Browse by Divisions pre August 2011

Barber, J.C.K., Zhang, S., Friend, N., Collins, A.L., Maloney, V.K., Hastings, R., Farren, B., Barnicoat, A., Polityko, A.D., Rumyantseva, N.V., Starke, H. and Ye, S. (2006) Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect. Cytogenetic and Genome Research, 114, (3-4), 351-358. (doi:10.1159/000094225).

Burkart, Kristin M., Barton, Sheila J., Holloway, John W., Yang, Ian A., Cakebread, Julie A., Cruikshank, William, Little, Frederic, Jin, Xiaoyi, Farrer, Lindsay A., Clough, Joanne B., Keith, Tim P., Holgate, Stephen, Center, David M. and O'Connor, George T. (2006) Association of asthma with a functional promoter polymorphism in the IL16 gene. Journal of Allergy and Clinical Immunology, 117, (1), 86-91. (doi:10.1016/j.jaci.2005.10.011).

Christensen, M.B., Lawlor, D.A., Gaunt, T.R., Howell, M.W., Davey Smith, G., Ebrahim, S. and Day, I.N.M. (2006) Genotype of galectin 2 (LGALS2) is associated with insulin-glucose profile in the British Women's Heart and Health Study. Diabetologia, 49, (4), 1-5. (doi:10.1007/s00125-006-0145-3).

Christensen, M.B., Lawlor, D.A., Gaunt, T.R., Howell, M.W., Davey Smith, G., Ebrahim, S. and Day, I.N.M. (2006) Genotype of galectin 2 (LGALS2) is associated with insulin-glucose profile in the British Women’s Heart and Health Study. Diabetologia, 49, (4), 673-677. (doi:10.1007/s00125-006-0145-3).

Chung, K. F., Hew, M., Score, J., Jones, A. V., Reiter, A., Cross, N. C. P. and Bain, B. J. (2006) Cough and hypereosinophilia due to FIP1L1-PDGFRA fusion gene with tyrosine kinase activity. European Respiratory Journal, 27, (1), 230-232. (doi:10.1183/09031936.06.00089405).

Cockwell, A. E., Maloney, V. K., Thomas, N. S., Smith, E. L., Gonda, P., Bass, P. and Crolla, J. A. (2006) Molecular investigation of a dicentric 13;17 chromosome found in a 21-week gestation fetus with multiple congenital abnormalities. Cytogenetic and Genome Research, 112, (1-2), 166-169. (doi:10.1159/000087530). (PMID:16276107).

Ennis, S., Murray, A., Youings, S., Brightwell, G., Herrick, D., Ring, S., Pembrey, M., Morton, N.E. and Jacobs, P. A. (2006) An investigation of FRAXA intermediate allele phenotype in a longitudinal sample. Annals of Human Genetics, 70, (2), 170-180. (doi:10.1111/j.1529-8817.2005.00220.x).

Ennis, Sarah, Ward, Daniel and Murray, Anna (2006) Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers. European Journal of Human Genetics, 14, (2), 253-255. (doi:10.1038/sj.ejhg.5201510).

Gaunt, Tom R., Hinks, Lesley J., Christensen, Mikkel B., Kiessling, Matthew and Day, Ian N.M. (2006) Experience applying light typerTM methodology to human SNPs relevant to growth and cardiovascular risk. In, Hecker, Karl H. (ed.) Genetic Variance Detection: Technologies for Pharmacogenomics. , DNA Press, 131-144. (Nuts & Bolts).

Gaunt, Tom R., Rodriguez, Santiago, Zapata, Carlos and Day, Ian N.M. (2006) MIDAS: software for analysis and visualisation of interallelic disequilibrium between multiallelic markers. BMC Bioinformatics, 7, 227. (doi: 10.1186/1471-2105-7-227).

Gavrilescu, L. Cristina, Cross, Nicholas C.P. and Van Etten, Richard A. (2006) Distinct leukemogenic activity and imatinib responsiveness of a BCR-PFGFRalpha fusion tyrosine kinase. Blood, 108, (11), p.1038A.

Gibson, Jane, Morton, Newton E. and Collins, Andrew (2006) Extended tracts of homozygosity in outbred human populations. Human Molecular Genetics, 15, (5), 789-795. (doi:10.1093/hmg/ddi493).

