Nature Reviews Genetics

Papers
(The H4-Index of Nature Reviews Genetics is 73. 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 2021-06-01 to 2025-06-01.)
ArticleCitations
The different faces of transcription factor sensitivity1332
High-resolution 3D genome characterization910
Explaining the male bias in cancers845
Single-cell expression profiling has its roots in in situ techniques819
Tightening the (neural) net for protein structure prediction748
Disentangling population structure in marine species652
Enhancing sustainable development through plant genetics641
The evolution of DNA sequencing with microfluidics628
SCOPE-ing out eukaryotic 6mA553
Weaponized genomics: potential threats to international and human security419
The evolution of modifier genes367
Getting organized with non-coding RNAs363
Interrogating epigenetic mechanisms with chemically customized chromatin358
Imprinted genes and the manipulation of parenting in mammals331
Means, mechanisms and consequences of adenine methylation in DNA301
Harnessing deep learning for population genetic inference278
Mining genomes to illuminate the specialized chemistry of life266
Pleiotropy, epistasis and the genetic architecture of quantitative traits213
Genomic insights into conifer evolution206
Unveiling the expanding protein universe of life204
Rapid pathogen surveillance: field-ready sequencing solutions200
The origin of animals and fungi198
Changes in cell-cycle rate drive diverging cell fates196
Progress in toxicogenomics to protect human health190
The epithelial–mesenchymal plasticity landscape: principles of design and mechanisms of regulation182
More than a decade of genetic research on the Denisovans182
Testing the super-enhancer concept175
Best practices for single-cell analysis across modalities175
CRISPR editing within microbial communities169
Abiotic stress responses in plants169
Shared genetic components of multimorbidity154
Layering epigenomic and transcriptomic space148
Revealing gene function with statistical inference at single-cell resolution147
Aneuploidy in the driving seat145
Mapping dosage145
Genomic transformations of Eurasian hunter-gatherer populations during the last Ice Age144
Mini-colons unlock tumour development outside the body143
Investigating spatial gene circuits and gene–phenotype mechanisms with Perturb-FISH134
Genomic landscape of cancer in racially and ethnically diverse populations134
Genetics of substance use disorders in the era of big data132
Intrinsically disordered regions as facilitators of the transcription factor target search131
Targeted genome-modification tools and their advanced applications in crop breeding125
Single cell–cell communication121
Inhibitors of bacterial immune systems: discovery, mechanisms and applications121
Epigenomes get personal119
Predicting the effects of multigene perturbations119
The hidden diversity of tumours117
CHIPping away at the genetic aetiology of clonal haematopoiesis116
Miller spreads and the power of observation115
Swapping genes within and beyond our bodies114
Fine-mapping causal variants — why finding ‘the one’ can be futile113
Mate choice through a genomic lens113
Cohesin and CTCF emerge as building blocks of 3D genome structure107
ADAR1 inhibits ZBP1 activation by endogenous Z-RNA102
Simultaneous single-cell sequencing of RNA and DNA at scale with DEFND-seq101
From computational models of the splicing code to regulatory mechanisms and therapeutic implications99
Scrambling the genome in cancer: causes and consequences of complex chromosome rearrangements99
Retrotransposons: still mobile in humans98
Genomic newborn screening for rare diseases97
The origin and evolution of Wnt signalling95
Social shifts in spiders91
The final pieces of the human genome86
Why geneticists should care about male infertility86
Fitness effects of mutations throughout evolution84
Global genomic diversity for All of Us84
Integrating model systems and genomic insights to decipher mechanisms of cancer metastasis82
The diversification of methods for studying cell–cell interactions and communication77
Fitness, growth and transmissibility of SARS-CoV-2 genetic variants76
High-throughput biochemistry in RNA sequence space: predicting structure and function74
The potential of mitochondrial genome engineering74
Effects of regulatory variants across pig tissues74
Targeting and engineering long non-coding RNAs for cancer therapy74
Indirect recognition of pathogen virulence proteins to activate plant immune receptors73
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