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 2020-11-01 to 2024-11-01.)
ArticleCitations
Navigating the DNA methylation landscape of cancer425
Emerging concepts of miRNA therapeutics: from cells to clinic342
DNA methylation: a historical perspective290
Mammalian SWI/SNF Chromatin Remodeling Complexes: Emerging Mechanisms and Therapeutic Strategies226
Where Are the Disease-Associated eQTLs?198
DNA Repair Pathway Choices in CRISPR-Cas9-Mediated Genome Editing168
To NMD or Not To NMD: Nonsense-Mediated mRNA Decay in Cancer and Other Genetic Diseases142
Crosstalk between epitranscriptomic and epigenetic mechanisms in gene regulation131
Histone Ubiquitination: An Integrative Signaling Platform in Genome Stability123
How genomics can help biodiversity conservation115
Classical and noncanonical functions of miRNAs in cancers114
Horizontal Gene Transfer in Eukaryotes: Not if, but How Much?103
The Nexus of cfDNA and Nuclease Biology101
Retention of duplicated genes in evolution100
Fast-forward breeding for a food-secure world91
The p53 network: cellular and systemic DNA damage responses in cancer and aging89
Polycomb Gene Silencing Mechanisms: PRC2 Chromatin Targeting, H3K27me3 'Readout', and Phase Separation-Based Compaction89
Hotspots of Human Mutation83
Taming transposable elements in vertebrates: from epigenetic silencing to domestication81
Extrachromosomal circular DNA in cancer: history, current knowledge, and methods78
Anything but Ordinary – Emerging Splicing Mechanisms in Eukaryotic Gene Regulation75
The Role of Noncoding Variants in Heritable Disease75
Genetic prediction of complex traits with polygenic scores: a statistical review71
Histone lactylation: epigenetic mark of glycolytic switch71
Forkhead Transcription Factors in Health and Disease70
Towards a Human Cell Atlas: Taking Notes from the Past67
Genetic Lesions of Type I Interferon Signalling in Human Antiviral Immunity61
Into the multiverse: advances in single-cell multiomic profiling61
The Branched Nature of the Nonsense-Mediated mRNA Decay Pathway60
The multifaceted effects of YTHDC1-mediated nuclear m6A recognition58
Impact of Parental Exposure on Offspring Health in Humans57
Beyond sequencing: machine learning algorithms extract biology hidden in Nanopore signal data56
Evolutionary cell type mapping with single-cell genomics56
New Approaches for Inferring Phylogenies in the Presence of Paralogs56
Role of Polycomb in the control of transposable elements53
Functions of PIWI Proteins in Gene Regulation: New Arrows Added to the piRNA Quiver53
Nonhomologous end joining: new accessory factors fine tune the machinery52
Transcriptional Silencers: Driving Gene Expression with the Brakes On52
ADAR1 and its implications in cancer development and treatment51
Deconstructing Sonic Hedgehog Medulloblastoma: Molecular Subtypes, Drivers, and Beyond50
Gene Regulation and Cellular Metabolism: An Essential Partnership50
WRKY transcription factors in plant defense50
Transcriptional Regulation at DSBs: Mechanisms and Consequences49
Polygenic Adaptation: Integrating Population Genetics and Gene Regulatory Networks49
Insights from multi-omics integration in complex disease primary tissues48
Therapeutic and prognostic insights from the analysis of cancer mutational signatures48
Epigenetic Regulators as the Gatekeepers of Hematopoiesis47
Host Polymorphisms May Impact SARS-CoV-2 Infectivity46
Noncanonical DNA structures are drivers of genome evolution44
Speed–Specificity Trade-Offs in the Transcription Factors Search for Their Genomic Binding Sites44
Bridging biological cfDNA features and machine learning approaches43
Genetic and epigenetic defects of the RNA modification machinery in cancer43
DNA Damage Triggers a New Phase in Neurodegeneration43
A TAD Skeptic: Is 3D Genome Topology Conserved?42
Somatic mutations provide important and unique insights into the biology of complex diseases41
From QTL to gene: C. elegans facilitates discoveries of the genetic mechanisms underlying natural variation41
Symbionts and gene drive: two strategies to combat vector-borne disease41
Genomics in the long-read sequencing era40
Spotlight on the Replisome: Aetiology of DNA Replication-Associated Genetic Diseases40
Emerging functions of circular RNA in aging40
Epimutations Define a Fast-Ticking Molecular Clock in Plants39
Genome structural variation in human evolution39
Base Editing Landscape Extends to Perform Transversion Mutation39
Molecular Clocks without Rocks: New Solutions for Old Problems39
Exploring the Alternative Splicing of Long Noncoding RNAs38
Networks of Resistance: Small RNA Control of Antibiotic Resistance36
Genetic disorders of cellular trafficking35
The H2A.Z-nucleosome code in mammals: emerging functions35
Plant Genetic Networks Shaping Phyllosphere Microbial Community34
The era of 3D and spatial genomics34
APOBECs orchestrate genomic and epigenomic editing across health and disease33
RNA Editing in Mitochondria and Plastids: Weird and Widespread33
Break-induced replication: unraveling each step33
Superspreading in the emergence of COVID-19 variants33
Site-Specific Recombination – How Simple DNA Inversions Produce Complex Phenotypic Heterogeneity in Bacterial Populations33
Anticipating and Identifying Collateral Damage in Genome Editing32
Polycomb-dependent histone H2A ubiquitination links developmental disorders with cancer32
State-of-the-art CRISPR for in vivo and cell-based studies in Drosophila32
