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Otago Medical School staff profiles

Dr Barry Palmer

PositionSenior Research Fellow
DepartmentDepartment of Medicine (UOC)
QualificationsBSc(Hons) PhD(Otago)
Research summaryCardioendocrinology

Research

  • Human Molecular Genetics
  • Genetics of the X-chromosome
  • Animal Molecular Genetics
  • Molecular Microbiology

Publications

Marks, E. C. A., Wilkinson, T. M., Frampton, C. M., Skelton, L., Pilbrow, A. P., Yandle, T. G., Pemberton, C. J., … Whalley, G. A., … Troughton, R. W., … Cameron, V. A., Richards, A. M., Gieseg, S. P., & Palmer, B. R. (2018). Plasma levels of soluble VEGF receptor isoforms, circulating pterins and VEGF system SNPs as prognostic biomarkers in patients with acute coronary syndromes. BMC Cardiovascular Disorders, 18, 169. doi: 10.1186/s12872-018-0894-1

Keogh, J. W. L., Palmer, B. R., Taylor, D., & Kilding, A. E. (2015). ACE and UCP2 gene polymorphisms and their association with baseline and exercise-related changes in the functional performance of older adults. PeerJ, 3, e980. doi: 10.7717/peerj.980

Palmer, B. R., Slow, S., Ellis, K. L., Pilbrow, A. P., Skelton, L., Frampton, C. M., Palmer, S. C., Troughton, R. W., Yandle, T. G., … Whalley, G. A., … Lever, M., George, P. M., Chambers, S. T., … Richards, A. M., & Cameron, V. A. (2014). Genetic polymorphism rs6922269 in the MTHFD1L gene is associated with survival and baseline active vitamin B12 levels in post-acute coronary syndromes patients. PLoS ONE, 9(3), e89029. doi: 10.1371/journal.pone.0089029

Stoner, L., Shultz, S. P., Lambrick, D. M., Krebs, J., Weatherall, M., Palmer, B. R., … Williams, M. A. (2013). The Combating Obesity in Māori and Pasifika Adolescent School-children Study: COMPASS methodology and study protocol. International Journal of Preventive Medicine, 4(5), 565-579. [Protocol/Methodology].

Palmer, B. R., Frampton, C. M., Skelton, L., Yandle, T. G., Doughty, R. N., Whalley, G. A., … Troughton, R. W., Richards, A. M., & Cameron, V. A. (2012). KCNE5 polymorphism rs697829 is associated with QT interval and survival in acute coronary syndromes patients. Journal of Cardiovascular Electrophysiology, 23(3), 319-324. doi: 10.1111/j.1540-8167.2011.02192.x

Journal - Research Article

Marks, E. C. A., Wilkinson, T. M., Frampton, C. M., Skelton, L., Pilbrow, A. P., Yandle, T. G., Pemberton, C. J., … Whalley, G. A., … Troughton, R. W., … Cameron, V. A., Richards, A. M., Gieseg, S. P., & Palmer, B. R. (2018). Plasma levels of soluble VEGF receptor isoforms, circulating pterins and VEGF system SNPs as prognostic biomarkers in patients with acute coronary syndromes. BMC Cardiovascular Disorders, 18, 169. doi: 10.1186/s12872-018-0894-1

Keogh, J. W. L., Palmer, B. R., Taylor, D., & Kilding, A. E. (2015). ACE and UCP2 gene polymorphisms and their association with baseline and exercise-related changes in the functional performance of older adults. PeerJ, 3, e980. doi: 10.7717/peerj.980

Palmer, B. R., Slow, S., Ellis, K. L., Pilbrow, A. P., Skelton, L., Frampton, C. M., Palmer, S. C., Troughton, R. W., Yandle, T. G., … Whalley, G. A., … Lever, M., George, P. M., Chambers, S. T., … Richards, A. M., & Cameron, V. A. (2014). Genetic polymorphism rs6922269 in the MTHFD1L gene is associated with survival and baseline active vitamin B12 levels in post-acute coronary syndromes patients. PLoS ONE, 9(3), e89029. doi: 10.1371/journal.pone.0089029

Palmer, B. R., Frampton, C. M., Skelton, L., Yandle, T. G., Doughty, R. N., Whalley, G. A., … Troughton, R. W., Richards, A. M., & Cameron, V. A. (2012). KCNE5 polymorphism rs697829 is associated with QT interval and survival in acute coronary syndromes patients. Journal of Cardiovascular Electrophysiology, 23(3), 319-324. doi: 10.1111/j.1540-8167.2011.02192.x

