Dr Peter H Dixon

Publications


Journals

  • Nicolaou M; Andress EJ; Zolnerciks JK; Dixon PH; Williamson C; Linton KJ. (Jan 2012). Canalicular ABC transporters and liver disease. J Pathol. 226:300-315. DOI.
  • Dixon PH; Trongwongsa P; Abu-Hayyah S; Ng SH; Akbar SA; Khawaja NP; Seckl MJ; Savage PM; et alFisher RA. (Mar 2012). Mutations in NLRP7 are associated with diploid biparental hydatidiform moles, but not androgenetic complete moles. J Med Genet. 49:206-211. DOI.
  • Groen A; Rodriguez Romero M; Kunne C; Hoosdally SJ; Dixon PH; Wooding C; Williamson C; Seppen J; et alvan den Oever K; Mok KS; Paulusma CC; Linton KJ; Elferink RPJO. (1 Nov 2011). Complementary Functions of the Flippase ATP8B1 and the Floppase ABCB4 in Maintaining Canalicular Membrane Integrity. GASTROENTEROLOGY. 141:1927-U523. DOI.
  • Geenes VL; Lim YH; Bowman N; Tailor H; Dixon PH; Chambers J; Brown L; Wyatt-Ashmead J; et alBhakoo K; Williamson C. (Dec 2011). A placental phenotype for intrahepatic cholestasis of pregnancy. Placenta. 32:1026-1032. DOI.
  • Kremer AE; Dixon PH; Ris-Stalpers C; Geenes V; Chambers J; van der Post JA; Williamson C; Beuers U; et alElferink RPJO. (1 Jan 2011). AUTOTAXIN IS A NOVEL DIAGNOSTIC MARKER FOR INTRAHEPATIC CHOLESTASIS OF PREGNANCY. ACTA DERMATO-VENEREOLOGICA. 91:625-625.
  • Lasecka L; Dixon PH; Molokhia M; Sharma N; Schleh A; Wang CM; Steel JH; Seckl MJ; et alSavage PM; Fisher RA. (Dec 2011). 667C>T and 1298A>C polymorphisms of MTHFR do not predict response to methotrexate in patients with gestational trophoblastic neoplasia. Gynecol Oncol. 123:605-609. DOI.
  • Wadsworth CA; Dixon PH; Wong JH; Chapman MH; McKay SC; Sharif A; Spalding DR; Pereira SP; et alThomas HC; Taylor-Robinson SD; Whittaker J; Williamson C; Khan SA. (2011). Genetic factors in the pathogenesis of cholangiocarcinoma. Dig Dis. 29:93-97. DOI.
  • Geenes VL; Dixon PH; Chambers J; Raguz S; Marin JJ; Bhakoo KK; Williamson C. (Jul 2011). Characterisation of the nuclear receptors FXR, PXR and CAR in normal and cholestatic placenta. Placenta. 32:535-537. DOI.
  • Wang CM; Dixon PH; Decordova S; Hodges MD; Sebire NJ; Ozalp S; Fallahian M; Sensi A; et alAshrafi F; Repiska V; Zhao J; Xiang Y; Savage PM; Seckl MJ; Fisher RA. (1 Aug 2009). Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region. JOURNAL OF MEDICAL GENETICS. 46:569-575. Author weblink DOI.
  • Dixon PH; van Mil SWC; Chambers J; Strautnieks S; Thompson RJ; Lammert F; Kubitz R; Keitel V; et alGlantz A; Mattsson L-A; Marschall H-U; Molokhia M; Moore GE; Linton KJ; Williamson C. (1 Apr 2009). Contribution of variant alleles of ABCB11 to susceptibility to intrahepatic cholestasis of pregnancy. GUT. 58:537-544. Author weblink DOI.
  • Owen BM; Van Mil SW; Boudjelal M; McLay I; Cairns W; Elias E; White R; Williamson C; et alDixon PH. (Oct 2008). Sequencing and functional assessment of hPXR (NR1I2) variants in intrahepatic cholestasis of pregnancy. Xenobiotica. 38:1289-1297. DOI.
