A case study of a strategic initiative in pediatric rehabilitation transition services: An insiders' perspective on team principles and practices von King, Gillian, Bowman, Laura R, Curran, C J, Oh, Anna, Thompson, Laura, McDougall, Carolyn, Menna-Dack, Dolly, Howson-Strong, Laura

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114: Bioequivalence of a Liquid vs Solid Formulation of Calcium Acetate von Greenberg, Jonathan, Howson, Laura, Hong-Ho, Chiang, Mullon, Claudy, Miller, Claude, Tuller, Sarah, Mico, Anila, Houlihan, Steve, Pirotsky, Vitaly, Diaz-Buxo, Jose

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A randomized, controlled, three-arm, open-label, cross-over bioequivalence study comparing calcium acetate oral solution and calcium acetate gelcaps in healthy volunteers von Diaz-Buxo, Jose A, Greenberg, Jonathan, Ho, Chiang-Hong, Howson, Laura, Sergeyeva, Olga, Hinsu, Punit, Mullon, Claudy

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Assessing the causal association of glycine with risk of cardio-metabolic diseases von Wittemans, Laura B. L., Lotta, Luca A., Oliver-Williams, Clare, Stewart, Isobel D., Surendran, Praveen, Karthikeyan, Savita, Day, Felix R., Koulman, Albert, Imamura, Fumiaki, Zeng, Lingyao, Erdmann, Jeanette, Schunkert, Heribert, Khaw, Kay-Tee, Griffin, Julian L., Forouhi, Nita G., Scott, Robert A., Wood, Angela M., Burgess, Stephen, Howson, Joanna M. M., Danesh, John, Wareham, Nicholas J., Butterworth, Adam S., Langenberg, Claudia

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Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases von Plagnol, Vincent, Howson, Joanna M M, Smyth, Deborah J, Walker, Neil, Hafler, Jason P, Wallace, Chris, Stevens, Helen, Jackson, Laura, Simmonds, Matthew J, Bingley, Polly J, Gough, Stephen C, Todd, John A

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Rare and common genetic determinants of metabolic individuality and their effects on human health von Surendran, Praveen, Stewart, Isobel D., Au Yeung, Victoria P. W., Pietzner, Maik, Raffler, Johannes, Wörheide, Maria A., Li, Chen, Smith, Rebecca F., Wittemans, Laura B. L., Bomba, Lorenzo, Menni, Cristina, Zierer, Jonas, Rossi, Niccolò, Sheridan, Patricia A., Watkins, Nicholas A., Mangino, Massimo, Hysi, Pirro G., Di Angelantonio, Emanuele, Falchi, Mario, Spector, Tim D., Soranzo, Nicole, Michelotti, Gregory A., Arlt, Wiebke, Lotta, Luca A., Denaxas, Spiros, Hemingway, Harry, Gamazon, Eric R., Howson, Joanna M. M., Wood, Angela M., Danesh, John, Wareham, Nicholas J., Kastenmüller, Gabi, Fauman, Eric B., Suhre, Karsten, Butterworth, Adam S., Langenberg, Claudia

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Improvements in Knife-boards von LAURA ELLEN HOWSON

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Integrating CMC document preparation into the development process for vaccine INDs von Hagen, Anna, Aunins, Anne, Howson, Laura, Janus, Tracy, LeGrow, Kathleen, Robinett, Robin, Thornton, Rachel, Sitrin, Robert

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Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene von Davison, Lucy J., Wallace, Chris, Cooper, Jason D., Cope, Nathan F., Wilson, Nicola K., Smyth, Deborah J., Howson, Joanna M.M., Saleh, Nada, Al-Jeffery, Abdullah, Angus, Karen L., Stevens, Helen E., Nutland, Sarah, Duley, Simon, Coulson, Richard M.R., Walker, Neil M., Burren, Oliver S., Rice, Catherine M., Cambien, Francois, Zeller, Tanja, Munzel, Thomas, Lackner, Karl, Blankenberg, Stefan, Fraser, Peter, Gottgens, Berthold, Todd, John A.

