Marcogliese, Paul C; Deal, Samantha L; Andrews, Jonathan; Harnish, J Michael; Bhavana, V Hemanjani; Graves, Hillary K; Jangam, Sharayu; Luo, Xi; Liu, Ning; Bei, Danqing; Chao, Yu-Hsin; Hull, Brooke; Lee, Pei-Tseng; Pan, Hongling; Bhadane, Pradnya; Huang, Mei-Chu; Longley, Colleen M; Chao, Hsiao-Tuan; Chung, Hyung-Lok; Haelterman, Nele A; Kanca, Oguz; Manivannan, Sathiya N; Rossetti, Linda Z; German, Ryan J; Gerard, Amanda; Schwaibold, Eva Maria Christina; Fehr, Sarah; Guerrini, Renzo; Vetro, Annalisa; England, Eleina; Murali, Chaya N; Barakat, Tahsin Stefan; van Dooren, Marieke F; Wilke, Martina; van Slegtenhorst, Marjon; Lesca, Gaetan; Sabatier, Isabelle; Chatron, Nicolas; Brownstein, Catherine A; Madden, Jill A; Agrawal, Pankaj B; Keren, Boris; Courtin, Thomas; Perrin, Laurence; Brugger, Melanie; Roser, Timo; Leiz, Steffen; Mau-Them, Frederic Tran; Delanne, Julian; Sukarova-Angelovska, Elena; Trajkova, Slavica; Rosenhahn, Erik; Strehlow, Vincent; Platzer, Konrad; Keller, Roberto; Pavinato, Lisa; Brusco, Alfredo; Rosenfeld, Jill A; Marom, Ronit; Wangler, Michael F; Yamamoto, Shinya     «

Marcogliese, Paul C; Deal, Samantha L; Andrews, Jonathan; Harnish, J Michael; Bhavana, V Hemanjani; Graves, Hillary K; Jangam, Sharayu; Luo, Xi; Liu, Ning; Bei, Danqing; Chao, Yu-Hsin; Hull, Brooke; Lee, Pei-Tseng; Pan, Hongling; Bhadane, Pradnya; Huang, Mei-Chu; Longley, Colleen M; Chao, Hsiao-Tuan; Chung, Hyung-Lok; Haelterman, Nele A; Kanca, Oguz; Manivannan, Sathiya N; Rossetti, Linda Z; German, Ryan J; Gerard, Amanda; Schwaibold, Eva Maria Christina; Fehr, Sarah; Guerrini, Renzo; Vetro, Ann...     »

Individuals with autism spectrum disorder (ASD) exhibit an increased burden of de novo mutations (DNMs) in a broadening range of genes. While these studies have implicated hundreds of genes in ASD pathogenesis, which DNMs cause functional consequences in vivo remains unclear. We functionally test the effects of ASD missense DNMs using Drosophila through "humanization" rescue and overexpression-based strategies. We examine 79 ASD variants in 74 genes identified in the Simons Simplex Collection and find 38% of them to cause functional alterations. Moreover, we identify GLRA2 as the cause of a spectrum of neurodevelopmental phenotypes beyond ASD in 13 previously undiagnosed subjects. Functional characterization of variants in ASD candidate genes points to conserved neurobiological mechanisms and facilitates gene discovery for rare neurodevelopmental diseases.      «

Individuals with autism spectrum disorder (ASD) exhibit an increased burden of de novo mutations (DNMs) in a broadening range of genes. While these studies have implicated hundreds of genes in ASD pathogenesis, which DNMs cause functional consequences in vivo remains unclear. We functionally test the effects of ASD missense DNMs using Drosophila through "humanization" rescue and overexpression-based strategies. We examine 79 ASD variants in 74 genes identified in the Simons Simplex Collection an...     »