hVps15, but not Ca2+/CaM, is required for the activity and regulation of hVps34 in mammalian cells von Yan, Ying, Flinn, Rory J, Wu, Haiyan, Schnur, Rachel S, Backer, Jonathan M

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Phosphatidylinositol-3,4,5-trisphosphate: Tool of choice for class I PI 3-kinases von Salamon, Rachel Schnur, Backer, Jonathan M.

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Phonological Retrieval Mediates the Relation Phonological Short-term Memory and Narrative Production von Zahn, Rachel, Schnur, Tatiana, Martin, Randi

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Cancer treatment experiences among survivors of childhood sexual abuse: A qualitative investigation of triggers and reactions to cumulative trauma von Schnur, Julie B., Dillon, Matthew J., Goldsmith, Rachel E., Montgomery, Guy H.

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De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy von Singh, Sakshi, Gupta, Aditi, Zech, Michael, Sigafoos, Ashley N., Clark, Karl J., Dincer, Yasemin, Wagner, Matias, Humberson, Jennifer B., Green, Sarah, van Gassen, Koen, Brandt, Tracy, Schnur, Rhonda E., Millan, Francisca, Si, Yue, Mall, Volker, Winkelmann, Juliane, Gavrilova, Ralitza H., Klee, Eric W., Engleman, Kendra, Safina, Nicole P., Slaugh, Rachel, Bryant, Emily M., Tan, Wen-Hann, Granadillo, Jorge, Misra, Sunita N., Schaefer, G. Bradley, Towner, Shelley, Brilstra, Eva H., Koeleman, Bobby P. C.

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Biallelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with spastic cerebral palsy and epilepsy von Calame, Daniel G., Bakhtiari, Somayeh, Logan, Rachel, Coban-Akdemir, Zeynep, Du, Haowei, Mitani, Tadahiro, Fatih, Jawid M., Hunter, Jill V., Herman, Isabella, Pehlivan, Davut, Jhangiani, Shalini N., Person, Richard, Schnur, Rhonda E., Jin, Sheng Chih, Bilguvar, Kaya, Posey, Jennifer E., Koh, Sookyong, Firouzabadi, Saghar G., Alehabib, Elham, Tafakhori, Abbas, Esmkhani, Sahra, Gibbs, Richard A., Noureldeen, Mahmoud M., Zaki, Maha S., Marafi, Dana, Darvish, Hossein, Kruer, Michael C., Lupski, James R.

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Through her eyes von Schnur, Julie B, Goldsmith, Rachel E

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Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder von Küry, Sébastien, Ebstein, Frédéric, Mollé, Alice, Besnard, Thomas, Lee, Ming-Kang, Vignard, Virginie, Hery, Tiphaine, Nizon, Mathilde, Mancini, Grazia M.S., Giltay, Jacques C., Cogné, Benjamin, McWalter, Kirsty, Deb, Wallid, Mor-Shaked, Hagar, Li, Hong, Schnur, Rhonda E., Wentzensen, Ingrid M., Denommé-Pichon, Anne-Sophie, Fourgeux, Cynthia, Verheijen, Frans W., Faurie, Eva, Schot, Rachel, Stevens, Cathy A., Smits, Daphne J., Barr, Eileen, Sheffer, Ruth, Bernstein, Jonathan A., Stimach, Chandler L., Kovitch, Eliana, Shashi, Vandana, Schoch, Kelly, Smith, Whitney, van Jaarsveld, Richard H., Hurst, Anna C.E., Smith, Kirstin, Baugh, Evan H., Bohm, Suzanne G., Vyhnálková, Emílie, Ryba, Lukáš, Delnatte, Capucine, Neira, Juanita, Bonneau, Dominique, Toutain, Annick, Rosenfeld, Jill A., Audebert-Bellanger, Séverine, Gilbert-Dussardier, Brigitte, Odent, Sylvie, Laumonnier, Frédéric, Berger, Seth I., Smith, Ann C.M., Bourdeaut, Franck, Stern, Marc-Henri, Redon, Richard, Krüger, Elke, Margueron, Raphaël, Bézieau, Stéphane, Poschmann, Jeremie, Isidor, Bertrand

