Journal Articles
Goldstein, Alisa M., Qin, Richard, Chu, Emily Y., Elder, David E., Massi, Daniela, Adams, David J., Harms, Paul W., Robles-Espinoza, Carla Daniela, Newton-Bishop, Julia A., Bishop, D. Timothy, Harland, Mark, Holland, Elizabeth A., Cust, Anne E., Schmid, Helen, Mann, Graham J., Puig, Susana, Potrony, Miriam, Alos, Llucia, Nagore, Eduardo, Millán-Esteban, David, Hayward, Nicholas K., Broit, Natasa, Palmer, Jane M., Nathan, Vaishnavi, Berry, Elizabeth G., Astiazaran-Symonds, Esteban, Yang, Xiaohong R., Tucker, Margaret A., Landi, Maria Teresa ... Sargen, Michael R. (2023). Association of germline variants in telomere maintenance genes (POT1, TERF2IP, ACD, and TERT) with spitzoid morphology in familial melanoma: a multi-center case series. JAAD International, 11, 43-51. doi: 10.1016/j.jdin.2023.01.013
Parsons, Michael, Anderson, Michael, Berkofsky-Fessler, Windy, Caputo, Sandrine, Chan, Raymond, Cline, Melissa, Couch, Fergus, de la Hoya, Miguel, Feng, Bing-Jian, Goldgar, David, Gomez-Garcia, Encarna, Hiraki, Susan, Holdren, Megan, Houdayer, Claude, James, Paul, Karam, Rachid, San Leong, Huei, Martins, Alexandra, Mensenkamp, Arjen, Monteiro, Alvaro, Nathan, Vaishnavi, O'Connor, Robert, Pesaran, Tina, Radice, Paolo, Richardson, Marcy, Schmidt, Gunnar, Pedersen, Inge Sokilde, Southey, Melissa, Tavtigian, Sean ... Spurdle, Amanda (2023). P076: The ClinGen ENIGMA BRCA1/2 expert panel: A dynamic framework for evidence-based recommendations to improve classification criteria for variants in BRCA1/2*. Genetics in Medicine Open, 1 (1) 100095, 100095. doi: 10.1016/j.gimo.2023.100095
Dalmasso, B., Pastorino, L., Nathan, V., Shah, N.N., Palmer, J.M., Howlie, M., Johansson, P.A., Freedman, N.D., Carter, B.D., Beane-Freeman, L., Hicks, B., Molven, A., Helgadottir, H., Sankar, A., Tsao, H., Stratigos, A.J., Helsing, P., Van Doorn, R., Gruis, N.A., Visser, M., Wadt, K.A.W., Mann, G., Holland, E.A., Nagore, E., Potrony, M., Puig, S., Menin, C., Peris, K., Fargnoli, M.C. ... Ghiorzo, P. (2021). Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia. Genetics in Medicine, 23 (11), 2087-2095. doi: 10.1038/s41436-021-01240-8
Nathan, Vaishnavi, Johansson, Peter A., Palmer, Jane M., Hamilton, Hayley R., Howlie, Madeleine, Brooks, Kelly M., Hayward, Nicholas K. and Pritchard, Antonia L. (2021). A rare missense variant in protection of telomeres 1 (POT1) predisposes to a range of haematological malignancies. British Journal of Haematology, 192 (2), e57-e60. doi: 10.1111/bjh.17218
Nathan, Vaishnavi, Palmer, Jane M, Johansson, Peter A, Hamilton, Hayley R, Warrier, Sunil K, Glasson, William, McGrath, Lindsay A, Kahl, Vivian F S, Vasireddy, Raja S, Pickett, Hilda A, Brooks, Kelly M, Pritchard, Antonia L and Hayward, Nicholas K (2020). Loss-of-function variants in POT1 predispose to uveal melanoma. Journal of Medical Genetics, 58 (4), jmedgenet-2020. doi: 10.1136/jmedgenet-2020-107098
