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Loss-of-function variants in MARK2 cause neurodevelopmental disorder Yang, Yunseon; Shim, Yoon-Kyung; Miyake, Noriko; Takada, Sanami; Silva, Sebastian; Peters-Foitzick, Alexander; Gupta, Abha R.; Neuhaus, Emily; Bradley, Catherine; Taylor, Cora; Russell, Bianca; Shrewsbury, Amanda; Michaelson, Jacob J.; Murali, Chaya N.; Gerard, Amanda; Geltzeiler, Alexa; Chung, Wendy K.; Chung, Hyung-lok Share Save
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Immune dysregulation in bipolar disorder Argue, Benney M. R.; Casten, Lucas G.; Mccool, Shaylah; Alrfooh, Aysheh; Richards, Jenny Gringer; Wemmie, John A.; Magnotta, Vincent A.; Williams, Aislinn J.; Michaelson, Jacob; Fiedorowicz, Jess G.; Scroggins, Sabrina M.; Gaine, Marie E. Share Save
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Force Field X: A computational microscope to study genetic variation and organic crystals using theory and experiment Gogal, Rose A.; Nessler, Aaron J.; Thiel, Andrew C.; Bernabe, Hernan V.; Corrigan Grove, Rae A.; Cousineau, Leah M.; Litman, Jacob M.; Miller, Jacob M.; Qi, Guowei; Speranza, Matthew J.; Tollefson, Mallory R.; Fenn, Timothy D.; Michaelson, Jacob J.; Okada, Okimasa; Piquemal, Jean-Philip; Ponder, Jay W.; Shen, Jana; Smith, Richard J. H.; Yang, Wei; Ren, Pengyu; Schnieders, Michael J. Share Save
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Using deep learning to quantify neuronal activation from single-cell and spatial transcriptomic data Bahl, Ethan; Chatterjee, Snehajyoti; Mukherjee, Utsav; Elsadany, Muhammad; Vanrobaeys, Yann; Lin, Li-Chun; Mcdonough, Miriam; Resch, Jon; Giese, K. Peter; Abel, Ted; Michaelson, Jacob J. Share Save
Cerebellar morphological differences and associations with extrinsic factors in bipolar disorder type I Harmata, Gail I. S.; Barsotti, Ercole John; Casten, Lucas G.; Fiedorowicz, Jess G.; Williams, Aislinn; Shaffer, Joseph J.; Richards, Jenny Gringer; Sathyaputri, Leela; Schmitz, Samantha L.; Christensen, Gary E.; Long, Jeffrey D.; Gaine, Marie E.; Xu, Jia; Michaelson, Jake J.; Wemmie, John A.; Magnotta, Vincent A. Share Save
The Gender Self-Report: A Multidimensional Gender Characterization Tool for Gender-Diverse and Cisgender Youth and Adults Strang, John F.; Wallace, Gregory L.; Michaelson, Jacob J.; Fischbach, Abigail L.; Thomas, Taylor R.; Jack, Allison; Shen, Jerry; Chen, Diane; Freeman, Andrew; Knauss, Megan; Corbett, Blythe A.; Kenworthy, Lauren; Tishelman, Amy C.; Willing, Laura; McQuaid, Goldie A.; Nelson, Eric E.; Toomey, Russell B.; McGuire, Jenifer K.; Fish, Jessica N.; Leibowitz, Scott F.; Nahata, Leena; Anthony, Laura G.; Slesaransky-Poe, Graciela; D'Angelo, Lawrence; Clawson, Ann; Song, Amber D.; Grannis, Connor; Sadikova, Eleonora; Pelphrey, Kevin A.; Mancilla, Michael; McClellan, Lucy S.; Csumitta, Kelsey D.; Winchenbach, Molly R.; Jilla, Amrita; Alemi, Farrokh; Yang, Ji Seung Share Save
