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Number of items: 86.

Weiner, Daniel J, Wigdor, Emilie M, Ripke, Stephan, Walters, Raymond K, Kosmicki, Jack A, Grove, Jakob, Samocha, Kaitlin E, Goldstein, Jacqueline I, Okbay, Aysu, Bybjerg-Grauholm, Jonas, Werge, Thomas, Hougaard, David M, Taylor, Jacob, Bækvad-Hansen, Marie, Dumont, Ashley, Hansen, Christine, Hansen, Thomas F, Howrigan, Daniel, Mattheisen, Manuel, Moran, Jennifer, Mors, Ole, Nordentoft, Merete, Nørgaard-Pedersen, Bent, Poterba, Timothy, Poulsen, Jesper, Stevens, Christine, Anttila, Verneri, Holmans, Peter Alan, Huang, Hailiang, Klei, Lambertus, Lee, Phil H, Medland, Sarah E, Neale, Benjamin, Weiss, Lauren A, Zwaigenbaum, Lonnie, Yu, Timothy W, Wittemeyer, Kerstin, Willsey, A Jeremy, Wijsman, Ellen M, Wassink, Thomas H, Waltes, Regina, Walsh, Christopher A, Wallace, Simon, Vorstman, Jacob A S, Vieland, Veronica J, Vicente, Astrid M, van Engeland, Herman, Tsang, Kathryn, Thompson, Ann P, Szatmari, Peter, Svantesson, Oscar, Steinberg, Stacy, Stefansson, Kari, Stefansson, Hreinn, State, Matthew W, Soorya, Latha, Silagadze, Teimuraz, Scherer, Stephen W, Schellenberg, Gerard D, Sandin, Sven, Saemundsen, Evald, Rouleau, Guy A, Rogé, Bernadette, Roeder, Kathryn, Roberts, Wendy, Reichert, Jennifer, Reichenberg, Abraham, Rehnström, Karola, Regan, Regina, Poustka, Fritz, Poultney, Christopher S, Piven, Joseph, Pinto, Dalila, Pericak-Vance, Margaret A, Pejovic-Milovancevic, Milica, Pedersen, Marianne G, Pedersen, Carsten B, Paterson, Andrew D, Parr, Jeremy R, Pagnamenta, Alistair T, Oliveira, Guiomar, Nurnberger, John I, Nordentoft, Merete, Murtha, Michael T, Mouga, Susana, Mors, Ole, Morrow, Eric M, De Luca, Daniel Moreno, Monaco, Anthony P, Minshew, Nancy, Merikangas, Alison, McMahon, William M, McGrew, Susan G, Mattheisen, Manuel, Martsenkovsky, Igor, Martin, Donna M, Mane, Shrikant M, Magnusson, Pall, Magalhaes, Tiago, Maestrini, Elena, Lowe, Jennifer K, Lord, Catherine, Levitt, Pat, Martin, Christa Lese, Ledbetter, David H, Leboyer, Marion, Le Couteur, Ann S, Ladd-Acosta, Christine, Kolevzon, Alexander, Klauck, Sabine M, Jacob, Suma, Iliadou, Bozenna, Hultman, Christina M, Hertz-Picciotto, Irva, Hendren, Robert, Hansen, Christine S, Haines, Jonathan L, Guter, Stephen J, Grice, Dorothy E, Green, Jonathan M, Green, Andrew, Goldberg, Arthur P, Gillberg, Christopher, Gilbert, John, Gallagher, Louise, Freitag, Christine M, Fombonne, Eric, Folstein, Susan E, Fernandez, Bridget, Fallin, M Daniele, Ercan-Sencicek, A Gulhan, Ennis, Sean, Duque, Frederico, Duketis, Eftichia, Delorme, Richard, De Rubeis, Silvia, De Jonge, Maretha V, Dawson, Geraldine, Cuccaro, Michael L, Correia, Catarina T, Conroy, Judith, Conceição, Inês C, Chiocchetti, Andreas G, Celestino-Soper, Patrícia B S, Casey, Jillian, Cantor, Rita M, Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F, Bölte, Sven, Bolshakova, Nadia, Betancur, Catalina, Bernier, Raphael, Beaudet, Arthur L, Battaglia, Agatino, Bal, Vanessa H, Baird, Gillian, Bailey, Anthony J, Bækvad-Hansen, Marie, Bader, Joel S, Bacchelli, Elena, Anagnostou, Evdokia, Amaral, David, Almeida, Joana, Buxbaum, Joseph D, Chakravarti, Aravinda, Cook, Edwin H, Coon, Hilary, Geschwind, Daniel H, Gill, Michael, Hakonarson, Hakon, Hallmayer, Joachim, Palotie, Aarno, Santangelo, Susan, Sutcliffe, James S, Arking, Dan E, Skuse, David, Devlin, Bernie, Anney, Richard, Sanders, Stephan J, Bishop, Somer, Mortensen, Preben Bo, Børglum, Anders D, Smith, George Davey, Daly, Mark J and Robinson, Elise B 2017. Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. Nature Genetics 49 (7) , pp. 978-985. 10.1038/ng.3863
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Vorstman, Jacob A. S., Parr, Jeremy R., Moreno-De-Luca, Daniel, Anney, Richard, Nurnberger Jr, John I. and Hallmayer, Joachim F. 2017. Autism genetics: opportunities and challenges for clinical translation. Nature Reviews Genetics 18 (6) , pp. 362-376. 10.1038/nrg.2017.4
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Connolly, Siobhan, Anney, Richard, Gallagher, Louise and Heron, Elizabeth A. 2017. A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3. European Journal of Human Genetics 25 (2) , pp. 234-239. 10.1038/ejhg.2016.153
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Cosgrove, D, Harold, D, Mothersill, O, Anney, Richard, Hill, Martin, Bray, Nicholas, Blokland, G, Petryshen, T, Donnelly, Peter, Bates, Lesley, Barroso, Ines, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Deloukas, Panos, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S, Mathew, Christopher G, Palmer, Colin N A, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas W, Spencer, Chris C A, Band, Gavin, Bellenguez, Céline, Freeman, Colin, Hellenthal, Garrett, Giannoulatou, Eleni, Hopkins, Lucinda, Pirinen, Matti, Pearson, Richard, Strange, Amy, Su, Zhan, Vukcevic, Damjan, Langford, Cordelia, Hunt, Sarah E, Edkins, Sarah, Gwilliam, Rhian, Blackburn, Hannah, Bumpstead, Suzannah J, Dronov, Serge, Gillman, Matthew, Gray, Emma, Hammond, Naomi, Jayakumar, Alagurevathi, McCann, Owen T, Liddle, Jennifer, Potter, Simon C, Ravindrarajah, Radhi, Ricketts, Michelle, Waller, Matthew, Weston, PaulWeston, Widaa, SaraWidaa, Whittaker, Pamela, Richards, Alexander, Mantripragada, Kiran, Owen, Michael, O'Donovan, Michael, Gill, M, Corvin, A, Morris, D W and Donohoe, G 2017. MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls. Translational Psychiatry 7 (1) , e1012. 10.1038/tp.2016.286
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Mooney, Michael A., McWeeney, Shannon K., Faraone, Stephen, Hinney, Anke, Hebebrand, Johannes, Nigg, Joel T., Wilmot, Beth, Thapar, Anita, Martin, Joanna, O'Donovan, Michael Conlon, Owen, Michael John, Williams, Nigel Melville, Anney, Richard, Langley, Kate, Holmans, Peter Alan and German ADHD GWAS Group, 2016. Pathway analysis in attention deficit hyperactivity disorder: an ensemble approach. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 (6) , pp. 815-826. 10.1002/ajmg.b.32446

Coleman, Ciara, Quinn, Emma M., Ryan, Anthony W., Conroy, Judith, Trimble, Valerie, Mahmud, Nasir, Kennedy, Nicholas, Corvin, Aiden P., Morris, Derek W., Donohoe, Gary, O'Morain, Colm, MacMathuna, Padraic, Byrnes, Valerie, Kiat, Clifford, Trynka, Gosia, Wijmenga, Cisca, Kelleher, Dermot, Ennis, Sean, Anney, Richard and McManus, Ross 2016. Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci. European Journal of Human Genetics 24 (2) , pp. 291-297. 10.1038/ejhg.2015.87
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Merikangas, A. K., Segurado, R., Heron, E. A., Anney, Richard, Paterson, A. D., Cook, E. H., Pinto, D., Scherer, S. W., Szatmari, P., Gill, M., Corvin, A. P. and Gallagher, L. 2015. The phenotypic manifestations of rare genic CNVs in autism spectrum disorder. Molecular Psychiatry 20 (11) , pp. 1366-1372. 10.1038/mp.2014.150

