Cocrystallization via planetary milling: Enhancing throughput of solid-state screening methods by Bysouth, Stephen R., Bis, Joanna A., Igo, David

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Pharmaceutical Co-Crystals by Vishweshwar, Peddy, McMahon, Jennifer A., Bis, Joanna A., Zaworotko, Michael J.

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Concomitant and Conformational Polymorphism, Conformational Isomorphism, and Phase Relationships in 4-Cyanopyridine·4,4‘-biphenol Cocrystals by Bis, Joanna A, Vishweshwar, Peddy, Middleton, Richard A, Zaworotko, Michael J

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The 2-Aminopyridinium-carboxylate Supramolecular Heterosynthon:  A Robust Motif for Generation of Multiple-Component Crystals by Bis, Joanna A, Zaworotko, Michael J

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Supramolecular Heterocatemers and Their Role in Cocrystal Design by Bis, Joanna A, McLaughlin, Olga L, Vishweshwar, Peddy, Zaworotko, Michael J

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Crystallization and Solid-State Characterization of the Hemihydrate of Albuterol Hemisulfate by Bis, Joanna A, Boyle, Paul D, Carino, Stephen A. R, Igo, David H, Katrincic, Lee M

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Discovery, Characterization, and Solid-State Quantification of the Racemic Compound of Guaifenesin by Bis, Joanna A., Graves, Briana N., Tarczynski, Frank J., Wojtas, Lukasz

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Hierarchy of Supramolecular Synthons:  Persistent Hydroxyl···Pyridine Hydrogen Bonds in Cocrystals That Contain a Cyano Acceptor by Bis, Joanna A., Vishweshwar, Peddy, Weyna, David, Zaworotko, Michael J.

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Hierarchy of supramolecular synthons: persistent hydroxyl...pyridine hydrogen bonds in cocrystals that contain a cyano acceptor by Bis, Joanna A, Vishweshwar, Peddy, Weyna, David, Zaworotko, Michael J

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Stroke genetics informs drug discovery and risk prediction across ancestries by Jürgenson, Tuuli, Namba, Shinichi, Posner, Daniel C., Kamanu, Frederick K., Koido, Masaru, He, Yunye, Caro, Ilana, Krebs, Kristi, Liaw, Yi-Ching, Parodi, Livia, Bae, Hee-Joon, Chong, Michael R., Tomppo, Liisa, Akinyemi, Rufus, Roshchupkin, Gennady V., Habib, Naomi, Jee, Yon Ho, Thomassen, Jesper Qvist, Abedi, Vida, Cárcel-Márquez, Jara, Nygaard, Marianne, Yonova-Doing, Ekaterina, Knol, Maria J., Lewis, Adam J., Judy, Renae L., Amouyel, Philippe, Bakker, Mark K., Bennett, David A., Bis, Joshua C., Bordes, Constance, Børte, Sigrid, Cain, Anael, Ridker, Paul M., Cho, Kelly, Chen, Zhengming, Cruchaga, Carlos, Cole, John W., de Cid, Rafael, Ferreira, Leslie E., He, Jing, Jeon, Christina E., Jern, Christina, Kamouchi, Masahiro, Keene, Keith L., Konuma, Takahiro, Kumar, Amit, Launer, Lenore J., Lee, Keon-Joo, Li, Jiang, Li, Liming, Manichaikul, Ani, Markus, Hugh S., Meitinger, Thomas, Mitchell, Braxton D., Morisaki, Takayuki, O’Donnell, Martin J., Onland-Moret, N. Charlotte, Ovbiagele, Bruce, Peters, Annette, Rosand, Jonathan, Sabatine, Marc S., Sacco, Ralph L., Saleheen, Danish, Schmidt, Carsten O., Smith, Nicholas L., Sloane, Kelly L., Sutoh, Yoichi, Tiwari, Hemant K., Wennberg, Patrik, Wilson, Peter W. F., Yang, Qiong, Yoon, Kyungheon, Gieger, Christian, Ninomiya, Toshiharu, Grabe, Hans J., Jukema, J. Wouter, Kim, Young Jin, Chen, Pei-Hsin, Mayerhofer, Ernst, Ikram, Mohammad A., Worrall, Bradford B., Lathrop, G. Mark, Riaz, Moeen, Simonsick, Eleanor M., Kõrv, Janika, Zand, Ramin, Prasad, Kameshwar, Frikke-Schmidt, Ruth, Liman, Thomas, Ruigrok, Ynte M., Bastarache, Lisa, Damrauer, Scott M., Rotter, Jerome I., Niiranen, Teemu J., Walters, Robin G., Owolabi, Mayowa O., Huffman, Jennifer E., Kamatani, Yoichiro, Dichgans, Martin, Debette, Stephanie

