Display screen or portion thereof with a graphical user interface von Kingery, Brian, Landefeld, Adam, Moss, Blaine, Willis, Chris

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Heparin-binding epidermal growth factor-like growth factor eliminates constraints on activated Kras to promote rapid onset of pancreatic neoplasia von Ray, K C, Moss, M E, Franklin, J L, Weaver, C J, Higginbotham, J, Song, Y, Revetta, F L, Blaine, S A, Bridges, L R, Guess, K E, Coffey, R J, Crawford, H C, Washington, M K, Means, A L

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What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia von Campbell, Ian M., Sheppard, Sarah E., Crowley, T. Blaine, McGinn, Daniel E., Bailey, Alice, McGinn, Michael J., Unolt, Marta, Homans, Jelle F., Chen, Erin Y., Salmons, Harold I., Gaynor, J. William, Goldmuntz, Elizabeth, Jackson, Oksana A., Katz, Lorraine E., Mascarenhas, Maria R., Deeney, Vincent F. X., Castelein, René M., Zur, Karen B., Elden, Lisa, Kallish, Staci, Kolon, Thomas F., Hopkins, Sarah E., Chadehumbe, Madeline A., Lambert, Michele P., Forbes, Brian J., Moldenhauer, Julie S., Schindewolf, Erica M., Solot, Cynthia B., Moss, Edward M., Gur, Raquel E., Sullivan, Kathleen E., Emanuel, Beverly S., Zackai, Elaine H., McDonald‐McGinn, Donna M.

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Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion von Engchuan, Worrawat, Hestand, Matthew S., Heung, Tracy, Johnston, H. Richard, Monfeuga, Thomas, McDonald-McGinn, Donna M., Gur, Raquel E., Morrow, Bernice E., Swillen, Ann, Vorstman, Jacob A. S., Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Warren, Stephen T., Chopra, Pankaj, Cutler, David J., Duncan, Richard, Mulle, Jennifer G., Voss, Anna J., Zwick, Michael E., Diacou, Alexander, Guo, Tingwei, Lin, Jhih-Rong, Wang, Tao, Zhang, Zhengdong, Zhao, Yingjie, Marshall, Christian, Jin, Andrea, Lilley, Brenna, Salmons, Harold I., Tran, Oanh, Pardinas, Antonio, Walters, James T. R., Demaerel, Wolfram, Boot, Erik, Butcher, Nancy J., Lowther, Chelsea, Evers, Rens, van Amelsvoort, Therese A. M. J., van Duin, Esther, Vingerhoets, Claudia, Breckpot, Jeroen, Devriendt, Koen, Vogels, Annick, Moss, Edward M., Sharkus, Robert J., Zackai, Elaine H., Calkins, Monica E., Gallagher, Robert S., Gur, Ruben C., Tang, Sunny X., Fritsch, Rosemarie, Ornstein, Claudia, Repetto, Gabriela M., Breetvelt, Elemi, Duijff, Sasja N., Fiksinski, Ania, Niarchou, Maria, Murphy, Kieran C., Prasad, Sarah E., Daly, Eileen M., Gudbrandsen, Maria, Murphy, Declan G., Buzzanca, Antonio, Digilio, Maria C., Pontillo, Maria, Marino, Bruno, Vicari, Stefano, Coleman, Karlene, Cubells, Joseph F., Ousley, Opal Y., Carmel, Miri, Mekori-Domachevsky, Ehud, Michaelovsky, Elena, Weinberger, Ronnie, Weizman, Abraham, Jalbrzikowski, Maria, Armando, Marco, Eliez, Stéphan, Sandini, Corrado, Béna, Frédérique Sloan, Antshel, Kevin M., Fremont, Wanda, Kates, Wendy R., Belzeaux, Raoul, Philip, Nicole, Campbell, Linda E., McCabe, Kathryn L., Hooper, Stephen R., Schoch, Kelly, Shashi, Vandana, Simon, Tony J., Tassone, Flora, Arango, Celso, García-Miñaúr, Sixto, Suñer, Damià H., Raventos-Simic, Jasna, Epstein, Michael P., Williams, Nigel M., Bassett, Anne S.