Walter, Klaudia, Min, Josine L., Huang, Jie, Crooks, Lucy, Memari, Yasin, McCarthy, Shane, Perry, John R. B., Xu, ChangJiang, Futema, Marta, Lawson, Daniel, Iotchkova, Valentina, Schiffels, Stephan, Hendricks, Audrey E., Danecek, Petr, Li, Rui, Floyd, James, Wain, Louise V., Barroso, Inês, Humphries, Steve E., Hurles, Matthew E., Zeggini, Eleftheria, Barrett, Jeffrey C., Plagnol, Vincent, Brent Richards, J., Greenwood, Celia M. T., Timpson, Nicholas J., Durbin, Richard, Soranzo, Nicole, Bala, Senduran, Clapham, Peter, Coates, Guy, Cox, Tony, Daly, Allan, Danecek, Petr, Du, Yuanping, Durbin, Richard, Edkins, Sarah, Ellis, Peter, Flicek, Paul, Guo, Xiaosen, Guo, Xueqin, Huang, Liren, Jackson, David K., Joyce, Chris, Keane, Thomas, Kolb-Kokocinski, Anja, Langford, Cordelia, Li, Yingrui, Liang, Jieqin, Lin, Hong, Liu, Ryan, Maslen, John, McCarthy, Shane, Muddyman, Dawn, Quail, Michael A., Stalker, Jim, Sun, Jianping, Tian, Jing, Wang, Guangbiao, Wang, Jun, Wang, Yu, Wong, Kim, Zhang, Pingbo, Barroso, Inês, Birney, Ewan, Boustred, Chris, Chen, Lu, Clement, Gail, Cocca, Massimiliano, Danecek, Petr, Davey Smith, George, Day, Ian N. M., Day-Williams, Aaron, Down, Thomas, Dunham, Ian, Durbin, Richard, Evans, David M., Gaunt, Tom R., Geihs, Matthias, Greenwood, Celia M. T., Hart, Deborah, Hendricks, Audrey E., Howie, Bryan, Huang, Jie, Hubbard, Tim, Hysi, Pirro, Iotchkova, Valentina, Jamshidi, Yalda, Karczewski, Konrad J., Kemp, John P., Lachance, Genevieve, Lawson, Daniel, Lek, Monkol, Lopes, Margarida, MacArthur, Daniel G., Marchini, Jonathan, Mangino, Massimo, Mathieson, Iain, McCarthy, Shane, Memari, Yasin, Metrustry, Sarah, Min, Josine L., Moayyeri, Alireza, Muddyman, Dawn, Northstone, Kate, Panoutsopoulou, Kalliope, Paternoster, Lavinia, Perry, John R. B., Quaye, Lydia, Brent Richards, J., Ring, Susan, Ritchie, Graham R. S., Schiffels, Stephan, Shihab, Hashem A., Shin, So-Youn, Small, Kerrin S., Soler Artigas, María, Soranzo, Nicole, Southam, Lorraine, Spector, Timothy D., St Pourcain, Beate, Surdulescu, Gabriela, Tachmazidou, Ioanna, Timpson, Nicholas J., Tobin, Martin D., Valdes, Ana M., Visscher, Peter M., Wain, Louise V., Walter, Klaudia, Ward, Kirsten, Wilson, Scott G., Wong, Kim, Yang, Jian, Zeggini, Eleftheria, Zhang, Feng, Zheng, Hou-Feng, Anney, Richard, Ayub, Muhammad, Barrett, Jeffrey C., Blackwood, Douglas, Bolton, Patrick F., Breen, Gerome, Collier, David A., Craddock, Nicholas John, Crooks, Lucy, Curran, Sarah, Curtis, David, Durbin, Richard, Gallagher, Louise, Geschwind, Daniel, Gurling, Hugh, Holmans, Peter Alan, Lee, Irene, Lönnqvist, Jouko, McCarthy, Shane, McGuffin, Peter, McIntosh, Andrew M., McKechanie, Andrew G., McQuillin, Andrew, Morris, James, Muddyman, Dawn, O'Donovan, Michael Conlon, Owen, Michael John, Palotie, Aarno, Parr, Jeremy R., Paunio, Tiina, Pietilainen, Olli, Rehnström, Karola, Sharp, Sally I., Skuse, David, St Clair, David, Suvisaari, Jaana, Walters, James Tynan Rhys, Williams, Hywel J., Barroso, Inês, Bochukova, Elena, Bounds, Rebecca, Dominiczak, Anna, Durbin, Richard, Farooqi, I. Sadaf, Hendricks, Audrey E., Keogh, Julia, Marenne, Gaëlle, McCarthy, Shane, Morris, Andrew, Muddyman, Dawn, O'Rahilly, Stephen, Porteous, David J., Smith, Blair H., Tachmazidou, Ioanna, Wheeler, Eleanor, Zeggini, Eleftheria, Al Turki, Saeed, Anderson, Carl A., Antony, Dinu, Barroso, Inês, Beales, Phil, Bentham, Jamie, Bhattacharya, Shoumo, Calissano, Mattia, Carss, Keren, Chatterjee, Krishna, Cirak, Sebahattin, Cosgrove, Catherine, Durbin, Richard, Fitzpatrick, David R., Floyd, James, Reghan Foley, A., Franklin, Christopher S., Futema, Marta, Grozeva, Detelina, Humphries, Steve E., Hurles, Matthew E., McCarthy, Shane, Mitchison, Hannah M., Muddyman, Dawn, Muntoni, Francesco, O'Rahilly, Stephen, Onoufriadis, Alexandros, Parker, Victoria, Payne, Felicity, Plagnol, Vincent, Lucy Raymond, F., Roberts, Nicola, Savage, David B., Scambler, Peter, Schmidts, Miriam, Schoenmakers, Nadia, Semple, Robert K., Serra, Eva, Spasic-Boskovic, Olivera, Stevens, Elizabeth, van Kogelenberg, Margriet, Vijayarangakannan, Parthiban, Walter, Klaudia, Williamson, Kathleen A., Wilson, Crispian, Whyte, Tamieka, Ciampi, Antonio, Greenwood, Celia M. T., Hendricks, Audrey E., Li, Rui, Metrustry, Sarah, Oualkacha, Karim, Tachmazidou, Ioanna, Xu, ChangJiang, Zeggini, Eleftheria, Bobrow, Martin, Bolton, Patrick F., Durbin, Richard, Fitzpatrick, David R., Griffin, Heather, Hurles, Matthew E., Kaye, Jane, Kennedy, Karen, Kent, Alastair, Muddyman, Dawn, Muntoni, Francesco, Lucy Raymond, F., Semple, Robert K., Smee, Carol, Spector, Timothy D., Timpson, Nicholas J., Charlton, Ruth, Ekong, Rosemary, Futema, Marta, Humphries, Steve E., Khawaja, Farrah, Lopes, Luis R., Migone, Nicola, Payne, Stewart J., Plagnol, Vincent, Pollitt, Rebecca C., Povey, Sue, Ridout, Cheryl K., Robinson, Rachel L., Scott, Richard H., Shaw, Adam, Syrris, Petros, Taylor, Rohan, Vandersteen, Anthony M., Barrett, Jeffrey C., Barroso, Inês, Davey Smith, George, Durbin, Richard, Farooqi, I. Sadaf, Fitzpatrick, David R., Hurles, Matthew E., Kaye, Jane, Kennedy, Karen, Langford, Cordelia, McCarthy, Shane, Muddyman, Dawn, Owen, Michael J., Palotie, Aarno, Brent Richards, J., Soranzo, Nicole, Spector, Timothy D., Stalker, Jim, Timpson, Nicholas J., Zeggini, Eleftheria, Amuzu, Antoinette, Pablo Casas, Juan, Chambers, John C., Cocca, Massimiliano, Dedoussis, George, Gambaro, Giovanni, Gasparini, Paolo, Gaunt, Tom R., Huang, Jie, Iotchkova, Valentina, Isaacs, Aaron, Johnson, Jon, Kleber, Marcus E., Kooner, Jaspal S., Langenberg, Claudia, Luan, Jian'an, Malerba, Giovanni, März, Winfried, Matchan, Angela, Min, Josine L., Morris, Richard, Nordestgaard, Børge G., Benn, Marianne, Ring, Susan, Scott, Robert A., Soranzo, Nicole, Southam, Lorraine, Timpson, Nicholas J., Toniolo, Daniela, Traglia, Michela, Tybjaerg-Hansen, Anne, van Duijn, Cornelia M., van Leeuwen, Elisabeth M., Varbo, Anette, Whincup, Peter, Zaza, Gianluigi, Zeggini, Eleftheria and Zhang, Weihua 2015. The UK10K project identifies rare variants in health and disease. Nature 526 , pp. 82-90.

