Attention-Deficit/Hyperactivity Disorder Polygenic Risk Scores Predict Attention Problems in a Population-Based Sample of Children von Groen-Blokhuis, Maria M., MD, PhD, Middeldorp, Christel M., MD, PhD, Kan, Kees-Jan, PhD, Abdellaoui, Abdel, MSc, van Beijsterveldt, Catharina E.M., PhD, Ehli, Erik A., PhD, Davies, Gareth E., PhD, Scheet, Paul A., PhD, Xiao, Xiangjun, MSc, Hudziak, James J., MD, Hottenga, Jouke-Jan, PhD, Neale, Ben M., PhD, Boomsma, Dorret I., PhD

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Reaction time performance in ADHD: improvement under fast-incentive condition and familial effects von ANDREOU, PENNY, NEALE, BEN M., CHEN, WAI, CHRISTIANSEN, HANNA, GABRIELS, ISABEL, HEISE, ALEXANDER, MEIDAD, SHEERA, MULLER, UELI C., UEBEL, HENRIK, BANASCHEWSKI, TOBIAS, MANOR, IRIS, OADES, ROBERT, ROEYERS, HERBERT, ROTHENBERGER, ARIBERT, SHAM, PAK, STEINHAUSEN, HANS-CHRISTOPH, ASHERSON, PHILIP, KUNTSI, JONNA

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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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SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse von Koopmans, Frank, van Nierop, Pim, Andres-Alonso, Maria, Bymes, Andrea, Cijsouw, Tony, Coba, Marcelo P, Cornelisse, L. Niels, Farrell, Ryan J, Goldschmidt, Hana L, Howrigan, Daniel P, Hussain, Natasha K, Imig, Cordelia, de Jong, Arthur P.H, Jung, Hwajin, Kohansalnodehi, Mandokht, Kramarz, Barbara, Lipstein, Noa, Lovering, Ruth C, MacGillavry, Harold, Mariano, Vittoria, Mi, Huaiyu, Ninov, Momchil, Osumi-Sutherland, David, Pielot, Rainer, Smalla, Karl-Heinz, Tang, Haiming, Tashman, Katherine, Toonen, Ruud F.G, Verpelli, Chiara, Reig-Viader, Rita, Watanabe, Kyoko, van Weering, Jan, Achsel, Tilmann, Ashrafi, Ghazaleh, Asi, Nimra, Brown, Tyler C, De Camilli, Pietro, Feuermann, Marc, Foulger, Rebecca E, Gaudet, Pascale, Joglekar, Anoushka, Kanellopoulos, Alexandros, Malenka, Robert, Nicoll, Roger A, Pulido, Camila, de Juan-Sanz, Jaime, Sheng, Morgan, Sudhof, Thomas C, Tilgner, Hagen U, Bagni, Claudia, Bayes, Alex, Biederer, Thomas, Brose, Nils, Chua, John Jia En, Dieterich, Daniela C, Gundelfinger, Eckart D, Hoogenraad, Casper, Huganir, Richard L, Jahn, Reinhard, Kaeser, Pascal S, Kim, Eunjoon, Kreutz, Michael R, McPherson, Peter S, Neale, Ben M, O'Connor, Vincent, Posthuma, Danielle, Ryan, Timothy A, Sala, Carlo, Feng, Guoping, Hyman, Steven E, Thomas, Paul D, Smit, August B, Verhage, Matthijs

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SynGO: An Evidence-Based, Expert-Curated Knowledge Base for the Synapse von Koopmans, Frank, van Nierop, Pim, Andres-Alonso, Maria, Byrnes, Andrea, Cijsouw, Tony, Coba, Marcelo P, Cornelisse, L Niels, Farrell, Ryan J, Goldschmidt, Hana L, Howrigan, Daniel P, Hussain, Natasha K, Imig, Cordelia, de Jong, Arthur P H, Jung, Hwajin, Kohansalnodehi, Mahdokht, Kramarz, Barbara, Lipstein, Noa, Lovering, Ruth C, MacGillavry, Harold, Mariano, Vittoria, Mi, Huaiyu, Ninov, Momchil, Osumi-Sutherland, David, Pielot, Rainer, Smalla, Karl-Heinz, Tang, Haiming, Tashman, Katherine, Toonen, Ruud F G, Verpelli, Chiara, Reig-Viader, Rita, Watanabe, Kyoko, van Weering, Jan, Achsel, Tilmann, Ashrafi, Ghazaleh, Asi, Nimra, Brown, Tyler C, De Camilli, Pietro, Feuermann, Marc, Foulger, Rebecca E, Gaudet, Pascale, Joglekar, Anoushka, Kanellopoulos, Alexandros, Malenka, Robert, Nicoll, Roger A, Pulido, Camila, de Juan-Sanz, Jaime, Sheng, Morgan, Südhof, Thomas C, Tilgner, Hagen U, Bagni, Claudia, Bayés, Àlex, Biederer, Thomas, Brose, Nils, Chua, John Jia En, Dieterich, Daniela C, Gundelfinger, Eckart D, Hoogenraad, Casper, Huganir, Richard L, Jahn, Reinhard, Kaeser, Pascal S, Kim, Eunjoon, Kreutz, Michael R, McPherson, Peter S, Neale, Ben M, O'Connor, Vincent, Posthuma, Danielle, Ryan, Timothy A, Sala, Carlo, Feng, Guoping, Hyman, Steven E, Thomas, Paul D, Smit, August B, Verhage, Matthijs