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Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome von Boot, Erik, Óskarsdóttir, Sólveig, Loo, Joanne C.Y., Crowley, Terrence Blaine, Orchanian-Cheff, Ani, Andrade, Danielle M., Arganbright, Jill M., Castelein, René M., Cserti-Gazdewich, Christine, de Reuver, Steven, Fiksinski, Ania M., Klingberg, Gunilla, Lang, Anthony E., Mascarenhas, Maria R., Moss, Edward M., Nowakowska, Beata Anna, Oechslin, Erwin, Palmer, Lisa, Repetto, Gabriela M., Reyes, Nikolai Gil D., Schneider, Maude, Silversides, Candice, Sullivan, Kathleen E., Swillen, Ann, van Amelsvoort, Therese A.M.J., Van Batavia, Jason P., Vingerhoets, Claudia, McDonald-McGinn, Donna M., Bassett, Anne S.

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Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness von Ching, Christopher R.K, Gutman, Boris A, Sun, Daqiang, Villalon Reina, Julio, Ragothaman, Anjanibhargavi, Isaev, Dmitry, Zavaliangos-Petropulu, Artemis, Lin, Amy, Jonas, Rachel K, Kushan, Leila, Pacheco-Hansen, Laura, Vajdi, Ariana, Forsyth, Jennifer K, Jalbrzikowski, Maria, Bakker, Geor, van Amelsvoort, Therese, Antshel, Kevin M, Fremont, Wanda, Kates, Wendy R, Campbell, Linda E, McCabe, Kathryn L, Craig, Michael C, Daly, Eileen, Gudbrandsen, Maria, Murphy, Clodagh M, Murphy, Declan G, Murphy, Kieran C, Fiksinski, Ania, Koops, Sanne, Vorstman, Jacob, Crowley, T. Blaine, Emanuel, Beverly S, Gur, Raquel E, McDonald-McGinn, Donna M, Roalf, David R, Ruparel, Kosha, Schmitt, J. Eric, Zackai, Elaine H, Durdle, Courtney A, Goodrich-Hunsaker, Naomi J, Simon, Tony J, Bassett, Anne S, Butcher, Nancy J, Chow, Eva W.C, Vila-Rodriguez, Fidel, Cunningham, Adam, Doherty, Joanne, Linden, David E, Moss, Hayley, Owen, Michael J, van den Bree, Marianne, Crossley, Nicolas A, Repetto, Gabriela M, Thompson, Paul M, Bearden, Carrie E

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Rapidly Enlarging Palatal Masses as a Novel Presentation of Scurvy von Xu, Summer, Stark, Courtney, Lapin, William Blaine, Hughes, Amy L, Balarezo, Fabiola, Moss, Kerry, Bezler, Natalie S, Cantor, Evan

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Early language measures associated with later psychosis features in 22q11.2 deletion syndrome von Solot, Cynthia B., Moore, Tyler M., Crowley, Terrence Blaine, Gerdes, Marsha, Moss, Edward, McGinn, Daniel E., Emanuel, Beverly S., Zackai, Elaine H., Gallagher, Sean, Calkins, Monica E., Ruparel, Kosha, Gur, Ruben C., McDonald‐McGinn, Donna M., Gur, Raquel E.

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Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs von Meer, Dennis, Agartz, Ingrid, Arango, Celso, Ayesa‐Arriola, Rosa, Bakker, Geor, Boomsma, Dorret I., Bülow, Robin, Butcher, Nancy J., Caspers, Svenja, Crespo‐Facorro, Benedicto, Dale, Anders M., Dazzan, Paola, Zubicaray, Greig I., Donohoe, Gary, Espeseth, Thomas, Fisher, Simon E., Ge, Tian, Glahn, David C., Grabe, Hans J., Gur, Raquel E., Håberg, Asta K., Hashimoto, Ryota, Hibar, Derrek P., Holmes, Avram J., Hulshoff Pol, Hilleke E., Kushan, Leila, Liu, Jingyu, Martin‐Brevet, Sandra, Martínez, Kenia, Mather, Karen A., Mathias, Samuel R., Medland, Sarah E., Modenato, Claudia, Mühleisen, Thomas W., Prieto, Carlos, Ragothaman, Anjanibhargavi, Reinbold, Céline S., Reis Marques, Tiago, Repetto, Gabriela M., Reymond, Alexandre, Sachdev, Perminder S., Schmitt, James E., Schofield, Peter R., Silva, Ana I., Stefansson, Hreinn, Stein, Dan J., Tamnes, Christian K., Ulfarsson, Magnus O., Vajdi, Ariana, Ent, Dennis, Bree, Marianne B. M., Vassos, Evangelos, Vázquez‐Bourgon, Javier, Vila‐Rodriguez, Fidel, Walters, G. Bragi, Wen, Wei, Zackai, Elaine H., Thompson, Paul M., Bearden, Carrie E., Blackburn, Nicholas B., Bøen, Rune, Zwarte, Sonja M. C., Forti, Marta Di, Frei, Oleksandr, Fukunaga, Masaki, Hehir‐Kwa, Jayne Y., Hoffmann, Per, Homuth, Georg, Jahanshad, Neda, Koops, Sanne, Kumar, Kuldeep, Kikuchi, Masataka, Le Hellard, Stephanie, Leu, Costin, Murray, Robin M, Nyberg, Lars, Shumskaya, Elena, Sisodiya, Sanjay M., Steen, Vidar M., Teumer, Alexander, Uhlmann, Anne, Wright, Margaret J., Campbell, Linda E., Crossley, Nicolas A., Crowley, T. Blaine, Daly, Eileen, Fiksinski, Ania M., Fremont, Wanda, Goodrich‐Hunsaker, Naomi J., Gudbrandsen, Maria, Jonas, Rachel K., Kates, Wendy R., Lin, Amy, Moss, Hayley, Murphy, Declan G., Murphy, Kieran C., Owen, Michael J., Simon, Tony. J., Amelsvoort, Therese, Vorstman, Jacob A. S.

