Trends in Genetics

Papers
(The median citation count of Trends in Genetics is 3. 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 2022-01-01 to 2026-01-01.)
ArticleCitations
Advisory Board and Contents766
Crossover recombination between homologous chromosomes in meiosis: recent progress and remaining mysteries664
Advisory Board and Contents295
Omics studies of DNA G-/C-quadruplexes in plants230
Epigenetic networks driving T cell identity and plasticity during immunosenescence224
Carcinoscorpius rotundicauda (mangrove horseshoe crab)205
Subscription and Copyright Information192
Advisory Board and Contents162
Genetic buffering mechanisms in SNF2-family translocases141
Assessing autosomal aneuploidy in ancient genomes132
Heritable epigenetic changes at single genes: challenges and opportunities in Caenorhabditis elegans123
Pursuing totipotency: authentic totipotent stem cells in culture119
Emerging regulatory mechanisms of noncoding RNAs in topologically associating domains117
The sound of silence: mechanisms and implications of HUSH complex function109
PCNA cycling dynamics during DNA replication and repair in mammals104
The complex universe of inactive PARP196
Intron retention: importance, challenges, and opportunities93
Advisory Board and Contents92
A new hypothesis to explain disease dominance87
A three-dimensional genomics view for speciation research83
The chromatin roots of abnormal splicing in autism82
Multi-omic genetic scores advance disease research77
Immunity and lifespan: answering long-standing questions with comparative genomics75
Histone lactylation: epigenetic mark of glycolytic switch72
m6A in the coding sequence: linking deposition, translation, and decay71
Genome structural variation in human evolution70
The molecular evolutionary basis of species formation revisited69
Evolution of piRNA-guided defense against transposable elements66
Clonal ants reveal a potentially hidden meiotic feature63
Canis familiaris (Great Dane domestic dog)62
Subscription and Copyright Information62
Advisory Board and Contents61
Advisory Board and Contents60
Advisory Board and Contents59
Animal origins: looping back in time59
Toward DNA-based taxonomy of prokaryotes and microeukaryotes58
The making and breaking of tRNAs by ribonucleases58
Ionizing radiation damage and repair from 3D-genomic perspective56
Dynamics of the Streptomyces chromosome: chance and necessity55
From genetic associations to genes: methods, applications, and challenges54
Features and biomedical relevance of circular RNA biogenesis51
Cis to trans: small ORF functions emerging through evolution51
Insights into Spt6: a histone chaperone that functions in transcription, DNA replication, and genome stability50
Progress and opportunities through use of genomics in animal production49
Finding functional microproteins47
Revealing microRNA regulation in single cells46
DNA base editing in nuclear and organellar genomes46
Pioneer factors: roles and their regulation in development45
Advisory Board and Contents44
Subscription and Copyright Information43
Subscription and Copyright Information42
Subscription and Copyright Information42
Does TFIIH move nucleosomes?41
Unraveling the diversity and cultural heritage of fruit crops through paleogenomics40
Extracellular vesicles as modifiers of epigenomic profiles39
In silico genome transplants and the cis-regulatory basis of biodiversity38
The illusion of clarity in familiar genetics diagrams37
Leveraging microbiome information for animal genetic improvement37
Exploring the world of small proteins in plant biology and bioengineering37
Wheat genomics: genomes, pangenomes, and beyond37
Genetic architecture of brain morphology and overlap with neuropsychiatric traits37
Protist genomics: key to understanding eukaryotic evolution37
Advisory Board and Contents36
Advisory Board and Contents36
Earth Biogenome Project: present status and future plans35
There is another: H3K27me3-mediated genomic imprinting35
Open practices in our science and our courtrooms35
Singling out motor neurons in the age of single-cell transcriptomics35
Mendel elucidated: Big Science comes to the humble garden pea35
Directing RNA-modifying machineries towards endogenous RNAs: opportunities and challenges34
Dissecting super-enhancer heterogeneity: time to re-examine cancer subtypes?34
mRNA-binding proteins and cell cycle progression33
Evolutionary impact of chimeric RNAs on generating phenotypic plasticity in human cells33
Positive-strand RNA virus genome replication organelles: structure, assembly, control32
Mapping cellular responses to DNA double-strand breaks using CRISPR technologies32
The origins and evolution of translation factors32
The H2A.Z-nucleosome code in mammals: emerging functions31
Clocks at sea: the genome-editing tide is rising31
Rare variants and handedness: spotlight on TUBB4B31
Architectural RNAs: blueprints for functional membraneless organelle assembly30
Clonal selection parallels between normal and cancer tissues30
Subscription and Copyright Information30
Sleeping less with a SIK3 mutation30
Cocos nucifera (coconut)30
Dosage compensation in non-model insects – progress and perspectives29
