Field study of pesticide leaching in a Himatangi sand (Manawatu) and in a Kiripaka bouldery clay loam (Northland). 1. Results von CLOSE, Murray E, LEE, Robert, MAGESAN, Gujja N, STEWART, Michael K, SKUSE, George, BEKESI, Gabor

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Field study of pesticide leaching in a Himatangi sand . 1. Results von Close, Murray E, Lee, Robert, Magesan, Gujja N, Stewart, Michael K, Skuse, George, Bekesi, Gabor

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Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development von Stergiakouli, Evie, Davey Smith, George, Martin, Joanna, Skuse, David H, Viechtbauer, Wolfgang, Ring, Susan M, Ronald, Angelica, Evans, David E, Fisher, Simon E, Thapar, Anita, St Pourcain, Beate

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Links Between Co-occurring Social-Communication and Hyperactive-Inattentive Trait Trajectories von St. Pourcain, Beate, Ph.D, Mandy, William P., Ph.D, Heron, Jon, Ph.D, Golding, Jean, Ph.D., D.Sc, Davey Smith, George, M.D., D.Sc, Skuse, David H., M.D

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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population von Robinson, Elise B, St Pourcain, Beate, Anttila, Verneri, Kosmicki, Jack A, Bulik-Sullivan, Brendan, Grove, Jakob, Maller, Julian, Samocha, Kaitlin E, Sanders, Stephan J, Ripke, Stephan, Martin, Joanna, Hollegaard, Mads V, Werge, Thomas, Hougaard, David M, Neale, Benjamin M, Evans, David M, Skuse, David, Mortensen, Preben Bo, Børglum, Anders D, Ronald, Angelica, Smith, George Davey, Daly, Mark J

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Timing, rates and spectra of human germline mutation von Rahbari, Raheleh, Wuster, Arthur, Lindsay, Sarah J, Hardwick, Robert J, Alexandrov, Ludmil B, Al Turki, Saeed, Dominiczak, Anna, Morris, Andrew, Porteous, David, Smith, Blair, Stratton, Michael R, Hurles, Matthew E

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Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling von Logan, Clare V, Szabadkai, György, Sharpe, Jenny A, Parry, David A, Torelli, Silvia, Childs, Anne-Marie, Kriek, Marjolein, Phadke, Rahul, Johnson, Colin A, Roberts, Nicola Y, Bonthron, David T, Pysden, Karen A, Whyte, Tamieka, Munteanu, Iulia, Foley, A Reghan, Wheway, Gabrielle, Szymanska, Katarzyna, Natarajan, Subaashini, Abdelhamed, Zakia A, Morgan, Joanne E, Roper, Helen, Santen, Gijs W E, Niks, Erik H, van der Pol, W Ludo, Lindhout, Dick, Raffaello, Anna, De Stefani, Diego, den Dunnen, Johan T, Sun, Yu, Ginjaar, Ieke, Sewry, Caroline A, Hurles, Matthew, Rizzuto, Rosario, Duchen, Michael R, Muntoni, Francesco, Sheridan, Eamonn

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Association Between a High-Risk Autism Locus on 5p14 and Social Communication Spectrum Phenotypes in the General Population von St. Pourcain, Beate, Wang, Kai, Glessner, Joseph T., Golding, Jean, Steer, Colin, Ring, Susan M., Skuse, David H., Grant, Struan F.A., Hakonarson, Hakon, Davey Smith, George

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Estimating telomere length from whole genome sequence data von Ding, Zhihao, Mangino, Massimo, Aviv, Abraham, Spector, Tim, Durbin, Richard

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Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability von Grozeva, Detelina, Carss, Keren, Spasic-Boskovic, Olivera, Tejada, Maria-Isabel, Gecz, Jozef, Shaw, Marie, Corbett, Mark, Haan, Eric, Thompson, Elizabeth, Friend, Kathryn, Hussain, Zaamin, Hackett, Anna, Field, Michael, Renieri, Alessandra, Stevenson, Roger, Schwartz, Charles, Floyd, James A.B., Bentham, Jamie, Cosgrove, Catherine, Keavney, Bernard, Bhattacharya, Shoumo, Hurles, Matthew, Raymond, F. Lucy

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Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence von St Pourcain, Beate, Skuse, David H, Mandy, William P, Wang, Kai, Hakonarson, Hakon, Timpson, Nicholas J, Evans, David M, Kemp, John P, Ring, Susan M, McArdle, Wendy L, Golding, Jean, Smith, George Davey

