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 2021-12-01 to 2025-12-01.)
ArticleCitations
Advisory Board and Contents733
Crossover recombination between homologous chromosomes in meiosis: recent progress and remaining mysteries639
Emerging regulatory mechanisms of noncoding RNAs in topologically associating domains285
Advisory Board and Contents220
Omics studies of DNA G-/C-quadruplexes in plants210
Epigenetic networks driving T cell identity and plasticity during immunosenescence194
Carcinoscorpius rotundicauda (mangrove horseshoe crab)188
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Superspreading in the emergence of COVID-19 variants142
Genetic buffering mechanisms in SNF2-family translocases138
Assessing autosomal aneuploidy in ancient genomes129
Heritable epigenetic changes at single genes: challenges and opportunities in Caenorhabditis elegans117
Pursuing totipotency: authentic totipotent stem cells in culture113
Intron retention: importance, challenges, and opportunities112
PCNA cycling dynamics during DNA replication and repair in mammals101
The sound of silence: mechanisms and implications of HUSH complex function99
Advisory Board and Contents92
The complex universe of inactive PARP192
Advisory Board and Contents90
A new hypothesis to explain disease dominance81
Evolution of piRNA-guided defense against transposable elements81
Variation on a theme: mapping microglial heterogeneity78
The chromatin roots of abnormal splicing in autism75
A three-dimensional genomics view for speciation research74
Immunity and lifespan: answering long-standing questions with comparative genomics69
m6A in the coding sequence: linking deposition, translation, and decay69
Multi-omic genetic scores advance disease research68
Genome structural variation in human evolution66
Histone lactylation: epigenetic mark of glycolytic switch64
The molecular evolutionary basis of species formation revisited62
Clonal ants reveal a potentially hidden meiotic feature60
Canis familiaris (Great Dane domestic dog)59
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Advisory Board and Contents59
Animal origins: looping back in time58
Advisory Board and Contents58
The making and breaking of tRNAs by ribonucleases57
Advisory Board and Contents57
Toward DNA-based taxonomy of prokaryotes and microeukaryotes55
Ionizing radiation damage and repair from 3D-genomic perspective54
DNA base editing in nuclear and organellar genomes50
From genetic associations to genes: methods, applications, and challenges48
Pioneer factors: roles and their regulation in development48
Progress and opportunities through use of genomics in animal production48
Insights into Spt6: a histone chaperone that functions in transcription, DNA replication, and genome stability46
Revealing microRNA regulation in single cells45
Dynamics of the Streptomyces chromosome: chance and necessity45
Cis to trans: small ORF functions emerging through evolution43
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Finding functional microproteins43
Advisory Board and Contents43
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Does TFIIH move nucleosomes?40
Protist genomics: key to understanding eukaryotic evolution39
Exploring the world of small proteins in plant biology and bioengineering39
Unraveling the diversity and cultural heritage of fruit crops through paleogenomics39
The illusion of clarity in familiar genetics diagrams38
Genetic architecture of brain morphology and overlap with neuropsychiatric traits37
Wheat genomics: genomes, pangenomes, and beyond37
In silico genome transplants and the cis-regulatory basis of biodiversity36
Leveraging microbiome information for animal genetic improvement36
Extracellular vesicles as modifiers of epigenomic profiles35
Advisory Board and Contents35
Advisory Board and Contents35
Open practices in our science and our courtrooms34
There is another: H3K27me3-mediated genomic imprinting34
Dissecting super-enhancer heterogeneity: time to re-examine cancer subtypes?34
The origins and evolution of translation factors34
A current guide to candidate gene association studies34
Mendel elucidated: Big Science comes to the humble garden pea33
Evolutionary impact of chimeric RNAs on generating phenotypic plasticity in human cells33
Mapping cellular responses to DNA double-strand breaks using CRISPR technologies33
Singling out motor neurons in the age of single-cell transcriptomics33
Directing RNA-modifying machineries towards endogenous RNAs: opportunities and challenges33
Positive-strand RNA virus genome replication organelles: structure, assembly, control32
