An organic chemical model of the acyl-.alpha.-chymotrypsin intermediate von Mallick, Ishwar M, D'Souza, Valerian T, Yamaguchi, Motowo, Lee, James, Chalabi, Phillip, Gadwood, Robert C, Bender, Myron L

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Synthesis of [ 3 H]CP‐93,129: A selective radioligand for the 5‐HT 1B receptor von Macor, John E, Ryan, Kevin, Chalabi, Phillip M., Windels, James C., Roth, Robert W.

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Reactions of formyl phosphate with linear and macrocyclic polyamines von Jiang, Zonghui, Chalabi, Phillip, Mertes, Kristin Bowman, Jahansouz, Hossain, Himes, Richard H., Mertes, Mathias P.

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Synthesis of [19-3H] herbimycin A von Dow, Robert L., Bechle, Bruce M., Chalabi, Phillip M., Windels, James H., Roth, Robert W.

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Synthesis of [3H]CP-93,129: A selective radioligand for the 5-HT1B receptor von Macor, John E, Ryan, Kevin, Chalabi, Phillip M., Windels, James C., Roth, Robert W.

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Synthesis of 5-(2,3-ditritiopropoxy)-3-(1,2,5,6-tetrahydropyrid-4-yl)indole ([3H]CP-96,501): A selective ligand for the serotonin (5-HT1B) receptor von Macor, John E., Burkhart, Carol A., Lebel, Lorraine A., Koe, B. Kenneth, Chalabi, Phillip M., Windels, James C., Roth, Robert W.

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Evaluation of risk factors in the development of hepatocellular carcinoma in autoimmune hepatitis: Implications for follow‐up and screening von Yeoman, Andrew D., Al‐Chalabi, Thawab, Karani, John B., Quaglia, Alberto, Devlin, John, Mieli‐Vergani, Giorgina, Bomford, Adrian, O'Grady, John G., Harrison, Phillip M., Heneghan, Michael A.

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NEK1 variants confer susceptibility to amyotrophic lateral sclerosis von Kenna, Kevin P, van Doormaal, Perry T C, Dekker, Annelot M, Ticozzi, Nicola, Kenna, Brendan J, Diekstra, Frank P, van Rheenen, Wouter, van Eijk, Kristel R, Jones, Ashley R, Keagle, Pamela, Shatunov, Aleksey, Sproviero, William, Smith, Bradley N, van Es, Michael A, Topp, Simon D, Kenna, Aoife, Miller, Jack W, Fallini, Claudia, Tiloca, Cinzia, McLaughlin, Russell L, Vance, Caroline, Troakes, Claire, Colombrita, Claudia, Mora, Gabriele, Calvo, Andrea, Verde, Federico, Al-Sarraj, Safa, King, Andrew, Calini, Daniela, de Belleroche, Jacqueline, Baas, Frank, van der Kooi, Anneke J, de Visser, Marianne, ten Asbroek, Anneloor L M A, Sapp, Peter C, McKenna-Yasek, Diane, Polak, Meraida, Asress, Seneshaw, Muñoz-Blanco, José Luis, Strom, Tim M, Meitinger, Thomas, Morrison, Karen E, Lauria, Giuseppe, Williams, Kelly L, Leigh, P Nigel, Nicholson, Garth A, Blair, Ian P, Leblond, Claire S, Dion, Patrick A, Rouleau, Guy A, Pall, Hardev, Shaw, Pamela J, Turner, Martin R, Talbot, Kevin, Taroni, Franco, Boylan, Kevin B, Van Blitterswijk, Marka, Rademakers, Rosa, Esteban-Pérez, Jesús, García-Redondo, Alberto, Van Damme, Phillip, Robberecht, Wim, Chio, Adriano, Gellera, Cinzia, Drepper, Carsten, Sendtner, Michael, Ratti, Antonia, Glass, Jonathan D, Mora, Jesús S, Basak, Nazli A, Hardiman, Orla, Ludolph, Albert C, Andersen, Peter M, Weishaupt, Jochen H, Brown, Robert H, Al-Chalabi, Ammar, Silani, Vincenzo, Shaw, Christopher E, van den Berg, Leonard H, Veldink, Jan H, Landers, John E

