Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder von Pagani, Lucia, St. Clair, Patricia A., Teshiba, Terri M., Service, Susan K., Fears, Scott C., Araya, Carmen, Araya, Xinia, Bejarano, Julio, Ramirez, Margarita, Castrillón, Gabriel, Gomez-Makhinson, Juliana, Lopez, Maria C., Montoya, Gabriel, Montoya, Claudia P., Aldana, Ileana, Navarro, Linda, Freimer, Daniel G., Safaie, Brian, Keung, Lap-Woon, Greenspan, Kiefer, Chou, Katty, Escobar, Javier I., Ospina-Duque, Jorge, Kremeyer, Barbara, Ruiz-Linares, Andres, Cantor, Rita M., Lopez-Jaramillo, Carlos, Macaya, Gabriel, Molina, Julio, Reus, Victor I., Sabatti, Chiara, Bearden, Carrie E., Takahashi, Joseph S., Freimer, Nelson B.

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Exome sequencing of Finnish isolates enhances rare-variant association power von Locke, Adam E., Steinberg, Karyn Meltz, Chiang, Charleston W. K., Service, Susan K., Havulinna, Aki S., Stell, Laurel, Pirinen, Matti, Abel, Haley J., Chiang, Colby C., Fulton, Robert S., Jackson, Anne U., Kang, Chul Joo, Kanchi, Krishna L., Koboldt, Daniel C., Larson, David E., Nelson, Joanne, Nicholas, Thomas J., Pietilä, Arto, Ramensky, Vasily, Ray, Debashree, Scott, Laura J., Stringham, Heather M., Vangipurapu, Jagadish, Welch, Ryan, Yajnik, Pranav, Yin, Xianyong, Eriksson, Johan G., Ala-Korpela, Mika, Järvelin, Marjo-Riitta, Männikkö, Minna, Laivuori, Hannele, Dutcher, Susan K., Stitziel, Nathan O., Wilson, Richard K., Hall, Ira M., Sabatti, Chiara, Palotie, Aarno, Salomaa, Veikko, Laakso, Markku, Ripatti, Samuli, Boehnke, Michael, Freimer, Nelson B.

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Mapping and characterization of structural variation in 17,795 human genomes von Abel, Haley J., Larson, David E., Regier, Allison A., Chiang, Colby, Das, Indraniel, Kanchi, Krishna L., Layer, Ryan M., Neale, Benjamin M., Salerno, William J., Reeves, Catherine, Buyske, Steven, Matise, Tara C., Muzny, Donna M., Zody, Michael C., Lander, Eric S., Dutcher, Susan K., Stitziel, Nathan O., Hall, Ira M.

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Recombination rates in admixed individuals identified by ancestry-based inference von Novembre, John, Wegmann, Daniel, Kessner, Darren E, Veeramah, Krishna R, Mathias, Rasika A, Nicolae, Dan L, Yanek, Lisa R, Sun, Yan V, Torgerson, Dara G, Rafaels, Nicholas, Mosley, Thomas, Becker, Lewis C, Ruczinski, Ingo, Beaty, Terri H, Kardia, Sharon L R, Meyers, Deborah A, Barnes, Kathleen C, Becker, Diane M, Freimer, Nelson B

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Systematic decoding of cis gene regulation defines context-dependent control of the multi-gene costimulatory receptor locus in human T cells von Mowery, Cody T., Freimer, Jacob W., Chen, Zeyu, Casaní-Galdón, Salvador, Umhoefer, Jennifer M., Arce, Maya M., Gjoni, Ketrin, Daniel, Bence, Sandor, Katalin, Gowen, Benjamin G., Nguyen, Vinh, Simeonov, Dimitre R., Garrido, Christian M., Curie, Gemma L., Schmidt, Ralf, Steinhart, Zachary, Satpathy, Ansuman T., Pollard, Katherine S., Corn, Jacob E., Bernstein, Bradley E., Ye, Chun Jimmie, Marson, Alexander

