Trends in Genetics

Papers
(The TQCC of Trends in Genetics is 15. 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 2020-07-01 to 2024-07-01.)
ArticleCitations
Navigating the DNA methylation landscape of cancer356
Emerging concepts of miRNA therapeutics: from cells to clinic284
DNA methylation: a historical perspective232
Mammalian SWI/SNF Chromatin Remodeling Complexes: Emerging Mechanisms and Therapeutic Strategies198
Where Are the Disease-Associated eQTLs?179
DNA Repair Pathway Choices in CRISPR-Cas9-Mediated Genome Editing142
To NMD or Not To NMD: Nonsense-Mediated mRNA Decay in Cancer and Other Genetic Diseases128
Crosstalk between epitranscriptomic and epigenetic mechanisms in gene regulation119
Histone Ubiquitination: An Integrative Signaling Platform in Genome Stability114
Classical and noncanonical functions of miRNAs in cancers102
Horizontal Gene Transfer in Eukaryotes: Not if, but How Much?93
Retention of duplicated genes in evolution87
Fast-forward breeding for a food-secure world86
The Nexus of cfDNA and Nuclease Biology86
How genomics can help biodiversity conservation83
Polycomb Gene Silencing Mechanisms: PRC2 Chromatin Targeting, H3K27me3 'Readout', and Phase Separation-Based Compaction81
Hotspots of Human Mutation78
The p53 network: cellular and systemic DNA damage responses in cancer and aging77
Taming transposable elements in vertebrates: from epigenetic silencing to domestication72
Anything but Ordinary – Emerging Splicing Mechanisms in Eukaryotic Gene Regulation71
Extrachromosomal circular DNA in cancer: history, current knowledge, and methods71
The Role of Noncoding Variants in Heritable Disease71
Transposable Elements: A Common Feature of Neurodevelopmental and Neurodegenerative Disorders68
Forkhead Transcription Factors in Health and Disease67
Relaxed Selection and the Rapid Evolution of Reproductive Genes67
Mitochondrial Diseases: A Diagnostic Revolution67
Genetic prediction of complex traits with polygenic scores: a statistical review65
Towards a Human Cell Atlas: Taking Notes from the Past63
Genetic Lesions of Type I Interferon Signalling in Human Antiviral Immunity59
The Branched Nature of the Nonsense-Mediated mRNA Decay Pathway59
Into the multiverse: advances in single-cell multiomic profiling56
New Approaches for Inferring Phylogenies in the Presence of Paralogs54
Impact of Parental Exposure on Offspring Health in Humans54
Histone lactylation: epigenetic mark of glycolytic switch54
Termination of Transcription by RNA Polymerase II: BOOM!54
Beyond sequencing: machine learning algorithms extract biology hidden in Nanopore signal data52
The multifaceted effects of YTHDC1-mediated nuclear m6A recognition52
Transcriptional Silencers: Driving Gene Expression with the Brakes On51
Evolutionary cell type mapping with single-cell genomics51
Role of Polycomb in the control of transposable elements50
Functions of PIWI Proteins in Gene Regulation: New Arrows Added to the piRNA Quiver50
Transcriptional Regulation at DSBs: Mechanisms and Consequences48
Nonhomologous end joining: new accessory factors fine tune the machinery48
Therapeutic and prognostic insights from the analysis of cancer mutational signatures46
Host Polymorphisms May Impact SARS-CoV-2 Infectivity45
Deconstructing Sonic Hedgehog Medulloblastoma: Molecular Subtypes, Drivers, and Beyond45
Insights from multi-omics integration in complex disease primary tissues44
Polygenic Adaptation: Integrating Population Genetics and Gene Regulatory Networks44
ADAR1 and its implications in cancer development and treatment42
Epigenetic Regulators as the Gatekeepers of Hematopoiesis42
Speed–Specificity Trade-Offs in the Transcription Factors Search for Their Genomic Binding Sites41
From QTL to gene: C. elegans facilitates discoveries of the genetic mechanisms underlying natural variation40
A TAD Skeptic: Is 3D Genome Topology Conserved?40
Gene Regulation and Cellular Metabolism: An Essential Partnership39
Base Editing Landscape Extends to Perform Transversion Mutation39
Emerging functions of circular RNA in aging39
WRKY transcription factors in plant defense38
Genome structural variation in human evolution38
DNA Damage Triggers a New Phase in Neurodegeneration38
Bridging biological cfDNA features and machine learning approaches38
Somatic mutations provide important and unique insights into the biology of complex diseases37
Symbionts and gene drive: two strategies to combat vector-borne disease36
Spotlight on the Replisome: Aetiology of DNA Replication-Associated Genetic Diseases36
Facilitating Complex Trait Analysis via Reduced Complexity Crosses36
Molecular Clocks without Rocks: New Solutions for Old Problems35
Exploring the Alternative Splicing of Long Noncoding RNAs35
Noncanonical DNA structures are drivers of genome evolution35
Epimutations Define a Fast-Ticking Molecular Clock in Plants35
The Y Chromosome as a Battleground for Intragenomic Conflict34
Superspreading in the emergence of COVID-19 variants32
Plant Genetic Networks Shaping Phyllosphere Microbial Community32
Anticipating and Identifying Collateral Damage in Genome Editing32
APOBECs orchestrate genomic and epigenomic editing across health and disease31
Taming the Turmoil Within: New Insights on the Containment of Transposable Elements30
RNA Editing in Mitochondria and Plastids: Weird and Widespread30
Hybrid sterility genes in mice (Mus musculus): a peculiar case of PRDM9 incompatibility30
Site-Specific Recombination – How Simple DNA Inversions Produce Complex Phenotypic Heterogeneity in Bacterial Populations30
State-of-the-art CRISPR for in vivo and cell-based studies in Drosophila29
