Mortality Rates during Cholera Epidemic, Haiti, 2010-2011 von Luquero, Francisco J, Rondy, Marc, Boncy, Jacques, Munger, André, Mekaoui, Helmi, Rymshaw, Ellen, Page, Anne-Laure, Toure, Brahima, Degail, Marie Amelie, Nicolas, Sarala, Grandesso, Francesco, Ginsbourger, Maud, Polonsky, Jonathan, Alberti, Kathryn P, Terzian, Mego, Olson, David, Porten, Klaudia, Ciglenecki, Iza

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Evaluation of a rapid test for the diagnosis of cholera in the absence of a gold standard von Page, Anne-Laure, Alberti, Kathryn P, Mondonge, Vital, Rauzier, Jean, Quilici, Marie-Laure, Guerin, Philippe J

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Geographic distribution and mortality risk factors during the cholera outbreak in a rural region of Haiti, 2010-2011 von Page, Anne-Laure, Ciglenecki, Iza, Jasmin, Ernest Robert, Desvignes, Laurence, Grandesso, Francesco, Polonsky, Jonathan, Nicholas, Sarala, Alberti, Kathryn P, Porten, Klaudia, Luquero, Francisco J

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Achievements and challenges for the use of killed oral cholera vaccines in the global stockpile era von Desai, Sachin N., Pezzoli, Lorenzo, Alberti, Kathryn P., Martin, Stephen, Costa, Alejandro, Perea, William, Legros, Dominique

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Malaria epidemics and interventions, Kenya, Burundi, southern Sudan, and Ethiopia, 1999-2004 von Checchi, Francesco, Cox, Jonathan, Balkan, Suna, Tamrat, Abiy, Priotto, Gerardo, Alberti, Kathryn P, Guthmann, Jean-Paul

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Use of Filter Paper as a Transport Medium for Laboratory Diagnosis of Cholera under Field Conditions von PAGE, Anne-Laure, ALBERTI, Kathryn P, GUENOLE, Alain, MONDONGUE, Vital, MAYELE, Sylvaine Lonlas, GUERIN, Philippe J, QUILICI, Marie-Laure

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Violence against civilians and access to health care in North Kivu, Democratic Republic of Congo: three cross-sectional surveys von Alberti, Kathryn P, Grellety, Emmanuel, Lin, Ya-Ching, Polonsky, Jonathan, Coppens, Katrien, Encinas, Luis, Rodrigue, Marie-Noëlle, Pedalino, Biagio, Mondonge, Vital

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Reactive vaccination as an effective tool for measles outbreak control in measles mortality reduction settings, Democratic Republic of Congo, 2005–2006 von Alberti, Kathryn P, King, Lisa A, Burny, Marie-Eve, Ilunga, Benoit Kebela, Grais, Rebecca F

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Geographic Distribution and Mortality Risk Factors during the Cholera Outbreak in a Rural Region of Haiti, 2010-2011: e0003605 von Page, Anne-Laure, Ciglenecki, Iza, Jasmin, Ernest Robert, Desvignes, Laurence, Grandesso, Francesco, Polonsky, Jonathan, Nicholas, Sarala, Alberti, Kathryn P, Porten, Klaudia, Luquero, Francisco J

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Malaria epidemics and interventions, Kenya, Burundi, southern Sudan, and Ethiopia, 1999-2004 von Checchi, Francesco, Cox, Jonathan, Balkan, Suna, Tamrat, Abiy, Priotto, Gerardo, Alberti, Kathryn P, Guthmann, Jean-Paul

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Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases von Stessman, Holly A F, Xiong, Bo, Coe, Bradley P, Wang, Tianyun, Hoekzema, Kendra, Fenckova, Michaela, Kvarnung, Malin, Gerdts, Jennifer, Trinh, Sandy, Cosemans, Nele, Vives, Laura, Lin, Janice, Turner, Tychele N, Santen, Gijs, Ruivenkamp, Claudia, Kriek, Marjolein, van Haeringen, Arie, Aten, Emmelien, Friend, Kathryn, Liebelt, Jan, Barnett, Christopher, Haan, Eric, Shaw, Marie, Gecz, Jozef, Anderlid, Britt-Marie, Nordgren, Ann, Lindstrand, Anna, Schwartz, Charles, Kooy, R Frank, Vandeweyer, Geert, Helsmoortel, Celine, Romano, Corrado, Alberti, Antonino, Vinci, Mirella, Avola, Emanuela, Giusto, Stefania, Courchesne, Eric, Pramparo, Tiziano, Pierce, Karen, Nalabolu, Srinivasa, Amaral, David G, Scheffer, Ingrid E, Delatycki, Martin B, Lockhart, Paul J, Hormozdiari, Fereydoun, Harich, Benjamin, Castells-Nobau, Anna, Xia, Kun, Peeters, Hilde, Nordenskjöld, Magnus, Schenck, Annette, Bernier, Raphael A, Eichler, Evan E