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Identification of common variants associated with human hippocampal and intracranial volumes von Vasquez, Alejandro Arias, Toro, Roberto, Bartecek, Richard, Bergmann, Ørjan, Bernard, Manon, Chakravarty, M Mallar, Grimm, Oliver, Homuth, Georg, Lopez, Lorna M, Hansell, Narelle K, Kim, Sungeun, Laje, Gonzalo, Lee, Phil H, Liu, Xinmin, Loth, Eva, Lourdusamy, Anbarasu, Mattingsdal, Morten, Mohnke, Sebastian, Maniega, Susana Muñoz, O'Brien, Carol, Pütz, Benno, Rasmussen, Jerod, Risacher, Shannon L, Rose, Emma J, Ryten, Mina, Sprooten, Emma, Teumer, Alexander, Trabzuni, Daniah, Turner, Jessica, van Eijk, Kristel, van Erp, Theo G M, van Tol, Marie-Jose, Wolf, Christiane, Aleman, Andre, Alhusaini, Saud, Binder, Elisabeth B, Brohawn, David G, Cantor, Rita M, Czisch, Michael, de Almeida, Marcio A A, Delanty, Norman, Dyer, Thomas D, Erk, Susanne, Fox, Peter T, Freimer, Nelson B, Hagler, Donald J, Hoogman, Martine, Johnson, Matthew P, Kasperaviciute, Dalia, Kent, Jack W, Kochunov, Peter, Lancaster, Jack L, Liewald, David C, Matarin, Mar, Mattheisen, Manuel, Moses, Eric K, Mühleisen, Thomas W, Nöthen, Markus M, Puls, Ralf, Reinvang, Ivar, Savitz, Jonathan, Schnack, Hugo G, Seiferth, Nina, Valdés Hernández, Maria C, Van Haren, Neeltje E M, Veltman, Joris A, Völzke, Henry, Westlye, Lars T, Whelan, Christopher D, Cavalleri, Gianpiero L, Dale, Anders M, Drevets, Wayne C, Heinz, Andreas, Le Hellard, Stephanie, Macciardi, Fabio, Montgomery, Grant W, Starr, John M, Gudnason, Vilmundur, Tzourio, Christophe, Vernooij, Meike W, Launer, Lenore J, Andreassen, Ole A, Bastin, Mark E, Blangero, John, Brunner, Han G, Buckner, Randy L, Coppola, Giovanni, de Zubicaray, Greig I, Fernández, Guillén, Glahn, David C, Hardy, John, Kahn, René S, McIntosh, Andrew M, Nichols, Thomas E, Ophoff, Roel A, Pausova, Zdenka, Potkin, Steven G, Smoller, Jordan W, Martin, Nicholas G, Thompson, Paul M

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A Genome-wide Association Study of Myasthenia Gravis von Renton, Alan E, Pliner, Hannah A, Provenzano, Carlo, Evoli, Amelia, Ricciardi, Roberta, Nalls, Michael A, Marangi, Giuseppe, Abramzon, Yevgeniya, Arepalli, Sampath, Chong, Sean, Hernandez, Dena G, Johnson, Janel O, Bartoccioni, Emanuela, Scuderi, Flavia, Maestri, Michelangelo, Gibbs, J. Raphael, Errichiello, Edoardo, Chiò, Adriano, Restagno, Gabriella, Sabatelli, Mario, Macek, Mark, Scholz, Sonja W, Corse, Andrea, Chaudhry, Vinay, Benatar, Michael, Barohn, Richard J, McVey, April, Pasnoor, Mamatha, Dimachkie, Mazen M, Rowin, Julie, Kissel, John, Freimer, Miriam, Kaminski, Henry J, Sanders, Donald B, Lipscomb, Bernadette, Massey, Janice M, Chopra, Manisha, Howard, James F, Koopman, Wilma J, Nicolle, Michael W, Pascuzzi, Robert M, Pestronk, Alan, Wulf, Charlie, Florence, Julaine, Blackmore, Derrick, Soloway, Aimee, Siddiqi, Zaeem, Muppidi, Srikanth, Wolfe, Gil, Richman, David, Mezei, Michelle M, Jiwa, Theresa, Oger, Joel, Drachman, Daniel B, Traynor, Bryan J

