Global functions of O‐glycosylation: promises and challenges in O‐glycobiology von Wandall, Hans H., Nielsen, Mathias A. I., King‐Smith, Sarah, Haan, Noortje, Bagdonaite, Ieva

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GATA2 deficiency syndrome: A decade of discovery von Homan, Claire C., Venugopal, Parvathy, Arts, Peer, Shahrin, Nur H., Feurstein, Simone, Rawlings, Lesley, Lawrence, David M., Andrews, James, King‐Smith, Sarah L., Harvey, Natasha L., Brown, Anna L., Scott, Hamish S., Hahn, Christopher N.

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Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1‐related syndrome von Arts, Peer, Garland, Jessica, Byrne, Alicia B., Hardy, Tristan S.E., Babic, Milena, Feng, Jinghua, Wang, Paul, Ha, Thuong, King‐Smith, Sarah L., Schreiber, Andreas W., Crawford, April, Manton, Nick, Moore, Lynette, Barnett, Christopher P., Scott, Hamish S.

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The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy von Homan, Claire C., King-Smith, Sarah L., Lawrence, David M., Arts, Peer, Feng, Jinghua, Andrews, James, Armstrong, Mark, Ha, Thuong, Dobbins, Julia, Drazer, Michael W., Yu, Kai, Bodor, Csaba, Cantor, Alan, Cazzola, Mario, Degelman, Erin, DiNardo, Courtney D., Duployez, Nicolas, Favier, Remi, Frohling, Stefan, Fitzgibbon, Jude, Klco, Jeffery M., Kramer, Alwin, Kurokawa, Mineo, Lee, Joanne, Malcovati, Luca, Morgan, Neil V., Natsoulis, Georges, Owen, Carolyn, Patel, Keyur P., Preudhomme, Claude, Raslova, Hana, Rienhoff, Hugh, Ripperger, Tim, Schulte, Rachael, Tawana, Kiran, Velloso, Elvira, Yan, Benedict, Liu, Paul, Godley, Lucy A., Schreiber, Andreas W., Hahn, Christopher N., Scott, Hamish S., Brown, Anna L.

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Glycoengineered keratinocyte library reveals essential functions of specific glycans for all stages of HSV-1 infection von Bagdonaite, Ieva, Marinova, Irina N., Rudjord-Levann, Asha M., Pallesen, Emil M. H., King-Smith, Sarah L., Karlsson, Richard, Rømer, Troels B., Chen, Yen-Hsi, Miller, Rebecca L., Olofsson, Sigvard, Nordén, Rickard, Bergström, Tomas, Dabelsteen, Sally, Wandall, Hans H.

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Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia von De Angelis, Carla, Byrne, Alicia B., Morrow, Rebecca, Feng, Jinghua, Ha, Thuong, Wang, Paul, Schreiber, Andreas W., Babic, Milena, Taranath, Ajay, Manton, Nick, King-Smith, Sarah L., Schwarz, Quenten, Arts, Peer, Scott, Hamish S., Barnett, Christopher

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RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML von Brown, Anna L., Arts, Peer, Carmichael, Catherine L., Babic, Milena, Dobbins, Julia, Chong, Chan-Eng, Schreiber, Andreas W., Feng, Jinghua, Phillips, Kerry, Wang, Paul P.S., Ha, Thuong, Homan, Claire C., King-Smith, Sarah L., Rawlings, Lesley, Vakulin, Cassandra, Dubowsky, Andrew, Burdett, Jessica, Moore, Sarah, McKavanagh, Grace, Henry, Denae, Wells, Amanda, Mercorella, Belinda, Nicola, Mario, Suttle, Jeffrey, Wilkins, Ella, Li, Xiao-Chun, Michaud, Joelle, Brautigan, Peter, Cannon, Ping, Altree, Meryl, Jaensch, Louise, Fine, Miriam, Butcher, Carolyn, D'Andrea, Richard J., Lewis, Ian D., Hiwase, Devendra K., Papaemmanuil, Elli, Horwitz, Marshall S., Natsoulis, Georges, Rienhoff, Hugh Y., Patton, Nigel, Mapp, Sally, Susman, Rachel, Morgan, Susan, Cooney, Julian, Currie, Mark, Popat, Uday, Bochtler, Tilmann, Izraeli, Shai, Bradstock, Kenneth, Godley, Lucy A., Krämer, Alwin, Fröhling, Stefan, Wei, Andrew H., Forsyth, Cecily, Mar Fan, Helen, Poplawski, Nicola K., Hahn, Christopher N., Scott, Hamish S.

