Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience von Willsey, Helen Rankin, Exner, Cameron R.T., Xu, Yuxiao, Everitt, Amanda, Sun, Nawei, Wang, Belinda, Dea, Jeanselle, Schmunk, Galina, Zaltsman, Yefim, Teerikorpi, Nia, Kim, Albert, Anderson, Aoife S., Shin, David, Seyler, Meghan, Nowakowski, Tomasz J., Harland, Richard M., Willsey, A. Jeremy, State, Matthew W.

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Genomics, convergent neuroscience and progress in understanding autism spectrum disorder von Willsey, Helen Rankin, Willsey, A. Jeremy, Wang, Belinda, State, Matthew W.

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Localized JNK signaling regulates organ size during development von Willsey, Helen Rankin, Zheng, Xiaoyan, Carlos Pastor-Pareja, José, Willsey, A Jeremy, Beachy, Philip A, Xu, Tian

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Xenopus leads the way: Frogs as a pioneering model to understand the human brain von Exner, Cameron R. T., Willsey, Helen Rankin

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Picroscope: low-cost system for simultaneous longitudinal biological imaging von Ly, Victoria T., Baudin, Pierre V., Pansodtee, Pattawong, Jung, Erik A., Voitiuk, Kateryna, Rosen, Yohei M., Willsey, Helen Rankin, Mantalas, Gary L., Seiler, Spencer T., Selberg, John A., Cordero, Sergio A., Ross, Jayden M., Rolandi, Marco, Pollen, Alex A., Nowakowski, Tomasz J., Haussler, David, Mostajo-Radji, Mohammed A., Salama, Sofie R., Teodorescu, Mircea

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Genomics, convergent neuroscience and progress in understanding autism spectrum disorder von Willsey, Helen Rankin, Willsey, A. Jeremy, Wang, Belinda, State, Matthew W.

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Modelling human genetic disorders in Xenopus tropicalis von Willsey, Helen Rankin, Seaby, Eleanor G, Godwin, Annie, Ennis, Sarah, Guille, Matthew, Grainger, Robert M

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DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract von Blackburn, Alexandria T. M., Bekheirnia, Nasim, Uma, Vanessa C., Corkins, Mark E., Xu, Yuxiao, Rosenfeld, Jill A., Bainbridge, Matthew N., Yang, Yaping, Liu, Pengfei, Madan-Khetarpal, Suneeta, Delgado, Mauricio R., Hudgins, Louanne, Krantz, Ian, Rodriguez-Buritica, David, Wheeler, Patricia G., Al-Gazali, Lihadh, Mohamed Saeed Mohamed Al Shamsi, Aisha, Gomez-Ospina, Natalia, Chao, Hsiao-Tuan, Mirzaa, Ghayda M., Scheuerle, Angela E., Kukolich, Mary K., Scaglia, Fernando, Eng, Christine, Willsey, Helen Rankin, Braun, Michael C., Lamb, Dolores J., Miller, Rachel K., Bekheirnia, Mir Reza

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Correction: DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract von Blackburn, Alexandria T.M., Bekheirnia, Nasim, Uma, Vanessa C., Corkins, Mark E., Xu, Yuxiao, Rosenfeld, Jill A., Bainbridge, Matthew N., Yang, Yaping, Liu, Pengfei, Madan-Khetarpal, Suneeta, Delgado, Mauricio R., Hudgins, Louanne, Krantz, Ian, Rodriguez-Buritica, David, Wheeler, Patricia G., Al-Gazali, Lihadh, Shamsi, Aisha Mohamed Saeed Mohamed Al, Gomez-Ospina, Natalia, Chao, Hsiao-Tuan, Mirzaa, Ghayda M., Scheuerle, Angela E., Kukolich, Mary K., Scaglia, Fernando, Eng, Christine, Willsey, Helen Rankin, Braun, Michael C., Lamb, Dolores J., Miller, Rachel K., Bekheirnia, Mir Reza

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Neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and brain size in Xenopus embryos von Willsey, Helen Rankin, Xu, Yuxiao, Everitt, Amanda, Dea, Jeanselle, Exner, Cameron R. T., Willsey, A. Jeremy, State, Matthew W., Harland, Richard M.

