Lipophilic but not hydrophilic statins selectively induce cell death in gynaecological cancers expressing high levels of HMGCoA reductase by Kato, S., Smalley, S., Sadarangani, A., Chen‐Lin, K., Oliva, B., Brañes, J., Carvajal, J., Gejman, R., Owen, G. I., Cuello, M.

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Postmenopausal androgen-secreting ovarian tumors: challenging differential diagnosis in two cases by Arteaga, E., Martinez, A., Jaramilo, J., Villaseca, P., Cuello, M., Valenzuela, P., Gejman, R., Blumel, J. E.

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A chilean case of chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (clippers): case report by Galilea izquierdo, A, Muñoz, F, Valenzuela, R, Gejman, R, Raue, M

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810 Simvastatin Inhibits Leptin-activated Signaling Pathways That Promote Migration and Invasiveness of Ovarian Cancer Cells by Cuello-Fredes, M, Kato, S, Diaz, D, Vecchiola, A, Branes, J, Barriga, M.I, Gejman, R, Owen, G.I

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P.9.9 A novel de novo mutation in ACTA1 causes a congenital myopathy with misleading type 1 fiber predominance and a peculiar MRI by Castiglioni, C, Cassandrini, D, Fattori, F, Bellacchio, E, Alvarez, K, D’Amico, A, Gejman, R, Díaz, J, Santorelli, F.M, Bevilacqua, J.A, Bertini, E

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REGISTRIES AND CARE OF NEUROMUSCULAR DISORDERS by Escobar, R., Gejman, R., Jaque, C., Beytia, M., Avila, D., Casar, J., Trujillo, O., Fadic, R.

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REGISTRIES AND CARE OF NEUROMUSCULAR DISORDERS: P.294Muscle biopsy in the study of muscle disease in pediatric population by Escobar, R., Gejman, R., Jaque, C., Beytia, M., Avila, D., Casar, J., Trujillo, O., Fadic, R.

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P2.03-01 Prevalence of EGFR Alterations in Chilean Lung Cancer Patients: A Retrospective Study by Gejman, R., Bravo, M.L., Muñoz, M., Retamal, I., Nervi, B., Sanchez, C., Ibañez, C., Peña, J., Madrid, J., Briones, J., Perez, P., Garrido, M., Pinto, M., Galindo, H.

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Temporal Lobe Epilepsy Surgery with Limited Resources: Results and Economic Considerations by Campos, M. G., Godoy, J., Mesa, M.T., Torrealba, G., Gejman, R., Huete, I.

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Mitochondrial DNA heteroplasmy of the m.3243A>G mutation in maternally inherited diabetes and deafness by Cataldo, Luis Rodrigo, Olmos, Pablo, Valerie Smalley, Susan, Díez, Alberto, Parada, Alejandra, Gejman, Roger, Fadic, Ricardo, Santos, José Luis

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Survival of patients with brain metastases by Lovo, Eduardo, Torrealba, Gonzalo, Villanueva, Pablo, Gejman, Roger, Tagle, Patricio

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Temporal lobe epilepsy surgery with limited resources: Results and economic considerations: Epilepsy surgery in developing countries by CAMPOS, M. G, GODOY, J, MESA, M. T, TORREALBA, G, GEJMAN, R, HUETE, I

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Silent adenoma type 3: the importance of the ultrastructural study in the differential diagnosis of pituitary adenoma associated with hyperprolactinemia in a case by Quevedo, I, Rodríguez, J A, Gejman, R, Méndez, J

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Genetics of Schizophrenia: New Findings and Challenges by Gejman, Pablo V, Sanders, Alan R, Kendler, Kenneth S

