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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.2006.09.018 243 403 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 30   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 91   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 10   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 14   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 120   6 Cited 4 times in Scopus4 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. 29 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 35   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 31   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.2006.01.005 659 916 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. 130   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.396 235   212 Cited 251 times in Scopus251 1
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. 6   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 37   53 Cited 59 times in Scopus59 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 54 6 17 Cited 17 times in Scopus17 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.2003.10.006 479 312 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.2004.04.019 428 484 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 9   Cited 10 times in Scopus10 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 32   45 Cited 51 times in Scopus51 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 50   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 17   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:10.1186/1471-2407-6-18 142   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 16   27 Cited 28 times in Scopus28 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 53 3 Cited 9 times in Scopus9 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 10   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 59   11 Cited 13 times in Scopus13 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 59   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 66   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. 204 120
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 279 940 60 Cited 71 times in Scopus71 0