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Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder von Moser, Gerhard, Agartz, Ingrid, Andreassen, Ole A., Anjorin, Adebayo, Bass, Nicholas, Bergen, Sarah E., Betancur, Catalina, Black, Donald W., Bloss, Cinnamon S., Buxbaum, Joseph D., Cantor, Rita M., Cormand, Bru, Coryell, William H., Craig, Ian W., Crosbie, Jennifer, Djurovic, Srdjan, Ebstein, Richard P., Etain, Bruno, Faraone, Stephen V., Farmer, Anne E., Ferrier, I. Nicol, Fombonne, Eric, Frank, Josef, Franke, Barbara, Freitag, Christine M., Friedl, Marion, Gershon, Elliot S., Gill, Michael, Gordon, Scott D., Green, Elaine K., De Haan, Lieuwe, Haines, Jonathan L., Hakonarson, Hakon, Hallmayer, Joachim, Hamilton, Steven P., Hamshere, Marian L., Hoogendijk, Witte J., Hottenga, Jouke-Jan, Hus, Vanessa, Jamain, Stéphane, Jones, Lisa, Kenny, Elaine, Krabbendam, Lydia, Kuntsi, Jonna, Landén, Mikael, Lesch, Klaus-Peter, Lichtenstein, Paul, Lieberman, Jeffrey A., Linszen, Don H., Loo, Sandra K., Lowe, Jennifer K., Lucae, Susanne, Magnusson, Patrik K.E., Mahon, Pamela B., Martin, Christa L., McGhee, Kevin A., McGuffin, Peter, McInnis, Melvin G., McIntosh, Andrew, McLean, Alan W., McMahon, William M., Meier, Sandra, Meng, Fan, Meyer, Jobst, Middeldorp, Christel M., Miranda, Ana, Montgomery, Grant W., Mühleisen, Thomas W., Neale, Benjamin M., Nyholt, Dale R., O’Donovan, Michael C., Olsen, Line, Penninx, Brenda W., Pergadia, Michele L., Pericak-Vance, Margaret A., Perlis, Roy H., Posthuma, Danielle, Rasmussen, Henrik B., Reif, Andreas, Ribasés, Marta, Rice, John P., Rossin, Lizzy, Sanders, Stephan J., Schachar, Russell, Schellenberg, Gerard D., Schumacher, Johannes, Scott, Laura J., Smalley, Susan L., Smit, Johannes H., Szelinger, Szabocls, Thapar, Anita, Thirumalai, Srinivasa, Treutlein, Jens, Visscher, Peter M., Willemsen, Gonneke, Young, Allan H., Zammit, Stanley, Zitman, Frans G., Potash, James B., Shi, Jianxin