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GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores by Mullins, Niamh, Bigdeli, Tim B, Børglum, Anders D, Coleman, Jonathan R.I, Demontis, Ditte, Mehta, Divya, Ripke, Stephan, Stahl, Eli A, Starnawska, Anna, Anjorin, Adebayo, Corvin, Aiden, Sanders, Alan R, Forstner, Andreas J, Reif, Andreas, Koller, Anna C, Świątkowska, Beata, Baune, Bernhard T, Müller-Myhsok, Bertram, Penninx, Brenda W.J.H, Pato, Carlos, Rujescu, Dan, Hougaard, David M, Quested, Digby, Levinson, Douglas F, Binder, Elisabeth B, Byrne, Enda M, Agerbo, Esben, Streit, Fabian, Mayoral, Fermin, Bellivier, Frank, Degenhardt, Franziska, Breen, Gerome, Morken, Gunnar, Turecki, Gustavo, Rouleau, Guy A, Grabe, Hans J, Jones, Ian, Agartz, Ingrid, Lawrence, Jacob, Walters, James T.R, Strohmaier, Jana, Shi, Jianxin, Hauser, Joanna, Biernacka, Joanna M, Vincent, John B, Kelsoe, John, Strauss, John S, Smoller, Jordan W, Guzman-Parra, José, Berger, Klaus, Scott, Laura J, Jones, Lisa A, Azevedo, M. Helena, Trzaskowski, Maciej, Kogevinas, Manolis, Rietschel, Marcella, Boks, Marco, Ising, Marcus, Grigoroiu-Serbanescu, Maria, Hamshere, Marian L, Leboyer, Marion, Nöthen, Markus M, Preisig, Martin, Boehnke, Michael, O’Donovan, Michael C, Owen, Michael J, Pato, Michele T, Renteria, Miguel E, Budde, Monika, Weissman, Myrna M, Wray, Naomi R, Bass, Nicholas, Craddock, Nicholas, Smeland, Olav B, Mors, Ole, Gejman, Pablo V, Sklar, Pamela, McGrath, Patrick, Hoffmann, Per, McGuffin, Peter, Lee, Phil H, Mortensen, Preben Bo, Kahn, René S, Ophoff, Roel A, Adolfsson, Rolf, Van der Auwera, Sandra, Djurovic, Srdjan, Heilmann-Heimbach, Stefanie, Jamain, Stéphane, Hamilton, Steven P, Lucae, Susanne, Schulze, Thomas G, Hansen, Thomas, Werge, Thomas, Air, Tracy M, Nimgaonkar, Vishwajit, Appadurai, Vivek, Cahn, Wiepke, McQuillin, Andrew, Lewis, Cathryn M

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Open Chromatin Profiling in hiPSC-Derived Neurons Prioritizes Functional Noncoding Psychiatric Risk Variants and Highlights Neurodevelopmental Loci by Forrest, Marc P., Zhang, Hanwen, Moy, Winton, McGowan, Heather, Leites, Catherine, Dionisio, Leonardo E., Xu, Zihui, Shi, Jianxin, Sanders, Alan R., Greenleaf, William J., Cowan, Chad A., Pang, Zhiping P., Gejman, Pablo V., Penzes, Peter, Duan, Jubao

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Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent by de Candia, Teresa R., Lee, S. Hong, Yang, Jian, Browning, Brian L., Gejman, Pablo V., Levinson, Douglas F., Mowry, Bryan J., Hewitt, John K., Goddard, Michael E., O’Donovan, Michael C., Purcell, Shaun M., Posthuma, Danielle, Visscher, Peter M., Wray, Naomi R., Keller, Matthew C.

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Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications by Levinson, Douglas F., Duan, Jubao, Oh, Sang, Wang, Kai, Sanders, Alan R., Shi, Jianxin, Zhang, Nancy, Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Kendler, Kenneth S., Freedman, Robert, Dudbridge, Frank, Pe'er, Itsik, Hakonarson, Hakon, Bergen, Sarah E., Fanous, Ayman H., Holmans, Peter A., Gejman, Pablo V.

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Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell–Derived Neurons by Parnell, Euan, Culotta, Lorenza, Forrest, Marc P., Jalloul, Hiba A., Eckman, Blair L., Loizzo, Daniel D., Horan, Katherine K.E., Dos Santos, Marc, Piguel, Nicolas H., Tai, Derek J.C., Zhang, Hanwen, Gertler, Tracy S., Simkin, Dina, Sanders, Alan R., Talkowski, Michael E., Gejman, Pablo V., Kiskinis, Evangelos, Duan, Jubao, Penzes, Peter

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CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 by Rees, Elliott, Walters, James T R, Chambert, Kimberly D, O'Dushlaine, Colm, Szatkiewicz, Jin, Richards, Alexander L, Georgieva, Lyudmila, Mahoney-Davies, Gerwyn, Legge, Sophie E, Moran, Jennifer L, Genovese, Giulio, Levinson, Douglas, Morris, Derek W, Cormican, Paul, Kendler, Kenneth S, O'Neill, Francis A, Riley, Brien, Gill, Michael, Corvin, Aiden, Sklar, Pamela, Hultman, Christina, Pato, Carlos, Pato, Michele, Sullivan, Patrick F, Gejman, Pablo V, McCarroll, Steven A, O'Donovan, Michael C, Owen, Michael J, Kirov, George

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