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Publications from S.Halford

  1. Stephanie Halford, Susana S Pires, Michael Turton, Lei Zheng, Irene Gonzalez-Menendez, Wayne L Davies, Stuart N Peirson, Jose M Garcia-Fernandez, Mark W Hankins and Russell G Foster (2009): VA opsin-based photoreceptors in the hypothalamus of birds. - Curr Biol, 19(16):1396-402.
  2. Susana S Pires, Steven Hughes, Michael Turton, Zare Melyan, Stuart N Peirson, Lei Zheng, Maria Kosmaoglou, James Bellingham, Michael E Cheetham, Robert J Lucas, Russell G Foster, Mark W Hankins and Stephanie Halford (2009): Differential expression of two distinct functional isoforms of melanopsin (Opn4) in the mammalian retina. - J Neurosci, 29(39):12332-42.
  3. Stuart N Peirson, Stephanie Halford and Russell G Foster (2009): The evolution of irradiance detection: melanopsin and the non-visual opsins. - Philos Trans R Soc Lond B Biol Sci, 364(1531):2849-65.
  4. Susana S Pires, Julia Shand, James Bellingham, Catherine Arrese, Michael Turton, Stuart Peirson, Russell G Foster and Stephanie Halford (2007): Isolation and characterization of melanopsin (Opn4) from the Australian marsupial Sminthopsis crassicaudata (fat-tailed dunnart). - Proc Biol Sci, 274(1627):2791-9.
  5. L Ocaka, C Spalluto, D I Wilson, D M Hunt and S Halford (2005): Chromosomal localization, genomic organization and evolution of the genes encoding human phosphatidylinositol transfer protein membrane-associated (PITPNM) 1, 2 and 3. - Cytogenet Genome Res, 108(4):293-302.
  6. E Zeggini, J R C Parkinson, S Halford, K R Owen, M Walker, G A Hitman, J C Levy, M J Sampson, T M Frayling, A T Hattersley and M I McCarthy (2005): Examining the relationships between the Pro12Ala variant in PPARG and Type 2 diabetes-related traits in UK samples. - Diabet Med, 22(12):1696-700.
  7. E Zeggini, C J Groves, J R C Parkinson, S Halford, K R Owen, T M Frayling, M Walker, G A Hitman, J C Levy, S O'Rahilly, A T Hattersley and M I McCarthy (2005): Large-scale studies of the association between variation at the TNF/LTA locus and susceptibility to type 2 diabetes. - Diabetologia, 48(10):2013-7.
  8. C Y Gregory-Evans, M J Williams, S Halford and K Gregory-Evans (2004): Ocular coloboma: a reassessment in the age of molecular neuroscience. - J Med Genet, 41(12):881-91.
  9. Mohamed F El-Ashry, Mai M Abd El-Aziz, Simon Wilkins, Michael E Cheetham, Susan E Wilkie, Alison J Hardcastle, Stephanie Halford, Ahmed Y Bayoumi, Linda A Ficker, Stephen Tuft, Shomi S Bhattacharya and Neil D Ebenezer (2002): Identification of novel mutations in the carbohydrate sulfotransferase gene (CHST6) causing macular corneal dystrophy. - Invest Ophthalmol Vis Sci, 43(2):377-82.
  10. S Halford, M S Freedman, J Bellingham, S L Inglis, S Poopalasundaram, B G Soni, R G Foster and D M Hunt (2001): Characterization of a novel human opsin gene with wide tissue expression and identification of embedded and flanking genes on chromosome 1q43. - Genomics, 72(2):203-8.
  11. S Murray, S Halford, N D Ebenezer, C Y Gregory-Evans and S S Bhattacharya (2001): Assignment of BCL2L11 to human chromosome band 2p13 with somatic cell and radiation hybrids. - Cytogenet Cell Genet, 92(3-4):353.
  12. S Halford, J Bellingham, L Ocaka, M Fox, S Johnson, R G Foster and D M Hunt (2001): Assignment of panopsin (OPN3) to human chromosome band 1q43 by in situ hybridization and somatic cell hybrids. - Cytogenet Cell Genet, 95(3-4):234-5.