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Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation von Tudini, Emma, Andrews, James, Lawrence, David M., King-Smith, Sarah L., Baker, Naomi, Baxter, Leanne, Beilby, John, Bennetts, Bruce, Beshay, Victoria, Black, Michael, Boughtwood, Tiffany F., Brion, Kristian, Cheong, Pak Leng, Christie, Michael, Christodoulou, John, Cox, Kathy, Davis, Mark R., Dejong, Lucas, Dinger, Marcel E., Doig, Kenneth D., Douglas, Evelyn, Dubowsky, Andrew, Ellul, Melissa, Fellowes, Andrew, Fisk, Katrina, Fortuno, Cristina, Friend, Kathryn, Gallagher, Renee L., Gao, Song, Hackett, Emma, Hadler, Johanna, Hipwell, Michael, Ho, Gladys, Hollway, Georgina, Hooper, Amanda J., Kassahn, Karin S., Krishnaraj, Rahul, Lau, Chiyan, Le, Huong, San Leong, Huei, Lundie, Ben, Lunke, Sebastian, Marty, Anthony, McPhillips, Mary, Nguyen, Lan T., Nones, Katia, Palmer, Kristen, Pearson, John V., Quinn, Michael C.J., Rawlings, Lesley H., Sadedin, Simon, Sanchez, Louisa, Schreiber, Andreas W., Sigalas, Emanouil, Simsek, Aygul, Soubrier, Julien, Stark, Zornitza, Thompson, Bryony A., U, James, Vakulin, Cassandra G., Wells, Amanda V., Wise, Cheryl A., Woods, Rick, Ziolkowski, Andrew, Brion, Marie-Jo, Scott, Hamish S., Thorne, Natalie P., Spurdle, Amanda B., Akesson, Lauren, Allcock, Richard, Ashton, Katie, Bell, Damon A., Brown, Anna, Buckley, Michael, Burrows, Linda, Byrne, Alicia, Chan, Eva, Cliffe, Corrina, Clifton-Bligh, Roderick, Dooley, Susan, Fernandez, Miriam Fanjul, Farnsworth, Elizabeth, Ha, Thuong, Henry, Denae, Holds, Duncan, Holman, Katherine, Jackson, Matilda, Kang, Sinlay, Luxford, Catherine, McManus, Sam, Mehrtens, Rachael, Meldrum, Cliff, Pantaleo, Sarah-Jane, Phelan, Dean, Pontikinas, Electra, Ravine, Anja, Roscioli, Tony, Scott, Rodney, Simons, Keryn, Vanwageningen, Oliver

