Professor Graham Mann

Professor and Associate Dean Research
Medicine, Westmead Clinical School
Westmead Millennium Institute for Medical Research

C24 - Westmead Hospital
The University of Sydney
NSW 2006 Australia

T: +61 2 9845 9056
F: +61 2 9845 9102

W: Related website

Biographical details

Research interests

Genetic and environmental causes of:

  • melanoma

  • breast cancer

  • non-melanoma skin cancer

  • prostate cancer.

Current national competitive grants*


Molecular determinants of risk, progression and treatment response in melanoma
Kefford R, Thompson J, Hersey P, Mann G, Scolyer R, Hayward N
NHMRC Program Grant ($12,065,000 over 5 years)

* Grants administered through the University of Sydney


2014 | 2013 | 2012 | 2011 | 2010 | 2009 | 2008


  • Watts, K., Meiser, B., Wakefield, C., Barratt, A., Howard, K., Cheah, B., Mann, G., Lobb, E., Gaff, C., Patel, M. (2014), Online Prostate Cancer Screening Decision Aid for At-Risk Men: A Randomized Trial. Health Psychology. 33(9), 986-997. [Abstract]
  • Moloney, F., Guitera, P., Coates, E., Haass, N., Ho, K., Khoury, R., O'Connell, R., Raudonikis, L., Schmid, H., Mann, G., Menzies, S. (2014), Detection of Primary Melanoma in Individuals at Extreme High Risk: A Prospective 5-Year Follow-Up Study. JAMA Dermatology. 150(8), 819-827. [Abstract]
  • Becker, T., Boyd, S., Mijatov, B., Gowrishankar, K., Snoyman, S., Pupo, G., Scolyer, R., Mann, G., Kefford, R., Zhang, X., Rizos, H. (2014), Mutant B-RAF-Mcl-1 survival signaling depends on the STAT3 transcription factor. Oncogene. 33, 1158¿1166. [Abstract]
  • Kaufman, K., Mactier, S., Armstrong, N., Mallawaaratchy, D., Byrne, S., Haydu, L., Jakrot, V., Thompson, J., Mann, G., Scolyer, R., Christopherson, R. (2014), Surface antigen profiles of leukocytes and melanoma cells in lymph node metastases are associated with survival in AJCC stage III melanoma patients. Clinical & Experimental Metastasis. 31, 407-421. [Abstract]
  • Dieng, M., Watts, C., Kasparian, N., Morton, R., Mann, G., Cust, A. (2014), Improving subjective perception of personal cancer risk: systematic review and meta-analysis of educational interventions for people with cancer or at high risk of cancer. Psycho-Oncology. 23(6), 613-625. [Abstract]