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Low-frequency variation in TP53 has large effects on head circumference and intracranial volume von Haworth, Simon, Shapland, Chin Yang, Hayward, Caroline, Prins, Bram P., Felix, Janine F., Medina-Gomez, Carolina, Rivadeneira, Fernando, Wang, Carol, Ahluwalia, Tarunveer S., Vrijheid, Martine, Guxens, Mònica, Sunyer, Jordi, Tachmazidou, Ioanna, Walter, Klaudia, Iotchkova, Valentina, Jackson, Andrew, Cleal, Louise, Huffmann, Jennifer, Min, Josine L., Sass, Lærke, Timmers, Paul R. H. J., Davey Smith, George, Fisher, Simon E., Wilson, James F., Cole, Tim J., Fernandez-Orth, Dietmar, Bønnelykke, Klaus, Bisgaard, Hans, Pennell, Craig E., Jaddoe, Vincent W. V., Dedoussis, George, Timpson, Nicholas, Zeggini, Eleftheria, Vitart, Veronique, St Pourcain, Beate

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Managing clinically significant findings in research: the UK10K example von Kaye, Jane, Hurles, Matthew, Griffin, Heather, Grewal, Jasote, Bobrow, Martin, Timpson, Nic, Smee, Carol, Bolton, Patrick, Durbin, Richard, Dyke, Stephanie, Fitzpatrick, David, Kennedy, Karen, Kent, Alastair, Muddyman, Dawn, Muntoni, Francesco, Raymond, Lucy F, Semple, Robert, Spector, Tim

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An interactive genome browser of association results from the UK10K cohorts project von Geihs, Matthias, Yan, Ying, Walter, Klaudia, Huang, Jie, Memari, Yasin, Min, Josine L, Mead, Daniel, Hubbard, Tim J, Timpson, Nicholas J, Down, Thomas A, Soranzo, Nicole

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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population von Robinson, Elise B, St. Pourcain, Beate, Anttila, Verneri, Kosmicki, Jack A, Bulik-Sullivan, Brendan, Grove, Jakob, Maller, Julian, Samocha, Kaitlin E, Sanders, Stephan J, Ripke, Stephan, Martin, Joanna, Hollegaard, Mads V, Werge, Thomas, Hougaard, David M, Neale, Benjamin M, Evans, David M, Skuse, David, Mortensen, Preben Bo, Børglum, Anders D, Ronald, Angelica, Smith, George Davey, Daly, Mark J

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Shared genetic influences between dimensional ASD and ADHD symptoms during child and adolescent development von Stergiakouli, Evie, Davey Smith, George, Martin, Joanna, Skuse, David H, Viechtbauer, Wolfgang, Ring, Susan M, Ronald, Angelica, Evans, David E, Fisher, Simon E, Thapar, Anita, St Pourcain, Beate

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Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity von Bochukova, Elena G, Bounds, Rebecca, Mistry, Vanisha, Langenberg, Claudia, Surendran, Praveen, Nordestgaard, Børge G, Nielsen, Sune F, Afzal, Shoaib, Papadia, Sofia, Ashford, Sofie, Zeggini, Eleftheria, Barroso, Inês, Farooqi, I. Sadaf, Burton, Jonathan, Buck, Nicholas, Kumari, Meena, Lynn, Peter, Rabe, Birgitta, Overvad, Kim, Clavel-Chapelon, Francoise, Matullo, Giuseppe, Boer, Jolanda Ma, Van Der Schouw, Yvonne, Moreno-Iribas, Conchi, Wennberg, Patrik, Key, Timothy J, Riboli, Elio, Al-Turki, Saeed, Antony, Dinu, Beales, Phil, Blackwooda, Douglas, Bobrow, Martin, Calissanoa, Mattia, Carss, Keren, Chatterjee, Krishna, Chen, Lu, Ciampia, Antonio, Cirak, Sebahattin, Clapham, Peter, Clement, Gail, Coates, Guy, Collier, David A, Coxa, Tony, Craddock, Nick, Curtis, David, Edkins, Sarah, Ellis, Peter, Evansa, David M, Flicek, Paul, Foley, A. Reghan, Franklin, Christopher S, Gallagher, Louise, Gaunt, Tom R, Grozeva, Detelina, Guo, Xiaosen, Holmans, Peter A, Huang, Liren, Iotchkova, Valentina, Jackson, David K, Karczewski, Konrad J, Kaye, Jane, Keane, Thomas, Kennedy, Karen, Khawaja, Farrah, Lee, Irene, Lek, Monkol, Mathieson, Iain, McKechanie, Andrew G, McQuillin, Andrew, Memari, Yasin, Metrustry, Sarah, Min, Josine L, Morris, Andrew D, O'Donovan, Michael C, Owen, Michael J, Palotie, Aarno, Paunio, Tiina, Payne, Stewart J, Plagnol, Vincent, Rehnström, Karola, Ridout, Cheryl K, Roberts, Nicola, Scott, Richard H, Sharp, Sally I, Shaw, Adam, Smee, Carol, Soranzo, Nicole, Spasic-Boskovic, Olivera, Spector, Timothy D, St Clair, David, Valdes, Ana M, Vandersteen, Anthony M, Vijayarangakannan, Parthiban, Visscher, Peter M, Wang, Guangbiao, Williams, Hywel J, Williamson, Kathleen A, Wilson, Scott G, Wong, Kim, Xu, Changjiang