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A European multicentre evaluation of detection and typing methods for human enteroviruses and parechoviruses using RNA transcripts von Hayes, A., Nguyen, D., Andersson, M., Antón, A., Bailly, J.‐L., Beard, S., Benschop, K. S. M., Berginc, N., Blomqvist, S., Cunningham, E., Davis, D., Dembinski, J. L., Diedrich, S., Dudman, S. G., Dyrdak, R., Eltringham, G. J. A., Gonzales‐Goggia, S., Gunson, R., Howson‐Wells, H. C., Jääskeläinen, A. J., López‐Labrador, F. X., Maier, M., Majumdar, M., Midgley, S., Mirand, A., Morley, U., Nordbø, S. A., Oikarinen, S., Osman, H., Papa, A., Pellegrinelli, L., Piralla, A., Rabella, N., Richter, J., Smith, M., Söderlund Strand, A., Templeton, K., Vipond, B., Vuorinen, T., Williams, C., Wollants, E., Zakikhany, K., Fischer, T. K., Harvala, H., Simmonds, P.

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Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference von Corbin, Laura J., Tan, Vanessa Y., Hughes, David A., Wade, Kaitlin H., Paul, Dirk S., Tansey, Katherine E., Butcher, Frances, Dudbridge, Frank, Howson, Joanna M., Jallow, Momodou W., John, Catherine, Kingston, Nathalie, Lindgren, Cecilia M., O’Donavan, Michael, O’Rahilly, Stephen, Owen, Michael J., Palmer, Colin N. A., Pearson, Ewan R., Scott, Robert A., van Heel, David A., Whittaker, John, Frayling, Tim, Tobin, Martin D., Wain, Louise V., Smith, George Davey, Evans, David M., Karpe, Fredrik, McCarthy, Mark I., Danesh, John, Franks, Paul W., Timpson, Nicholas J.

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The Polygenic and Monogenic Basis of Blood Traits and Diseases von Vuckovic, Dragana, Bao, Erik L., Akbari, Parsa, Mousas, Abdou, Jiang, Tao, Chen, Ming-Huei, Raffield, Laura M., Huffman, Jennifer E., Ritchie, Scott C., Megy, Karyn, Ponstingl, Hannes, Penkett, Christopher J., Albers, Patrick K., Wigdor, Emilie M., Sakaue, Saori, Moscati, Arden, Manansala, Regina, Lo, Ken Sin, Qian, Huijun, Akiyama, Masato, Bartz, Traci M., Beswick, Andrew, Bork-Jensen, Jette, Bottinger, Erwin P., van Rooij, Frank J.A., Chitrala, Kumaraswamy N., Wilson, Peter W.F., Choquet, Hélène, Danesh, John, Di Angelantonio, Emanuele, Dimou, Niki, Ding, Jingzhong, Elliott, Paul, Esko, Tõnu, Evans, Michele K., Felix, Stephan B., Floyd, James S., Grarup, Niels, Guo, Michael H., Guo, Qi, Greinacher, Andreas, Haessler, Jeff, Howson, Joanna M.M., Huang, Wei, Kacprowski, Tim, Kähönen, Mika, Kamatani, Yoichiro, Kanai, Masahiro, Karthikeyan, Savita, Koskeridis, Fotios, Lange, Leslie A., Lehtimäki, Terho, Linneberg, Allan, Liu, Yongmei, Lyytikäinen, Leo-Pekka, Manichaikul, Ani, Matsuda, Koichi, Mohlke, Karen L., Mononen, Nina, Murakami, Yoshinori, Nikus, Kjell, Pankratz, Nathan, Pedersen, Oluf, Preuss, Michael, Psaty, Bruce M., Rich, Stephen S., Rodriguez, Benjamin A.T., Rosen, Jonathan D., Rotter, Jerome I., Spracklen, Cassandra N., Surendran, Praveen, Tang, Hua, Tardif, Jean-Claude, Ghanbari, Mohsen, Völzke, Henry, Watkins, Nicholas A., Cai, Na, Kundu, Kousik, Watt, Stephen B., Walter, Klaudia, Zonderman, Alan B., Cho, Kelly, Li, Yun, Loos, Ruth J.F., Knight, Julian C., Georges, Michel, Stegle, Oliver, Evangelou, Evangelos, Okada, Yukinori, Roberts, David J., Inouye, Michael, Johnson, Andrew D., Auer, Paul L., Astle, William J., Reiner, Alexander P., Butterworth, Adam S., Ouwehand, Willem H., Lettre, Guillaume, Sankaran, Vijay G., Soranzo, Nicole