Evolving a favorable distribution for mutation effects29
Chromoanagenesis in plants: triggers, mechanisms, and potential impact28
Beyond sequencing: machine learning algorithms extract biology hidden in Nanopore signal data28
Complex genomic rearrangements: an underestimated cause of rare diseases28
Molecular circuits for genomic recording of cellular events28
Genetics of human handedness: microtubules and beyond27
The influence of transposable elements on animal colouration26
Mitochondrial-derived microproteins: from discovery to function26
Convergent evolution for antibiotic biosynthesis in bacteria and animals26
Complexities of mammalian transcriptome revealed by targeted RNA enrichment techniques25
Is it time to reassess variant annotation?25
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Long-read transcriptome sequencing reveals allele-specific variants at high resolution25
The rare-to-common disease journey: a winding road to new therapies24
Pathway-level convergence: an underexplored aspect of convergent evolution24
Emerging insights into the genetics and evolution of human same-sex sexual behavior24
Subscription and Copyright Information23
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A new Down syndrome rat model races forward23
The versatile relationships between eIF4E and eIF4E-interacting proteins23
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Advisory Board and Contents23
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Repetitive elements in aging and neurodegeneration22
Into the multiverse: advances in single-cell multiomic profiling22
Predicting genome organisation and function with mechanistic modelling22
Complex diseases meet deep phenotyping and generative AI22
Integration of DNA damage responses with dynamic spatial genome organization22
Current concepts, advances, and challenges in deciphering the human microbiota with metatranscriptomics20
The impact of IDR phosphorylation on the RNA binding profiles of proteins20
In search of a cure: PACS1 Research Foundation as a model of rare disease therapy development20
Genomic newborn screening: exploring opportunities and navigating pitfalls while ensuring inclusivity19
Bear essentials19
The essential but enigmatic regulatory role of HERVH in pluripotency19
The ribosome’s comeback: new role in body weight regulation19
Are phenome-wide association studies feasible in a developing country?19
Across the North Sea and beyond19
DNA lesions piece together impossible trees18
Dynamics of replication timing during mammalian development18
Zebrafish and idiopathic scoliosis: the ‘unknown knowns’18
Subscription and Copyright Information18
Advisory Board and Contents18
Noncanonical DNA structures are drivers of genome evolution17
Mitochondria and G-quadruplex evolution: an intertwined relationship17
Genome stability from the perspective of telomere length17
Computational methods for allele-specific expression in single cells17
DNA methylation: a historical perspective17
Cross-kingdom RNA communication in plant–bacterial interaction17
Mendelian randomization analyses for PCOS: evidence, opportunities, and challenges17
Maturation and application of phenome-wide association studies16
Modeling the origin of cells16
Honeybees’ novel complementary sex-determining system: function and origin16
Advisory Board and Contents16
Emerging functions of mitochondria-encoded noncoding RNAs16
Optimizing homology-directed repair for gene editing: the potential of single-stranded DNA donors16
Approaches and challenges in genome-wide circular RNA identification and quantification16
Chromatin accessibility provides a window into the genetic etiology of human brain disease15
Subscription and Copyright Information15
AlphaGenome: a Swiss-army knife for exploring non-coding DNA15
Insights from multi-omics integration in complex disease primary tissues15
Mitochondrial-derived microproteins: from discovery to function15
The wild side of grape genomics15
Whole-genome doubling in tissues and tumors15
Opportunities and tradeoffs in single-cell transcriptomic technologies15
The searchable chromosome15
Beyond the gene: decoding alternative isoforms15
Advisory Board and Contents14
Subscription and Copyright Information14
Advisory Board and Contents14
Advancing evolutionary medicine with complete primate genomes and advanced biotechnologies14
Advisory Board and Contents14
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Yes, polygenic sex determination is a thing!13
Breakage in breakage–fusion–bridge cycle: an 80-year-old mystery13
Genetic adaptations for the oceanic success of fish eggs13
Finding genes and pathways that underlie coral adaptation12
Spatial omics enters the microscopic realm: opportunities and challenges12
Advisory Board and Contents12
Noncoding snoRNA host genes are a distinct subclass of long noncoding RNAs12
iPSC-derived organ-on-a-chip models for personalized human genetics and pharmacogenomics studies12
Every gene can (and possibly will) be associated with cancer12
Intragenomic mutational heterogeneity: structural and functional insights from gene evolution12
