School of Medicine
  • Print
   
   

School staff listing

People listings by divisions

 

Image of Amanda Henry

Amanda Henry

Research Fellow, Faculty of Medicine & Health Sciences

Contact

Recent Publications

  • LIU B, BILLINGTON CK, HENRY AP, BHAKER SK, KHEIRALLAH AK, SWAN C and HALL IP, 2018. Chloride intracellular channel 1 (CLIC1) contributes to modulation of cyclic AMP-activated whole-cell chloride currents in human bronchial epithelial cells. Physiological reports. 6(2),
  • WAIN LV, SHRINE N, ARTIGAS MS, ERZURUMLUOGLU AM, NOYVERT B, BOSSINI-CASTILLO L, OBEIDAT M, HENRY AP, PORTELLI MA, HALL RJ, BILLINGTON CK, RIMINGTON TL, FENECH AG, JOHN C, BLAKE T, JACKSON VE, ALLEN RJ, PRINS BP, , CAMPBELL A, PORTEOUS DJ, JARVELIN MR, WIELSCHER M, JAMES AL, HUI J, WAREHAM NJ, ZHAO JH, WILSON JF, JOSHI PK, STUBBE B, RAWAL R, SCHULZ H, IMBODEN M, PROBST-HENSCH NM, KARRASCH S, GIEGER C, DEARY IJ, HARRIS SE, MARTEN J, RUDAN I, ENROTH S, GYLLENSTEN U, KERR SM, POLASEK O, KÄHÖNEN M, SURAKKA I, VITART V, HAYWARD C, LEHTIMÄKI T, RAITAKARI OT, EVANS DM, HENDERSON AJ, PENNELL CE, WANG CA, SLY PD, WAN ES, BUSCH R, HOBBS BD, LITONJUA AA, SPARROW DW, GULSVIK A, BAKKE PS, CRAPO JD, BEATY TH, HANSEL NN, MATHIAS RA, RUCZINSKI I, BARNES KC, BOSSÉ Y, JOUBERT P, VAN DEN BERGE M, BRANDSMA CA, PARÉ PD, SIN DD, NICKLE DC, HAO K, GOTTESMAN O, DEWEY FE, BRUSE SE, CAREY DJ, KIRCHNER HL, , JONSSON S, THORLEIFSSON G, JONSDOTTIR I, GISLASON T, STEFANSSON K, SCHURMANN C, NADKARNI G, BOTTINGER EP, LOOS RJ, WALTERS RG, CHEN Z, MILLWOOD IY, VAUCHER J, KURMI OP, LI L, HANSELL AL, BRIGHTLING C, ZEGGINI E, CHO MH, SILVERMAN EK, SAYERS I, TRYNKA G, MORRIS AP, STRACHAN DP, HALL IP and TOBIN MD, 2017. Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. Nature genetics. (In Press.)
  • WARE JS, WAIN LV, CHANNAVAJJHALA SK, JACKSON VE, EDWARDS E, LU R, SIEW K, JIA W, SHRINE N, KINNEAR S, JALLAND M, HENRY AP, CLAYTON J, O'SHAUGHNESSY KM, TOBIN MD, SCHUSTER V, COOK S, HALL IP and GLOVER M, 2017. Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia. The Journal of clinical investigation. (In Press.)
  • ALLEN RJ, PORTE J, BRAYBROOKE R, FLORES C, FINGERLIN TE, OLDHAM JM, GUILLEN-GUIO B, MA SF, OKAMOTO T, JOHN AE, OBEIDAT M, YANG IV, HENRY A, HUBBARD RB, NAVARATNAM V, SAINI G, THOMPSON N, BOOTH HL, HART SP, HILL MR, HIRANI N, MAHER TM, MCANULTY RJ, MILLAR AB, MOLYNEAUX PL, PARFREY H, RASSL DM, WHYTE MKB, FAHY WA, MARSHALL RP, OBALLA E, BOSSÉ Y, NICKLE DC, SIN DD, TIMENS W, SHRINE N, SAYERS I, HALL IP, NOTH I, SCHWARTZ DA, TOBIN MD, WAIN LV and JENKINS RG, 2017. Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. The Lancet. Respiratory medicine. (In Press.)