Van Rooij, Nicholas, Adams, Agnieszka, De’Ambrosis, Brian, Nathan, Vaishnavi, Hayward, Nicholas and Whiteman, David (2020). Cluster of pregnancy‐associated melanoma: A case report and brief update. The Journal of Dermatology, 47 (9) 1346-8138.15455, 1054-1057. doi: 10.1111/1346-8138.15455
Johansson, Peter A., Brooks, Kelly, Newell, Felicity, Palmer, Jane M., Wilmott, James S., Pritchard, Antonia L., Broit, Natasa, Wood, Scott, Carlino, Matteo S., Leonard, Conrad, Koufariotis, Lambros T., Nathan, Vaishnavi, Beasley, Aaron B., Howlie, Madeleine, Dawson, Rebecca, Rizos, Helen, Schmidt, Chris W., Long, Georgina V., Hamilton, Hayley, Kiilgaard, Jens F., Isaacs, Timothy, Gray, Elin S., Rolfe, Olivia J., Park, John J., Stark, Andrew, Mann, Graham J., Scolyer, Richard A., Pearson, John V., van Baren, Nicolas ... Hayward, Nicholas K. (2020). Whole genome landscapes of uveal melanoma show an ultraviolet radiation signature in iris tumours. Nature Communications, 11 (1) 2408, 2408. doi: 10.1038/s41467-020-16276-8
Johansson, Peter A., Nathan, Vaishnavi, Bourke, Lauren M., Palmer, Jane M., Zhang, Tongwu, Symmons, Judith, Howlie, Madeleine, Patch, Ann-Marie, Read, Jazlyn, Holland, Elizabeth A., Schmid, Helen, Warrier, Sunil, Glasson, William, Höiom, Veronica, Wadt, Karin, Jönsson, Göran, Olsson, Håkan, Ingvar, Christian, Mann, Graham, Brown, Kevin M., Hayward, Nicholas K. and Pritchard, Antonia L. (2019). Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma. Melanoma Research, 29 (5), 483-490. doi: 10.1097/cmr.0000000000000613
Nathan, Vaishnavi, Johansson, Peter A., Palmer, Jane M., Howlie, Madeleine, Hamilton, Hayley R., Wadt, Karin, Jönsson, Göran, Brooks, Kelly M., Pritchard, Antonia L. and Hayward, Nicholas K. (2019). Germline variants in oculocutaneous albinism genes and predisposition to familial cutaneous melanoma. Pigment Cell & Melanoma Research, 32 (6) pcmr.12804, 854-863. doi: 10.1111/pcmr.12804
Bennett, Dorothy C., Hayward, N. K., Nathan, V., Orlic-Milacic, M. and Rizos, H. (2019). Diseases of cellular senescence. Reactome - a curated knowledgebase of biological pathways, 69. doi: 10.3180/r-hsa-9630747.1
Pritchard, Antonia L., Johansson, Peter A., Nathan, Vaishnavi, Howlie, Madeleine, Symmons, Judith, Palmer, Jane M. and Hayward, Nicholas K. (2018). Germline mutations in candidate predisposition genes in individuals with cutaneous melanoma and at least two independent additional primary cancers. Plos One, 13 (4) e0194098, e0194098. doi: 10.1371/journal.pone.0194098
Larsen, Jill E., Nathan, Vaishnavi, Osborne, Jihan K., Farrow, Rebecca K., Deb, Dhruba, Sullivan, James P., Dospoy, Patrick D., Augustyn, Alexander, Hight, Suzie K., Sato, Mitsuo, Girard, Luc, Behrens, Carmen, Wistuba, Ignacio I., Gazdar, Adi F., Hayward, Nicholas K. and Minna, John D. (2016). ZEB1 drives epithelial-to-mesenchymal transition in lung cancer. Journal of Clinical Investigation, 126 (9), 3219-3235. doi: 10.1172/JCI76725
Thesis
Nathan, Vaishnavi (2021). Functional assessment of candidate melanoma susceptibility genes. PhD Thesis, Faculty of Medicine, The University of Queensland. doi: 10.14264/7187c16