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SHWAN NA, LOUZADA S, YANG F and ARMOUR JA, 2017. Recurrent Rearrangements of Human Amylase Genes Create Multiple Independent CNV Series. Human mutation. (In Press.)
AI Z, LI M, LIU W, FOO JN, MANSOURI O, YIN P, ZHOU Q, TANG X, DONG X, FENG S, XU R, ZHONG Z, CHEN J, WAN J, LOU T, YU J, ZHOU Q, FAN J, MAO H, GALE D, BARRATT J, ARMOUR JA, LIU J and YU X, 2016. Low α-defensin gene copy number increases the risk for IgA nephropathy and renal dysfunction. Science translational medicine. 8(345), 345ra88
INCHLEY CE, LARBEY CD, SHWAN NA, PAGANI L, SAAG L, ANT?O T, JACOBS G, HUDJASHOV G, METSPALU E, MITT M, EICHSTAEDT CA, MALYARCHUK B, DERENKO M, WEE J, ABDULLAH S, RICAUT FX, MORMINA M, M?GI R, VILLEMS R, METSPALU M, JONES MK, ARMOUR JA and KIVISILD T, 2016. Selective sweep on human amylase genes postdates the split with Neanderthals. Scientific reports. 6, 37198
TYSON J and ARMOUR JA, 2016. Analysis of Multiallelic CNVs by Emulsion Haplotype Fusion PCR. Methods in molecular biology (Clifton, N.J.). 1492, 155-165
FERNáNDEZ-GRANDON GM, GEZAN SA, ARMOUR JAL, PICKETT JA and LOGAN JG, 2015. Heritability of attractiveness to mosquitoes. PloS one. 10(4), e0122716
CARPENTER D, DHAR S, MITCHELL LM, FU B, TYSON J, SHWAN NAA, YANG F, THOMAS MG and ARMOUR JAL, 2015. Obesity, starch digestion and amylase: association between copy number variants at human salivary (AMY1) and pancreatic (AMY2) amylase genes. Human molecular genetics. 24(12), 3472-80
ARMOUR JA, DAVISON A and MCMANUS IC, 2014. Genome-wide association study of handedness excludes simple genetic models. Heredity. 112(3), 221-5
CARPENTER D, TAYPE C, GOULDING J, LEVIN M, ELEY B, ANDERSON S, SHAW M and ARMOUR JAL, 2014. CCL3L1 copy number, CCR5 genotype and susceptibility to tuberculosis. BMC Medical Genetics. 15, 5
BLACK HA, KHAN FF, TYSON J and ARMOUR JAL, 2014. Inferring mechanisms of copy number change from haplotype structures at the human DEFA1A3 locus. BMC Genomics. 15, 614
MCMANUS IC, DAVISON A and ARMOUR JAL, 2013. Multilocus genetic models of handedness closely resemble single-locus models in explaining family data and are compatible with genome-wide association studies. Annals of the New York Academy of Sciences. 1288, 48-58
KHAN FF, CARPENTER D, MITCHELL L, MANSOURI O, BLACK HA, TYSON J and ARMOUR JA, 2013. Accurate measurement of gene copy number for human alpha-defensin DEFA1A3. BMC genomics. 14(1), 719
CARPENTER D, MCINTOSH RS, PLEASS RJ and ARMOUR JAL, 2012. Functional effects of CCL3L1 copy number. Genes and immunity. 13(5), 374-9
CARPENTER D, F?RNERT A, ROOTH I, ARMOUR JAL and SHAW M, 2012. CCL3L1 copy number and susceptibility to malaria. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases. 12(5), 1147-54
STUART PE, HüFFMEIER U, NAIR RP, PALLA R, TEJASVI T, SCHALKWIJK J, ELDER JT, REIS A and ARMOUR JAL, 2012. Association of β-defensin copy number and psoriasis in three cohorts of european origin. The journal of investigative dermatology. 132, 2407-2413
NORDANG GBN, CARPENTER D, VIKEN MK, KVIEN TK, ARMOUR JAL and LIE BA, 2012. Association analysis of the CCL3L1 copy number locus by paralogue ratio test in norwegian rheumatoid arthritis patients and healthy controls. Genes and immunity. 13, 579-582
