Green M.R., Gandhi M.K., Camilleri E., Marlton P., Lea R.A. & Griffiths L.R.(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):731-4 (IF 2.48)

Broadley S.A., Vanags D., Williams B., Johnson B., Feeney D., Griffiths L.R., Shakib S., Brown G, Coulthardt A., Mullins P and Kneebone C. (2009). Results of a phase IIa clinical trial of an anti-inflammatory molecule, chaperonin 10, in multiple sclerosis. Multiple Sclerosis (IF 3.260) 15(3):329-336

Day G., Szvetko A., Griffiths L.R., McPhee I., Tuffley J., Labrom R., Askin G., Woodland P., McClosky E., Ian T., Tomlinson F. (2009). Shox gene is expressed in vertebral body growth plates in idiopathic and congenital scoliosis: Implications for the aetiology of scoliosis in Turner Syndrome.J Orthop Res 27(6):807-13 (IF 2.437)

Cox H., Bellis C., Quinlan S., Dyer T., Lea R.A. Blangero J. & Griffiths L.R.(2009). Principal component and linkage analysis of cardiovascular risk traits in Norfolk Islanders. Human Heredity (IF 2.155) 68(1):55-64

Szvetko A., Jones A., Mackenzie J., Tajouri L., Csurhes P., Greer J., Pender M. And Griffiths L.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 (IF 2.494) 1255:148-52

Fernandez, F. Colson N., Quinlan S., MacMillan J., Lea R.A., Griffiths L.R.(2009). Association between a functional polymorphism at the dopamine á-hydroxylase (DBH) locus and migraine. Neurogenetics (IF 4.281) 10(3):199-208

Mackenzie J., Tajouri L., Szvetko A., Weth V., Moreau J., Greer J.M., Csurhes P.A., Pender M.P. and Griffiths L.R. (2009). Study of leukemia inhibitory factor polymorphism within an Australian Multiple Sclerosis population.Journal of the Neurological Sciences 280. (IF 2.315) (1-2):62-4

Green M, Camilleri E, Gandhi M, Griffiths L.R.. (2009). Genetic susceptibility to complex traits: moving towards informed analysis of whole-genome screens. In F. Columbus (Ed) The Human Genome: Features, Variations and Genetic Disorders 167-180 Hauppage, NY: Nova Science Publishers.

Grealy R. & Griffiths L.R. (2009). Current status of pharmacogenomics testing for anti-tumour drug therapies: approaches to non-melanoma skin cancer: Molecular Diagnosis and Therapy (IF 2.139) 13(2):65-72

Lea, R.A., Colson, N., Quinlan, S., Macmillan, J and Griffiths, L.R. (2009). The effects of vitamin supplementation and MTHFR (C677T) genotype on homocysteine- lowering and migraine disability. Pharmacogenetics and Genomics (IF 5.775) 19(6):422-8.

Green M., Gandhi M., Courtney M.J, Marlton P. and Griffiths L.R. (2009). Relative abundance of full-length and truncated FOXP1 isoforms is associated with differential NFkB activity in follicular lymphoma. Leukemia Research (IF 2.39) 33(12):1699-1702.

Haupt L.M. and Griffith L.R. (2009). Heparan sulfate proteoglycans, tumour progression and the cancer stem cell niche. Current Cancer Therapy Reviews5(4):256-260.

Macgregor S., Bellis C., Lea R.A., Cox H.C., Dyer T., Blangero J., Visscher P.,Griffiths L.R. (2009). Legacy of mutiny on the bounty: Founder effect and admixture on Norfolk Island. European Journal of Human Genetics (IF 3.925) 18(1):67-72

Hsieh S., Smith R.A., Lintell N.A., Hunter K.W. and Griffith L.R. (2009). Polymorphisms of the SIPA1 gene and sporadic breast cancer susceptibility.BMC Cancer (IF 3.01) 9(1):331-337

McEvoy B.P., Zhao Z.Z., Macgregor S., Bellis C., Lea R.A., Cox H., Montgomery G.W., Griffiths L.R. & Visscher P.M. (2009). European and Polynesian admixture in the Norfolk Island population. Heredity (IF 4.22) 105(2):229-34.