  • Van Mil SWC; Milona A; Dixon PH; Mullenbach R; Geenes VL; Chambers J; Shevchuk V; Moore GE; et alLammert F; Glantz AG; Mattsson L-A; Whittaker J; Parker MG; White R; Williamson C. (1 Aug 2007). Functional variants of the central bile acid sensor FXR identified in intrahepatic cholestasis of pregnancy. GASTROENTEROLOGY. 133:507-516. Author weblink DOI.
  • Mumm S; Christie PT; Finnegan P; Jones J; Dixon PH; Pannett AAJ; Harding B; Gottesman GS; et alThakker RV; Whyte MP. (1 Sep 2000). A 5-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a 6-generation Arkansas kindred. JOURNAL OF BONE AND MINERAL RESEARCH. 15:S212-S212. Author weblink.
  • Dixon PH; Ahmed SF; Bonthron DT; Barr DGD; Kelnar CJH; Thakker RV. (1 Aug 1996). Mutational analysis of the GNAS1 gene in pseudohypoparathyroidism. JOURNAL OF BONE AND MINERAL RESEARCH. 11:S494-S494. Author weblink.
  • Dixon PH; Trump D; Wooding C; Mumm S; Schlessinger D; Whyte MP; Thakker RV. (1 Aug 1996). Genetic mapping studies of the X-linked recessive hypoparathyroid gene on the X chromosome (Xq27). JOURNAL OF BONE AND MINERAL RESEARCH. 11:169-169. Author weblink.
  • Dixon PH; Wooding C; Trump D; Schlessinger D; Whyte MP; Thakker RV. (1 Aug 1996). Seven novel mutations in the PEX gene indicate molecular heterogeneity for X-linked hypophosphataemic rickets. JOURNAL OF BONE AND MINERAL RESEARCH. 11:165-165. Author weblink.
  • Dixon PH; Wooding C; Cristie P; Thakker RV. (1 Aug 1997). X-linked hypophosphataemic rickets in a Saudi Arabian kindred results from a nonsense mutation of the PEX gene. JOURNAL OF BONE AND MINERAL RESEARCH. 12:S528-S528. Author weblink.
  • Dixon PH; Wooding C; Christie P; Grieff M; Schlessinger D; Whyte MP; Thakker RV. (1 Aug 1997). Mutations of the PEX regulatory and C-terminal regions cause X-linked hypophosphataemia. JOURNAL OF BONE AND MINERAL RESEARCH. 12:101-101. Author weblink.
  • Whyte MP; Christie PT; Podgornik MN; Dixon PH; Eddy MC; Wooding C; Trump D; Grieff M; et alMumm S; Schlessinger D. (1 Sep 1999). X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype. JOURNAL OF BONE AND MINERAL RESEARCH. 14:S448-S448. Author weblink.
  • Williamson C; Weerasekera N; Dixon PH; Donaldson O; Chambers J; Egginton E; Weaver J; Nelson-Piercy C; et alde Swiet M; Elias E; Johnson DG; McCarthy MI. (1 Oct 1999). Obstetric cholestasis in a woman with no family history of progressive familial intrahepatic cholestasis caused by a novel mutation in the MDR3 gene. AMERICAN JOURNAL OF HUMAN GENETICS. 65:A472-A472. Author weblink.
  • Weerasekera N; Dixon PH; Lumley J; Williamson C. (1 Oct 1999). Allele loss from chromosome 1p and from the von Hippel-Lindau locus in a patient with a sporadic carotid body tumour. AMERICAN JOURNAL OF HUMAN GENETICS. 65:A329-A329. Author weblink.