  • MILLER S, HENRY AP, HODGE E, KHEIRALLAH AK, BILLINGTON CK, RIMINGTON TL, BHAKER SK, OBEIDAT M, MELÉN E, MERID SK, SWAN C, GOWLAND C, NELSON CP, STEWART CE, BOLTON CE, KILTY I, MALARSTIG A, PARKER SG, MOFFATT MF, WARDLAW AJ, HALL IP and SAYERS I, 2016. The Ser82 RAGE Variant Affects Lung Function and Serum RAGE in Smokers and sRAGE Production In Vitro. PloS one. 11(10), e0164041
  • GARSED, K., CHERNOVA, J., HASTINGS, M., LAM, C., MARCIANI, L., SINGH, G., HENRY, A., HALL, I., WHORWELL, P. and SPILLER, R., 2014. A randomised trial of ondansetron for the treatment of irritable bowel syndrome with diarrhoea: Gut Gut. 63(10), 1617-25
  • HODGE E, NELSON CP, MILLER S, BILLINGTON CK, STEWART CE, SWAN C, MALARSTIG A, HENRY AP, GOWLAND C, MELÉN E, HALL IP and SAYERS I, 2013. HTR4 gene structure and altered expression in the developing lung Respiratory research. 14, 77
  • OBEIDAT M, MILLER S, PROBERT K, BILLINGTON CK, HENRY AP, HODGE E, NELSON CP, STEWART CE, SWAN C, WAIN LV, ARTIGAS MS, MELÉN E, USHEY K, HAO K, LAMONTAGNE M, BOSSÉ Y, POSTMA DS, TOBIN MD, SAYERS I and HALL IP, 2013. GSTCD and INTS12 Regulation and Expression in the Human Lung PloS one. 8(9), e74630
  • GLOVER M, WARE JS, HENRY A, WOLLEY M, WALSH R, WAIN LV, XU S, VAN'T HOFF WG, TOBIN MD, HALL IP, COOK S, GORDON RD, STOWASSER M and O'SHAUGHNESSY KM, 2013. Detection of mutations in KLHL3 and CUL3 in families with Familial Hyperkalaemic Hypertension (FHHt or Gordon Syndrome). Clinical science (London, England : 1979). (In Press.)
  • HANCOCK DB, ARTIGAS MS, GHARIB SA, HENRY A, MANICHAIKUL A, RAMASAMY A, LOTH DW, IMBODEN M, KOCH B, MCARDLE WL, SMITH AV, SMOLONSKA J, SOOD A, TANG W, WILK JB, ZHAI G, ZHAO JH, ASCHARD H, BURKART KM, CURJURIC I, EIJGELSHEIM M, ELLIOTT P, GU X, HARRIS TB, JANSON C, HOMUTH G, HYSI PG, LIU JZ, LOEHR LR, LOHMAN K, LOOS RJF, MANNING AK, MARCIANTE KD, OBEIDAT M, POSTMA DS, ALDRICH MC, BRUSSELLE GG, CHEN T, EIRIKSDOTTIR G, FRANCESCHINI N, HEINRICH J, ROTTER JI, WIJMENGA C, WILLIAMS OD, BENTLEY AR, HOFMAN A, LAURIE CC, LUMLEY T, MORRISON AC, JOUBERT BR, RIVADENEIRA F, COUPER DJ, KRITCHEVSKY SB, LIU Y, WJST M, WAIN LV, VONK JM, UITTERLINDEN AG, ROCHAT T, RICH SS, PSATY BM, O'CONNOR GT, NORTH KE, MIREL DB, MEIBOHM B, LAUNER LJ, KHAW K, HARTIKAINEN A, HAMMOND CJ, GLÄSER S, MARCHINI J, KRAFT P, WAREHAM NJ, VÖLZKE H, STRICKER BHC, SPECTOR TD, PROBST-HENSCH NM, JARVIS D, JARVELIN M, HECKBERT SR, GUDNASON V, BOEZEN HM, BARR RG, CASSANO PA, STRACHAN DP, FORNAGE M, HALL IP, DUPUIS J, TOBIN MD and LONDON SJ, 2012. Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. PLoS genetics. 8(12), e1003098