  13. S Halford, P Spencer, J Greenwood, H Winton, D M Hunt and P Adamson (2000): Assignment of claudin-1 (CLDN1) to human chromosome 3q28-->q29 with somatic cell hybrids. - Cytogenet Cell Genet, 88(3-4):217.
  14. S Halford, K S Dulai, S C Daw, J Fitzgibbon and D M Hunt (1998): Isolation and chromosomal localization of two human CDP-diacylglycerol synthase (CDS) genes. - Genomics, 54(1):140-4.
  15. H Sirotkin, H O'Donnell, R DasGupta, S Halford, B St Jore, A Puech, S Parimoo, B Morrow, A Skoultchi, S M Weissman, P Scambler and R Kucherlapati (1997): Identification of a new human catenin gene family member (ARVCF) from the region deleted in velo-cardio-facial syndrome. - Genomics, 41(1):75-83.
  16. C Roberts, S C Daw, S Halford and P J Scambler (1997): Cloning and developmental expression analysis of chick Hira (Chira), a candidate gene for DiGeorge syndrome. - Hum Mol Genet, 6(2):237-45.
  17. R Wadey, S Daw, C Taylor, U Atif, S Kamath, S Halford, H O'Donnell, D Wilson, J Goodship and J Burn (1995): Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome. - Hum Mol Genet, 4(6):1027-33.
  18. S Halford, M G Mattei, S Daw and P J Scambler (1995): A novel C2H2 zinc-finger protein gene (ZNF160) maps to human chromosome 19q13.3-q13.4. - Genomics, 25(1):322-3.
  19. M G Mattei, S Halford and P J Scambler (1994): Mapping of the Tuple1 gene to mouse chromosome 16A-B1. - Genomics, 23(3):717-8.
  20. M Ramsay, R Williamson, X Estivill, B J Wainwright, M F Ho, S Halford, J Kere, E Savilahti, A de la Chapelle and M Schwartz (1993): Haplotype analysis to determine the position of a mutation among closely linked DNA markers. - Hum Mol Genet, 2(7):1007-14.
  21. C Desmaze, P Scambler, M Prieur, S Halford, D Sidi, F Le Deist and A Aurias (1993): Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization. - Hum Genet, 90(6):663-5.
  22. R Wadey, S Daw, A Wickremasinghe, C Roberts, D Wilson, J Goodship, J Burn, S Halford and P J Scambler (1993): Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134). - J Med Genet, 30(10):818-21.
  23. S Halford, E Lindsay, M Nayudu, A H Carey, A Baldini and P J Scambler (1993): Low-copy-number repeat sequences flank the DiGeorge/velo-cardio-facial syndrome loci at 22q11. - Hum Mol Genet, 2(2):191-6.
  24. S Halford, D I Wilson, S C Daw, C Roberts, R Wadey, S Kamath, A Wickremasinghe, J Burn, J Goodship and M G Mattei (1993): Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome. - Hum Mol Genet, 2(10):1577-82.
  25. E A Lindsay, S Halford, R Wadey, P J Scambler and A Baldini (1993): Molecular cytogenetic characterization of the DiGeorge syndrome region using fluorescence in situ hybridization. - Genomics, 17(2):403-7.
  26. S Halford, R Wadey, C Roberts, S C Daw, J A Whiting, H O'Donnell, I Dunham, D Bentley, E Lindsay and A Baldini (1993): Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease. - Hum Mol Genet, 2(12):2099-107.
  27. J R Dorin, P Dickinson, E Emslie, A R Clarke, L Dobbie, M L Hooper, S Halford, B J Wainwright and D J Porteous (1992): Successful targeting of the mouse cystic fibrosis transmembrane conductance regulator gene in embryonal stem cells. - Transgenic Res, 1(2):101-5.
  28. A H Carey, D Kelly, S Halford, R Wadey, D Wilson, J Goodship, J Burn, T Paul, A Sharkey and J Dumanski (1992): Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome. - Am J Hum Genet, 51(5):964-70.
  29. F Tata, P Stanier, C Wicking, S Halford, H Kruyer, N J Lench, P J Scambler, C Hansen, J C Braman and R Williamson (1991): Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene. - Genomics, 10(2):301-7.
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