Distress Levels and Self-Reported Treatment Rates for Medicine, Law, Psychology and Mechanical Engineering Tertiary Students: Cross-Sectional Study by Leahy, Catherine M., Peterson, Ray F., Wilson, Ian G., Newbury, Jonathan W., Tonkin, Anne L., Turnbull, Deborah

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Sarcopenia: a potential cause and consequence of type 2 diabetes in Australia's ageing population? by Li, Joule J, Newbury, Jonathan W, Adams, Robert J

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Vitamin D insufficiency in Aboriginal Australians by Vanlint, Simon J, Morris, Howard A, Newbury, Jonathan W, Crockett, Alan J

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Randomised controlled trial of health assessments for older Australian veterans and war widows by Byles, Julie E, Tavener, Meredith, Higginbotham, Nick H, Francis, Lyn, Marley, John E, O'Connell, Rachel L, Nair, Balakrishnan R, Goodger, Brendan G, Jackson, Claire L, McKernon, Mary E, Heller, Richard F, Newbury, Jonathan

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Should we still give our asthmatic patients written individualised management plans? by Thornett, Andrew M, Newbury, Jonathan W, Duszynski, Andre J

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The LINKIN Health Census process: design and implementation by Hoon-Leahy, Catherine Elizabeth, Newbury, Jonathan, Kitson, Alison, Whitford, Deirdre, Wilson, Anne, Karnon, Jonathan, Baker, Jenny, Jamrozik, Konrad, Beilby, Justin

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A randomised controlled trial of the outcome of health assessment of people aged 75 years and over by Newbury, Jonathan W, Marley, John E, Beilby, Justin J

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Should we still give our asthmatic patients written individualised management plans? by Thornett, Andrew M, Newbury, Jonathan W, Duszynski, Andre J

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A checklist for comprehensive health assessment for the over 70's by Byles, Julie E., Tavener, Meredith A., Fitzgerald, Patrick E B., Hair, Balakrishnan R., Higginbotham, Nick, Jackson, Claire L., Heller, Richard F., Newbury, Jonathan W.

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Prevalence and architecture of de novo mutations in developmental disorders by McRae, Jeremy F, Clayton, Stephen, Mason, Laura E, Tivey, Adrian R, Ahmed, Munaza, Awada, Jana, Balasubramanian, Meena, Banka, Siddharth, Bennett, Chris, Bernhard, Birgitta, Bevan, A. Paul, Blair, Edward, Blyth, Moira, Burn, John, Castle, Bruce, Clasper, Susan, Collins, Amanda, Collinson, Morag N, Dabir, Tabib, Davidson, Rosemarie, Davies, Sally, Dean, John, Donnai, Dian, Ellard, Sian, Ellis, Ian, Everest, Sarah, Foulds, Nicola, Fryer, Alan, Gaunt, Lorraine, Goudie, David, Gray, Emma, Greene, Philip, Gribble, Susan, Henderson, Alex, Hildyard, Lucy, Holden, Simon, Holder, Muriel, Ingram, Stuart, Jackson, Andrew, Kaemba, Beckie, Kazembe, Sandra, Kinning, Esther, Kraus, Alison, Kumar, V. K. Ajith, Lachlan, Katherine, Lam, Wayne, Lim, Derek, Longman, Cheryl, Lynch, Sally A, Maher, Eddy, Maye, Una, McKay, Kirsten, McWilliam, Catherine, Metcalfe, Kay, Morgan, Sian, Murday, Victoria, Murphy, Helen, Nemeth, Andrea, Nevitt, Louise, Newbury-Ecob, Ruth, Park, Soo-Mi, Paterson, Joan, Payne, Stewart, Perrett, Daniel, Pratt, Norman, Quarrell, Oliver, Randall, Josh, Rankin, Julia, Raymond, Lucy, Robert, Leema, Roberts, Paul, Saggar, Anand, Samant, Shalaka, Sampson, Julian, Sandford, Richard, Selby, Ann, Sequeira, Cheryl, Shearing, Emma, Smith, Audrey, Smith, Kath, Splitt, Miranda, Suri, Mohnish, Sutton, Vivienne, Tatton-Brown, Kate, Temple, I. Karen, Turner, Claire, Varghese, Vinod, Vasudevan, Pradeep, Vogt, Julie, Wakeling, Emma, Wilcox, Sarah, Williams, Denise, Williams, Nicola, Wilson, Louise, Wright, Michael, Yates, Laura, Yau, Michael, Wright, Caroline F, FitzPatrick, David R, Barrett, Jeffrey C