  • WILK, J.B., SHRINE, N.R.G., LOEHR, L.R., ZHAO, J.H., MANICHAIKUL, A., LOPEZ, L.M., SMITH, A.V., HECKBERT, S.R., SMOLONSKA, J., TANG, W., LOTH, D.W., CURJURIC, I., HUI, J., CHO, M.H., LATOURELLE, J.C., HENRY, A.P., ALDRICH, M., BAKKE, P., BEATY, T.H., BENTLEY, A.R., BORECKI, I.B., BRUSSELLE, G.G., BURKART, K.M., CHEN, T., COUPER, D., CRAPO, J.D., DAVIES, G., DUPUIS, J., FRANCESCHINI, N., GULSVIK, A., HANCOCK, D.B., HARRIS, T.B., HOFMAN, A., IMBODEN, M., JAMES, A.L., KHAW, K., LAHOUSSE, L., LAUNE,R L.J., LITONJUA, A., LIU, Y., LOHMAN, K.K., LOMAS, D.A., LUMLEY, T., MARCIANTE, K.D., MCARDLE, W.L., MEIBOHM, B., MORRISON, A.C., MUSK, A.W., MYERS, R.H., NORTH, K.E., POSTMA, D.S., PSATY, B.M., RICH, S.S., RIVADENEIRA, F., ROCHAT, T., ROTTER, J.I., ARTIGAS, M.S., STARR, J.M., UITTERLINDEN, A.G., WAREHAM, N.J., WIJMENGA, C., ZANEN, P., PROVINCE, M.A., SILVERMAN, E.K., DEARY, I.J., PALMER, L.J., CASSANO, P.A., GUDNASON, V., BARR, R.G., LOOS, R.J.F., STRACHAN, D.P., LONDON, S.J., BOEZEN, H.M., PROBST-HENSCH, N., GHARIB, S.A., HALL, I.P., O'CONNOR, G.T., TOBIN, M.D. and STRICKER, B.H., 2012. Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. American journal of respiratory and critical care medicine. 186(7), 622-32
  • HALAPI E, GUDBJARTSSON DF, JONSDOTTIR GM, BJORNSDOTTIR US, THORLEIFSSON G, HELGADOTTIR H, WILLIAMS C, KOPPELMAN GH, HEINZMANN A, BOEZEN HM, JONASDOTTIR A, BLONDAL T, GUDJONSSON SA, JONASDOTTIR A, THORLACIUS T, HENRY AP, ALTMUELLER J, KRUEGER M, SHIN HD, UH S, CHEONG HS, JONSDOTTIR B, LUDVIKSSON BR, LUDVIKSDOTTIR D, GISLASON D, PARK C, DEICHMANN K, THOMPSON PJ, WJST M, HALL IP, POSTMA DS, GISLASON T, KONG A, JONSDOTTIR I, THORSTEINSDOTTIR U and STEFANSSON K, 2010. A Sequence Variant On 17Q21 Is Associated With Age At Onset And Severity Of Asthma. European Journal Of Human Genetics : Ejhg. 18(8), 902-8
  • SAYERS,, HAWLEY,, STEWART,, BILLINGTON,, HENRY,, LEIGHTON-DAVIES,, CHARLTON, and HALL,, 2009. Pharmacogenetic characterization of indacaterol, a novel beta(2)-adrenoceptor agonist. British journal of pharmacology.
  • BARTON, S.J., KOPPELMAN, G.H., VONK, J.M., BROWNING, C.A., NOLTE, I.M., STEWART, C.E., BAINBRIDGE, S., MUTCH, S., ROSE-ZERILLI, M.J., POSTMA, D.S., MANIATIS, N., HENRY, A.P., HALL, I.P., HOLGATE, S.T., TIGHE, P., HOLLOWAY, J.W. and SAYERS, I., 2009. PLAUR polymorphisms are associated with asthma, PLAUR levels, and lung function decline Journal of Allergy and Clinical Immunology. 123(6), 1391-1400.e17
