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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Brief Report: Associations Between Self-injurious Behaviors and Abdominal Pain Among Individuals with ASD-Associated Disruptive Mutations von Kurtz-Nelson, Evangeline C., Tham, See Wan, Ahlers, Kaitlyn, Cho, Daniel, Wallace, Arianne S., Eichler, Evan E., Bernier, Raphael A., Earl, Rachel K.

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Clinical Phenotypes of Carriers of Mutations in CHD8 or Its Conserved Target Genes von Beighley, Jennifer S, Hudac, Caitlin M, Arnett, Anne B, Peterson, Jessica L, Gerdts, Jennifer, Wallace, Arianne S, Mefford, Heather C, Hoekzema, Kendra, Turner, Tychele N, O’Roak, Brian J, Eichler, Evan E, Bernier, Raphael A

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The autism spectrum phenotype in ADNP syndrome von Arnett, Anne B., Rhoads, Candace L., Hoekzema, Kendra, Turner, Tychele N., Gerdts, Jennifer, Wallace, Arianne S., Bedrosian‐Sermone, Sandra, Eichler, Evan E., Bernier, Raphael A.

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Trauma and Autism Spectrum Disorder: Review, Proposed Treatment Adaptations and Future Directions von Peterson, Jessica L., Earl, Rachel K., Fox, Emily A., Ma, Ruqian, Haidar, Ghina, Pepper, Micah, Berliner, Lucy, Wallace, Arianne S., Bernier, Raphael A.

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Comorbid symptoms of inattention, autism, and executive cognition in youth with putative genetic risk von Arnett, Anne B., Cairney, Brianna E., Wallace, Arianne S., Gerdts, Jennifer, Turner, Tychele N., Eichler, Evan E., Bernier, Raphael A.

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Auditory perception is associated with implicit language learning and receptive language ability in autism spectrum disorder von Arnett, Anne B., Hudac, Caitlin M., DesChamps, Trent D., Cairney, Brianna E., Gerdts, Jennifer, Wallace, Arianne S., Bernier, Raphael A., Webb, Sara J.

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Longitudinal report of child with de novo 16p11.2 triplication von Wallace, Arianne S., Hudac, Caitlin M., Steinman, Kyle J., Peterson, Jessica L., DesChamps, Trent D., Duyzend, Michael H., Nuttle, Xander, Eichler, Evan E., Bernier, Raphael A.

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Associations between Self-Injurious Behaviors and Abdominal Pain among Individuals with ASD-Associated Disruptive Mutations von Kurtz-Nelson, Evangeline C., Wan Tham, See, Ahlers, Kaitlyn, Cho, Daniel, Wallace, Arianne S., Eichler, Evan E., Bernier, Raphael A., Earl, Rachel K.

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Longitudinal report of child with de novo 16p11.2 triplication von Wallace, Arianne S, Hudac, Caitlin M, Steinman, Kyle J, Peterson, Jessica L, DesChamps, Trent D, Duyzend, Michael H, Nuttle, Xander, Eichler, Evan E, Bernier, Raphael A

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The Cognitive and Behavioral Phenotype of the 16p11.2 Deletion in a Clinically Ascertained Population von Hanson, Ellen, Bernier, Raphael, Porche, Ken, Jackson, Frank I, Goin-Kochel, Robin P, Snyder, LeeAnne Green, Snow, Anne V, Wallace, Arianne Stevens, Campe, Katherine L, Zhang, Yuan, Chen, Qixuan, D’Angelo, Debra, Moreno-De-Luca, Andres, Orr, Patrick T, Boomer, K.B, Evans, David W, Kanne, Stephen, Berry, Leandra, Miller, Fiona K, Olson, Jennifer, Sherr, Elliot, Martin, Christa L, Ledbetter, David H, Spiro, John E, Chung, Wendy K

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Clinical phenotype of the recurrent 1q21.1 copy-number variant von Bernier, Raphael, Steinman, Kyle J., Reilly, Beau, Wallace, Arianne Stevens, Sherr, Elliott H., Pojman, Nicholas, Mefford, Heather C., Gerdts, Jennifer, Earl, Rachel, Hanson, Ellen, Goin-Kochel, Robin P., Berry, Leandra, Kanne, Stephen, Snyder, LeeAnne Green, Spence, Sarah, Ramocki, Melissa B., Evans, David W., Spiro, John E., Martin, Christa L., Ledbetter, David H., Chung, Wendy K.

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Health-Related Quality of Life in Pediatric Patients With Demyelinating Diseases: Relevance of Disability, Relapsing Presentation, and Fatigue von Self, Mariella M, Fobian, Aaron, Cutitta, Katherine, Wallace, Arianne, Lotze, Timothy E

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Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication von Green Snyder, LeeAnne, D’Angelo, Debra, Chen, Qixuan, Bernier, Raphael, Goin-Kochel, Robin P., Wallace, Arianne Stevens, Gerdts, Jennifer, Kanne, Stephen, Berry, Leandra, Blaskey, Lisa, Kuschner, Emily, Roberts, Timothy, Sherr, Elliot, Martin, Christa L., Ledbetter, David H., Spiro, John E., Chung, Wendy K., Hanson, Ellen

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Developmental trajectories for young children with 16p11.2 copy number variation von Bernier, Raphael, Hudac, Caitlin M., Chen, Qixuan, Zeng, Chubing, Wallace, Arianne Stevens, Gerdts, Jennifer, Earl, Rachel, Peterson, Jessica, Wolken, Anne, Peters, Alana, Hanson, Ellen, Goin‐Kochel, Robin P., Kanne, Stephen, Snyder, LeeAnne Green, Chung, Wendy K.

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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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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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