Psychometric Study of the Social Responsiveness Scale in Phelan–McDermid Syndrome von Gergoudis, Kellie, Weinberg, Alan, Templin, Jonathan, Farmer, Cristan, Durkin, Alison, Weissman, Jordana, Siper, Paige, Foss‐Feig, Jennifer, Pilar Trelles, Maria, Bernstein, Jonathan A., Buxbaum, Joseph D., Berry‐Kravis, Elizabeth, Powell, Craig M., Sahin, Mustafa, Soorya, Latha, Thurm, Audrey, Kolevzon, Alexander

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Posttraumatic Stress Disorder in a Child with Autism Spectrum Disorder: Challenges in Management von Trelles Thorne, Maria del Pilar, Khinda, Navjot, Coffey, Barbara J

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Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations von De Rubeis, Silvia, Siper, Paige M, Durkin, Allison, Weissman, Jordana, Muratet, François, Halpern, Danielle, Trelles, Maria Del Pilar, Frank, Yitzchak, Lozano, Reymundo, Wang, A Ting, Holder, Jr, J Lloyd, Betancur, Catalina, Buxbaum, Joseph D, Kolevzon, Alexander

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Reduced engagement of visual attention in children with autism spectrum disorder von McLaughlin, Christopher S, Grosman, Hannah E, Guillory, Sylvia B, Isenstein, Emily L, Wilkinson, Emma, Trelles, Maria del Pilar, Halpern, Danielle B, Siper, Paige M, Kolevzon, Alexander, Buxbaum, Joseph D, Wang, A Ting, Foss-Feig, Jennifer H

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Prospective investigation of FOXP1 syndrome von Siper, Paige M, De Rubeis, Silvia, Trelles, Maria Del Pilar, Durkin, Allison, Di Marino, Daniele, Muratet, François, Frank, Yitzchak, Lozano, Reymundo, Eichler, Evan E, Kelly, Morgan, Beighley, Jennifer, Gerdts, Jennifer, Wallace, Arianne S, Mefford, Heather C, Bernier, Raphael A, Kolevzon, Alexander, Buxbaum, Joseph D

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Sensory Reactivity Symptoms Are a Core Feature of ADNP Syndrome Irrespective of Autism Diagnosis von Siper, Paige M, Layton, Christina, Levy, Tess, Lurie, Stacey, Benrey, Nurit, Zweifach, Jessica, Rowe, Mikaela, Tang, Lara, Guillory, Sylvia, Halpern, Danielle, Giserman-Kiss, Ivy, Del Pilar Trelles, Maria, Foss-Feig, Jennifer H, De Rubeis, Silvia, Tavassoli, Teresa, Buxbaum, Joseph D, Kolevzon, Alexander

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Ageusia and anosmia, a common sign of COVID-19? A case series from four countries von Vargas-Gandica, Jair, Winter, Daniel, Schnippe, Rainer, Rodriguez-Morales, Andrea G., Mondragon, Johana, Escalera-Antezana, Juan Pablo, Trelles-Thorne, María del Pilar, Bonilla-Aldana, D. Katterine, Rodriguez-Morales, Alfonso J., Paniz-Mondolfi, Alberto

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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism von Fu, Jack M., Satterstrom, F. Kyle, Peng, Minshi, Brand, Harrison, Collins, Ryan L., Dong, Shan, Wamsley, Brie, Klei, Lambertus, Wang, Lily, Hao, Stephanie P., Stevens, Christine R., Cusick, Caroline, Babadi, Mehrtash, Banks, Eric, Collins, Brett, Dodge, Sheila, Gabriel, Stacey B., Gauthier, Laura, Lee, Samuel K., Liang, Lindsay, Ljungdahl, Alicia, Mahjani, Behrang, Sloofman, Laura, Smirnov, Andrey N., Barbosa, Mafalda, Betancur, Catalina, Brusco, Alfredo, Chung, Brian H. Y., Cook, Edwin H., Cuccaro, Michael L., Domenici, Enrico, Ferrero, Giovanni Battista, Gargus, J. Jay, Herman, Gail E., Hertz-Picciotto, Irva, Maciel, Patricia, Manoach, Dara S., Passos-Bueno, Maria Rita, Persico, Antonio M., Renieri, Alessandra, Sutcliffe, James S., Tassone, Flora, Trabetti, Elisabetta, Campos, Gabriele, Cardaropoli, Simona, Carli, Diana, Chan, Marcus C. Y., Fallerini, Chiara, Giorgio, Elisa, Girardi, Ana Cristina, Hansen-Kiss, Emily, Lee, So Lun, Lintas, Carla, Ludena, Yunin, Nguyen, Rachel, Pavinato, Lisa, Pericak-Vance, Margaret, Pessah, Isaac N., Schmidt, Rebecca J., Smith, Moyra, Costa, Claudia I. S., Trajkova, Slavica, Wang, Jaqueline Y. T., Yu, Mullin H. C., Cutler, David J., De Rubeis, Silvia, Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J., Talkowski, Michael E.

