Fracture analysis of a total hip prosthesis based on reverse engineering von Babić, Milena, Verić, Ozren, Božić, Željko, Sušić, Aleksandar

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Finite element modelling and fatigue life assessment of a cemented total hip prosthesis based on 3D scanning von Babić, Milena, Verić, Ozren, Božić, Željko, Sušić, Aleksandar

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Reverse engineering based integrity assessment of a total hip prosthesis von Babić, Milena, Verić, Ozren, Božić, Željko, Sušić, Aleksandar

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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 von 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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The mutational burden of therapy-related myeloid neoplasms is similar to primary myelodysplastic syndrome but has a distinctive distribution von Singhal, Deepak, Wee, Li Yan A., Kutyna, Monika M., Chhetri, Rakchha, Geoghegan, Joel, Schreiber, Andreas W., Feng, Jinghua, Wang, Paul P.-S., Babic, Milena, Parker, Wendy T., Hiwase, Smita, Edwards, Suzanne, Moore, Sarah, Branford, Susan, Kuzmanovic, Teodora, Singhal, Nimit, Gowda, Raghu, Brown, Anna L., Arts, Peer, To, Luen B., Bardy, Peter G., Lewis, Ian D., D’Andrea, Richard J., Maciejewski, Jaroslaw P., Scott, Hamish S., Hahn, Christopher N., Hiwase, Devendra K.

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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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A novel germline SAMD9L mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemia von 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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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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Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss von 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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Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies von Lewinsohn, Maya, Brown, Anna L., Weinel, Luke M., Phung, Connie, Rafidi, George, Lee, Ming K., Schreiber, Andreas W., Feng, Jinghua, Babic, Milena, Chong, Chan-Eng, Lee, Young, Yong, Agnes, Suthers, Graeme K., Poplawski, Nicola, Altree, Meryl, Phillips, Kerry, Jaensch, Louise, Fine, Miriam, D'Andrea, Richard J., Lewis, Ian D., Medeiros, Bruno C., Pollyea, Daniel A., King, Mary-Claire, Walsh, Tom, Keel, Siobán, Shimamura, Akiko, Godley, Lucy A., Hahn, Christopher N., Churpek, Jane E., Scott, Hamish S.

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Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia von Scott, Hamish S, Hahn, Christopher N, Chong, Chan-Eng, Carmichael, Catherine L, Wilkins, Ella J, Brautigan, Peter J, Li, Xiao-Chun, Babic, Milena, Lin, Ming, Carmagnac, Amandine, Lee, Young K, Kok, Chung H, Gagliardi, Lucia, Friend, Kathryn L, Ekert, Paul G, Butcher, Carolyn M, Brown, Anna L, Lewis, Ian D, To, L Bik, Timms, Andrew E, Storek, Jan, Moore, Sarah, Altree, Meryl, Escher, Robert, Bardy, Peter G, Suthers, Graeme K, D'Andrea, Richard J, Horwitz, Marshall S

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In depth analysis of the Sox4 gene locus that consists of sense and natural antisense transcripts von Ling, King-Hwa, Brautigan, Peter J., Moore, Sarah, Fraser, Rachel, Leong, Melody Pui-Yee, Leong, Jia-Wen, Zainal Abidin, Shahidee, Lee, Han-Chung, Cheah, Pike-See, Raison, Joy M., Babic, Milena, Lee, Young Kyung, Daish, Tasman, Mattiske, Deidre M., Mann, Jeffrey R., Adelson, David L., Thomas, Paul Q., Hahn, Christopher N., Scott, Hamish S.

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Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature von Kazenwadel, Jan, Secker, Genevieve A., Liu, Yajuan J., Rosenfeld, Jill A., Wildin, Robert S., Cuellar-Rodriguez, Jennifer, Hsu, Amy P., Dyack, Sarah, Fernandez, Conrad V., Chong, Chan-Eng, Babic, Milena, Bardy, Peter G., Shimamura, Akiko, Zhang, Michael Y., Walsh, Tom, Holland, Steven M., Hickstein, Dennis D., Horwitz, Marshall S., Hahn, Christopher N., Scott, Hamish S., Harvey, Natasha L.