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Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption von Schumann, Gunter, Coin, Lachlan J, Lourdusamy, Anbarasu, Charoen, Pimphen, Berger, Karen H, Stacey, David, Desrivières, Sylvane, Aliev, Fazil A, Khan, Anokhi A, Aulchenko, Yurii S, Bakalkin, Georgy, Bakker, Stephan J, Balkau, Beverley, Beulens, Joline W, Bilbao, Ainhoa, de Boer, Rudolf A, Beury, Delphine, Bots, Michiel L, Cauchi, Stéphane, Cavalcanti-Proença, Christine, Chambers, John C, Clarke, Toni-Kim, Dahmen, Norbert, de Geus, Eco J, Dick, Danielle, Ducci, Francesca, Easton, Alanna, Esk, Tõnu, Foroud, Tatiana, Freimer, Nelson B, Girault, Jean-Antoine, Grobbee, Diederick E, Guarrera, Simonetta, Gudbjartsson, Daniel F, Hartikainen, Anna-Liisa, Heath, Andrew C, Hesselbrock, Victor, Hottenga, Jouke-Jan, Kaprio, Jaakko, Khaw, Kay-Tee, Kuehnel, Brigitte, Laitinen, Jaana, Luan, Jian'an, Mangino, Massimo, Maroteaux, Matthieu, Matullo, Giuseppe, Mueller, Christian, Navis, Gerjan, Numans, Mattijs E, Núñez, Alejandro, Nyholt, Dale R, Onland-Moret, Charlotte N, Oostra, Ben A, O'Reilly, Paul F, Palkovits, Miklos, Penninx, Brenda W, Polidoro, Silvia, Pouta, Anneli, Prokopenko, Inga, Ricceri, Fulvio, Santos, Eugenio, Smit, Johannes H, Soranzo, Nicole, Song, Kijoung, Sovio, Ulla, Stumvoll, Michael, Surakk, Ida, Thorgeirsson, Thorgeir E, Thorsteinsdottir, Unnur, Troakes, Claire, Tyrfingsson, Thorarinn, Tönjes, Anke, Uiterwaal, Cuno S, Uitterlinden, Andre G, van der Harst, Pim, van der Schouw, Yvonne T, Staehlin, Oliver, Waeber, Gerard, Wareham, Nicholas J, Wichmann, Erich H, Witteman, Jacqueline C, Yuan, Xin, Zhai, Guangju, Zhao, Jing H, Zhang, Weihua, Martin, Nicholas G, Metspalu, Andres, Doering, Angela, Scott, James, Spector, Tim D, Loos, Ruth J, Boomsma, Dorret I, Peltonen, Leena, van Duijn, Cornelia M, Vineis, Paolo, Kooner, Jaspal S, Spanagel, Rainer, Heberlein, Ulrike A, Jarvelin, Marjo-Riitta, Elliott, Paul

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Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power von Locke, Adam E., Steinberg, Karyn Meltz, Chiang, Charleston W. K., Service, Susan K., Havulinna, Aki S., Stell, Laurel, Pirinen, Matti, Abel, Haley J., Chiang, Colby C., Fulton, Robert S., Jackson, Anne U., Kang, Chul Joo, Kanchi, Krishna L., Koboldt, Daniel C., Larson, David E., Nelson, Joanne, Nicholas, Thomas J., Pietilä, Arto, Ramensky, Vasily, Ray, Debashree, Scott, Laura J., Stringham, Heather M., Vangipurapu, Jagadish, Welch, Ryan, Yajnik, Pranav, Yin, Xianyong, Eriksson, Johan G., Ala-Korpela, Mika, Järvelin, Marjo-Riitta, Männikkö, Minna, Laivuori, Hannele, Dutcher, Susan K., Stitziel, Nathan O., Wilson, Richard K., Hall, Ira M., Sabatti, Chiara, Palotie, Aarno, Salomaa, Veikko, Laakso, Markku, Ripatti, Samuli, Boehnke, Michael, Freimer, Nelson B.

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Genetic evidence of assortative mating in humans von Robinson, Matthew R., Kleinman, Aaron, Graff, Mariaelisa, Vinkhuyzen, Anna A. E., Couper, David, Miller, Michael B., Peyrot, Wouter J., Abdellaoui, Abdel, Zietsch, Brendan P., Nolte, Ilja M., van Vliet-Ostaptchouk, Jana V., Snieder, Harold, Medland, Sarah E., Martin, Nicholas G., Magnusson, Patrik K. E., Iacono, William G., McGue, Matt, North, Kari E., Yang, Jian, Visscher, Peter M.

