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Tajouri, Lotti, Fernandez, Francesca, Tajouri, Sophie, Detriche, Geraldine, Szvetko, Attila, Colson, Natalie, Csurhes, Peter, Pender, M. P. and Griffiths, Lyn R. (2007) Allelic Variation Investigation of the Estrogen Receptor Within an Australian Multiple Sclerosis Population. Journal of the Neurological Sciences, 252 1: 9-12. doi:10.1016/j.jns.2006.09.018 246 418 2 Cited 4 times in Scopus4 0
Green, Michael R., Jardine, Paul, Wood, Peter, Wellwood, Jeremy, Lea, Rod A., Marlton, Paula and Griffiths, Lyn R. (2010) A new method to detect loss of heterozygosity using cohort heterozygosity comparisions. Bmc Cancer, 10 195.1-195.8. doi:10.1186/1471-2407-10-195 34   4 Cited 3 times in Scopus3 0
Szvetko, Attila L., Jones, Ashleigh, Mackenzie, Jason, Tajouri, Lotti, Csurhes, Peter A., Greer, Judith M., Pender, Michael P. and Griffiths, Lyn R. (2009) An investigation of the C77G and C772T variations within the human protein tyrosine phosphatase receptor type C gene for association with multiple sclerosis in an Australian population. Brain Research, 1255 148-152. doi:10.1016/j.brainres.2008.12.017 93   6 Cited 8 times in Scopus8 0
Okolicsanyi, Rachel K., Buffiere, Anne, Jacinto, Jose M. E., Chacon-Cortes, Diego, Chambers, Suzanne K., Youl, Philippa H., Haupt, Larisa M. and Griffiths, Lyn R. (2014) Association of heparan sulfate proteoglycans SDC1 and SDC4 polymorphisms with breast cancer in an Australian Caucasian population. Tumor Biology, . doi:10.1007/s13277-014-2774-3 12   Cited 0 times in Scopus0 2
Okolicsanyi, Rachel K., Faure, Marion, Jacinto, Jose M.E., Chacon-Cortes, Diego, Chambers, Suzanne, Youl, Philippa H., Haupt, Larisa M. and Griffiths, Lyn R. (2014) Association of the SNP rs2623047 in the HSPG modification enzyme SULF1 with an Australian Caucasian breast cancer cohort. Gene, 547 1: 50-54. doi:10.1016/j.gene.2014.06.009 15   0 Cited 0 times in Scopus0 2
Lill, Christina M., Liu, Tian, Schjeide, Brit-Marem, Roehr, Johannes T., Akkad, Denis A., Damotte, Vincent, Alcina, Antonio, Ortiz, Migual A., Arroyo, Rafa, Lopez de Lapuente, Aitzkoa, Blaschke, Paul, Winkelmann, Alexander, Gerdes, Lisa-Ann, Luessi, Felix, Fernadez, Oscar, Izquierdo, Guillermo, Antiguedad, Alfredo, Hoffjan, Sabine, Cournu-Reibeix, Isabelle, Gromoller, Silvana, Faber, Hans, Liebsch, Maria, Meissner, Esther, Chanvillard, Coralie, Touze, Emmanuel, Pico, Fernando, Corcia, Philippe, 19ANZgene Consortium, Bahlo, Melanie, Booth, David R., Broadley, Simon A., Brown, Matthew A., Browning, Brian L., Browning, Sharon R., Butzkueven, Helmut, Carroll, William M., Cox, Mathew B., Chapman, Caron, Clarke, Glynnis, Danoy, Patrick, Drysdale, Karen, Field, Judith, Foote, Simon J., Greer, Judith M., Griffiths, Lyn R., Hadler, Johanna, Jensen, Cathy J., Johnson, Laura J., Kermode, Allan G., Heard, Rober N., Kilpatrick, Trevor J., Lechner-Scott, Jeanette, Marriott, Mark, Mason, Deborah, Moscato, Pablo, Pender, Michael P., Perreau, Victoria M., Rubio, Justin P., Scott, Rodney J., Slee, Mark, Stankovich, Jim, Stewart, Graeme J., Tajouri, Lotfi, Taylor, Bruce V., Wiley, James, Wilkins, Ella J., Dorner, Thomas, Steinhagen-Thiessen, Elisabeth, Baeckman, Lars, Heekeren, Hauke R., Li, Shu-Chen, Lindenberger, Ulman, Chan, Andrew, Hartung, Hans-Peter, Aktas, Orhan, Lohse, Peter, Kumpfel, Tania, Kubisch, Christian, Epplen, Joerg T., Zettl, Uwe K., Fontaine, Bertrand, Vandenbroeck, Koen, Matesanz, Fuencisla, Urcelay, Elena, Bertram, Lars and Zipp, Frauke (2012) Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects. Journal of Medical Genetics, 49 9: 558-562. doi:10.1136/jmedgenet-2012-101175 127   7 Cited 5 times in Scopus5 1
