Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer by Singhal, Deepak, Hahn, Christopher N., Feurstein, Simone, Wee, Li Yan A., Moma, Luke, Kutyna, Monika M., Chhetri, Rakchha, Eshraghi, Leila, Schreiber, Andreas W., Feng, Jinghua, Wang, Paul P-S., Babic, Milena, Parker, Wendy T., Gao, Song, Moore, Sarah, Das, Soma, Thomas, David, Pattnaik, Swetansu, Brown, Anna L., D’Andrea, Richard J., Poplawski, Nicola K., Thomas, Daniel, Scott, Hamish S., Godley, Lucy A., Hiwase, Devendra K.

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Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition by Zerella, Jiarna R., Homan, Claire C., Arts, Peer, Lin, Xuzhu, Spinelli, Sam J., Venugopal, Parvathy, Babic, Milena, Brautigan, Peter J., Truong, Lynda, Arriola-Martinez, Luis, Moore, Sarah, Hollins, Rachel, Parker, Wendy T., Nguyen, Hung, Kassahn, Karin S., Branford, Susan, Feurstein, Simone, Larcher, Lise, Sicre de Fontbrune, Flore, Demirdas, Serwet, de Munnik, Sonja, Antoine-Poirel, Hélène, Brichard, Benedicte, Mansour, Sahar, Gordon, Kristiana, Baliakas, Panagiotis, Blombery, Piers, Fox, Lucy C., Donadieu, Jean, Rio-Machin, Ana, Steinberg-Shemer, Orna, Morgan, Neil V., Ngeow, Joanne Y. Y., Skokowa, Julia, Pinese, Mark, Cowley, Mark J., Wlodarski, Marcin W., Koppayi, Ashwin, Dobbins, Sara, Mutsaers, Pim G. N. J., Nichols, Kim E., Oak, Ninad, DeMille, Desiree, Mao, Rong, Crawford, Ali, McCarrier, Julie, Basel, Donald, Flores-Daboub, Josue, Drazer, Michael W., Phillips, Kerry, Poplawski, Nicola K., Birdsey, Graeme M., Pirri, Daniela, Ostergaard, Pia, Simons, Annet, Godley, Lucy A., Ross, David M., Hiwase, Devendra K., Soulier, Jean, Brown, Anna L., Carmichael, Catherine L., Scott, Hamish S., Hahn, Christopher N.

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Integrated Guidance for Enhancing the Care of Familial Hypercholesterolaemia in Australia by Watts, Gerald F., Sullivan, David R., Hare, David L., Kostner, Karam M., Horton, Ari E., Bell, Damon A., Brett, Tom, Trent, Ronald J., Poplawski, Nicola K., Martin, Andrew C., Srinivasan, Shubha, Justo, Robert N., Chow, Clara K., Pang, Jing, Ademi, Zanfina, Ardill, Justin J., Barnett, Wendy, Bates, Timothy R., Beilin, Lawrence J., Bishop, Warrick, Black, J. Andrew, Brett, Peter, Brown, Alex, Burnett, John R., Bursill, Christina A., Colley, Alison, Clifton, Peter M., Ekinci, Elif I., Elias, Luke, Figtree, Gemma A., Forge, Brett H., Garton-Smith, Jacquie, Graham, Dorothy F., Hamilton-Craig, Ian, Hamilton-Craig, Christian R., Heal, Clare, Hespe, Charlotte M., Hooper, Amanda J., Howes, Laurence G., Ingles, Jodie, Irvin, John, Janus, Edward D., Kangaharan, Nadarajah, Keech, Anthony C., Kirke, Andrew B., Kritharides, Leonard, Kyle, Campbell V., Lacaze, Paul, Lambert, Kirsten, Li, Stephen C.H., Malan, Wynand, Maticevic, Stjepana, McQuillan, Brendan M., Mirzaee, Sam, Mori, Trevor A., Morton, Allison C., Colquhoun, David M., Moullin, Joanna C., Nestel, Paul J., Nowak, Kristen J., O'Brien, Richard C., Pachter, Nicholas, Page, Michael M., Pedrotti, Annette, Psaltis, Peter J., Radford, Jan, Reid, Nicola J., Robertson, Elizabeth N., Ryan, Jacqueline D.M., Sarkies, Mitchell N., Schultz, Carl J., Scott, Russell S., Semsarian, Christopher, Simons, Leon A., Spinks, Catherine, Tonkin, Andrew M., van Bockxmeer, Frank, Waddell-Smith, Kathryn E., Ward, Natalie C., White, Harvey D., Wilson, Andrew M., Winship, Ingrid, Woodward, Ann Marie, Nicholls, Stephen J.