Mendelian randomization analyses for PCOS: evidence, opportunities, and challenges32
Future of DNA-based insect monitoring31
Optogenetics for transcriptional programming and genetic engineering31
Hybrid sterility genes in mice (Mus musculus): a peculiar case of PRDM9 incompatibility31
The Toll gene in Drosophila pattern formation30
Complex genomic rearrangements: an underestimated cause of rare diseases30
A devil's bargain with transposable elements in plant pathogens30
Evolution of Diverse Strategies for Promoter Regulation29
Intricacies of single-cell multi-omics data integration29
A decade of molecular cell atlases28
The sound of silence: mechanisms and implications of HUSH complex function28
Metabolic Microenvironments Drive Microbial Differentiation and Antibiotic Resistance28
Advancing human disease research with fish evolutionary mutant models27
Long Noncoding RNAs at the Crossroads of Cell Cycle and Genome Integrity27
ATRX, a guardian of chromatin27
Multiple sclerosis: doubling down on MHC27
DNA N6-methyldeoxyadenosine in mammals and human disease27
Splicing to Keep Cycling: The Importance of Pre-mRNA Splicing during the Cell Cycle27
Emerging functions of mitochondria-encoded noncoding RNAs26
iPSC-derived organ-on-a-chip models for personalized human genetics and pharmacogenomics studies25
Elucidation of Biological Networks across Complex Diseases Using Single-Cell Omics25
Uncovering the impact of noncoding variants in neurodegenerative brain diseases24
The evolution of the GALactose utilization pathway in budding yeasts24
Every gene can (and possibly will) be associated with cancer24
Horizontal Gene Transfer in Vertebrates: A Fishy Tale24
All Creatures Great and Small: New Approaches for Understanding Down Syndrome Genetics24
Genetics in Light of Transcriptional Adaptation23
Emerging Insights into the Distinctive Neuronal Methylome23
Genetically transitional disease: a new concept in genomic medicine23
Intron retention: importance, challenges, and opportunities23
Underappreciated Roles of DNA Polymerase δ in Replication Stress Survival23
There is another: H3K27me3-mediated genomic imprinting22
Mitochondria and G-quadruplex evolution: an intertwined relationship22
Dynamic Chromatin Structure and Epigenetics Control the Fate of Malaria Parasites22
Evolutionary conservation in noncoding genomic regions22
SWEET Genes for Disease Resistance in Plants22
The PDE-Opathies: Diverse Phenotypes Produced by a Functionally Related Multigene Family22
Mitochondrial genome engineering coming-of-age22
Throwing away DNA: programmed downsizing in somatic nuclei21
Regulatory mechanisms ensuring coordinated expression of functionally related genes21
Machine learning approaches to explore digenic inheritance20
First discovered, long out of sight, finally visible: ribosomal DNA20
Repetitive elements in aging and neurodegeneration20
Feralization: Confronting the Complexity of Domestication and Evolution20
Germline Variants That Affect Tumor Progression20
Biosensing Detection of the SARS-CoV-2 D614G Mutation20
DNA base editing in nuclear and organellar genomes20
Virus-Based CRISPR/Cas9 Genome Editing in Plants20
The cell as a bag of RNA19
miRNA biogenesis and inherited disorders: clinico-molecular insights19
Rare variants and the oligogenic architecture of autism19
'Fly-ing' from rare to common neurodegenerative disease mechanisms19
A proposed metric set for evaluation of genome assembly quality18
Mouse Genetic Reference Populations: Cellular Platforms for Integrative Systems Genetics18
Gene product diversity: adaptive or not?18
Potato trait development going fast-forward with genome editing18
Pioneer factors: roles and their regulation in development18
Alternative Synaptonemal Complex Structures: Too Much of a Good Thing?17
Biology in balance: human diploid genome integrity, gene dosage, and genomic medicine17
Sperm mosaicism: implications for genomic diversity and disease17
Trash Talk: Mammalian Proteasome Regulation at the Transcriptional Level16
Clinical progress in genome-editing technology and in vivo delivery techniques16
Breakage in breakage–fusion–bridge cycle: an 80-year-old mystery16
Deciphering pathogenicity of variants of uncertain significance with CRISPR-edited iPSCs16
Integration of DNA damage responses with dynamic spatial genome organization16
Selective Xi reactivation and alternative methods to restore MECP2 function in Rett syndrome16
Recursive Test of Hardy-Weinberg Equilibrium in Tetraploids16
Current concepts, advances, and challenges in deciphering the human microbiota with metatranscriptomics16
Autosomal Clonal Monoallelic Expression: Natural or Artifactual?16
Take a walk on the KRAB side16
Interpreting omics data with pathway enrichment analysis16
Chromatin and Nuclear Architecture: Shaping DNA Replication in 3D16
Phenotype-aware prioritisation of rare Mendelian disease variants15
Chromatin modules and their implication in genomic organization and gene regulation15
Tissue specificity of DNA repair: the CRISPR compass15
CD225 Proteins: A Family Portrait of Fusion Regulators15
Quantitative genetics: pan-genomes, SVs, and k-mers for GWAS15
The essential but enigmatic regulatory role of HERVH in pluripotency15
Transgenerational epigenetic impacts of parental infection on offspring health and disease susceptibility15
Ginkgo biloba15
The Emerging Roles of Cytosine-5 Methylation in mRNAs15
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