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CDK19-related disorder results from both loss-of-function and gain-of-function de novo missense variants von Zarate, Yuri A., Uehara, Tomoko, Abe, Kota, Oginuma, Masayuki, Harako, Sora, Ishitani, Shizuka, Lehesjoki, Anna-Elina, Bierhals, Tatjana, Kloth, Katja, Ehmke, Nadja, Horn, Denise, Holtgrewe, Manuel, Anderson, Katherine, Viskochil, David, Edgar-Zarate, Courtney L., Sacoto, Maria J. Guillen, Schnur, Rhonda E., Morrow, Michelle M., Sanchez-Valle, Amarilis, Pappas, John, Rabin, Rachel, Muona, Mikko, Anttonen, Anna-Kaisa, Platzer, Konrad, Luppe, Johannes, Gburek-Augustat, Janina, Kaname, Tadashi, Okamoto, Nobuhiko, Mizuno, Seiji, Kaido, Yusaku, Ohkuma, Yoshiaki, Hirose, Yutaka, Ishitani, Tohru, Kosaki, Kenjiro

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Cancer Victim Identity for Individuals with Histories of Cancer and Childhood Sexual Abuse von McDonnell, Glynnis A., Sucala, Madalina, Goldsmith, Rachel E., Montgomery, Guy H., Schnur, Julie B.

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Development of the Healthcare Triggering Questionnaire in Adult Sexual Abuse Survivors von Schnur, Julie B, Chaplin, William F, Khurshid, Kiran, Mogavero, Jazmin N, Goldsmith, Rachel E, Lee, Young-Sun, Litman, Leib, Montgomery, Guy H

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De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy von Singh, Sakshi, Gupta, Aditi, Zech, Michael, Sigafoos, Ashley N, Clark, Karl J, Dincer, Yasemin, Wagner, Matias, Humberson, Jennifer B, Green, Sarah, van Gassen, Koen, Brandt, Tracy, Schnur, Rhonda E, Millan, Francisca, Si, Yue, Mall, Volker, Winkelmann, Juliane, Gavrilova, Ralitza H, Klee, Eric W, Engleman, Kendra, Safina, Nicole P, Slaugh, Rachel, Bryant, Emily M, Tan, Wen-Hann, Granadillo, Jorge, Misra, Sunita N, Schaefer, G Bradley, Towner, Shelley, Brilstra, Eva H, Koeleman, Bobby P C

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Economically Disadvantaged Students in a School for the Academically Gifted: A Postpositivist Inquiry into Individual and Family Adjustment von Borland, James H., Schnur, Rachel, Wright, Lisa

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Optimizing Patient Throughput: PACU to Inpatient Unit Transfer Process von Schnur, Maureen, Micalizzi, Rosella, Banks, Cathy, Connolly, Kelly, Hogan, Kristin, Castricone, Rachel, Chase, Lynnette Delano, Dennen, Kristen, Healy, Shauna, Higgins, Marcia, Mudarri, Shelby, Pignataro, Shelly, Rivello, Sharon, Romaniak, Maura, Rossetti, Jill, Sawyer, Mary

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De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy von Singh, Sakshi, Gupta, Aditi, Zech, Michael, Sigafoos, Ashley N, Clark, Karl J, Dincer, Yasemin, Wagner, Matias, Humberson, Jennifer B, Green, Sarah, van Gassen, Koen, Brandt, Tracy, Schnur, Rhonda E, Millan, Francisca, Si, Yue, Mall, Volker, Winkelmann, Juliane, Gavrilova, Ralitza H, Klee, Eric W, Engleman, Kendra, Safina, Nicole P, Slaugh, Rachel, Bryant, Emily M, Tan, Wen-Hann, Granadillo, Jorge, Misra, Sunita N, Schaefer, G. Bradley, Towner, Shelley, Brilstra, Eva H, Koeleman, Bobby P. C

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