  • Schramm, S., Menzies, A., Mann, G. (2013), Molecular biomarkers of prognosis in melanoma: how far are we from the clinic?. Melanoma Research. 23, 423-425. [Abstract]
  • Boyd, S., Mijatov, B., Pupo, G., Tran, S., Gowrishankar, K., Shaw, H., Goding, C., Scolyer, R., Mann, G., Kefford, R., Rizos, H., Becker, T. (2013), Oncogenic B-RAF(V600E) Signaling Induces the T-Box3 Transcriptional Repressor to Repress E-Cadherin and Enhance Melanoma Cell Invasion. The Journal of Investigative Dermatology. 133(5), 1269-1277. [Abstract]
  • Dutton-Regester, K., Kakavand, H., Aoude, L., Stark, M., Gartside, M., Johansson, P., O'Connor, L., Lanagan, C., Tembe, V., Pupo, G., Haydu, L., Schmidt, C., Mann, G., Thompson, J., Scolyer, R., Hayward, N. (2013), Melanomas of unknown primary have a mutation profile consistent with cutaneous sun-exposed melanoma. Pigment Cell & Melanoma Research. 26(6), 852-860. [Abstract]
  • Schramm, S., Jayaswal, V., Goel, A., Li, S., Yang, Y., Mann, G., Wilkins, M. (2013), Molecular interaction networks for the analysis of human disease: utility, limitations, and considerations. Proteomics. 13(23-24), 3393-3405. [Abstract]
  • Cust, A., Goumas, C., Vuong, K., Davies, J., Barrett, J., Holland, E., Schmid, H., Agha-Hamilton, C., Armstrong, B., Kefford, R., Aitken, J., Giles, G., Bishop, D., Newton-Bishop, J., Hopper, J., Mann, G., Jenkins, M. (2013), MC1R genotype as a predictor of early-onset melanoma, compared with self-reported and physician-measured traditional risk factors: an Australian case-control-family study. BMC Cancer. 13(1), 406. [Abstract]
  • Kakavand, H., Scolyer, R., Thompson, J., Mann, G. (2013), Identification of new prognostic biomarkers for Stage III metastatic melanoma patients. Oncoimmunology. 2(9), e25564. [Abstract]
  • McLoone, J., Menzies, S., Meiser, B., Mann, G., Kasparian, N. (2013), Psycho-educational interventions for melanoma survivors: a systematic review. Psycho-Oncology. 22(7), 1444-1456. [Abstract]
  • Mann, G., Pupo, G., Campain, A., Carter, C., Schramm, S., Pianova, S., Gerega, S., De Silva, C., Lai, K., Wilmott, J., Synnott, M., Hersey, P., Kefford, R., Thompson, J., Yang, Y., Scolyer, R. (2013), BRAF Mutation, NRAS Mutation, and the Absence of an Immune-Related Expressed Gene Profile Predict Poor Outcome in Patients with Stage III Melanoma. The Journal of Investigative Dermatology. 133(2), 509-517. [Abstract]
  • Mar, V., Wong, S., Li, J., Scolyer, R., McLean, C., Papenfuss, A., Tothill, R., Kakavand, H., Mann, G., Thompson, J., Behren, A., Cebon, J., Wolfe, R., Kelly, J., Dobrovic, A., McArthur, G. (2013), BRAF/NRAS Wild-Type Melanomas Have a High Mutation Load Correlating with Histologic and Molecular Signatures of UV Damage. Clinical Cancer Research. 19(17), 4589-4598. [Abstract]
  • Schramm, S., Li, S., Jayaswal, V., Fung, D., Campain, A., Pang, C., Scolyer, R., Yang, Y., Mann, G., Wilkins, M. (2013), Disturbed protein-protein interaction networks in metastatic melanoma are associated with worse prognosis and increased functional mutation burden. Pigment Cell & Melanoma Research. 26, 708-722. [Abstract]
  • Qian, J., Liu, H., Wei, S., Liu, Z., Li, Y., Wang, L., Chen, W., Amos, C., Lee, J., Iles, M., Law, M., Cust, A., Barrett, J., Montgomery, G., Taylor, J., Bishop, J., Macgregor, S., Bishop, D., Mann, G., Hayward, N., Wei, Q. (2013), Association between putative functional variants in the PSMB9 gene and risk of melanoma--re-analysis of published melanoma genome-wide association studies. Pigment Cell & Melanoma Research. 26(3), 392-401. [Abstract]
  • Liu, H., Wang, L., Liu, Z., Chen, W., Amos, C., Lee, J., Iles, M., Law, M., Barrett, J., Montgomery, G., Taylor, J., MacGregor, S., Cust, A., Newton Bishop, J., Hayward, N., Bishop, D., Mann, G., Affleck, P., Wei, Q. (2013), Association between functional polymorphisms in genes involved in the MAPK signaling pathways and cutaneous melanoma risk. Carcinogenesis. 34(4), 885-892. [Abstract]
  • Iles, M., Law, M., Stacey, S., Han, J., Fang, S., Pfeiffer, R., Harland, M., Macgregor, S., Taylor, J., Aben, K., Akslen, L., Avril, M., Azizi, E., Bakker, B., Benediktsdottir, K., Bergman, W., Scarrà, G., Brown, K., Calista, D., Chaudru, V., Fargnoli, M., Cust, A., Demenais, F., de Waal, A., DÄ¿bniak, T., Elder, D., Friedman, E., Galan, P., Ghiorzo, P., Gillanders, E., Goldstein, A., Gruis, N., Hansson, J., Helsing, P., Hočevar, M., Höiom, V., Hopper, J., Ingvar, C., Janssen, M., Jenkins, M., Kanetsky, P., Kiemeney, L., Lang, J., Lathrop, G., Leachman, S., Lee, J., LubiÅ¿ski, J., Mackie, R., Mann, G., Martin, N., Mayordomo, J., Molven, A., Mulder, S., Nagore, E., NovakoviÄ¿, S., Okamoto, I., Olafsson, J., Olsson, H., Pehamberger, H., Peris, K., Grasa, M., Planelles, D., Puig, S., Puig-Butille, J., Randerson-Moor, J., Requena, C., Rivoltini, L., Rodolfo, M., Santinami, M., Sigurgeirsson, B., Snowden, H., Song, F., Sulem, P., Thorisdottir, K., Tuominen, R., Van Belle, P., van der Stoep, N., van Rossum, M., Wei, Q., Wendt, J., Zelenika, D., Zhang, M., Landi, M., Thorleifsson, G., Bishop, D., Amos, C., Hayward, N., Stefansson, K., Bishop, J., Barrett, J. (2013), A variant in FTO shows association with melanoma risk not due to BMI. Nature Genetics. 45(4), 428-432, 432e1. [Abstract]
  • McLoone, J., Watts, K., Menzies, S., Barlow-Stewart, K., Mann, G., Kasparian, N. (2013), Melanoma survivors at high risk of developing new primary disease: a qualitative examination of the factors that contribute to patient satisfaction with clinical care. Psycho-Oncology. 22(9), 1994-2000. [Abstract]
  • Jayaswal, V., Schramm, S., Mann, G., Wilkins, M., Yang, Y. (2013), VAN: an R package for identifying biologically perturbed networks via differential variability analysis. BMC Research Notes. 6(1), 430. [Abstract]