  • Whyte MP; Christie PT; Podgornik MN; Dixon PH; Eddy MC; Wooding C; Trump D; Grieff M; et alMumm S; Shlessinger D; Thakker RV. (1 Oct 1999). X-linked hypophosphatemia (XLH): Mutations compromising PHEX structure reflect a severe phenotype. AMERICAN JOURNAL OF HUMAN GENETICS. 65:A114-A114. Author weblink.
  • Mumm S; Christie PT; Finnegan P; Jones J; Dixon PH; Pannett AAJ; Harding B; Gottesman GS; et alThakker RV; Whyte MP. (1 Sep 2000). A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. 85:3343-3347. Author weblink DOI.
  • Trump D; Pilia G; Dixon PH; Wooding C; Thakrar R; Leigh SE; Nagaraja R; Whyte MP; et alSchlessinger D; Thakker RV. (Jan 1996). Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1. Hum Genet. 97:60-68.
  • Dixon PH; Christie PT; Wooding C; Trump D; Grieff M; Holm I; Gertner JM; Schmidtke J; et alShah B; Shaw N; Smith C; Tau C; Schlessinger D; Whyte MP; Thakker RV. (Oct 1998). Mutational analysis of PHEX gene in X-linked hypophosphatemia. J Clin Endocrinol Metab. 83:3615-3623.
  • Trump D; Dixon PH; Mumm S; Wooding C; Davies KE; Schlessinger D; Whyte MP; Thakker RV. (Nov 1998). Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27. J Med Genet. 35:905-909.
  • Ahmed SF; Dixon PH; Bonthron DT; Stirling HF; Barr DG; Kelnar CJ; Thakker RV. (Oct 1998). GNAS1 mutational analysis in pseudohypoparathyroidism. Clin Endocrinol (Oxf). 49:525-531.
  • Lloyd SE; Pannett AA; Dixon PH; Whyte MP; Thakker RV. (Jan 1999). Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13. Am J Hum Genet. 64:189-195. DOI.
  • Williamson C; Cavaco BM; Jauch A; Dixon PH; Forbes S; Harding B; Holtgreve-Grez H; Schoell B; et alPereira MC; Font AP; Loureiro MM; Sobrinho LG; Santos MA; Thakker RV. (Feb 1999). Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31. J Bone Miner Res. 14:230-239. DOI.
  • Dixon PH; Weerasekera N; Linton KJ; Donaldson O; Chambers J; Egginton E; Weaver J; Nelson-Piercy C; et alde Swiet M; Warnes G; Elias E; Higgins CF; Johnston DG; McCarthy MI; Williamson C. (1 May 2000). Heterozygous MDR3 missense mutation associated with intrahepatic cholestasis of pregnancy: evidence for a defect in protein trafficking. Hum Mol Genet. 9:1209-1217.

Conferences

  • Kremer AE; Dixon PH; Ris-Stalpers C; Geenes V; Chambers J; van der Post JA; Williamson C; Beuers U; et alElferink RPO. AUTOTAXIN IS A NOVEL DIAGNOSTIC MARKER FOR INTRAHEPATIC CHOLESTASIS OF PREGNANCY. 46th Annual Meeting of the European-Association-for-the-Study-of-the-Liver (EASL), 2011. 54:S11-S12. ELSEVIER SCIENCE BV (1 Mar 2011).
  • Wadsworth CA; Dixon PH; Zabron AA; Wong JH; Chapman MH; McKay SC; Sharif AW; Spalding DR; et alPereira SP; Wasan HS; Thomas HC; Taylor-Robinson SD; Whittaker JC; Williamson C; Khan SA. GENETIC VARIATION IN BILIARY TRANSPORTERS AS A SUSCEPTIBILITY FACTOR FOR CHOLANGIOCARCINOMA. 46th Annual Meeting of the European-Association-for-the-Study-of-the-Liver (EASL), 2011. 54:S109-S109. ELSEVIER SCIENCE BV (1 Mar 2011). Author weblink.