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SynGO: an evidence-based, expert-curated knowledgebase for the synapse von Koopmans, Frank, van Nierop, Pim, Andres-Alonso, Maria, Byrnes, Andrea, Cijsouw, Tony, Coba, Marcelo P., Cornelisse, L. Niels, Farrell, Ryan J., Goldschmidt, Hana L., Howrigan, Daniel P., Hussain, Natasha K., Imig, Cordelia, de Jong, Arthur P.H., Jung, Hwajin, Kohansalnodehi, Mahdokht, Kramarz, Barbara, Lipstein, Noa, Lovering, Ruth C., MacGillavry, Harold, Mariano, Vittoria, Mi, Huaiyu, Ninov, Momchil, Osumi-Sutherland, David, Pielot, Rainer, Smalla, Karl-Heinz, Tang, Haiming, Tashman, Katherine, Toonen, Ruud F.G., Verpelli, Chiara, Reig-Viader, Rita, Watanabe, Kyoko, van Weering, Jan, Achsel, Tilmann, Ashrafi, Ghazaleh, Asi, Nimra, Brown, Tyler C., De Camilli, Pietro, Feuermann, Marc, Foulger, Rebecca E., Gaudet, Pascale, Joglekar, Anoushka, Kanellopoulos, Alexandros, Malenka, Robert, Nicoll, Roger A., Pulido, Camila, de Juan-Sanz, Jaime, Sheng, Morgan, Südhof, Thomas C., Tilgner, Hagen U., Bagni, Claudia, Bayés, Àlex, Biederer, Thomas, Brose, Nils, En Chua, John Jia, Dieterich, Daniela C., Gundelfinger, Eckart D., Hoogenraad, Casper, Huganir, Richard L., Jahn, Reinhard, Kaeser, Pascal S., Kim, Eunjoon, Kreutz, Michael R., McPherson, Peter S., Neale, Ben M., O’Connor, Vincent, Posthuma, Danielle, Ryan, Timothy A., Sala, Carlo, Feng, Guoping, Hyman, Steven E., Thomas, Paul D., Smit, August B., Verhage, Matthijs

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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, Schizophrenia Psychiatric Genome-Wide Association Study Consortium

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Reaction time performance in ADHD: improvement under fast-incentive condition and familial effects von Andreou, Penny, Neale, Ben M, Chen, Wai, Christiansen, Hanna, Gabriels, Isabel, Heise, Alexander, Meidad, Sheera, Müller, Ueli C, Uebel, Henrik, Banaschewski, Tobias, Manor, Iris, Oades, Robert, Roeyers, Herbert, Rothenberger, Aribert, Sham, Pak, Steinhausen, Hans-Christoph, Asherson, Philip, Kuntsi, Jonna

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Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort von Moen, Gunn-Helen, Brumpton, Ben, Willer, Cristen, Åsvold, Bjørn Olav, Birkeland, Kåre I., Wang, Geng, Neale, Michael C., Freathy, Rachel M., Smith, George Davey, Lawlor, Deborah A., Kirkpatrick, Robert M., Warrington, Nicole M., Evans, David M.

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Analysis of protein-coding genetic variation in 60,706 humans von 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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A structural variation reference for medical and population genetics von Collins, Ryan L., Brand, Harrison, Karczewski, Konrad J., Zhao, Xuefang, Alföldi, Jessica, Francioli, Laurent C., Khera, Amit V., Lowther, Chelsea, Gauthier, Laura D., Wang, Harold, Watts, Nicholas A., Solomonson, Matthew, O’Donnell-Luria, Anne, Baumann, Alexander, Munshi, Ruchi, Walker, Mark, Whelan, Christopher W., Huang, Yongqing, Brookings, Ted, Sharpe, Ted, Stone, Matthew R., Valkanas, Elise, Fu, Jack, Tiao, Grace, Laricchia, Kristen M., Ruano-Rubio, Valentin, Stevens, Christine, Gupta, Namrata, Cusick, Caroline, Margolin, Lauren, Taylor, Kent D., Lin, Henry J., Rich, Stephen S., Post, Wendy S., Chen, Yii-Der Ida, Rotter, Jerome I., Nusbaum, Chad, Philippakis, Anthony, Lander, Eric, Gabriel, Stacey, Neale, Benjamin M., Kathiresan, Sekar, Daly, Mark J., Banks, Eric, MacArthur, Daniel G., Talkowski, Michael E.

