| Prevalence, incidence and carrier frequency of 5q–linked spinal muscular atrophy–a literature review IEC Verhaart, A Robertson, IJ Wilson, A Aartsma-Rus, S Cameron, ... Orphanet journal of rare diseases 12, 1-15, 2017 | 592 | 2017 |
| Universal heteroplasmy of human mitochondrial DNA BAI Payne, IJ Wilson, P Yu-Wai-Man, J Coxhead, D Deehan, R Horvath, ... Human molecular genetics 22 (2), 384-390, 2013 | 416 | 2013 |
| Genealogical inference from microsatellite data IJ Wilson, DJ Balding Genetics 150 (1), 499-510, 1998 | 338 | 1998 |
| Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease R Soemedi, IJ Wilson, J Bentham, R Darlay, A Töpf, D Zelenika, ... The American Journal of Human Genetics 91 (3), 489-501, 2012 | 334 | 2012 |
| A predominantly neolithic origin for European paternal lineages P Balaresque, GR Bowden, SM Adams, HY Leung, TE King, ZH Rosser, ... PLoS Biology 8 (1), e1000285, 2010 | 319 | 2010 |
| Inferences from DNA data: population histories, evolutionary processes and forensic match probabilities IJ Wilson, ME Weale, DJ Balding Journal of the Royal Statistical Society Series A: Statistics in Society 166 …, 2003 | 304 | 2003 |
| Mitochondrial aging is accelerated by anti-retroviral therapy through the clonal expansion of mtDNA mutations BAI Payne, IJ Wilson, CA Hateley, R Horvath, M Santibanez-Koref, ... Nature genetics 43 (8), 806-810, 2011 | 271 | 2011 |
| Filaggrin null mutations and childhood atopic eczema: a population-based case-control study SJ Brown, CL Relton, H Liao, Y Zhao, A Sandilands, IJ Wilson, J Burn, ... Journal of allergy and clinical immunology 121 (4), 940-946. e3, 2008 | 189 | 2008 |
| Inferring Population History From Microsatellite and Enzyme Data in Serially Introduced Cane Toads, Bufo marinus A Estoup, IJ Wilson, C Sullivan, JM Cornuet, C Moritz Genetics 159 (4), 1671-1687, 2001 | 173 | 2001 |
| The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care BT Wilson, Z Stark, RE Sutton, S Danda, AV Ekbote, SM Elsayed, ... Genetics in medicine 18 (5), 483-493, 2016 | 171 | 2016 |
| Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance G Pfeffer, GS Gorman, H Griffin, M Kurzawa-Akanbi, EL Blakely, I Wilson, ... Brain 137 (5), 1323-1336, 2014 | 171 | 2014 |
| Recent mitochondrial DNA mutations increase the risk of developing common late-onset human diseases G Hudson, A Gomez-Duran, IJ Wilson, PF Chinnery PLoS genetics 10 (5), e1004369, 2014 | 168 | 2014 |
| Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism ME Hurles, R Veitia, E Arroyo, M Armenteros, J Bertranpetit, ... The American Journal of Human Genetics 65 (5), 1437-1448, 1999 | 164 | 1999 |
| Assignment of paternity groups without access to parental genotypes: multiple mating and developmental plasticity in squid AM Emery, IJ Wilson, S Craig, PR Boyle, LR Noble Molecular Ecology 10 (5), 1265-1278, 2001 | 137 | 2001 |
| Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls R Soemedi, A Topf, IJ Wilson, R Darlay, T Rahman, E Glen, D Hall, ... Human molecular genetics 21 (7), 1513-1520, 2012 | 132 | 2012 |
| Genealogies and geography NH Barton, I Wilson Philosophical Transactions of the Royal Society of London. Series B …, 1995 | 131 | 1995 |
| Phenotypic heterogeneity in m. 3243A> G mitochondrial disease: the role of nuclear factors SJ Pickett, JP Grady, YS Ng, GS Gorman, AM Schaefer, IJ Wilson, ... Annals of clinical and translational neurology 5 (3), 333-345, 2018 | 115 | 2018 |
| Mitochondrial DNA point mutations and relative copy number in 1363 disease and control human brains W Wei, MJ Keogh, I Wilson, J Coxhead, S Ryan, S Rollinson, H Griffin, ... Acta neuropathologica communications 5, 1-8, 2017 | 100 | 2017 |
| Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot HJ Cordell, A Töpf, C Mamasoula, AV Postma, J Bentham, D Zelenika, ... Human molecular genetics 22 (7), 1473-1481, 2013 | 98 | 2013 |
| Extreme-depth re-sequencing of mitochondrial DNA finds no evidence of paternal transmission in humans A Pyle, G Hudson, IJ Wilson, J Coxhead, T Smertenko, M Herbert, ... PLoS genetics 11 (5), e1005040, 2015 | 92 | 2015 |
