Large-scale discovery of novel genetic causes of developmental disorders by van Kogelenberg, M, Goudie, D, Gray, E, Harrison, L, Hawkins, R, Henderson, A, Holder, S, Irving, M, Bayzetinova, T, Jones, D, Kini, U, Kinning, E, Kirby, G, Kirk, C, Kumar, D, Lachlan, K, Lees, M, Lim, D, Coomber, E L, Lowther, G, Lynch, S A, Maher, E, Mansour, S, Maye, U, McCann, E, McMullan, D J, McNerlan, S, Metcalfe, K, Mohammed, S, Jones, P, Moore, D, Morton, J, Mugalaasi, H, Newbury-Ecob, R, Ogilvie, C, Park, S, Parker, M J, Patel, C, Porteous, D, Mason, L E, Ragge, N, Rankin, J, Raymond, L, Rosser, E, Miller, R, Sarkar, A, Scott, C, Scott, R, Selby, A, Shannon, N, Simpkin, D, Singzon, R, Skitt, Z, Rajan, D, Splitt, M, Stewart, F, Swaminathan, G J, Tatton-Brown, K, Temple, I K, Torokwa, A, Turner, C, Turnpenny, P, Tysoe, C, Vandersteen, A, Walker, D, Ahmed, M, Widaa, S, Williams, N, Wragg, C, Yau, M, FitzPatrick, D R, Anjum, U, Balasubramanian, M, Banerjee, R, Baralle, D, Baty, D, Bennett, C, Berg, J, Bevan, A P, Bourdon, L, Brady, A, Burton, J, Chandler, K, Cooper, N, Cross, G, D'Alessandro, M, Dabir, T, Davidson, R, Davies, S, Dean, J, Deshpande, C, Donnelly, C, Douglas, A, Eason, J, Edkins, S, Foulds, N, Fryer, A, Gardiner, C, Pereira, S L Gomes, Goodship, J

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Global change effects on plant communities are magnified by time and the number of global change factors imposed by Komatsu, Kimberly J., Avolio, Meghan L., Lemoine, Nathan P., Isbell, Forest, Grman, Emily, Houseman, Gregory R., Koerner, Sally E., Johnson, David S., Wilcox, Kevin R., Alatalo, Juha M., Anderson, John P., Aerts, Rien, Baer, Sara G., Baldwin, Andrew H., Bates, Jonathan, Beierkuhnlein, Carl, Belote, R. Travis, Blair, John, Bloor, Juliette M. G., Bohlen, Patrick J., Bork, Edward W., Boughton, Elizabeth H., Bowman, William D., Britton, Andrea J., Cahill, James F., Chaneton, Enrique, Chiariello, Nona R., Cheng, Jimin, Collins, Scott L., Cornelissen, J. Hans C., Du, Guozhen, Eskelinen, Anu, Firn, Jennifer, Foster, Bryan, Gough, Laura, Gross, Katherine, Hallett, Lauren M., Han, Xingguo, Harmens, Harry, Hovenden, Mark J., Jagerbrand, Annika, Jentsch, Anke, Kern, Christel, Klanderud, Kari, Knapp, Alan K., Kreyling, Juergen, Li, Wei, Luo, Yiqi, McCulley, Rebecca L., McLaren, Jennie R., Megonigal, J. Patrick, Morgan, John W., Onipchenko, Vladimir, Pennings, Steven C., Prevéy, Janet S., Price, Jodi N., Reich, Peter B., Robinson, Clare H., Russell, F. Leland, Sala, Osvaldo E., Seabloom, Eric W., Smith, Melinda D., Soudzilovskaia, Nadejda A., Souza, Lara, Suding, Katherine, Suttle, K. Blake, Svejcar, Tony, Tilman, David, Tognetti, Pedro, Turkington, Roy, White, Shannon, Xu, Zhuwen, Yahdjian, Laura, Yu, Qiang, Zhang, Pengfei, Zhang, Yunhai

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Evidence for 28 genetic disorders discovered by combining healthcare and research data by Kaplanis, Joanna, Samocha, Kaitlin E, Wiel, Laurens, Zhang, Zhancheng, Arvai, Kevin J, Eberhardt, Ruth Y, Gallone, Giuseppe, Lelieveld, Stefan H, Martin, Hilary C, McRae, Jeremy F, Short, Patrick J, Torene, Rebecca I, de Boer, Elke, Danecek, Petr, Gardner, Eugene J, Huang, Ni, Lord, Jenny, Martincorena, Iñigo, Pfundt, Rolph, Reijnders, Margot R F, Yeung, Alison, Yntema, Helger G, Vissers, Lisenka E L M, Juusola, Jane, Wright, Caroline F, Brunner, Han G, Firth, Helen V, FitzPatrick, David R, Barrett, Jeffrey C, Hurles, Matthew E, Gilissen, Christian, Retterer, Kyle

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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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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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Enabling precision manufacturing of active pharmaceutical ingredients: workflow for seeded cooling continuous crystallisations by Brown, Cameron J., McGlone, Thomas, Yerdelen, Stephanie, Srirambhatla, Vijay, Mabbott, Fraser, Gurung, Rajesh, L. Briuglia, Maria, Ahmed, Bilal, Polyzois, Hector, McGinty, John, Perciballi, Francesca, Fysikopoulos, Dimitris, MacFhionnghaile, Pól, Siddique, Humera, Raval, Vishal, Harrington, Tomás S., Vassileiou, Antony D., Robertson, Murray, Prasad, Elke, Johnston, Andrea, Johnston, Blair, Nordon, Alison, Srai, Jagjit S., Halbert, Gavin, ter Horst, Joop H., Price, Chris J., Rielly, Chris D., Sefcik, Jan, Florence, Alastair J.

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Genetic correlation between amyotrophic lateral sclerosis and schizophrenia by McLaughlin, Russell L, Schijven, Dick, van Rheenen, Wouter, van Eijk, Kristel R, O'Brien, Margaret, Kahn, René S, Ophoff, Roel A, Goris, An, Bradley, Daniel G, Al-Chalabi, Ammar, van den Berg, Leonard H, Luykx, Jurjen J, Hardiman, Orla, Veldink, Jan H

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Harmonized cross-species cell atlases of trigeminal and dorsal root ganglia by Bhuiyan, Shamsuddin A., Xu, Mengyi, Yang, Lite, Semizoglou, Evangelia, Bhatia, Parth, Pantaleo, Katerina I., Tochitsky, Ivan, Jain, Aakanksha, Erdogan, Burcu, Blair, Steven, Cat, Victor, Mwirigi, Juliet M., Sankaranarayanan, Ishwarya, Tavares-Ferreira, Diana, Green, Ursula, McIlvried, Lisa A., Copits, Bryan A., Bertels, Zachariah, Del Rosario, John S., Widman, Allie J., Slivicki, Richard A., Yi, Jiwon, Sharif-Naeini, Reza, Woolf, Clifford J., Lennerz, Jochen K., Whited, Jessica L., Price, Theodore J., Robert W. Gereau IV, Renthal, William

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Zidovudine (AZT) monotherapy selects for the A360V mutation in the connection domain of HIV-1 reverse transcriptase by Brehm, Jessica H, Scott, Yanille, Koontz, Dianna L, Perry, Steven, Hammer, Scott, Katzenstein, David, Mellors, John W, Sluis-Cremer, Nicolas

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