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Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis von Ghaoui, Roula, Ha, Thuong T., Kerkhof, Jennifer, McConkey, Haley, Gao, Song, Babic, Milena, King, Rob, Ravenscroft, Gianina, Koszyca, Barbara, Otto, Sophia, Laing, Nigel G., Scott, Hamish, Sadikovic, Bekim, Kassahn, Karin S.

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Al‐Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2‐Related Disorders von Batkovskyte, Dominyka, McKenzie, Fiona, Taylan, Fulya, Simsek‐Kiper, Pelin Ozlem, Nikkel, Sarah M, Ohashi, Hirofumi, Stevenson, Roger E, Ha, Thuong, Cavalcanti, Denise P, Miyahara, Hiroyuki, Skinner, Steven A, Aguirre, Miguel A, Akçören, Zühal, Utine, Gulen Eda, Chiu, Tillie, Shimizu, Kenji, Hammarsjö, Anna, Boduroglu, Koray, Moore, Hannah W, Louie, Raymond J, Arts, Peer, Merrihew, Allie N, Babic, Milena, Jackson, Matilda R, Papadogiannakis, Nikos, Lindstrand, Anna, Nordgren, Ann, Barnett, Christopher P, Scott, Hamish S, Chagin, Andrei S, Nishimura, Gen, Grigelioniene, Giedre

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ERG Is a New Predisposition Gene for Bone Marrow Failure and Hematological Malignancy von Scott, Hamish S, Zerella, Jiarna, Homan, Claire, Arts, Peer, Lin, Steve, Spinelli, Sam J, Babic, Milena, Brautigan, Peter J, Truong, Lynda, Arriola-Martinez, Luis, Venugopal, Parvathy, Feurstein, Simone K, Larcher, Lise, Sicre De Fontbrune, Flore, Demirdas, Serwet, De Munnik, Sonja, Poirel, Hélène, Brichard, Benedicte, Dobbins, Sara, Mutsaers, Pim, DeMille, Desiree S, Flores-Daboub, Josue, Drazer, Michael W, Crawford, Alison, McCarrier, Julie, Basel, Donald G, Phillips, Kerry, Poplawski, Nicola K, Birdsey, Graeme, Pirri, Daniela, Ostergaard, Pia, Simons, Annet, Godley, Lucy, Ross, David M., Hiwase, Devendra, Soulier, Jean, Brown, Anna, Carmichael, Catherine, Hahn, Christopher N.

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Familial Clustering of Hematological Malignancies: Harbingers of Wider Germline Cancer Susceptibility von Brown, Anna L, Babic, Milena, Schreiber, Andreas, Feng, Jinghua, Dobbins, Julia, Arts, Peer, Wang, Paul, Phillips, Kerry, Hiwase, Devendra K, Venugopal, Parvathy, Branford, Susan, Poplawski, Nicola, Hahn, Christopher N, Scott, Hamish S

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Australian Familial Haematological Cancer Study - Findings from 15 Years of Aggregated Clinical, Genomic and Transcriptomic Data von Hahn, Christopher N, Babic, Milena, Brautigan, Peter J, Venugopal, Parvathy, Phillips, Kerry, Dobbins, Julia, Arts, Peer, Wee, Amilia, Singhal, Deepak, Hiwase, Devendra K, Feng, Jinghua, Schreiber, Andreas W, D'Andrea, Richard J, Poplawski, Nicola, Brown, Anna L, Scott, Hamish S

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AN INTEGRATIVE GENOMIC APPROACH TO EXAMINE MUTATIONS AND BIOLOGICAL PATHWAYS ASSOCIATED WITH HAEMATOLOGICAL MALIGNANCY DEVELOPMENT IN DDX41 MUTATED FAMILIES von Cheah, Jesse, Brown, Anna, Eshraghi, Leila, Feng, Jinghua, Schreiber, Andreas, Babic, Milena, Homan, Claire, Fine, Miriam, Philips, Kerry, Poplawski, Nicola, Hahn, Christopher, Scott, Hamish

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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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