  • Wadsworth CA; Dixon PH; Zabron AA; Wong JH; Chapman MH; McKay SC; Spalding DR; Pereira SP; et alWasan HS; Thomas HC; Taylor-Robinson SD; Whittaker JC; Williamson C; Khan SA. COMMON GENETIC VARIATION IN NATURAL KILLER CELL RECEPTOR PROTEIN G2D DOES NOT MODIFY SUSCEPTIBILITY TO SPORADIC CHOLANGIOCARCINOMA. 46th Annual Meeting of the European-Association-for-the-Study-of-the-Liver (EASL), 2011. 54:S108-S109. ELSEVIER SCIENCE BV (1 Mar 2011). Author weblink.
  • Dixon PH; Wadsworth CA; Chambers J; Donnelly JC; Cooley SM; Kubitz R; Lammert F; Marschall H-U; et alGlantz A; Khan SA; Whittaker J; Geary M; Williamson C. DOES COMMON GENETIC VARIATION AROUND THE PREGNANE-X RECEPTOR INFLUENCE SUSCEPTIBILITY TO INTRAHEPATIC CHOLESTASIS OF PREGNANCY?. 62nd Annual Meeting of the American-Association-for-the-Study-of-Liver-Diseases (AASLD), 4 Nov 2011 - 8 Nov 2011. 54:924A-924A. WILEY-BLACKWELL (1 Oct 2011). Author weblink.
  • Dixon PH; Wadsworth CA; Chambers J; Donnelly J; Cooley SM; Jarvis S; Kubitz R; Lammert F; et alMarschall H-U; Glantz A; Khan SA; Whittaker J; Geary M; Williamson C. THE ROLE OF COMMON GENETIC VARIATION AROUND SIX CANDIDATE LOCI FOR SUSCEPTIBILITY TO INTRAHEPATIC CHOLESTASIS OF PREGNANCY. 61st Annual Meeting of the American-Association-for-the-Study-of-Liver-Diseases, 29 Oct 2010 - 2 Nov 2010. 52:479A-479A. WILEY-BLACKWELL (1 Oct 2010). Author weblink.
  • Wadsworth CA; Dixon PH; Zabron AA; Wong JH; Chapman MH; McKay SC; Spalding DR; Pereira SP; et alWasan HS; Thomas HC; Taylor-Robinson SD; Whittaker JC; Williamson C; Khan SA. GENETIC VARIATION IN NATURAL KILLER CELL RECEPTOR PROTEIN G2D DOES NOT MODIFY SUSCEPTIBILITY TO SPORADIC CHOLANGIOCARCINOMA. Annual Meeting on British-Society-of-Gasenterology, 14 Mar 2011 - 17 Mar 2011. 60. B M J PUBLISHING GROUP (1 Apr 2011). DOI.
  • Pattni S; Pathmasrirengan S; Dixon PH; Williamson C; Walters JRF. A STUDY OF THE PREVALENCE OF GENETIC POLYMORPHISMS IN BILE ACID DIARRHOEA PATIENTS. Annual Meeting on British-Society-of-Gasenterology, 14 Mar 2011 - 17 Mar 2011. 60:A89-A89. B M J PUBLISHING GROUP (1 Apr 2011). DOI.
  • Dixon PH; van Mil S; Strautnieks S; Thompson R; Lammert F; Kubitz R; Keitel V; Glantz A; et alMattsson L-A; Marschall H-U; Molokhia M; Williamson C. The role of ABCB11 (BSEP) variation in susceptibility to intrahepatic cholestasis of pregnancy. 20th International Bile Acid Meeting, 13 Jun 2008 - 14 Jun 2008. 165:46-50. SPRINGER (1 Jan 2009). Author weblink DOI.
  • van Mil S; Dixon PH; Christian M; Mullenbach R; Shevchuk L; Chambers J; Cheng F; White R; et alParker M; Williamson C. FXR mutations in intrahepatic cholestasis of pregnancy. 56th Annual Meeting of the American-Association-for-the-Study-of-Liver-Diseases. 42:461A-461A. (Oct 2005).
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