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De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome von Chen, Yuyang, Kim, Hyung Chul, Ljungdahl, Alicia, Stenton, Sarah L., Lord, Jenny, Lemire, Gabrielle, Martin-Geary, Alexandra C., Ganesh, Vijay S., Ma, Jialan, Ellingford, Jamie M., Delage, Erwan, D’Souza, Elston N., Dong, Shan, Adams, David R., Allan, Kirsten, Bakshi, Madhura, Baldwin, Erin E., Berger, Seth I., Brown, Natasha J., Burrage, Lindsay C., Chapman, Kimberly, Coman, David J., Compton, Alison G., Cunningham, Chloe A., D’Souza, Precilla, Danecek, Petr, Délot, Emmanuèle C., Dias, Kerith-Rae, Elias, Ellen R., Elmslie, Frances, Evans, Care-Anne, Ezell, Kimberly, Fraser, Jamie L., Gallacher, Lyndon, Genetti, Casie A., Grant, Christina L., Haack, Tobias, Higgs, Jenny E., Hinch, Anjali G., Hurles, Matthew E., Kuechler, Alma, Lecoquierre, François, Fevre, Anna Le, Leventer, Richard J., Liebelt, Jan E., Lindsay, Sarah, Lockhart, Paul J., Ma, Alan S., Macnamara, Ellen F., Mendez, Hector R., Metcalfe, Kay, Montgomery, Stephen B., Moosajee, Mariya, Nassogne, Marie-Cécile, Neumann, Serena, O’Donoghue, Michael, O’Leary, Melanie, Palmer, Elizabeth E., Pattani, Nikhil, Pitsava, Georgia, Pysar, Ryan, Rehm, Heidi L., Reuter, Chloe M., Revencu, Nicole, Riess, Angelika, Rodan, Lance, Roscioli, Tony, Rosenfeld, Jill A., Sachdev, Rani, Shaw-Smith, Charles J., Simons, Cas, Sisodiya, Sanjay M., Snell, Penny, St Clair, Laura, Stewart, Helen S., Tan, Natalie B., Temple, Suzanna E. L., Thorburn, David R., Tifft, Cynthia J., VanNoy, Grace E., Vilain, Eric, Viskochil, David H., Wedd, Laura, Wheeler, Matthew T., White, Susan M., Wojcik, Monica, Wolfe, Lynne A., Wolfenson, Zoe, Wright, Caroline F., Xiao, Changrui, Zocche, David, Rubenstein, John L., Markenscoff-Papadimitriou, Eirene, Fica, Sebastian M., Baralle, Diana, Depienne, Christel, MacArthur, Daniel G., Sanders, Stephan J., O’Donnell-Luria, Anne, Whiffin, Nicola

