Newborn Discharge Timing and Readmissions: California, 1992-1995 von Danielsen, Beate, Castles, Anne G, Damberg, Cheryl L, Gould, Jeffrey B

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Using employer purchasing power to improve the quality of perinatal care von Castles, A G, Milstein, A, Damberg, C L

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Retirement and Sexual Satisfaction von Henning, Georg, Segel-Karpas, Dikla, Praetorius Björk, Marcus, Bjälkebring, Pär, Berg, Anne Ingeborg

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Comprehensive Control of Human Papillomavirus Infections and Related Diseases von Bosch, F. Xavier, Broker, Thomas R, Forman, David, Moscicki, Anna-Barbara, Gillison, Maura L, Doorbar, John, Stern, Peter L, Stanley, Margaret, Arbyn, Marc, Poljak, Mario, Cuzick, Jack, Castle, Philip E, Schiller, John T, Markowitz, Lauri E, Fisher, William A, Canfell, Karen, Denny, Lynette A, Franco, Eduardo L, Steben, Marc, Kane, Mark A, Schiffman, Mark, Meijer, Chris J.L.M, Sankaranarayanan, Rengaswamy, Castellsagué, Xavier, Kim, Jane J, Brotons, Maria, Alemany, Laia, Albero, Ginesa, Diaz, Mireia, Sanjosé, Silvia de

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Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype von Tatton-Brown, Katrina, Murray, Anne, Hanks, Sandra, Douglas, Jenny, Armstrong, Ruth, Banka, Siddharth, Bird, Lynne M., Clericuzio, Carol L., Cormier-Daire, Valerie, Cushing, Tom, Flinter, Frances, Jacquemont, Marie-Line, Joss, Shelagh, Kinning, Esther, Lynch, Sally Ann, Magee, Alex, McConnell, Vivienne, Medeira, Ana, Ozono, Keiichi, Patton, Michael, Rankin, Julia, Shears, Debbie, Simon, Marleen, Splitt, Miranda, Strenger, Volker, Stuurman, Kyra, Taylor, Clare, Titheradge, Hannah, Van Maldergem, Lionel, Temple, I. Karen, Cole, Trevor, Seal, Sheila, Rahman, Nazneen

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Comprehensive Control of Human Papillomavirus Infections and Related Diseases von Bosch, F. Xavier, Broker, Thomas R, Forman, David, Moscicki, Anna-Barbara, Gillison, Maura L, Doorbar, John, Stern, Peter L, Stanley, Margaret, Arbyn, Marc, Poljak, Mario, Cuzick, Jack, Castle, Philip E, Schiller, John T, Markowitz, Lauri E, Fisher, William A, Canfell, Karen, Denny, Lynette A, Franco, Eduardo L, Steben, Marc, Kane, Mark A, Schiffman, Mark, Meijer, Chris J.L.M, Sankaranarayanan, Rengaswamy, Castellsagué, Xavier, Kim, Jane J, Brotons, Maria, Alemany, Laia, Albero, Ginesa, Diaz, Mireia, Sanjosé, Silvia de

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A Neuroethics Framework for the Australian Brain Initiative von Carter, Adrian, Richards, Linda J., Apthorp, Deborah, Azghadi, Mostafa Rahimi, Badcock, David R., Balleine, Bernard, Bekkers, John M., Berk, Michael, Bourne, James A., Bradley, Andrew P., Breakspear, Michael, Brichta, Alan, Carter, Olivia, Castles, Anne, Chakli, Khaled, Cohen-Woods, Sarah, Conn, Simon J., Cornish, Jennifer, Cornish, Kim, de Zubicaray, Greg, Egan, Gary F., Enticott, Peter G., Fitzgibbon, Bernadette M., Forlini, Cynthia, Fornito, Alex, Griffiths, Lyn, Gullifer, Judith, Hall, Wayne, Halliday, Glenda, Hannan, Anthony J., Harrer, Stefan, Harvey, Alan, Hatherly, Chris, Hickie, Ian B., Kennett, Jeanette, Kiernan, Matthew, Kilpatrick, Trevor, Kiral-Kornek, Isabell, Korgaonkar, Mayuresh S., Lawrence, Andrew J., Leventer, Rick, Levy, Neil, Licinio, Julio, Lovell, Nigel, Mackellar, Geoff, Malcolm, Lynne, Mason, Alice, Mattingley, Jason B., Medland, Sarah E., Michie, Patricia T., Nithianantharajah, Jess, Parker, John, Payne, Jonathan M., Poole-Warren, Laura, Sah, Pankaj, Sarnyai, Zoltan, Schofield, Peter R., Shimoni, Olga, Shum, David H.K., Silk, Tim, Slee, Mark, Smith, Ashleigh E., Soulis, Tina, Sriram, Sharath, Stuart, Greg J., Tapson, Jonathan, Thompson, Matthew B., van Schaik, André, Vincent, Nicole A., Vissel, Bryce, Waters, Allison