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The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos von Willsey, Helen Rankin, Xu, Yuxiao, Everitt, Amanda, Dea, Jeanselle, Exner, Cameron R T, Willsey, A Jeremy, State, Matthew W, Harland, Richard M

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Pleiotropy of autism-associated chromatin regulators von Lasser, Micaela, Sun, Nawei, Xu, Yuxiao, Wang, Sheng, Drake, Sam, Law, Karen, Gonzalez, Silvano, Wang, Belinda, Drury, Vanessa, Castillo, Octavio, Zaltsman, Yefim, Dea, Jeanselle, Bader, Ethel, McCluskey, Kate E, State, Matthew W, Willsey, A Jeremy, Willsey, Helen Rankin

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Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience von Willsey, Helen Rankin, Exner, Cameron R T, Xu, Yuxiao, Everitt, Amanda, Sun, Nawei, Wang, Belinda, Dea, Jeanselle, Schmunk, Galina, Zaltsman, Yefim, Teerikorpi, Nia, Kim, Albert, Anderson, Aoife S, Shin, David, Seyler, Meghan, Nowakowski, Tomasz J, Harland, Richard M, Willsey, A Jeremy, State, Matthew W

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Correction: The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos von Willsey, Helen Rankin, Xu, Yuxiao, Everitt, Amanda, Dea, Jeanselle, Exner, Cameron R T, Willsey, A Jeremy, State, Matthew W, Harland, Richard M

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Deep learning is widely applicable to phenotyping embryonic development and disease von Naert, Thomas, Çiçek, Özgün, Ogar, Paulina, Bürgi, Max, Shaidani, Nikko-Ideen, Kaminski, Michael M, Xu, Yuxiao, Grand, Kelli, Vujanovic, Marko, Prata, Daniel, Hildebrandt, Friedhelm, Brox, Thomas, Ronneberger, Olaf, Voigt, Fabian F, Helmchen, Fritjof, Loffing, Johannes, Horb, Marko E, Willsey, Helen Rankin, Lienkamp, Soeren S

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Repurposing of a gill gene regulatory program for outer ear evolution von Thiruppathy, Mathi, Teubner, Lauren, Roberts, Ryan R, Lasser, Micaela, Moscatello, Alessandra, Chen, Ya-Wen, Hochstim, Christian, Ruffins, Seth, Sarkar, Arijita, Tassey, Jade, Evseenko, Denis, Lozito, Thomas P, Willsey, Helen Rankin, Gillis, J Andrew, Crump, J Gage

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Katanin-like protein Katnal2 is required for ciliogenesis and brain development in Xenopus embryos von Willsey, Helen Rankin, Walentek, Peter, Exner, Cameron R.T., Xu, Yuxiao, Lane, Andrew B., Harland, Richard M., Heald, Rebecca, Santama, Niovi

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A convergent molecular network underlying autism and congenital heart disease von Rosenthal, Sara Brin, Willsey, Helen Rankin, Xu, Yuxiao, Mei, Yuan, Dea, Jeanselle, Wang, Sheng, Curtis, Charlotte, Sempou, Emily, Khokha, Mustafa K., Chi, Neil C., Willsey, Arthur Jeremy, Fisch, Kathleen M., Ideker, Trey

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Deep learning is widely applicable to phenotyping embryonic development and disease von Naert, Thomas, Çiçek, Özgün, Ogar, Paulina, Bürgi, Max, Shaidani, Nikko-Ideen, Kaminski, Michael M, Xu, Yuxiao, Grand, Kelli, Vujanovic, Marko, Prata, Daniel, Hildebrandt, Friedhelm, Brox, Thomas, Ronneberger, Olaf, Voigt, Fabian F, Helmchen, Fritjof, Loffing, Johannes, Horb, Marko E, Willsey, Helen Rankin, Lienkamp, Soeren S

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Deep learning is widely applicable to phenotyping embryonic development and disease von Naert, Thomas, Cicek, Ozgun, Ogar, Paulina, Burgi, Max, Shaidani, Nikko-Ideen, Kaminski, Michael M, Xu, Yuxiao, Grand, Kelli, Vujanovic, Marko, Prata, Daniel, Hildebrandt, Friedhelm, Brox, Thomas, Ronneberger, Olaf, Voigt, Fabian F, Helmchen, Fritjof, Loffing, Johannes, Horb, Marko E, Willsey, Helen Rankin, Lienkamp, Soeren S

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