  • GUDBJARTSSON, D.F., BJORNSDOTTIR, U.S., HALAPI, E., HELGADOTTIR, A., SULEM, P., JONSDOTTIR, G.M., THORLEIFSSON, G., HELGADOTTIR, H., STEINTHORSDOTTIR, V., STEFANSSON, H., WILLIAMS, C., HUI, J., BEILBY, J., WARRINGTON, N.M., JAMES, A., PALMER, L.J., KOPPELMAN, G.H., HEINZMANN, A., KRUEGER, M., BOEZEN, H.M., WHEATLEY, A., ALTMULLER, J., SHIN, H.D., UH, S.-T., CHEONG, H.S., JONSDOTTIR, B., GISLASON, D., PARK, C.-S., RASMUSSEN, L.M., PORSBJERG, C., HANSEN, J.W., BACKER, V., WERGE, T., JANSON, C., JÖNSSON, U.-B., NG, M.C.Y., CHAN, J., SO, W.Y., MA, R., SHAH, S.H., GRANGER, C.B., QUYYUMI, A.A., LEVEY, A.I., VACCARINO, V., REILLY, M.P., RADER, D.J., WILLIAMS, M.J.A., RIJ, A.M. VAN, JONES, G.T., TRABETTI, E., MALERBA, G., PIGNATTI, P.F., BONER, A., PESCOLLDERUNGG, L., GIRELLI, D., OLIVIERI, O., MARTINELLI, N., LUDVIKSSON, B.R., LUDVIKSDOTTIR, D., EYJOLFSSON. G.I., ARNAR, D., THORGEIRSSON, G., DEICHMANN, K., THOMPSON, P.J., WJST, M., HALL, I.P., POSTMA, D.S., GISLASON, T., GULCHER, J., KONG, A., JONSDOTTIR, I., THORSTEINSDOTTIR, U. and STEFANSSON, K., 2009. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Nature Genetics. 41(3), 342-347
  • GUDBJARTSSON, DANIEL F., BJORNSDOTTIR, UNNUR S., HALAPI, EVA, HELGADOTTIR, ANNA, SULEM, PATRICK, JONSDOTTIR, GUDRUN M., THORLEIFSSON, GUDMAR, HELGADOTTIR, HAFDIS, STEINTHORSDOTTIR, VALGERDUR, STEFANSSON, HREINN, WILLIAMS, CAROLYN, HUI, JENNIE, BEILBY, JOHN, WARRINGTON, NICOLE M., JAMES, ALAN, PALMER, LYLE J., KOPPELMAN, GERARD H., HEINZMANN, ANDREA, KRUEGER, MARCUS, BOEZEN, H. MARIKE, WHEATLEY, AMANDA, ALTMULLER, JANINE, SHIN, HYOUNG DOO, UH, SOO-TAEK, CHEONG, HYUN SUB, JONSDOTTIR, BRYNJA, GISLASON, DAVID, PARK, CHOON-SIK, RASMUSSEN, LINDA M., PORSBJERG, CELESTE, HANSEN, JAKOB W., BACKER, VIBEKE, WERGE, THOMAS, JANSON, CHRISTER, JOENSSON, ULLA-BRITT, NG, MAGGIE C. Y., CHAN, JULIANA, SO, WING YEE, MA, RONALD, SHAH, SVATI H., GRANGER, CHRISTOPHER B., QUYYUMI, ARSHED A., LEVEY, ALLAN I., VACCARINO, VIOLA, REILLY, MUREDACH P., RADER, DANIEL J., WILLIAMS, MICHAEL J. A., VAN RIJ, ANDRE M., JONES, GREGORY T., TRABETTI, ELISABETTA, MALERBA, GIOVANNI, PIGNATTI, PIER FRANCO, BONER, ATTILIO, PESCOLLDERUNGG, LYDIA, GIRELLI, DOMENICO, OLIVIERI, OLIVIERO, MARTINELLI, NICOLA, LUDVIKSSON, BJORN R., LUDVIKSDOTTIR, DORA, EYJOLFSSON, GUDMUNDUR I., ARNAR, DAVID, THORGEIRSSON, GUDMUNDUR, DEICHMANN, KLAUS, THOMPSON, PHILIP J., WJST, MATTHIAS, HALL, IAN P., POSTMA, DIRKJE S., GISLASON, THORARINN, GULCHER, JEFFREY, KONG, AUGUSTINE, JONSDOTTIR, INGILEIF, THORSTEINSDOTTIR, UNNUR and STEFANSSON, KARI, 2009. Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction NATURE GENETICS. 41(3), 342-347