  • Kim, J., McCarthy, S., Thompson, J., Pupo, G., Vonthethoff, L., Nash, P., Mann, G., Scolyer, R. (2012), Cellular blue naevus involving the urinary bladder. Pathology. 44(7), 664-668. [Abstract]
  • Cust, A., Goumas, C., Holland, E., Agha-Hamilton, C., Aitken, J., Armstrong, B., Giles, G., Kefford, R., Schmid, H., Hopper, J., Mann, G., Jenkins, M. (2012), MC1R genotypes and risk of melanoma before age 40 years: A population-based case-control-family study. International Journal of Cancer. 131(3), E269-281. [Abstract]
  • Dutton-Regester, K., Aoude, L., Nancarrow, D., Stark, M., O'Connor, L., Lanagan, C., Pupo, G., Tembe, V., Carter, C., O'Rourke, M., Scolyer, R., Mann, G., Schmidt, C., Herington, A., Hayward, N. (2012), Identification of TFG (TRK-fused gene) as a putative metastatic melanoma tumor suppressor gene. Genes, Chromosomes & Cancer. 51(5), 452-461. [Abstract]
  • Dutton-Regester, K., Irwin, D., Hunt, P., Aoude, L., Tembe, V., Pupo, G., Lanagan, C., Carter, C., O'Connor, L., O'Rourke, M., Scolyer, R., Mann, G., Schmidt, C., Herington, A., Hayward, N. (2012), A high-throughput panel for identifying clinically relevant mutation profiles in melanoma. Molecular Cancer Therapeutics. 11(4), 888-897. [Abstract]
  • Schramm, S., Campain, A., Scolyer, R., Yang, Y., Mann, G. (2012), Review and Cross-Validation of Gene Expression Signatures and Melanoma Prognosis. The Journal of investigative dermatology. 132(2), 274-83. [Abstract]
  • Law, M., Montgomery, G., Brown, K., Martin, N., Mann, G., Hayward, N., Macgregor, S. (2012), Meta-Analysis Combining New and Existing Data Sets Confirms that the TERT-CLPTM1L Locus Influences Melanoma Risk. Journal of Investigative Dermatology. 132(2), 485-487. [Abstract]
  • Kasparian, N., Sansom-Daly, U., McDonald, R., Meiser, B., Butow, P., Mann, G. (2012), The nature and structure of psychological distress in people at high risk for melanoma: a factor analytic study. Psycho-Oncology. 21(8), 845-856. [Abstract]
  • Howard, K., Salkeld, G., Mann, G., Patel, M., Cunich, M., Pignone, M. (2012), The COMPASs Study: Community Preferences for Prostate cAncer Screening. Protocol for a quantitative preference study. BMJ Open. 2(1), e000587. [Abstract]


