Endometrial echo complex thickness in postmenopausal endometrial cancer von Chandavarkar, Uma, Kuperman, Julie M, Muderspach, Laila I, Opper, Neisha, Felix, Juan C, Roman, Lynda

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Alpha-2 Adrenoceptor Activation Inhibits Phencyclidine-Induced Deficits of Spatial Working Memory in Rats von MARRS, William, KUPERMAN, Julie, AVEDIAN, Tahlin, ROTH, Robert H, JENTSCH, J. David

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Effect of Contraception Decisional Aid on Postpartum Contraceptive Choice: A Replicated Time Series Study [20G] von Sridhar, Aparna, Kuperman, Julie, Hulugalle, Avanthi

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Alpha-2 Adrenoceptor Activation Inhibits Phencyclidine-Induced Deficits of Spatial Working Memory in Rats: Preclinical Research von Marrs, William, Kuperman, Julie, Avedian, Tahlin, Roth, Robert H, Jentsch, J David

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Effects of individual differences in verbal skills on eye-movement patterns during sentence reading von Kuperman, Victor, Van Dyke, Julie A.

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Reassessing Word Frequency as a Determinant of Word Recognition for Skilled and Unskilled Readers von Kuperman, Victor, Van Dyke, Julie A

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Long-Term Use of Everolimus in Patients with Tuberous Sclerosis Complex: Final Results from the EXIST-1 Study von Franz, David N, Belousova, Elena, Sparagana, Steven, Bebin, E Martina, Frost, Michael D, Kuperman, Rachel, Witt, Olaf, Kohrman, Michael H, Flamini, J Robert, Wu, Joyce Y, Curatolo, Paolo, de Vries, Petrus J, Berkowitz, Noah, Niolat, Julie, Jóźwiak, Sergiusz

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Everolimus for subependymal giant cell astrocytoma in patients with tuberous sclerosis complex: 2-year open-label extension of the randomised EXIST-1 study von Franz, David Neal, Dr Prof, Belousova, Elena, Prof, Sparagana, Steven, MD, Bebin, E Martina, MD, Frost, Michael, MD, Kuperman, Rachel, MD, Witt, Olaf, Prof, Kohrman, Michael H, Prof, Flamini, J Robert, MD, Wu, Joyce Y, MD, Curatolo, Paolo, Prof, de Vries, Petrus J, Prof, Berkowitz, Noah, MD, Anak, Oezlem, MD, Niolat, Julie, MSc, Jozwiak, Sergiusz, Prof

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Contributions of Reader- and Text-Level Characteristics to Eye-Movement Patterns During Passage Reading von Kuperman, Victor, Matsuki, Kazunaga, Van Dyke, Julie A.

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CompLex: an eye-movement database of compound word reading in English von Schmidtke, Daniel, Van Dyke, Julie A., Kuperman, Victor

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Individual Variability in the Semantic Processing of English Compound Words von Schmidtke, Daniel, Van Dyke, Julie A, Kuperman, Victor

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Improving Acceptance of Computerized Prescribing Alerts in Ambulatory Care von Shah, Nidhi R., Seger, Andrew C., Seger, Diane L., Fiskio, Julie M., Kuperman, Gilad J., Blumenfeld, Barry, Recklet, Elaine G., Bates, David W., Gandhi, Tejal K.

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Potential Unintended Consequences of Health Information Exchange von Kuperman, Gilad J., McGowan, Julie J.

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DerLex: An eye-movement database of derived word reading in English von Schmidtke, Daniel, Van Dyke, Julie A., Kuperman, Victor

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Oculomotor planning in RAN and reading: a strong test of the visual scanning hypothesis von Henry, Regina, Van Dyke, Julie A., Kuperman, Victor

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Investigation of gene–environment interactions in relation to tic severity von Abdulkadir, Mohamed, Yu, Dongmei, Osiecki, Lisa, King, Robert A., Fernandez, Thomas V., Brown, Lawrence W., Cheon, Keun-Ah, Coffey, Barbara J., Garcia-Delgar, Blanca, Gilbert, Donald L., Grice, Dorothy E., Hagstrøm, Julie, Hedderly, Tammy, Heyman, Isobel, Hong, Hyun Ju, Huyser, Chaim, Ibanez-Gomez, Laura, Kim, Young Key, Kim, Young-Shin, Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Leventhal, Bennett, Madruga-Garrido, Marcos, Maras, Athanasios, Mir, Pablo, Morer, Astrid, Münchau, Alexander, Plessen, Kerstin J., Roessner, Veit, Shin, Eun-Young, Song, Dong-Ho, Song, Jungeun, Visscher, Frank, Zinner, Samuel H., Mathews, Carol A., Scharf, Jeremiah M., Tischfield, Jay A., Heiman, Gary A., Dietrich, Andrea, Hoekstra, Pieter J.