  • ASLAM, A, LEWIS, R J, WHEATLEY, A, PLEASS, R J and SAYERS, I, 2008. The secretory tailpiece isoform of IgE is not associated with allergy. Allergy. 63(7), 942-3
  • HALL, I.P., BLAKEY, J.D., AL BALUSHI, K.A., WHEATLEY, A., SAYERS, I., PEMBREY, M.E., RING, S.M., MCARDLE, W.L. and STRACHAN, D.P., 2006. β2-adrenoceptor polymorphisms and asthma from childhood to middle age in the British 1958 birth cohort: a genetic association study Lancet. 368(9537), 771-779
  • HORAN, M, NEWSWAY, V., YASMIN,, LEWIS, M.D., EASTER, T.E., REES, D.A., MAHTO, A., MILLAR, D.S., PROCTER, A.M., SCANLON, M.F., WILKINSON, I.B., HALL, I.P., WHEATLEY, A., BLAKEY, J., BATH, P.M.W., COCKCROFT, J.R., KRAWCZAK, M. and COOPER, D.N., 2006. Genetic variation at the growth hormone (GH1) and growth hormone receptor (GHR) loci as a risk factor for hypertension and stroke. Human Genetics. 119(5), 527-540
  • BLAKEY, J., HALAPI, E., BJORNSDOTTIR, U.S., WHEATLEY, A., KRISTINSSON, S., UPMANYU, R., STEFANSSON, K., HAKONARSON, H. and HALL, I.P., 2005. Contribution of ADAM33 polymorphisms to the population risk of asthma Thorax. 60(4), 274-276
  • WHEATLEY, A.P., BOLLAND, D.J., HEWITT, J.E., DEWAR, J.C. and HALL, I.P., 2002. Identification of the autoantigen SART-1 as a candidate gene for the development of atopy Human Molecular Genetics. 11(18), 2143-2146
  • FOWLER, S.J., HALL, I.P., WILSON, A.M., WHEATLEY, A.P. and LIPWORTH, B.J., 2002. 5-Lipoxygenase polymorphism and in-vivo response to leukotriene receptor antagonists European Journal of Clinical Pharmacology. 58(3), 187-190
  • LIPWORTH, B, KOPPELMAN, G H, WHEATLEY, A P, LE JEUNE, I, COUTIE, W, MEURS, H, KAUFFMAN, H F, POSTMA, D S and HALL, I P, 2002. Beta2 adrenoceptor promoter polymorphisms: extended haplotypes and functional effects in peripheral blood mononuclear cells. Thorax. 57(1), 61-6
  • CHO, S.H., HALL, I.P., WHEATLEY, A., DEWAR, J., ABRAHA, D., DEL MUNDO, J., LEE, H. and OH, C.K., 2001. Possible role of the 4G/5G polymorphism of the plasminogen activator inhibitor 1 gene in the development of asthma Journal of Allergy and Clinical Immunology. 108(2), 212-214
  • COCKCROFT JR, GAZIS AG, CROSS DJ, WHEATLEY A, DEWAR J, HALL IP and NOON JP, 2000. Beta(2)-adrenoceptor polymorphism determines vascular reactivity in humans. Hypertension (Dallas, Tex. : 1979). 36(3), 371-5
  • CANDY G, SAMANI N, NORTON G, WOODIWISS A, RADEVSKI I, WHEATLEY A, COCKCROFT J and HALL IP, 2000. Association analysis of beta2 adrenoceptor polymorphisms with hypertension in a Black African population. Journal of hypertension. 18(2), 167-72
