| # | Title | Journal | Year | Citations |
|---|
| 1 | No saturation in the accumulation of alien species worldwide | Nature Communications | 2017 | 1,543 |
| 2 | Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 | Autophagy | 2021 | 1,430 |
| 3 | Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility | Nature Genetics | 2014 | 959 |
| 4 | Identification of common variants associated with human hippocampal and intracranial volumes | Nature Genetics | 2012 | 594 |
| 5 | Cardioprotection by S-nitrosation of a cysteine switch on mitochondrial complex I | Nature Medicine | 2013 | 521 |
| 6 | Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study | Lancet, The | 2013 | 485 |
| 7 | Linking the influence and dependence of people on biodiversity across scales | Nature | 2017 | 474 |
| 8 | Restoration of vision after transplantation of photoreceptors | Nature | 2012 | 447 |
| 9 | Life history and spatial traits predict extinction risk due to climate change | Nature Climate Change | 2014 | 341 |
| 10 | Genome-wide meta-analysis identifies new susceptibility loci for migraine | Nature Genetics | 2013 | 338 |
| 11 | Global hotspots and correlates of alien species richness across taxonomic groups | Nature Ecology and Evolution | 2017 | 315 |
| 12 | Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation | Nature Genetics | 2015 | 294 |
| 13 | A holidic medium for Drosophila melanogaster | Nature Methods | 2014 | 291 |
| 14 | Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses | Human Mutation | 2012 | 273 |
| 15 | Gene-centric Association Signals for Lipids and Apolipoproteins Identified via the HumanCVD BeadChip | American Journal of Human Genetics | 2009 | 183 |
| 16 | Late Pleistocene climate change and the global expansion of anatomically modern humans | Proceedings of the National Academy of Sciences of the United States of America | 2012 | 157 |
| 17 | Endocrine regulation of aging and reproduction in Drosophila | Molecular and Cellular Endocrinology | 2009 | 152 |
| 18 | Mutations in the autoregulatory domain of β‐tubulin 4a cause hereditary dystonia | Annals of Neurology | 2013 | 148 |
| 19 | First report of Mycobacterium bovis DNA in human remains from the Iron Age | Microbiology (United Kingdom) | 2007 | 141 |
| 20 | A histone H3K36 chromatin switch coordinates DNA double-strand break repair pathway choice | Nature Communications | 2014 | 134 |
| 21 | Exome sequencing identifiesDYNC2H1mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement | Journal of Medical Genetics | 2013 | 127 |
| 22 | The RNA-binding protein HuR is essential for the B cell antibody response | Nature Immunology | 2015 | 125 |
| 23 | Defining the Integration Capacity of Embryonic Stem Cell-Derived Photoreceptor Precursors | Stem Cells | 2012 | 119 |
| 24 | Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis | Brain | 2009 | 116 |
| 25 | Gene therapy with a promoter targeting both rods and cones rescues retinal degeneration caused by AIPL1 mutations | Gene Therapy | 2010 | 114 |
| 26 | CNOT3 Is a Modifier of PRPF31 Mutations in Retinitis Pigmentosa with Incomplete Penetrance | PLoS Genetics | 2012 | 109 |
| 27 | The ‘mitoflash’ probe cpYFP does not respond to superoxide | Nature | 2014 | 109 |
| 28 | A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia | American Journal of Human Genetics | 2015 | 109 |
| 29 | Cystatin C and Cardiovascular Disease | Journal of the American College of Cardiology | 2016 | 109 |
| 30 | Exploring long non-coding RNAs through sequencing | Seminars in Cell and Developmental Biology | 2012 | 108 |
| 31 | Mutations in the Gene Encoding IFT Dynein Complex Component WDR34 Cause Jeune Asphyxiating Thoracic Dystrophy | American Journal of Human Genetics | 2013 | 108 |
| 32 | Adult Ciliary Epithelial Cells, Previously Identified as Retinal Stem Cells with Potential for Retinal Repair, Fail to Differentiate into New Rod Photoreceptors | Stem Cells | 2010 | 107 |
| 33 | Effective Transplantation of Photoreceptor Precursor Cells Selected via Cell Surface Antigen Expression | Stem Cells | 2011 | 107 |
| 34 | Population genetics of sexual conflict in the genomic era | Nature Reviews Genetics | 2017 | 106 |
| 35 | Whole exome sequencing of familial hypercholesterolaemia patients negative forLDLR/APOB/PCSK9mutations | Journal of Medical Genetics | 2014 | 104 |
| 36 | The Tight Junction Associated Signalling Proteins ZO-1 and ZONAB Regulate Retinal Pigment Epithelium Homeostasis in Mice | PLoS ONE | 2010 | 104 |
| 37 | The global avian invasions atlas, a database of alien bird distributions worldwide | Scientific Data | 2017 | 103 |
| 38 | Cone and rod photoreceptor transplantation in models of the childhood retinopathy Leber congenital amaurosis using flow-sorted Crx-positive donor cells | Human Molecular Genetics | 2010 | 96 |
| 39 | Adonia variegata (Coleoptera: Coccinellidae) bears maternally inherited Flavobacteria that kill males only | Parasitology | 1999 | 89 |
| 40 | A radiation of arboreal basal eutherian mammals beginning in the Late Cretaceous of India | Proceedings of the National Academy of Sciences of the United States of America | 2011 | 87 |
| 41 | Patterns of contribution to citizen science biodiversity projects increase understanding of volunteers’ recording behaviour | Scientific Reports | 2016 | 85 |
| 42 | RNA polymerase III limits longevity downstream of TORC1 | Nature | 2017 | 83 |
| 43 | A Transcriptomic Signature of the Hypothalamic Response to Fasting and BDNF Deficiency in Prader-Willi Syndrome | Cell Reports | 2018 | 81 |
| 44 | CENP-B preserves genome integrity at replication forks paused by retrotransposon LTR | Nature | 2011 | 79 |
| 45 | Phage ϕC2 Mediates Transduction of Tn 6215 , Encoding Erythromycin Resistance, between Clostridium difficile Strains | MBio | 2013 | 79 |
| 46 | Use of targeted exome sequencing as a diagnostic tool for Familial Hypercholesterolaemia | Journal of Medical Genetics | 2012 | 74 |
| 47 | Two forms of death in ageing Caenorhabditis elegans | Nature Communications | 2017 | 73 |
| 48 | Long-Term Preservation of Cones and Improvement in Visual Function Following Gene Therapy in a Mouse Model of Leber Congenital Amaurosis Caused by Guanylate Cyclase-1 Deficiency | Human Gene Therapy | 2011 | 70 |
| 49 | What causes inefficient transmission of male-killing Wolbachia in Drosophila? | Heredity | 2001 | 67 |
| 50 | Dog10K: an international sequencing effort to advance studies of canine domestication, phenotypes and health | National Science Review | 2019 | 65 |
