Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci by Yin, Xianyong, Chan, Lap Sum, Bose, Debraj, Jackson, Anne U., VandeHaar, Peter, Locke, Adam E., Fuchsberger, Christian, Stringham, Heather M., Welch, Ryan, Yu, Ketian, Fernandes Silva, Lilian, Service, Susan K., Zhang, Daiwei, Hector, Emily C., Young, Erica, Ganel, Liron, Das, Indraniel, Abel, Haley, Erdos, Michael R., Bonnycastle, Lori L., Kuusisto, Johanna, Stitziel, Nathan O., Hall, Ira M., Wagner, Gregory R., Kang, Jian, Morrison, Jean, Burant, Charles F., Collins, Francis S., Ripatti, Samuli, Palotie, Aarno, Freimer, Nelson B., Mohlke, Karen L., Scott, Laura J., Wen, Xiaoquan, Fauman, Eric B., Laakso, Markku, Boehnke, Michael

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Genetic background of extreme violent behavior by Tiihonen, J, Rautiainen, M-R, Ollila, H M, Repo-Tiihonen, E, Virkkunen, M, Palotie, A, Pietiläinen, O, Kristiansson, K, Joukamaa, M, Lauerma, H, Saarela, J, Tyni, S, Vartiainen, H, Paananen, J, Goldman, D, Paunio, T

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Mono- and biallelic variant effects on disease at biobank scale by Heyne, H. O., Karjalainen, J., Karczewski, K. J., Lemmelä, S. M., Zhou, W., Havulinna, A. S., Kurki, M., Rehm, H. L., Palotie, A., Daly, M. J.

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GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium by Trampush, J W, Yang, M L Z, Yu, J, Knowles, E, Davies, G, Liewald, D 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, A, 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, E, Poldrack, R A, Sabb, F W, Congdon, E, Conley, E D, Scult, M A, Dickinson, D, Straub, R E, Donohoe, G, Morris, D, Corvin, A, Gill, M, Hariri, A R, Weinberger, D R, Pendleton, N, Bitsios, P, Rujescu, D, Lahti, J, Le Hellard, S, Keller, M C, Andreassen, O A, Deary, I J, Glahn, D C, Malhotra, A K, Lencz, T

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Genome-wide association study of antisocial personality disorder by Rautiainen, M-R, Paunio, T, Repo-Tiihonen, E, Virkkunen, M, Ollila, H M, Sulkava, S, Jolanki, O, Palotie, A, Tiihonen, J

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Systematic review of genome-wide expression studies in multiple sclerosis by Kemppinen, A K, Kaprio, J, Palotie, A, Saarela, J

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Toward a roadmap in global biobanking for health by HARRIS, Jennifer R, BURTON, Paul, FORTIER, Isabel, HAINAUT, Pierre, HEWITT, Robert, KAYE, Jane, LITTON, Jan-Eric, METSPALU, Andres, OLLIER, Bill, PALMER, Lyle J, PALOTIE, Aarno, PASTERK, Markus, KNOPPERS, Bartha Maria, PEROLA, Markus, RIEGMAN, Peter Hj, OMMEN, Gert-Janvan, YUILLE, Martin, ZATLOUKAL, Kurt, LINDPAINTNER, Klaus, BLEDSOE, Marianna, BROOKES, Anthony J, BUDIN-LJØSNE, Isabelle, CHISHOLM, Rex, COX, David, DESCHENES, Mylène

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Genetic associations of protein-coding variants in human disease by Sun, Benjamin B., Kurki, Mitja I., Foley, Christopher N., Mechakra, Asma, Chen, Chia-Yen, Marshall, Eric, Wilk, Jemma B., Chahine, Mohamed, Chevalier, Philippe, Christé, Georges, Palotie, Aarno, Daly, Mark J., Runz, Heiko