Gilling, Mette, Dullinger, Jörn S., Gesk, Stefan, Metzke-Heidemann, Simone, Siebert, Reiner, Meyer, Thomas, Brondum-Nielsen, Karen, Tommerup, Niels, Ropers, Hans-Hilger, Tümer, Zeynep, Kalscheuer, Vera M. and Thomas, N. Simon (2006) Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)(p11.2q21.2) mutation among northern Europeans. American Journal of Human Genetics, 78, (5), 878-883. (doi:10.1086/503632).

Gloyn, Anna L., Mackay, Deborah J.G., Weedon, Michael N., McCarthy, Mark I., Walker, Mark, Hitman, Graham, Knight, Bridget A., Owen, Katharine R., Hattersley, Andrew T. and Frayling, Timothy M. (2006) Assessment of the role of common genetic variation in the transient neonatal diabetes mellitus (TNDM) region in type 2 diabetes: a comparative genomic and tagging single nucleotide polymorphism approach. Diabetes, 55, (8), 2272-2276. (doi:10.2337/db06-0216).

Gosgnach, S., Lanuza, G.M., Butt, S.J.B., Saueressig, H., Zhang, Y., Velasquez, T., Riethmacher, D., Callaway, E.M., Kiehn, O. and Goulding, M. (2006) V1 spinal neurons regulate the speed of vertebrate locomotor outputs. Nature, 440, (7081), 215-219. (doi:10.1038/nature04545).

Goto, Masahiro, Piper Hanley, Karen Piper, Marcos, Josep, Wood, Peter J., Wright, Sarah, Postle, Anthony D., Cameron, Iain T., Mason, J. Ian, Wilson, David I. and Hanley, Neil A. (2006) In humans, early cortisol biosynthesis provides a mechanism to safeguard female sexual development. Journal of Clinical Investigation, 116, (4), 953-960. (doi:10.1172/JCI25091).

Hearle, N.C.M., Rudd, M.F., Lim, W., Murday, V., Lim, A.G., Phillips, R.K., Lee, P.W., O'Donohue, J., Morrison, P.J., Norman, A., Hodgson, S.V., Lucassen, A. and Houlston, R.S. (2006) Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome. Journal of Medical Genetics, 43, (4), e15-[4pp]. (doi:10.1136/jmg.2005.036830).

Holgate, S.T., Davies, D.E., Powell, R.M. and Holloway, J.W. (2006) ADAM33: a newly identified protease involved in airway remodelling. Pulmonary Pharmacology & Therapeutics, 19, (1), 3-11. (doi:10.1016/j.pupt.2005.02.008).

Hoornaert, K.P., Dewinter, C., Vereecke, I., Beemer, F.A., Courtens, W., Fryer, A., Fryssira, H., Lees, M., Mullner-Eidenbock, A., Rimoin, D.L., Siderius, L., Superti-Furga, A., Temple, K., Willems, P.J., Zankl, A., Zweier, C., De Paepe, A., Coucke, P. and Mortier, G.R. (2006) The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene. Journal of Medical Genetics, 43, (5), 406-413. (doi:10.1136/jmg.2005.035717).

Houghton, Franchesca D. (2006) Energy metabolism of the inner cell mass and trophectoderm of the mouse blastocyst. Differentiation, 74, (1), 11-18. (doi:10.1111/j.1432-0436.2006.00052.x).

Houlden, Henry, King, Rosalind, Blake, Julian, Groves, Mike, Love, Seth, Woodward, Cathy, Hammans, Simon, Nicoll, James A., Lennox, Graham, O'Donovan, Dominic G., Gabriel, Carolyn, Thomas, P.K. and Reilly, Mary M. (2006) Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I). Brain, 129, (2), 411-425. (doi:10.1093/brain/awh712).

Howell, W.M. and Rose-Zerilli, M.J. (2006) Interleukin-10 polymorphisms, cancer susceptibility and prognosis. Familial Cancer, 5, (2), 143-149. (doi:10.1007/s10689-005-0072-3).

Huang, Shuwen, Chen, Xiao-he and Day, Ian N.M. (2006) Combination of 768-well microplate array diagonal gel electrophoresis with duplex PCR of X and Y chromosome markers for quality control of epidemiological DNA banks. Electrophoresis, 27, (15), 3038-3041. (doi:10.1002/elps.200500745).