Ning, Zhenfei, McLellan, Andrew S., Ball, Melanie, Wynne, Freda, O'Neill, Cora, Mills, Walter, Quinn, John P., Kleinjan, Dirk A., Anney, Richard, Carmody, Ruaidhre J., O'Keeffe, Gerard and Moore, Tom 2015. Regulation of SPRY3 by X chromosome and PAR2-linked promoters in an autism susceptibility region. Human Molecular Genetics 24 (18) , pp. 5126-5141. 10.1093/hmg/ddv231

Huang, Jie, Howie, Bryan, McCarthy, Shane, Memari, Yasin, Walter, Klaudia, Min, Josine L., Danecek, Petr, Malerba, Giovanni, Trabetti, Elisabetta, Zheng, Hou-Feng, Al Turki, Saeed, Amuzu, Antoinette, Anderson, Carl A., Anney, Richard, Antony, Dinu, Artigas, María Soler, Ayub, Muhammad, Bala, Senduran, Barrett, Jeffrey C., Barroso, Inês, Beales, Phil, Benn, Marianne, Bentham, Jamie, Bhattacharya, Shoumo, Birney, Ewan, Blackwood, Douglas, Bobrow, Martin, Bochukova, Elena, Bolton, Patrick F., Bounds, Rebecca, Boustred, Chris, Breen, Gerome, Calissano, Mattia, Carss, Keren, Pablo Casas, Juan, Chambers, John C., Charlton, Ruth, Chatterjee, Krishna, Chen, Lu, Ciampi, Antonio, Cirak, Sebahattin, Clapham, Peter, Clement, Gail, Coates, Guy, Cocca, Massimiliano, Collier, David A., Cosgrove, Catherine, Cox, Tony, Craddock, Nicholas John, Crooks, Lucy, Curran, Sarah, Curtis, David, Daly, Allan, Day, Ian N. M., Day-Williams, Aaron, Dedoussis, George, Down, Thomas, Du, Yuanping, van Duijn, Cornelia M., Dunham, Ian, Edkins, Sarah, Ekong, Rosemary, Ellis, Peter, Evans, David M., Farooqi, I. Sadaf, Fitzpatrick, David R., Flicek, Paul, Floyd, James, Foley, A. Reghan, Franklin, Christopher S., Futema, Marta, Gallagher, Louise, Gasparini, Paolo, Gaunt, Tom R., Geihs, Matthias, Geschwind, Daniel, Greenwood, Celia, Griffin, Heather, Grozeva, Detelina, Guo, Xiaosen, Guo, Xueqin, Gurling, Hugh, Hart, Deborah, Hendricks, Audrey E., Holmans, Peter Alan, Huang, Liren, Hubbard, Tim, Humphries, Steve E., Hurles, Matthew E., Hysi, Pirro, Iotchkova, Valentina, Isaacs, Aaron, Jackson, David K., Jamshidi, Yalda, Johnson, Jon, Joyce, Chris, Karczewski, Konrad J., Kaye, Jane, Keane, Thomas, Kemp, John P., Kennedy, Karen, Kent, Alastair, Keogh, Julia, Khawaja, Farrah, Kleber, Marcus E., van Kogelenberg, Margriet, Kolb-Kokocinski, Anja, Kooner, Jaspal S., Lachance, Genevieve, Langenberg, Claudia, Langford, Cordelia, Lawson, Daniel, Lee, Irene, van Leeuwen, Elisabeth M., Lek, Monkol, Li, Rui, Li, Yingrui, Liang, Jieqin, Lin, Hong, Liu, Ryan, Lönnqvist, Jouko, Lopes, Luis R., Lopes, Margarida, Luan, Jian'an, MacArthur, Daniel G., Mangino, Massimo, Marenne, Gaëlle, März, Winfried, Maslen, John, Matchan, Angela, Mathieson, Iain, McGuffin, Peter, McIntosh, Andrew M., McKechanie, Andrew G., McQuillin, Andrew, Metrustry, Sarah, Migone, Nicola, Mitchison, Hannah M., Moayyeri, Alireza, Morris, James, Morris, Richard, Muddyman, Dawn, Muntoni, Francesco, Nordestgaard, Børge G., Northstone, Kate, O'Donovan, Michael Conlon, O'Rahilly, Stephen, Onoufriadis, Alexandros, Oualkacha, Karim, Owen, Michael John, Palotie, Aarno, Panoutsopoulou, Kalliope, Parker, Victoria, Parr, Jeremy R., Paternoster, Lavinia, Paunio, Tiina, Payne, Felicity, Payne, Stewart J., Perry, John R. B., Pietilainen, Olli, Plagnol, Vincent, Pollitt, Rebecca C., Povey, Sue, Quail, Michael A., Quaye, Lydia, Raymond, Lucy, Rehnström, Karola, Ridout, Cheryl K., Ring, Susan, Ritchie, Graham R. S., Roberts, Nicola, Robinson, Rachel L., Savage, David B., Scambler, Peter, Schiffels, Stephan, Schmidts, Miriam, Schoenmakers, Nadia, Scott, Richard H., Scott, Robert A., Semple, Robert K., Serra, Eva, Sharp, Sally I., Shaw, Adam, Shihab, Hashem A., Shin, So-Youn, Skuse, David, Small, Kerrin S., Smee, Carol, Smith, George Davey, Southam, Lorraine, Spasic-Boskovic, Olivera, Spector, Timothy D., St Clair, David, St Pourcain, Beate, Stalker, Jim, Stevens, Elizabeth, Sun, Jianping, Surdulescu, Gabriela, Suvisaari, Jaana, Syrris, Petros, Tachmazidou, Ioanna, Taylor, Rohan, Tian, Jing, Tobin, Martin D., Toniolo, Daniela, Traglia, Michela, Tybjaerg-Hansen, Anne, Valdes, Ana M., Vandersteen, Anthony M., Varbo, Anette, Vijayarangakannan, Parthiban, Visscher, Peter M., Wain, Louise V., Walters, James Tynan Rhys, Wang, Guangbiao, Wang, Jun, Wang, Yu, Ward, Kirsten, Wheeler, Eleanor, Whincup, Peter, Whyte, Tamieka, Williams, Hywel J., Williamson, Kathleen A., Wilson, Crispian, Wilson, Scott G., Wong, Kim, Xu, ChangJiang, Yang, Jian, Zaza, Gianluigi, Zeggini, Eleftheria, Zhang, Feng, Zhang, Pingbo, Zhang, Weihua, Gambaro, Giovanni, Richards, J. Brent, Durbin, Richard, Timpson, Nicholas J., Marchini, Jonathan and Soranzo, Nicole 2015. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel. Nature Communications 6 , 8111. 10.1038/ncomms9111