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Unrecognised actionability for breast cancer risk variants identified in a national-level review of Australian familial cancer centres by Fortuno, Cristina, Cops, Elisa J., Davidson, Aimee L., Hadler, Johanna, Innella, Giovanni, McKenzie, Maddison E., Parsons, Michael, Campbell, Ainsley M., Dubowsky, Andrew, Fargas, Verna, Field, Michael J., Mar Fan, Helen G., Nichols, Cassandra B., Poplawski, Nicola K., Warwick, Linda, Williams, Rachel, Beshay, Victoria, Edwards, Caitlin, Johns, Andrea, McPhillips, Mary, Kumar, Vanessa Siva, Scott, Rodney, Williams, Mark, Scott, Hamish, James, Paul A., Spurdle, Amanda B.

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Integrated guidance to enhance the care of children and adolescents with familial hypercholesterolaemia: Practical advice for the community clinician by Horton, Ari E, Martin, Andrew C, Srinivasan, Shubha, Justo, Robert N, Poplawski, Nicola K, Sullivan, David, Brett, Tom, Chow, Clara K, Nicholls, Stephen J, Pang, Jing, Watts, Gerald F

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Survey of germline variants in cancer‐associated genes in young adults with colorectal cancer by Mikaeel, Reger R., Young, Joanne P., Li, Yun, Smith, Eric, Horsnell, Mehgan, Uylaki, Wendy, Tapia Rico, Gonzalo, Poplawski, Nicola K., Hardingham, Jennifer E., Tomita, Yoko, Townsend, Amanda R., Feng, Jinghua, Zibat, Arne, Kaulfuß, Silke, Müller, Christian, Yigit, Gökhan, Wollnik, Bernd, Price, Timothy J.

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A synonymous GATA2 variant underlying familial myeloid malignancy with striking intrafamilial phenotypic variability by Fox, Lucy C., Tan, Michelle, Brown, Anna L., Arts, Peer, Thompson, Ella, Ryland, Georgina L., Lickiss, Jennifer, Scott, Hamish S., Poplawski, Nicola K., Phillips, Kerry, Came, Neil A., James, Paul, Ting, Stephen B., Ritchie, David S., Szer, Jeff, Hahn, Christopher N., Schwarer, Anthony, Blombery, Piers

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Identification of monogenic diabetes in an Australian cohort using the Exeter maturity-onset diabetes of the young (MODY) probability calculator and next-generation sequencing gene... by De Sousa, Sunita M. C., Wu, Kathy H. C., Colclough, Kevin, Rawlings, Lesley, Dubowsky, Andrew, Monnik, Melissa, Poplawski, Nicola, Scott, Hamish S., Horowitz, Michael, Torpy, David J.

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RNF43 pathogenic Germline variant in a family with colorectal cancer by Mikaeel, Reger R., Young, Joanne P., Li, Yun, Poplawski, Nicola K., Smith, Eric, Horsnell, Mehgan, Uylaki, Wendy, Tomita, Yoko, Townsend, Amanda R., Feng, Jinghua, Zibat, Arne, Kaulfuß, Silke, Müller, Christian, Yigit, Gökhan, Wollnik, Bernd, Scott, Hamish, Rawlings, Lesley, Henry, Denae, Vakulin, Cassandra, Dubowsky, Andrew, Price, Timothy J.

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Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss by Venugopal, Parvathy, Gagliardi, Lucia, Forsyth, Cecily, Feng, Jinghua, Phillips, Kerry, Babic, Milena, Poplawski, Nicola K, Rienhoff, Jr, Hugh Young, Schreiber, Andreas W, Hahn, Christopher N, Brown, Anna L, Scott, Hamish S

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A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia by Cheah, Jesse J C, Brown, Anna L, Schreiber, Andreas W, Feng, Jinghua, Babic, Milena, Moore, Sarah, Young, Chun-Chun, Fine, Miriam, Phillips, Kerry, Guandalini, Michael, Wilson, Peter, Poplawski, Nicola, Hahn, Christopher N, Scott, Hamish S

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Essentials of a new clinical practice guidance on familial hypercholesterolaemia for physicians by Watts, Gerald F., Sullivan, David R., Hare, David L., Kostner, Karam M., Horton, Ari E., Bell, Damon A., Brett, Tom, Trent, Ronald J., Poplawski, Nicola K., Martin, Andrew C., Srinivasan, Shubha, Justo, Robert N., Chow, Clara K., Pang, Jing

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BAP1 Tumour Predisposition Syndrome Due to Whole BAP1 Gene Deletion by Pandithan, Dinusha, Klebe, Sonja, McKavanagh, Grace, Rawlings, Lesley, Yu, Sui, Nicholl, Jillian, Poplawski, Nicola

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Autosomal dominant hypocalcaemia due to a novel CASR mutation: clinical and genetic implications by Gagliardi, Lucia, Burt, Morton G., Feng, Jinghua, Poplawski, Nicola K., Scott, Hamish S.