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Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function von Hagenaars, Saskia P., Liewald, David C. M., Ahola-Olli, Ari V., Barnes, Catriona L. K., Bertram, Lars, Bis, Joshua C., Burdick, Katherine E., Christoforou, Andrea, Espeseth, Thomas, Giakoumaki, Stella, Giddaluru, Sudheer, Gustavson, Daniel E., Lahti, Jari, Leber, Markus, Melle, Ingrid, Oldmeadow, Christopher, Reynolds, Chandra A., Scholz, Markus, Smith, Jennifer A., Smith, Albert V., Thalamuthu, Anbupalam, Trompet, Stella, van der Lee, Sven J., Ware, Erin B., Yang, Jingyun, Ames, David, Armstrong, Nicola J., Assareh, Amelia A., Böhmer, Anne C., Campbell, Harry, Cannon, Tyrone D., Corley, Janie, Cox, Simon R., Dale, Anders M., Dick, Danielle, Evangelou, Evangelos, Faul, Jessica D., Ford, Ian, Gao, He, Giegling, Ina, Gillespie, Nathan A., Gordon, Scott D., Gottesman, Rebecca F., Griswold, Michael E., Hatzimanolis, Alex, Heiss, Gerardo, Joshi, Peter K., Kähönen, Mika, Kleineidam, Luca, Kochan, Nicole A., Le Hellard, Stephanie, Lee, Teresa, Lill, Christina M., Longstreth, Will T., Lopez, Oscar L., Loukola, Anu, Lyytikäinen, Leo-Pekka, Martin, Nicholas G., Murray, Alison D., Need, Anna C., Ollier, William, Polasek, Ozren, Riedel-Heller, Steffi G., Rose, Richard J., Rovio, Suvi P., Schmid, Matthias, Scott, Rodney J., Scult, Matthew A., Simino, Jeannette, Straub, Richard E., Tzoulaki, Ioanna, Uitterlinden, André, Vitart, Veronique, Wagner, Michael, Weinhold, Leonie, Wen, K. Hoyan, Adams, Hieab H. H., Arking, Dan E., Chiba-Falek, Ornit, Debette, Stéphanie, Donohoe, Gary, Elliott, Paul, Gill, Michael, Hägg, Sara, Hansell, Narelle K., Vuoksimaa, Eero, Pendleton, Neil, Porteous, David J., Rudan, Igor, Dan Rujescu, Schmidt, Reinhold, Schofield, Peter W., Steen, Vidar M., Van Duijn, Cornelia M., Villringer, Arno, Weinberger, Daniel R., McIntosh, Andrew M., Gale, Catharine R., Mosley, Thomas H., Lencz, Todd

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Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations von Guo, Xiuqing, Bis, Joshua C., Yang, Min-Lee, Ehret, Georg, Sijbrands, Eric J., Eiriksdottir, Gudny, Pihur, Vasyl, Vasan, Ramachandran S., Gateva, Vesela, Tobin, Martin D., Bochud, Murielle, Zhao, Jing Hua, Heath, Simon C., Eyheramendy, Susana, Zhang, Feng, Farrall, Martin, Wallace, Chris, Khaw, Kay-Tee, Nilsson, Peter, Polidoro, Silvia, Grobbee, Diederick E., Onland-Moret, N. Charlotte, Teumer, Alexander, Luan, Jian’an, Burton, Paul R., McArdle, Wendy L., Brown, Morris, Newhouse, Stephen J., Webster, John, Zeggini, Eleftheria, Bergmann, Sven, Song, Kijoung, Waeber, Gerard, Yuan, Xin, Groop, Leif, Di Gregorio, Alessandra, Guarrera, Simonetta, Panico, Salvatore, Romanazzi, Valeria, Vineis, Paolo, Luben, Robert N., Crawford, Gabriel J., Boehnke, Michael, Collins, Francis S., Jackson, Anne U., Stringham, Heather M., Morken, Mario A., Gieger, Christian, Wichmann, H. Erich, O’Donnell, Christopher J., Siscovick, David S., O’Reilly, Paul F., Peltonen, Leena, Pouta, Anneli, van Gilst, Wiek H., Clarke, Robert, Goel, Anuj, Syvänen, Ann-Christine, Scheet, Paul, Scuteri, Angelo, Ernst, Florian, Felix, Stephan B., Lorbeer, Roberto, Völker, Uwe, Hercberg, Serge, Zeleneka, Diana, Deloukas, Panos, Soranzo, Nicole, Zhai, Guangju, Laakso, Markku, Forouhi, Nita G., Völzke, Henry, Numans, Mattijs E., Navis, Gerjan, Paterson, Andrew D., Bandinelli, Stefania, Spector, Tim D., Altshuler, David, Strachan, David P., Jarvelin, Marjo-Riitta, Melander, Olle, Loos, Ruth J.F., Caulfield, Mark, Raffel, Leslie J., Amin, Najaf, Rotter, Jerome I., Launer, Lenore J., Caulfield, Mark, Morrison, Alanna C., Li, Guo, Harris, Tamara B., Zhang, He, Siscovick, David S., Gao, Wei, Rivadeneira, Fernando, Willer, Cristen J., Huo, Yong, Palmas, Walter, van Duijn, Cornelia, Fornage, Myriam