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Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41 von Homan, Claire C., Drazer, Michael W., Yu, Kai, Lawrence, David M., Feng, Jinghua, Arriola-Martinez, Luis, Pozsgai, Matthew J., McNeely, Kelsey E., Ha, Thuong, Venugopal, Parvathy, Arts, Peer, King-Smith, Sarah L., Cheah, Jesse, Armstrong, Mark, Wang, Paul, Bödör, Csaba, Cantor, Alan B., Cazzola, Mario, Degelman, Erin, DiNardo, Courtney D., Duployez, Nicolas, Favier, Remi, Fröhling, Stefan, Rio-Machin, Ana, Klco, Jeffery M., Krämer, Alwin, Kurokawa, Mineo, Lee, Joanne, Malcovati, Luca, Morgan, Neil V., Natsoulis, Georges, Owen, Carolyn, Patel, Keyur P., Preudhomme, Claude, Raslova, Hana, Rienhoff, Hugh, Ripperger, Tim, Schulte, Rachael, Tawana, Kiran, Velloso, Elvira, Yan, Benedict, Kim, Erika, Sood, Raman, Hsu, Amy P., Holland, Steven M., Phillips, Kerry, Poplawski, Nicola K., Babic, Milena, Wei, Andrew H., Forsyth, Cecily, Mar Fan, Helen, Lewis, Ian D., Cooney, Julian, Susman, Rachel, Fox, Lucy C., Blombery, Piers, Singhal, Deepak, Hiwase, Devendra, Phipson, Belinda, Schreiber, Andreas W., Hahn, Christopher N., Scott, Hamish S., Liu, Paul, Godley, Lucy A., Brown, Anna L.

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Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations von Drazer, Michael W., Homan, Claire C., Yu, Kai, Cavalcante de Andrade Silva, Marcela, McNeely, Kelsey E., Pozsgai, Matthew J., Acevedo-Mendez, Maria G., Segal, Jeremy P., Wang, Peng, Feng, Jinghua, King-Smith, Sarah L., Kim, Erika, Korotev, Sophia, Lawrence, David M., Schreiber, Andreas W., Hahn, Christopher N., Scott, Hamish S., Sood, Raman, Velloso, Elvira D.R.P., Brown, Anna L., Liu, Paul P., Godley, Lucy A.

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Parental experiences of ultrarapid genomic testing for their critically unwell infants and children von Brett, Gemma R., Martyn, Melissa, Lynch, Fiona, de Silva, Michelle G., Ayres, Samantha, Gallacher, Lyndon, Boggs, Kirsten, Baxendale, Anne, Schenscher, Sarah, King-Smith, Sarah, Fowles, Lindsay, Springer, Amanda, Lunke, Sebastian, Vasudevan, Anand, Krzesinski, Emma, Pinner, Jason, Sandaradura, Sarah A., Barnett, Christopher, Patel, Chirag, Wilson, Meredith, Stark, Zornitza

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Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death von Byrne, Alicia B., Arts, Peer, Ha, Thuong T., Kassahn, Karin S., Pais, Lynn S., O’Donnell-Luria, Anne, Babic, Milena, Frank, Mahalia S. B., Feng, Jinghua, Wang, Paul, Lawrence, David M., Eshraghi, Leila, Arriola, Luis, Toubia, John, Nguyen, Hung, McGillivray, George, Pinner, Jason, McKenzie, Fiona, Morrow, Rebecca, Lipsett, Jill, Manton, Nick, Khong, T. Yee, Moore, Lynette, Liebelt, Jan E., Schreiber, Andreas W., King-Smith, Sarah L., Hardy, Tristan S. E., Jackson, Matilda R., Barnett, Christopher P., Scott, Hamish S.

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Cover, Volume 42, Issue 11 von Homan, Claire C., Venugopal, Parvathy, Arts, Peer, Shahrin, Nur H., Feurstein, Simone, Rawlings, Lesley, Lawrence, David M., Andrews, James, King‐Smith, Sarah L., Harvey, Natasha L., Brown, Anna L., Scott, Hamish S., Hahn, Christopher N.

