Incorporation of additives into protective coatings von Clancy, Sean Owen, Su, Tining, Cox, Bronwyn, Yun, Yang, Cao, Liulei

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INCORPORATION OF ADDITIVES INTO PROTECTIVE COATINGS von YUN YANG, COX BRONWYN, CLANCY SEAN OWEN, CAO LIULEI, SU TINING

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INCORPORATION OF ADDITIVES INTO PROTECTIVE COATINGS von COX, BRONWYN, YUN, YANG, CAO, LIULEI, SU, TINING, CLANCY, SEAN, OWEN

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Ecological momentary interventions for mental health: A scoping review von Balaskas, Andreas, Schueller, Stephen M, Cox, Anna L, Doherty, Gavin

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Extreme drilling environment forces evolution of rotary steerable systems and bits von COX, Bronwyn, ROMO, Louis, CHAMPION, Brett, MAUNG, Osman, CARD, Kirk, BARTON, Steve

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Enrolment of the first paediatric cohort into the Australian lupus registry and biobank: A single-centre experience von Power, Bronwyn D, Kandane-Rathnayake, Rangi, Tiller, Georgina, Renton, William D, Cox, Angela, Johnstone, Lilian, Hoi, Alberta, Gowdie, Peter

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Preoperative biomarker evaluation for the prediction of cardiovascular events after major vascular surgery von Chan, William, Kingwell, Bronwyn A., Schneider, Hans G., Cox, Geoffrey, Natoli, Alaina, Starr, Jenny, Croft, Kevin D., Dart, Anthony M., Duffy, Stephen J.

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Design and implementation of multiplexed amplicon sequencing panels to serve genomic epidemiology of infectious disease: A malaria case study von LaVerriere, Emily, Schwabl, Philipp, Carrasquilla, Manuela, Taylor, Aimee R., Johnson, Zachary M., Shieh, Meg, Panchal, Ruchit, Straub, Timothy J., Kuzma, Rebecca, Watson, Sean, Buckee, Caroline O., Andrade, Carolina M., Portugal, Silvia, Crompton, Peter D., Traore, Boubacar, Rayner, Julian C., Corredor, Vladimir, James, Kashana, Cox, Horace, Early, Angela M., MacInnis, Bronwyn L., Neafsey, Daniel E.

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Genome-wide association study identifies novel breast cancer susceptibility loci von Meyer, Kerstin B, Pharoah, Paul D. P, Kataja, Vesa, Haiman, Christopher A, Lissowska, Jolanta, Ko, Yon-Dschun, Hall, Per, Olson, Janet E, Beesley, Jonathan, Zhang, Jinghui, Fagerholm, Rainer, Cox, David G, Meijers-Heijboer, Hanne, Wang, Hui-Chun, Hankinson, Susan E, Field, Helen, Rahman, Nazneen, Le Marchand, Loic, Peplonska, Beata, Gaborieau, Valerie, Hunter, David J, Gonzalez-Neira, Anna, Chenevix-Trench, Georgia, Kang, Daehee, Dörk, Thilo, Jacobi, Catharina E, Bojesen, Stig E, Nordestgaard, Børge G, Alexander, Bruce H, Shen, Chen-Yang, Bogdanova, Natalia, Pooley, Karen A, Brock, Ian W, Goode, Ellen L, Healey, Catherine S, Stratton, Michael R, Cox, David R, Dunning, Alison M, Odefrey, Fabrice, Wu, Pei-Ei, Noh, Dong-Young, Morrison, Jonathan, Bowman, Richard, Cox, Angela, Fletcher, Olivia, Luben, Robert, Couch, Fergus J, Ballinger, Dennis G, Brennan, Paul, Peto, Julian, Tollenaar, Rob A. E. M, Hopper, John L, Easton, Douglas F, Seal, Sheila, Eerola, Hannaleena, Ponder, Bruce A. J, Hartikainen, Jaana, Reed, Malcolm W. R, Klijn, Jan G. M, Wareham, Nicholas, Kosma, Veli-Matti, Low, Yen-Ling, Doody, Michele M, Eccles, Diana, Brinton, Louise, Brauch, Hiltrud, Spurdle, Amanda B, Sigurdson, Alice J, Sangrajrang, Suleeporn, Hamann, Ute, Ahn, Sei-Hyun, Schürmann, Peter, Schroen, Chris, McCredie, Margaret, Evans, D. Gareth, Milne, Roger L, Nevanlinna, Heli, Devilee, Peter, Justenhoven, Christina, Thompson, Deborah, Mannermaa, Arto, Day, Nicholas E, Rivadeneira, Fernando, Kolonel, Laurence K, Benitez, Javier, Ribas, Gloria, Axelsson, Christen K, Giles, Graham G, Yoo, Keun-Young, Chen, Xiaoqing, Southey, Melissa, Uitterlinden, André, Liu, Jianjun, Johnson, Nichola, van den Ouweland, Ans, Chanock, Stephen, MacPherson, Gordon, Henderson, Brian E, Ahmed, Shahana, Wedren, Sara

