Ms Jenny Berkman
PhD student & Casual Senior Genetic Counsellor
Frazer Institute
Affiliate of Dermatology Research Centre
Dermatology Research Centre
Journal Articles
McGahan, Ella, Berkman, Jennifer, Milne, David, Terrill, Bronwyn, Gear, Russell, Gardiner, Susan, Eckstein, Lisa, Nicol, Dianne, Taylor, Natalie, Winship, Ingrid, McWhirter, Rebekah, Nisselle, Amy, Lodge, Jason and McInerney-Leo, Aideen (2025). Empowering human research ethics committees to review genomics applications: evaluating the utility of a custom online education resource. European Journal of Human Genetics 5, 1-11. doi: 10.1038/s41431-025-01846-5
Debortoli, Emily, McGahan, Ella, Yanes, Tatiane, Berkman, Jennifer, Fuentes-Bolanos, Noemi, Milch, Vivienne, Steinberg, Julia and Mcinerney-Leo, Aideen (2025). Utility of genomic testing in children, adolescents, and young adults with cancer. JNCI: Journal of the National Cancer Institute, 117 (4), 601-610. doi: 10.1093/jnci/djae233
Berkman, Jennifer, DeBortoli, Emily, Steinberg, Julia, Milch, Vivienne, Yanes, Tatiane and McInerney‐Leo, Aideen (2025). Mainstreaming cancer genomic testing: a scoping review of the acceptability, efficacy, and impact. Clinical Genetics, 107 (2), 123-135. doi: 10.1111/cge.14660
McInerney-Leo, A., DeBortoli, E., Primiero, C., Wallingford, C., Berkman, J., Yanes, T., Finnane, A. and Soyer, H.P. (2025). Mainstreaming melanoma genetic testing: Participant outcomes comparable when testing is provided by dermatologists and genetic counsellors. EJC Skin Cancer, 3 100505, 100505. doi: 10.1016/j.ejcskn.2025.100505
Dane, Aimee, Berkman, Jennifer, DeBortoli, Emily, Wallingford, Courtney K., Yanes, Tatiane and McInerney‐Leo, Aideen (2024). Narrative therapy and family therapy in genetic counseling: a scoping review. Journal of Genetic Counseling, 34 (2) e1938. doi: 10.1002/jgc4.1938
Hoskins, Cass, Gaff, Clara, McEwen, Alison, Macciocca, Ivan, Pearn, Amy, Shalhoub, Carolyn, Salvemini, Hayley, Berkman, Jennifer, Riley, Kate E., Williams, Rachel, Milward, Michael and Young, Mary-Anne (2021). Professional regulation for Australasian genetic counselors. Journal of Genetic Counseling, 30 (2), 361-369. doi: 10.1002/jgc4.1344
Lammerts van Bueren, Kelly, Bennetts, Jennifer S., Fowles, Lindsay F., Berkman, Jennifer L., Simpson, Fiona and Wicking, Carol (2007). Murine embryonic expression of the gene for the UV-responsive protein p15(PAF). Gene Expression Patterns, 7 (1-2), 47-50. doi: 10.1016/j.modgep.2006.05.006
Bennetts, Jennifer S., Fowles, Lindsay F., Berkman, Jennifer L., Lammerts van Bueren, Kelly, Richman, Joy M., Simpson, Fiona and Wicking, Carol (2006). Evolutionary conservation and murine embryonic expression of the gene encoding the SERTA domain-containing protein CDCA4 (HEPP). Gene, 374 (1-2), 153-165. doi: 10.1016/j.gene.2006.01.027
Bennetts, Jennifer S., Fowles, Lindsay F., Butterfield, Natalie C., Berkman, Jennifer L., Teasdale, Rohan D., Simpson, Fiona and Wicking, Carol (2006). Identification and analysis of novel genes expressed in the mouse embryonic facial primordia. Frontiers In Bioscience, 11 (SUPPL. 2), 2631-2646. doi: 10.2741/1997
Ruf, R. G., Xu, P. X., Silvius, D., Otto, E. A., Beekmann, F., Muerb, U. T., Kumar, S., Neuhaus, T. J., Kemper, M. J., Raymond, R. M., Brophy, P. D., Berkman, J., Gattas, M., Hyland, V., Ruf, E. M., Schwartz, C., Chang, E. H., Smith, R. J. H., Stratakis, C. A., Weil, D., Petit, C. and Hildebrandt, F. (2004). SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes. Proceedings of the National Academy of Sciences of the United States of America, 101 (21), 8090-8095. doi: 10.1073/pnas.0308475101