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The Australian Genomics Mitochondrial Flagship: A National Program Delivering Mitochondrial Diagnoses von Rius, Rocio, Compton, Alison G., Baker, Naomi L., Balasubramaniam, Shanti, Best, Stephanie, Bhattacharya, Kaustuv, Boggs, Kirsten, Boughtwood, Tiffany, Braithwaite, Jeffrey, Bratkovic, Drago, Bray, Alessandra, Brion, Marie-Jo, Burke, Jo, Casauria, Sarah, Chong, Belinda, Coman, David, Cowie, Shannon, Cowley, Mark, de Silva, Michelle G., Delatycki, Martin B., Edwards, Samantha, Ellaway, Carolyn, Fahey, Michael C., Finlay, Keri, Fletcher, Janice, Frajman, Leah E., Frazier, Ann E., Gayevskiy, Velimir, Ghaoui, Roula, Goel, Himanshu, Goranitis, Ilias, Haas, Matilda, Hock, Daniella H., Howting, Denise, Jackson, Matilda R., Kava, Maina P., Kemp, Madonna, King-Smith, Sarah, Lake, Nicole J., Lamont, Phillipa J., Lee, Joy, Long, Janet C., MacShane, Mandi, Madelli, Evanthia O., Martin, Ellenore M., Marum, Justine E., Mattiske, Tessa, McGill, Jim, Metke, Alejandro, Murray, Sean, Panetta, Julie, Phillips, Liza K., Quinn, Michael C.J., Ryan, Michael T., Schenscher, Sarah, Simons, Cas, Smith, Nicholas, Stroud, David A., Tchan, Michel C., Tom, Melanie, Wallis, Mathew, Ware, Tyson L., Welch, AnneMarie E., Wools, Christine, Wu, You, Christodoulou, John, Thorburn, David R.

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Author Correction: Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death von Byrne, Alicia B., Arts, Peer, Ha, Thuong T., Kassahn, Karin S., Pais, Lynn S., O’Donnell-Luria, Anne, Babic, Milena, Frank, Mahalia S. B., Feng, Jinghua, Wang, Paul, Lawrence, David M., Eshraghi, Leila, Arriola, Luis, Toubia, John, Nguyen, Hung, McGillivray, George, Pinner, Jason, McKenzie, Fiona, Morrow, Rebecca, Lipsett, Jill, Manton, Nick, Khong, T. Yee, Moore, Lynette, Liebelt, Jan E., Schreiber, Andreas W., King-Smith, Sarah L., Hardy, Tristan S. E., Jackson, Matilda R., Barnett, Christopher P., Scott, Hamish S.

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Somatic Mutational Landscape of Hereditary Hematopoietic Malignancies Associated with Germline Variants in RUNX1, GATA2 and DDX41 von Brown, Anna L., Homan, Claire, Drazer, Michael W., Yu, Kai, Lawrence, David, Feng, Jinghua, Arriola-Martinez, Luis, Pozsgai, Matthew, McNeely, Kelsey, Ha, Thuong, Venugopal, Parvathy, Arts, Peer, King-Smith, Sarah, Cheah, Jesse JC, Armstrong, Mark, Bödör, Csaba, Wang, Paul, Cantor, Alan B., Cazzola, Mario, Degelman, Erin, DiNardo, Courtney D., Duployez, Nicolas, Favier, Remi, Fröhling, Stefan, Rio-Machin, Ana, Klco, Jeffery M., Krämer, Alwin, Kurokawa, Mineo, Lee, Joanne, Malcovati, Luca, Morgan, Neil V, Natsoulis, Georges, Owen, Carolyn, Patel, Keyur P., Preudhomme, Claude, Raslova, Hana, Rienhoff, Hugh Young, Ripperger, Tim, Schulte, Rachael, Tawana, Kiran, Velloso, Elvira Deolinda Rodrigues Pereira, Yan, Benedict, Sood, Raman, Hsu, Amy, Holland, Steven M., Phillips, Kerry, Poplawski, Nicola, Babic, Milena, Kwon Kim, Erika M, Wei, Andrew H., Forsyth, Cecily, Mar Fan, Helen, Lewis, Ian D, Cooney, Julian, Susman, Rachel, Fox, Lucy C, Blombery, Piers, Singhal, Deepak, Hiwase, Devendra, Schreiber, Andreas W, Hahn, Christopher N, Scott, Hamish S, Liu, Paul P., Godley, Lucy A.