mRNA-binding proteins and cell cycle progression32
Earth Biogenome Project: present status and future plans32
Rare variants and handedness: spotlight on TUBB4B31
Sleeping less with a SIK3 mutation30
Clocks at sea: the genome-editing tide is rising30
Clonal selection parallels between normal and cancer tissues30
Convergent evolution for antibiotic biosynthesis in bacteria and animals30
Cocos nucifera (coconut)29
Chromoanagenesis in plants: triggers, mechanisms, and potential impact28
The H2A.Z-nucleosome code in mammals: emerging functions28
Subscription and Copyright Information28
The influence of transposable elements on animal colouration28
Dosage compensation in non-model insects – progress and perspectives27
Architectural RNAs: blueprints for functional membraneless organelle assembly27
Complex genomic rearrangements: an underestimated cause of rare diseases27
The cell as a bag of RNA27
Molecular circuits for genomic recording of cellular events27
Evolving a favorable distribution for mutation effects26
Genetics of human handedness: microtubules and beyond26
Beyond sequencing: machine learning algorithms extract biology hidden in Nanopore signal data26
Mitochondrial-derived microproteins: from discovery to function25
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Is it time to reassess variant annotation?24
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A new Down syndrome rat model races forward24
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Pathway-level convergence: an underexplored aspect of convergent evolution24
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Advisory Board and Contents23
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The versatile relationships between eIF4E and eIF4E-interacting proteins23
Complexities of mammalian transcriptome revealed by targeted RNA enrichment techniques22
Predicting genome organisation and function with mechanistic modelling22
Integration of DNA damage responses with dynamic spatial genome organization22
In search of a cure: PACS1 Research Foundation as a model of rare disease therapy development22
The impact of IDR phosphorylation on the RNA binding profiles of proteins22
Long-read transcriptome sequencing reveals allele-specific variants at high resolution22
Complex diseases meet deep phenotyping and generative AI21
Into the multiverse: advances in single-cell multiomic profiling20
Repetitive elements in aging and neurodegeneration20
The rare-to-common disease journey: a winding road to new therapies20
Emerging insights into the genetics and evolution of human same-sex sexual behavior20
The essential but enigmatic regulatory role of HERVH in pluripotency20
Current concepts, advances, and challenges in deciphering the human microbiota with metatranscriptomics20
Genomic newborn screening: exploring opportunities and navigating pitfalls while ensuring inclusivity19
Across the North Sea and beyond19
The ribosome’s comeback: new role in body weight regulation19
Bear essentials19
Are phenome-wide association studies feasible in a developing country?19
Advisory Board and Contents19
DNA lesions piece together impossible trees18
Computational methods for allele-specific expression in single cells18
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Cross-kingdom RNA communication in plant–bacterial interaction18
Advisory Board and Contents18
Zebrafish and idiopathic scoliosis: the ‘unknown knowns’18
Dynamics of replication timing during mammalian development17
Noncanonical DNA structures are drivers of genome evolution17
Emerging functions of mitochondria-encoded noncoding RNAs17
Genome stability from the perspective of telomere length17
Maturation and application of phenome-wide association studies16
Advisory Board and Contents16
Mitochondria and G-quadruplex evolution: an intertwined relationship16
Mendelian randomization analyses for PCOS: evidence, opportunities, and challenges16
DNA methylation: a historical perspective16
Modeling the origin of cells16
The wild side of grape genomics15
Optimizing homology-directed repair for gene editing: the potential of single-stranded DNA donors15
Opportunities and tradeoffs in single-cell transcriptomic technologies15
Mitochondrial-derived microproteins: from discovery to function15
The searchable chromosome15
Chromatin accessibility provides a window into the genetic etiology of human brain disease15
Honeybees’ novel complementary sex-determining system: function and origin15
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