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The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder von Smith, Bradley N, Newhouse, Stephen, Shatunov, Aleksey, Vance, Caroline, Topp, Simon, Johnson, Lauren, Miller, Jack, Lee, Younbok, Troakes, Claire, Scott, Kirsten M, Jones, Ashley, Gray, Ian, Wright, Jamie, Hortobágyi, Tibor, Al-Sarraj, Safa, Rogelj, Boris, Powell, John, Lupton, Michelle, Lovestone, Simon, Sapp, Peter C, Weber, Markus, Nestor, Peter J, Schelhaas, Helenius J, Asbroek, Anneloor Alm Ten, Silani, Vincenzo, Gellera, Cinzia, Taroni, Franco, Ticozzi, Nicola, Van den Berg, Leonard, Veldink, Jan, Van Damme, Phillip, Robberecht, Wim, Shaw, Pamela J, Kirby, Janine, Pall, Hardev, Morrison, Karen E, Morris, Alex, de Belleroche, Jacqueline, Vianney de Jong, J M B, Baas, Frank, Andersen, Peter M, Landers, John, Brown, Jr, Robert H, Weale, Michael E, Al-Chalabi, Ammar, Shaw, Christopher E

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Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials von van Eijk, Ruben P.A, Jones, Ashley R, Sproviero, William, Shatunov, Aleksey, Shaw, Pamela J, Leigh, P Nigel, Young, Carolyn A, Shaw, Christopher E, Mora, Gabriele, Mandrioli, Jessica, Borghero, Giuseppe, Volanti, Paolo, Diekstra, Frank P, van Rheenen, Wouter, Verstraete, Esther, Eijkemans, Marinus J.C, Veldink, Jan H, Chio, Adriano, Al-Chalabi, Ammar, van den Berg, Leonard H, van Es, Michael A

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Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries von Skoric-Milosavljevic, Doris, Tadros, Rafik, Bosada, Fernanda M, Tessadori, Federico, van Weerd, Jan Hendrik, Woudstra, Odilia, Tjong, Fleur V.Y, Lahrouchi, Najim, Bajolle, Fanny, Cordell, Heather J, Agopian, A.J, Blue, Gillian M, Barge-Schaapveld, Daniela Q.C.M, Gewillig, Marc, Preuss, Christoph, Lodder, Elisabeth M, Barnett, Phil, Ilgun, Aho, Beekman, Leander, van Duijvenboden, Karel, Bokenkamp, Regina, Muller-Nurasyid, Martina, Vliegen, Hubert W, Konings, Thelma C, van Melle, Joost P, van Dijk, Arie P.J, van Kimmenade, Roland R.J, Roos-Hesselink, Jolien W, Sieswerda, Gertjan, Meijboom, Folkert, Abdul-Khaliq, Hashim, Berger, Felix, Dittrich, Sven, Hitz, Marc-Phillip, Moosmann, Julia, Riede, Frank-Thomas, Schubert, Stephan, Galan, Pilar, Lathrop, Mark, Munter, Hans Markus, Al-Chalabi, Ammar, Shaw, Christopher E, Shaw, Pamela J, Morrison, Karen E, Veldink, Jan H, van den Berg, Leonard H, Evans, Sylvia, Nobrega, Marcelo A, Aneas, Ivy, Radivojkov-Blagojevic, Milena, Meitinger, Thomas, Oechslin, Erwin, Mondal, Tapas, Bergin, M. Lynn, Smythe, John F, Altamirano-Diaz, Luis, Lougheed, Jane, Bouma, Berto J, Chaix, Marie A, Kline, Jennie, Bassett, Anne S, Andelfinger, Gregor, van der Palen, Roel L.F, Bouvagnet, Patrice, Clur, Sally-Ann B, Breckpot, Jeroen, Kerstjens-Frederikse, Wilhelmina S, Winlaw, David S, Bauer, Ulrike M.M, Mital, Seema, Goldmuntz, Elizabeth, Keavney, Bernard, Bonnet, Damien, Mulder, Barbara J, Tanck, Michael W.T, Bakkers, Jeroen, Christoffels, Vincent M, Boogerd, Cornelis J, Postma, Alex, Bezzina, Connie R