Hume, G.E., Fowler, El.V., Doecke, J., Simms, L.A., Huang, N., Palmieri, O.,Griffiths, L.R., Florin, T.H.J., Annese, A. ad Radford-Smith, G.L. (2008). A novel NOD2 haplotype strengthens the association between TLR4 Asp299Gly and Crohn?s disease in an Australian cohort. Inflammatory Bowel Disease(5):585-90 (IF 3.912)

Haupt, L., Irving, R.E., Weinstein, S.R. Irving, M.G. and Griffiths, L.R.(2008). Matrix metalloproteinase localisation by In Situ-RT-PCR in archival human breast biopsy material. Molecular and Cellular Probes (22): 83-89 (IF 2.016)

Colson, N.J., Fernandez, F. and Griffiths, L.R. (2008). Migraine Genetics and Prospects for Pharmacotherapy. Drug Development Research. 68: 282-293

Bellis, C. Lea, R.A., Burgner, D., Ovcaric, M., Heath, S., Blangero, J. &Griffiths, L.R. (2008). Linkage disequilibrium analysis in the genetically isolated Norfolk Island population. Heredity (4): 366-73 (IF 2.872)

Carless, M.A., Kraska, T., Neale, R.E., Green, A.C. and Griffiths, L.R. (2008). Polymorphisms of the VDR gene are associated with presence of solar keratoses on the skin. British Journal of Dermatology 159(4):804-10 (IF 3.662)

Carless, M.A., Griffiths, L.R. (2008). Cytogenetics of melanoma and nonmelanoma skin cancer. Advances in experimental medicine and biology,624: 227-240

Tran H., Nourse J., Hall S., Green M., Griffiths, L.R. & Gandhi M. (2008). Immunodeficiency-related lymphomas. Blood Reviews 22(5): 261-81 (IF 5.756)

Smith, R.A., Curtain, R., Ovcaric, M., Tajouri, L., MacMillan, J. & Griffiths, L.R. (2008). Investigation of the NOTCH3 and TNFSF7 Genes on C19p13 as Candidates for Migraine. Open Neurol J 2:1-7

Chikhani, S., Fernandez, F., Poetter, K., Toohey, B., Harvey, R., Griffiths, L.R. (2008). Investigation Between the S377G3 GATA-4 Polymorphism and Migraine. Open Neurology Journal 2:35-38.

Lymbury R, Tinggi U, Griffiths L.R., Rosenfeldt F and Perkins AV. (2008). Selenium status of the Australian population: effect of age, gender and cardiovascular disease. Biol Trace Elem Res. : 126 Suppl 1:S1-10

Bellis C., Cox H.C., Dyer T.D., Charlesworth J.C., Begley K.N., Quinlan S., Lea R.A., Heath S.C., Blangero J. & Griffiths L.R. (2008). Linkage mapping of CVD risk traits in the isolated Norfolk Island population. Human Genetics 124 (5): 543-552 (IF 3.974)

Fernandez F., Esposito T., Lea R., Colson., Ciccodicola A., Gianfrancesco F. andGriffiths L.R. (2008). Investigation of GABA A Receptor Genes and Migraine Susceptibility. BMC Medical Genetics 9:109 (IF 2.419)


Szvetko, A.L., Fowder, J., Nelson, J., Colson, N.J., Tajouri, L. Csurhes, P., Pender, M.P. & Griffiths, L.R. (2007). No association between MTHFR A1298C and MTRR A66G polymorphisms, and MS in an Australian Cohort. J Neurol Sci 252:49-52 (IF 2.412)

Tajouri, L., Fernandez, F., Tajouri, S., Detrich, G., Szvetko, A., Colson, N., Csurhes, P., & Griffiths, L.R. (2007). Allelic variation investigation of the estrogen receptor within an Australian multiple sclerosis population. J Neurol Sci 252(1):9-12 (IF 2.412)

Colson, N.J., Lea, R.A. and Griffiths, L.R. (2007). The search for migraine genes: an overview of current knowledge. Cell. Mol. Life Sciences 64(3):331-44 (IF 4.582)

McCallum, L.K., Fernandez, F., Quinlan, S., Lea, R.A., Griffiths, L.R. (2007). Association study of a functional variant in Intron 8 of the dopamine transporter gene and migraine susceptibility. European Journal of Neurology14:706-707 (IF 2.437)

Carless M.A. and Griffiths, L.R. (2007). Cytogenetics of melanoma and non- melanoma skin cancer in: Sunlight, Vitamin D and Skin Cancer. 624:227-240