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An international survey of surveillance schemes for unaffected BRCA1 and BRCA2 mutation carriers by Madorsky-Feldman, Dana, Sklair-Levy, Miri, Perri, Tamar, Laitman, Yael, Paluch-Shimon, Shani, Schmutzler, Rita, Rhiem, Kerstin, Lester, Jenny, Karlan, Beth Y., Singer, Christian F., Van Maerken, Tom, Claes, Kathleen, Brunet, Joan, Izquierdo, Angel, Teulé, Alex, Lee, Jong Won, Kim, Sung-Won, Arun, Banu, Jakubowska, Anna, Lubinski, Jan, Tucker, Katherine, Poplawski, Nicola K., Varesco, Liliana, Bonelli, Luigina Ada, Buys, Saundra S., Mitchell, Gillian, Tischkowitz, Marc, Gerdes, Anne-Marie, Seynaeve, Caroline, Robson, Mark, Kwong, Ava, Tung, Nadine, Tessa, Nalven, Domchek, Susan M., Godwin, Andrew K., Rantala, Johanna, Arver, Brita, Friedman, Eitan

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Young‐onset colorectal cancer is associated with a personal history of type 2 diabetes by Mikaeel, Reger R., Symonds, Erin L., Kimber, James, Smith, Eric, Horsnell, Mehgan, Uylaki, Wendy, Tapia Rico, Gonzalo, Hewett, Peter J., Yong, Jonathan, Tonkin, Darren, Jesudason, David, Poplawski, Nicola K., Ruszkiewicz, Andrew R., Drew, Paul A., Hardingham, Jenny E., Wong, Stephanie, Frank, Oliver, Tomita, Yoko, Patel, Dainik, Vatandoust, Sina, Townsend, Amanda R., Roder, David, Young, Graeme P., Parry, Susan, Tomlinson, Ian P., Wittert, Gary, Wattchow, David, Worthley, Daniel L., Brooks, William J., Price, Timothy J., Young, Joanne P.

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Familial GATA6 mutation causing variably expressed diabetes mellitus and cardiac and renal abnormalities by Du, Yang Timothy, Moore, Lynette, Poplawski, Nicola K, De Sousa, Sunita M C

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Corrigendum to Synopsis of an integrated guidance for enhancing the care of familial hypercholesterolaemia: An Australian perspective [American Journal of Preventive Cardiology 6 (... by Watts, Gerald F., Sullivan, David R., Hare, David L., Kostner, Karam M., Horton, Ari E., Bell, Damon A., Brett, Tom, Trent, Ronald J., Poplawski, Nicola K., Martin, Andrew C., Srinivasan, Shubha, Justo, Robert N., Chow, Clara K., Pang, Jing

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Implementation and Evaluation of a National Multidisciplinary Kidney Genetics Clinic Network Over 10 Years by Jayasinghe, Kushani, Biros, Erik, Harris, Trudie, Wood, Alasdair, O’Shea, Rosie, Hill, Lauren, Fowles, Lindsay, Wardrop, Louise, Shalhoub, Carolyn, Hahn, Deirdre, Rangan, Gopala, Kevin, Lucy, Tchan, Michel, Snelling, Paul, Sandow, Rhiannon, Sundaram, Madhivan, Chaturvedi, Swasti, Trnka, Peter, Faull, Randall, Poplawski, Nicola K., Huntley, Vanessa, Garza, Denisse, Wallis, Mathew, Jose, Matthew, Leaver, Anna, Trainer, Alison H., Wilkins, Ella J., White, Sue, Elbaum, Yoni, Prawer, Yael, Krzesinski, Emma, Valente, Giulia, Winship, Ingrid, Ryan, Jessica, Whitlam, John, Nicholls, Kathy, West, Kirsty, Donaldson, Liz, Johnstone, Lilian, Lewit-Mendes, Miranda, Kerr, Peter G., Bodek, Simon, Chakera, Aron, MacShane, Mandi, Mincham, Christine, Stackpoole, Elaine, Willis, Francis, Soraru, Jacqueline, Pachter, Nick, Bennetts, Bruce, Forbes, Thomas A., Mallawaarachchi, Amali, Quinlan, Catherine, Patel, Chirag, McCarthy, Hugh, Goranitis, Illias, Best, Stephanie, Alexander, Stephen, Stark, Zornitza, Mallett, Andrew J.

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Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort by Rosty, Christophe, Clendenning, Mark, Walsh, Michael D, Eriksen, Stine V, Southey, Melissa C, Winship, Ingrid M, Macrae, Finlay A, Boussioutas, Alex, Poplawski, Nicola K, Parry, Susan, Arnold, Julie, Young, Joanne P, Casey, Graham, Haile, Robert W, Gallinger, Steven, Le Marchand, Loïc, Newcomb, Polly A, Potter, John D, DeRycke, Melissa, Lindor, Noralane M, Thibodeau, Stephen N, Baron, John A, Win, Aung Ko, Hopper, John L, Jenkins, Mark A, Buchanan, Daniel D

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