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Runs of homozygosity implicate autozygosity as a schizophrenia risk factor von Keller, Matthew C, Simonson, Matthew A, Ripke, Stephan, Neale, Ben M, Gejman, Pablo V, Howrigan, Daniel P, Lee, Sang Hong, Lencz, Todd, Levinson, Douglas F, Sullivan, Patrick F

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Multi-Trait Analysis of GWAS and Biological Insights Into Cognition: A Response to Hill (2018) von Lam, Max, Trampush, Joey W., Yu, Jin, Knowles, Emma, Djurovic, Srdjan, Melle, Ingrid, Sundet, Kjetil, Christoforou, Andrea, Reinvang, Ivar, DeRosse, Pamela, Lundervold, Astri J., Steen, Vidar M., Espeseth, Thomas, Räikkönen, Katri, Widen, Elisabeth, Palotie, Aarno, Eriksson, Johan G., Giegling, Ina, Konte, Bettina, Roussos, Panos, Giakoumaki, Stella, Burdick, Katherine E., Payton, Antony, Ollier, William, Chiba-Falek, Ornit, Attix, Deborah K., Need, Anna C., Cirulli, Elizabeth T., Voineskos, Aristotle N., Stefanis, Nikos C., Avramopoulos, Dimitrios, Hatzimanolis, Alex, Arking, Dan E., Smyrnis, Nikolaos, Bilder, Robert M., Freimer, Nelson A., Cannon, Tyrone D., London, Edythe, Poldrack, Russell A., Sabb, Fred W., Congdon, Eliza, Conley, Emily Drabant, Scult, Matthew A., Dickinson, Dwight, Straub, Richard E., Donohoe, Gary, Morris, Derek, Corvin, Aiden, Gill, Michael, Hariri, Ahmad R., Weinberger, Daniel R., Pendleton, Neil, Bitsios, Panos, Rujescu, Dan, Lahti, Jari, Hellard, Stephanie Le, Keller, Matthew C., Andreassen, Ole A., Glahn, David C., Malhotra, Anil K., Lencz, Todd

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Multifocal motor neuropathy: Response to human immune globulin von Chaudhry, Vinay, Corse, Andrea M., Cornblath, David R., Kuncl, Ralph W., Drachman, Daniel B., Freimer, Miriam L., Miller, Robert G., Griffin, John W.

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Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function von Lam, Max, Trampush, Joey W, Luciano, Michelle, Hagenaars, Saskia P, Ritchie, Stuart J, Okely, Judith A, Bertram, Lars, Christoforou, Andrea, Djurovic, Srdjan, Giakoumaki, Stella, Giddaluru, Sudheer, Karlsson, Robert, Knowles, Emma, Lahti, Jari, Leber, Markus, Li, Shuo, Mather, Karen A, Melle, Ingrid, Palviainen, Teemu, Petrovic, Katja, Reynolds, Chandra A, Sargurupremraj, Muralidharan, Scholz, Markus, Smith, Albert V, Thalamuthu, Anbupalam, van der Lee, Sven J, Ware, Erin B, Wright, Margaret J, Yu, Jin, Attix, Deborah, Avramopoulos, Dimitrios, Böhmer, Anne C, Boyle, Patricia A, Cirulli, Elizabeth T, Conley, Emily Drabant, Corley, Janie, Dale, Anders M, Dehghan, Abbas, Dickinson, Dwight, Evangelou, Evangelos, Faul, Jessica D, Giegling, Ina, Harris, Tamara B, Holliday, Elizabeth G, Karlsson, Ida, Knopman, David S, Kochan, Nicole A, Le Hellard, Stephanie, Liu, Tian, London, Edythe, Longstreth, Will T, Loukola, Anu, Montgomery, Grant W, Noordam, Raymond, Nyberg, Lars, Papenberg, Goran, Pattie, Alison, Psaty, Bruce M, Riedel-Heller, Steffi G, Roussos, Panos, Schmid, Matthias, Scult, Matthew A, Soumaré, Aïcha, Stefanis, Nikos C, Straub, Richard E, Taylor, Adele M, Taylor, Kent D, Tzourio, Christophe, Uitterlinden, André, Kaprio, Jaakko, Wagner, Holger, Weinhold, Leonie, Wen, K. Hoyan, Widen, Elisabeth, Zhao, Wei, Arking, Dan E, Bilder, Robert M, Boerwinkle, Eric, Chiba-Falek, Ornit, Corvin, Aiden, Debette, Stéphanie, Donohoe, Gary, Elliott, Paul, Fitzpatrick, Annette L, Hägg, Sara, Vuoksimaa, Eero, Keller, Matthew C, Kremen, William S, Palotie, Aarno, Pedersen, Nancy L, Schofield, Peter W, Schofield, Peter R, Trollor, Julian N, Turner, Steven T, Van Duijn, Cornelia M, Villringer, Arno, Weir, David R, Wilson, James F, Seshadri, Sudha, Bressler, Jan