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Luis Antonio Trelles Montero (3 de setiembre 1942 - 23 de febrero 2001) von Trelles Thorne, María del Pilar

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Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism von Satterstrom, F. Kyle, Breen, Michael S., Grove, Jakob, Klei, Lambertus, Xu, Xinyi, Norman, Utku, Brand, Harrison, Schwartz, Grace, Barbosa, Mafalda, Bybjerg-Grauholm, Jonas, Carracedo, Angel, Chiocchetti, Andreas G., Chung, Brian H.Y., Coon, Hilary, Cuccaro, Michael L., Dalla Bernardina, Bernardo, Domenici, Enrico, Dong, Shan, Freitag, Christine M., González-Peñas, Javier, Guter, Stephen, He, Xin, Herman, Gail E., Hertz-Picciotto, Irva, Hougaard, David M., Ionita-Laza, Iuliana, Jacob, Suma, Jamison, Jesslyn, Jugessur, Astanand, Kolevzon, Alexander, Kushima, Itaru, Lee, So Lun, Lehtimäki, Terho, Lim, Elaine T., Lipkin, W. Ian, Lopergolo, Diego, Lopes, Fátima, Ludena, Yunin, Maciel, Patricia, Meiri, Gal, Menashe, Idan, Miller, Judith, Montenegro, Eduarda M.S., Muglia, Pierandrea, Nordentoft, Merete, Ozaki, Norio, Palotie, Aarno, Parellada, Mara, Passos-Bueno, Maria Rita, Persico, Antonio M., Pessah, Isaac, Puura, Kaija, Renieri, Alessandra, Riberi, Evelise, Robinson, Elise B., Samocha, Kaitlin E., Sandin, Sven, Santangelo, Susan L., Schellenberg, Gerry, Scherer, Stephen W., Schmitt, Lauren, Silva, Isabela M.W., Singh, Tarjinder, Siper, Paige M., Soares, Gabriela, Susser, Ezra, Szatmari, Peter, Tang, Lara, Tassone, Flora, Teufel, Karoline, Trelles, Maria del Pilar, Werge, Thomas, Werling, Donna M., Wigdor, Emilie M., Yu, Mullin H.C., Zachi, Elaine, Agerbo, Esben, Als, Thomas Damm, Bækvad-Hansen, Marie, Belliveau, Rich, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Maller, Julian, Mattheisen, Manuel, Moran, Jennifer, Pallesen, Jonatan, Poulsen, Jesper Buchhave, Ripke, Stephan, Gallagher, Louise, Gill, Michael, Zwick, Michael E., State, Matthew W., Daly, Mark J., Buxbaum, Joseph D.

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Strong evidence for genotype–phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium von Levy, Tess, Foss-Feig, Jennifer H, Betancur, Catalina, Siper, Paige M, Trelles-Thorne, Maria del Pilar, Halpern, Danielle, Frank, Yitzchak, Lozano, Reymundo, Layton, Christina, Britvan, Bari, Bernstein, Jonathan A, Buxbaum, Joseph D, Berry-Kravis, Elizabeth, Powell, Craig M, Srivastava, Siddharth, Sahin, Mustafa, Soorya, Latha, Thurm, Audrey, Kolevzon, Alexander

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Genetic and epigenetic signatures associated with plasma oxytocin levels in children and adolescents with autism spectrum disorder von Siecinski, Stephen K., Giamberardino, Stephanie N., Spanos, Marina, Hauser, Annalise C., Gibson, Jason R., Chandrasekhar, Tara, Trelles, Maria del Pilar, Rockhill, Carol M., Palumbo, Michelle L., Cundiff, Allyson Witters, Montgomery, Alicia, Siper, Paige, Minjarez, Mendy, Nowinski, Lisa A., Marler, Sarah, Kwee, Lydia C., Shuffrey, Lauren C., Alderman, Cheryl, Weissman, Jordana, Zappone, Brooke, Mullett, Jennifer E., Crosson, Hope, Hong, Natalie, Luo, Sheng, She, Lilin, Bhapkar, Manjushri, Dean, Russell, Scheer, Abby, Johnson, Jacqueline L., King, Bryan H., McDougle, Christopher J., Sanders, Kevin B., Kim, Soo‐Jeong, Kolevzon, Alexander, Veenstra‐VanderWeele, Jeremy, Hauser, Elizabeth R., Sikich, Linmarie, Gregory, Simon G.