Tajouri L., Fernandez F. and Griffiths L.R. (2007). Gene expression studies in Multiple Sclerosis. Current Genomics 8(3):181-189

Smith R., Lea R.A., Weinstein S.R. & Griffiths L.R. (2007). Progesterone, glucocorticoid, but not estrogen receptor mRNA is altered in breast cancer stroma. Cancer Letters. 255(1):77-84 (IF 3.277)

Fernandez F., Colson N and Griffiths L.R. (2007). Pharmacogenetics of migraine: genetic variants and their role in migraine therapy.Pharmacogenomics 8(6):609-22 (IF 3.957)

Kirk, E.P., Sunde, M., Costa, M.W., Rankin, S.A., Castro, L., Butler, T.L., Hyun, Changbaig, Guo, G., Otway, R., Mackay, J.P., Waddell, L.B., Cole, A.D., Hayward, C., Keogh, A., Macdonald, P., Griffiths, L.R., et al (2007). Mutations in cardiac factor gene are associated with diverse cardiac pathologies including defects of septation and valvulogenesis, and cardiomyopathy. Am J Human Genetics 81 (2):280-91 (IF 12.629)

Johnson, M.P., Fernandez, F., Colson, N. and Griffiths. L.R. (2007). A pharmacogenomic evaluation of migraine therapy. Expert Opinion on Pharmacotherapy 8(12):1821-35.

Colson N., Lea R., Fernandez F. and Griffiths L.R. (2007). Expert Commentary A & Chapter 1: The Genetics of Migraine. Migraine Disorders Research Trends. Nova Science Publishers, Editor Laura B. Clarke ISBN 978-1-60021-553-7

Lintell N.A., Maguire D.J., Griffiths L.R. & McCabe M. (2007). Analysis of SDHD and MMP12 in an affected solar keratosis and control cohort. Adv Exp Med Biol 599:79-85

Hsieh S.M., Maguire D.J., Lintell N.A., McCabe M. & Griffiths L.R. (2007). PTEN and NDUFB8 aberrations in cervical cancer tissue. Adv Exp Med Biol599:31- 36

F.Fernandez, R.P. Curtain, M. Colson, N.J., Ovcaric, J. MacMillan and L.R. Griffiths (2007). Association analysis of chromosome 1 migraine candidate genes BMC Medical Genetics 8(1):57-64 (IF 2.86)


Curtain, R., Tajouri, L., Lea, R., MacMillan, J., and Griffiths, L.R. (2006). No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree. European Journal of Medical Genetics 49:57-62 (IF 1.614)

Colson, N.J., Lea, R.A., Quinlan, S. and Griffiths, L.R. (2006). No role for the Estrogen Reception 1 Gene Intron 1 Pvu II and Exon 4 C325G Polymorphisms in Migraine Susceptibility. BMC Medical Genetics 7:12 (IF 2.86)

Colson N.J., Lea R.A., Quinlan S. & Griffiths L.R. (2006). The role of vascular and hormonal genes in migraine susceptibility. Molecular Genetics and Metabolism 88:107-113 (IF 2.502)

Curtain R. P., Smith R., Ovcaric M., Griffiths L.R. (2006). Minor head trauma induced Sporadic Hemiplegic Migraine (SHM) coma: A case report. Pediatric Neurology 34(4):329-32.

Haupt, L.M., Thompson, E.W., Trezise, A.E.O., Irving, R., Irving, M.G. andGriffiths, L.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 (IF 2.290)

Tajouri, L., Martin, V., Gasparini, C., Ovcaric, M., Curtain, R., Lea, R., Csurhes, P., Pender, M.P. and Griffiths, L.R. (2006). Genetic investigation of methylenetetrahydroxyfolate reductase (MTHFR) and catechol-o-methyl transferase (COMT) in multiple sclerosis. Brain Research Bulletin 69:327-331 (IF 2.429)

Lintell, N.A., Maguire, D.J., Griffiths, L.R. & McCabe, M. (2006). Focusing on genomic and phenomic aberrations in non-melanotic skin cancers. Adv. Exp. Med. Biol. 578:381-6

Fernandez, F., Lea, R.A., Colson, N.J., Bellis, C., Quinlan, S. & Griffiths, L.R.(2006). Association between a 19bp deletion polymorphism at the Dopamine-?-hydroxylase (D?H) locus and migraine with aura. J Neurol Sci251(1-2):118-23 (IF 2.412)