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Refining analyses of copy number variation identifies specific genes associated with developmental delay von Coe, Bradley P, Witherspoon, Kali, Rosenfeld, Jill A, van Bon, Bregje W M, Vulto-van Silfhout, Anneke T, Bosco, Paolo, Friend, Kathryn L, Baker, Carl, Buono, Serafino, Vissers, Lisenka E L M, Schuurs-Hoeijmakers, Janneke H, Hoischen, Alex, Pfundt, Rolph, Krumm, Nik, Carvill, Gemma L, Li, Deana, Amaral, David, Brown, Natasha, Lockhart, Paul J, Scheffer, Ingrid E, Alberti, Antonino, Shaw, Marie, Pettinato, Rosa, Tervo, Raymond, de Leeuw, Nicole, Reijnders, Margot R F, Torchia, Beth S, Peeters, Hilde, Thompson, Elizabeth, O'Roak, Brian J, Fichera, Marco, Hehir-Kwa, Jayne Y, Shendure, Jay, Mefford, Heather C, Haan, Eric, Gécz, Jozef, de Vries, Bert B A, Romano, Corrado, Eichler, Evan E

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A randomised comparison of deferasirox versus deferoxamine for the treatment of transfusional iron overload in sickle cell disease von Vichinsky, Elliott, Onyekwere, Onyinye, Porter, John, Swerdlow, Paul, Eckman, James, Lane, Peter, Files, Beatrice, Hassell, Kathryn, Kelly, Patrick, Wilson, Felicia, Bernaudin, Françoise, Forni, Gian Luca, Okpala, Iheanyi, Ressayre‐Djaffer, Catherine, Alberti, Daniele, Holland, Jaymes, Marks, Peter, Fung, Ellen, Fischer, Roland, Mueller, Brigitta U., Coates, Thomas

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Convergent genetic and expression data implicate immunity in Alzheimer's disease von Jones, Lesley, Wang, Li-San, Choi, Seung-Hoan, Vedernikov, Alexey, Escott-Price, Valentina, Richards, Alexander, Naj, Adam C., Sims, Rebecca, Gerrish, Amy, Jun, Gyungah, Beecham, Gary W., Grenier-Boley, Benjamin, Smith, Albert V., Chouraki, Vincent, Thomas, Charlene, Zelenika, Diana, Vardarajan, Badri N., Kamatani, Yoichiro, Bihoreau, Marie-Thérèse, Reitz, Christiane, Pasquier, Florence, Hanon, Olivier, Buxbaum, Joseph D., Campion, Dominique, Crane, Paul K., Gudnason, Vilmundur, Cruchaga, Carlos, Craig, David, Berr, Claudine, Lopez, Oscar L., De Jager, Philip L., Deramecourt, Vincent, Evans, Denis, Tárraga, Lluís, Sleegers, Kristel, Gill, Michael, Emilsson, Valur, Keller, Lina, Barberger-Gateau, Pascale, McGuinness, Bernadette, Larson, Eric B., Myers, Amanda J., Dufouil, Carole, Todd, Stephen, Love, Seth, Kehoe, Pat, Rogaeva, Ekaterina, Gallacher, John, Tsuang, Debby W., Yu, Lei, Sorbi, Sandro, Fox, Nick, Hardy, John, Deniz Naranjo, Maria Candida, Clarke, Robert, Mancuso, Michelangelo, Mecocci, Patrizia, del Zompo, Maria, Maier, Wolfgang, Pilotto, Alberto, Bullido, Maria, Caffarra, Paolo, Gilbert, John R., Mayhaus, Manuel, Lannfelt, Lars, Pichler, Sabrina, Ingelsson, Martin, Beekly, Duane, Valladares, Otto, Coto, Eliecer, Hamilton-Nelson, Kara L., Owen, Michael J., Faber, Kelley M., O'Donovan, Michael C., Soininen, Hilkka, Mead, Simon, de Bruijn, Renee F.A.G., Rotter, Jerome I., Brice, Alexis, Morgan, Kevin, Foroud, Tatiana M., Hannequin, Didier, Powell, John F., Nalls, Michael A., Ritchie, Karen, Riemenschneider, Matthias, Boada, Mercè, Hiltunen, Mikko, Pastor, Pau, Mayeux, Richard, Graff, Caroline, Psaty, Bruce M., Haines, Jonathan L., Lathrop, Mark, Pericak-Vance, Margaret A., Launer, Lenore J., Farrer, Lindsay A., van Duijn, Cornelia M., Williams, Julie, Holmans, Peter A.

