is a Susceptibility Factor for Neurodevelopmental Delay0
Comparative Cytogenetic Analysis of Diploid and Triploid Pacific Abalone, <i>Haliotis discus hannai</i>0
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
Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia0
Identification of Centromere-Specific Repeats in the Zebra Finch Genome0
Front & Back Matter0
Subject Index0
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
Girl-Boy Twins with Developmental Delay from 16p11.2 Triplication due to Biparental Inheritance from Two Parents with 16p11.2 Duplication0
Transcriptional Analysis of Microsatellites in Velvetbean Caterpillar Anticarsia gemmatalis Hübner, 18180
Front & Back Matter0
Radiation-Induced Gene Expression Changes Used for Biodosimetry and Clinical Outcome Prediction: Challenges and Promises0
Comparison of Isolated Lymphocyte and Whole Blood-Based CBMN Assays for Radiation Triage0
Biased Clonal Evolution in Acute Promyelocytic Leukemia through Imbalances Affecting the der(17) but Not the der(15) Chromosome: Report of Two Cases0
Recurrent Mutations in Refractory/Relapsed Diffuse Large B-Cell Lymphoma by Targeted Gene Sequencing0
Application of the Cytokinesis-Block Micronucleus Assay for High-Dose Exposures Using Imaging Flow Cytometry0
Front & Back Matter0
B-Cell Acute Lymphoblastic Leukemia with iAMP21 in a Patient with Constitutional Ring Chromosome 210
Molecular Cytogenetic Characterization of the Murine Melanoma Cell Lines S91 Clone M3 and B16-F1 with Variant B16-4A50
Prelims0
Biomarkers for Biodosimetry and Their Role in Predicting Radiation Injury0
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