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Genes From a Translational Analysis Support a Multifactorial Nature of White Matter Hyperintensities by Lopez, Lorna M, Hill, W David, Harris, Sarah E, Valdes Hernandez, Maria, Munoz Maniega, Susana, Bastin, Mark E, Bailey, Emma, Smith, Colin, McBride, Martin, McClure, John, Graham, Delyth, Dominiczak, Anna, Yang, Qiong, Fornage, Myriam, Ikram, M Arfan, Debette, Stephanie, Launer, Lenore, Bis, Joshua C, Schmidt, Reinhold, Seshadri, Sudha, Porteous, David J, Starr, John, Deary, Ian J, Wardlaw, Joanna M

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Comparison of bicuspid and tricuspid aortic valve repair by Gocoł, Radosław, Bis, Jarosław, Malinowski, Marcin, Ciosek, Joanna, Hudziak, Damian, Morkisz, Łukasz, Jasiński, Marek, Deja, Marek A

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Building a collaborative cloud platform to accelerate heart, lung, blood, and sleep research by Ahalt, Stan, Avillach, Paul, Boyles, Rebecca, Bradford, Kira, Cox, Steven, Davis-Dusenbery, Brandi, Grossman, Robert L, Krishnamurthy, Ashok, Manning, Alisa, Paten, Benedict, Philippakis, Anthony, Borecki, Ingrid, Chen, Shu Hui, Kaltman, Jon, Ladwa, Sweta, Schwartz, Chip, Thomson, Alastair, Davis, Sarah, Leaf, Alison, Lyons, Jessica, Sheets, Elizabeth, Bis, Joshua C, Conomos, Matthew, Culotti, Alessandro, Desain, Thomas, Digiovanna, Jack, Domazet, Milan, Gogarten, Stephanie, Gutierrez-Sacristan, Alba, Harris, Tim, Heavner, Ben, Jain, Deepti, O'Connor, Brian, Osborn, Kevin, Pillion, Danielle, Pleiness, Jacob, Rice, Ken, Rupp, Garrett, Serret-Larmande, Arnaud, Smith, Albert, Stedman, Jason P, Stilp, Adrienne, Barsanti, Teresa, Cheadle, John, Erdmann, Christopher, Farlow, Brandy, Gartland-Gray, Allie, Hayes, Julie, Hiles, Hannah, Kerr, Paul, Lenhardt, Chris, Madden, Tom, Mieczkowska, Joanna O, Miller, Amanda, Patton, Patrick, Rathbun, Marcie, Suber, Stephanie, Asare, Joe

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Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies by Traylor, Matthew, MSc, Farrall, Martin, FRCPath, Holliday, Elizabeth G, PhD, Sudlow, Cathie, FRCP, Hopewell, Jemma C, PhD, Cheng, Yu-Ching, PhD, Fornage, Myriam, PhD, Ikram, M Arfan, MD, Malik, Rainer, PhD, Bevan, Steve, PhD, Thorsteinsdottir, Unnur, PhD, Nalls, Mike A, PhD, Longstreth, WT, MD, Wiggins, Kerri L, MS, Yadav, Sunaina, MSc, Parati, Eugenio A, MD, DeStefano, Anita L, PhD, Worrall, Bradford B, MD, Kittner, Steven J, MD, Khan, Muhammad Saleem, MSc, Reiner, Alex P, MD, Helgadottir, Anna, MD, Achterberg, Sefanja, PhD, Fernandez-Cadenas, Israel, PhD, Abboud, Sherine, MD, Schmidt, Reinhold, MD, Walters, Matthew, MD, Chen, Wei-Min, PhD, Ringelstein, E Bernd, MD, O'Donnell, Martin, MD, Ho, Weang Kee, PhD, Pera, Joanna, MD, Lemmens, Robin, MD, Norrving, Bo, MD, Higgins, Peter, MRCP, Benn, Marianne, MD, Sale, Michele, PhD, Kuhlenbäumer, Gregor, MD, Doney, Alexander S F, PhD, Vicente, Astrid M, PhD, Delavaran, Hossein, MD, Algra, Ale, MD, Davies, Gail, PhD, Oliveira, Sofia A, PhD, Palmer, Colin N A, PhD, Deary, Ian, PhD, Schmidt, Helena, MD, Pandolfo, Massimo, MD, Montaner, Joan, MD, Carty, Cara, PhD, de Bakker, Paul I W, PhD, Kostulas, Konstantinos, MD, Ferro, Jose M, MD, van Zuydam, Natalie R, MSc, Valdimarsson, Einar, MD, Nordestgaard, Børge G, MD, Lindgren, Arne, MD, Thijs, Vincent, MD, Slowik, Agnieszka, MD, Saleheen, Danish, MD, Paré, Guillaume, MD, Berger, Klaus, MD, Thorleifsson, Gudmar, PhD, Hofman, Albert, MD, Mosley, Thomas H, PhD, Mitchell, Braxton D, PhD, Furie, Karen, MD, Clarke, Robert, FRCP, Levi, Christopher, MD, Seshadri, Sudha, MD, Gschwendtner, Andreas, MD, Boncoraglio, Giorgio B, MD, Sharma, Pankaj, PhD, Bis, Joshua C, PhD, Gretarsdottir, Solveig, PhD, Psaty, Bruce M, Rothwell, Peter M, FMedSci, Rosand, Jonathan, MD, Meschia, James F, MD, Stefansson, Kari, MD, Dichgans, Martin, MD, Markus, Hugh S, Dr