Schmidts, Miriam, Hou, Yuqing, Cortés, Claudio R., Mans, Dorus A., Huber, Celine, Boldt, Karsten, Patel, Mitali, van Reeuwijk, Jeroen, Plaza, Jean-Marc, van Beersum, Sylvia E. C., Yap, Zhi Min, Letteboer, Stef J. F., Taylor, S. Paige, Herridge, Warren, Johnson, Colin A., Scambler, Peter J., Ueffing, Marius, Kayserili, Hulya, Krakow, Deborah, King, Stephen M., Beales, Philip L., Al-Gazali, Lihadh, Wicking, Carol, Cormier-Daire, Valerie, Roepman, Ronald, Mitchison, Hannah M., Witman, George B., Al-Turki, Saeed, Anderson, Carl, Anney, Richard, Antony, Dinu, Asimit, Jennifer, Ayub, Mohammad, Barrett, Jeff, Barroso, Inês, Bentham, Jamie, Bhattacharya, Shoumo, Blackwood, Douglas, Bobrow, Martin, Bochukova, Elena, Bolton, Patrick, Boustred, Chris, Breen, Gerome, Brion, Marie-Jo, Brown, Andrew, Calissano, Mattia, Carss, Keren, Chatterjee, Krishna, Chen, Lu, Cirak, Sebhattin, Clapham, Peter, Clement, Gail, Coates, Guy, Collier, David, Cosgrove, Catherine, Cox, Tony, Craddock, Nicholas John, Crooks, Lucy, Curran, Sarah, Daly, Allan, Danecek, Petr, Smith, George Davey, Day-Williams, Aaron, Day, Ian, Durbin, Richard, Edkins, Sarah, Ellis, Peter, Evans, David, Farooqi, I. Sadaf, Fatemifar, Ghazaleh, Fitzpatrick, David, Flicek, Paul, Floyd, Jamie, Foley, A. Reghan, Franklin, Chris, Futema, Marta, Gallagher, Louise, Gaunt, Tom, Geschwind, Daniel, Greenwood, Celia, Grozeva, Detelina, Guo, Xiaosen, Gurling, Hugh, Hart, Deborah, Hendricks, Audrey, Holmans, Peter Alan, Huang, Jie, Humphries, Steve E., Hurles, Matt, Hysi, Pirro, Jackson, David, Jamshidi, Yalda, Jewell, David, Chris, Joyce, Kaye, Jane, Keane, Thomas, Kemp, John, Kennedy, Karen, Kent, Alastair, Kolb-Kokocinski, Anja, Lachance, Genevieve, Langford, Cordelia, Lee, Irene, Li, Rui, Li, Yingrui, Ryan, Liu, Lönnqvist, Jouko, Lopes, Margarida, MacArthur, Daniel G., Massimo, Mangino, Marchini, Jonathan, Maslen, John, McCarthy, Shane, McGuffin, Peter, McIntosh, Andrew, McKechanie, Andrew, McQuillin, Andrew, Memari, Yasin, Metrustry, Sarah, Min, Josine, Moayyeri, Alireza, Morris, James, Muddyman, Dawn, Muntoni, Francesco, Northstone, Kate, O'Donovan, Michael Conlon, O?Rahilly, Stephen, Onoufriadis, Alexandros, Oualkacha, Karim, Owen, Michael John, Palotie, Aarno, Panoutsopoulou, Kalliope, Parker, Victoria, Parr, Jeremy, Paternoster, Lavinia, Paunio, Tiina, Payne, Felicity, Perry, John, Pietilainen, Olli, Plagnol, Vincent, Quail, Michael A., Quaye, Lydia, Raymond, Lucy, Rehnström, Karola, Brent Richards, J., Ring, Sue, Ritchie, Graham R S, Savage, David B., Schoenmakers, Nadia, Semple, Robert K., Serra, Eva, Shihab, Hashem, Shin, So-Youn, Skuse, David, Small, Kerrin, Smee, Carol, Soler, Artigas María, Soranzo, Nicole, Southam, Lorraine, Spector, Tim, St Pourcain, Beate, St. Clair, David, Stalker, Jim, Surdulescu, Gabriela, Suvisaari, Jaana, Tachmazidou, Ioanna, Tian, Jing, Timpson, Nic, Tobin, Martin, Valdes, Ana, van Kogelenberg, Margriet, Vijayarangakannan, Parthiban, Wain, Louise, Walter, Klaudia, Wang, Jun, Ward, Kirsten, Wheeler, Ellie, Whittall, Ros, Williams, Hywel, Williamson, Kathy, Wilson, Scott G., Wong, Kim, Whyte, Tamieka, ChangJiang, Xu, Zeggini, Eleftheria, Zhang, Feng and Zheng, Hou-Feng 2015. TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport. Nature Communications 6 , 7074. 10.1038/ncomms8074

Connolly, S., Anney, Richard, Gallagher, L. and Heron, E. 2015. Investigation of assortative mating in autism spectrum disorders [Conference Abstract]. Human Heredity 79 (1) , p. 31. 10.1159/000381109

O'Dushlaine, Colm, Rossin, Lizzy, Lee, Phil H, Duncan, Laramie, Parikshak, Neelroop N, Newhouse, Stephen, Ripke, Stephan, Neale, Benjamin M, Purcell, Shaun M, Posthuma, Danielle, Nurnberger, John I, Lee, S Hong, Faraone, Stephen V, Perlis, Roy H, Mowry, Bryan J, Thapar, Anita, Goddard, Michael E, Witte, John S, Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A, Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E, Asherson, Philip, Azevedo, Maria H, Backlund, Lena, Badner, Judith A, Bailey, Anthony J, Banaschewski, Tobias, Barchas, Jack D, Barnes, Michael R, Barrett, Thomas B, Bass, Nicholas, Battaglia, Agatino, Bauer, Michael, Bayés, Mònica, Bellivier, Frank, Bergen, Sarah E, Berrettini, Wade, Betancur, Catalina, Bettecken, Thomas, Biederman, Joseph, Binder, Elisabeth B, Black, Donald W, Blackwood, Douglas H R, Bloss, Cinnamon S, Boehnke, Michael, Boomsma, Dorret I, Breuer, René, Bruggeman, Richard, Cormican, Paul, Buccola, Nancy G, Buitelaar, Jan 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Cochrane, Lynne E., Tansey, Katherine E., Gill, Michael, Gallagher, Louise and Anney, Richard 2010. Lack of association between markers in the ITGA3, ITGAV, ITGA6 and ITGB3 and autism in an Irish sample. Autism Research 3 (6) , pp. 342-344. 10.1002/aur.157

Merikangas, Alison K., Heron, Elizabeth A., Anney, Richard, Corvin, Aiden P. and Gallagher, Louise 2010. Investigating the association between rare copy number variation and developmental anomalies in autism spectrum disorders [Conference Abstract]. Genetic Epidemiology 34 (8) , p. 929. 10.1002/gepi.20553