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Tracking devices reduce wandering frequency, risk among children with autism von Bortz, Katherine, Park, Chung-Hyuk, Thorne, Maria del Pilar Trelles

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Luis Antonio Trelles Montero: 3 de setiembre 1942 - 23 de febrero 2001 von Trelles Thorne, María del Pilar

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Additional file 2: of Prospective investigation of FOXP1 syndrome von Siper, Paige, Rubeis, Silvia De, Trelles, Maria Del Pilar, Durkin, Allison, Marino, Daniele Di, FrançOis Muratet, Frank, Yitzchak, Reymundo Lozano, Eichler, Evan, Kelly, Morgan, Beighley, Jennifer, Gerdts, Jennifer, Wallace, Arianne, Mefford, Heather, Bernier, Raphael, Kolevzon, Alexander, Buxbaum, Joseph

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Additional file 3: of Prospective investigation of FOXP1 syndrome von Siper, Paige, Rubeis, Silvia De, Trelles, Maria Del Pilar, Durkin, Allison, Marino, Daniele Di, FrançOis Muratet, Frank, Yitzchak, Reymundo Lozano, Eichler, Evan, Kelly, Morgan, Beighley, Jennifer, Gerdts, Jennifer, Wallace, Arianne, Mefford, Heather, Bernier, Raphael, Kolevzon, Alexander, Buxbaum, Joseph

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Additional file 1: of Prospective investigation of FOXP1 syndrome von Siper, Paige, Rubeis, Silvia De, Trelles, Maria Del Pilar, Durkin, Allison, Marino, Daniele Di, FrançOis Muratet, Frank, Yitzchak, Reymundo Lozano, Eichler, Evan, Kelly, Morgan, Beighley, Jennifer, Gerdts, Jennifer, Wallace, Arianne, Mefford, Heather, Bernier, Raphael, Kolevzon, Alexander, Buxbaum, Joseph

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174 - BÚSQUEDA DE UN PATRÓN CLÍNICO PARA LA PREDICCIÓN DE COLONOSCOPIA PATOLÓGICA EN LOS PACIENTES PARTICIPANTES DE LAS 2 PRIMERAS RONDAS DEL PROGRAMA DE DETECCIÓN PRECOZ DE CÁNCER... von Guzmán, Marita Trelles, del Pilar Roca, María, Sastre-Serra, Jorge, Moreno, José Reyes

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Result of the first two rounds of the colorectal cancer screening program in the Balearic Islands (Spain) von Trelles Guzmán, Marita Grimanesa, Novella Duran, Maria Teresa, Heredia Centeno, M Luisa, Florido Garcia, Monica, Sanchez-Contador Escudero, Maria Del Carmen, Iyo Miyashiro, Eduardo Yun, Ortega Moya, Silvia Patricia, Miro Viamonte, Elisa, Artigues Vives, Guillem, Gelabert Zornoza, Joan, Garcia Cortez, Paul David, Lucero Pizones, Juan Antonio, Rodriguez Hidalgo, Carolina, Ruiz Rubi, Alicia, Roca Salom, María Del Pilar, Sastre-Serra, Jorge, Reyes Moreno, Jose

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Resultado de las 2 primeras rondas del programa de cribado de cáncer colorrectal en las Islas Baleares (España) von Trelles Guzmán, Marita Grimanesa, Novella Duran, Maria Teresa, Heredia Centeno, M. Luisa, Florido Garcia, Monica, Sanchez-Contador Escudero, Maria del Carmen, Iyo Miyashiro, Eduardo Yun, Ortega Moya, Silvia Patricia, Miro Viamonte, Elisa, Artigues Vives, Guillem, Gelabert Zornoza, Joan, Garcia Cortez, Paul David, Lucero Pizones, Juan Antonio, Rodriguez Hidalgo, Carolina, Ruiz Rubi, Alicia, Roca Salom, María del Pilar, Sastre-Serra, Jorge, Reyes Moreno, Jose

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