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A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease by Scott, Robert A, Freitag, Daniel F, Li, Li, Chu, Audrey Y, Surendran, Praveen, Young, Robin, Grarup, Niels, Stancáková, Alena, Chen, Yuning, Varga, Tibor V, Yaghootkar, Hanieh, Luan, Jian'an, Zhao, Jing Hua, Willems, Sara M, Wessel, Jennifer, Wang, Shuai, Maruthur, Nisa, Michailidou, Kyriaki, Pirie, Ailith, van der Lee, Sven J, Gillson, Christopher, Al Olama, Ali Amin, Amouyel, Philippe, Arriola, Larraitz, Arveiler, Dominique, Aviles-Olmos, Iciar, Balkau, Beverley, Barricarte, Aurelio, Barroso, Inês, Garcia, Sara Benlloch, Bis, Joshua C, Blankenberg, Stefan, Boehnke, Michael, Boeing, Heiner, Boerwinkle, Eric, Borecki, Ingrid B, Bork-Jensen, Jette, Bowden, Sarah, Caldas, Carlos, Caslake, Muriel, Cupples, L Adrienne, Cruchaga, Carlos, Czajkowski, Jacek, den Hoed, Marcel, Dunn, Janet A, Earl, Helena M, Ehret, Georg B, Ferrannini, Ele, Ferrieres, Jean, Foltynie, Thomas, Ford, Ian, Forouhi, Nita G, Gianfagna, Francesco, Gonzalez, Carlos, Grioni, Sara, Hiller, Louise, Jansson, Jan-Håkan, Jørgensen, Marit E, Jukema, J Wouter, Kaaks, Rudolf, Kee, Frank, Kerrison, Nicola D, Key, Timothy J, Kontto, Jukka, Kote-Jarai, Zsofia, Kraja, Aldi T, Kuulasmaa, Kari, Kuusisto, Johanna, Linneberg, Allan, Liu, Chunyu, Marenne, Gaëlle, Mohlke, Karen L, Morris, Andrew P, Muir, Kenneth, Müller-Nurasyid, Martina, Munroe, Patricia B, Navarro, Carmen, Nielsen, Sune F, Nilsson, Peter M, Nordestgaard, Børge G, Packard, Chris J, Palli, Domenico, Panico, Salvatore, Peloso, Gina M, Perola, Markus, Peters, Annette, Poole, Christopher J, Quirós, J Ramón, Rolandsson, Olov, Sacerdote, Carlotta, Salomaa, Veikko, Sánchez, María-José, Sattar, Naveed, Sharp, Stephen J, Sims, Rebecca, Slimani, Nadia, Smith, Jennifer A, Thompson, Deborah J, Trompet, Stella, Tumino, Rosario

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Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate by Mishra, Aniket, Duplaà, Cécile, Vojinovic, Dina, Suzuki, Hideaki, Sargurupremraj, Muralidharan, Zilhão, Nuno R, Li, Shuo, Bartz, Traci M, Jian, Xueqiu, Zhao, Wei, Hofer, Edith, Wittfeld, Katharina, Harris, Sarah E, van der Auwera-Palitschka, Sandra, Luciano, Michelle, Bis, Joshua C, Adams, Hieab H H, Satizabal, Claudia L, Gottesman, Rebecca F, Gampawar, Piyush G, Bülow, Robin, Weiss, Stefan, Yu, Miao, Bastin, Mark E, Lopez, Oscar L, Vernooij, Meike W, Beiser, Alexa S, Völker, Uwe, Kacprowski, Tim, Soumare, Aicha, Smith, Jennifer A, Knopman, David S, Morris, Zoe, Zhu, Yicheng, Rotter, Jerome I, Dufouil, Carole, Valdés Hernández, Maria, Muñoz Maniega, Susana, Lathrop, Mark, Boerwinkle, Erik, Schmidt, Reinhold, Ihara, Masafumi, Mazoyer, Bernard, Yang, Qiong, Joutel, Anne, Tournier-Lasserve, Elizabeth, Launer, Lenore J, Deary, Ian J, Mosley, Thomas H, Amouyel, Philippe, DeCarli, Charles S, Psaty, Bruce M, Tzourio, Christophe, Kardia, Sharon L R, Grabe, Hans J, Teumer, Alexander, van Duijn, Cornelia M, Schmidt, Helena, Wardlaw, Joanna M, Ikram, M Arfan, Fornage, Myriam, Gudnason, Vilmundur, Seshadri, Sudha, Matthews, Paul M, Longstreth, William T, Couffinhal, Thierry, Debette, Stephanie