Ismail, A.R., Lachlan, K.L., Mumford, A.D., Temple, I.K. and Hodgkins, P.R. (2006) Hereditary hyperferritinemia cataract syndrome: ocular, genetic, and biochemical findings. European Journal of Ophthalmology, 16, (1), 153-160.

Jenner, Matthew W., Leone, Paola E., Walker, Brian A., Johnson, David C., Chiecchio, Laura, Cabanas, Elisabet Dachs, Dagrada, Gian Paolo, Nightingale, Mathew, Protheroe, Rebecca K.M., Stockley, David, Else, Monica, Ross, Fiona M., Cross, Nicholas C.P., Davies, Faith E. and Morgan, Gareth J. (2006) Abnormalities of 16q in multiple myeloma are associated with poor prognosis: 500K gene mapping and expression correlations identify two potential tumor suppressor genes, WWOX and CYLD. Blood, 108, (11), p.37A.

Jerjes, Walid K., Peters, Timothy J., Taylor, Norman F., Wood, Peter J., Wessely, Simon and Cleare, Anthony J. (2006) Diurnal excretion of urinary cortisol, cortisone, and cortisol metabolites in chronic fatigue syndrome. Journal of Psychosomatic Research, 60, (2), 145-153. (doi:10.1016/j.jpsychores.2005.07.008).

Jones, Amy V., Silver, Richard T., Waghorn, Katherine, Curtis, Claire, Kreil, Sebastian, Zoi, Katerina, Hochhaus, Andreas, Oscier, David, Metzgeroth, Georgia, Lengfelder, Eva, Reiter, Andreas, Chase, Andrew and Cross, Nicholas C. (2006) Minimal molecular response in polycythemia vera patients treated with imatinib or interferon alpha. Blood, 107, (8), 3339-3341. (doi:10.1182/blood-2005-09-3917).

Jovanovic, J., Score, J., Waghorn, K., Reiter, A., Gottardi, E., Saglio, G., Apperley, J., Martinelli, G., Preudhomme, C., Hehlmann, R., Grimwade, D. and Cross, N.C.P. (2006) Low-dose imatinib therapy leads to rapid induction of major molecular responses with achievement of molecular remission in FIP1L1 -PDGFRA associated hypereosinophilic syndrome. British Journal of Haematology, 133, (s1), p.13. (doi:10.1111/j.1365-2141.2006.06027.x).

Khatkar, Mehar S., Collins, Andrew, Cavanagh, Julie A.L., Hawken, Rachel J., Hobbs, Matthew, Zenger, Kyall R., Barris, Wes, McClintock, Alexander E., Thomson, Peter C., Nicholas, Frank W. and Raadsma, Herman W. (2006) A first-generation metric linkage disequilibrium map of bovine chromosome. Genetics, 174, (1), 79-85. (doi:10.1534/genetics.106.060418).

Khorashad, Jamshid S., Lipton, Jeffrey H., Marin, David, Milojkovic, Dragana, Cross, Nicholas C.P., Dibb, Nicholas, Melo, Junia V., Kamel-Reid, Suzanne, Goldman, John M., Apperley, Jane F. and Kaeda, Jaspal S. (2006) Abnormally small BCR-ABL transcripts in CML patients before and during imatinib treatment. Blood, 108, (11), p.611A.

Kralovicova, Jana, Gaunt, Tom R., Rodriguez, Santiago, Wood, Peter J., Day, Ian N.M. and Vorechovsky, Igor (2006) Variants in the human insulin gene that affect Pre-mRNA splicing: is -23HphI a functional single nucleotide polymorphism at IDDM2? Diabetes, 55, (1), 260-264. (doi:10.2337/diabetes.55.01.06.db05-0773).

Kralovicova, Jana and Vorechovsky, Igor (2006) Position-dependent repression and promotion of DQB1 intron 3 splicing by GGGG motifs. Journal of Immunology, 176, (4), 2381-2388.

Kreil, Sebastian, Waghorn, Katherine, Pfirrmann, Markus, Reiter, Andreas, Hehlmann, Rudiger, Hochhaus, Andreas and Cross, Nicholas C.P. (2006) Heterogeneous prognostic impact of 9q+ deletions in patients with chronic myelogenous leukemia. Blood, 108, (11), p.599A.

Lachlan, K.L., Youings, S., Costa, T., Jacobs, P.A. and Thomas, N.S. (2006) A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions. Human Genetics, 118, (5), 640-651. (doi:10.1007/s00439-005-0081-1).

