Parent Opinion of Sexuality Education in a State with Mandated Abstinence Education: Does Policy Match Parental Preference? von Ito, Kristin E., Gizlice, Ziya, Owen-O’Dowd, Judy, Foust, Evelyn, Leone, Peter A., Miller, William C.

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To friend or not to friend: using new media for adolescent health promotion von Ito, Kristin E, Brown, Jane D

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10: Factors Affecting Avatar Use in a STI Prevention CD-ROM von Ito, Kristin E., MD, MPH, Kalyanaraman, Sri, PhD, Brown, Jane D., PhD, Miller, William C., MD, MPH, PhD

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Examining the social ecology of a bar-crawl: An exploratory pilot study von Clapp, John D, Madden, Danielle R, Mooney, Douglas D, Dahlquist, Kristin E

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Kinetic and Structural Basis for Acyl-Group Selectivity and NAD+ Dependence in Sirtuin-Catalyzed Deacylation von Feldman, Jessica L, Dittenhafer-Reed, Kristin E, Kudo, Norio, Thelen, Julie N, Ito, Akihiro, Yoshida, Minoru, Denu, John M

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Cell types and neuronal circuitry underlying female aggression in Drosophila von Schretter, Catherine E, Aso, Yoshinori, Robie, Alice A, Dreher, Marisa, Dolan, Michael-John, Chen, Nan, Ito, Masayoshi, Yang, Tansy, Parekh, Ruchi, Branson, Kristin M, Rubin, Gerald M

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ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies von Lemire, Gabrielle, Ito, Yoko A., Marshall, Aren E., Chrestian, Nicolas, Stanley, Valentina, Brady, Lauren, Tarnopolsky, Mark, Curry, Cynthia J., Hartley, Taila, Mears, Wendy, Derksen, Alexa, Rioux, Nadie, Laflamme, Nataly, Hutchison, Harrol T., Pais, Lynn S., Zaki, Maha S., Sultan, Tipu, Dane, Adrie D., Gleeson, Joseph G., Vaz, Frédéric M., Kernohan, Kristin D., Bernard, Geneviève, Boycott, Kym M.

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Effect of Occupational Therapy-Led Playgroups in Early Intervention on Child Playfulness and Caregiver Responsiveness: A Repeated-Measures Design von Fabrizi, Sarah E, Ito, Max A, Winston, Kristin

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Belantamab Mafodotin, Pomalidomide, and Dexamethasone in Multiple Myeloma von Dimopoulos, Meletios Athanasios, Beksac, Meral, Pour, Ludek, Delimpasi, Sosana, Vorobyev, Vladimir, Quach, Hang, Spicka, Ivan, Radocha, Jakub, Robak, Pawel, Kim, Kihyun, Cavo, Michele, Suzuki, Kazuhito, Morris, Kristin, Pompilus, Farrah, Phillips-Jones, Amy, Zhou, Xiaoou L., Fulci, Giulia, Sule, Neal, Kremer, Brandon E., Opalinska, Joanna, Mateos, María-Victoria, Trudel, Suzanne

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Biallelic variants in the ectonucleotidase ENTPD1 cause a complex neurodevelopmental disorder with intellectual disability, hypomyelination, and spastic paraplegia von Calame, Daniel G., Herman, Isabella, Marshall, Aren E., Maroofian, Reza, Donis, Karina Carvalho, Fatih, Jawid M., Mitani, Tadahiro, Du, Haowei, Grochowski, Christopher M., Sousa, Sergio, Bakhtiari, Somayeh, Ito, Yoko A., Rocca, Clarissa, Hunter, Jill V., Sutton, V. Reid, Emrick, Lisa T., Boycott, Kym M., Lossos, Alexander, Fellig, Yakov, Prus, Eugenia, Kalish, Yosef, Meiner, Vardiella, Suerink, Manon, Ruivenkamp, Claudia, Muirhead, Kayla, Saadi, Nebal W., Zaki, Maha S., Skidmore, David L., Osmond, Matthew, Silva, Thiago Oliveira, Houlden, Henry, Murphy, David, Ghayoorarimiani, Ehsan, Jamshidi, Yalda, Jaddoa, Asaad Ghanim, Tajsharghi, Homa, Jin, Sheng Chih, Coban-Akdemir, Zeynep, Travaglini, Lorena, Nicita, Francesco, Jhangiani, Shalini N., Gibbs, Richard A., Posey, Jennifer E., Kruer, Michael C., Kernohan, Kristin D., Morales Saute, Jonas A., Vanderver, Adeline, Pehlivan, Davut, Marafi, Dana, Lupski, James R.