Evolution of Diverse Strategies for Promoter Regulation29
The era of 3D and spatial genomics29
Networks of Resistance: Small RNA Control of Antibiotic Resistance29
Genetic and epigenetic defects of the RNA modification machinery in cancer29
A devil's bargain with transposable elements in plant pathogens29
Break-induced replication: unraveling each step28
DNA Damage Response and Metabolic Reprogramming in Health and Disease28
Optogenetics for transcriptional programming and genetic engineering27
Deregulated Regulators: Disease-Causing cis Variants in Transcription Factor Genes27
Genomics in the long-read sequencing era27
Polycomb-dependent histone H2A ubiquitination links developmental disorders with cancer27
Intricacies of single-cell multi-omics data integration26
Mendelian randomization analyses for PCOS: evidence, opportunities, and challenges26
Multiple sclerosis: doubling down on MHC26
Future of DNA-based insect monitoring26
Principles of Epigenetic Homeostasis Shared Between Flowering Plants and Mammals26
Splicing to Keep Cycling: The Importance of Pre-mRNA Splicing during the Cell Cycle26
Genetic disorders of cellular trafficking26
The H2A.Z-nucleosome code in mammals: emerging functions26
The Toll gene in Drosophila pattern formation26
Elucidation of Biological Networks across Complex Diseases Using Single-Cell Omics25
Every gene can (and possibly will) be associated with cancer25
Metabolic Microenvironments Drive Microbial Differentiation and Antibiotic Resistance25
A decade of molecular cell atlases24
Genetics and Epigenetics of Sex Bias: Insights from Human Cancer and Autoimmunity24
Quo vadis microRNAs?24
Complex genomic rearrangements: an underestimated cause of rare diseases24
Advancing human disease research with fish evolutionary mutant models24
Underappreciated Roles of DNA Polymerase δ in Replication Stress Survival23
DNA N6-methyldeoxyadenosine in mammals and human disease23
Long Noncoding RNAs at the Crossroads of Cell Cycle and Genome Integrity23
All Creatures Great and Small: New Approaches for Understanding Down Syndrome Genetics23
Transcriptional and Epigenetic Regulation of Autophagy in Plants22
Emerging functions of mitochondria-encoded noncoding RNAs22
Emerging Insights into the Distinctive Neuronal Methylome22
Horizontal Gene Transfer in Vertebrates: A Fishy Tale22
ATRX, a guardian of chromatin22
Monarch Butterfly Migration Moving into the Genetic Era22
Uncovering the impact of noncoding variants in neurodegenerative brain diseases22
Mitochondrial genome engineering coming-of-age22
The evolution of the GALactose utilization pathway in budding yeasts22
Genetics in Light of Transcriptional Adaptation21
Unraveling the Epigenetic Basis of Liver Development, Regeneration and Disease21
iPSC-derived organ-on-a-chip models for personalized human genetics and pharmacogenomics studies21
Dynamic Chromatin Structure and Epigenetics Control the Fate of Malaria Parasites21
Throwing away DNA: programmed downsizing in somatic nuclei21
Feralization: Confronting the Complexity of Domestication and Evolution20
Intron retention: importance, challenges, and opportunities20
There is another: H3K27me3-mediated genomic imprinting20
Genetically transitional disease: a new concept in genomic medicine20
SWEET Genes for Disease Resistance in Plants20
The PDE-Opathies: Diverse Phenotypes Produced by a Functionally Related Multigene Family20
Biosensing Detection of the SARS-CoV-2 D614G Mutation20
Simple Repeats as Building Blocks for Genetic Computers19
'Fly-ing' from rare to common neurodegenerative disease mechanisms19
Machine learning approaches to explore digenic inheritance19
Meiotic Executioner Genes Protect the Y from Extinction19
Germline Variants That Affect Tumor Progression18
The sound of silence: mechanisms and implications of HUSH complex function18
First discovered, long out of sight, finally visible: ribosomal DNA18
SpRY: Engineered CRISPR/Cas9 Harnesses New Genome-Editing Power18
Regulatory mechanisms ensuring coordinated expression of functionally related genes18
Virus-Based CRISPR/Cas9 Genome Editing in Plants18
DNA base editing in nuclear and organellar genomes17
The cell as a bag of RNA17
Potato trait development going fast-forward with genome editing17
Evolutionary conservation in noncoding genomic regions17
A proposed metric set for evaluation of genome assembly quality16
Trash Talk: Mammalian Proteasome Regulation at the Transcriptional Level16
Sperm mosaicism: implications for genomic diversity and disease16
Biology in balance: human diploid genome integrity, gene dosage, and genomic medicine16
Mouse Genetic Reference Populations: Cellular Platforms for Integrative Systems Genetics16
Mediator Roles Going Beyond Transcription15
Phenotype-aware prioritisation of rare Mendelian disease variants15
Mitochondria and G-quadruplex evolution: an intertwined relationship15
Tissue specificity of DNA repair: the CRISPR compass15
Alternative Synaptonemal Complex Structures: Too Much of a Good Thing?15
miRNA biogenesis and inherited disorders: clinico-molecular insights15
Deciphering pathogenicity of variants of uncertain significance with CRISPR-edited iPSCs15
Current concepts, advances, and challenges in deciphering the human microbiota with metatranscriptomics15
Rare variants and the oligogenic architecture of autism15
Is CpG Density the Link between Epigenetic Aging and Lifespan?15
Genetic Variants Affecting Skeletal Morphology in Domestic Dogs15
Chromatin and Nuclear Architecture: Shaping DNA Replication in 3D15
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