Lawlor, Debbie A., Gaunt, Tom R., Hinks, Lesley J., Smith, George Davey, Timpson, Nick, Day, Ian N.M. and Ebrahim, Shah (2006) The association of the PON1 Q192R polymorphism with complications and outcomes of pregnancy: findings from the British Women's Heart and Health cohort study. Paediatric and Perinatal Epidemiology, 20, (3), 244-250. (doi:10.1111/j.1365-3016.2006.00716.x).

Lawlor, Debbie A., Timpson, Nick, Ebrahim, Shah, Day, Ian N.M. and Smith, George Davey (2006) The association of oestrogen receptor alpha-haplotypes with cardiovascular risk factors in the British Women's Heart and Health Study. European Heart Journal, 27, (13), 1597-1604. (doi:10.1093/eurheartj/ehi833).

Lewis, S.J., Lawlor, D.A., Davey Smith, G., Araya, R., Timpson, N., Day, I.N.M. and Ebrahim, S. (2006) The thermolabile variant of MTHFR is associated with depression in the British Women's Heart and Health Study and a meta-analysis. Molecular Psychiatry, 11, (4), 352-360. (doi:10.1038/sj.mp.4001790).

Lotery, Andrew J., Baas, Dominique, Ridley, Caroline, Jones, Richard P.O., Klaver, Caroline C.W., Stone, Edwin, Nakamura, Tomoyuki, Luff, Andrew, Griffiths, Helen, Wang, Tao, Bergen, Arthur A.B. and Trump, Dorothy (2006) Reduced secretion of fibulin 5 in age related macular degeneration and cutis laxa. Human Mutation, 27, (6), 568-574. (doi:10.1002/humu.20344).

Mackay, D.J.G., Boonen, S.E., Clayton-Smith, J., Goodship, J., Hahnemann, J.M.D., Kant, S.G., Njølstad, P.R., Robin, N.H., Robinson, D.O., Siebert, R., Shield, J.P.H., White, H.E. and Temple, I.K. (2006) A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus. Human Genetics, 120, (2), 262-269. (doi:10.1007/s00439-006-0205-2).

Mackay, D.J.G., Hahnemann, J.M.D., Boonen, S.E., Poerksen, S., Bunyan, D.J., White, H.E., Durston, V.J., Thomas, N.S., Robinson, D.O., Shield, J.P.H., Clayton-Smith, J. and Temple, I.K. (2006) Epimutation of the TNDM locus and the Beckwith-Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus. Human Genetics, 119, (1-2), 179-184. (doi:10.1007/s00439-005-0127-4).

Manser, Rosemary C. and Houghton, Franchesca D. (2006) Ca2+ -linked upregulation and mitochondrial production of nitric oxide in the mouse preimplantation embryo. Journal of Cell Science, 119, (10), 2048-2055. (doi:10.1242/jcs.02927).

McCormick, James, Barry, Sean P., Sivarajah, Ahila, Stefanutti, Giorgio, Townsend, Paul A., Lawrence, Kevin M., Eaton, Simon, Knight, Richard A., Thiemermann, Christoph, Latchman, David S. and Stephanou, Anastasis (2006) Free radical scavenging inhibits STAT phosphorylation following in vivo ischemia/reperfusion injury. Federation of American Societies for Experimental Biology (FASEB) Journal, 20, (12), 2115-2117. (doi:10.1096/fj.06-6188fje).

Morton, Newton E. (2006) Fifty years of genetic epidemiology, with special reference to Japan. Journal of Human Genetics (doi:10.1007/s10038-006-0366-9).

Raponi, M., Upadhyaya, M. and Baralle, D. (2006) Functional splicing assay shows a pathogenic intronic mutation in neurofibromatosis type 1 (NF1) due to intronic sequence exonization. Human Mutation, 27, (3), 294-295. (doi:10.1002/humu.9412).

Renwick, Anthony, Thompson, Deborah, Seal, Sheila, Kelly, Patrick, Chagtai, Tasnim, Ahmed, Munaza, North, Bernard, Jayatilake, Hiran, Barfoot, Rita, Spanova, Katarina, McGuffog, Lesley, Evans, D. Gareth, Eccles, Diana, Easton, Douglas F., Stratton, Michael R. and Rahman, Nazneen Breast Cancer Susceptibility Collaboration (UK) (2006) ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles. Nature Genetics, 38, (8), 873-875. (doi:10.1038/ng1837).