Anney, Richard, Klei, Lambertus, Pinto, Dalila, Regan, Regina, Conroy, Judith, Magalhaes, Tiago R., Correia, Catarina, Abrahams, Brett S., Sykes, Nuala, Pagnamenta, Alistair T., Almeida, Joana, Bacchelli, Elena, Bailey, Anthony J., Baird, Gillian, Battaglia, Agatino, Berney, Tom, Bolshakova, Nadia, Boelte, Sven, Bolton, Patrick F., Bourgeron, Thomas, Brennan, Sean, Brian, Jessica, Carson, Andrew R., Casallo, Guillermo, Casey, Jillian, Chu, Su H., Cochrane, Lynne, Corsello, Christina, Crawford, Emily L., Crossett, Andrew, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Drmic, Irene, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A., Folstein, Susan E., Fombonne, Eric, Freitag, Christine M., Gilbert, John, Gillberg, Christopher, Glessner, Joseph T., Goldberg, Jeremy, Green, Jonathan, Guter, Stephen J., Hakonarson, Hakon, Heron, Elizabeth A., Hill, Matthew, Holt, Richard, Howe, Jennifer L., Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Kim, Cecilia, Klauck, Sabine M., Kolevzon, Alexander, Korvatska, Olena, Kustanovich, Vlad, Lajonchere, Clara M., Lamb, Janine A., Laskawiec, Magdalena, Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L., Lionel, Anath C., Liu, Xiao-Qing, Lord, Catherine, Lotspeich, Linda, Lund, Sabata C., Maestrini, Elena, Mahoney, William, Mantoulan, Carine, Marshall, Christian R., McConachie, Helen, McDougle, Christopher J., McGrath, Jane, McMahon, William M., Melhem, Nadine M., Merikangas, Alison, Migita, Ohsuke, Minshew, Nancy J., Mirza, Ghazala K., Munson, Jeff, Nelson, Stanley F., Noakes, Carolyn, Noor, Abdul, Nygren, Gudrun, Oliveira, Guiomar, Papanikolaou, Katerina, Parr, Jeremy R., Parrini, Barbara, Paton, Tara, Pickles, Andrew, Piven, Joseph, osey, David J., Poustka, Annemarie, Poustka, Fritz, Prasad, Aparna, Ragoussis, Jiannis, Renshaw, Katy, Rickaby, Jessica, Roberts, Wendy, Roeder, Kathryn, Roge, Bernadette, Rutter, Michael L., Bierut, Laura J., Rice, John P., Salt, Jeff, Sansom, Katherine, Sato, Daisuke, Segurado, Ricardo, Senman, Lili, Shah, Naisha, Sheffield, Val C., Soorya, Latha, Sousa, Ines, Stoppioni, Vera, Strawbridge, Christina, Tancredi, Raffaella, Tansey, Katherine, Thiruvahindrapduram, Bhooma, Thompson, Ann P., Thomson, Susanne, Tryfon, Ana, Tsiantis, John, Van Engeland, Herman, Vincent, John B., Volkmar, Fred, Wallace, Simon, Wang, Kai, Wang, Zhouzhi, Wassink, Thomas H., Wing, Kirsty, Wittemeyer, Kerstin, Wood, Shawn, Yaspan, Brian L., Zurawiecki, Danielle, Zwaigenbaum, Lonnie, Betancur, Catalina, Buxbaum, Joseph D., Cantor, Rita M., Cook, Edwin H., Coon, Hilary, Cuccaro, Michael L., Gallagher, Louise, Geschwind, Daniel H., Gill, Michael, Haines, Jonathan L., Miller, Judith, Monaco, Anthony P., Nurnberger, John I., Paterson, Andrew D., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Scherer, Stephen W., Sutcliffe, James S., Szatmari, Peter, Vicente, Astrid M., Vieland, Veronica J., Wijsman, Ellen M., Devlin, Bernie, Ennis, Sean and Hallmayer, Joachim 2010. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics 19 (20) , pp. 4072-4082. 10.1093/hmg/ddq307

Hill, M., Anney, Richard, Gill, M. and Hawi, Z. 2010. Functional analysis of intron 8 and 3 ' UTR variable number of tandem repeats of SLC6A3: differential activity of intron 8 variants. Pharmacogenomics Journal 10 (5) , pp. 442-447. 10.1038/tpj.2009.66

Sobanski, Esther, Banaschewski, Tobias, Asherson, Philip, Buitelaar, Jan, Chen, Wai, Franke, Barbara, Holtmann, Martin, Krumm, Bertram, Sergeant, Joseph, Sonuga-Barke, Edmund J. S., Stringaris, Argyris, Taylor, Eric, Anney, Richard, Ebstein, Richard P., Gill, Michael, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Steinhausen, Hans-Christoph and Faraone, Stephen V. 2010. Emotional lability in children and adolescents with attention deficit/hyperactivity disorder (ADHD): clinical correlates and familial prevalence. Journal of Child Psychology and Psychiatry 51 (8) , pp. 915-923. 10.1111/j.1469-7610.2010.02217.x

Pinto, Dalila, Pagnamenta, Alistair T., Klei, Lambertus, Anney, Richard, Merico, Daniele, Regan, Regina, Conroy, Judith, Magalhaes, Tiago R., Correia, Catarina, Abrahams, Brett S., Almeida, Joana, Bacchelli, Elena, Bader, Gary D., Bailey, Anthony J., Baird, Gillian, Battaglia, Agatino, Berney, Tom, Bolshakova, Nadia, Boelte, Sven, Bolton, Patrick F., Bourgeron, Thomas, Brennan, Sean, Brian, Jessica, Bryson, Susan E., Carson, Andrew R., Casallo, Guillermo, Casey, Jillian, Chung, Brian H. Y., Cochrane, Lynne, Corsello, Christina, Crawford, Emily L., Crossett, Andrew, Cytrynbaum, Cheryl, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Drmic, Irene, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A., Folstein, Susan E., Fombonne, Eric, Freitag, Christine M., Gilbert, John, Gillberg, Christopher, Glessner, Joseph T., Goldberg, Jeremy, Green, Andrew, Green, Jonathan, Guter, Stephen J., Hakonarson, Hakon, Heron, Elizabeth A., Hill, Matthew, Holt, Richard, Howe, Jennifer L., Hughes, Gillian, Hus, Vanessa, Igliozzi, Roberta, Kim, Cecilia, Klauck, Sabine M., Kolevzon, Alexander, Korvatska, Olena, Kustanovich, Vlad, Lajonchere, Clara M., Lamb, Janine A., Laskawiec, Magdalena, Leboyer, Marion, Le Couteur, Ann, Leventhal, Bennett L., Lionel, Anath C., Liu, Xiao-Qing, Lord, Catherine, Lotspeich, Linda, Lund, Sabata C., Maestrini, Elena, Mahoney, William, Mantoulan, Carine, Marshall, Christian R., McConachie, Helen, McDougle, Christopher J., McGrath, Jane, McMahon, William M., Merikangas, Alison, Migita, Ohsuke, Minshew, Nancy J., Mirza, Ghazala K., Munson, Jeff, Nelson, Stanley F., Noakes, Carolyn, Noor, Abdul, Nygren, Gudrun, Oliveira, Guiomar, Papanikolaou, Katerina, Parr, Jeremy R., Parrini, Barbara, Paton, Tara, Pickles, Andrew, Pilorge, Marion, Piven, Joseph, Ponting, Chris P., Posey, David J., Poustka, Annemarie, Poustka, Fritz, Prasad, Aparna, Ragoussis, Jiannis, Renshaw, Katy, Rickaby, Jessica, Roberts, Wendy, Roeder, Kathryn, Roge, Bernadette, Rutter, Michael L., Bierut, Laura J., Rice, John P., Salt, Jeff, Sansom, Katherine, Sato, Daisuke, Segurado, Ricardo, Sequeira, Ana F., Senman, Lili, Shah, Naisha, Sheffield, Val C., Soorya, Latha, Sousa, Ines, Stein, Olaf, Sykes, Nuala, Stoppioni, Vera, Strawbridge, Christina, Tancredi, Raffaella, Tansey, Katherine, Thiruvahindrapduram, Bhooma, Thompson, Ann P., Thomson, Susanne, Tryfon, Ana, Tsiantis, John, Van Engeland, Herman, Vincent, John B., Volkmar, Fred, Wallace, Simon, Wang, Kai, Wang, Zhouzhi, Wassink, Thomas H., Webber, Caleb, Weksberg, Rosanna, Wing, Kirsty, Wittemeyer, Kerstin, Wood, Shawn, Wu, Jing, Yaspan, Brian L., Zurawiecki, Danielle, Zwaigenbaum, Lonnie, Buxbaum, Joseph D., Cantor, Rita M., Cook, Edwin H., Coon, Hilary, Cuccaro, Michael L., Devlin, Bernie, Ennis, Sean, Gallagher, Louise, Geschwind, Daniel H., Gill, Michael, Haines, Jonathan L., Hallmayer, Joachim, Miller, Judith, Monaco, Anthony P., Nurnberger, John I., Paterson, Andrew D., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Szatmari, Peter, Vicente, Astrid M., Vieland, Veronica J., Wijsman, Ellen M., Scherer, Stephen W., Sutcliffe, James S. and Betancur, Catalina 2010. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 466 (7304) , pp. 368-372. 10.1038/nature09146

Nijmeijer, Judith S., Arias-Vasquez, Alejandro, Rommelse, Nanda N. J., Altink, Marieke E., Anney, Richard, Asherson, Philip, Banaschewski, Tobias, Buschgens, Cathelijne J. M., Fliers, Ellen A., Gill, Michael, Minderaa, Ruud B., Poustka, Luise, Sergeant, Joseph A., Buitelaar, Jan K., Franke, Barbara, Ebstein, Richard P., Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sonuga-Barke, Edmund J. S., Steinhausen, Hans-Christoph, Faraone, Stephen. V., Hartman, Catharina A. and Hoekstra, Pieter J. 2010. Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach. Journal of the American Academy of Child & Adolescent Psychiatry 49 (7) , pp. 675-685. 10.1016/j.jaac.2010.03.015