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Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function von Lam, Max, Trampush, Joey W, Luciano, Michelle, Hagenaars, Saskia P, Ritchie, Stuart J, Okely, Judith A, Bertram, Lars, Christoforou, Andrea, Derosse, Pamela, Djurovic, Srdjan, Giakoumaki, Stella, Giddaluru, Sudheer, Karlsson, Robert, Knowles, Emma, Lahti, Jari, Leber, Markus, Li, Shuo, Mather, Karen A, Melle, Ingrid, Palviainen, Teemu, Petrovic, Katja, Reynolds, Chandra A, Sargurupremraj, Muralidharan, Scholz, Markus, Smith, Albert V, Thalamuthu, Anbupalam, van der Lee, Sven J, Ware, Erin B, Wright, Margaret J, Yu, Jin, Attix, Deborah, Avramopoulos, Dimitrios, Böhmer, Anne C, Boyle, Patricia A, Cirulli, Elizabeth T, Conley, Emily Drabant, Dehghan, Abbas, Dickinson, Dwight, Evangelou, Evangelos, Faul, Jessica D, Giegling, Ina, Harris, Tamara B, Holliday, Elizabeth G, Karlsson, Ida, Knopman, David S, Kochan, Nicole A, Le Hellard, Stephanie, Liu, Tian, London, Edythe, Longstreth, Will T, Loukola, Anu, Montgomery, Grant W, Noordam, Raymond, Nyberg, Lars, Papenberg, Göran, Pattie, Alison, Psaty, Bruce M, Riedel-Heller, Steffi G, Roussos, Panos, Schmid, Matthias, Scult, Matthew A, Soumaré, Aïcha, Straub, Richard E, Taylor, Adele M, Taylor, Kent D, Tzourio, Christophe, Uitterlinden, André, Kaprio, Jaakko, Wagner, Holger, Weinhold, Leonie, Wen, K. Hoyan, Zhao, Wei, Adams, Hieab H.H, Arking, Dan E, Bilder, Robert M, Boerwinkle, Eric, Chiba-Falek, Ornit, Corvin, Aiden, Debette, Stéphanie, Donohoe, Gary, Elliott, Paul, Fitzpatrick, Annette L, Hägg, Sara, Hariri, Ahmad, Vuoksimaa, Eero, Keller, Matthew C, Kremen, William S, Palotie, Aarno, Pedersen, Nancy L, Rujescu, Dan, Schofield, Peter W, Schofield, Peter R, Steen, Vidar Martin, Turner, Steven T, Van Duijn, Cornelia M, Villringer, Arno, Weir, David R, Wilson, James F, Seshadri, Sudha, Bressler, Jan