TYSON J and ARMOUR JA, 2012. Determination of haplotypes at structurally complex regions using emulsion haplotype fusion PCR. BMC genomics. 13(1), 693
PARK, J.J, OH, B.R, KIM, J.Y, PARK, J.A, KIM, C, LEE, Y.J, SONG, Y.W and ARMOUR, J.A.L. AND LEE, E.B., 2011. Copy number variation of β-defensin genes in Beh?et's disease. Clinical and experimental rheumatology. 29((4 Suppl 67)), S20-3
CARPENTER D, WALKER S, PRESCOTT N, SCHALKWIJK J and ARMOUR JA, 2011. Accuracy And Differential Bias In Copy Number Measurement Of Ccl3l1 In Association Studies With Three Auto-Immune Disorders. Bmc Genomics. 12, 418
RIVEIRA-MUNOZ E, HE S, ESCARAMíS G, STUART PE, HüFFMEIER U, LEE C, KIRBY B, OKA A, GIARDINA E, LIAO W, BERGBOER J, KAINU K, DE CID R, MUNKHBAT B, ZEEUWEN PLJM, ARMOUR JAL, POON A, MABUCHI T, OZAWA A, ZAWIRSKA A, BURDEN AD, BARKER JN, CAPON F, TRAUPE H, SUN L, CUI Y, YIN X, CHEN G, LIM HW, NAIR RP, VOORHEES JJ, TEJASVI T, PUJOL R, MUNKHTUVSHIN N, FISCHER J, KERE J, SCHALKWIJK J, BOWCOCK A, KWOK P, NOVELLI G, INOKO H, RYAN AW, TREMBATH RC, REIS A, ZHANG X, ELDER JT and ESTIVILL X, 2011. Meta-Analysis Confirms The Lce3c_Lce3b Deletion As A Risk Factor For Psoriasis In Several Ethnic Groups And Finds Interaction With Hla-Cw6. The Journal Of Investigative Dermatology. 131(5), 1105-9
GRANADOS-RIVERON, J.T., GHOSH, T,K., POPE, M., BU'LOCK, F., THORNBOROUGH, C., EASON, J., KIRK, E.P., FATKIN, D., FENELEY, M.P., HARVEY, R.P., ARMOUR, J.A.L. and BROOK, J.D., 2010. ?-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects Human Molecular Genetics. 19(20), 4007-4016
TYSON, J, MAJERUS T.M.O and WALKER, S. AND ARMOUR, J.A.L., 2010. Screening for common copy-number variants in cancer genes. Cancer Genetics & Cytogenetics. 203(2), 316-323
HüFFMEIER, U, BERGBOER, J.G, BECKER, T, ARMOUR, J.A.L, TRAUPE, H, ESTIVILL, X, RIVEIRA-MUNOZ, E, M?SSNER, R, REICH, K, KURRAT, W, WIENKER, T.F, SCHALKWIJK, J, ZEEUWEN, P.L and REIS, A., 2010. Replication of LCE3C-LCE3B CNV as a Risk Factor for Psoriasis and Analysis of Interaction with Other Genetic Risk Factors. Journal of Investigative Dermatology. 130, 979–984
BERGBOER, JGM, ZEEUWEN, PLJM, IRVINE, AD, WEIDINGER, S, GIARDINA, E, NOVELLI, G, DEN HEIJER, M, RODRIGUEZ, E, ILLIG, T, RIVEIRA-MUNOZ, E, CAMPBELL, LE, TYSON, J, DANNHAUSER, EN, O'REGAN, GM, GALLI, E, KLOPP, N, KOPPELMAN, GH, NOVAK, N, ESTIVILL, X, MCLEAN, WHI, POSTMA, DS, ARMOUR, JAL AND SCHALKWIJK and J, 2010. Deletion of Late Cornified Envelope 3B and 3C Genes Is Not Associated with Atopic Dermatitis. The Journal of investigative dermatology. 130, 2057-2061
ALDHOUS, M.C., ABU BAKAR, S., PRESCOTT, N.J., PALLA, R., SOO, K., MANSFIELD, J.C., MATHEW, C.G., SATSANGI, J. and ARMOUR, J.A.L., 2010. Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease Human Molecular Genetics. 19(24), 4930-4938
TYSON, J, MAJERUS, T.M.O and WALKER, S. AND ARMOUR, J.A.L., 2009. Quadruplex MAPH: improvement of throughput in high-resolution copy number screening. BMC Genomics. 10, 453
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