| Psoriasis is associated with increased β-defensin genomic copy number EJ Hollox, U Huffmeier, PLJM Zeeuwen, R Palla, J Lascorz, ... Nature genetics 40 (1), 23-25, 2008 | 821 | 2008 |
| Complex gene conversion events in germline mutation at human minisatellites AJ Jeffreys, K Tamaki, A MacLeod, DG Monckton, DL Neil, JAL Armour Nature genetics 6 (2), 136-145, 1994 | 640 | 1994 |
| Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis R De Cid, E Riveira-Munoz, PLJM Zeeuwen, J Robarge, W Liao, ... Nature genetics 41 (2), 211-215, 2009 | 617 | 2009 |
| Extensive normal copy number variation of a β-defensin antimicrobial-gene cluster EJ Hollox, JAL Armour, JCK Barber The American Journal of Human Genetics 73 (3), 591-600, 2003 | 488 | 2003 |
| Isolation of human simple repeat loci by hybridization selection JAL Armour, R Neumann, S Gobert, AJ Jeffreys Human molecular genetics 3 (4), 599-605, 1994 | 484 | 1994 |
| Uniparental paternal disomy in Angelman's syndrome S Malcolm, J Clayton-Smith, M Nichols, ME Pembrey, JAL Armour, ... The Lancet 337 (8743), 694-697, 1991 | 377 | 1991 |
| The frequency of uniparental disomy in Prader-Willi syndrome: implications for molecular diagnosis MJ Mascari, W Gottlieb, PK Rogan, MG Butler, DA Waller, JAL Armour, ... New England Journal of Medicine 326 (24), 1599-1607, 1992 | 288 | 1992 |
| Measurement of locus copy number by hybridisation with amplifiable probes JAL Armour, C Sismani, PC Patsalis, G Cross Nucleic acids research 28 (2), 605-609, 2000 | 286 | 2000 |
| The retinoblastoma gene is frequently altered leading to loss of expression in primary breast tumours. JM Varley, J Armour, JE Swallow, AJ Jeffreys, BA Ponder, A T'ang, ... Oncogene 4 (6), 725-729, 1989 | 284 | 1989 |
| Genomic copy number variation, human health, and disease LV Wain, JAL Armour, MD Tobin The Lancet 374 (9686), 340-350, 2009 | 252 | 2009 |
| β-Defensin-2 protein is a serum biomarker for disease activity in psoriasis and reaches biologically relevant concentrations in lesional skin PAM Jansen, D Rodijk-Olthuis, EJ Hollox, M Kamsteeg, GS Tjabringa, ... PloS one 4 (3), e4725, 2009 | 244 | 2009 |
| Minisatellite diversity supports a recent African origin for modern humans JAL Armour, T Anttinen, CA May, EE Vega, A Sajantila, JR Kidd, KK Kidd, ... Nature genetics 13 (2), 154-160, 1996 | 242 | 1996 |
| Copy number polymorphism and expression level variation of the human α-defensin genes DEFA1 and DEFA3 PMR Aldred, EJ Hollox, JAL Armour Human molecular genetics 14 (14), 2045-2052, 2005 | 237 | 2005 |
| Systematic cloning of human minisatellites from ordered array charomid libraries JAL Armour, S Povey, S Jeremiah, AJ Jeffreys Genomics 8 (3), 501-512, 1990 | 208 | 1990 |
| Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4 B Coyle, R Coffey, JAL Armour, E Gausden, Z Hochberg, A Grossman, ... Nature genetics 12 (4), 421-423, 1996 | 195 | 1996 |
| Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy J Clapp, LM Mitchell, DJ Bolland, J Fantes, AE Corcoran, PJ Scotting, ... The American Journal of Human Genetics 81 (2), 264-279, 2007 | 188 | 2007 |
| Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats JAL Armour, R Palla, PLJM Zeeuwen, M Heijer, J Schalkwijk, EJ Hollox Nucleic acids research 35 (3), e19-e19, 2007 | 184 | 2007 |
| α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects JT Granados-Riveron, TK Ghosh, M Pope, F Bu'Lock, C Thornborough, ... Human molecular genetics 19 (20), 4007-4016, 2010 | 169 | 2010 |
| Multilocus genetic models of handedness closely resemble single‐locus models in explaining family data and are compatible with genome‐wide association studies IC McManus, A Davison, JAL Armour Annals of the New York Academy of Sciences 1288 (1), 48-58, 2013 | 168 | 2013 |
| The detection of large deletions or duplications in genomic DNA JAL Armour, DE Barton, DJ Cockburn, GR Taylor Human Mutation 20 (5), 325-337, 2002 | 164 | 2002 |