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The mutational constraint spectrum quantified from variation in 141,456 humans von 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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Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses von Brumpton, Ben, Sanderson, Eleanor, Heilbron, Karl, Hartwig, Fernando Pires, Harrison, Sean, Vie, Gunnhild Åberge, Cho, Yoonsu, Howe, Laura D., Hughes, Amanda, Boomsma, Dorret I., Havdahl, Alexandra, Hopper, John, Neale, Michael, Nivard, Michel G., Pedersen, Nancy L., Reynolds, Chandra A., Tucker-Drob, Elliot M., Grotzinger, Andrew, Howe, Laurence, Morris, Tim, Li, Shuai, Auton, Adam, Windmeijer, Frank, Chen, Wei-Min, Bjørngaard, Johan Håkon, Hveem, Kristian, Willer, Cristen, Evans, David M., Kaprio, Jaakko, Davey Smith, George, Åsvold, Bjørn Olav, Hemani, Gibran, Davies, Neil M.

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Controlling the {111}/{110} Surface Ratio of Cuboidal Ceria Nanoparticles von Castanet, Uli, Feral-Martin, Cédric, Demourgues, Alain, Neale, Rachel L, Sayle, Dean C, Caddeo, Francesco, Flitcroft, Joseph M, Caygill, Robert, Pointon, Ben J, Molinari, Marco, Majimel, Jerome

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Evaluating drug targets through human loss-of-function genetic variation von Minikel, Eric Vallabh, Karczewski, Konrad J., Martin, Hilary C., Cummings, Beryl B., Whiffin, Nicola, Rhodes, Daniel, Alföldi, Jessica, Trembath, Richard C., van Heel, David A., Daly, Mark J., Schreiber, Stuart L., MacArthur, Daniel G.

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The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia von Nehme, Ralda, Pietiläinen, Olli, Artomov, Mykyta, Tegtmeyer, Matthew, Valakh, Vera, Lehtonen, Leevi, Bell, Christina, Singh, Tarjinder, Trehan, Aditi, Sherwood, John, Manning, Danielle, Peirent, Emily, Malik, Rhea, Guss, Ellen J., Hawes, Derek, Beccard, Amanda, Bara, Anne M., Hazelbaker, Dane Z., Zuccaro, Emanuela, Genovese, Giulio, Loboda, Alexander A., Neumann, Anna, Lilliehook, Christina, Kuismin, Outi, Hamalainen, Eija, Kurki, Mitja, Hultman, Christina M., Kähler, Anna K., Paulo, Joao A., Ganna, Andrea, Madison, Jon, Cohen, Bruce, McPhie, Donna, Adolfsson, Rolf, Perlis, Roy, Dolmetsch, Ricardo, Farhi, Samouil, McCarroll, Steven, Hyman, Steven, Neale, Ben, Barrett, Lindy E., Harper, Wade, Palotie, Aarno, Daly, Mark, Eggan, Kevin

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Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes von Wang, Qingbo, Pierce-Hoffman, Emma, Cummings, Beryl B., Alföldi, Jessica, Francioli, Laurent C., Gauthier, Laura D., Hill, Andrew J., O’Donnell-Luria, Anne H., Karczewski, Konrad J., MacArthur, Daniel G.

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Transcript expression-aware annotation improves rare variant interpretation von Cummings, Beryl B., Karczewski, Konrad J., Kosmicki, Jack A., Seaby, Eleanor G., Watts, Nicholas A., Singer-Berk, Moriel, Mudge, Jonathan M., Karjalainen, Juha, Satterstrom, F. Kyle, O’Donnell-Luria, Anne H., Poterba, Timothy, Seed, Cotton, Solomonson, Matthew, Alföldi, Jessica, Daly, Mark J., MacArthur, Daniel G.

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Psychiatric Genomics: An Update and an Agenda von Sullivan, Patrick F, Agrawal, Arpana, Bulik, Cynthia M, Andreassen, Ole A, Børglum, Anders D, Breen, Gerome, Cichon, Sven, Edenberg, Howard J, Faraone, Stephen V, Gelernter, Joel, Mathews, Carol A, Nievergelt, Caroline M, Smoller, Jordan W, O’Donovan, Michael C

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Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap von Gandal, Michael J, Haney, Jillian R, Parikshak, Neelroop N, Leppa, Virpi, Ramaswami, Gokul, Hartl, Chris, Schork, Andrew J, Appadurai, Vivek, Buil, Alfonso, Werge, Thomas M, Liu, Chunyu, White, Kevin P, Horvath, Steve, Geschwind, Daniel H

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