RichardDavidBagnallMD

PubMed

• Postmortem review and genetic analysis in sudden infant death syndrome: an 11-year review
  Angharad Evans, Richard D. Bagnall, Johan Duflou, Christopher Semsarian> ;Human Pathology. 2013 Sep 1
• Genetic Basis of Familial Valvular Heart Disease
  Ratnasari Padang, Richard D. Bagnall, Christopher Semsarian> ;Circulation-cardiovascular Genetics. 2012 Oct 1
• Rare non-synonymous variations in the transcriptional activation domains of GATA5 in bicuspid aortic valve disease
  Ratnasari Padang, Richard D. Bagnall, David R. Richmond, Paul G. Bannon, Christopher Semsarian> ;Journal of Molecular and Cellular Cardiology. 2012 Aug 1
• A polymorphic miR-155 binding site in AGTR1 is associated with cardiac hypertrophy in Friedreich ataxia.
  Matthew Kelly, Richard D. Bagnall, Roger E. Peverill, Lesley Donelan, Louise A. Corben, Martin B. Delatycki, Christopher Semsarian> ;Journal of Molecular and Cellular Cardiology. 2011 Nov 1
• GENETIC ANALYSIS OF HYPERPOLARISATION-ACTIVATED CYCLIC NUCLEOTIDE-GATED CATION (HCN) CHANNELS IN SUDDEN UNEXPECTED DEATH IN EPILEPSY (SUDEP) CASES.
  Tu, E., Waterhouse, L., Duflou, J., Bagnall, R.D., Semsarian, C.> ;Brain Pathol. 2011 Nov
• Molecular Diagnostics of Cardiomyopathies The Future Is Here
  Richard D. Bagnall, Jodie Ingles, Christopher Semsarian> ;Circulation-cardiovascular Genetics. 2011 Apr 1
• Post‐Mortem Review and Genetic Analysis of Sudden Unexpected Death in Epilepsy (SUDEP) Cases
  Emily Tu, Richard D. Bagnall, Johan Duflou, Christopher Semsarian> ;Brain Pathology. 2011 Mar 1
• Analysis of the Z-disc genes PDLIM3 and MYPN in patients with hypertrophic cardiomyopathy.
  Richard D. Bagnall, Laura Yeates, Christopher Semsarian> ;International Journal of Cardiology. 2010 Dec 3
• The role of large gene deletions and duplications in MYBPC3 and TNNT2 in patients with hypertrophic cardiomyopathy.
  Richard D. Bagnall, Laura Yeates, Christopher Semsarian> ;International Journal of Cardiology. 2010 Nov 5
• Mutations in Alpha-Actinin-2 Cause Hypertrophic Cardiomyopathy: A Genome-Wide Analysis
  Christine L Chiu, Richard D. Bagnall, Jodie Ingles, Laura Yeates, Marina L. Kennerson, Jennifer A. Donald, Mika Jormakka, Joanne M. Lind, Christopher Semsarian> ;Journal of the American College of Cardiology. 2010 Mar 16
• Post-mortem pathologic and genetic studies in "dead in bed syndrome" cases in type 1 diabetes mellitus.
  Emily Tu, Richard D. Bagnall, Johan Duflou, Matthew J Lynch, Stephen M. Twigg, Christopher Semsarian> ;Human Pathology. 2010 Mar 1
• Impact of multiple gene mutations in determining the severity of cardiomyopathy and heart failure.
  Tatiana Tsoutsman, Richard D. Bagnall, Christopher Semsarian> ;Clinical and Experimental Pharmacology and Physiology. 2008 Nov 1
• Haemophilia A mutations in the UK: results of screening one-third of the population.
  Peter M. Green, Richard Bagnall, Naushin Waseem, Francesco Giannelli> ;British Journal of Haematology. 2008 Oct 1
• Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation.
  Richard Bagnall, Roland G. Roberts, Muddassar M. Mirza, Toshihiko Torigoe, Natalie J. Prescott, Christopher G. Mathew> ;European Journal of Human Genetics. 2008 Jan 23
• Identification, evolution, and association study of a novel promoter and first exon of the human NOD2 (CARD15) gene ☆
  Katherine S. King, Richard Bagnall, Sheila A. Fisher, Faisal Sheikh, Andrew Cuthbert, Sipin Tan, Nicholas I. Mundy, Philip Rosenstiel, Stefan Schreiber, Christopher G....> ;Genomics. 2007 Oct 1
• Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.
  Miles Parkes, Jeffrey C. Barrett, Natalie J. Prescott, Mark Tremelling, Carl A. Anderson, Sheila A. Fisher, Roland G. Roberts, Elaine R. Nimmo, Fraser Cummings, Dianne...> ;Nature Genetics. 2007 Jul 1
• A nonsynonymous SNP in ATG16L1 predisposes to ileal Crohn's disease and is independent of CARD15 and IBD5.
  Natalie J. Prescott, Sheila A. Fisher, Andre Franke, Jochen Hampe, Clive M. Onnie, Dianne Soars, Richard Bagnall, Muddassar M. Mirza, Jeremy D. Sanderson, Alastair For...> ;Gastroenterology. 2007 May 1
• Int22h‐related inversions causing hemophilia A: a novel insight into their origin and a new more discriminant PCR test for their detection
  Richard Bagnall, Francesco Giannelli, Peter M. Green> ;Journal of Thrombosis and Haemostasis. 2006 Mar 1
• Gene conversion and evolution of Xq28 duplicons involved in recurring inversions causing severe hemophilia A
  Richard Bagnall, Karen L. Ayres, Peter M. Green, Francesco Giannelli> ;Genome Research. 2005 Feb 1
• Mutation detection in factor VIII cDNA from lymphocytes of hemophilia A patients by solid phase fluorescent chemical cleavage of mismatch.
  Naushin Waseem, Richard Bagnall, Peter M. Green, Francesco Giannelli> ;Methods of Molecular Biology. 2002 Jan 1
• Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A.
  Richard Bagnall, Naushin Waseem, Peter M. Green, Francesco Giannelli> ;Blood. 2002 Jan 1
• Creation of a novel donor splice site in intron 1 of the factor VIII gene leads to activation of a 191 bp cryptic exon in two haemophilia A patients
  Richard Bagnall, Naushin Waseem, Peter M. Green, B. T. Colvin, Christine A. Lee, Francesco Giannelli> ;British Journal of Haematology. 1999 Dec 1
• Start of UK Confidential Haemophilia A Database: Analysis of 142 Patients by Solid Phase Fluorescent Chemical Cleavage of Mismatch
  Naushin Waseem, Richard Bagnall, Peter M. Green, Francesco Giannelli> ;Thrombosis and Haemostasis. 1999 Jun 1
• Detection of mutations in hemophilia a patients by chemical cleavage of mismatch method.
  Naushin H. Waseem, Richard D. Bagnall, Peter M. Green, Francesco Giannelli> ;Methods in molecular medicine. 1999 Jan 1
• A serological survey of leptospirosis in cattle of rural communities in the province of KwaZulu-Natal, South Africa.
  Hesterberg, U. W., Bagnall, R., Bosch, B., Perrett, K., Horner, R., Gummow, B.> ;J S Afr Vet Assoc. 2009 Mar 01
• Join now to see all