Ellis, K. L., Palmer, B. R., Frampton, C. M., Troughton, R. W., Doughty, R. N., Whalley, G. A., … Pilbrow, A. P., Skelton, L., Yandle, T. G., Richards, A. M., & Cameron, V. A. (2012). Genetic variation in the renin-angiotensin-aldosterone system is associated with cardiovascular risk factors and early mortality in established coronary heart disease. Journal of Human Hypertension, 27, 237-244. doi: 10.1038/jhh.2012.24

Ellis, K. L., Pilbrow, A. P., Potter, H. C., Frampton, C. M., Doughty, R. N., Whalley, G. A., … Palmer, B. R., Skelton, L., Yandle, T. G., Troughton, R. W., Richards, A. M., & Cameron, V. A. (2012). Association between endothelin type A receptor haplotypes and mortality in coronary heart disease. Personalized Medicine, 9(3), 341-349. doi: 10.2217/PME.12.10

Jarvis, M. D., Palmer, B. R., Pilbrow, A. P., Ellis, K. L., Frampton, C. M., Skelton, L., … Whalley, G. A., … Yandle, T. G., Richards, A. M., & Cameron, V. A. (2010). CYP1A1 MSPI (T6235C) gene polymorphism is associated with mortality in acute coronary syndrome patients. Clinical & Experimental Pharmacology & Physiology, 37(2), 193-198. doi: 10.1111/j.1440-1681.2009.05261.x

Ellis, K. L., Pilbrow, A. P., Frampton, C. M., Doughty, R. N., Whalley, G. A., Ellis, C. J., Palmer, B. R., Skelton, L., Yandle, T. G., Palmer, S. C., Troughton, R. W., Richards, A. M., & Cameron, V. A. (2010). A common variant at chromosome 9P21.3 is associated with age of onset of coronary disease but not subsequent mortality. Circulation: Cardiovascular Genetics, 3(3), 286-293. doi: 10.1161/circgenetics.109.917443

Palmer, B. R., Devereaux, C. L., Dhamrait, S. S., Mocatta, T. J., Pilbrow, A. P., Frampton, C. M., Skelton, L., Yandle, T. G., Winterbourn, C. C., Richards, A. M., … Cameron, V. A. (2009). The common G-866A polymorphism of the UCP2 gene and survival in diabetic patients following myocardial infarction. Cardiovascular Diabetology, 8. doi: 10.1186/1475-2840-8-31

Palmer, B. R., Pilbrow, A. P., Frampton, C. M., Yandle, T. G., Skelton, L., Nicholls, M. G., & Richards, A. M. (2008). Plasma aldosterone levels during hospitalization are predictive of survival post-myocardial infarction. European Heart Journal, 29, 2489-2496. doi: 10.1093/eurheartj/ehn383

Palmer, B. R., Jarvis, M. D., Pilbrow, A. P., Ellis, K. L., Frampton, C. M., Skelton, L., Yandle, T. G., … Whalley, G. A., … Troughton, R. W., Richards, A. M., & Cameron, V. A. (2008). Angiotensin-converting enzyme 2 A1075G polymorphism is associated with survival in an acute coronary syndromes cohort. American Heart Journal, 156(4), 752-758. doi: 10.1016/j.ahj.2008.06.013

Littlejohn, M. D., Palmer, B. R., Richards, A. M., Frampton, C. M., Pilbrow, A. P., Troughton, R. W., Cameron, V. A., & Kennedy, M. A. (2008). Ile164 variant of β2-adrenoceptor does not influence outcome in heart failure but may interact with β blocker treatment. European Journal of Heart Failure, 10(1), 55-59. doi: 10.1016/j.ejheart.2007.10.011

Baird, T. E., Palmer, B. R., Frampton, C. M., Yandle, T. G., Skelton, L., Richards, A. M., & Cameron, V. A. (2007). Association of the aldosterone synthase gene C-344T polymorphism with risk factors and survival in a post-myocardial infarction cohort. Journal of Human Hypertension, 21, 256-258.

Pilbrow, A. P., Palmer, B. R., Frampton, C. M., Yandle, T. G., Troughton, R. W., Campbell, E., Skelton, L., Lainchbury, J. G., Richards, A. M., & Cameron, V. A. (2007). Angiotensinogen M235T and T174M gene polymorphisms in combination doubles the risk of mortality in heart failure. Hypertension, 49(2), 322-327.