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Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries von Škorić-Milosavljević, Doris, Tadros, Rafik, Bosada, Fernanda M., Tessadori, Federico, van Weerd, Jan Hendrik, Woudstra, Odilia I., Tjong, Fleur V.Y., Lahrouchi, Najim, Bajolle, Fanny, Cordell, Heather J., Agopian, A. J., Blue, Gillian M., Barge-Schaapveld, Daniela Q.C.M., Gewillig, Marc, Preuss, Christoph, Lodder, Elisabeth M., Barnett, Phil, Ilgun, Aho, Beekman, Leander, van Duijvenboden, Karel, Bokenkamp, Regina, Müller-Nurasyid, Martina, Vliegen, Hubert W., Konings, Thelma C., van Melle, Joost P., van Dijk, Arie P.J., van Kimmenade, Roland R.J., Roos-Hesselink, Jolien W., Sieswerda, Gertjan T., Meijboom, Folkert, Abdul- Khaliq, Hashim, Berger, Felix, Dittrich, Sven, Hitz, Marc-Phillip, Moosmann, Julia, Riede, Frank-Thomas, Schubert, Stephan, Galan, Pilar, Lathrop, Mark, Munter, Hans M., Al-Chalabi, Ammar, Shaw, Christopher E., Shaw, Pamela J., Morrison, Karen E., Veldink, Jan H., van den Berg, Leonard H., Evans, Sylvia, Nobrega, Marcelo A., Aneas, Ivy, Radivojkov-Blagojević, Milena, Meitinger, Thomas, Oechslin, Erwin, Mondal, Tapas, Bergin, Lynn, Smythe, John F., Altamirano-Diaz, Luis, Lougheed, Jane, Bouma, Berto J., Chaix, Marie-A., Kline, Jennie, Bassett, Anne S., Andelfinger, Gregor, van der Palen, Roel L.F., Bouvagnet, Patrice, Clur, Sally-Ann B., Breckpot, Jeroen, Kerstjens-Frederikse, Wilhelmina S., Winlaw, David S., Bauer, Ulrike M.M., Mital, Seema, Goldmuntz, Elizabeth, Keavney, Bernard, Bonnet, Damien, Mulder, Barbara J., Tanck, Michael W.T., Bakkers, Jeroen, Christoffels, Vincent M., Boogerd, Cornelis J., Postma, Alex V., Bezzina, Connie R.

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Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation von Hemani, Gibran, Dekkers, Koen F, Luijk, René, Carnero-Montoro, Elena, Burrows, Kimberley, Richardson, Tom G, Klughammer, Johanna, Iotchkova, Valentina, Sharp, Gemma, Al Khleifat, Ahmad, Shatunov, Aleksey, Iacoangeli, Alfredo, McArdle, Wendy L, Ho, Karen M, Kumar, Ashish, Söderhäll, Cilla, Kazmi, Nabila, McRae, Allan F, Kasela, Silva, Cardona, Alexia, Cugliari, Giovanni, Viberti, Clara, Guarrera, Simonetta, Lerro, Michael, Zeng, Yanni, Clarke, Toni-Kim, Walker, Rosie M, Schmoll, Vanessa, Czamara, Darina, Ruiz-Arenas, Carlos, Marioni, Riccardo E, Lin, Tian, Awaloff, Yvonne, Germain, Marine, Aïssi, Dylan, Dekker, Annelot, van Dongen, Jenny, Hottenga, Jouke-Jan, Barturen, Guillermo, Català-Moll, Francesc, Wang, Carol, Melton, Phillip, Elliott, Hannah R, Shin, Jean, Yet, Idil, Smart, Melissa, Shaw, Chris, Ring, Susan M, Melén, Erik, Roquer, Jaume, Lawlor, Deborah A, Wright, John, Montgomery, Grant W, Moffitt, Terrie E, Poulton, Richie, Esko, Tõnu, Perry, John R. B, Ong, Ken K, Wareham, Nicholas J, Sacerdote, Carlotta, Panico, Salvatore, Caspi, Avshalom, Arseneault, Louise, Gagnon, France, Felix, Janine F, Rivadeneira, Fernando, Uitterlinden, André G, Jaddoe, Vincent W. V, Evans, Kathryn L, Murray, Alison, Räikkönen, Katri, Sørensen, Thorkild I. A, Morgen, Camilla S, Binder, Elisabeth B, Lucae, Susanne, Bustamante, Mariona, Sunyer, Jordi, Holloway, John W, Karmaus, Wilfried, Zhang, Hongmei, Deary, Ian J, Wray, Naomi R, Beekman, Marian, van Heemst, Diana, Slagboom, P. Eline, Veldink, Jan H, Davies, Gareth E, de Geus, Eco J. C, Boomsma, Dorret I, Vonk, Judith M, Brunekreef, Bert, Koppelman, Gerard H, Pennell, Craig E, Ikram, M. Arfan, Chaturvedi, Nish, Spector, Timothy D, Schalkwyk, Leonard C, Davey Smith, George, Mill, Jonathan, Relton, Caroline L