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Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes von Scala, Marcello, Nishikawa, Masashi, Ito, Hidenori, Tabata, Hidenori, Khan, Tayyaba, Accogli, Andrea, Davids, Laura, Ruiz, Anna, Chiurazzi, Pietro, Cericola, Gabriella, Schulte, Björn, Monaghan, Kristin G, Begtrup, Amber, Torella, Annalaura, Pinelli, Michele, Denommé-Pichon, Anne Sophie, Vitobello, Antonio, Racine, Caroline, Mancardi, Maria Margherita, Kiss, Courtney, Guerin, Andrea, Wu, Wendy, Gabau Vila, Elisabeth, Mak, Bryan C, Martinez-Agosto, Julian A, Gorin, Michael B, Duz, Bugrahan, Bayram, Yavuz, Carvalho, Claudia M B, Vengoechea, Jaime E, Chitayat, David, Tan, Tiong Yang, Callewaert, Bert, Kruse, Bernd, Bird, Lynne M, Faivre, Laurence, Zollino, Marcella, Biskup, Saskia, Striano, Pasquale, Nigro, Vincenzo, Severino, Mariasavina, Capra, Valeria, Costain, Gregory, Nagata, Koh ichi, Undiagnosed Diseases Network, [missing], Telethon Undiagnosed Diseases Program, [missing]

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PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementation von Chelban, Viorica, Wilson, Matthew P, Chardon, Jodi Warman, Vandrovcova, Jana, Zanetti, M. Natalia, Zamba-Papanicolaou, Eleni, Efthymiou, Stephanie, Pope, Simon, Conte, Maria R, Abis, Giancarlo, Liu, Yo-Tsen, Tribollet, Eloise, Haridy, Nourelhoda A, Botía, Juan A, Ryten, Mina, Nicolaou, Paschalis, Minaidou, Anna, Christodoulou, Kyproula, Kernohan, Kristin D, Eaton, Alison, Osmond, Matthew, Ito, Yoko, Bourque, Pierre, Jepson, James E.C, Bello, Oscar, Bremner, Fion, Cordivari, Carla, Reilly, Mary M, Foiani, Martha, Heslegrave, Amanda, Zetterberg, Henrik, Heales, Simon J.R, Wood, Nicholas W, Rothman, James E, Boycott, Kym M, Mills, Philippa B, Clayton, Peter T, Houlden, Henry, Care4Rare Canada Consortium, the SYNaPS Study Group

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PDXK mutations cause polyneuropathy responsive to pyridoxal 5 '-phosphate supplementation von Chelban, Viorica, Wilson, Matthew P, Chardon, Jodi Warman, Vandrovcova, Jana, Zanetti, M. Natalia, Zamba-Papanicolaou, Eleni, Efthymiou, Stephanie, Pope, Simon, Conte, Maria R, Abis, Giancarlo, Liu, Yo-Tsen, Tribollet, Eloise, Haridy, Nourelhoda A, Botia, Juan A, Ryten, Mina, Nicolaou, Paschalis, Minaidou, Anna, Christodoulou, Kyproula, Kernohan, Kristin D, Eaton, Alison, Osmond, Matthew, Ito, Yoko, Bourque, Pierre, Jepson, James E.C, Bello, Oscar, Bremner, Fion, Cordivari, Carla, Reilly, Mary M, Foiani, Martha, Heslegrave, Amanda, Zetterberg, Henrik, Heales, Simon J.R, Wood, Nicholas W, Rothman, James E, Boycott, Kym M, Mills, Philippa B, Clayton, Peter T, Houlden, Henry

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Seizures in Extremely Low Birth Weight Infants Are Associated with Adverse Outcome von Davis, Alexis S., MD, Hintz, Susan R., MD, MS (Epi), Van Meurs, Krisa P., MD, Li, Lei, PhD, Das, Abhik, PhD, Stoll, Barbara J., MD, Walsh, Michele C., MD, MS, Pappas, Athina, MD, Bell, Edward F., MD, Laptook, Abbot R., MD, Higgins, Rosemary D., MD

