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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
Published in Journal of the American Academy of Child and Adolescent Psychiatry (01.10.2014)
Published in Journal of the American Academy of Child and Adolescent Psychiatry (01.10.2014)
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Reaction time performance in ADHD: improvement under fast-incentive condition and familial effects
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
Published in Psychological medicine (01.12.2007)
Published in Psychological medicine (01.12.2007)
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Runs of homozygosity implicate autozygosity as a schizophrenia risk factor
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
Published in PLoS genetics (01.04.2012)
Published in PLoS genetics (01.04.2012)
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SynGO: an evidence-based, expert-curated knowledgebase for the synapse
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
Published in Neuron (Cambridge, Mass.) (03.06.2019)
Published in Neuron (Cambridge, Mass.) (03.06.2019)
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Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families
Werling, Donna M, Brand, Harrison, Joon-Yong, An, Stone, Matthew R, Glessner, Joseph T, Zhu, Lingxue, Collins, Ryan L, Dong, Shan, Layer, Ryan M, Markenscoff-Papadimitriou, Eiriene-Chloe, Farrell, Andrew, Schwartz, Grace B, Currall, Benjamin B, Jeanselle Dea, Duhn, Clif, Erdman, Carolyn, Gilson, Michael, Handsaker, Robert E, Kashin, Seva, Klei, Lambertus, Mandell, Jeffrey D, Nowakowski, Tomasz J, Liu, Yuwen, Pochareddy, Sirisha, Smith, Louw, Walker, Michael F, Wang, Harold Z, Waterman, Mathew J, He, Xin, Kriegstein, Arnold R, Rubenstein, John L, Sestan, Nenad, Mccarroll, Steven A, Neale, Ben M, Coon, Hilary, Willsey, A Jeremy, Buxbaum, Joseph D, Daly, Mark J, State, Matthew W, Quinlan, Aaron, Marth, Gabor T, Roeder, Kathryn, Devlin, Bernie, Talkowski, Michael E, Sanders, Stephan J
Published in bioRxiv (13.04.2017)
Published in bioRxiv (13.04.2017)
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