Cenozoic deformation in the Otway Basin, southern Australian margin: implications for the origin and nature of post-breakup compression at rifted margins von Holford, Simon P., Tuitt, Adrian K., Hillis, Richard R., Green, Paul F., Stoker, Martyn S., Duddy, Ian R., Sandiford, Mike, Tassone, David R.

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Quantification of Cretaceous-Cenozoic exhumation in the Otway Basin using sonic velocities and implications for hydrocarbon exploration von Tassone, David R., Holford, Simon P., Hillis, Richard R.

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Sequencing the unsequenceable: expanded CGG-repeat alleles of the fragile X gene von Loomis, Erick W, Eid, John S, Peluso, Paul, Yin, Jun, Hickey, Luke, Rank, David, McCalmon, Sarah, Hagerman, Randi J, Tassone, Flora, Hagerman, Paul J

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Anti-DKK1 mAb (BHQ880) as a potential therapeutic agent for multiple myeloma von Fulciniti, Mariateresa, Tassone, Pierfrancesco, Hideshima, Teru, Vallet, Sonia, Nanjappa, Puru, Ettenberg, Seth A., Shen, Zhenxin, Patel, Nipun, Tai, Yu-tzu, Chauhan, Dharminder, Mitsiades, Constantine, Prabhala, Rao, Raje, Noopur, Anderson, Kenneth C., Stover, David R., Munshi, Nikhil C.

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A case of vagal paraganglioma initially diagnosed as metastatic thyroid cancer from fine-needle aspiration von Barry, Elsie, Gilley, David R., Tassone, Patrick

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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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Blood Proteome Profiling Reveals Biomarkers and Pathway Alterations in Fragile X PM at Risk for Developing FXTAS von Zafarullah, Marwa, Li, Jie, Salemi, Michelle R, Phinney, Brett S, Durbin-Johnson, Blythe P, Hagerman, Randi, Hessl, David, Rivera, Susan M, Tassone, Flora

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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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AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome von Yrigollen, Carolyn M., Durbin-Johnson, Blythe, Gane, Louise, Nelson, David L., Hagerman, Randi, Hagerman, Paul J., Tassone, Flora

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Metabolic profiling reveals dysregulated lipid metabolism and potential biomarkers associated with the development and progression of Fragile X‐Associated Tremor/Ataxia Syndrome (F... von Zafarullah, Marwa, Palczewski, Grzegorz, Rivera, Susan M., Hessl, David R., Tassone, Flora

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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome von Davies, Robert W., Fiksinski, Ania M., Breetvelt, Elemi J., Williams, Nigel M., Hooper, Stephen R., Monfeuga, Thomas, Bassett, Anne S., Owen, Michael J., Gur, Raquel E., Morrow, Bernice E., McDonald-McGinn, Donna M., Swillen, Ann, Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., van Amelsvoort, Therese, Arango, Celso, Armando, Marco, Campbell, Linda E., Cubells, Joseph F., Eliez, Stephan, Garcia-Minaur, Sixto, Gothelf, Doron, Kates, Wendy R., Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan G., Philip, Nicole, Repetto, Gabriela M., Shashi, Vandana, Simon, Tony J., Suñer, Damiàn Heine, Vicari, Stefano, Scherer, Stephen W., Bearden, Carrie E., Vorstman, Jacob A. S.

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Mechanistic Study of Shape-Anisotropic Nanomaterials Synthesized via Spontaneous Galvanic Displacement von Strand, Matthew B, Leong, G. Jeremy, Tassone, Christopher J, Larsen, Brian, Neyerlin, K. C, Gorman, Brian, Diercks, David R, Pylypenko, Svitlana, Pivovar, Bryan, Richards, Ryan M

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Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion von Loesch, D. Z., Bui, M. Q., Hammersley, E., Schneider, A., Storey, E., Stimpson, P., Burgess, T., Francis, D., Slater, H., Tassone, F., Hagerman, R. J., Hessl, D.

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A case of parapharyngeal space salivary duct cyst with fine needle biopsy suspicious for squamous cell carcinoma von Gilley, David R., Clark, Andrew, Tassone, Patrick

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A randomized double-blind, placebo-controlled trial of ganaxolone in children and adolescents with fragile X syndrome von Ligsay, Andrew, Van Dijck, Anke, Nguyen, Danh V, Lozano, Reymundo, Chen, Yanjun, Bickel, Erika S, Hessl, David, Schneider, Andrea, Angkustsiri, Kathleen, Tassone, Flora, Ceulemans, Berten, Kooy, R Frank, Hagerman, Randi J

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Metabolomic Biomarkers Are Associated With Area of the Pons in Fragile X Premutation Carriers at Risk for Developing FXTAS von Zafarullah, Marwa, Durbin-Johnson, Blythe, Fourie, Emily S., Hessl, David R., Rivera, Susan M., Tassone, Flora

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Mitochondrial dysfunction in brain tissues and Extracellular Vesicles Fragile X‐associated tremor/ataxia syndrome von Yao, Pamela J., Manolopoulos, Apostolos, Eren, Erden, Rivera, Susan Michelle, Hessl, David R., Hagerman, Randi, Martinez‐Cerdeno, Veronica, Tassone, Flora, Kapogiannis, Dimitrios

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Total and Regional White Matter Lesions Are Correlated With Motor and Cognitive Impairments in Carriers of the FMR1 Premutation von Hocking, Darren R, Loesch, Danuta Z, Trost, Nicholas, Bui, Minh Q, Hammersley, Eleanor, Francis, David, Tassone, Flora, Storey, Elsdon

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The Autism Spectrum Disorders Stem Cell Resource at Children's Hospital of Orange County: Implications for Disease Modeling and Drug Discovery von Brick, David J., Nethercott, Hubert E., Montesano, Samantha, Banuelos, Maria G., Stover, Alexander E., Schutte, Soleil Sun, O'Dowd, Diane K., Hagerman, Randi J., Ono, Michele, Hessl, David R., Tassone, Flora, Schwartz, Philip H.

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Progression of tremor and ataxia in male carriers of the FMR1 premutation von Leehey, Maureen A., Berry-Kravis, Elizabeth, Min, Sung-Joon, Hall, Deborah A., Rice, Cathlin D., Zhang, Lin, Grigsby, Jim, Greco, Claudia M., Reynolds, Ann, Lara, Rebecca, Cogswell, Jennifer, Jacquemont, Sebastien, Hessl, David R., Tassone, Flora, Hagerman, Randi, Hagerman, Paul J.

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