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Language and reading impairments are associated with increased prevalence of non-right-handedness Abbondanza, Filippo; Dale, Philip S.; Wang, Carol A.; Hayiou-Thomas, Marianna E.; Toseeb, Umar; Koomar, Tanner S.; Wigg, Karen G.; Feng, Yu; Price, Kaitlyn M.; Kerr, Elizabeth N.; Guger, Sharon L.; Lovett, Maureen W.; Strug, Lisa J.; van Bergen, Elsje; Dolan, Conor V.; Tomblin, J. Bruce; Moll, Kristina; Schulte-Koerne, Gerd; Neuhoff, Nina; Warnke, Andreas; Fisher, Simon E.; Barr, Cathy L.; Michaelson, Jacob J.; Boomsma, Dorret I.; Snowling, Margaret J.; Hulme, Charles; Whitehouse, Andrew J. O.; Pennell, Craig E.; Newbury, Dianne F.; Stein, John; Talcott, Joel B.; Bishop, Dorothy V. M.; Paracchini, Silvia Share Save
Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism (vol 11, 3650, 2014) Corominas, Roser; Yang, Xinping; Lin, Guan Ning; Kang, Shuli; Shen, Yun; Ghamsari, Lila; Broly, Martin; Rodriguez, Maria; Tam, Stanley; Wanamaker, Shelly A.; Fan, Changyu; Yi, Song; Tasan, Murat; Lemmens, Irma; Kuang, Xingyan; Zhao, Nan; Malhotra, Dheeraj; Michaelson, Jacob J.; Vacic, Vladimir; Calderwood, Michael A.; Roth, Frederick P.; Tavernier, Jan; Horvath, Steve; Salehi-Ashtiani, Kourosh; Korkin, Dmitry; Sebat, Jonathan; Hill, David E.; Hao, Tong; Vidal, Marc; Iakoucheva, Lilia M. Share Save
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities Price, Kaitlyn M.; Wigg, Karen G.; Eising, Else; Feng, Yu; Blokland, Kirsten; Wilkinson, Margaret; Kerr, Elizabeth N.; Guger, Sharon L.; Abbondanza, Filippo; Allegrini, Andrea G.; Andlauer, Till F. M.; Bates, Timothy C.; Bernard, Manon; Bonte, Milene; Boomsma, Dorret I.; Bourgeron, Thomas; Brandeis, Daniel; Carreiras, Manuel; Ceroni, Fabiola; Csepe, Valeria; Dale, Philip S.; DeFries, John C.; de Jong, Peter F.; Demonet, Jean Francois; de Zeeuw, Eveline L.; Franken, Marie-Christine J.; Francks, Clyde; Gerritse, Margot; Gialluisi, Alessandro; Gordon, Scott D.; Gruen, Jeffrey R.; Hayiou-Thomas, Marianna E.; Hernandez-Cabrera, Juan; Hottenga, Jouke-Jan; Hulme, Charles; Jansen, Philip R.; Kere, Juha; Koomar, Tanner; Landerl, Karin; Leonard, Gabriel T.; Liao, Zhijie; Luciano, Michelle; Lyytinen, Heikki; Martin, Nicholas G.; Martinelli, Angela; Maurer, Urs; Michaelson, Jacob J.; Mirza-Schreiber, Nazanin; Moll, Kristina; Monaco, Anthony P.; Morgan, Angela T.; Mueller-Myhsok, Bertram; Newbury, Dianne F.; Noethen, Markus M.; Olson, Richard K.; Paracchini, Silvia; Paus, Tomas; Pausova, Zdenka; Pennell, Craig E.; Pennington, Bruce F.; Plomin, Robert J.; Ramus, Franck; Reilly, Sheena; Richer, Louis; Rimfeld, Kaili; Schulte-Korne, Gerd; Shapland, Chin Yang; Simpson, Nuala H.; Smith, Shelley D.; Snowling, Margaret J.; St Pourcain, Beate; Stein, John F.; Talcott, Joel B.; Tiemeier, Henning; Tomblin, J. Bruce; Truong, Dongnhu T.; van Bergen, Elsje; van der Schroeff, Marc P.; Van Donkelaar, Marjolein; Verhoef, Ellen; Wang, Carol A.; Watkins, Kate E.; Whitehouse, Andrew J. O.; Willcutt, Erik G.; Wright, Margaret J.; Zhu, Gu; Fisher, Simon E.; Lovett, Maureen W.; Strug, Lisa J.; Barr, Cathy L. Share Save
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