  • HALL IP, WHEATLEY AP and DEWAR JC, 2000. Genetic polymorphisms of adrenergic receptors. Methods in molecular biology (Clifton, N.J.). 126, 117-26
  • SCOTT, M.G.H., SWAN, C., WHEATLEY, A.P. and HALL, I.P., 1999. Identification of' novel polymorphisms within the promoter region of the human ~2 adrenergic receptor gene British Journal of Pharmacology. 126(4), 841-844
  • LIPWORTH BJ, HALL IP, AZIZ I, TAN KS and WHEATLEY A, 1999. Beta2-adrenoceptor polymorphism and bronchoprotective sensitivity with regular short- and long-acting beta2-agonist therapy. Clinical science (London, England : 1979). 96(3), 253-9
  • HALL IP, WHEATLEY A, CHRISTIE G, MCDOUGALL C, HUBBARD R and HELMS PJ, 1999. Association of CCR5 delta32 with reduced risk of asthma. Lancet (London, England). 354(9186), 1264-5
  • HOPES E, MCDOUGALL C, CHRISTIE G, DEWAR J, WHEATLEY A, HALL IP and HELMS PJ, 1998. Association of glutamine 27 polymorphism of beta 2 adrenoceptor with reported childhood asthma: population based study. BMJ (Clinical research ed.). 316(7132), 664
  • DEWAR JC, WHEATLEY AP, VENN A, MORRISON JF, BRITTON J and HALL IP, 1998. Beta2-adrenoceptor polymorphisms are in linkage disequilibrium, but are not associated with asthma in an adult population. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 28(4), 442-8
  • DEWAR J, WHEATLEY A, WILKINSON J, HOLGATE ST, THOMAS NS, LIO P, MORTON NE and HALL IP, 1997. Association of the Gln 27 beta 2-adrenoceptor polymorphism and IgE variability in asthmatic families. Chest. 111(6 Suppl), 78S-79S
  • DEWAR JC, WILKINSON J, WHEATLEY A, THOMAS NS, DOULL I, MORTON N, LIO P, HARVEY JF, LIGGETT SB, HOLGATE ST and HALL IP, 1997. The glutamine 27 beta2-adrenoceptor polymorphism is associated with elevated IgE levels in asthmatic families. The Journal of allergy and clinical immunology. 100(2), 261-5
  • HALL IP, WHEATLEY A, DEWAR J, WILKINSON J and MORRISON J, 1996. Fc epsilon RI-beta polymorphisms unlikely to contribute substantially to genetic risk of allergic disease. BMJ (Clinical research ed.). 312(7026), 311
  • DEWAR JC and WHEATLEY AP, 1996. The heritability of allergic disease. Monographs in allergy. 33, 4-34
  • HALL IP, WHEATLEY A, WILDING P and LIGGETT SB, 1995. Association of Glu 27 beta 2-adrenoceptor polymorphism with lower airway reactivity in asthmatic subjects. Lancet (London, England). 345(8959), 1213-4

School of Medicine

University of Nottingham
Medical School
Nottingham, NG7 2UH

Contacts: Please see our 'contact us' page for further details