Ruf, R. G., Berkman, J., Wolf, M. T. F., Nurnberg, P., Gattas, M., Ruf, E. M., Hyland, V., Kromberg, J., Glass, I., Macmillan, J., Otto, E., Nurnberg, G., Lucke, B., Hennies, H. C. and Hildebrandt, F. (2003). A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3. Journal of Medical Genetics, 40 (7), 515-519. doi: 10.1136/jmg.40.7.515
Fowles, L. F., Bennetts, J. S., Berkman, J. L., Williams, E., Koopman, P., Teasdale, R. D. and Wicking, C. (2003). Genomic screen for genes involved in mammalian craniofacial development. Genesis, 35 (2), 73-87. doi: 10.1002/gene.10165
Kunchaparty, S., Palcso, M., Berkman, J., Velázquez, H., Desir, G. V., Bernstein, P., Reilly, R. F. and Ellison, D. H. (1999). Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome. American Journal of Physiology-Renal Physiology, 277 (4), F643-F649. doi: 10.1152/ajprenal.1999.277.4.f643
Bowles, Josephine, Cooper, Leanne, Berkman, Jennifer and Koopman, Peter (1999). Sry requires a CAG repeat domain for male sex determination in Mus musculus. Nature Genetics, 22 (4), 405-408. doi: 10.1038/11981
Wicking, C., Breen, M., Negus, K., Berkman, J., Evdokiou, A., Cowled, P., Chenevix-Trench, G. and Wainwright, B. (1995). The human growth-arrest-specific gene gas 1 maps outside the candidate region of the gene for nevoid basal-cell carcinoma syndrome. Cytogenetics and Cell Genetics, 68 (1-2), 119-121. doi: 10.1159/000133904
Wicking C., Berkman J., Wainwright B. and Chenevix-Trench G. (1994). Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome. Genomics, 22 (3), 505-511. doi: 10.1006/geno.1994.1423
Berkman, Jenny, Armour, John A.L., Chenevix-trench, Georgia, Wicking, Carol and Wainwright, Brandon (1994). Simple repeat polymorphism at the D9S151 locus. Human Molecular Genetics, 3 (1), 211-211. doi: 10.1093/hmg/3.1.211
Chenevix-Trench, Georgia, Wicking, Carol, Berkman, Jenny, Sharpe, Helen, Hockey, A., Haan, Eric, Oley, Christine, Ravine, David, Turner, Anne, Goldgar, David, Searle, Jeffrey and Wainwright, Brandon (1993). Further localization of the gene for nevoid basal-cell carcinoma syndrome (NBCCS) in15 Australasian families - linkage and loss of heterozygosity. American Journal of Human Genetics, 53 (3), 760-767.
Conference Papers
Simpson, F., van Bueren, Lammerts K., Fowles, L., Berkman, J., Butterfield, N., Bowles, J., Adolphe, C., Simms, L., Young, J., Walsh, M. and Wicking, C. (2005). The PCNA-associated factor KIAA0101/p15(PAF) binds the potential tumour suppressor product p33ING1. Unknown, Unknown, Unknown. Amsterdam, Netherlands: Elsevier Science.
Bennetts, J., Fowles, L., Butterfield, N., van Bueren, Lammerts K., Berkman, J., Simpson, F. and Wicking, C. (2005). Identification and characterisation of novel genes with developmental significance. Unknown, Unknown, Unknown. Shannon, Co. Clare, Ireland: Elsevier Ireland.
Sabath, E., Meade, P., Berkman, J., de los Heros, P., Moreno, E., Bobadilla, N. A., Vázquez, N., Ellison, D. H. and Gamba, G. (2004). Pathophysiology of functional mutations of the thiazide-sensitive Na-Cl cotransporter in Gitelman disease. 35th Annual Meeting of the American Society of Nephrology, Philadelphia, PA, United States, 30 October-6 November 2002. Rockville, MD, United States: American Physiological Society. doi: 10.1152/ajprenal.00044.2004
Bowles, J., Cooper, L., Berkman, J. and Koopman, P. (1999). Mouse SRY requires a CAG repeat domain for male sex determination. -, -, 1999. Chicago, IL United States: University of Chicago Press.