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Detailed metabolic and genetic characterization reveals new associations for 30 known lipid loci by TUKIAINEN, Taru, KETTUNEN, Johannes, POUTA, Anneli, JULA, Antti, LEHTIMÄKI, Terho, KÄHÖNEN, Mika, VIIKARI, Jorma, TASKINEN, Marja-Riitta, JAUHIAINEN, Matti, ERIKSSON, Johan G, RAITAKARI, Olli, SALOMAA, Veikko, KANGAS, Antti J, JÄRVELIN, Marjo-Riitta, PEROLA, Markus, PALOTIE, Aarno, ALA-KORPELA, Mika, RIPATTI, Samuli, LYYTIKÄINEN, Leo-Pekka, SOININEN, Pasi, SARIN, Antti-Pekka, TIKKANEN, Emmi, O'REILLY, Paul F, SAVOLAINEN, Markku J, KASKI, Kimmo

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Candidate-gene association study searching for genetic factors involved in migraine chronification by Louter, MA, Fernandez-Morales, J, de Vries, B, Winsvold, B, Anttila, V, Fernandez-Cadenas, I, Vila-Pueyo, M, Sintas, C, van Duijn, CM, Cormand, B, Álvarez-Sabin, J, Montaner, J, Ferrari, MD, van den Maagdenberg, AMJM, Palotie, A, Zwart, JA, Macaya, A, Terwindt, GM, Pozo-Rosich, P

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The mutational constraint spectrum quantified from variation in 141,456 humans by Karczewski, Konrad J., Francioli, Laurent C., Tiao, Grace, Cummings, Beryl B., Alföldi, Jessica, Wang, Qingbo, Collins, Ryan L., Laricchia, Kristen M., Ganna, Andrea, Birnbaum, Daniel P., Gauthier, Laura D., Brand, Harrison, Solomonson, Matthew, Watts, Nicholas A., Rhodes, Daniel, Singer-Berk, Moriel, England, Eleina M., Seaby, Eleanor G., Kosmicki, Jack A., Walters, Raymond K., Tashman, Katherine, Farjoun, Yossi, Banks, Eric, Poterba, Timothy, Wang, Arcturus, Seed, Cotton, Whiffin, Nicola, Chong, Jessica X., Samocha, Kaitlin E., Pierce-Hoffman, Emma, Zappala, Zachary, O’Donnell-Luria, Anne H., Minikel, Eric Vallabh, Weisburd, Ben, Lek, Monkol, Ware, James S., Vittal, Christopher, Armean, Irina M., Bergelson, Louis, Cibulskis, Kristian, Connolly, Kristen M., Covarrubias, Miguel, Donnelly, Stacey, Ferriera, Steven, Gabriel, Stacey, Gentry, Jeff, Gupta, Namrata, Jeandet, Thibault, Kaplan, Diane, Llanwarne, Christopher, Munshi, Ruchi, Novod, Sam, Petrillo, Nikelle, Roazen, David, Ruano-Rubio, Valentin, Saltzman, Andrea, Schleicher, Molly, Soto, Jose, Tibbetts, Kathleen, Tolonen, Charlotte, Wade, Gordon, Talkowski, Michael E., Neale, Benjamin M., Daly, Mark J., MacArthur, Daniel G.

