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Amanda Henry

Research Fellow, Faculty of Medicine & Health Sciences

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Recent Publications

  • 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

School of Medicine

University of Nottingham
Medical School
Nottingham, NG7 2UH

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