Riethmacher, Dieter, Lim, Filip and Schimmang, Thomas (2006) Efficient transfer of HSV-1 amplicon vectors into embryonic stem cells and their derivatives. Methods in Molecular Biology, 329, 265-272. (doi:10.1385/1-59745-037-5:265).

Rivera, H., Yala-Madrigal, M.L., Barros-Nunez, J.P., Rnaud-Lopez, L., Maloney, V. and Crolla, J.A. (2006) A highly complex rea(2;3;11) and aniridia by position effect. Cytogenetic and Genome Research, 114, (1), 83-88. (doi:10.1159/000091933).

Rodriguez, Santiago, Huang, Shuwen, Chen, Xiao-he, Gaunt, Tom R., Syddall, Holly E., Gilg, Julie A., Miller, George J., Cooper, Cyrus C., Cook, Derek G., Whincup, Peter H. and Day, Ian N.M. (2006) A study of TH01 and IGF2-INS-TH haplotypes in relation to smoking initiation in three independent surveys. Pharmacogenetics and Genomics, 16, (1), 15-23.

Score, J., Curtis, C., Waghorn, K., Stalder, M., Jotterand, M., Grand, F.H. and Cross, N.C. (2006) Identification of a novel imatinib responsive KIF5B-PDGFRA fusion gene following screening for PDGFRA overexpression in patients with hypereosinophilia. Leukemia, 20, (5), 827-832. (doi:10.1038/sj.leu.2404154).

Self, James Edward, Ennis, Sarah, Collins, Andrew, Shawkat, Fatima, Harris, Christopher Mark, Mackey, David Anthony, Hodgkins, Peter Robert, Temple, Isabelle Karen, Chen, Xiaoli and Lotery, Andrew John (2006) Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3. Molecular Vision, 12, 1211-1216.

Service, Susan, DeYoung, Joseph, Karayiorgou, Maria, Roos, J. Louw, Pretorious, Herman, Bedoya, Gabriel, Ospina, Jorge, Ruiz-Linares, Andres, Macedo, António, Palha, Joana Almeida, Heutink, Peter, Aulchenko, Yurii, Oostra, Ben, van Duijn, Cornelia, Jarvelin, Marjo-Riitta, Varilo, Teppo, Peddle, Lynette, Rahman, Proton, Piras, Giovanna, Monne, Maria, Murray, Sarah, Galver, Luana, Peltonen, Leena, Sabatti, Chiara, Collins, Andrew and Freimer, Nelson (2006) Letter. Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies. Nature Genetics, 38, (5), 556-560. (doi:10.1038/ng1770).

Smith, Mathew J., Alharbi, Khalid K., Aldahmesh, Mohammed A., Pante-de-Sousa, Gabriella, Hou, Guangwei, Chen, Xiao-he, Gaunt, Tom R., Eccles, Diana M., Fox, Keith R. and Day, Ian N.M. (2006) Madge-based technologies for identification of unknown mutations at the population level: MeltMADGE and EndoVII-MADGE. In, Hecker, Karl H. (ed.) Genetic Variance Detection: Technologies for Pharmacogenomics. , DNA Press, 146-152. (Nuts & Bolts).

Thomas, N. Simon, Durkie, Miranda, Potts, Gemma, Sandford, Richard, Van Zyl, Berendine, Youings, Sheila, Dennis, Nicholas R. and Jacobs, Patricia A. (2006) Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11. European Journal of Human Genetics, 14, (7), 831-837. (doi:10.1038/sj.ejhg.5201617).

Thomas, N. Simon, Durkie, Miranda, Van Zyl, Berendine, Sanford, Richard, Potts, Gemma, Youings, Sheila, Dennis, Nicholas and Jacobs, Patricia (2006) Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in man. Human Genetics, 119, (4), 444-450. (doi:10.1007/s00439-006-0157-6).

Ticho, Benjamin H., Hilchie-Schmidt, Clair, Egel, Robert T., Traboulsi, Elias I., Howarth, Rachel J. and Robinson, David (2006) Ocular findings in Gillespie-like syndrome: Association with a new PAX6 mutation. Ophthalmic Genetics, 27, (4), 145-149. (doi:10.1080/13816810600976897).