  • Amos, C., Wang, L., Lee, J., Gershenwald, J., Chen, W., Fang, S., Kosoy, R., Zhang, M., Qureshi, A., Vattathil, S., Schacherer, C., Gardner, J., Wang, Y., Tim Bishop, D., Barrett, J., Macgregor, S., Hayward, N., Martin, N., Duffy, D., Mann, G., Cust, A., Hopper, J., Brown, K., Grimm, E., Xu, Y., Han, Y., Jing, K., McHugh, C., Laurie, C., Doheny, K., Pugh, E., Seldin, M., Han, J., Wei, Q. (2011), Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Human Molecular Genetics. 20(24), 5012-5023. [Abstract]
  • Yokoyama, S., Woods, S., Boyle, G., Aoude, L., MacGregor, S., Zismann, V., Gartside, M., Cust, A., Haq, R., Harland, M., Taylor, J., Duffy, D., Holohan, K., Dutton-Regester, K., Palmer, J., Bonazzi, V., Stark, M., Symmons, J., Law, M., Schmidt, C., Lanagan, C., O'Connor, L., Holland, E., Schmid, H., Maskiell, J., Jetann, J., Ferguson, M., Jenkins, M., Kefford, R., Giles, G., Armstrong, B., Aitken, J., Hopper, J., Whiteman, D., Pharoah, P., Easton, D., Dunning, A., Newton-Bishop, J., Montgomery, G., Martin, N., Mann, G., Bishop, D., Tsao, H., Trent, J., Fisher, D., Hayward, N., Brown, K. (2011), A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Nature. 480(7375), 99-103. [Abstract]
  • Scurr, L., McKenzie, H., Becker, T., Irvine, M., Lai, K., Mann, G., Scolyer, R., Kefford, R., Rizos, H. (2011), Selective Loss of Wild-Type p16(INK4a) Expression in Human Nevi. The Journal of Investigative Dermatology. 131(11), 2329-2332. [Abstract]
  • Barrett, J., Iles, M., Harland, M., Taylor, J., Aitken, J., Andresen, P., Akslen, L., Armstrong, B., Avril, M., Azizi, E., Bakker, B., Bergman, W., Bianchi-Scarrà, G., Bressac-de Paillerets, B., Calista, D., Cannon-Albright, L., Corda, E., Cust, A., Dębniak, T., Duffy, D., Dunning, A., Easton, D., Friedman, E., Galan, P., Ghiorzo, P., Giles, G., Hansson, J., Hocevar, M., Höiom, V., Hopper, J., Ingvar, C., Janssen, B., Jenkins, M., Jönsson, G., Kefford, R., Landi, G., Landi, M., Lang, J., Lubiński, J., Mackie, R., Malvehy, J., Martin, N., Molven, A., Montgomery, G., van Nieuwpoort, F., Novakovic, S., Olsson, H., Pastorino, L., Puig, S., Puig-Butille, J., Randerson-Moor, J., Snowden, H., Tuominen, R., Van Belle, P., van der Stoep, N., Whiteman, D., Zelenika, D., Han, J., Fang, S., Lee, J., Wei, Q., Lathrop, G., Gillanders, E., Brown, K., Goldstein, A., Kanetsky, P., Mann, G., Macgregor, S., Elder, D., Amos, C., Hayward, N., Gruis, N., Demenais, F., Bishop, J., Bishop, D. (2011), Genome-wide association study identifies three new melanoma susceptibility loci. Nature genetics. 43(11), 1108-13. [Abstract]
  • Macgregor, S., Montgomery, G., Liu, J., Zhao, Z., Henders, A., Stark, M., Schmid, H., Holland, E., Duffy, D., Zhang, M., Painter, J., Nyholt, D., Maskiell, J., Jetann, J., Ferguson, M., Cust, A., Jenkins, M., Whiteman, D., Olsson, H., Puig, S., Bianchi-Scarrà, G., Hansson, J., Demenais, F., Landi, M., Dębniak, T., Mackie, R., Azizi, E., Bressac-de Paillerets, B., Goldstein, A., Kanetsky, P., Gruis, N., Elder, D., Newton-Bishop, J., Bishop, D., Iles, M., Helsing, P., Amos, C., Wei, Q., Wang, L., Lee, J., Qureshi, A., Kefford, R., Giles, G., Armstrong, B., Aitken, J., Han, J., Hopper, J., Trent, J., Brown, K., Martin, N., Mann, G., Hayward, N. (2011), Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. Nature Genetics. 43(11), 1114-1118. [Abstract]
  • Schramm, S., Mann, G. (2011), Melanoma Prognosis: A REMARK-based systematic review and bioinformatic analysis of immunohistochemical and gene microarray studies. Molecular cancer therapeutics. 10(8), 1520-8. [Abstract]
  • Cust, A., Jenkins, M., Goumas, C., Armstrong, B., Schmid, H., Aitken, J., Giles, G., Kefford, R., Hopper, J., Mann, G. (2011), Early-life sun exposure and risk of melanoma before age 40 years. Cancer causes & control : CCC. 22(6), 885-97. [Abstract]
  • Cust, A., Armstrong, B., Goumas, C., Jenkins, M., Schmid, H., Hopper, J., Kefford, R., Giles, G., Aitken, J., Mann, G. (2011), Sunbed use during adolescence and early adulthood is associated with increased risk of early-onset melanoma. International journal of cancer. Journal international du cancer. 128(10), 2425-35. [Abstract]
  • Long, G., Menzies, A., Nagrial, A., Haydu, L., Hamilton, A., Mann, G., Hughes, T., Thompson, J., Scolyer, R., Kefford, R. (2011), Prognostic and Clinicopathologic Associations of Oncogenic BRAF in Metastatic Melanoma. Journal of Clinical Oncology. 29(10), 1239-1246. [Abstract]
  • Cust, A., Harland, M., Makalic, E., Schmidt, D., Dowty, J., Aitken, J., Agha-Hamilton, C., Armstrong, B., Barrett, J., Chan, M., Chang, Y., Gascoyne, J., Giles, G., Holland, E., Kefford, R., Kukalizch, K., Lowery, J., Randerson-Moor, J., Schmid, H., Taylor, C., Whitaker, L., Hopper, J., Newton-Bishop, J., Mann, G., Bishop, D., Jenkins, M. (2011), Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UK. Journal of medical genetics. 48(4), 266-72. [Abstract]
  • Wakefield, C., Watts, K., Meiser, B., Sansom-Daly, U., Barratt, A., Mann, G., Lobb, E., Gaff, C., Howard, K., Patel, M. (2011), Development and pilot testing of an online screening decision aid for men with a family history of prostate cancer. Patient Education and Counseling. 83(1), 64-72. [Abstract]
  • Hersey, P., Smalley, K., Weeraratna, A., Bosenberg, M., Zhang, X., Haass, N., Paton, E., Mann, G., Scolyer, R. (2011), Meeting report from the 7th International Melanoma Congress, Sydney, November, 2010. Pigment Cell & Melanoma Research. 24(1), e1-e15. [Abstract]


