Paternal Origin of FGFR2 Mutations in Sporadic Cases of Crouzon Syndrome and Pfeiffer Syndrome von Glaser, Rivka L., Jiang, Wen, Boyadjiev, Simeon A., Tran, Alissa K., Zachary, Andrea A., Van Maldergem, Lionel, Johnson, David, Walsh, Sinead, Oldridge, Michael, Wall, Steven A., Wilkie, Andrew O.M., Jabs, Ethylin Wang

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Structure-based classification predicts drug response in EGFR-mutant NSCLC von Robichaux, Jacqulyne P., Le, Xiuning, Vijayan, R. S. K., Hicks, J. Kevin, Heeke, Simon, Elamin, Yasir Y., Lin, Heather Y., Udagawa, Hibiki, Skoulidis, Ferdinandos, Tran, Hai, Varghese, Susan, He, Junqin, Zhang, Fahao, Nilsson, Monique B., Hu, Lemei, Poteete, Alissa, Rinsurongkawong, Waree, Zhang, Xiaoshan, Ren, Chenghui, Liu, Xiaoke, Hong, Lingzhi, Zhang, Jianjun, Diao, Lixia, Madison, Russell, Schrock, Alexa B., Saam, Jennifer, Raymond, Victoria, Fang, Bingliang, Wang, Jing, Ha, Min Jin, Cross, Jason B., Gray, Jhanelle E., Heymach, John V.

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NAB2::STAT6 fusions and genome‐wide DNA methylation profiling: Predictors of patient outcomes in meningeal solitary fibrous tumors von Eschbacher, Kathryn L., Tran, Quynh T., Moskalev, Evgeny A., Jenkins, Sarah, Fritchie, Karen, Stoehr, Robert, Caron, Alissa, Link, Michael J., Brown, Paul D., Guajardo, Andrew, Brat, Daniel J., Wu, Ashley, Santagata, Sandro, Louis, David N., Brastianos, Priscilla K., Kaplan, Alexander B., Alexander, Brian, Rossi, Sabrina, Ferrarese, Fabio, Raleigh, David R., Nguyen, Minh P., Gross, John, Velazquez Vega, Jose, Rodriguez, Fausto, Perry, Arie, Martinez‐Lage, Maria, Orr, Brent A., Haller, Florian, Giannini, Caterina

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Interpregnancy interval and prevalence of selected birth defects: A multistate study von Liberman, Rebecca F., Heinke, Dominique, Petersen, Julie M., Parker, Samantha E., Nestoridi, Eirini, Van Zutphen, Alissa R., Nembhard, Wendy N., Ramirez, Glenda M., Ethen, Mary K., Tran, Tri, Kirby, Russell S., Getz, Kelly D., Nance, Amy E., Yazdy, Mahsa M.

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