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Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci von Liu, Mengzhen, Jackson, Victoria E., Melbourne, Carl A., Young, Robin, Batini, Chiara, Afaq, Saima, Agrawal, Arpana, Antoniou, Antonis C., Baumbach, Clemens, Boehnke, Michael, Brazel, David M, Chen, Chu, Corley, Janie, Chou, Yi-Ling, David, Sean P., de Boer, Rudolf A., Dennis, Joe G., Easton, Douglas F., Eaton, Charles, Goate, Alison, Grabe, Hans J., Haessler, Jeff, Hallmans, Göran, Harris, Sarah E., Hattersley, Andrew, Heath, Andrew, Kapoor, Manav, Karpe, Fredrik, Kooner, Jaspal S., Kooperberg, Charles, Laakso, Markku, Langenberg, Claudia, Luan, Jian’an, Madden, Pamela A. F., Mangino, Massimo, Marouli, Eirini, Marten, Jonathan, McGue, Matt, Moayyeri, Alireza, Moitry, Marie, Naheed, Aliya, Nauck, Matthias, Neville, Matthew J., Nielsen, Sune Fallgaard, Perola, Markus, Pharoah, Paul D. P., Rasheed, Asif, Renström, Frida, Rice, John, Rohde, Rebecca, Samuel, Maria, Scholte, Steven H, Scott, Robert A., Shao, Yaming, Smith, Jennifer A., Starr, John M., Stram, Danielle, Stringham, Heather M., Tachmazidou, Ioanna, Tardif, Jean-Claude, Thompson, Deborah J., Tindle, Hilary A., Tragante, Vinicius, Trompet, Stella, Turcot, Valerie, Tyrrell, Jessica, van der Leij, Andries R, van der Meer, Peter, Verweij, Niek, Warren, Helen R., Weiss, Stefan, Wetherill, Leah, Yaghootkar, Hanieh, Jiang, Yu, Chen, Fang, Zhan, Xiaowei, Zhang, Weihua, Zhao, Wei, Zhao, Wei, Zhou, Kaixin, Amouyel, Philippe, Blankenberg, Stefan, Caulfield, Mark J., Chowdhury, Rajiv, Cucca, Francesco, Deary, Ian J., Deloukas, Panos, Ferrario, Marco, Frossard, Philippe, Hall, Ian P., Jansson, Jan-Håkan, Kee, Frank, Munroe, Patricia B., Palmer, Colin N. A., Sattar, Naveed, Spector, Timothy, Zeggini, Eleftheria, Saleheen, Danish, Danesh, John, Tobin, Martin D.

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Origins of stereoselectivity in optically pure phenylethaniminopyridine tris-chelates M(NN')3(n+) (M = Mn, Fe, Co, Ni and Zn) von Howson, Suzanne E, Allan, Laura E N, Chmel, Nikola P, Clarkson, Guy J, Deeth, Robert J, Faulkner, Alan D, Simpson, Daniel H, Scott, Peter

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Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data von Romagnoni, Alberto, Jégou, Simon, Van Steen, Kristel, Wainrib, Gilles, Hugot, Jean-Pierre

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Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use von Jiang, Yu, Hughey, Jordan M., Zhan, Xiaowei, Gong, Jian, Batini, Chiara, Liu, MengZhen, Surendran, Praveen, Young, Robin, Nielsen, Sune Fallgaard, Kontto, Jukka, Perola, Markus, Caslake, Muriel, Reily, Dermot F., Vogt, Thomas, Sattar, Naveed, Ford, Ian, Alam, Dewan S., Majumder, Abdulla al Shafi, Di Angelantonio, Emanuele, Chowdhury, Rajiv, Arveiler, Dominique, Blankenberg, Stefan, Veronesi, Giovanni, EPIC-CVD Consortium, Frossard, Philippe, Nordestgaard, Børge Grønne, Saleheen, Danish, Danesh, John, Butterworth, Adam S., Warren, Helen R., Tragante, Vinicius, Altmaier, Elisabeth, Luan, Jian’an, Scott, Robert A., Stirrups, Kathleen, Marouli, Eirini, Karpe, Fredrik, Poulter, Neil, Rolandsson, Olov, Chambers, John C., Kooner, Jaspal S., Wareham, Nicholas J., Renström, Frida, Hallmans, Göran, Marioni, Riccardo E., Corley, Janie, Starr, John M., van der Meer, Peter, Yavas, Ersin, Vaartjes, Ilonca, Asselbergs, Folkert W., Grabe, Hans J., Nauck, Matthias, Pharoah, Paul D.P., Dunning, Alison M., Dennis, Joe G., Tyrrell, Jessica, Mihailov, Evelin, Metspalu, Andres, Palmer, Colin N.A., Hall, Ian P., Strachan, David P., Understanding Society Scientific Group, Munroe, Patricia B., Jansson, Jan-Håkan, Franks, Paul W., Deloukas, Panos, Chou, Yi-Ling, Faul, Jessica D., Hammerschlag, Anke R., Hsu, Chris, Lai, Dongbing, Le, Nhung, Loukola, Anu, Mangino, Massimo, Melbourne, Carl A., Pistis, Giorgio, Qaiser, Beenish, Stringham, Heather, Wetherill, Leah, Bierut, Laura, Chen, Chu, Eaton, Charles B., Iacono, William G., Polderman, Tinca J., Schlessinger, David, Scholte, H. Steven, Smith, Jennifer A., Boehnke, Michael, Cucca, Francesco, David, Sean P., Foroud, Tatiana, Kardia, Sharon L.R., Madden, Pamela, McGue, Matt, Posthuma, Danielle, Spector, Timothy, Stram, Daniel, Kaprio, Jaakko, Vrieze, Scott