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Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height von Tatton-Brown, Katrina, Hanks, Sandra, Ruark, Elise, Zachariou, Anna, Duarte, Silvana Del Vecchio, Ramsay, Emma, Snape, Katie, Murray, Anne, Perdeaux, Elizabeth R, Seal, Sheila, Loveday, Chey, Banka, Siddharth, Clericuzio, Carol, Flinter, Frances, Magee, Alex, McConnell, Vivienne, Patton, Michael, Raith, Wolfgang, Rankin, Julia, Splitt, Miranda, Strenger, Volker, Taylor, Clare, Wheeler, Patricia, Temple, Karen I, Cole, Trevor, Douglas, Jenny, Rahman, Nazneen

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A Haplotype Spanning KIAA0319 and TTRAP Is Associated with Normal Variation in Reading and Spelling Ability von Luciano, Michelle, Lind, Penelope A, Duffy, David L, Castles, Anne, Wright, Margaret J, Montgomery, Grant W, Martin, Nicholas G, Bates, Timothy C

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A Neuroethics Framework for the Australian Brain Initiative von Carter, Adrian, Richards, Linda J., Apthorp, Deborah, Azghadi, Mostafa Rahimi, Badcock, David R., Balleine, Bernard, Bekkers, John M., Berk, Michael, Bourne, James A., Bradley, Andrew P., Breakspear, Michael, Brichta, Alan, Carter, Olivia, Castles, Anne, Chakli, Khaled, Cohen-Woods, Sarah, Conn, Simon J., Cornish, Jennifer, Cornish, Kim, de Zubicaray, Greg, Egan, Gary F., Enticott, Peter G., Fitzgibbon, Bernadette M., Forlini, Cynthia, Fornito, Alex, Griffiths, Lyn, Gullifer, Judith, Hall, Wayne, Halliday, Glenda, Hannan, Anthony J., Harrer, Stefan, Harvey, Alan, Hatherly, Chris, Hickie, Ian B., Kennett, Jeanette, Kiernan, Matthew, Kilpatrick, Trevor, Kiral-Kornek, Isabell, Korgaonkar, Mayuresh S., Lawrence, Andrew J., Leventer, Rick, Levy, Neil, Licinio, Julio, Lovell, Nigel, Mackellar, Geoff, Malcolm, Lynne, Mason, Alice, Mattingley, Jason B., Medland, Sarah E., Michie, Patricia T., Nithianantharajah, Jess, Parker, John, Payne, Jonathan M., Poole-Warren, Laura, Sah, Pankaj, Sarnyai, Zoltan, Schofield, Peter R., Shimoni, Olga, Shum, David H.K., Silk, Tim, Slee, Mark, Smith, Ashleigh E., Soulis, Tina, Sriram, Sharath, Stuart, Greg J., Tapson, Jonathan, Thompson, Matthew B., van Schaik, André, Vincent, Nicole A., Vissel, Bryce, Waters, Allison

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Comprehensive Control of Human Papillomavirus Infections and Related Diseases von Bosch, F. Xavier, Broker, Thomas R, Forman, David, Moscicki, Anna-Barbara, Gillison, Maura L, Doorbar, John, Stern, Peter L, Stanley, Margaret, Arbyn, Marc, Poljak, Mario, Cuzick, Jack, Castle, Philip E, Schiller, John T, Markowitz, Lauri E, Fisher, William A, Canfell, Karen, Denny, Lynette A, Franco, Eduardo L, Steben, Marc, Kane, Mark A, Schiffman, Mark, Meijer, Chris J.L.M, Sankaranarayanan, Rengaswamy, Castellsagué, Xavier, Kim, Jane J, Brotons, Maria, Alemany, Laia, Albero, Ginesa, Diaz, Mireia, Sanjosé, Silvia de

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Behaviour genetic analyses of reading and spelling: A component processes approach von Bates, Timothy C., Castles, Anne, Coltheart, Max, Gillespie, Nathan, Wright, Margie, Martin, Nicholas G.

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Can contrast sensitivity functions in dyslexia be explained by inattention rather than a magnocellular deficit? von Stuart, Geoffrey W, McAnally, Ken I, Castles, Anne

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Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17 von Bates, Timothy C, Luciano, Michelle, Castles, Anne, Coltheart, Max, Wright, Margaret J, Martin, Nicholas G

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Contrast sensitivity in subgroups of developmental dyslexia von Williams, Monica J., Stuart, Geoffrey W., Castles, Anne, McAnally, Ken I.

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Genetic and Environmental Bases of Reading and Spelling: A Unified Genetic Dual Route Model von Bates, Timothy C, Castles, Anne, Luciano, Michelle, Wright, Margaret J, Coltheart, Max, Martin, Nicholas G

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Cognitive modelling and the behaviour genetics of reading von Castles, Anne, Bates, Timothy, Coltheart, Max, Luciano, Michelle, Martin, Nicholas G.

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Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17 von Bates, Timothy C, Luciano, Michelle, Castles, Anne, Coltheart, Max, Wright, Margaret J, Martin, Nicholas G

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Original Article: A Haplotype Spanning KIAA0319 and TTRAP Is Associated with Normal Variation in Reading and Spelling Ability von Luciano, Michelle, Lind, Penelope A, Duffy, David L, Castles, Anne, Wright, Margaret J, Montgomery, Grant W, Martin, Nicholas G, Bates, Timothy C

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Morphological Processing and Visual Word Recognition Evidence from Acquired Dyslexia von Castles Max Coltheart Greg Savage Andree Bates Lauren Reid, Anne

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