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Whole-genome sequence-based analysis of thyroid function von Taylor, Peter N, Porcu, Eleonora, Campbell, Purdey J, Brown, Suzanne J, Mullin, Benjamin H, Min, Josine, Memari, Yasin, Charoen, Pimphen, Danecek, Petr, Greenwood, Celia, McCarthy, Shane, Panicker, Vijay, Relton, Caroline, Schlessinger, David, Abecasis, Goncalo, Cucca, Francesco, Surdulescu, Gabriela L, Dayan, Colin M, Spector, Tim, Davey Smith, George, Brent Richards, J, Turki, Saeed Al, Anderson, Carl, Artigas, Maria Soler, Balasubramaniam, Senduran, Bhattacharya, Shoumo, Birney, Ewan, Bounds, Rebecca, Breen, Gerome, Calissano, Mattia, Chatterjee, Krishna, Chen, Lu, Cirak, Sebhattin, Clapham, Peter, Clement, Gail, Collier, David, Curran, Sarah, Day, Ian N.M, Dunham, Ian, Edkins, Sarah, Ellis, Peter, Evans, David, Faroogi, Sadaf, Fitzpatrick, David R, Foley, A. Reghan, Futema, Marta, Griffin, Heather, Hendricks, Audrey, Howie, Bryan, Humphries, Steve E, Hurles, Matthew E, Hysi, Pirro, Kaye, Jane, Lachance, Genevieve, Lawson, Daniel, Lee, Irene, Liang, Jieqin, Lin, Hong, Lönnqvist, Jouko, Lopes, Margarida, Lotchkova, Valentina, Marchini, Jonathan, Mathieson, Iain, McQuillin, Andrew, Mitchison, Hannah, Moayyeri, Alireza, Morris, James, Muntoni, Francesco, O'Donnovan, Michael, Palotie, Aarno, Panoutsopoulou, Kalliope, Paternoster, Lavinia, Paunio, Tiina, Plagnol, Vincent, Quai, Michael A, Rehnström, Karola, Ring, Susan, Savage, David B, Scambler, Peter, Semple, Robert K, Serra, Eva, Sharp, Sally I, Shin, So-Youn, Skuse, David, Spasic-Boskovic, Olivera, Clair, David St, Stevens, Elizabeth, Pourcian, Beate St, Sun, Jianping, Tachmazidou, Ionna, Valdes, Ana, Vijayarangakannan, Parthiban, Visscher, Peter M, Wain, Louise V, Wang, Yu, Whyte, Tamieka, Williams, Hywel, Xu, ChangJiang, Yang, Jian, Zhang, Fend