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C9orf72 expansion differentially affects males with spinal onset amyotrophic lateral sclerosis von Rooney, James, Fogh, Isabella, Westeneng, Henk-Jan, Vajda, Alice, McLaughlin, Russell, Heverin, Mark, Jones, Ashley, van Eijk, Ruben, Calvo, Andrea, Mazzini, Letizia, Shaw, Christopher, Morrison, Karen, Shaw, Pamela J, Robberecht, Wim, Van Damme, Phillip, Al-Chalabi, Ammar, van den Berg, Leonard, Chiò, Adriano, Veldink, Jan, Hardiman, Orla

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Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries von Škorić-Milosavljević, Doris, Tadros, Rafik, Bosada, Fernanda M, Tessadori, Federico, Weerd, Jan Hendrik van, Woudstra, Odilia I, Tjong, Fleur V.Y, Lahrouchi, Najim, Bajolle, Fanny, Cordell, Heather J, Agopian, A.J, Blue, Gillian M, Barge-Schaapveld, Daniela Q.C.M, Gewillig, Marc, Preuss, Christoph, Lodder, Elisabeth M, Barnett, Phil, Ilgun, Aho, Beekman, Leander, Duijvenboden, Karel van, Bokenkamp, Regina, Müller-Nurasyid, Martina, Vliegen, Hubert W, Konings, Thelma C, Melle, Joost P. van, Dijk, Arie P. J. van, Kimmenade, Roland R .J. van, Roos-Hesselink, Jolien W, Sieswerda, Gertjan T, Meijboom, Folkert, Abdul-Khaliq, Hashim, Berger, Felix, Dittrich, Sven, Hitz, Marc-Phillip, Moosmann, Julia, Riede, Frank-Thomas, Schubert, Stephan, Galan, Pilar, Lathrop, Mark, Munter, Hans M, Al-Chalabi, Ammar, Shaw, Christopher E, Shaw, Pamela J, Morrison, Karen E, Veldink, Jan H, Berg, Leonard H. van den, Evans, Sylvia, Nobrega, Marcelo A, Aneas, Ivy, Radivojkov-Blagojević, Milena, Meitinger, Thomas, Oechslin, Erwin, Mondal, Tapas, Bergin, Lynn, Smythe, John F, Altamirano-Diaz, Luis, Lougheed, Jane, Bouma, Berto J, Chaix, Marie-A, Kline, Jennie, Bassett, Anne S, Andelfinger, Gregor, Palen, Roel L. F. van der, Bouvagnet, Patrice, Clur, Sally-Ann B, Breckpot, Jeroen, Kerstjens-Frederikse, Wilhelmina S, Winlaw, David S, Bauer, Ulrike M.M, Mital, Seema, Goldmuntz, Elizabeth, Keavney, Bernard, Bonnet, Damien, Mulder, Barbara J, Tanck, Michael W. T, Bakkers, Jeroen, Christoffels, Vincent M, Boogerd, Cornelis J, Postma, Alex V, Bezzina, Connie R

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