Quinn, Emma M., Hill, Matthew, Anney, Richard, Gill, Michael, Corvin, Aiden P. and Morris, Derek W. 2010. Evidence for cis-acting regulation of ANK3 and CACNA1C gene expression. Bipolar Disorders 12 (4) , pp. 440-445. 10.1111/j.1399-5618.2010.00817.x

Tansey, Katherine E., Brookes, Keeley J., Hill, Matthew J., Cochrane, Lynne E., Gill, Michael, Skuse, David, Correia, Catarina, Vicente, Astrid, Kent, Lindsey, Gallagher, Louise and Anney, Richard 2010. Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: Genetic and molecular studies. Neuroscience Letters 474 (3) , pp. 163-167. 10.1016/j.neulet.2010.03.035

Lasky-Su, Jessica, Won, Sungho, Mick, Eric, Anney, Richard, Franke, Barbara, Neale, Benjamin, Biederman, Joseph, Smalley, Susan L., Loo, Sandra K., Todorov, Alexandre, Faraone, Stephen V., Weiss, Scott T. and Lange, Christoph 2010. On genome-wide association studies for family-based designs: an integrative analysis approach combining ascertained family samples with unselected controls. American Journal of Human Genetics 86 (4) , pp. 573-580. 10.1016/j.ajhg.2010.02.019

Olsson, C. A., Foley, D. L., Parkinson-Bates, M., Byrnes, G., McKenzie, M., Patton, G. C., Morley, R., Anney, Richard, Craig, J. M. and Saffery, R. 2010. Prospects for epigenetic research within cohort studies of psychological disorder: A pilot investigation of a peripheral cell marker of epigenetic risk for depression. Biological Psychology 83 (2) , pp. 159-165. 10.1016/j.biopsycho.2009.12.003

Hawi, Z., Kent, L., Hill, M., Anney, Richard, Brookes, K. J., Barry, E., Franke, B., Banaschewski, T., Buitelaar, J., Ebstein, R., Miranda, A., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E. J. S., Steinhausen, H. -C., Faraone, S. V., Asherson, P. and Gill, M. 2010. ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (1) , pp. 97-102. 10.1002/ajmg.b.30960

Neale, Benjamin M., Medland, Sarah, Ripke, Stephan, Anney, Richard, Asherson, Philip, Buitelaar, Jan, Franke, Barbara, Gill, Michael, Kent, Lindsey, Holmans, Peter Alan, Middleton, Frank, Thapar, Anita, Lesch, Klaus-Peter, Daly, Mark, Nguyen, Thuy Trang, Schäfer, Helmut, Steinhausen, Hans-Christoph, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Walitza, Susanne, Freitag, Christine, Meyer, Jobst, Palmason, Haukur, Rothenberger, Aribert, Hawi, Ziarih, Sergeant, Joseph, Roeyers, Herbert, Mick, Eric and Biederman, Joseph 2010. Case-control genome-wide association study of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child & Adolescent Psychiatry 49 (9) , pp. 906-920. 10.1016/j.jaac.2010.06.007

Neale, Benjamin M., Medland, Sarah E., Ripke, Stephan, Asherson, Philip, Franke, Barbara, Lesch, Klaus-Peter, Faraone, Stephen V., Nguyen, Thuy Trang, Schäfer, Helmut, Holmans, Peter Alan, Daly, Mark, Steinhausen, Hans-Christoph, Freitag, Christine, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Walitza, Susanne, Warnke, Andreas, Meyer, Jobst, Palmason, Haukur, Buitelaar, Jan, Vasquez, Alejandro Arias, Lambregts-Rommelse, Nanda, Gill, Michael, Anney, Richard, Langley, Kate, O'Donovan, Michael Conlon, Williams, Nigel Melville, Owen, Michael John, Thapar, Anita, Kent, Lindsey, Sergeant, Joseph, Roeyers, Herbert, Mick, Eric, Biederman, Joseph, Doyle, Alysa, Smalley, Susan, Loo, Sandra, Hakonarson, Hakon, Elia, Josephine, Todorov, Alexandre, Ana, Miranda, Mulas, Fernando, Ebstein, Richard P., Rothenberger, Aribert, Banaschewski, Tobias, Oades, Richard D., Sonuga-Barke, Edmund, McGough, James, Nisenbaum, Laura, Middleton, Frank, Hu, Xiaolan and Nelson, Stan 2010. Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Journal of the American Academy of Child & Adolescent Psychiatry 49 (9) , pp. 884-897. 10.1016/j.jaac.2010.06.008

Sonuga-Barke, Edmund J. S., Oades, Robert D., Psychogiou, Lamprini, Chen, Wai, Franke, Barbara, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard P., Gil, Michael, Anney, Richard, Miranda, Ana, Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans Christoph, Thompson, Margaret, Asherson, Philip and Faraone, Stephen V. 2009. Dopamine and serotonin transporter genotypes moderate sensitivity to maternal expressed emotion: the case of conduct and emotional problems in attention deficit/hyperactivity disorder. Journal of Child Psychology and Psychiatry 50 (9) , pp. 1052-1063. 10.1111/j.1469-7610.2009.02095.x

Anney, Richard and Lasky-Su, J. 2009. S.18.05 Molecular-genetics of aggression and antisocial behaviour in clinical populations [Conference abstract]. European Neuropsychopharmacology 19 , S203-S203. 10.1016/S0924-977X(09)70264-0

Conroy, Judith, Cochrane, Lynne, Anney, Richard, Sutcliffe, James S., Carthy, Paula, Dunlop, Adam, Mullarkey, Marice, O'hlci, Bronagh, Green, Andrew J., Ennis, Sean, Gill, Michael and Gallagher, Louise 2009. Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (4) , pp. 535-544. 10.1002/ajmg.b.30854

Xu, X., Duman, E. A., Anney, Richard, Brookes, K., Franke, B., Zhou, K., Buschgens, C., Chen, W., Christiansen, H., Eisenberg, J., Gabriels, I., Manor, I., Marco, R., Mueller, U. C., Mulligan, A., Rommelse, N., Thompson, M., Uebel, H., Banaschewski, T., Buitelaar, J., Ebstein, R., Gill, M., Miranda, A., Mulas, F., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E. J. S., Steinhausen, H. -C., Taylor, E., Faraone, S. V. and Asherson, P. 2009. No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder [Erratum]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (2) , p. 307. 10.1002/ajmg.b.30921

Mulligan, Aisling, Anney, Richard, O'Regan, Myra, Chen, Wai, Butler, Louise, Fitzgerald, Michael, Buitelaar, Jan, Steinhausen, Hans-Christoph, Rothenberger, Aribert, Minderaa, Ruud, Nijmeijer, Judith, Hoekstra, Pieter J., Oades, Robert D., Roeyers, Herbert, Buschgens, Cathelijne, Christiansen, Hanna, Franke, Barbara, Gabriels, Isabel, Hartman, Catharina, Kuntsi, Jonna, Marco, Rafaela, Meidad, Sheera, Mueller, Ueli, Psychogiou, Lamprini, Rommelse, Nanda, Thompson, Margaret, Uebel, Henrik, Banaschewski, Tobias, Ebstein, Richard, Eisenberg, Jacques, Manor, Iris, Miranda, Ana, Mulas, Fernando, Sergeant, Joseph, Sonuga-Barke, Edmund J. S., Asherson, Phil, Faraone, Stephen V. and Gill, Michael 2009. Autism symptoms in attention-deficit/hyperactivity disorder: a familial trait which correlates with conduct, oppositional defiant, language and motor disorders. Journal of Autism and Developmental Disorders 39 (2) , pp. 197-209. 10.1007/s10803-008-0621-3

Xu, X., Duman, E. A., Anney, Richard, Brookes, K., Franke, B., Zhou, K., Buschgens, C., Chen, W., Christiansen, H., Eisenberg, J., Gabriels, I., Manor, I., Marco, R., Mueller, U. C., Mulligan, A., Rommelse, N., Thompson, M., Uebel, H., Banaschewski, T., Buitelaar, J., Ebstein, R., Gill, M., Miranda, A., Mulas, F., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E. J. S., Steinhausen, H. -C., Taylor, E., Faraone, S. V. and Asherson, P. 2009. No association between two polymorphisms of the serotonin transporter gene and combined type attention deficit hyperactivity disorder [Erratum]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (1) , p. 154. 10.1002/ajmg.b.30892