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Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome von Óskarsdóttir, Sólveig, Boot, Erik, Crowley, Terrence Blaine, Loo, Joanne C.Y., Arganbright, Jill M., Armando, Marco, Baylis, Adriane L., Breetvelt, Elemi J., Castelein, René M., Chadehumbe, Madeline, Cielo, Christopher M., de Reuver, Steven, Eliez, Stephan, Fiksinski, Ania M., Forbes, Brian J., Gallagher, Emily, Hopkins, Sarah E., Jackson, Oksana A., Levitz-Katz, Lorraine, Klingberg, Gunilla, Lambert, Michele P., Marino, Bruno, Mascarenhas, Maria R., Moldenhauer, Julie, Moss, Edward M., Nowakowska, Beata Anna, Orchanian-Cheff, Ani, Putotto, Carolina, Repetto, Gabriela M., Schindewolf, Erica, Schneider, Maude, Solot, Cynthia B., Sullivan, Kathleen E., Swillen, Ann, Unolt, Marta, Van Batavia, Jason P., Vingerhoets, Claudia, Vorstman, Jacob, Bassett, Anne S., McDonald-McGinn, Donna M.

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Relationship between intelligence quotient measures and computerized neurocognitive performance in 22q11.2 deletion syndrome von Gur, Ruben C., Moore, Tyler M., Weinberger, Ronnie, Mekori‐Domachevsky, Ehud, Gross, Raz, Emanuel, Beverly S., Zackai, Elaine H., Moss, Edward, Gallagher, Robert Sean, McGinn, Daniel E., Crowley, Terrence Blaine, McDonald‐McGinn, Donna, Gothelf, Doron, Gur, Raquel E.

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Prioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics von Forsyth, Jennifer K, Mennigen, Eva, Lin, Amy, Sun, Daqiang, Vajdi, Ariana, Kushan-Wells, Leila, Ching, Christopher R K, Villalon-Reina, Julio E, Thompson, Paul M, Bearden, Carrie E

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Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome von McGinn, Daniel E, Crowley, T Blaine, Heung, Tracy, Tran, Oanh, Moss, Edward, Zackai, Elaine H, Emanuel, Beverly S, Chow, Eva W C, Morrow, Bernice E, Swillen, Ann, Bassett, Anne S, McDonald-McGinn, Donna M

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The impact of hypocalcemia on full scale IQ in patients with 22q11.2 deletion syndrome von Grand, Katheryn, Levitt Katz, Lorraine E., Crowley, T. Blaine, Moss, Edward, Lessig, Megan, Bamba, Vaneeta, Lord, Katherine, Zackai, Elaine H., Emanuel, Beverly S., Valverde, Kathleen, McDonald‐McGinn, Donna M.

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Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome von Boot, Erik, Óskarsdóttir, Sólveig, Loo, Joanne C.Y, Crowley, Terrence Blaine, Orchanian-Cheff, Ani, Andrade, Danielle M, Arganbright, Jill M, Castelein, René M, Cserti-Gazdewich, Christine, de Reuver, Steven, Fiksinski, Ania M, Klingberg, Gunilla, Lang, Anthony E, Mascarenhas, Maria R, Moss, Edward M, Nowakowska, Beata Anna, Oechslin, Erwin, Palmer, Lisa, Repetto, Gabriela M, Reyes, Nikolai Gil D, Schneider, Maude, Silversides, Candice, Sullivan, Kathleen E, Swillen, Ann, van Amelsvoort, Therese A.M.J, Van Batavia, Jason P, Vingerhoets, Claudia, McDonald-McGinn, Donna M, Bassett, Anne S