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TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport von Hou, Yuqing, Boldt, Karsten, van Reeuwijk, Jeroen, Plaza, Jean-Marc, Letteboer, Stef J. F, Johnson, Colin A, Kayserili, Hulya, King, Stephen M, Wicking, Carol, Cormier-Daire, Valerie, Roepman, Ronald, Anderson, Carl, Ayub, Mohammad, Barroso, Inês, Bentham, Jamie, Bhattacharya, Shoumo, Bochukova, Elena, Bolton, Patrick, Boustred, Chris, Breen, Gerome, Calissano, Mattia, Carss, Keren, Chatterjee, Krishna, Chen, Lu, Cirak, Sebhattin, Coates, Guy, Collier, David, Craddock, Nick, Crooks, Lucy, Daly, Allan, Smith, George Davey, Day-Williams, Aaron, Edkins, Sarah, Fitzpatrick, David, Floyd, Jamie, Futema, Marta, Gallagher, Louise, Grozeva, Detelina, Hendricks, Audrey, Holmans, Peter, Humphries, Steve E, Hurles, Matt, Jackson, David, Jamshidi, Yalda, Chris, Joyce, Keane, Thomas, Kennedy, Karen, Kolb-Kokocinski, Anja, Lachance, Genevieve, Lee, Irene, Li, Rui, Ryan, Liu, Lönnqvist, Jouko, Lopes, Margarida, MacArthur, Daniel G, Massimo, Mangino, Marchini, Jonathan, Maslen, John, McKechanie, Andrew, Metrustry, Sarah, Moayyeri, Alireza, Muddyman, Dawn, Muntoni, Francesco, Northstone, Kate, O'Rahilly, Stephen, Onoufriadis, Alexandros, Oualkacha, Karim, Panoutsopoulou, Kalliope, Parr, Jeremy, Paternoster, Lavinia, Paunio, Tiina, Pietilainen, Olli, Plagnol, Vincent, Quaye, Lydia, Raymond, Lucy, Rehnström, Karola, Brent Richards, J, Ring, Sue, Ritchie, Graham R S, Serra, Eva, Shin, So-Youn, Small, Kerrin, Soranzo, Nicole, St Pourcain, Beate, St. Clair, David, Surdulescu, Gabriela, Suvisaari, Jaana, Tian, Jing, Timpson, Nic, Valdes, Ana, van Kogelenberg, Margriet, Wang, Jun, Ward, Kirsten, Wheeler, Ellie, Williams, Hywel, Williamson, Kathy, Wilson, Scott G, Whyte, Tamieka, ChangJiang, Xu, Zeggini, Eleftheria

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A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans von Timpson, Nicholas J, Walter, Klaudia, Min, Josine L, Malerba, Giovanni, Chen, Lu, Iotchkova, Valentina, Cocca, Massimiliano, McCarthy, Shane, Muddyman, Dawn, Mangino, Massimo, Menni, Cristina, Ring, Susan M, Gaye, Amadou, Farmaki, Aliki-Eleni, Talmud, Philippa J, Gambaro, Giovanni, Spector, Tim D, Smith, George Davey, Durbin, Richard, Richards, J Brent, Humphries, Steve E, Zeggini, Eleftheria, Soranzo, Nicole, Al Turki, Saeed, Bhattacharya, Shoumo, Bobrow, Martin, Bounds, Rebecca, Breen, Gerome, Calissano, Mattia, Chatterjee, Krishna, Ciampi, Antonio, Cirak, Sebhattin, Clapham, Peter, Clement, Gail, Coates, Guy, Collier, David, Cosgrove, Catherine, Curran, Sarah, Day, Ian N. M, Dunham, Ian, Ellis, Peter, Evans, David, Faroogi, Sadaf, Fitzpatrick, David R, Flyod, James, Foley, A Reghan, Gallagher, Louise, Guo, Xiaosen, Gurling, Hugh, Hubbard, Tim, Hurles, Matthew E, Hysi, Pirro, Jing, Tian, Joyce, Chris, Kaye, Jane, Keane, Thomas, Kennedy, Karen, Lachance, Genevieve, Lee, Irene, Lin, Hong, Liu, Ryan, Lönnqvist, Jouko, Lotchkova, Valentina, Mathieson, Iain, McGuffin, Peter, McQuillin, Andrew, Moayyeri, Alireza, Palotie, Aarno, Panoutsopoulou, Kalliope, Parker, Victoria, Paternoster, Lavinia, Paunio, Tiina, Payne, Felicity, Perry, John, Pietilainen, Olli, Quaye, Lydia, Raymond, Lucy, Rehnström, Karola, Ritchie, Graham R. S, Schiffels, Stephen, Shihab, Hasheem, Skuse, David, Spector, Tim, Stevens, Elizabeth, St Pourcian, Beate, Suvisaari, Jaana, Timpson, Nicholas, Tobin, Martin D, Van Kogelenberg, Margriet, Walters, James T. R, Wang, Jun, Ward, Kirsten, Williamson, Kathleen A, Wilson, Crispian, Wilson, Scott G, Wong, Kim, Xu, ChangJiang, Yang, Jian, Zhang, Fend, Zheng, Hou-Feng

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