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Revision of RUNX1 variant curation rules von Feurstein, Simone, Luo, Xi, Shah, Mancy, Walker, Taylor, Mehta, Nikita, Wu, David, Godley, Lucy A.

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Somatic mutational landscape of hereditary hematopoietic malignancies caused by germ line RUNX1, GATA2, and DDX41 variants von Homan, Claire C, Drazer, Michael W, Yu, Kai, Lawrence, David Michael, Feng, Jinghua, Arriola-Martinez, Luis Alberto, Pozsgai, Matthew J, McNeely, Kelsey E, Ha, Thuong Thi, Venugopal, Parvathy, Arts, Peer, King-Smith, Sarah, Cheah, Jesse Jc, Armstrong, Mark, Wang, Paul, Bödör, Csaba, Cantor, Alan B, Cazzola, Mario, Degelman, Erin S, DiNardo, Courtney D, Duployez, Nicolas, Favier, Rémi, Fröhling, Stefan, Rio-Machin, Ana, Klco, Jeffery M, Krämer, Alwin, Kurokawa, Mineo, Lee, Joanne, Malcovati, Luca, Morgan, Neil V, Georges, Natsoulis, Owen, Carolyn, Patel, Keyur P, Preudhomme, Claude, Raslova, Hana, Rienhoff, Hugh Young, Ripperger, Tim, Schulte, Rachael R, Tawana, Kiran, Velloso, Elvira, Benedict, Yan, Kim, Erika Mijin Kwon, Sood, Raman, Hsu, Amy P, Holland, Steven M, Phillips, Kerry, Poplawski, Nicola, Babic, Milena, Wei, Andrew H, Forsyth, Cecily J, Mar Fan, Helen, Lewis, Ian, Cooney, Julian P, Susman, Rachel, Fox, Lucy C, Blombery, Piers, Singhal, Deepak, Hiwase, Devendra K, Phipson, Belinda, Schreiber, Andreas W, Hahn, Christopher N, Scott, Hamish S, Liu, Paul P, Godley, Lucy A, Brown, Anna L

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Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1-related syndrome von Arts, Peer, Garland, Jessica, Byrne, Alicia B, Hardy, Tristan S E, Babic, Milena, Feng, Jinghua, Wang, Paul, Ha, Thuong, King-Smith, Sarah L, Schreiber, Andreas W, Crawford, April, Manton, Nick, Moore, Lynette, Barnett, Christopher P, Scott, Hamish S

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Comparative genomics of Cluster O mycobacteriophages von Cresawn, Steven G, Pope, Welkin H, Jacobs-Sera, Deborah, Bowman, Charles A, Russell, Daniel A, Dedrick, Rebekah M, Adair, Tamarah, Anders, Kirk R, Ball, Sarah, Bollivar, David, Breitenberger, Caroline, Burnett, Sandra H, Butela, Kristen, Byrnes, Deanna, Carzo, Sarah, Cornely, Kathleen A, Cross, Trevor, Daniels, Richard L, Dunbar, David, Findley, Ann M, Gissendanner, Chris R, Golebiewska, Urszula P, Hartzog, Grant A, Hatherill, J Robert, Hughes, Lee E, Jalloh, Chernoh S, De Los Santos, Carla, Ekanem, Kevin, Khambule, Sphindile L, King, Rodney A, King-Smith, Christina, Klyczek, Karen, Krukonis, Greg P, Laing, Christian, Lapin, Jonathan S, Lopez, A Javier, Mkhwanazi, Sipho M, Molloy, Sally D, Moran, Deborah, Munsamy, Vanisha, Pacey, Eddie, Plymale, Ruth, Poxleitner, Marianne, Reyna, Nathan, Schildbach, Joel F, Stukey, Joseph, Taylor, Sarah E, Ware, Vassie C, Wellmann, Amanda L, Westholm, Daniel, Wodarski, Donna, Zajko, Michelle, Zikalala, Thabiso S, Hendrix, Roger W, Hatfull, Graham F

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