Jarvis, M. D., Rademaker, M. T., Ellmers, L. J., Currie, M. J., McKenzie, J. L., Palmer, B. R., Frampton, C. M., Richards, A. M., & Cameron, V. A. (2006). Comparison of infarct-derived and control ovine cardiac myofibroblasts in culture: Response to cytokines and natriuretic peptide receptor expression profiles. American Journal of Physiology: Heart & Circulatory Physiology, 291, H1952-H1958. doi: 10.1152/ajpheart.00764.2005

Collins, R. P., Palmer, B. R., Pilbrow, A. P., Frampton, C. M., Troughton, R. W., Yandle, T. G., Skelton, L., Richards, A. M., & Cameron, V. A. (2006). Evaluation of AMPD1 C34T genotype as a predictor of mortality in heart failure and post-myocardial infarction patients. American Heart Journal, 152(2), 312-320.

Palmer, B. R., Pilbrow, A. P., Yandle, T. G., Frampton, C. M., Richards, A. M., Nicholls, M. G., & Cameron, V. A. (2003). Angiotensin-converting enzyme gene polymorphism interacts with left ventricular ejection fraction and brain natriuretic peptide levels to predict mortality after myocardial infarction. JACC, 41(5), 729-736. doi: 10.1016/S0735-1097(02)02927-3

Cameron, V. A., & Palmer, B. R. (2003). Reply to letter to the editor Angiotensin-converting enzyme polymorphism (I/D) and coronary heart disease in young adults. JACC, 42(10), 1864.

Ilian, M. A., Morton, J. D., Bekhit, A. E.-D., Roberts, N., Palmer, B. R., Sorimachi, H., & Bickerstaffe, R. (2001). Effect of preslaughter feed withdrawal period on longissimus tenderness and the expression of calpains in the ovine. Journal of Agricultural & Food Chemistry, 49(4), 1990-1998.

Su, H.-Y., Palmer, B. R., Wellby, M. P., Bickerstaffe, R., & Hickford, J. G. H. (2001). Differential expression of a gene homologous to a G-α protein gene in neonatal mouse skin during development of hair follicles. Journal of Dermatological Science, 25(1), 10-19.

Palmer, B. R., Su, H.-Y., Roberts, N., Hickford, J. G. H., & Bickerstaffe, R. (2000). Single nucleotide polymorphisms in an intron of the ovine calpastatin gene. Animal Biotechnology, 11(1), 63-67.

Palmer, B. R., Roberts, N., Hickford, J. G. H., & Bickerstaffe, R. (1998). PCR-RFLPs for MspI and NcoI in the ovine calpastatin gene. Journal of Animal Science, 76, 1499-1500.

Wu, R., Palmer, B. R., & Cole, A. L. J. (1998). Phenotypic variation and survival of genetically marked Pseudomonas tolaasii in mushroom compost. Canadian Journal of Microbiology, 44(4), 373-377.

Palmer, B. R., & Marinus, M. G. (1994). The dam and dcm strains of Escherichia coli: A review. Gene, 143(1), 1-12.

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Journal - Research Other

Stoner, L., Shultz, S. P., Lambrick, D. M., Krebs, J., Weatherall, M., Palmer, B. R., … Williams, M. A. (2013). The Combating Obesity in Māori and Pasifika Adolescent School-children Study: COMPASS methodology and study protocol. International Journal of Preventive Medicine, 4(5), 565-579. [Protocol/Methodology].

Palmer, B. R., Frampton, C. M., Richards, A. M., & Cameron, V. A. (2007). AMPD1 gene polymorphism and survival in patients with stable congestive heart failure [Letter to the editor]. American Heart Journal, 153, e13. Retrieved from http://www.sciencedirect.com/science?_ob=PublicationURL&_tockey=%23TOC%236683%232007%23998469994%23650294%23FLA%23&_cdi=6683&_pubType=J&_auth=y&_acct=C000007718&_version=1&_urlVersion=0&_userid=100241&md5=724a2d0db54e3f555bbfcbe8269e42c5

Palmer, B. R., Frampton, C. M., Richards, A. M., Cameron, V. A., & Nakayama, T. (2004). Absence of a NPR-A gene functional deletion allele in a postmyocardial infarction cohort from New Zealand [Letter to the editor]. Circulation Research, 94(10), e86.

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