关注
John Armour
John Armour
未知所在单位机构
在 nottingham.ac.uk 的电子邮件经过验证
标题
引用次数
引用次数
年份
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
8182008
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
6421994
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
6212009
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
4932003
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
4821994
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
3761991
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
2931992
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
2862000
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
2811989
Genomic copy number variation, human health, and disease
LV Wain, JAL Armour, MD Tobin
The Lancet 374 (9686), 340-350, 2009
2522009
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
2492009
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
2411996
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
2372005
Systematic cloning of human minisatellites from ordered array charomid libraries
JAL Armour, S Povey, S Jeremiah, AJ Jeffreys
Genomics 8 (3), 501-512, 1990
2011990
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
1961996
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
1892007
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
1832007
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
1732013
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
1712010
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
1622002
系统目前无法执行此操作,请稍后再试。
文章 1–20