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Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome von Boot, Erik, Oskarsdottir, Solveig, Loo, Joanne C.Y, Crowley, Terrence Blaine, Orchanian-Cheff, Ani, Andrade, Danielle M, Arganbright, Jill M, Castelein, Rene M, Cserti-Gazdewich, Christine, de Reuver, Steven, Fiksinski, Ania M, Klingberg, Gunilla, Lang, Anthony E, Mascarenhas, Maria R, Moss, Edward M, Nowakowska, Beata Anna, Oechslin, Erwin, Palmer, Lisa, Repetto, Gabriela M, Reyes, Nikolai Gil D, Schneider, Maude, Silversides, Candice, Sullivan, Kathleen E, Swillen, Ann, van Amelsvoort, Therese A.M.J, Van Batavia, Jason P, Vingerhoets, Claudia, McDonald-McGinn, Donna M, Bassett, Anne S

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Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome von Oskarsdottir, Solveig, Boot, Erik, Crowley, Terrence Blaine, Loo, Joanne C.Y, Arganbright, Jill M, Armando, Marco, Baylis, Adriane L, Breetvelt, Elemi J, Castelein, Rene M, Chadehumbe, Madeline, Cielo, Christopher M, de Reuver, Steven, Eliez, Stephan, Fiksinski, Ania M, Forbes, Brian J, Gallagher, Emily, Hopkins, Sarah E, Jackson, Oksana A, Levitz-Katz, Lorraine, Klingberg, Gunilla, Lambert, Michele P, Marino, Bruno, Mascarenhas, Maria R, Moldenhauer, Julie, Moss, Edward M, Nowakowska, Beata Anna, Orchanian-Cheff, Ani, Putotto, Carolina, Repetto, Gabriela M, Schindewolf, Erica, Schneider, Maude, Solot, Cynthia B, Sullivan, Kathleen E, Swillen, Ann, Unolt, Marta, Van Batavia, Jason P, Vingerhoets, Claudia, Vorstman, Jacob, Bassett, Anne S, McDonald-McGinn, Donna M

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Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome von Óskarsdóttir, Sólveig, Boot, Erik, Crowley, Terrence Blaine, Loo, Joanne C.Y, Arganbright, Jill M, Armando, Marco, Baylis, Adriane L, Breetvelt, Elemi J, Castelein, René M, Chadehumbe, Madeline, Cielo, Christopher M, de Reuver, Steven, Eliez, Stephan, Fiksinski, Ania M, Forbes, Brian J, Gallagher, Emily, Hopkins, Sarah E, Jackson, Oksana A, Levitz-Katz, Lorraine, Klingberg, Gunilla, Lambert, Michele P, Marino, Bruno, Mascarenhas, Maria R, Moldenhauer, Julie, Moss, Edward M, Nowakowska, Beata Anna, Orchanian-Cheff, Ani, Putotto, Carolina, Repetto, Gabriela M, Schindewolf, Erica, Schneider, Maude, Solot, Cynthia B, Sullivan, Kathleen E, Swillen, Ann, Unolt, Marta, Van Batavia, Jason P, Vingerhoets, Claudia, Vorstman, Jacob, Bassett, Anne S, McDonald-McGinn, Donna M

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Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome von McGinn, Daniel E, Crowley, T. Blaine, Heung, Tracy, Oanh, Tran, Moss, Edward, Zackai, Elaine H, Emanuel, Beverly S, Chow, Eva W.C, Morrow, Bernice E, Swillen, Ann, Bassett, Anne S, McDonald-McGinn, Donna M

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Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects von Zhao, Yingjie, Diacou, Alexander, Johnston, H. Richard, Musfee, Fadi I, McDonald-McGinn, Donna M, McGinn, Daniel, Crowley, T. Blaine, Repetto, Gabriela M, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R, Kates, Wendy R, Digilio, M. Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne, Moss, Hayley, Owen, Michael J, Murphy, Kieran C, Murphy, Clodagh M, Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J, Shprintzen, Robert J, Campbell, Linda, Philip, Nicole, Heine-Suner, Damian, Garcia-Minaur, Sixto, Fernandez, Luis, Bearden, Carrie E, Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob A.S, Gothelf, Doron, Zackai, Elaine, Agopian, A.J, Gur, Raquel E, Bassett, Anne S, Emanuel, Beverly S, Goldmuntz, Elizabeth, Mitchell, Laura E, Wang, Tao, Morrow, Bernice E

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