  • Balleine, R., Provan, P., Pupo, G., Pathmanathan, N., Cummings, M., Farshid, G., Salisbury, E., Bilous, A., Byth, K., Mann, G. (2010), Familial concordance of breast cancer pathology as an indicator of genotype in multiple-case families. Genes, chromosomes & cancer. 49(12), 1082-94. [Abstract]
  • Kasparian, N., McLoone, J., Meiser, B., Butow, P., Simpson, J., Mann, G. (2010), Skin cancer screening behaviours among individuals with a strong family history of malignant melanoma. British journal of cancer. 103(10), 1502-9. [Abstract]
  • Demenais, F., Mohamdi, H., Chaudru, V., Goldstein, A., Newton Bishop, J., Bishop, D., Kanetsky, P., Hayward, N., Gillanders, E., Elder, D., Avril, M., Azizi, E., van Belle, P., Bergman, W., Bianchi-Scarrà, G., Bressac-de Paillerets, B., Calista, D., Carrera, C., Hansson, J., Harland, M., Hogg, D., Höiom, V., Holland, E., Ingvar, C., Landi, M., Lang, J., Mackie, R., Mann, G., Ming, M., Njauw, C., Olsson, H., Palmer, J., Pastorino, L., Puig, S., Randerson-Moor, J., Stark, M., Tsao, H., Tucker, M., van der Velden, P., Yang, X., Gruis, N. (2010), Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study. Journal of the National Cancer Institute. 102(20), 1568-83. [Abstract]
  • Kaufman, K., Belov, L., Huang, P., Mactier, S., Scolyer, R., Mann, G., Christopherson, R. (2010), An extended antibody microarray for surface profiling metastatic melanoma. Journal of immunological methods. 358(1-2), 23-34. [Abstract]
  • McKenzie, H., Fung, C., Becker, T., Irvine, M., Mann, G., Kefford, R., Rizos, H. (2010), Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A. Human mutation. 31(6), 692-701. [Abstract]
  • Scurr, L., Pupo, G., Becker, T., Lai, K., Schrama, D., Haferkamp, S., Irvine, M., Scolyer, R., Mann, G., Becker, J., Kefford, R., Rizos, H. (2010), IGFBP7 is not required for B-RAF-induced melanocyte senescence. Cell. 141(4), 717-727. [Abstract]