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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism by Satterstrom, F. Kyle, Breen, Michael S., Grove, Jakob, Klei, Lambertus, Xu, Xinyi, Norman, Utku, Brand, Harrison, Schwartz, Grace, Barbosa, Mafalda, Bybjerg-Grauholm, Jonas, Carracedo, Angel, Chiocchetti, Andreas G., Chung, Brian H.Y., Coon, Hilary, Cuccaro, Michael L., Dalla Bernardina, Bernardo, Domenici, Enrico, Dong, Shan, Freitag, Christine M., González-Peñas, Javier, Guter, Stephen, He, Xin, Herman, Gail E., Hertz-Picciotto, Irva, Hougaard, David M., Ionita-Laza, Iuliana, Jacob, Suma, Jamison, Jesslyn, Jugessur, Astanand, Kolevzon, Alexander, Kushima, Itaru, Lee, So Lun, Lehtimäki, Terho, Lim, Elaine T., Lipkin, W. Ian, Lopergolo, Diego, Lopes, Fátima, Ludena, Yunin, Maciel, Patricia, Meiri, Gal, Menashe, Idan, Miller, Judith, Montenegro, Eduarda M.S., Muglia, Pierandrea, Nordentoft, Merete, Ozaki, Norio, Palotie, Aarno, Parellada, Mara, Passos-Bueno, Maria Rita, Persico, Antonio M., Pessah, Isaac, Puura, Kaija, Renieri, Alessandra, Riberi, Evelise, Robinson, Elise B., Samocha, Kaitlin E., Sandin, Sven, Santangelo, Susan L., Schellenberg, Gerry, Scherer, Stephen W., Schmitt, Lauren, Silva, Isabela M.W., Singh, Tarjinder, Siper, Paige M., Soares, Gabriela, Susser, Ezra, Szatmari, Peter, Tang, Lara, Tassone, Flora, Teufel, Karoline, Trelles, Maria del Pilar, Werge, Thomas, Werling, Donna M., Wigdor, Emilie M., Yu, Mullin H.C., Zachi, Elaine, Agerbo, Esben, Als, Thomas Damm, Bækvad-Hansen, Marie, Belliveau, Rich, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Maller, Julian, Mattheisen, Manuel, Moran, Jennifer, Pallesen, Jonatan, Poulsen, Jesper Buchhave, Ripke, Stephan, Gallagher, Louise, Gill, Michael, Zwick, Michael E., State, Matthew W., Daly, Mark J., Buxbaum, Joseph D.

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Transcriptome and genome sequencing uncovers functional variation in humans by Lappalainen, Tuuli, Sammeth, Michael, Friedländer, Marc R., ‘t Hoen, Peter A. C., Monlong, Jean, Rivas, Manuel A., Gonzàlez-Porta, Mar, Kurbatova, Natalja, Griebel, Thasso, Ferreira, Pedro G., Barann, Matthias, Wieland, Thomas, Greger, Liliana, van Iterson, Maarten, Almlöf, Jonas, Ribeca, Paolo, Pulyakhina, Irina, Esser, Daniela, Giger, Thomas, Tikhonov, Andrew, Sultan, Marc, Bertier, Gabrielle, MacArthur, Daniel G., Lek, Monkol, Lizano, Esther, Buermans, Henk P. J., Padioleau, Ismael, Schwarzmayr, Thomas, Karlberg, Olof, Ongen, Halit, Kilpinen, Helena, Beltran, Sergi, Gut, Marta, Kahlem, Katja, Amstislavskiy, Vyacheslav, Stegle, Oliver, Pirinen, Matti, Montgomery, Stephen B., Donnelly, Peter, McCarthy, Mark I., Flicek, Paul, Strom, Tim M., Lehrach, Hans, Schreiber, Stefan, Sudbrak, Ralf, Carracedo, Ángel, Antonarakis, Stylianos E., Häsler, Robert, Syvänen, Ann-Christine, van Ommen, Gert-Jan, Brazma, Alvis, Meitinger, Thomas, Rosenstiel, Philip, Guigó, Roderic, Gut, Ivo G., Estivill, Xavier, Dermitzakis, Emmanouil T.

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Investigation of multiple dyslipidemias in a large Austrian pedigree by genetic risk scores and exome sequencing by Nikkola, E, Ko, A, Cantor, R.M, Muxel, R, Matikainen, N, Söderlund, S, Motazacker, M.M, Kuivenhoven, J.A, Boren, J, Kronenberg, F, Schneider, W, Palotie, A, Laakso, M, Taskinen, M.R, Pajukanta, P

