Microscopical lesions in coccidiostat and mycotoxin intoxication in selected organs in turkeys: A case report by Szarek, J., Babińska, I., Dzikowski, A., Wąsowicz, K., Szynaka, B., Popławski, K., Kimel, A., Gulda, D.

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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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Trends in European Veterinary Pathology in Recent Years in Light of the Congresses of the European Society of Veterinary Pathology and European College of Veterinary Pathologists by Szarek, J., Dzikowski, A., Babińska, I., Felsmann, M.Z., Popławski, K., Gulda, D., Wąsowicz, K., Szynaka, B.

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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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Opinions of Veterinary Experts on Animals Issued in 1995–2015 by Babińska, I., Szarek, J., Kusiak, D., Lis, A., Łyko, A., Szweda, M., Maciejewska, M., Popławski, K., Felsmann, M.Z.

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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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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 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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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 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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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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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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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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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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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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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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Unraveling facets of MECOM-associated syndrome: somatic genetic rescue, clonal hematopoiesis, and phenotype expansion by Venugopal, Parvathy, Arts, Peer, Fox, Lucy C., Simons, Annet, Hiwase, Devendra K., Bardy, Peter G., Swift, Annette, Ross, David M., van Vulpen, Lize F. D., Buijs, Arjan, Bolton, Kelly L., Getta, Bartlomiej, Furlong, Eliska, Carter, Tina, Krapels, Ingrid, Hoeks, Marlijn, Al Kindy, Adila, Al Kindy, Farah, de Munnik, Sonja, Evans, Pamela, Frank, Mahalia S. B., Bournazos, Adam M., Cooper, Sandra T., Ha, Thuong Thi, Jackson, Matilda R., Arriola-Martinez, Luis, Phillips, Kerry, Brennan, Yvonne, Bakshi, Madhura, Ambler, Karen, Gao, Song, Kassahn, Karin S., Kenyon, Rosalie, Hung, Kevin, Babic, Milena, McGovern, Alan, Rawlings, Lesley, Vakulin, Cassandra, Dejong, Lucas, Fathi, Rema, McRae, Simon, Myles, Nicholas, Ladon, Dariusz, Jongmans, Marjolijn, Kuiper, Roland P., Poplawski, Nicola K., Barbaro, Pasquale, Blombery, Piers, Brown, Anna L., Hahn, Christopher N., Scott, Hamish S.

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