Smith R.A., Lea R.A., Weinstein S.R., Griffiths L.R. (2006). Detection of mRNA levels for the estrogen alpha, estrogen beta and androgen nuclear receptor genes in archival breast cancer tissue. Cancer Letters 237 (2): 248-255 (IF 3.398)

Bellis C., Hughes R.M., Begley K.N., Quinlan S., Lea R.A., Heath S.C., Blangero J., Griffiths L.R. (2006). Phenotypical characterisation of the isolated Norfolk Island population focusing on epidemiological indicators of cardiovascular disease, Human Heredity 60 :211-9 (IF 2.155)


Ashton, K.J., Carless, M.A. & Griffiths, L.R. (2005). Cytogenetic Alterations in Non-Melanoma Skin Cancer: A Review. Genes, Chromosomes and Cancer43:239- 248 (IF 4.276) (5 citations)

Colson, N.J, Lea, R.A., Quinlan, S., MacMillian, J., Griffiths, L.R. (2005). Investigation of Hormone Receptor Genes in Migraine. Neurogenetics6(1):17-23 (IF 3.115)

Griffiths, L.R., (2005). Authors’ response to: Critique of “Sibpair Studies Implicate Chromosome 18 in essential Hypertension”. American Journal of Medical Genetics 132:458-460 (IF 2.440)

Kammerer, S., Roth, R.B., Hoyal, C.R., Reneland, R., Marnellos, G., Kiechle, M., Schwarz- Boeger, U., Griffiths, L.R., Ebner, F., Rehbock, J., Cantor, C.R., Nelson, M.R. & Braun, A. (2005). Association of the NuMA region on chromosome 11q13 with breast cancer susceptibility. PNAS 102(6):2004-2009 (IF 10.452)

Lea, R.A., Nyholt, D.R., Curtain R., Ovcaric, M, Sciascia R., Bellis, C., MacMillan J., Quinlan S., Gibson, R.A., McCarthy L.C., Riley, J.H., Smithies Y.J., Kinade S., and Griffiths L.R. (2005). A genome-wide Scan provides evidence for loci influencing a severe heritable form of common migraine. Neurogenetics 6(2): 67-72 (IF 3.115)

Lea, R.A., Ovcaric, M., Sundholm, J., Solyom, L., MacMillan, J. and Griffiths, L.R. (2005). Genetic Varients of Angiotensin Converting Enzyme and Methylene Tetrahydrofolate Reductase may act in combination to increase migraine susceptibility. Molecular Brain Research 136:112-117. (IF 1.711)

Hoyal, C.R., Kammerer, S., Roth, R.B., Reneland, R., Marnelloa, G., Kiechle, M., Schwarz- Boeger, U., Griffiths, L.R., Ebner, F., Rehbock, J., Nelson, M.R., Braun, A. (2005). Genetic polymorphisms in DPF3 associated with risk of breast cancer and lymph node metastases. Journal of Carcinogenesis19(4):13 (IF 5.406)

Curtain R., Sundholm J., Lea R., Ovcaric M., MacMillan J., Griffiths L.R.(2005). Association analysis of a highly polymorphic CAG repeat in the human potassium channel gene KCNN3 and migraine susceptibility. BMC Medical Genetics 14(6):32 (IF 2.86)

Johnson, M.P., Lea, R.A., Colson, N.J., MacMillan, J.C and Griffiths, L.R.(2005). A Population Genomics Overview of the Neuronal Nitric Oxide Synthase (nNOS) Gene and it’s Relationship to Migraine Susceptibility.Cellular and Molecular Biology 51: 285-292

Tajouri, L., Ovcaric, M., Curtain, R., Lea, R., Johnson, M., Csurhes, P., Pender, M.P., and Griffiths, L.R. (2005). Variation in the Vitamin D Receptor Gene is Associated with Multiple Sclerosis in an Australian Population. Journal of Neurogenetics 19(1):25-38 (IF 1.583)

Tajouri, L., Mellick, A.S., Tourtellotte, W.W., Nagra, R.M., Griffiths, L.R.(2005). An examination of MS candidate genes identified as differentially regulated in MS plaque tissue, using absolute and comparative real time Q-PCR analysis. Brain Research 15(2):79-91