  • Cust, A., Schmid, H., Maskiell, J., Jetann, J., Ferguson, M., Holland, E., Agha-Hamilton, C., Jenkins, M., Kelly, J., Kefford, R., Giles, G., Armstrong, B., Aitken, J., Hopper, J., Mann, G. (2009), Population-based, case-control-family design to investigate genetic and environmental influences on melanoma risk: Australian Melanoma Family Study. American Journal of Epidemiology. 170(12), 1541-1554. [Abstract]
  • Leachman, S., Carucci, J., Kohlmann, W., Banks, K., Asgari, M., Bergman, W., Bianchi-Scarrà, G., Brentnall, T., Bressac-de Paillerets, B., Bruno, W., Curiel-Lewandrowski, C., de Snoo, F., Debniak, T., Demierre, M., Elder, D., Goldstein, A., Grant-Kels, J., Halpern, A., Ingvar, C., Kefford, R., Lang, J., MacKie, R., Mann, G., Mueller, K., Newton-Bishop, J., Olsson, H., Petersen, G., Puig, S., Rigel, D., Swetter, S., Tucker, M., Yakobson, E., Zitelli, J., Tsao, H. (2009), Selection criteria for genetic assessment of patients with familial melanoma. Journal of the American Academy of Dermatology. 61(4), 677.e1-677.e14. [Abstract]
  • Howard, K., Barratt, A., Mann, G., Patel, M. (2009), A model of prostate-specific antigen screening outcomes for low- to high-risk men: information to support informed choices. Archives of Internal Medicine. 169(17), 1603-1610. [Abstract]
  • Bishop, D., Demenais, F., Iles, M., Harland, M., Taylor, J., Corda, E., Randerson-Moor, J., Aitken, J., Avril, M., Azizi, E., Bakker, B., Bianchi-Scarrà, G., Bressac-de Paillerets, B., Calista, D., Cannon-Albright, L., Chin-A-Woeng, T., Debniak, T., Galore-Haskel, G., Ghiorzo, P., Gut, I., Hansson, J., Hocevar, M., Höiom, V., Hopper, J., Ingvar, C., Kanetsky, P., Kefford, R., Landi, M., Lang, J., Lubiński, J., Mackie, R., Malvehy, J., Mann, G., Martin, N., Montgomery, G., van Nieuwpoort, F., Novakovic, S., Olsson, H., Puig, S., Weiss, M., van Workum, W., Zelenika, D., Brown, K., Goldstein, A., Gillanders, E., Boland, A., Galan, P., Elder, D., Gruis, N., Hayward, N., Lathrop, G., Barrett, J., Bishop, J. (2009), Genome-wide association study identifies three loci associated with melanoma risk. Nature Genetics. 41(8), 920-925. [Abstract]
  • Kasparian, N., Meiser, B., Butow, P., Simpson, J., Mann, G. (2009), Genetic testing for melanoma risk: a prospective cohort study of uptake and outcomes among Australian families. Genetics in Medicine. 11(4), 265-278. [Abstract]
  • Scaini, M., Rossi, E., Torres, P., Zullato, D., Callegaro, M., Casella, C., Quaggio, M., Agata, S., Malacrida, S., Chiarion-Sileni, V., Vecchiato, A., Alaibac, M., Montagna, M., Mann, G., Menin, C., D'Andrea, E. (2009), Functional impairment of p16(INK4A) due to CDKN2A p.Gly23Asp missense mutation. Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis. 671(1-2), 26-32. [Abstract]
  • Becker, T., Haferkamp, S., Dijkstra, M., Scurr, L., Frausto, M., Diefenbach, E., Scolyer, R., Reisman, D., Mann, G., Kefford, R., Rizos, H. (2009), The chromatin remodelling factor BRG1 is a novel binding partner of the tumor suppressor p16INK4a. Molecular Cancer. 8, 4. [Abstract]
  • Morey, A., Murali, R., McCarthy, S., Mann, G., Scolyer, R. (2009), Diagnosis of cutaneous melanocytic tumours by four-colour fluorescence in situ hybridisation. Pathology. 41(4), 383-7. [Abstract]
  • Gartside, M., Chen, H., Ibrahimi, O., Byron, S., Curtis, A., Wellens, C., Bengston, A., Yudt, L., Eliseenkova, A., Ma, J., Curtin, J., Hyder, P., Harper, U., Riedesel, E., Mann, G., Trent, J., Bastian, B., Meltzer, P., Mohammadi, M., Pollock, P. (2009), Loss-of-function fibroblast growth factor receptor-2 mutations in melanoma. Molecular Cancer Research. 7(1), 41-54. [Abstract]