ATRX, a guardian of chromatin12
ReNU syndrome – a newly discovered prevalent neurodevelopmental disorder12
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Advances in methods for tRNA sequencing and quantification11
Genetic and epigenetic defects of the RNA modification machinery in cancer11
Interplay between regulatory elements and chromatin topology in cellular lineage determination11
Cis-regulatory dynamics in plant domestication11
Selective REcruitmeNt of plant DNA polymerases by geminivirus11
Epigenetic perspectives on wheat speciation, adaptation, and development11
Selective Xi reactivation and alternative methods to restore MECP2 function in Rett syndrome11
Aneuploidy in human cancer: new tools and perspectives11
Starships: a new frontier for fungal biology11
Interruptions impact clinical features of repeat expansion diseases, but how are they gained and lost?11
New insights into oocyte cytoplasmic lattice-associated proteins11
Chromatin-centric insights into DNA replication11
A multi-epigenomic map of endurance exercise training11
An updated view of the kinetochore architecture11
miRNA biogenesis and inherited disorders: clinico-molecular insights10
People with disability and privacy in precision medicine research: what’s at stake?10
Recent insights into eukaryotic double-strand DNA break repair unveiled by single-molecule methods10
Transposon–host arms race: a saga of genome evolution10
ADAR1 and its implications in cancer development and treatment10
Contributions of epigenomic and epitranscriptomic methylation to animal colouration10
Chromosome-scale haplotype-resolved pangenomics10
Take a walk on the KRAB side10
Advisory Board and Contents10
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Fun-sized and fundamental10
A blood drop through the pore: nanopore sequencing in hematology10
Molecular animations in genomics education: designing for whom?9
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Advisory Board and Contents9
Patient privacy in AI-driven omics methods9
FIRRM and FIGNL1: partners in the regulation of homologous recombination9
Leveraging spatial multiomics to unravel tissue architecture in embryo development9
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Genetic disorders of cellular trafficking9
Gene-dosage issues: a recurrent theme in whole genome duplication events9
The impact of human accelerated regions on neuronal development9
Emerging links between phase separation and transcription factor haploinsufficiency9
Haldane’s duel: intragenomic conflict, selfish Y chromosomes and speciation9
Unraveling brain complexity: from single-cell to spatial m6A technologies8
Preventing excess replication origin activation to ensure genome stability8
Duplicated gene networks promote ‘hopeful’ phenotypic variation8
Functional characterization of human genomic variation linked to polygenic diseases8
Out of the dark: the emerging roles of lncRNAs in pain8
The evolution of the GALactose utilization pathway in budding yeasts8
A dive into the unknome7
Genetic and epigenetic landscape of male infertility7
Achieve your research goals: a project management toolkit for graduate studies7
Advisory Board and Contents7
RNAPII driven post-translational modifications of nucleosomal histones7
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The impact of human accelerated regions on neuronal development7
Bridging biological cfDNA features and machine learning approaches7
Advisory Board and Contents7
Single-cell omics sequencing technologies: the long-read generation7
Retrotransposon renaissance in early embryos7
DEAD/DEAH-box RNA helicases shape the risk of neurodevelopmental disorders7
Time is ticking faster for long genes in aging7
From darkness to discovery: evolutionary, adaptive, and translational genetic insights from cavefish7
Epigenetic control of muscle stem cells: time for a new dimension7
Picochlorum sp. SENEW37
Exploring the role of phage plasmids in gene transfers6
Aegilops tauschii presents a genetic roadmap for hexaploid wheat improvement6
The evolution of aging and lifespan6
We must not ignore eugenics in our genetics curriculum6
Advisory Board and Contents6
Strategies for dissecting the complexity of neurodevelopmental disorders6
Therapeutic and prognostic insights from the analysis of cancer mutational signatures6
Single-cell dissection of tumor microenvironmental response and resistance to cancer therapy6
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Supergenes promote ecological stasis in a keystone species6
The very early evolution of biological complexity6
New mechanism of chromatin compartmentalization by BRD26
The multifaceted effects of YTHDC1-mediated nuclear m6A recognition6
Structure-specific nucleases: role in Okazaki fragment maturation6
Gene reporters for magnetic resonance imaging6
Alternative paths for genetics, then and now: Q&A with Gregory Radick about Disputed Inheritance6
Homologous recombination counteracts mismatch repair to promote fertility and genetic diversity6
Gene product diversity: adaptive or not?5
Conditional mutagenesis strategies in zebrafish5
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