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Characteristics and consequences of drug allergy alert overrides in a computerized physician order entry system von Hsieh, Tyken C., Kuperman, Gilad J., Jaggi, Tonushree, Hojnowski-Diaz, Patricia, Fiskio, Julie, Williams, Deborah H., Bates, David W., Gandhi, Tejal K.

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Whole-exome sequencing identifies genes associated with Tourette’s disorder in multiplex families von Cao, Xiaolong, Zhang, Yeting, Abdulkadir, Mohamed, Deng, Li, Fernandez, Thomas V., Garcia-Delgar, Blanca, Hagstrøm, Julie, Hoekstra, Pieter J., King, Robert A., Koesterich, Justin, Kuperman, Samuel, Morer, Astrid, Nasello, Cara, Plessen, Kerstin J., Thackray, Joshua K., Zhou, Lisheng, Dietrich, Andrea, Tischfield, Jay A., Heiman, Gary A., Xing, Jinchuan

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Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome von Jain, Pritesh, Yang, Zhiyu, Yu, Dongmei, Tumer, Zeynep, Hartmann, Andreas, Müller-Vahl, Kirsten R., Boomsma, Dorret I., Wolanczyk, Tomasz, Nemoda, Zsofia, Padmanabhuni, Shanmukha S., Grice, Dorothy, Glennon, Jeffrey, Stefansson, Hreinn, Stamatoyannopoulos, John A., Benaroya-Milshtein, Noa, Cardona, Francesco, Heyman, Isobel, Mir, Pablo, Munchau, Alexander, Plessen, Kerstin J., Roessner, Veit, Martino, Davide, Barr, Cathy L., Batterson, James R., Budman, Cathy L., Coppola, Giovanni, Darrow, Sabrina, Freimer, Nelson B., Grados, Marco A., Greenberg, Erica, Huang, Alden Y., Illmann, Cornelia, Kurlan, Roger, Leckman, James F., Malaty, Irene A., McMahon, William M., Neale, Benjamin M., Osiecki, Lisa, Rouleau, Guy A., Sul, Jae Hoon, Androutsos, Christos, Basha, Entela, Farkas, Luca, Janik, Piotr, Kapisyzi, Mira, Karagiannidis, Iordanis, Koumoula, Anastasia, Nagy, Peter, Puchala, Joanna, Szymanska, Urszula, Apter, Alan, Bodmer, Benjamin, Bognar, Emese, Buse, Judith, Fremer, Carolin, Garcia-Delgar, Blanca, Hagen, Annelieke, Hagstrøm, Julie, Madruga-Garrido, Marcos, Silvestri, Paola Rosaria, Skov, Liselotte, Steinberg, Tamar, Turner, Victoria L., Alexander, John, Aranyi, Tamas, Fan, Siyan, Forde, Natalie J., Gerasch, Sarah, Kanaan, Ahmad S., Möller, Harald E., Poelmans, Geert, Pouwels, Petra J.W., Rizzo, Francesca, Veltman, Dick J., van der Werf, Ysbrand D., Widomska, Joanna, Zilhäo, Nuno R., Brown, Lawrence W., Cheon, Keun-Ah, Fernandez, Thomas V., Kim, Eun-Joo, Kim, Young Key, Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Maras, Athanasios, Murphy, Tara L., Shin, Eun-Young, Song, Dong-Ho, State, Matthew W., Visscher, Frank, Heiman, Gary A., Willsey, A. Jeremy, Dietrich, Andrea, Davis, Lea K., Crowley, James J., Scharf, Jeremiah M., Georgitsi, Marianthi, Hoekstra, Pieter J., Paschou, Peristera

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Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD von Wang, Sheng, Wang, Belinda, Drury, Vanessa, Drake, Sam, Sun, Nawei, Alkhairo, Hasan, Arbelaez, Juan, Duhn, Clif, Bal, Vanessa H., Langley, Kate, Martin, Joanna, Hoekstra, Pieter J., Dietrich, Andrea, Xing, Jinchuan, Heiman, Gary A., Tischfield, Jay A., Fernandez, Thomas V., Owen, Michael J., O’Donovan, Michael C., Thapar, Anita, State, Matthew W., Willsey, A. Jeremy

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