Curtain, R., Lea, R.A., Tajouri, L., Haupt, L., Ovcaric, M., MacMillan, J., andGriffiths, L.R. (2005). Analysis of chromosome 1 microsatellite markers and the FHM-2 (ATP1A2 ) gene mutations in Migraine pedigrees. Neurological Research 27(6):647-652 (IF 1.634)

Smith, R.A., Lea, R.A., Weinstein, S.R., Griffiths, L.R. (2005). Detection of mRNA Levels for the Estrogen Alpha, Estrogen Beta and Androgen Nuclear Receptor Genes Archival Breast Cancer Tissue. Cancer Letters 237(2):248-55 (IF 2.938)

Johnson, M.P. & Griffiths, L.R. (2005). A genetic analysis of serotonergic biosynthetic and metabolic enzymes in migraine using a DNA pooling approach. Journal of Human Genetics 50(12):607-610 (IF 2.316)

Maguire, D.J., Lintell, N.A., McCabe, M. and Griffiths, L.R. (2005). Focusing on genomic and phenomic correlations in respiration of non-melanotic skin cancers. Adv Exp Med Biol 566:375-80


Rutherford, S., Johnson, M.P. and Griffiths, L.R., (2004). Sibpair studies implicate Chromosome 18 in essential hypertension. American Journal of Medical Genetics 126(3): 241-7. (IF 2.0)

Tajouri, L. Ferreira, L., Ovcaric, M., Curtain, R., Lea, R.A., Csurhes, P., Pender, M., and Griffiths, L.R. (2004). Investigation of a neuronal nitric oxide synthase gene (NOS1) polymorphism in a multiple sclerosis population.Journal of the Neurological Sciences ERA B 218;(1-2) 25-8 (IF 2.366)

Jenner, T.L., Mellick, A.S., Harrison, G.J., Griffiths, L.R. and Rose’Meyer, R.B. (2004). Age related changes in adenosine receptor expression. Mechanisms of Ageing and Development. 125(3); 211-7. (IF 2.866)

Johnson, M.P., Haupt, L.M., and Griffiths, L.R. (2004). Locked nucleic acid (LNA) single nucleotide polymorphism (SNP) genotype analysis and validation using real-time PCR. Nucleic Acids Research 32(6) e55: 1-9 (IF 7.260)

Lea, R.A., Ovcaric, M., Sundholm, J., MacMillan, J. and Griffiths, L.R. (2004). The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura. BMC Medicine 2(1):3:1-8 (IF 3.21)

Colson, N., Lea R.A., Quinlan S., Brimage P., MacMillan J., and Griffiths, L.R.(2004). The estrogen receptor (Er?) G594A polymorphism is associated with migraine susceptibility in two independent caucasian populations.Neurogenetics 5(2):129-33 Epub 2004 (IF 3.115)

Wright, K., Tajouri, L., Lea, R.A., Ovcaric, M., Heux, S., Headrick, J., andGriffiths, L.R. (2004). The role of adenosine-related genes variants in susceptibility to essential hypertension. Journal of Hypertension 22(8): 1519-22 (IF 4.871)

Tajouri, L., Martin, V., Ovcaric, M., Curtain, R., Lea, R.A., Csurhes, P., Pender, M., and Griffiths, L.R. (2004). Investigation of an inducible nitric oxide synthase gene (NOS2A) polymorphism in a multiple sclerosis population.Brain Research Bulletin 64(1):9-13 (IF 2.429)

Selvey, S. Haupt, L.M., Thompson, E.W., Matthaei, K.I., Irving, M.G. andGriffiths, L.R. (2004). Stimulation of MMP-11 (stromelysin-3) expression in mouse fibroblasts by cytokines, collagen and co-culture with human breast cancer cell lines. BMC Cancer 4(1):40-9 (IF 2.290)

Curtain, R., Lea, R.A., Quinlan, S., Bellis., Tajouri, L., Hughes, R., MacMillan, J., and Griffiths, L.R. (2004). Investigation of the Low Density Lipoprotein Receptor Gene and Cholesterol as a Risk Factor for Migraine. Journal of the Neurological Sciences 227(1):95-100 (IF 2.366)

Heux, S., Morin, F., Lea, R.A., Ovcaric, M., Tajouri, L., and Griffiths, L.R.(2004). The methylentetrahydrofolate reductase (MTHFR) gene variant (C677T) as a risk factor for essential hypertension. Hypertension Research27(9):663-7 (IF 1.731)

