Multiplex, single-cell CRISPRa screening for cell type specific regulatory elements by Chardon, FM, McDiarmid, TA, Page, NF, Daza, RM, Martin, BK, Domcke, S, Regalado, SG, Lalanne, J, Calderon, D, Li, X, Starita, LM, Sanders, SJ, Ahituv, N, Shendure, J

Astrocytic β-catenin signaling via TCF7L2 regulates synapse development and social behavior by Szewczyk, LM, Lipiec, MA, Liszewska, E, Meyza, K, Urban-Ciecko, J, Kondrakiewicz, L, Goncerzewicz, A, Rafalko, K, Krawczyk, TG, Bogaj, K, Vainchtein, ID, Nakao-Inoue, H, Puscian, A, Knapska, E, Sanders, SJ, Jan Nowakowski, T, Molofsky, AV, Wisniewska, MB

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. by Walters, RK, Kosmicki, JA, Grove, J, Samocha, KE, Goldstein, JI, Okbay, A, Bybjerg-Grauholm, J, Werge, T, Hougaard, DM, Taylor, J, iPSYCH-Broad Autism Group, Psychiatric Genomics Consortium Autism Group, Skuse, D, Devlin, B, Anney, R, Sanders, SJ, Bishop, S, Mortensen, PB, Børglum, AD, Smith, GD, Daly, MJ, Robinson, EB

The Human Phenotype Ontology in 2024: phenotypes around the world by Gargano, MA, Matentzoglu, N, Coleman, B, Addo-Lartey, EB, Anagnostopoulos, A, Anderton, J, Avillach, P, Bagley, AM, Bakštein, E, Balhoff, JP, Baynam, G, Bello, SM, Berk, M, Bertram, H, Bishop, S, Blau, H, Bodenstein, DF, Botas, P, Boztug, K, Čady, J, Callahan, TJ, Cameron, R, Carbon, S, Castellanos, F, Sanders, SJ

A comprehensive AI model development framework for consistent Gleason grading by Huo, X, Ong, KH, Lau, KW, Gole, L, Young, DM, Tan, CL, Zhu, X, Zhang, C, Zhang, Y, Li, L, Han, H, Lu, H, Zhang, J, Hou, J, Zhao, H, Gan, H, Yin, L, Wang, X, Chen, X, Lv, H, Cao, H, Yu, X, Shi, Y, Huang, Z, Sanders, SJ

De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome by Chen, Y, Dawes, R, Kim, HC, Ljungdahl, A, Stenton, SL, Walker, S, Lord, J, Lemire, G, Martin-Geary, AC, Ganesh, VS, Ma, J, Ellingford, JM, Delage, E, D’Souza, EN, Dong, S, Adams, DR, Allan, K, Bakshi, M, Baldwin, EE, Berger, SI, Bernstein, JA, Bhatnagar, I, Blair, E, Brown, NJ, Goriely, A, Hinch, AG, Stewart, HS, Fica, SM, Sanders, SJ, Whiffin, N

Missense variants in the histone acetyltransferase complex component gene TRRAP cause autism and syndromic intellectual disability by Cogné, B, Ehresmann, S, Beauregard-Lacroix, E, Rousseau, J, Besnard, T, Garcia, T, Petrovski, S, Avni, S, McWalter, K, Blackburn, PR, Sanders, SJ, Uguen, K, Harris, J, Cohen, JS, Blyth, M, Lehman, A, Berg, J, Li, MH, Kini, U, Joss, S, von der Lippe, C, Gordon, CT, Humberson, JB, Robak, L, Scott, DA, Sutton, VR, Skraban, CM, Johnston, JJ, Poduri, A, Nordenskjöld, M, Shashi, V, Gerkes, EH, Bongers, EMHF, Gilissen, C, Zarate, YA, Kvarnung, M, Lally, KP, Kulch, PA, Daniels, B, Hernandez-Garcia, A, Stong, N, McGaughran, J, Retterer, K, Tveten, K, Sullivan, J, Geisheker, MR, Stray-Pedersen, A, Tarpinian, JM, Klee, EW, Nellaker, C, Sapp, JC

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia by Anney, RJL, Ripke, S, Anttila, V, Grove, J, Holmans, P, Huang, H, Klei, L, Lee, PH, Medland, SE, Neale, B, Robinson, E, Weiss, LA, Zwaigenbaum, L, Yu, TW, Wittemeyer, K, Willsey, AJ, Wijsman, EM, Werge, T, Wassink, TH, Waltes, R, Walsh, CA, Wallace, S, Vorstman, JAS, Vieland, VJ, Vicente, AM, vanEngeland, H, Tsang, K, Thompson, AP, Szatmari, P, Svantesson, O, Steinberg, S, Stefansson, K, Stefansson, H, State, MW, Soorya, L, Silagadze, T, Scherer, SW, Schellenberg, GD, Sandin, S, Sanders, SJ, Saemundsen, E, Rouleau, GA, Roge, B, Roeder, K, Roberts, W, Reichert, J, Reichenberg, A, Rehnstrom, K, Regan, R, Poustka, F, Poultney, CS, Piven, J, Pinto, D, Pericak-Vance, MA, Pejovic-Milovancevic, M, Pedersen, MG, Pedersen, CB, Paterson, AD, Parr, JR, Pagnamenta, AT, Oliveira, G, Nurnberger, JI, Nordentoft, M, Murtha, MT, Mouga, S, Mortensen, PB, Mors, O, Morrow, EM, Moreno-De-Luca, D, Monaco, AP, Minshew, N, Merikangas, A, McMahon, WM, McGrew, SG, Mattheisen, M, Martsenkovsky, I, Martin, DM, Mane, SM, Magnusson, P, Magalhaes, T, Maestrini, E, Lowe, JK, Lord, C, Levitt, P, LeseMartin, C, Ledbetter, DH, Leboyer, M, LeCouteur, AS, Ladd-Acosta, C, Kolevzon, A, Klauck, SM, Jacob, S, Iliadou, B, Hultman, CM, Hougaard, DM, Hertz-Picciotto, I, Hendren, R, Hansen, CS, Haines, JL, Guter, SJ, Grice, DE, Green, JM, Green, A, Goldberg, AP, Gillberg, C, Gilbert, J, Gallagher, L, Freitag, CM, Fombonne, E, Folstein, SE, Fernandez, B, Fallin, MD, Ercan-Sencicek, AG, Ennis, S, Duque, F, Duketis, E, Delorme, R, DeRubeis, S, DeJonge, MV, Dawson, G, Cuccaro, ML, Correia, CT, Conroy, J, Conceicao, IC, Chiocchetti, AG, Celestino-Soper, PBS, Casey, J, Cantor, RM, Cafe, C, Bybjerg-Grauholm, J, Brennan, S, Bourgeron, T, Bolton, PF, Boelte, S, Bolshakova, N, Betancur, C, Bernier, R, Beaudet, AL, Battaglia, A, Bal, VH, Baird, G, Bailey, AJ, Baekvad-Hansen, M, Bader, JS, Bacchelli, E, Anagnostou, E, Amaral, D, Almeida, J, Borglum, AD, Buxbaum, JD, Chakravarti, A, Cook, EH, Coon, H, Geschwind, DH, Gill, M, Hakonarson, H, Hallmayer, J, Palotie, A, Santangelo, S, Sutcliffe, JS, Arking, DE, Devlin, B, Daly, MJ