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An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression von Wyszynski, Asaf, Hong, Chi-Chen, Lam, Kristin, Michailidou, Kyriaki, Lytle, Christian, Yao, Song, Zhang, Yali, Bolla, Manjeet K, Wang, Qin, Dennis, Joe, Hopper, John L, Southey, Melissa C, Schmidt, Marjanka K, Broeks, Annegien, Muir, Kenneth, Lophatananon, Artitaya, Fasching, Peter A, Beckmann, Matthias W, Peto, Julian, Dos-Santos-Silva, Isabel, Sawyer, Elinor J, Tomlinson, Ian, Burwinkel, Barbara, Marme, Frederik, Guénel, Pascal, Truong, Thérèse, Bojesen, Stig E, Nordestgaard, Børge G, González-Neira, Anna, Benitez, Javier, Neuhausen, Susan L, Brenner, Hermann, Dieffenbach, Aida Karina, Meindl, Alfons, Schmutzler, Rita K, Brauch, Hiltrud, Nevanlinna, Heli, Khan, Sofia, Matsuo, Keitaro, Ito, Hidemi, Dörk, Thilo, Bogdanova, Natalia V, Lindblom, Annika, Margolin, Sara, Mannermaa, Arto, Kosma, Veli-Matti, Wu, Anna H, Van Den Berg, David, Lambrechts, Diether, Wildiers, Hans, Chang-Claude, Jenny, Rudolph, Anja, Radice, Paolo, Peterlongo, Paolo, Couch, Fergus J, Olson, Janet E, Giles, Graham G, Milne, Roger L, Haiman, Christopher A, Henderson, Brian E, Dumont, Martine, Teo, Soo Hwang, Wong, Tien Y, Kristensen, Vessela, Zheng, Wei, Long, Jirong, Winqvist, Robert, Pylkäs, Katri, Andrulis, Irene L, Knight, Julia A, Devilee, Peter, Seynaeve, Caroline, García-Closas, Montserrat, Figueroa, Jonine, Klevebring, Daniel, Czene, Kamila, Hooning, Maartje J, van den Ouweland, Ans M.W, Darabi, Hatef, Shu, Xiao-Ou, Gao, Yu-Tang, Cox, Angela, Blot, William, Signorello, Lisa B, Shah, Mitul, Kang, Daehee, Choi, Ji-Yeob, Hartman, Mikael, Miao, Hui, Hamann, Ute, Jakubowska, Anna, Lubinski, Jan, Sangrajrang, Suleeporn, McKay, James, Toland, Amanda E, Yannoukakos, Drakoulis, Shen, Chen-Yang, Wu, Pei-Ei, Swerdlow, Anthony, Orr, Nick

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Biallelic Variants in the Ectonucleotidase ENTPD1 Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic Paraple... von Calame, Daniel G, Herman, Isabella, Maroofian, Reza, Marshall, Aren E, Donis, Karina Carvalho, Fatih, Jawid M, Mitani, Tadahiro, Du, Haowei, Grochowski, Christopher M, Sousa, Sergio B, Gijavanekar, Charul, Bakhtiari, Somayeh, Ito, Yoko A, Rocca, Clarissa, Hunter, Jill, Sutton, V Reid, Emrick, Lisa T, Boycott, Kym M, Lossos, Alexander, Fellig, Yakov, Prus, Eugenia, Kalish, Yosef, Meiner, Vardiella, Suerink, Manon, Ruivenkamp, Claudia, Muirhead, Kayla, Saadi, Nebal W, Zaki, Maha S, Bouman, Arjan, Barakat, Tahsin Stefan, Skidmore, David L, Osmond, Matthew, Silva, Thiago Oliveira, Murphy, David, Karimiani, Ehsan Ghayoor, Jamshidi, Yalda, Jaddoa, Asaad Ghanim, Tajsharghi, Homa, Jin, Sheng Chih, Abbaszadegan, Mohammad Reza, Ebrahimzadeh-Vesal, Reza, Hosseini, Susan, Alavi, Shahryar, Bahreini, Amir, Zarean, Elahe, Salehi, Mohammad Mehdi, Al-Sannaa, Nouriya Abbas, Zifarelli, Giovanni, Bauer, Peter, Robson, Simon C, Coban-Akdemir, Zeynep, Travaglini, Lorena, Nicita, Francesco, Jhangiani, Shalini N, Gibbs, Richard A, Posey, Jennifer E, Kruer, Michael C, Kernohan, Kristin D, Morales Saute, Jonas A, Houlden, Henry, Vanderver, Adeline, Elsea, Sarah H, Pehlivan, Davut, Marafi, Dana, Lupski, James R