Lasky-Su, Jessica, Neale, Benjamin M., Franke, Barbara, Anney, Richard, Zhou, Kaixin, Maller, Julian B., Arias Vasquez, Alejandro, Chen, Wai, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Gill, Michael, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund J. S., Steinhausen, Hans Christoph, Taylor, Eric, Daly, Mark, Laird, Nan, Lange, Christoph and Faraone, Stephen V. 2008. Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1345-1354. 10.1002/ajmg.b.30867

Brookes, K. J., Xu, X., Anney, Richard, Franke, B., Zhou, K., Chen, Wai, Banaschewski, T., Buitelaar, J., Ebstein, R., Eisenberg, J., Gill, M., Miranda, A., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E. J. S., Steinhausen, H. -C., Taylor, E., Faraone, S. V. and Asherson, P. 2008. Association of ADHD with genetic variants in the 5'-region of the dopamine transporter gene: evidence for allelic heterogeneity. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1519-1523. 10.1002/ajmg.b.30782

Anney, Richard, Lasky-Su, Jessica, O'Dushlaine, Colm, Kenny, Elaine, Neale, Benjamin M., Mulligan, Aisling, Franke, Barbara, Zhou, Kaixin, Chen, Wai, Christiansen, Hanna, Arias-Vasquez, Alejandro, Banaschewski, Tobias, Buitelaar, Jan, Ebstein, Richard, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund J. S., Steinhausen, Hans, Asherson, Philip, Faraone, Stephen V. and Gill, Michael 2008. Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1369-1378. 10.1002/ajmg.b.30871

Neale, Benjamin M., Lasky-Su, Jessica, Anney, Richard, Franke, Barbara, Zhou, Kaixin, Maller, Julian B., Arias Vasquez, Alejandro, Asherson, Philip, Chen, Wai, Banasehewski, Tobias, Buitelaar, Jan, Ebstein, Richard, Gill, Michael, Miranda, Ana, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans Christoph, Sonuga-Barke, Edmund J. S., Mulas, Fernando, Taylor, Eric, Laird, Nan, Lange, Christoph, Daly, Mark and Faraone, Stephen V. 2008. Genome-wide association scan of attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1337-1344. 10.1002/ajmg.b.30866

Anney, Richard, Hawi, Ziarih, Sheehan, Karen, Mulligan, Aisling, Pinto, Carlos, Brookes, Keeley J., Xu, Xiaohui, Zhou, Kaixin, Franke, Barbara, Buitelaar, Jan, Vermeulen, Sita H., Banaschewski, Tobias, Sonuga-Barke, Edmund J. S., Ebstein, Richard, Manor, Iris, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rommelse, Nanda, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans-Christoph, Taylor, Eric, Thompson, Margaret, Asherson, Philip, Faraone, Stephen V. and Gill, Michael 2008. Parent of Origin Effects in Attention/Deficit Hyperactivity Disorder (ADHD): Analysis of Data From the International Multicenter ADHD Genetics (IMAGE) Program. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1495-1500. 10.1002/ajmg.b.30659

Xu, X., Hawi, Z., Brookes, K. J., Anney, Richard, Bellgrove, M., Franke, B., Barry, E., Chen, W., Kuntsi, J., Banaschewski, T., Buitelaar, J., Ebstein, R., Fitzgerald, M., Miranda, A., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E. J. S., Steinhausen, H. -C., Faraone, S. V., Gill, M. and Asherson, P. 2008. Replication of a Rare Protective Allele in the Noradrenaline Transporter Gene and ADHD. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1564-1567. 10.1002/ajmg.b.30872

Sonuga-Barke, Edmund J. S., Lasky-Su, Jessica, Neale, Benjamin M., Oades, Robert, Chen, Wai, Franke, Barbara, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Gill, Michael, Anney, Richard, Miranda, Ana, Mulas, Fernando, Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans Christoph, Thompson, Margaret, Asherson, Philip and Faraone, Stephen V. 2008. Does Parental Expressed Emotion Moderate Genetic Effects in ADHD? An Exploration Using a Genome Wide Association Scan. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1359-1368. 10.1002/ajmg.b.30860

Lasky-Su, Jessica, Anney, Richard, Neale, Benjamin M., Franke, Barbara, Zhou, Kaixin, Maller, Julian B., Arias Vasquez, Alejandro, Chen, Wai, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Gill, Michael, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund J. S., Steinhausen, Hans Christoph, Taylor, Eric, Daly, Mark, Laird, Nan, Lange, Christoph and Faraone, Stephen V. 2008. Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1355-1358. 10.1002/ajmg.b.30869

Anney, Richard, Kenny, Elaine, O'Dushlaine, Colm T., Lasky-Su, Jessica, Franke, Barbara, Morris, Derek W., Neale, Benjamin M., Asherson, Philip, Faraone, Stephen V. and Gill, Michael 2008. Non-random error in genotype calling procedures: implications for family-based and case-control genome-wide association studies. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (8) , pp. 1379-1386. 10.1002/ajmg.b.30836

Oades, Robert D., Lasky-Su, Jessica, Christiansen, Hanna, Faraone, Stephen V., Sonuga-Barke, Edmund J. S., Banaschewski, Tobias, Chen, Wai, Anney, Richard, Buitelaar, Jan K., Ebstein, Richard P., Franke, Barbara, Gill, Michael, Miranda, Ana, Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph A., Steinhausen, Hans-Christoph, Taylor, Eric A., Thompson, Margaret and Asherson, Philip 2008. The influence of serotonin- and other genes on impulsive behavioral aggression and cognitive impulsivity in children with attention-deficit/hyperactivity disorder (ADHD): Findings from a family-based association test (FBAT) analysis. Behavioral and Brain Functions : BBF 4 , p. 48. 10.1186/1744-9081-4-48

Xu, X., Aysimi, E., Anney, Richard, Brookes, K., Franke, B., Zhou, K., Buschgens, C., Chen, W., Christiansen, H., Eisenberg, J., Gabriels, I., Manor, I., Marco, R., Muller, U. C., Mulligan, A., Rommelse, N., Thompson, M., Uebel, H., Banaschewski, T., Buitelaar, J., Ebstein, R., Gill, M., Miranda, A., Mulas, F., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Sonuga-Barke, E. J. S., Steinhausen, H. -C., Taylor, E., Faraone, S. V. and Asherson, P. 2008. No Association Between Two Polymorphisms of the Serotonin Transporter Gene and Combined Type Attention Deficit Hyperactivity Disorder. American Journal of Medical Genetics. Part B 147B (7) , pp. 1306-1309. 10.1002/ajmg.b.30737

Zhou, Kaixin, Asherson, Philip, Sham, Pak, Franke, Barbara, Anney, Richard, Buitelaar, Jan, Ebstein, Richard, Gill, Michael, Brookes, Keeley, Buschgens, Cathelijne, Campbell, Desmond, Chen, Wai, Christiansen, Hanna, Fliers, Ellen, Gabris, Isabel, Johansson, Lena, Marco, Rafaela, Mulas, Fernando, Mueller, Ueli, Mulligan, Aisling, Neale, Benjamin M., Rijsdijk, Fruhling, Rommelse, Nanda, Uebel, Henrik, Psychogiou, Lamprini, Xu, Xiaohui, Banaschewski, Tobias, Sonuga-Barke, Edmund J. S., Eisenberg, Jacques, Manor, Iris, Miranda, Ana, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans-Christoph, Taylor, Eric, Thompson, Margaret and Faraone, Stephen V. 2008. Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings. Biological psychiatry 64 (7) , pp. 571-576. 10.1016/j.biopsych.2008.02.024

Altink, Marieke E., Arias-Vasquez, Alejandro, Franke, Barbara, Slaats-Willemse, Dorine I. E., Buschgens, Cathelijne J. M., Rommelse, Nanda N. J., Fliers, Ellen A., Anney, Richard, Brookes, Keeley-Joanne, Chen, Wai, Gill, Michael, Mulligan, Aisling, Sonuga-Barke, Edmund J. S., Thompson, Margaret, Sergeant, Joseph A., Faraone, Stephen V., Asherson, Philip and Buitelaar, Jan K. 2008. The dopamine receptor D4 7-repeat allele and prenatal smoking in ADHD-affected children and their unaffected siblings: no gene-environment interaction. Journal of Child Psychology and Psychiatry 49 (10) , pp. 1053-1060. 10.1111/j.1469-7610.2008.01998.x