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Analysis of protein-coding genetic variation in 60,706 humans by Lek, Monkol, Karczewski, Konrad J., Minikel, Eric V., Samocha, Kaitlin E., Banks, Eric, Fennell, Timothy, O’Donnell-Luria, Anne H., Ware, James S., Hill, Andrew J., Cummings, Beryl B., Tukiainen, Taru, Birnbaum, Daniel P., Kosmicki, Jack A., Duncan, Laramie E., Estrada, Karol, Zhao, Fengmei, Zou, James, Pierce-Hoffman, Emma, Berghout, Joanne, Cooper, David N., Deflaux, Nicole, DePristo, Mark, Do, Ron, Flannick, Jason, Fromer, Menachem, Gauthier, Laura, Goldstein, Jackie, Gupta, Namrata, Howrigan, Daniel, Kiezun, Adam, Kurki, Mitja I., Moonshine, Ami Levy, Natarajan, Pradeep, Orozco, Lorena, Peloso, Gina M., Poplin, Ryan, Rivas, Manuel A., Ruano-Rubio, Valentin, Rose, Samuel A., Ruderfer, Douglas M., Shakir, Khalid, Stenson, Peter D., Stevens, Christine, Thomas, Brett P., Tiao, Grace, Tusie-Luna, Maria T., Weisburd, Ben, Won, Hong-Hee, Yu, Dongmei, Altshuler, David M., Ardissino, Diego, Boehnke, Michael, Danesh, John, Donnelly, Stacey, Elosua, Roberto, Florez, Jose C., Gabriel, Stacey B., Getz, Gad, Glatt, Stephen J., Hultman, Christina M., Kathiresan, Sekar, Laakso, Markku, McCarroll, Steven, McCarthy, Mark I., McGovern, Dermot, McPherson, Ruth, Neale, Benjamin M., Palotie, Aarno, Purcell, Shaun M., Saleheen, Danish, Scharf, Jeremiah M., Sklar, Pamela, Sullivan, Patrick F., Tuomilehto, Jaakko, Tsuang, Ming T., Watkins, Hugh C., Wilson, James G., Daly, Mark J., MacArthur, Daniel G.

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Mapping and characterization of structural variation in 17,795 human genomes by 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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Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia by Rees, E, Kirov, G, Walters, J T, Richards, A L, Howrigan, D, Kavanagh, D H, Pocklington, A J, Fromer, M, Ruderfer, D M, Georgieva, L, Carrera, N, Gormley, P, Palta, P, Williams, H, Dwyer, S, Johnson, J S, Roussos, P, Barker, D D, Banks, E, Milanova, V, Rose, S A, Chambert, K, Mahajan, M, Scolnick, E M, Moran, J L, Tsuang, M T, Glatt, S J, Chen, W J, Hwu, H -G, Neale, B M, Palotie, A, Sklar, P, Purcell, S M, McCarroll, S A, Holmans, P, Owen, M J, O'Donovan, M C

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A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales by Service, S K, Verweij, K J H, Lahti, J, Congdon, E, Ekelund, J, Hintsanen, M, Räikkönen, K, Lehtimäki, T, Kähönen, M, Widen, E, Taanila, A, Veijola, J, Heath, A C, Madden, P A F, Montgomery, G W, Sabatti, C, Järvelin, M-R, Palotie, A, Raitakari, O, Viikari, J, Martin, N G, Eriksson, J G, Keltikangas-Järvinen, L, Wray, N R, Freimer, N B

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Common candidate gene variants are associated with QT interval duration in the general population by Marjamaa, A., Newton‐Cheh, C., Porthan, K., Reunanen, A., Lahermo, P., Väänänen, H., Jula, A., Karanko, H., Swan, H., Toivonen, L., Nieminen, M. S., Viitasalo, M., Peltonen, L., Oikarinen, L., Palotie, A., Kontula, K., Salomaa, V.

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Trait Components Provide Tools to Dissect the Genetic Susceptibility of Migraine by Anttila, V., Kallela, M., Oswell, G., Kaunisto, M.A., Nyholt, D.R., Hämäläinen, E., Havanka, H., Ilmavirta, M., Terwilliger, J., Sobel, E., Peltonen, L., Kaprio, J., Färkkilä, M., Wessman, M., Palotie, A.

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