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Abstract P13: Faster Treatment Speed is Not Associated With Bleeds: Intravenous Alteplase Treatment in the Ultra-Early Time Window is Safe von Provencher, Michelle, Scherman, Ashley, Baraban, Elizabeth, Jackson, Robert, Stuchiner, Tamela L, Cox, Kailey L, McDonald, Kristen, Tarpley, Jason W, Kansara, Amit, Rogers, Bronwyn S, Van Horn, Christine, Teeter, Lisa, Fitzgerald, Darcie D, Cowell, Leigh

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Human candidate gene polymorphisms and risk of severe malaria in children in Kilifi, Kenya: a case-control association study von Ndila, Carolyne M, Shebe, Mohammed, Awuondo, Kennedy O, Mturi, Neema, Rowlands, Kate, Jeffreys, Anna, Mackinnon, Margaret, Abubakar, Ismaela, Aiyegbo, Mohammed, Amenga-Etego, Lucas, Anchang-Kimbi, Judith, Ansah, Patrick, Ansong, Daniel, Atuguba, Frank, Auburn, Sarah, Bauni, Evasius, Bull, Susan, Busby, George, Camara, Landing, Campino, Susana, Carter, Richard, Carucci, Dan, Ceesay, Ndey, Chau, Tran, Chuong, Ly, Cole-Ceesay, Ramou, Cook, Katharine, Craik, Rachel, Day, Nicholas, Deloukas, Panos, Dembele, Awa, deVries, Jantina, Diss, Andrea, Djimdé, Abdoulaye, Dolo, Amagana, Doumbo, Ogobara, Drury, Eleanor, Elzein, Abier, Evans, Jennifer, Green, Angie, Hien, Tran, Hubbart, Christina, Ishengoma, Deus, Jaiteh, Jula, Jammeh, Kebba, Jasseh, Momodou, Joseph, Sarah, Kachala, David, Kanyi, Haddy, Karunajeewa, Harin, Kokwaro, Gilbert, Leffler, Ellen, Lemnge, Martha, Lin, Enmoore, Ly, Alioune, Macharia, Alexander, MacInnis, Bronwyn, Makani, Julie, Malangone, Cinzia, Manjurano, Alphaxard, Manske, Magnus, Marsh, Vicki, Mbunwe, Eric, McCreight, Marilyn, Mead, Daniel, Mohamed, Hiba, Moore, Mike, Mugri, Regina, Munthali, Annie, Nadjm, Behzad, Newton, Charles, Njie, Jalimory, Nyirongo, Vysaul, O'Brien, John, Ofori, Alex, Olaosebikan, Rasaq, Oluoch, Tom, Onykwelu, Emmanuel, Opi, Daniel, Oyola, Samuel, Pensulo, Paul, Quyen, Nguyen, Rasheed, Oba, Rodford, Joanne, Rowlands, Kate, Saidy-Khan, Momodou, Saine, Horeja, Sakuntabhai, Anavaj, Siba, Peter, Sisay-Joof, Fatoumatta, Small, Kerrin, Somaskantharajah, Elilan, Suriyaphol, Prapat, Thera, Mahamadou, Titanji, Vincent, Usen, Stanley, Vanderwal, Aaron, Wangai, Hannah, Wilson, Michael, Yamoah, Lawrence

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Mutations in PHF6 are associated with Börjeson-Forssman -Lehmann syndrome von de Vries, Bert B. A, Ross, Shelley, Gécz, Jozef, Grompe, Markus, Clayton-Smith, Jill, Stewart, Helen, Lampe, Anne K, Gedeon, Ági K, White, Susan M, Thomas, Paul, Mulley, John C, Lower, Karen M, Turner, Gillian, Mathews, Katherine D, Schelley, Susan, van Ravenswaay, Conny M. A, Kerr, Bronwyn A, Shaw, Marie A, Hoyme, H. Eugene, Delatycki, Martin B, Cox, Barbara

