Genomic and epigenetic evidence for oxytocin receptor deficiency in autism von Gregory, Simon G, Connelly, Jessica J, Towers, Aaron J, Johnson, Jessica, Biscocho, Dhani, Markunas, Christina A, Lintas, Carla, Abramson, Ruth K, Wright, Harry H, Ellis, Peter, Langford, Cordelia F, Worley, Gordon, Delong, G Robert, Murphy, Susan K, Cuccaro, Michael L, Persico, Antonello, Pericak-Vance, Margaret A

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A low-cost socially assistive robot and robot-assisted intervention for children with autism spectrum disorder: field trials and lessons learned von Boccanfuso, Laura, Scarborough, Sarah, Abramson, Ruth K., Hall, Alicia V., Wright, Harry H., O’Kane, Jason M.

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Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways von GRISWOLD, Anthony J, DEQIONG MA, WRIGHT, Harry H, ABRAMSON, Ruth K, WILLIAMS, Scott M, MENON, Ramkumar, MARTIN, Eden R, HAINES, Jonathan L, GILBERT, John R, CUCCARO, Michael L, PERICAK-VANCE, Margaret A, CUKIER, Holly N, NATIONS, Laura D, SCHMIDT, Mike A, CHUNG, Ren-Hua, JAWORSKI, James M, SALYAKINA, Daria, KONIDARI, Loanna, WHITEHEAD, Patrice L

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Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk von Salyakina, Daria, Cukier, Holly N, Lee, Joycelyn M, Sacharow, Stephanie, Nations, Laura D, Ma, Deqiong, Jaworski, James M, Konidari, Ioanna, Whitehead, Patrice L, Wright, Harry H, Abramson, Ruth K, Williams, Scott M, Menon, Ramkumar, Haines, Jonathan L, Gilbert, John R, Cuccaro, Michael L, Pericak-Vance, Margaret A

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Pharmacotherapy of Autism Spectrum Disorder: Results from the Randomized BAART Clinical Trial von DeVane, C. Lindsay, Charles, Jane M., Abramson, Ruth K., Williams, John E., Carpenter, Laura A., Raven, Sarah, Gwynette, Frampton, Stuck, Craig A., Geesey, Mark E., Bradley, Catherine, Donovan, Jennifer L., Hall, Alicia G., Sherk, Shelley T., Powers, Nancy R., Spratt, Eve, Kinsman, Anne, Kruesi, Markus J., Bragg, John E.

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Common SNP-Based Haplotype Analysis of the 4p16.3 Huntington Disease Gene Region von Lee, Jong-Min, Gillis, Tammy, Mysore, Jayalakshmi Srinidhi, Ramos, Eliana Marisa, Myers, Richard H., Hayden, Michael R., Morrison, Patrick J., Nance, Martha, Ross, Christopher A., Margolis, Russell L., Squitieri, Ferdinando, Griguoli, Annamaria, Di Donato, Stefano, Gomez-Tortosa, Estrella, Ayuso, Carmen, Suchowersky, Oksana, Trent, Ronald J., McCusker, Elizabeth, Novelletto, Andrea, Frontali, Marina, Jones, Randi, Ashizawa, Tetsuo, Frank, Samuel, Saint-Hilaire, Marie-Helene, Hersch, Steven M., Rosas, Herminia D., Lucente, Diane, Harrison, Madaline B., Zanko, Andrea, Abramson, Ruth K., Marder, Karen, Sequeiros, Jorge, MacDonald, Marcy E., Gusella, James F.

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The Expanding Role of MBD Genes in Autism: Identification of a MECP2 Duplication and Novel Alterations in MBD5, MBD6, and SETDB1 von Cukier, Holly N., Lee, Joycelyn M., Ma, Deqiong, Young, Juan I., Mayo, Vera, Butler, Brittany L., Ramsook, Sandhya S., Rantus, Joseph A., Abrams, Alexander J., Whitehead, Patrice L., Wright, Harry H., Abramson, Ruth K., Haines, Jonathan L., Cuccaro, Michael L., Pericak-Vance, Margaret A., Gilbert, John R.

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Three Brothers With Autism Carry a Stop‐Gain Mutation in the HPA‐Axis Gene NR3C2 von Cukier, Holly N., Griswold, Anthony J., Hofmann, Natalia K., Gomez, Lissette, Whitehead, Patrice L., Abramson, Ruth K., Gilbert, John R., Cuccaro, Michael L., Dykxhoorn, Derek M., Pericak‐Vance, Margaret A.

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A Genome‐wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1 von Ma, Deqiong, Salyakina, Daria, Jaworski, James M., Konidari, Ioanna, Whitehead, Patrice L., Andersen, Ashley N., Hoffman, Joshua D., Slifer, Susan H., Hedges, Dale J., Cukier, Holly N., Griswold, Anthony J., McCauley, Jacob L., Beecham, Gary W., Wright, Harry H., Abramson, Ruth K., Martin, Eden R., Hussman, John P., Gilbert, John R., Cuccaro, Michael L., Haines, Jonathan L., Pericak‐Vance, Margaret A.