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Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains von Geisheker, Madeleine R, Heymann, Gabriel, Wang, Tianyun, Coe, Bradley P, Turner, Tychele N, Stessman, Holly A F, Hoekzema, Kendra, Kvarnung, Malin, Shaw, Marie, Friend, Kathryn, Liebelt, Jan, Barnett, Christopher, Thompson, Elizabeth M, Haan, Eric, Guo, Hui, Anderlid, Britt-Marie, Nordgren, Ann, Lindstrand, Anna, Vandeweyer, Geert, Alberti, Antonino, Avola, Emanuela, Vinci, Mirella, Giusto, Stefania, Pramparo, Tiziano, Pierce, Karen, Nalabolu, Srinivasa, Michaelson, Jacob J, Sedlacek, Zdenek, Santen, Gijs W E, Peeters, Hilde, Hakonarson, Hakon, Courchesne, Eric, Romano, Corrado, Kooy, R Frank, Bernier, Raphael A, Nordenskjöld, Magnus, Gecz, Jozef, Xia, Kun, Zweifel, Larry S, Eichler, Evan E

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Review of Solar Energetic Particle Prediction Models von Whitman, Kathryn, Egeland, Ricky, Richardson, Ian G, Allison, Clayton, Quinn, Philip, Barzilla, Janet, Kitiashvili, Irina, Sadykov, Viacheslav, Bain, Hazel M, Dierckxsens, Mark, Mays, M. Leila, Tadesse, Tilaye, Lee, Kerry T, Semones, Edward, Luhmann, Janet G, Nunez, Marlon, White, Stephen M, Kahler, Stephen W, Ling, Alan G, Smart, Don F, Shea, Margaret A, Tenishev, Valeriy, Boubrahimi, Soukaina F, Aydin, Berkay, Martens, Petrus, Angryk, Rafal, Marsh, Michael S, Dalla, Silvia, Crosby, Norma, Schwadron, Nathan A, Kozarev, Kamen, Gorby, Matthew, Young, Matthew A, Laurenza, Monica, Cliver, Edward W, Alberti, Tommaso, Stumpo, Mirko, Benella, Simone, Papaioannou, Athanasios, Anastasiadis, Anastasios, Sandberg, Ingmar, Georgoulis, Manolis K, Ji, Anli, Kempton, Dustin, Pandey, Chetraj, Li, Gang, Hu, Junxiang, Zank, Gary P, Lavasa, Eleni, Giannopoulos, Giorgos, Falconer, David, Kadadi, Yash, Fernandes, Ian, Dayeh, Maher A, Munoz-Jaramillo, Andres, Chatterjee, Subhamoy, Moreland, Kimberly D, V. Sokolov, Igor, Roussev, Ilia I, Taktakishvili, Aleksandre, Effenberger, Frederic, Gombosi, Tamas, Huang, Zhenguang, Zhao, Lulu, Wijsen, Nicolas, Aran, Angels, Poedts, Stefaan, Kouloumvakos, Athanasios, Paassilta, Miikka, Vainio, Rami, Belov, Anatoly, Eroshenko, Eugenia A, Abunina, Maria A, Abunin, Artem A, Balch, Christopher C, Malandraki, Olga, Karavolos, Michalis, Heber, Bernd, Labrenz, Johannes, Kuhl, Patrick, Kosovichev, Alexander G, Oria, Vincent, Nita, Gelu M, Illarionov, Egor, O'Keefe, Patrick M, Jiang, Yucheng, Fereira, Sheldon H, Ali, Aatiya, Paouris, Evangelos, Aminalragia-Giamini, Sigiava, Jiggens, Piers, Jin, Meng, Lee, Christina O, Palmerio, Erika, Bruno, Alessandro, Kasapis, Spiridon, Wang, Xiantong, Chen, Yang, Sanahuja, Blai, Lario, David