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Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study von Johnson, Nichola, Dudbridge, Frank, Orr, Nick, Gibson, Lorna, Jones, Michael E, Schoemaker, Minouk J, Folkerd, Elizabeth J, Haynes, Ben P, Hopper, John L, Southey, Melissa C, Dite, Gillian S, Apicella, Carmel, Schmidt, Marjanka K, Broeks, Annegien, Van't Veer, Laura J, Atsma, Femke, Muir, Kenneth, Lophatananon, Artitaya, Fasching, Peter A, Beckmann, Matthias W, Ekici, Arif B, Renner, Stefan P, Sawyer, Elinor, Tomlinson, Ian, Kerin, Michael, Miller, Nicola, Burwinkel, Barbara, Marme, Frederik, Schneeweiss, Andreas, Sohn, Christof, Guénel, Pascal, Truong, Therese, Cordina, Emilie, Menegaux, Florence, Bojesen, Stig E, Nordestgaard, Børge G, Flyger, Henrik, Milne, Roger, Zamora, M Pilar, Arias Perez, Jose Ignacio, Benitez, Javier, Bernstein, Leslie, Anton-Culver, Hoda, Ziogas, Argyrios, Clarke Dur, Christina, Brenner, Hermann, Müller, Heiko, Arndt, Volker, Dieffenbach, Aida Karina, Meindl, Alfons, Heil, Joerg, Bartram, Claus R, Schmutzler, Rita K, Brauch, Hiltrud, Justenhoven, Christina, Ko, Yon-Dschun, Nevanlinna, Heli, Muranen, Taru A, Aittomäki, Kristiina, Blomqvist, Carl, Matsuo, Keitaro, Dörk, Thilo, Bogdanova, Natalia V, Antonenkova, Natalia N, Lindblom, Annika, Mannermaa, Arto, Kataja, Vesa, Kosma, Veli-Matti, Hartikainen, Jaana M, Chenevix-Trench, Georgia, Beesley, Jonathan, Wu, Anna H, Van den Berg, David, Tseng, Chiu-Chen, Lambrechts, Diether, Smeets, Dominiek, Neven, Patrick, Wildiers, Hans, Chang-Claude, Jenny, Rudolph, Anja, Nickels, Stefan, Flesch-Janys, Dieter, Radice, Paolo, Peterlongo, Paolo, Bonanni, Bernardo, Pensotti, Valeria, Couch, Fergus J, Olson, Janet E, Wang, Xianshu, Fredericksen, Zachary, Pankratz, Vernon S, Giles, Graham G, Severi, Gianluca, Baglietto, Laura, Haiman, Chris, Simard, Jacques, Goldberg, Mark S, Labrèche, France, Dumont, Martine, Soucy, Penny

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Evaluation of a Practice-Development Initiative to Improve Breastfeeding Rates von Barnes, Margaret, Cox, Julie, Doyle, Bronwyn, Reed, Rachel

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The Shwachman–Bodian–Diamond syndrome gene mutations cause a neonatal form of spondylometaphysial dysplasia (SMD) resembling SMD Sedaghatian type von Nishimura, Gen, Nakashima, Eiji, Hirose, Yuichiro, Cole, Trevor, Cox, Phillip, Cohn, Daniel H, Rimoin, David L, Lachman, Ralph S, Miyamoto, Yoshinari, Kerr, Bronwyn, Unger, Sheila, Ohashi, Hirofumi, Superti-Furga, Andrea, Ikegawa, Shiro

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Structure of mouse kallikrein gene family suggests a role in specific processing of biologically active peptides von Mason, Anthony J, Evans, Bronwyn A, Cox, David R, Shine, John, Richards, Robert I

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Design and implementation of multiplexed amplicon sequencing panels to serve genomic epidemiology of infectious disease: A malaria case study von LaVerriere, Emily, Schwabl, Philipp, Carrasquilla, Manuela, Taylor, Aimee R, Johnson, Zachary M, Shieh, Meg, Panchal, Ruchit, Straub, Timothy J, Kuzma, Rebecca, Watson, Sean, Buckee, Caroline O, Andrade, Carolina M, Portugal, Silvia, Crompton, Peter D, Traore, Boubacar, Rayner, Julian C, Corredor, Vladimir, James, Kashana, Cox, Horace, Early, Angela M, MacInnis, Bronwyn L, Neafsey, Daniel E

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Mutations in PHF6 are associated with Boerjeson-Forssman-Lehmann syndrome von Lower, K M, Turner, G, Kerr, BA, Mathews, K D, Shaw, MA, Gedeon, A K, Schelley, S, Hoyme, HE, White, S M, Delatycki, M B, Lampe, A K, Clayton-Smith, J, Stewart, H, Gecz, J

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