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An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males von Chung, Ren-Hua, Ma, Deqiong, Wang, Kai, Hedges, Dale J, Jaworski, James M, Gilbert, John R, Cuccaro, Michael L, Wright, Harry H, Abramson, Ruth K, Konidari, Ioanna, Whitehead, Patrice L, Schellenberg, Gerard D, Hakonarson, Hakon, Haines, Jonathan L, Pericak-Vance, Margaret A, Martin, Eden R

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Uric Acid Causes Vascular Smooth Muscle Cell Proliferation by Entering Cells via a Functional Urate Transporter von Kang, Duk-Hee, Han, Lin, Ouyang, Xiaosen, Kahn, Andrew M., Kanellis, John, Li, Ping, Feng, Lili, Nakagawa, Takahiko, Watanabe, Susumu, Hosoyamada, Makoto, Endou, Hitoshi, Lipkowitz, Michael, Abramson, Ruth, Mu, Wei, Johnson, Richard J.

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Exploring the Relationship Between Autism Spectrum Disorder and Epilepsy Using Latent Class Cluster Analysis von Cuccaro, Michael L., Tuchman, Roberto F., Hamilton, Kara L., Wright, Harry H., Abramson, Ruth K., Haines, Jonathan L., Gilbert, John R., Pericak-Vance, Margaret

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Factor Analysis of the Aberrant Behavior Checklist in Individuals with Autism Spectrum Disorders von Brinkley, Jason, Nations, Laura, Abramson, Ruth K, Hall, Alicia, Wright, Harry H, Gabriels, Robin, Gilbert, John R, Pericak-Vance, Margaret A. O, Cuccaro, Michael L

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Investigation of autism and GABA receptor subunit genes in multiple ethnic groups von COLLINS, Ann L, DEQIONG MA, PERICAK-VANCE, Margaret A, WHITEHEAD, Patrice L, MARTIN, Eden R, WRIGHT, Harry H, ABRAMSON, Ruth K, HUSSMAN, John P, HAINES, Jonathan L, CUCCARO, Michael L, GILBERT, John R

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Accelerated head growth in early development of individuals with autism von Dementieva, Yulia A., Vance, Danica D., Donnelly, Shannon L., Elston, Leigh A., Wolpert, Chantelle M., Ravan, Sarah A., DeLong, G. Robert, Abramson, Ruth K., Wright, Harry H., Cuccaro, Michael L.

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Novel variants identified in methyl-CpG-binding domain genes in autistic individuals von Cukier, Holly N., Rabionet, Raquel, Konidari, Ioanna, Rayner-Evans, Melissa Y., Baltos, Mary L., Wright, Harry H., Abramson, Ruth K., Martin, Eden R., Cuccaro, Michael L., Pericak-Vance, Margaret A., Gilbert, John R.

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Genomic screen and follow-up analysis for autistic disorder von Shao, Yujun, Wolpert, Chantelle M., Raiford, Kimberly L., Menold, Marisa M., Donnelly, Shannon L., Ravan, Sarah A., Bass, Meredyth P., McClain, Cate, von Wendt, Lennart, Vance, Jeffery M., Abramson, Ruth H., Wright, Harry H., Ashley-Koch, Allison, Gilbert, John R., DeLong, Robert G., Cuccaro, Michael L., Pericak-Vance, Margaret A.

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Evaluating Mitochondrial DNA Variation in Autism Spectrum Disorders von Hadjixenofontos, Athena, Schmidt, Michael A., Whitehead, Patrice L., Konidari, Ioanna, Hedges, Dale J., Wright, Harry H., Abramson, Ruth K., Menon, Ramkumar, Williams, Scott M., Cuccaro, Michael L., Haines, Jonathan L., Gilbert, John R., Pericak‐Vance, Margaret A., Martin, Eden R., McCauley, Jacob L.

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Factor analysis of restricted and repetitive behaviors in Autism using the Autism Diagnostic interview-R von CUCCARO, Michael L, YUJAN SHAO, PERICAK-VANCE, Margaret A, GRUBBER, Janet, SLIFER, Michael, WOLPERT, Chantelle M, DONNELLY, Shannon L, ABRAMSON, Ruth K, RAVAN, Sarah A, WRIGHT, Harry H, DELONG, G. Robert

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A Genome Scan for Modifiers of Age at Onset in Huntington Disease: The HD MAPS Study von Li, Jian-Liang, Hayden, Michael R., Almqvist, Elisabeth W., Brinkman, Ryan R., Durr, Alexandra, Dodé, Catherine, Morrison, Patrick J., Suchowersky, Oksana, Ross, Christopher A., Margolis, Russell L., Rosenblatt, Adam, Gómez-Tortosa, Estrella, Cabrero, David Mayo, Novelletto, Andrea, Frontali, Marina, Nance, Martha, Trent, Ronald J.A., McCusker, Elizabeth, Jones, Randi, Paulsen, Jane S., Harrison, Madeline, Zanko, Andrea, Abramson, Ruth K., Russ, Ana L., Knowlton, Beth, Djoussé, Luc, Mysore, Jayalakshmi S., Tariot, Suzanne, Gusella, Michael F., Wheeler, Vanessa C., Atwood, Larry D., Cupples, L. Adrienne, Saint-Hilaire, Marie, Cha, Jang-Ho J., Hersch, Steven M., Koroshetz, Walter J., Gusella, James F., MacDonald, Marcy E., Myers, Richard H.

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