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Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains von Geisheker, Madeleine R, Heymann, Gabriel, Wang, Tianyun, Coe, Bradley P, Turner, Tychele N, Stessman, Holly A.F, Hoekzema, Kendra, Kvarnung, Malin, Shaw, Marie, Friend, Kathryn, Liebelt, Jan, Barnett, Christopher, Thompson, Elizabeth M, Haan, Eric, Guo, Hui, Anderlid, Britt-Marie, Nordgren, Ann, Lindstrand, Anna, Vandeweyer, Geert, Alberti, Antonino, Avola, Emanuela, Vinci, Mirella, Giusto, Stefania, Pramparo, Tiziano, Pierce, Karen, Nalabolu, Srinivasa, Michaelson, Jacob J, Sedlacek, Zdenek, Santen, Gijs W.E, Peeters, Hilde, Hakonarson, Hakon, Courchesne, Eric, Romano, Corrado, Kooy, R. Frank, Bernier, Raphael A, Nordenskjöld, Magnus, Gecz, Jozef, Xia, Kun, Zweifel, Larry S, Eichler, Evan E

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Hotspots of missense mutation identify novel neurodevelopmental disorder genes and functional domains von Geisheker, Madeleine R., Heymann, Gabriel, Wang, Tianyun, Coe, Bradley P., Turner, Tychele N., Stessman, Holly A.F., Hoekzema, Kendra, Kvarnung, Malin, Shaw, Marie, Friend, Kathryn, Liebelt, Jan, Barnett, Christopher, Thompson, Elizabeth M., Haan, Eric, Guo, Hui, Anderlid, Britt-Marie, Nordgren, Ann, Lindstrand, Anna, Vandeweyer, Geert, Alberti, Antonino, Avola, Emanuela, Vinci, Mirella, Giusto, Stefania, Pramparo, Tiziano, Pierce, Karen, Nalabolu, Srinivasa, Michaelson, Jacob J., Sedlacek, Zdenek, Santen, Gijs W.E., Peeters, Hilde, Hakonarson, Hakon, Courchesne, Eric, Romano, Corrado, Kooy, R. Frank, Bernier, Raphael A., Nordenskjöld, Magnus, Gecz, Jozef, Xia, Kun, Zweifel, Larry S., Eichler, Evan E.

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Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases von Stessman, Holly A.F, Xiong, Bo, Coe, Bradley P, Wang, Tianyun, Hoekzema, Kendra, Fenckova, Michaela, Kvarnung, Malin, Gerdts, Jennifer, Trinh, Sandy, Cosemans, Nele, Vives, Laura, Lin, Janice, Turner, Tychele N, Santen, Gijs, Ruivenkamp, Claudia, Kriek, Marjolein, van Haeringen, Arie, Aten, Emmelien, Friend, Kathryn, Liebelt, Jan, Barnett, Christopher, Haan, Eric, Shaw, Marie, Gecz, Jozef, Anderlid, Britt-Marie, Nordgren, Ann, Lindstrand, Anna, Schwartz, Charles, Kooy, R. Frank, Vandeweyer, Geert, Helsmoortel, Celine, Romano, Corrado, Alberti, Antonino, Vinci, Mirella, Avola, Emanuela, Giusto, Stefania, Courchesne, Eric, Pramparo, Tiziano, Pierce, Karen, Nalabolu, Srinivasa, Amaral, David G, Scheffer, Ingrid E, Delatycki, Martin B, Lockhart, Paul J, Hormozdiari, Fereydoun, Harich, Benjamin, Castells-Nobau, Anna, Xia, Kun, Peeters, Hilde, Nordenskjöld, Magnus, Schenck, Annette, Bernier, Raphael A, Eichler, Evan E

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Refining analyses of copy number variation identifies specific genes associated with developmental delay von Coe, Bradley P, Witherspoon, Kali, Rosenfeld, Jill A, van Bon, Bregje W.M, Vulto-van Silfhout, Anneke T, Bosco, Paolo, Friend, Kathryn L, Baker, Carl, Buono, Serafino, Vissers, Lisenka E.L.M, Schuurs-Hoeijmakers, Janneke H, Hoischen, Alex, Pfundt, Rolph, Krumm, Nik, Carvill, Gemma L, Li, Deana, Amaral, David, Brown, Natasha, Lockhart, Paul J, Scheffer, Ingrid E, Alberti, Antonino, Shaw, Marie, Pettinato, Rosa, Tervo, Raymond, de Leeuw, Nicole, Reijnders, Margot R.F, Torchia, Beth S, Peeters, Hilde, Thompson, Elizabeth, O'Roak, Brian J, Fichera, Marco, Hehir-Kwa, Jayne Y, Shendure, Jay, Mefford, Heather C, Haan, Eric, Gécz, Jozef, de Vries, Bert B.A, Romano, Corrado, Eichler, Evan E

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