Hume, Georgia E., Fowler, Elizabeth V., Griffiths, Lyn R., Doecke, James D. and Radford-Smith, Graham L. (2012) Common PPAR gamma variants C161T and Pro12Ala are not Associated with Inflammatory Bowel Disease in an Australian Cohort. Journal of Gastrointestinal and Liver Diseases, 21 4: 349-355. 31 5 0 Cited 0 times in Scopus0
Cameron, Cate M., Scuffham, Paul A., Spinks, Anneliese, Scott, Rani, Sipe, Neil, Ng, ShuKay, Wilson, Andrew, Searle, Judy, Lyons, Ronan A., Kendall, Elizabeth, Halford, Kim, Griffiths, Lyn R., Homel, Ross and McClure, Roderick J. (2012) Environments for Healthy Living (EFHL) Griffith birth cohort study: background and methods. Maternal and Child Health Journal, 16 9: 1896-1905. doi:10.1007/s10995-011-0940-4 38   Cited 6 times in Scopus6 0
Ghassabian, Sussan, Rethwan, Nur Syazwani Ahmad, Griffiths, Lyn and Smith, Maree T. (2014) Fully validated LC–MS/MS method for quantification of homocysteine concentrations in samples of human serum: a new approach. Journal of Chromatography B, 972 14-21. doi:10.1016/j.jchromb.2014.09.032 47   0 Cited 0 times in Scopus0 0
Tajouri, Lotti, Martin, Virginie, Gasparini, Claudia, Ovcaric, Micky, Curtain, Rob, Lea, Rod A., Haupt, Larisa M., Csurhes, Peter, Pender, Michael P. and Griffiths, Lyn R. (2006) Genetic Investigation of Methylenetetrahydrofolate Reductase (MTHFR) and Catechol-O-Methyl Transferase (COMT) in Multiple Sclerosis. Brain Research Bulletin, 69 3: 327-331. doi:10.1016/j.brainresbull.2006.01.005 668 951 12 Cited 11 times in Scopus11 0
Green, Michael R., Camilleri, Emily, Gandhi, Maher K. and Griffiths, Lyn R. (2009). Genetic susceptibility to complex traits: moving towards informed analysis of whole-genome screens. In Akio Matsumoto and Mai Nakano (Ed.), Human genome: features, variations and genetic disorders (pp. 167-180) New York, NY, United States: Nova Science. 133   0
Bahlo, Melanie, Booth, David R., Broadley, Simon A., Brown, Matthew A., Foote, Simon J., Griffiths, Lyn R., Kilpatrick, Trevour J., Lechner-Scott, Jeanette, Moscato, Pablo, Perreau, Victoria M., Rubio, Justin P., Scott, Rodney J., Stankovich, Jim, Stewart, Graeme J., Taylor, Bruce V., Wiley, James, Clarke, Glynnis, Cox, Mathew B., Csurhes, Peter A., Danoy, Patrick, Drysdale, Karen, Field, Judith, Foote, Simon J., Greer, Judith M., Griffiths, Lyn R, Hadler, Johanna, McMorran, Brendan J., Jensen, Cathy J., Johnson, Laura J., McCallum, Ruth, Merriman, Marilyn, Merriman, Tony, Pryce, Karena, Tajouri, Lotfi, Wilkins, Ella J., Browning, Brian L., Browning, Sharon R., Perera, Devindri, Butzkueven, Helmut, Carroll, William M., Chapman, Caron, Kermode, Allan G., Marriott, Mark, Mason, Deborah, Heard, Robert N., Pender, Michael P., Slee, Mark, Tubridy, Niall and Willoughby, Ernest (2009) Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. Nature Genetics, 41 7: 824-828. doi:10.1038/ng.396 240   219 Cited 256 times in Scopus256 4
Green, Michael, Gandhi, Maher K, Camilleri, Emily, Marlton, Paula, Lea, Rod and Griffiths, Lyn (2009) High levels of BACH2 associated with lower levels of BCL2 transcript abundance in t(14;18)(q21;q34) translocation positive non-Hodgkin's lymphoma. Leukemia Research, 33 5: 731-734. doi:10.1016/j.leukres.2008.09.007 40   7 Cited 7 times in Scopus7 0
Camilleri, Emily T., Aya-Bonilla, Carlos A., Brown, Philip J., Banham, Alison, Marlton, Paula, Gandhi, Maher K. and Griffiths, Lyn R. (2012). Identification of FOXP1 Transcriptional Targets in Diffuse Large B Cell Lymphoma. In: Blood. 54th Annual Meeting and Exposition of the American-Society-of-Hematology (ASH), Atlanta Ga, (). Dec 08-11, 2012. 5   0