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Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution von Justice, Anne E., Young, Kristin L., Lu, Yingchang, Turcot, Valérie, Winkler, Thomas W., Medina-Gomez, Carolina, Mudgal, Poorva, Ng, Maggie C. Y., Willems, Sara M., Abecasis, Goncalo, Allison, Matthew, Balkau, Beverley, Bastarache, Lisa, Bergmann, Sven, Bielak, Lawrence F., Blüher, Matthias, Boeing, Heiner, Bottinger, Erwin P., Bowden, Donald W., Butterworth, Adam S., Chambers, John C., Chen, Yii-Der Ida, Chowdhury, Rajiv, Chu, Audrey Y., Cox, Amanda J., Danesh, John, Denny, Josh C., Di Angelantonio, Emanuele, Drenos, Fotios, Dubé, Marie-Pierre, Evangelou, Evangelos, Ferrannini, Ele, Ferrieres, Jean, Florez, Jose C., Gan, Wei, Giedraitis, Vilmantas, Grove, Megan L., Howson, Joanna M. M., Ikram, M. Arfan, Ingelsson, Erik, Jackson, Anne U., Jarvik, Gail P., Kitajima, Hidetoshi, Krämer, Bernhard K., Laakso, Markku, Lamparter, David, Lee, Wen-Jane, Li, Huaixing, Li, Jin, Lin, Xu, Linneberg, Allan, Liu, Ching-Ti, MacGregor, Stuart, Männistö, Satu, Masca, Nicholas G. D., Moitry, Marie, Müller-Nurasyid, Martina, Munroe, Patricia B., Neville, Matt, Perola, Markus, Pers, Tune H., Reilly, Dermot F., Ridker, Paul M., Rivas, Manuel A., Robertson, Neil R., Rudan, Igor, Saleheen, Danish, Samani, Nilesh J., Schreiner, Pamela J., Scott, Robert A., Slater, Andrew J., Speliotes, Elizabeth K., Steinthorsdottir, Valgerdur, Sun, Liang, Taylor, Kent D., Thorleifsson, Gudmar, Tönjes, Anke, Tsafantakis, Emmanouil, Uusitupa, Matti, Vermeulen, Sita H., Vitart, Veronique, Vuckovic, Dragana, Wagenknecht, Lynne E., Walker, Mark, Wallentin, Lars, Waterworth, Dawn M., Wu, Ying, Zeggini, Eleftheria, Zhan, Xiaowei, Zhao, Jing Hua, Zhao, Wei, Zhou, Wei, Rivadeneira, Fernando, Pospisilik, J. Andrew, Mohlke, Karen L., Rotter, Jerome I., Hirschhorn, Joel N., Cupples, L. Adrienne, Loos, Ruth J. F., North, Kari E.

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Publisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus von Stacey, David, Chen, Lingyan, Stanczyk, Paulina J., Howson, Joanna M. M., Mason, Amy M., Burgess, Stephen, MacDonald, Stephen, Langdown, Jonathan, McKinney, Harriett, Downes, Kate, Farahi, Neda, Peters, James E., Basu, Saonli, Pankow, James S., Tang, Weihong, Pankratz, Nathan, Sabater-Lleal, Maria, de Vries, Paul S., Smith, Nicholas L., Gelinas, Amy D., Schneider, Daniel J., Janjic, Nebojsa, Samani, Nilesh J., Ye, Shu, Summers, Charlotte, Chilvers, Edwin R., Danesh, John, Paul, Dirk S.

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Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data von Chen, Guo-Bo, Lee, Sang Hong, Brion, Marie-Jo A, Montgomery, Grant W, Wray, Naomi R, Radford-Smith, Graham L, Visscher, Peter M

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