Kammerer, S., Roth, R.B, Reneland, R., Marnellos, G., Hoyal, C.R., Markward, N.J., Ebner, F., Kiechle, M., Schwarz-Boeger, U., Griffiths, L.R., Ulbrich, C., Chrobok, K., Forster, G., Praetorius, G.M., Meyer, P., Rehbock, J., Cantor, C.R., Nelson, M.R., Braun, A. (2004). Large-scale association study identifies ICAM gene region as breast and prostate cancer susceptibility locus. Cancer Research 64(24) 8906-10 (IF 7.690)

Carless, M., Ashton, K., Griffiths, L.R. (2004). Cytogenetic Analysis of Basal Cell Carcinoma and Squamous Cell Carcinoma. Molecular Mechanisms of Basal Cell and Squamous Cell Carcinomas. J”rg Reichrath (Publication date 2004-10-01 ISBN 1-58706- 198-8)


Smith RA, Curran JE, Weinstein ST, Griffiths LR, (2003). Expression of glucocorticoid and progesterone nuclear receptor genes in archival breast tumour tissue. Breast Cancer Research 5:9-12 (IF 2.975)

Johnson, M.P., Lea, R.A., Curtain, R.P., MacMillan, J.C., and Griffiths, L.R.(2003). An investigation of the 5-HT2c receptor gene as a migraine candidate gene. Am J of Medical Genetics B 117:86-9 (IF 2.0)

Grice, I.D., Garhnam, B., Pierens, G., Rogers, K., Tindal, D., & Griffiths, L.R.(2003). Isolation of two phenylethanoid glycosides from eremophila gilesii. J. of Ethnopharmacology 86:123-5.

Rose’Meyer, R.B., Mellick, A.S., Garnham, B.G., Massa, H.M. and Griffiths, L.R. 2003. The measurement of adenosine and estrogen receptor expression in rat brains following ovariectomy using quantitative PCR analysis. Brain Research Protoc. 11:9-18. (IF 1.818)

Bellis, C., Ashton, K.J., Freney, B., Blair, B., and Griffiths, L.R. (2003). A molecular genetic approach for forensic animal species identification. Forensic Science International 134: 99-108 (IF 2.015)

Ashton, K.J., Weinstein, S.R., Maguire, D.J., Griffiths, L.R. (2003). Chromosomal aberrations in squamous cell carcinoma and solar keratoses revealed by comparative genomic hybridization. Archives of Dermatology.139:876-82. (IF 3.187)

Rogers, K.L., Lea, R.A., and Griffiths, L.R., (2003). Molecular mechanisms of migraine: prospects for pharmacogenomics. American Journal of Pharmacogenomics 3:329-43

Lea, R.A., Hilton, D.A., MacMillan, J.C. and Griffiths, L.R. (2003). An analysis of clinical characteristics in migraine affected pedigrees. Cephalalgia 23:808-813 (IF 3.133)

Mellick, A.S., Blackmore, D., Weinstein, S.R., and Griffiths, L.R. (2003). An assessment of MMP and TIMP gene expression in cell lines and stroma-tumor differences in microdissected breast cancer biopsies. Tumour Biology 7 24:258-270 (IF 2.34)

Tajouri, L., Mellick, A.S., Ashton, K., Tannenberg, A.E., Tourtellotte, W., andGriffiths, L.R. (2003). Quantitative and qualitative changes in gene expression patterns characterize the activity of plaques in multiple sclerosis.Molecular Brain Research 119:170-183 (IF 1.997)

Hyun, C., Filippich, L., Lea, R.A., Shepherd, G., Hughes, I., and Griffiths, L.R.(2003). Prospects for whole genome linkage disequilibrium mapping in domestic dog breeds. Mammalian Genome 14:640-9 (IF 2.658)

Maguire, D.J., Lintell, N.J., McCabe, M., Griffiths, L.R., and Ashton, K. (2003). Genomic and phenomic correlations in respiration of basal cell carcinomas. Adv. Exp. Med. Biol. 540:251-6

Purdam C.R., Crichton K., Fehrmann M., Grant M., Griffiths L.R., Harcourt P., Kellaway D., Kiss Z., Tress B., Cook J.L., Visentini P., Wark J., Young D., Hopper D.M., Khan K.M., Barlett J., Bass S., Bonar F., Coleman B. (2003). Discriminative ability of functional loading tests for adolescent jumper’s knee,Physical Therapy in Sport 4 (1) 3-9


Griffiths, L.R., (2002). Authors response to: Critique of “Chromosome 17 and inducible nitric oxide synthase gene in human essential hypertension” by Rutherford et. al Human Genetics (IF 4.328) 2002 110(1):100-3

Shepherd, A.G., Lea, R.A., Hutchins, C., Jordan, K., Brimage, P.J. andGriffiths, L.R. (2002). Dopamine receptor genes and migraine with or without aura: an association study. Headache (IF 2.307) 42(5):346-351.