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Publisher Correction: Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus by 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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Publisher Correction: Stroke genetics informs drug discovery and risk prediction across ancestries by Jürgenson, Tuuli, Namba, Shinichi, Posner, Daniel C., Kamanu, Frederick K., Koido, Masaru, He, Yunye, Caro, Ilana, Krebs, Kristi, Liaw, Yi-Ching, Parodi, Livia, Bae, Hee-Joon, Chong, Michael R., Tomppo, Liisa, Akinyemi, Rufus, Roshchupkin, Gennady V., Habib, Naomi, Jee, Yon Ho, Thomassen, Jesper Qvist, Abedi, Vida, Cárcel-Márquez, Jara, Nygaard, Marianne, Yonova-Doing, Ekaterina, Knol, Maria J., Lewis, Adam J., Judy, Renae L., Amouyel, Philippe, Bakker, Mark K., Bennett, David A., Bis, Joshua C., Bordes, Constance, Børte, Sigrid, Cain, Anael, Ridker, Paul M., Cho, Kelly, Chen, Zhengming, Cruchaga, Carlos, Cole, John W., de Cid, Rafael, Ferreira, Leslie E., He, Jing, Jeon, Christina E., Jern, Christina, Kamouchi, Masahiro, Keene, Keith L., Konuma, Takahiro, Kumar, Amit, Launer, Lenore J., Lee, Keon-Joo, Li, Jiang, Li, Liming, Manichaikul, Ani, Markus, Hugh S., Meitinger, Thomas, Mitchell, Braxton D., Morisaki, Takayuki, O’Donnell, Martin J., Onland-Moret, N. Charlotte, Ovbiagele, Bruce, Peters, Annette, Rosand, Jonathan, Sabatine, Marc S., Sacco, Ralph L., Saleheen, Danish, Schmidt, Carsten O., Smith, Nicholas L., Sloane, Kelly L., Sutoh, Yoichi, Tiwari, Hemant K., Wennberg, Patrik, Wilson, Peter W. F., Yang, Qiong, Yoon, Kyungheon, Gieger, Christian, Ninomiya, Toshiharu, Grabe, Hans J., Jukema, J. Wouter, Kim, Young Jin, Chen, Pei-Hsin, Mayerhofer, Ernst, Ikram, Mohammad A., Worrall, Bradford B., Lathrop, G. Mark, Riaz, Moeen, Simonsick, Eleanor M., Kõrv, Janika, Zand, Ramin, Prasad, Kameshwar, Frikke-Schmidt, Ruth, Liman, Thomas, Ruigrok, Ynte M., Bastarache, Lisa, Damrauer, Scott M., Rotter, Jerome I., Niiranen, Teemu J., Walters, Robin G., Owolabi, Mayowa O., Huffman, Jennifer E., Kamatani, Yoichiro, Dichgans, Martin, Debette, Stephanie

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Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus by 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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Meta-analysis of epigenome-wide association studies of carotid intima-media thickness by Portilla-Fernández, Eliana, Hwang, Shih-Jen, Wilson, Rory, Maddock, Jane, Hill, W. David, Teumer, Alexander, Mishra, Pashupati P., Brody, Jennifer A., Joehanes, Roby, Ligthart, Symen, Ghanbari, Mohsen, Kavousi, Maryam, Roks, Anton J. M., Danser, A. H. Jan, Levy, Daniel, Peters, Annette, Ghasemi, Sahar, Schminke, Ulf, Dörr, Marcus, Grabe, Hans J., Lehtimäki, Terho, Kähönen, Mika, Hurme, Mikko A., Bartz, Traci M., Sotoodehnia, Nona, Bis, Joshua C., Thiery, Joachim, Koenig, Wolfgang, Ong, Ken K., Bell, Jordana T., Meisinger, Christine, Wardlaw, Joanna M., Starr, John M., Seissler, Jochen, Then, Cornelia, Rathmann, Wolfgang, Ikram, M. Arfan, Psaty, Bruce M., Raitakari, Olli T., Völzke, Henry, Deary, Ian J., Wong, Andrew, Waldenberger, Melanie, O’Donnell, Christopher J., Dehghan, Abbas

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