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Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes von Scala, Marcello, Nishikawa, Masashi, Ito, Hidenori, Tabata, Hidenori, Khan, Tayyaba, Accogli, Andrea, Davids, Laura, Ruiz, Anna, Chiurazzi, Pietro, Cericola, Gabriella, Schulte, Björn, Monaghan, Kristin G, Begtrup, Amber, Torella, Annalaura, Pinelli, Michele, Denommé-Pichon, Anne Sophie, Vitobello, Antonio, Racine, Caroline, Mancardi, Maria Margherita, Kiss, Courtney, Guerin, Andrea, Wu, Wendy, Gabau, Elisabeth, Mak, Bryan C, Martinez-Agosto, Julian A, Gorin, Michael B, Duz, Bugrahan, Bayram, Yavuz, Carvalho, Claudia M B, Vengoechea, Jaime E, Chitayat, David, Tan, Tiong Yang, Callewaert, Bert, Kruse, Bernd, Bird, Lynne M, Faivre, Laurence, Zollino, Marcella, Biskup, Saskia, Striano, Pasquale, Nigro, Vincenzo, Severino, Mariasavina, Capra, Valeria, Costain, Gregory, Nagata, Koh ichi, Universitat Autònoma de Barcelona

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Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes von Scala, Marcello, Nishikawa, Masashi, Ito, Hidenori, Tabata, Hidenori, Khan, Tayyaba, Accogli, Andrea, Davids, Laura, Ruiz, Anna, Chiurazzi, Pietro, Cericola, Gabriella, Schulte, Björn, Monaghan, Kristin G, Begtrup, Amber, Torella, Annalaura, Pinelli, Michele, Denommé-Pichon, Anne Sophie, Vitobello, Antonio, Racine, Caroline, Mancardi, Maria Margherita, Kiss, Courtney, Guerin, Andrea, Wu, Wendy, Gabau, Elisabeth, Mak, Bryan C, Martinez-Agosto, Julian A, Gorin, Michael B, Duz, Bugrahan, Bayram, Yavuz, Carvalho, Claudia M B, Vengoechea, Jaime E, Chitayat, David, Tan, Tiong Yang, Callewaert, Bert, Kruse, Bernd, Bird, Lynne M, Faivre, Laurence, Zollino, Marcella, Biskup, Saskia, Striano, Pasquale, Nigro, Vincenzo, Severino, Mariasavina, Capra, Valeria, Costain, Gregory, Nagata, Koh-ichi, Universitat Autònoma de Barcelona

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Coverings of Open Books von Ito, Tetsuya, Kawamuro, Keiko

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An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression von Wyszynski, Asaf, Hong, Chi-Chen, Lam, Kristin, Michailidou, Kyriaki, Lytle, Christian, Yao, Song, Wang, Qin, Dennis, Joe, Hopper, John L, Southey, Melissa C, Schmidt, Marjanka K, Broeks, Annegien, Muir, Kenneth, Lophatananon, Artitaya, Fasching, Peter A, Beckmann, Matthias W, Peto, Julian, Dos-Santos-Silva, Isabel, Sawyer, Elinor J, Tomlinson, Ian, Burwinkel, Barbara, Marme, Frederik, Guénel, Pascal, Bojesen, Stig E, Nordestgaard, Børge G, González-Neira, Anna, Benitez, Javier, Neuhausen, Susan L, Brenner, Hermann, Dieffenbach, Aida Karina, Meindl, Alfons, Schmutzler, Rita K, Brauch, Hiltrud, GENICA Network, Nevanlinna, Heli, Khan, Sofia, Matsuo, Keitaro, Ito, Hidemi, Dörk, Thilo, Bogdanova, Natalia V, Lindblom, Annika, Margolin, Sara, Mannermaa, Arto, Australian Ovarian Cancer Study Group, Wu, Anna H, Van Den Berg, David, Lambrechts, Diether, Wildiers, Hans, Rudolph, Anja, Radice, Paolo, Peterlongo, Paolo, Couch, Fergus J, Olson, Janet E, Giles, Graham G, Milne, Roger L, Haiman, Christopher A, Henderson, Brian E, Dumont, Martine, Teo, Soo Hwang, Wong, Tien Y, Kristensen, Vessela, Zheng, Wei, Long, Jirong, Winqvist, Robert, Pylkäs, Katri, Andrulis, Irene L, Knight, Julia A, Devilee, Peter, Seynaeve, Caroline, García-Closas, Montserrat, Klevebring, Daniel, Czene, Kamila, Hooning, Maartje J, van den Ouweland, Ans MW, Shu, Xiao-Ou, Gao, Yu-Tang, Cox, Angela, Signorello, Lisa B, Shah, Mitul, Choi, Ji-Yeob, Hartman, Mikael, Miao, Hui, Jakubowska, Anna, Lubinski, Jan, Sangrajrang, Suleeporn, McKay, James, Toland, Amanda E, Yannoukakos, Drakoulis, Wu, Pei-Ei, Swerdlow, Anthony, Orr, Nick, Simard, Jacques, Pharoah, Paul DP, Dunning, Alison M, Chenevix-Trench, Georgia, Hall, Per, Bandera, Elisa, Amos, Chris, Ambrosone, Christine, Easton, Douglas F

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