Lea, R.A., Shepherd, A.G., Curtain, R.P., Nyholt, D.R., Quinlan, S., Brimage, P.J. and Griffiths, L.R. (2002). A typical migraine susceptibility region localises to chromosome 1q31. Neurogenet (IF 3.115) 4:17-22.

Rogers, K.L., Fong, W. F, Redburn, J., Griffiths, L.R. (2002). Fluorescence detection of plant extracts that affect neuronal voltage-gated Ca 2+ channels. Eur J Pharm Sc (IF 1.949) 15: 321-330.

Mellick, A.S., Day, C.J., Weinstein, S.R., Griffiths, L.R. and Morrison, N.A. (2002). Differential gene expression in breast cancer cell lines and stroma tumour differences in microdissected breast cancer biopsies revealed by display array analysis. Int Journal of Cancer (IF 4.416) 100: 172-180 (22 Citations)

Curran, J.E., Weinstein, S.R. and Griffiths, L.R. (2002). Polymorphic variants of NFKB1 and its inhibitory protein NFKBIA and their involvement in sporadic breast cancer. Cancer Letters (IF 2.938) 188: 103-107.

Carless, M.A., Lea, R.A., Curran, J.E., Appleyard, B., Gaffney, P., Green, A. andGriffiths, L.R. (2002). The GSTM1 null genotype confers an increased risk for solar keratosis development in an Australian caucasian population. Journal of Investigative Dermatology. (IF 4.238) 119:1373-8.


Lea, R.A., Curtain, R.P., Shepherd, A.G., Brimage, P.J. and Griffiths, L.R.(2001). No evidence for involvement of the human inducible nitric oxide synthase (iNOS) gene in susceptibility for typical migraine. Am. J. Med. Genet.(IF 3.659) 105: 110 – 113.

Cook, J.L., Khan, K.M., Kiss, Z.S., Purdam, C.R. and Griffiths, L.R. (2001). Reproducibility and clinical utility of tendon palpation to detect patellar tendinopathy in young basketball players. Br. J. Sports Med. 35: 65 – 69.

Box, N.F., Duffy, D.L., Irving, R., Russell, A., Chen, W., Griffiths, L.R., Parsons, P.G., Green, A.C., Sturm, R.A. (2001). Melanocortin ? 1 receptor genotype is a risk factor for basal and squamous cell carcinoma. Journal of Investigative Dermatology (IF 4.238) 116(2): 224 – 229.

Carless, M.A., Curran, J.E., Gaffney, P., Weinstein, S.R. and Griffiths, L.R.(2001). Association analysis of somatostatin receptor (SSTR1 and SSTR2) in susceptibility to breast cancer and solar keratosis. Cancer Letters (IF 2.938) 166: 193-197.

Curran, J.E., Lea, R.A., Rutherford, S., Weinstein, S.R. and Griffiths, L.R.(2001). Association of Estrogen Receptor and Glucocorticoid Receptor Gene Poymorphisms with Sporadic Breast Cancer. International Journal of Cancer(IF 4.416) 95(4):271-5.

Grice, I.D., Ferreira, L.A. and Griffiths, L.R. (2001). Identification and simultaneous analysis of harmane, harmine, harmol, isovitexin and vitexin in Passiflora incarnta extracts using a novel HPLC method. J. Liq. Chromato. Rel. Tech. 24(16): 2513-2523.

Ashton, K.J., Williams, B.F., Weinstein, S.R., Maguire, D.J. and Griffiths, L.R.(2001). Molecular cytogenetic analysis of basal cell carcinoma representative DNA using comparative genomic hybridisation. Journal of Investigative Dermatology (IF 4.238) 117(3): 683-686.

Rogers, K.L., Grice, I.D. and Griffiths, L.R. (2001). Modulation of In-Vitro Platelet 5-HT Release by Species of Erythrina and Cymbopogon. Life Sciences(IF 2.158) 69: 1817-1829.

