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| An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56-65, 2012 | 8291 | 2012 |
| Variation in the mutation rate across mammalian genomes A Hodgkinson, A Eyre-Walker Nature Reviews Genetics 12 (11), 756-766, 2011 | 518 | 2011 |
| Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy KT Kahle, ND Merner, P Friedel, L Silayeva, B Liang, A Khanna, Y Shang, ... EMBO reports 15 (7), 766-774, 2014 | 191 | 2014 |
| ffrench-Constant RH, Reynolds SE: Prior infection of Manduca sexta with non-pathogenic Escherichia coli elicits immunity to pathogenic Photorhabdus luminescens: roles of immune … I Eleftherianos, J Marokhazi, PJ Millichap, AJ Hodgkinson, A Sriboonlert Insect Biochem Mol Biol 36 (6), 517-525, 2006 | 146* | 2006 |
| Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia ME Samuels, J Majewski, N Alirezaie, I Fernandez, F Casals, N Patey, ... Journal of medical genetics 50 (5), 324-329, 2013 | 139 | 2013 |
| Cryptic variation in the human mutation rate A Hodgkinson, E Ladoukakis, A Eyre-Walker PLoS biology 7 (2), e1000027, 2009 | 134 | 2009 |
| Gene-by-environment interactions in urban populations modulate risk phenotypes MJ Favé, FC Lamaze, D Soave, A Hodgkinson, H Gauvin, V Bruat, ... Nature communications 9 (1), 827, 2018 | 119 | 2018 |
| High-Resolution Genomic Analysis of Human Mitochondrial RNA Sequence Variation A Hodgkinson, Y Idaghdour, E Gbeha, JC Grenier, E Hip-Ki, V Bruat, ... Science 344 (6182), 413-415, 2014 | 109 | 2014 |
| Human triallelic sites: evidence for a new mutational mechanism? A Hodgkinson, A Eyre-Walker Genetics 184 (1), 233-241, 2010 | 109 | 2010 |
| Recombination affects accumulation of damaging and disease-associated mutations in human populations JG Hussin, A Hodgkinson, Y Idaghdour, JC Grenier, JP Goulet, E Gbeha, ... Nature genetics 47 (4), 400-404, 2015 | 102 | 2015 |
| Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans F Casals, A Hodgkinson, J Hussin, Y Idaghdour, V Bruat, T de Maillard, ... PLoS genetics 9 (9), e1003815, 2013 | 99 | 2013 |
| The large‐scale distribution of somatic mutations in cancer genomes A Hodgkinson, Y Chen, A Eyre‐Walker Human mutation 33 (1), 136-143, 2012 | 98 | 2012 |
| Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis CS Leblond, Z Gan-Or, D Spiegelman, SB Laurent, A Szuto, ... Neurobiology of aging 37, 209. e17-209. e21, 2016 | 78 | 2016 |
| Nuclear genetic regulation of the human mitochondrial transcriptome AT Ali, L Boehme, G Carbajosa, VC Seitan, KS Small, A Hodgkinson eLife 8, e41927, 2019 | 76 | 2019 |
| Relaxed selection during a recent human expansion S Peischl, I Dupanloup, A Foucal, M Jomphe, V Bruat, JC Grenier, A Gouy, ... Genetics, genetics. 300551.2017, 2017 | 60 | 2017 |
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| Gain-of-function missense variant in SLC12A2, encoding the bumetanide-sensitive NKCC1 cotransporter, identified in human schizophrenia ND Merner, A Mercado, AR Khanna, A Hodgkinson, V Bruat, P Awadalla, ... Journal of psychiatric research 77, 22-26, 2016 | 49 | 2016 |
| Integrated genomic analysis of mitochondrial RNA processing in human cancers Y Idaghdour, A Hodgkinson Genome Medicine 9 (1), 36, 2017 | 34 | 2017 |
| The genomic distribution and local context of coincident SNPs in human and chimpanzee A Hodgkinson, A Eyre-Walker Genome biology and evolution 2, 547-557, 2010 | 33 | 2010 |