Turner, C.L.S., Skinner, A.C., Castle, B.M. and Wellesley, D.G. (2006) Mid-trimester hyperechogenic bowel in a fetus of Japanese origin: caution in interpreting reported CFTR mutation (L548Q). Prenatal Diagnosis, 26, (9), 875-876. (doi:10.1002/pd.1535).

Turnpenny, Lee W., Spalluto, Cosma M., Perrett, Rebecca M., O'Shea, Marie, Piper Hanley, Karen, Cameron, Iain T., Wilson, David I. and Hanley, Neil A. (2006) Evaluating human embryonic germ cells: concord and conflict as pluripotent stem cells. Stem Cells, 24, (2), 212-220. (doi:10.1634/stemcells.2005-0255).

Valentim, Lauren, Laurence, Kevin M., Townsend, Paul A., Carroll, Christopher J., Soond, Surinder, Scarabelli, Tiziano M., Knight, Richard A., Latchman, David S. and Stephanou, Anastasis (2006) Urocortin inhibits Beclin1-mediated autophagic cell death in cardiac myocytes exposed to ischaemia/reperfusion injury. Journal of Molecular and Cellular Cardiology, 40, (6), 846-852. (doi:10.1016/j.yjmcc.2006.03.428).

Vizmanos, J.L., Ormazábal, C., Larráyoz, M.J., Cross, N.C.P. and Calasanz, M.J. (2006) JAK2 V617F mutation in classic chronic myeloproliferative diseases: a report on a series of 349 patients. Leukemia, 20, (3), 534-535. (doi:10.1038/sj.leu.2404086).

Walker, Brian A., Leone, Paola E., Jenner, Matthew W., Li, Cheng, Gonzalez, David, Johnson, David C., Ross, Fiona M., Davies, Faith E. and Morgan, Gareth J. (2006) Integration of global SNP-based mapping and expression arrays reveals key regions, mechanisms and genes important in the pathogenesis of multiple myeloma. Blood, 108, (5), 1733-1743. (doi:10.1182/blood-2006-02-005496).

Walz, Christoph, Metzgeroth, Georgia, Schoch, Claudia, Haferlach, Torsten, Hehlmann, Rudiger, Hochhaus, Andreas, Cross, Nicholas C.P. and Reiter, Andreas (2006) Characterization of two new imatinib-responsive fusion genes generated by disruption of PDGFRB in eosinophilia-associated chronic myeloproliferative disorders. Blood, 108, (11), p.200A.

White, H., Hall, V.J., Boyle, T., Warner, J., McLuskey, J., Sibbring, J., Hamilton, S., Diack, J., Allen, S., Jones, M. and Cross, N.C.P. (2006) NGRL (Wessex) evaluation of CE marked in vitro diagnostic test kits for prenatal diagnosis of aneuploidy. Journal of Medical Genetics, 43, pp.S91.

White, Helen E., Durston, Victoria J., Harvey, John F. and Cross, Nicholas C. (2006) Quantitative analysis of SNRPN [correction of SRNPN] gene methylation by pyrosequencing as a diagnostic test for Prader-Willi syndrome and Angelman syndrome. Clinical Chemistry, 52, (6), 1005-1013. (doi:10.1373/clinchem.2005.065086).

Yang, I.A., Fong, K.M., Holgate, S.T. and Holloway, J.W. (2006) The role of Toll-like receptors and related receptors of the innate immune system in asthma. Current Opinion in Allergy and Clinical Immunology, 6, (1), 23-28.

Ye, Shu (2006) Influence of matrix metalloproteinase genotype on cardiovascular disease susceptibility and outcome. Cardiovascular research, 69, (3), 636-645. (doi:10.1016/j.cardiores.2005.07.015).

Zhang, Ling Yan, Smith, Matthew L., Schultheis, Beate, Fitzgibbon, Jude, Lister, T. Andrew, Melo, Junia V., Cross, Nicholas C.P. and Cavenagh, Jamie D. (2006) A novel K509I mutation of KIT identified in familial mastocytosis—in vitro and in vivo responsiveness to imatinib therapy. Leukemia Research, 30, (4), 373-378. (doi:10.1016/j.leukres.2005.08.015).

Zhang, Ling-Yan, Xu, Gong-Li and Cross, Nicholas C.P. (2006) [Application of denaturing high performance liquid chromatography to mutation detection of the c-kit gene in mastocytosis]. Zhongguo shi yan xue ye xue za zhi [Journal of Experimental Hematology], 14, (5), 981-984.