Tran, Huy, Nourse, Jamie, Hall, Sara, Green, Michael, Griffiths, Lyn and Gandhi, Maher K. (2008) Immunodeficiency-associated lymphomas. Blood Reviews, 22 5: 261-281. doi:10.1016/j.blre.2008.03.009 39   53 Cited 59 times in Scopus59 3
Aya-Bonilla, Carlos, Camilleri, Emily, Haupt, Larisa M., Lea, Rod, Gandhi, Maher K. and Griffiths, Lyn R. (2014) In silico analyses reveal common cellular pathways affected by loss of heterozygosity (LOH) events in the lymphomagenesis of Non-Hodgkin’s lymphoma (NHL). BMC Genomics, 15 390: 1-12. doi:10.1186/1471-2164-15-390 10   0 Cited 0 times in Scopus0 0
Green, Michael R., Aya-Bonilla, Carlos, Gandhi, Maher K., Lea, Rod A., Wellwood, Jeremy, Wood, Peter, Marlton, Paula and Griffiths, Lyn R. (2011) Integrative genomic profiling reveals conserved genetic mechanisms for tumorigenesis in common entities of non-Hodgkin's lymphoma. Genes Chromosomes and Cancer, 50 5: 313-326. doi:10.1002/gcc.20856 55 6 20 Cited 20 times in Scopus20 0
Tajouri, Lotti, Ferreira, Linda, Ovcaric, Micky, Curtain, Rob, Lea, Rod, Csurhes, Peter A., Pender, Michael P. and Griffiths, Lyn R. (2004) Investigation of a Neuronal Nitric Oxide Synthase Gene (NOS1) Polymorphism in a Multiple Sclerosis Population. Journal of the Neurological Sciences, 218 1-2: 25-28. doi:10.1016/j.jns.2003.10.006 483 317 3 Cited 7 times in Scopus7 0
Tajouri, Lotti, Martin, Virginie, Ovcaric, Micky, Curtain, Rob P., Lea, Rod A., Csurhes, Peter, Pender, Michael P. and Griffiths, Lyn R. (2004) Investigation Of An Inducible Nitric Oxide Synthase Gene (NOS2A) Polymorphism In A Multiple Sclerosis Population. Brain Research Bulletin, 64 1: 9-13. doi:10.1016/j.brainresbull.2004.04.019 431 496 7 Cited 11 times in Scopus11 0
Fowdar, Javed Y., Larson, Marta V., Szvetko, Attila L., Lea, Rodney A. and Griffiths, Lyn R. (2012) Investigation of homocysteine-pathway-related variants in essential hypertension.. International Journal of Hypertension, 2012 1-9. doi:10.1155/2012/190923 12   Cited 11 times in Scopus11 0
Colson, Natalie J., Lea, Rod A., Quinlan, Sharon, MacMillan, John and Griffiths, Lyn R. (2005) Investigation of hormone receptor genes in migraine. Neurogenetics, 6 1: 17-23. doi:10.1007/s10048-004-0205-0 34   46 Cited 52 times in Scopus52 0
Szvetko, Attila, Jones, Ashleigh, Mackenzie, Jason, Tajouri, Lotti, Csurhes, Peter, Greer, Judith, Pender, Michael and Griffiths, Lyn (2010) Investigation of the [-/A](8) and C1236T genetic variations within the human toll-like receptor 3 gene for association with multiple sclerosis. Neurological Research [electronic resource], 32 4: 438-441. doi:10.1179/174313209X405155 55   0 Cited 0 times in Scopus0 0
Chen, Timothy, Murrell, Melanie, Fowdar, Javed, Roy, Bishakha, Grealy, Rebecca and Griffiths, Lyn R. (2012) Investigation of the role of the GABRG2 gene variant in migraine. Journal of the Neurological Sciences, 318 1-2: 112-114. doi:10.1016/j.jns.2012.03.014 20   2 Cited 2 times in Scopus2 0
Haupt, Larisa M., Thompson, Erik W., Trezise, Ann E. O., Irving, Rachel E., Irving, Michael G. and Griffiths, Lyn R. (2006) In vitro and in vivo MMP gene expression localisation by In Situ-RT-PCR in cell culture and paraffin embedded human breast cancer cell line xenografts. BMC Cancer, 6 18-1-18-10. doi:10.1186/1471-2407-6-18 145   12 Cited 12 times in Scopus12 0
