Multi-model functionalization of disease-associated PTEN missense mutations identifies multiple molecular mechanisms underlying protein dysfunction von Post, Kathryn L., Belmadani, Manuel, Ganguly, Payel, Meili, Fabian, Dingwall, Riki, McDiarmid, Troy A., Meyers, Warren M., Herrington, Caitlin, Young, Barry P., Callaghan, Daniel B., Rogic, Sanja, Edwards, Matthew, Niciforovic, Ana, Cau, Alessandro, Rankin, Catharine H., O’Connor, Timothy P., Bamji, Shernaz X., Loewen, Christopher J. R., Allan, Douglas W., Pavlidis, Paul, Haas, Kurt

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Whole transcriptome sequencing reveals recurrent NOTCH1 mutations in mantle cell lymphoma von Kridel, Robert, Meissner, Barbara, Rogic, Sanja, Boyle, Merrill, Telenius, Adele, Woolcock, Bruce, