Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants by Hojlo, Margaret A, Ghebrelul, Merhawi, Genetti, Casie A, Smith, Richard, Rockowitz, Shira, Deaso, Emma, Beggs, Alan H, Agrawal, Pankaj B, Glahn, David C, Gonzalez-Heydrich, Joseph, Brownstein, Catherine A

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Unexplained regression in Down syndrome: Management of 51 patients in an international patient database by Santoro, Stephanie L., Baumer, Nicole T., Cornacchia, Michelle, Franklin, Catherine, Hart, Sarah J., Haugen, Kelsey, Hojlo, Margaret A., Horick, Nora, Kishnani, Priya S., Krell, Kavita, McCormick, Andrew, Milliken, Anna L., Oreskovic, Nicolas M., Pawlowski, Katherine G., Sargado, Sabrina, Torres, Amy, Valentini, Diletta, Vellody, Kishore, Skotko, Brian G.

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Similar Rates of Deleterious Copy Number Variants in Early-Onset Psychosis and Autism Spectrum Disorder by Brownstein, Catherine A., Douard, Elise, Mollon, Josephine, Smith, Richard, Hojlo, Margaret A., Das, Ananth, Goldman, Maria, Garvey, Emily, Cabral, Kristin, Li, Jianqiao, Bowen, Joshua, Rao, Abhijit S., Genetti, Casie, Carroll, Devon, Knowles, Emma E. M., Deaso, Emma, Agrawal, Pankaj B., Beggs, Alan H., D’Angelo, Eugene, Almasy, Laura, Alexander-Bloch, Aaron, Saci, Zohra, Moreau, Clara A., Huguet, Guillaume, Deo, Anthony J., Jacquemont, Sébastien, Glahn, David C., Gonzalez-Heydrich, Joseph

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Development and implementation of a longitudinal clinical database for down syndrome in a large pediatric specialty clinic: Methodology and feasibility by Baumer, Nicole T., Hojlo, Margaret A., Lombardo, Angela M., Milliken, Anna L., Pawlowski, Katherine G., Sargado, Sabrina, Soccorso, Cara, Davidson, Emily J., Barbaresi, William J.

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Co‐occurring conditions in Down syndrome: Findings from a clinical database by Baumer, Nicole T., Hojlo, Margaret A., Pawlowski, Katherine G., Milliken, Anna L., Lombardo, Angela M., Sargado, Sabrina, Soccorso, Cara, Davidson, Emily J., Barbaresi, William J.

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RCL1 copy number variants are associated with a range of neuropsychiatric phenotypes by Brownstein, Catherine A., Smith, Richard S., Rodan, Lance H., Gorman, Mark P., Hojlo, Margaret A., Garvey, Emily A., Li, Jianqiao, Cabral, Kristin, Bowen, Joshua J., Rao, Abhijit S., Genetti, Casie A., Carroll, Devon, Deaso, Emma A., Agrawal, Pankaj B., Rosenfeld, Jill A., Bi, Weimin, Howe, Jennifer, Stavropoulos, Dimitri J., Hansen, Adam W., Hamoda, Hesham M., Pinard, Ferne, Caracansi, Annmarie, Walsh, Christopher A., D’Angelo, Eugene J., Beggs, Alan H., Zarrei, Mehdi, Gibbs, Richard A., Scherer, Stephen W., Glahn, David C., Gonzalez-Heydrich, Joseph

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Response to Letter to the Editor by Palffy and Ghaziuddin by Santoro, Stephanie L., Baumer, Nicole T., Cornacchia, Michelle, Franklin, Catherine, Hart, Sarah J., Haugen, Kelsey, Hojlo, Margaret A., Horick, Nora, Kishnani, Priya S., Krell, Kavita, McCormick, Andrew, Milliken, Anna L., Oreskovic, Nicolas M., Pawlowski, Katherine G., Sargado, Sabrina, Torres, Amy, Valentini, Diletta, Vellody, Kishore, Skotko, Brian G.

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Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study by Li, Jianqiao, Hojlo, Margaret A, Chennuri, Sampath, Gujral, Nitin, Paterson, Heather L, Shefchek, Kent A, Genetti, Casie A, Cohn, Emily L, Sewalk, Kara C, Garvey, Emily A, Buttermore, Elizabeth D, Anderson, Nickesha C, Beggs, Alan H, Agrawal, Pankaj B, Brownstein, John S, Haendel, Melissa A, Holm, Ingrid A, Gonzalez-Heydrich, Joseph, Brownstein, Catherine A

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Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders by Wang, Tianyun, Hoekzema, Kendra, Vecchio, Davide, Wu, Huidan, Sulovari, Arvis, Coe, Bradley P., Gillentine, Madelyn A., Wilfert, Amy B., Perez-Jurado, Luis A., Kvarnung, Malin, Sleyp, Yoeri, Earl, Rachel K., Rosenfeld, Jill A., Geisheker, Madeleine R., Han, Lin, Du, Bing, Barnett, Chris, Thompson, Elizabeth, Shaw, Marie, Carroll, Renee, Friend, Kathryn, Catford, Rachael, Palmer, Elizabeth E., Zou, Xiaobing, Ou, Jianjun, Li, Honghui, Guo, Hui, Gerdts, Jennifer, Avola, Emanuela, Calabrese, Giuseppe, Elia, Maurizio, Greco, Donatella, Lindstrand, Anna, Nordgren, Ann, Anderlid, Britt-Marie, Vandeweyer, Geert, Van Dijck, Anke, Van der Aa, Nathalie, McKenna, Brooke, Hancarova, Miroslava, Bendova, Sarka, Havlovicova, Marketa, Malerba, Giovanni, Bernardina, Bernardo Dalla, Muglia, Pierandrea, van Haeringen, Arie, Hoffer, Mariette J. V., Franke, Barbara, Cappuccio, Gerarda, Delatycki, Martin, Lockhart, Paul J., Manning, Melanie A., Liu, Pengfei, Scheffer, Ingrid E., Brunetti-Pierri, Nicola, Rommelse, Nanda, Amaral, David G., Santen, Gijs W. E., Trabetti, Elisabetta, Sedláček, Zdeněk, Michaelson, Jacob J., Pierce, Karen, Courchesne, Eric, Kooy, R. Frank, Nordenskjöld, Magnus, Romano, Corrado, Peeters, Hilde, Bernier, Raphael A., Gecz, Jozef, Xia, Kun, Eichler, Evan E.

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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders by Gillentine, Madelyn A, Wang, Tianyun, Hoekzema, Kendra, Rosenfeld, Jill, Liu, Pengfei, Guo, Hui, Kim, Chang N, De Vries, Bert B A, Vissers, Lisenka E L M, Nordenskjold, Magnus, Kvarnung, Malin, Lindstrand, Anna, Nordgren, Ann, Gecz, Jozef, Iascone, Maria, Cereda, Anna, Scatigno, Agnese, Maitz, Silvia, Zanni, Ginevra, Bertini, Enrico, Zweier, Christiane, Schuhmann, Sarah, Wiesener, Antje, Pepper, Micah, Panjwani, Heena, Torti, Erin, Abid, Farida, Anselm, Irina, Srivastava, Siddharth, Atwal, Paldeep, Bacino, Carlos A, Bhat, Gifty, Cobian, Katherine, Bird, Lynne M, Friedman, Jennifer, Wright, Meredith S, Callewaert, Bert, Petit, Florence, Mathieu, Sophie, Afenjar, Alexandra, Christensen, Celenie K, White, Kerry M, Elpeleg, Orly, Berger, Itai, Espineli, Edward J, Fagerberg, Christina, Brasch-Andersen, Charlotte, Hansen, Lars Kjærsgaard, Feyma, Timothy, Hughes, Susan, Thiffault, Isabelle, Sullivan, Bonnie, Yan, Shuang, Keller, Kory, Keren, Boris, Mignot, Cyril, Kooy, Frank, Meuwissen, Marije, Basinger, Alice, Kukolich, Mary, Philips, Meredith, Ortega, Lucia, Drummond-Borg, Margaret, Lauridsen, Mathilde, Sorensen, Kristina, Lehman, Anna, Lopez-Rangel, Elena, Levy, Paul, Lessel, Davor, Lotze, Timothy, Madan-Khetarpal, Suneeta, Sebastian, Jessica, Vento, Jodie, Vats, Divya, Benman, L Manace, Mckee, Shane, Mirzaa, Ghayda M, Muss, Candace, Pappas, John, Peeters, Hilde, Romano, Corrado, Elia, Maurizio, Galesi, Ornella, Simon, Marleen E H, van Gassen, Koen L I, Simpson, Kara, Stratton, Robert, Syed, Sabeen, Thevenon, Julien, Palafoll, Irene Valenzuela, Vitobello, Antonio, Bournez, Marie, Faivre, Laurence, Xia, Kun, Earl, Rachel K, Nowakowski, Tomasz, Bernier, Raphael A, Eichler, Evan E

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Rate of Deleterious Copy Number Variants Similar in Early Onset Psychosis and Autism Spectrum Disorders: Implications for Clinical Practice by Brownstein, Catherine A., Douard, Elise, Mollon, Josephine, Smith, Richard, Hojlo, Margaret A., Das, Ananth, Goldman, Maria, Garvey, Emily, Cabral, Kristin, Li, Jianqiao, Bowen, Joshua, Rao, Abhijit S., Genetti, Casie, Carroll, Devon, Knowles, Emma E. M., Deaso, Emma, Agrawal, Pankaj B, Beggs, Alan H., D’Angelo, Eugene, Almasy, Laura, Alexander-Bloch, Aaron, Saci, Zohra, Moreau, Clara A., Huguet, Guillaume, Deo, Anthony, Jacquemont, Sébastien, Glahn, David C., Gonzalez-Heydrich, Joseph

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Children with Early-Onset Psychosis Have Increased Burden of Rare IGRIN2A/I Variants by Hojlo, Margaret A, Ghebrelul, Merhawi, Genetti, Casie A, Smith, Richard, Rockowitz, Shira, Deaso, Emma, Beggs, Alan H, Agrawal, Pankaj B, Glahn, David C, Gonzalez-Heydrich, Joseph, Brownstein, Catherine A

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Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders by Wang, Tianyun, Hoekzema, Kendra, Vecchio, Davide, Wu, Huidan, Sulovari, Arvis, Coe, Bradley P., Gillentine, Madelyn A., Wilfert, Amy B., Perez-Jurado, Luis A., Kvarnung, Malin, Sleyp, Yoeri, Earl, Rachel K., Rosenfeld, Jill A., Geisheker, Madeleine R., Han, Lin, Du, Bing, Barnett, Chris, Thompson, Elizabeth, Shaw, Marie, Carroll, Renee, Friend, Kathryn, Catford, Rachael, Palmer, Elizabeth E., Zou, Xiaobing, Ou, Jianjun, Li, Honghui, Guo, Hui, Gerdts, Jennifer, Avola, Emanuela, Calabrese, Giuseppe, Elia, Maurizio, Greco, Donatella, Lindstrand, Anna, Nordgren, Ann, Anderlid, Britt-Marie, Vandeweyer, Geert, Van Dijck, Anke, Van der Aa, Nathalie, McKenna, Brooke, Hancarova, Miroslava, Bendova, Sarka, Havlovicova, Marketa, Malerba, Giovanni, Bernardina, Bernardo Dalla, Muglia, Pierandrea, van Haeringen, Arie, Hoffer, Mariette J. V., Franke, Barbara, Cappuccio, Gerarda, Delatycki, Martin, Lockhart, Paul J., Manning, Melanie A., Liu, Pengfei, Scheffer, Ingrid E., Brunetti-Pierri, Nicola, Rommelse, Nanda, Amaral, David G., Santen, Gijs W. E., Trabetti, Elisabetta, Sedláček, Zdeněk, Michaelson, Jacob J., Pierce, Karen, Courchesne, Eric, Kooy, R. Frank, Nordenskjöld, Magnus, Romano, Corrado, Peeters, Hilde, Bernier, Raphael A., Gecz, Jozef, Xia, Kun, Eichler, Evan E.

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Development, education, and services in children with Down syndrome: a cohort analysis from a clinical database by Soccorso, Cara, Hojlo, Margaret, Pawlowski, Katherine, Lombardo, Angela, Davidson, Emily, Sargado, Sabrina, DePillis, Rafael, Baumer, Nicole

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Characterization of pain and somatization and its relationship with psychopathology in early onset psychosis by van der Heijden, Hanne, Goldman, Maria, Ray, Aliza, Golden, Emma, Petty, Carter R., Deaso, Emma, Hojlo, Margaret, Sethna, Navil, Glahn, David C., Gonzalez-Heydrich, Joseph, Upadhyay, Jaymin

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Prevalence of Rate of Deleterious Copy Number Variants Similar in Early Onset Psychosis and Autism Spectrum Disorders: Implications for Clinical Practice by Brownstein, Catherine, Douard, Elise, Mollon, Josephine, Smith, Richard, Hojlo, Margaret, Garvey, Emily, Cabral, Kristin, Bowen, Joshua, Deaso, Emma, Rao, Abhijit, Genetti, Casie, Carroll, Devon, Knowles, Emma, Agrawal, Pankaj, Beggs, Alan, D’Angelo, Eugene, Almasy, Laura, Saci, Zohra, Moreau, Clara, Huguet, Guillaume, Jacquemont, Sébastien, Glahn, David, Gonzalez-Heydrich, Joseph

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Burden Experienced by Primary Caregivers of Children With Psychotic Disorders and at Clinical High Risk for Psychosis by Carroll, Devon, Wales, Meghan, Rintell, L. Sophia, Hojlo, Margaret, Gonzalez-Heydrich, Joseph, Berbert, Laura, Fitzpatrick, Molly, D’Angelo, Eugene, Reed, Mary P.

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