  • Gallagher, S., Thompson, J., Indsto, J., Scurr, L., Lett, M., Gao, B., Dunleavey, R., Mann, G., Kefford, R., Rizos, H. (2008), p16INK4a expression and absence of activated B-RAF are independent predictors of chemosensitivity in melanoma tumors. Neoplasia. 10(11), 1231-1239. [Abstract]
  • Brown, K., Macgregor, S., Montgomery, G., Craig, D., Zhao, Z., Iyadurai, K., K Henders, A., Homer, N., Campbell, M., Stark, M., Thomas, S., Schmid, H., Holland, E., Gillanders, E., Duffy, D., Maskiell, J., Jetann, J., Ferguson, M., Stephan, D., Cust, A., Whiteman, D., Green, A., Olsson, H., Puig, S., Ghiorzo, P., Hansson, J., Demenais, F., Goldstein, A., Gruis, N., Elder, D., Bishop, J., Kefford, R., Giles, G., Armstrong, B., Aitken, J., Hopper, J., Martin, N., Trent, J., Mann, G., Hayward, N. (2008), Common sequence variants on 20q11.22 confer melanoma susceptibility. Nature genetics. 40(7), 838-40. [Abstract]
  • Wakefield, C., Meiser, B., Gaff, C., Barratt, A., Patel, M., Suthers, G., Lobb, E., Ramsay, J., Mann, G. (2008), Issues Faced by Unaffected Men With a Family History of Prostate Cancer: A Multidisciplinary Overview. The Journal of urology. 180(1), 38-46; discussion 46. [Abstract]
  • Harland, M., Goldstein, A., Kukalizch, K., Taylor, C., Hogg, D., Puig, S., Badenas, C., Gruis, N., ter Huurne, J., Bergman, W., Hayward, N., Stark, M., Tsao, H., Tucker, M., Landi, M., Scarra, G., Ghiorzo, P., Kanetsky, P., Elder, D., Mann, G., Holland, E., Bishop, D., Bishop, J. (2008), A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL). European journal of cancer. 44(9), 1269-1274. [Abstract]
  • Kasparian, N., Butow, P., Meiser, B., Mann, G. (2008), High- and average-risk individuals' beliefs about, and perceptions of, malignant melanoma: an Australian perspective. Psycho-oncology. 17(3), 270-9. [Abstract]
  • Kasparian, N., Meiser, B., Butow, P., Simpson, J., Mann, G. (2008), Predictors of psychological distress among individuals with a strong family history of malignant melanoma. Clinical genetics. 73(2), 121-131. [Abstract]
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