Wang, Joanne H., Pappas, Derek, De Jager, Philip L., Pelletier, Daniel, de Bakker, Paul I. W., Kappos, Ludwig, Polman, Chris H., The Australian and New Zealand Multiple Sclerosis Genetics Consortium, Bahlo, Melanie, Booth, David R., Broadley, Simon A., Brown, Matthew A., Foote, Simon J., Griffiths, Lyn R., Kilpatrick, Trevor J., Lechner-Scott, Jeanette, Moscato, Pablo, Perreau, Victoria M., Rubio, Justin P., Scott, Rodney J., Stankovich, Jim, Stewart, Graeme J., Taylor, Bruce V., Wiley, James, Danoy, Patrick, Butzkueven, Helmut, Slee, Mark, Greer, Judith M., Kermode, Allan, Carroll, William, Chibnik, Lori B., Hafler, David A., Matthews, Paul M., Hauser, Stephen L, Baranzini, Sergio E. and Oksenberg, Jorge R. (2011) Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data.. Genome Medicine, 3 1: 3.1-3.10. doi:10.1186/gm217 17   31 Cited 31 times in Scopus31 0
Bissessor, Naylin, Wong, Allison W., Hourigan, Lisa A., Jayasinghe, Rohan S., Scalia, Greg S., Burstow, Darryl J., Griffiths, Lyn R., Savage, Michael and Walters, Darren L. (2011) Percutaneous patent foramen ovale closure: Outcomes with the Premere and Amplatzer devices. Cardiovascular Revascularization Medicine, 12 3: 164-169. doi:10.1016/j.carrev.2010.06.001 54 3 Cited 9 times in Scopus9 0
Nasir, Bushra Farah, Griffiths, Lyn, Nasir, Aslam, Roberts, Rebecca, Barclay, Murray, Gearry, Richard and Lea, Rodney A. (2013) Perianal disease combined with NOD2 genotype predicts need for IBD-related surgery in Crohn's disease patients from a population-based cohort. Journal of Clinical Gastroenterology, 47 3: 242-245. doi:10.1097/MCG.0b013e318258314d 2   2 Cited 3 times in Scopus3 0
Morrison, Nigel A., Stephens, Alexandre S., Osato, Motomi, Pasco, Julie A., Fozzard, Nicolette, Stein, Gary S., Polly, Patsie, Griffiths, Lyn R. and Nicholson, Geoff C. (2013) Polyalanine repeat polymorphism in RUNX2 is associated with site-specific fracture in post-menopausal females. PLoS ONE, 8 9: e72740.1-e72740.8. doi:10.1371/journal.pone.0072740 11   1 Cited 0 times in Scopus0 0
Green, Michael R., Gandhi, Maher K., Courtney, Mark J., Marlton, Paula and Griffiths, Lyn (2009) Relative abundance of full-length and truncated FOXP1 isoforms is associated with differential NF kappa B activity in Follicular Lymphoma. Leukemia Research, 33 12: 1699-1702. doi:10.1016/j.leukres.2009.05.004 62   13 Cited 14 times in Scopus14 0
Day, Gregory, Szvetko, Attila, Griffiths, Lyn, McPhee, I. Bruce, Tuffley, John, LaBrom, Robert, Askin, Geoffrey, Woodland, Peter, McClosky, Eamonn, Torode, Ian and Tomlinson, Francis (2009) SHOX Gene Is Expressed in Vertebral Body Growth Plates in Idiopathic and Congenital Scoliosis: Implications for the Etiology of Scoliosis in Turner Syndrome. Journal of Orthopaedic Research, 27 6: 807-813. doi:10.1002/jor.20801 67   2 Cited 3 times in Scopus3 0
Mackenzie, Jason, Tajouri, Lotti, Szvetko, Attila, Weth, Verena, Moreau, Julie, Greer, Judith M., Csurhes, Peter A., Pender, Michael P. and Griffiths, Lyn R. (2009) Study of leukemia inhibitory factor polymorphism within an Australian multiple sclerosis population. Journal of the Neurological Sciences, 280 1-2: 62-64. doi:10.1016/j.jns.2009.01.026 69   0 Cited 0 times in Scopus0 0
McClintock, Alasdair. and Griffiths, Lyn. UQ projects - the Hay days, 1996-2007. St. Lucia, Qld: Properties and Facilities Division, The University of Queensland, 2007. 206 127
Tajouri, Lotti, Ovcaric, Micky, Curtain, Rob, Johnson, Matthew P., Griffiths, Lyn R., Csurhes, Peter, Pender, Michael P. and Lea, Rod A. (2005) Variation in The Vitamin D Receptor Gene is Associated With Multiple Sclerosis in an Australian Population. Journal of Neurogenetics, 19 1: 25-38. doi:10.1080/01677060590949692 282 1004 63 Cited 73 times in Scopus73 0