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Variants in CLDN5 cause a syndrome characterized by seizures, microcephaly and brain calcifications by Deshwar, Ashish R, Cytrynbaum, Cheryl, Murthy, Harsha, Zon, Jessica, Chitayat, David, Volpatti, Jonathan, Newbury-Ecob, Ruth, Ellard, Sian, Allen, Hana Lango, Yu, Emily P, Noche, Ramil, Walker, Suzi, Scherer, Stephen W, Mahida, Sonal, Elitt, Christopher M, Nicolas, Gaël, Goldenberg, Alice, Saugier-Veber, Pascale, Lecoquierre, Francois, Dabaj, Ivana, Meddaugh, Hannah, Marble, Michael, Keppler-Noreuil, Kim M, Drayson, Lucy, Barañano, Kristin W, Chassevent, Anna, Agre, Katie, Létard, Pascaline, Bilan, Frederic, Le Guyader, Gwenaël, Laquerrière, Annie, Ramsey, Keri, Henderson, Lindsay, Brady, Lauren, Tarnopolsky, Mark, Bainbridge, Matthew, Friedman, Jennifer, Capri, Yline, Athayde, Larissa, Kok, Fernando, Gurgel-Giannetti, Juliana, Ramos, Luiza L P, Blaser, Susan, Dowling, James J, Weksberg, Rosanna

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CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language by Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language by Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language by Blok, Lot Snijders, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

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Abdominal adiposity and obstructive airway disease: testing insulin resistance and sleep disordered breathing mechanisms by Haren, Matthew T, Misan, Gary, Paterson, Tracey-Jayne, Ruffin, Richard E, Grant, Janet F, Buckley, Jonathan D, Howe, Peter R C, Newbury, Jonathan, Taylor, Anne W, McDermott, Robyn A

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The Biomedical Research Infrastructure Software as a Service Kit (BRISSKit): technical description by Butters, Oliver W., Issa, Shajid, Lusted, Jeff, Newbury, Malcolm, Parsloe, Russ, Holden, Nick, Free, Robert C., Beck, Tim, Wilson, Rebecca C., Burton, Paul R., Tedds, Jonathan A.

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Book Reviews by Cartledge, Paul, Ranger, Terence, Braund, David, Shepard, Jonathan, Treadgold, Warren, Shatzmiller, Joseph, Bradbury, Jim, Mackenzie, John M., Peers, Douglas M., Liebel-Weckowicz, Helen, Perry, John R., Steele, Ian K., Trani, Eugene P., Craton, Michael, Severn, John K., Connelly, Owen, Rothenberg, Gunther E., Victor Koschmann, J., Ashton, Rosemary, Newbury, Colin, Saab, Ann Pottinger, Ferris, Norman B., Dosal, Paul J., Wooley, Wesley T., Betts, Raymond F., Johnson, Robert David, Halpern, Paul G., Wilcox, Craig, Herwig, Holger H., Jacobson, Jon, Marks, Sally, Tarling, Nicholas, Deshmukh, Marion F., Lowe, Peter, Haslam, Jonathan, Conroy, Hilary, Brands, H. W., Mackenzie, S. P., Rodina, Matthew E., Beckett, Ian F. W., Katz, Steven J., Gillingham, John, Lora, Ronald, Little, Douglas, Harbutt, Fraser J., Buteux, Paul, Cell, John W., Aronsen, Lawrence, Canning, Paul, Holland, Robert, Carroll, Francis M., Frank, Willard C., Adamec, Ludwig W., Gann, L. H., McNeill, William H., Donaghy, Greg, Holden, Robert H., Conro, Hilary, Thomson, Janice E., Modelski, George

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Book Reviews by Cartledge, Paul, Ranger, Terence, Braund, David, Shepard, Jonathan, Treadgold, Warren, Shatzmiller, Joseph, Bradbury, Jim, Mackenzie, John M., Peers, Douglas M., Liebel-Weckowicz, Helen, Perry, John R., Steele, Ian K., Trani, Eugene P., Craton, Michael, Severn, John K., Connelly, Owen, Rothenberg, Gunther E., Victor Koschmann, J., Ashton, Rosemary, Newbury, Colin, Saab, Ann Pottinger, Ferris, Norman B., Dosal, Paul J., Wooley, Wesley T., Betts, Raymond F., Johnson, Robert David, Halpern, Paul G., Wilcox, Craig, Herwig, Holger H., Jacobson, Jon, Marks, Sally, Tarling, Nicholas, Deshmukh, Marion F., Lowe, Peter, Haslam, Jonathan, Conroy, Hilary, Brands, H. W., Mackenzie, S. P., Rodina, Matthew E., Beckett, Ian F. W., Katz, Steven J., Gillingham, John, Lora, Ronald, Little, Douglas, Harbutt, Fraser J., Buteux, Paul, Cell, John W., Aronsen, Lawrence, Canning, Paul, Holland, Robert, Carroll, Francis M., Frank, Willard C., Adamec, Ludwig W., Gann, L. H., McNeill, William H., Donaghy, Greg, Holden, Robert H., Conro, Hilary, Thomson, Janice E., Modelski, George

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