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GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function:a report from the COGENT consortium von Trampush, Joey W, Yang, M L Z, Yu, J, Knowles, E, Davies, G, Liewald, David C, Starr, J M, Djurovic, S, Melle, I, Sundet, K, Christoforou, A, Reinvang, I, DeRosse, P, Lundervold, A. J, Steen, V. M, Espeseth, T, Räikkönen, K, Widen, E, Palotie, A, Eriksson, J G, Giegling, I, Konte, B, Roussos, P, Giakoumaki, S, Burdick, K. E, Payton, Antony, Ollier, W, Horan, M, Chiba-Falek, O, Attix, D K, Need, A C, Cirulli, E T, Voineskos, A N, Stefanis, N C, Avramopoulos, D, Hatzimanolis, A, Arking, D E, Smyrnis, N, Bilder, R M, Freimer, N A, Cannon, T D, London, Edythe D, Poldrack, R A, Sabb, F W, Congdon, E, Conley, E D, Scult, M A, Dickinson, D, Straub, Richard E, Donohoe, G, Morris, D, Corvin, A, Gill, M, Hariri, A R, Weinberger, Daniel R, Pendleton, N, Bitsios, P, Rujescu, D, Lahti, J, Le Hellard, S, Keller, Matthew C, Andreassen, Ole A, Deary, I. J, Glahn, D. C, Malhotra, Anil K, Lencz, T

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Editorial by concerned physicians: Unintended effect of the orphan drug act on the potential cost of 3,4-diaminopyridine: Editorial von Burns, Ted M., Smith, Gordon A., Allen, Jeffrey A., Amato, Anthony A., Arnold, W. David, Barohn, Richard, Benatar, Michael, Bird, Shawn J., Bromberg, Mark, Chahin, Nizar, Ciafaloni, Emma, Cohen, Jeffrey A., Corse, Andrea, Crum, Brian A., David, William S., Dimberg, Elliot, Sousa, Eduardo A. De, Donofrio, Peter D., Dyck, P. James B., Engel, Andrew G., Ensrud, Erik R., Ferrante, Mark, Freimer, Miriam, Gable, Karissa L., Gibson, Summer, Gilchrist, James M., Goldstein, Jonathan M., Gooch, Clifton L., Goodman, Brent P., Gorelov, Dmitri, Gospe, Sidney M., Goyal, Namita A., Guidon, Amanda C., Guptill, Jeffrey T., Gutmann, Laurie, Gutmann, Ludwig, Gwathmey, Kelly, Harati, Yadollah, Harper, C. Michel, Hehir, Michael K., Hobson-Webb, Lisa D., Howard, James F., Jackson, Carlayne E., Johnson, Nicholas, Jones, Sarah M., Juel, Vern C., Kaminski, Henry J., Karam, Chafic, Kennelly, Kathleen D., Khella, Sami, Khoury, Julie, Kincaid, John C., Kissel, John T., Kolb, Noah, Lacomis, David, Ladha, Shafeeq, Larriviere, Daniel, Lewis, Richard A., Li, Yuebing, Litchy, William J., Logigian, Eric, Lou, Jau-Shin, MacGowen, Daniel J.L., Maselli, Ricardo, Massey, Janice M., Mauermann, Michelle L., Mathews, Katherine D., Meriggioli, Matthew N., Miller, Robert G., Moon, Joon-Shik, Mozaffar, Tahseen, Nations, Sharon P., Nowak, Richard J., Ostrow, Lyle W., Pascuzzi, Robert M., Peltier, Amanda, Ruzhansky, Katherine, Richman, David P., Ross, Mark A., Rubin, DEVON I., Russell, James A., Sachs, George M., Salajegheh, Mohammad Kian, Saperstein, David S., Scelsa, Stephen, Selcen, Duygu, Shaibani, Aziz, Shieh, Perry B., Silvestri, Nicholas J., Singleton, J. Rob, Smith, Benn E., So, Yuen T., Solorzano, Guillermo, Sorenson, Eric J., Srinivasen, Jayashri, Tavee, Jinny, Tawil, Rabi, Thaisetthawatkul, Pariwat, Thornton, Charles, Trivedi, Jaya

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