Sonuga-Barke, Edmund J. S., Brookes, Keeley-Joanne, Buitelaar, Jan, Anney, Richard, Bitsakou, Paraskevi, Baeyens, Dieter, Buschgens, Cathelijne, Chen, Wai, Christiansen, Hanna, Eisenberg, Jacques, Kuntsi, Jonna, Manor, Iris, Melia, Amanda, Mulligan, Aisling, Rommelse, Nanda, Mueller, Ueli C., Uebel, Henrik, Banaschewski, Tobias, Ebstein, Richard, Franke, Barbara, Gill, Michael, Miranda, Ana, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans Christoph, Thompson, Margaret, Taylor, Eric, Asherson, Philip and Faraone, Stephen V. 2008. Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder [Erratum]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (5) , p. 670. 10.1002/ajmg.b.30820

Asherson, P., Zhou, K., Anney, Richard, Franke, B., Buitelaar, J., Ebstein, R., Gill, M., Altink, M., Arnold, R., Boer, F., Brookes, K., Buschgens, C., Butler, L., Cambell, D., Chen, W., Christiansen, H., Feldman, L., Fleischman, K., Fliers, E., Howe-Forbes, R., Goldfarb, A., Heise, A., Gabrieels, I., Johansson, L., Lubetzki, I., Marco, R., Medad, S., Minderaa, R., Mulas, F., Mueller, U., Mulligan, A., Neale, B., Rijsdijk, F., Rabin, K., Rommelse, N., Sethna, V., Sorohan, J., Uebel, H., Psychogiou, L., Weeks, A., Barrett, R., Xu, X., Banaschewski, T., Sonuga-Barke, E. J. S., Eisenberg, J., Manor, I., Miranda, A., Oades, R. D., Roeyers, H., Rothenberger, A., Sergeant, J., Steinhausen, H-C, Taylor, E., Thompson, M. and Faraone, S. V. 2008. A high-density SNP linkage scan with 142 combined subtype ADHD sib pairs identifies linkage regions on chromosomes 9 and 16. Molecular Psychiatry 13 (5) , pp. 514-521. 10.1038/sj.mp.4002140

Sonuga-Barke, Edmund J. S., Brookes, Keeley-Joanne, Buitelaar, Jan, Anney, Richard, Bitsakou, Paraskevi, Baeyens, Dieter, Buschgens, Cathelijne, Chen, Wai, Christiansen, Hanna, Eisenberg, Jacques, Kuntsi, Jonna, Manor, Iris, Melia, Amanda, Mulligan, Aisling, Rommelse, Nanda, Mueller, Ueli C., Uebel, Henrik, Banaschewski, Tobias, Ebstein, Richard, Franke, Barbara, Gill, Michael, Miranda, Ana, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Steinhausen, Hans Christoph, Thompson, Margaret, Taylor, Eric, Asherson, Philip and Faraone, Stephen V. 2008. Intelligence in DSM-IV combined type attention-deficit/hyperactivity disorder is not predicted by either dopamine receptor/transporter genes or other previously identified risk alleles for attention-deficit/hyperactivity disorder. American Journal of Medical Genetics. Part B 147B (3) , pp. 316-319. 10.1002/ajmg.b.30596

Olsson, C. A., Byrnes, G. B., Anney, Richard, Collins, V., Hemphill, S. A., Williamson, R. and Patton, G. C. 2007. COMT Val(158)Met and 5HTTLPR functional loci interact to predict persistence of anxiety across adolescence: results from the Victorian Adolescent Health Cohort Study. Genes Brain and Behavior 6 (7) , pp. 647-652. 10.1111/j.1601-183X.2007.00313.x

Anney, Richard, Lotfi-Miri, Mehrnoush, Olsson, Craig A., Reid, Sophie C., Hemphill, Sheryl A. and Patton, George C. 2007. Variation in the gene coding for the M5 Muscarinic receptor (CHRM5) influences cigarette dose but is not associated with dependence to drugs of addiction: evidence from a prospective population based cohort study of young adults. BMC Genetics 8 , p. 46. 10.1186/1471-2156-8-46

Brookes, K., Xu, X., Chen, W., Zhou, K., Neale, B., Lowe, N., Anney, Richard, Franke, B., Gill, M., Ebstein, R., Buitelaar, J., Sham, P., Campbell, D., Knight, J., Andreou, P., Altink, M., Arnold, R., Boer, F., Buschgens, C., Butler, L., Christiansen, H., Feldman, L., Fleischman, K., Fliers, E., Howe-Forbes, R., Goldfarb, A., Heise, A., Gabriels, I., Korn-Lubetzki, I., Johansson, L., Marco, R., Medad, S., Minderaa, R., Mulas, F., Mueller, U., Mulligan, A., Rabin, K., Rommelse, N., Sethna, V., Sorohan, J., Uebel, H., Psychogiou, L., Weeks, A., Barrett, R., Craig, I., Banaschewski, T., Sonuga-Barke, E. J. S., Eisenberg, J., Kuntsi, J., Manor, I., McGuffin, P., Miranda, A., D Oades, R., Plomin, R., Roeyers, H., Rothenberger, A., Sergeant, J., Steinhausen, H-C, Taylor, E., Thompson, M., Faraone, S. V. and Asherson, P. 2006. The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Molecular Psychiatry 11 (12) , pp. 934-953. 10.1038/sj.mp.4001869

Anney, Richard, Hawi, Ziarah, Sheehan, Karen, Brookes, Keeley, Zhou, Kaixin, Banaschewski, Tobias, Buitelaar, Jan, Ebstein, Richard. P., Miranda, Ana, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund J. S. and Steinhausen, Hans-Christoph 2006. Epigenetic effects in ADHD: Parent-of-origin effects in image sample [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (7) , pp. 736-737. 10.1002/ajmg.b.30408

Mulligan, A., Anney, Richard, Chen, W., Butler, L., Fitzgerald, M. and Gill, M. 2006. Autistic symptoms in ADHD- A report from the International Multi-Center ADHD Gene Project (IMAGE) [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141B (7) , p. 687. 10.1002/ajmg.b.30408

Olsson, CA, Byrnes, GB, Lotfi-Miri, M, Collins, V, Williamson, R, Patton, C and Anney, Richard 2005. Association between 5-HTTLPR genotypes and persisting patterns of anxiety and alcohol use: results from a 10-year longitudinal study of adolescent mental health. Molecular Psychiatry 10 (9) , pp. 868-876. 10.1038/sj.mp.4001677

Olsson, CA, Anney, Richard, Lotfi-Miri, M, Byrnes, GB, Williamson, R and Patton, GC 2005. Association between the COMT Val158Met polymorphism and propensity to anxiety in an Australian population-based longitudinal study of adolescent health. Psychiatric Genetics 15 (2) , pp. 109-115.

Staddon, Susan, Arranz, Maria J., Mancama, Dalu, Perez-Nievas, Fernando, Arrizabalaga, Iñaki, Anney, Richard, Buckland, Paul Robert, Elkin, Amanda, Osborne, Sarah, Munro, Janet, Mata, Ignacio and Kerwin, Robert W. 2005. Association between dopamine D3 receptor gene polymorphisms and schizophrenia in an isolate population. Schizophrenia Research 73 (1) , pp. 49-54. 10.1016/j.schres.2004.06.011

Anney, Richard, Rees, Mark I., Bryan, E., Spurlock, Gillian, Williams, Nigel Melville, Norton, Nadine, Williams, Hywel John, Cardno, Alastair George, Zammit, Stanley, Jones, S., Jones, G., Hoogendoorn, Bastiaan, Smith, K. J., Hamshere, Marian Lindsay, Coleman, Sharon Louise, Guy, Carol, O'Donovan, Michael Conlon, Owen, Michael John and Buckland, Paul Robert 2002. Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia. Molecular psychiatry 7 (5) , pp. 493-502. 10.1038/sj.mp.4001003

This list was generated on Mon Oct 23 03:57:12 2017 BST.