Rutherford, S., Johnson, M.P., Curtain, R.P. and Griffiths, L.R. (2001). Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension. Hum. Genet. (IF 4.328) 109: 408-415.

Selvey, S., Thompson, E.W., Matthaei, K., Irving, M.G. and Griffiths, L.R.(2001). ?-actin – An unsuitable internal control for RT-PCR. Mol. Cell. Probes(IF 2.019) 15(5): 307-311

Lea, R.A., Curtain, R.P., Hutchins, C., Brimage, P.J. and Griffiths, L.R.(2001) An investigation of the CACNA1A gene as a candidate for typical migraine susceptibility. Am. J. Med. Genet. (IF 3.659) 105(8): 707-712.

McCarthy, L.C., Hosford, D.A., Riley, J.H., Bird, M.I., White, N.J., Hewitt, D.R., Peroutka, S., Griffiths, L.R., Boyd, P.R., Lea, R.A., Bhatti, S.M., Hosking, L.K., Hood, C.M., Jones, K.W., Handley, A.R., Rallan, R., Lewis, K.F., Yeo, A.J.M., Williams, P.M., Priest, R.C., Khan, P., Donnelly, C., Lumsden, S.M., O’Sullivan, J., See, C.G., Smart, D.H., Shaw- Hawkins, S., Patel, J., Lnagrish, T.C., Feniuk, W., Knowles, R.G., Thomas, M., Libir, V., Montgomery, D.S., Manasco, P.K., Xu, C., Dykes, C., Humphrey, P.P.A., Roses, A.D., and Purvis, I.J. (2001) Single nucleotide polymorphism (SNP) alleles in the INSR gene are associated with typical migraine. Genomics (IF 3.840) 78(3): 135-149.

Smith, R.A., Curran, J.E., Weinstein, S.R. and Griffiths, L.R. (2001). Investigation of glutathione S-transferase zeta and the development of sporadic breast cancer. Breast Cancer Research (IF 2.975) 3: 409-411

Cook, J.L., Khan, K.M. Kiss, Z.S., Coleman, B.D. and Griffiths, L.R. (2001). Asymptomatic hypoechoic regions on patellar tendon ultrasound: A 4-year clinical and ultrasound follow up of 46 tendons. Scand J Med Sci Sports (IF 1.717) 11: 321-327.


Rogers, K.L., Grice, I.D. and Griffiths, L.R. (2000). Inhibition of platelet aggregation and 5-HT release by extracts of Australian plants used traditionally as headache treatments. European Journal of Pharmaceutical Sciences (IF 1.949) 9:(4) 355-363.

Curran, J.E., Weinstein, S.R. and Griffiths, L.R. (2000). Polymorphisms of glutathione S-transferase genes (GSTM1, GSTP1 and GSTT1) and breast cancer susceptibility. Cancer Letters (IF 2.938) 153; 113 ? 120

Cook, J.L., Khan, K.M., Kiss, Z.S., Purdam, C.R., Griffiths, L.R. (2000). Prospective imaging study of asymptomatic patellar tendinopathy in elite junior basketball players. J Ultrasound Med. 19(7):473-9.

Cook, J.L., Khan, K.M., Kiss, Z.S., Griffiths, L.R. (2000). Patellar tendinopathy in junior basketball players: a controlled clinical and ultrasonographic study of 268 patellar tendons in players aged 14-18 years.Scand J Med Sci Sports 10(4):216-20.

Nyholt, D.R., Curtain, R.P. and Griffiths, L.R. (2000). Familial typical migraine: Significant linkage and localisation of a gene to Xq24-28. Human Genetics (IF 4.328) 107:18 – 23.

Lea, R.A., Dohy, A., Jordan, K., Quinlan, S., Brimage, P.J. and Griffiths, L.R.(2000). Evidence for allelic association of the Dopamine B-Hydroxylase Gene (DBH) with susceptibility to typical migraine. Neurogenetics (IF 3.11) 3:35 – 40.

Grigg, R.F., Lea, R.A., Sullivan, A.A., Curtain, R.P., MacMillan, J. and Griffiths, L.R. (2000). Identification of a Novel C144F Mutation in the Notch3 Gene in an Australian CADASIL pedigree. Human Mutation (IF 6.845) 16(5): 449 – 50.