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1 : Bidwell, JL, Clay, TM, Wood, NAP, Pursall, MC, Martin, AF, Bradley, BA and Hui, KM (1993) Rapid HLA-DR-Dw and DP matching by PCR fingerprinting and related DNA heteroduplex technologies. pp 99-116 in: Handbook of HLA Typing Techniques [Eds KM Hui & JL Bidwell] CRC Press: Boca Raton, Florida.
2 : Wood, N, Tyfield, L, Bidwell, J (1993) Rapid classification of phenylketonuria genotypes by analysis of heteroduplexes generated by PCR-amplifiable synthetic DNA. Human Mutation 2: 131-137.
3 : Bidwell, JL, Wood, NAP, Tyfield, LA, Clay, TM, Culpan, D, Evans, JM, Pursall, MC, Bradley, BA (1993) Universal heteroduplex generators: reagents for genotyping of HLA and of human diseases. Molecular Bases of Human Diseases (Ed. E.E.Polli). pp27-34. Elsevier/North-Holland, Amsterdam.
4 : Wood, N, Standen, G, Hows, J, Bradley, B, Bidwell, J. (1993) diagnosis of sickle cell disease with a universal heteroduplex generator. Lancet 342: 1519-1520.
6 : Clay, TM, Cuplan, D, Howell, WM, Sage, DA, Bradley, BA, Bidwell, JL. (1994) UHG crossmatching: a comparison with PCR-SSO typing in the selection of HLA-DPB1-compatible bone marrow donors. Transplantation 58: 200-207.
7 : Bidwell, JL. (1994) Advances in DNA-based HLA-typing methods. Immunology Today 15: 303-307.
8 : Tyfield, LA, Stephenson, A, Bidwell, JL, Wood, NAP, Cockburn, F, Harvie, A, Smith, I. (1994) Mutation analysis of the phenylalanine hydroxylase gene using heteroduplex analysis with synthetic DNA constructs. Acta Paediatrica 83: 47-48.
9 : Savage, DA, Wood, NAP, Bidwell, JL, Hui, KM. (1995) HLA-DRB1*01 subtyping by heteroduplex analysis. Tissue Antigens 45: 120-124.
10 : Wood, N, Standen, G, Murray, EW, Lillicrap, D, Holmberg, L, Peake, IR, Bidwell, J. (1995) Rapid genotype analysis in type 2B von Willebrand's disease using a universal heteroduplex generator. Brit J Haematol 89: 152-156
11 : Wood, N, Standen, G, Old, J, Bidwell, J. (1995) Optimisation and properties of a UHG for genotypng of haemoglobins S and C. Hum Mutation 5: 166-172.
12 : Savage, DA, Wood, NAP, Bidwell, JL, Fitches, A, Old, JM, Hui, KM. (1995) Detection of b-thalassaemia mutations using DNA heteroduplex generator molecules. Brit J Haematol 90: 564-571.
13 : Tyfield, LA, Zschocke, J, Stephenson, A, Cockburn, F, Harvie, A, Bidwell, JL, Wood, NAP, Hunt, LP. (1995) Discordant phenylketonuria phenotypes in one family: the relationship between genotype and clinical outcome is a function of multiple effects. J Med Genet 32: 132-136.
14 : Wood, NAP, Bidwell, JL. (1996) UHG: heteroduplex and universal heteroduplex generator analysis. In: Laboratory protocols for mutation detection (ed Landegren, U), pp 105-112. Oxford University Press for the Human Genome Organisation.
15 : Wood, N, Bidwell, J. (1996) Genetic screening and testing by induced heteroduplex formation. Electrophoresis 17: 247-254.
17 : Savage, DA, Tang, JP, Wood, NAP, Evans, J, Bidwell, JL, Wee, JLK, Oei, AA, Hui, KM (1996) A rapid HLA-DRB1*04 subtyping method using PCR and DNA heteroduplex generators. Tissue Antigens 47: 284-292.
21 : Tyfield, LA, Stephenson, A, Cockburn, F, Harvie, A, Bidwell, JL, Wood, NAP, Pilz, DT, Harper, P, Smith, I (1997) Sequence variation at the phenylalanine hydroxylase gene in the British Isles. Am J Hum Genet 60: 388-396
22 : Enayat, MS, Theophilus, BDM, Hill, FGH, Rose, PE, Culpan, D, Bidwell, J, Standen, GR (1998) A new candidate mutation (K755E) causing Type 2A Von Willebrand’s disease identified by UHG analysis. Br J Haematol 79:240
23 : Culpan, D, Goodeve, A, Bowen, DJ, Standen, G, Bidwell, J (1988) Rapid genotypic diagnosis of type 2A von Willebrand’s disease by heteroduplex analysis. Clin. Lab. Haem 20: 177-178.
24 : Bowen, DJ, Standen, GR, Mazurier, C, Gaucher, C, Cumming, A, Keeney, S, Bidwell, J (1998) Type 2N von Willebrand disease: rapid genetic diagnosis of G2811A (R854Q), C2696T (R816W), T2701A (H817Q) and G2823T (C858F) - detection of a novel candidate type 2N mutation: C2801T (R854W). Thromb Haemost 80: 32-36.
27 : Wood, NAP, Thompson, SC, Smith, RM, Bidwell, JL (2000) Identification of human TGF-b1 signal (leader) sequence polymorphisms by PCR-RFLP. J Immunol Methods 234: 117-122.
28 : Bidwell, JL, Olomolaiye, OO, Keen, LJ, Wood, NAP, Morse, HR, Laundy, GJ, Thompson, SJ (2000) Cytokine gene polymorphism. In: Human Blood Cells: Consequences of Genetic Polymorphism (Ed. King, M-J), pp375-400. Imperial College Press, London.
33 : Cardoso SP, Keen L, Bidwell J. (2004) Identification of two novel single nucleotide polymorphisms in the promoter of the human IL-18 receptor alpha gene. European Journal of Immunogenetics 31: 27-29
38 : Medford AR, Keen LJ, Bidwell JL, Millar AB. (2005) Vascular endothelial growth factor gene polymorphism and acute respiratory distress syndrome. Thorax 60:244-248.
39 : Smith AJ, Elson CJ, Perry MJ, Bidwell JL. (2005) Accuracy of haplotype association studies is enhanced by increasing number of polymorphic loci examined: comment on the article by Meulenbelt et al. Arthritis Rheum. 52:675
40 : Atan D, Turner SJ, Kilmartin DJ, Forrester JV, Bidwell J, Dick AD, Churchill AJ. (2005) Cytokine gene polymorphism in sympathetic ophthalmia. Inv Ophthal Visual Sci (in press)
41 : Spink CF, Gray LC, Davies FE, Cohen D, Hawkins K, Morgan GJ, Bidwell, JL (2005) Haplotypic structure across the IκBa gene (NFKBIA) and association with multiple myeloma. Cancer Letters (in press)
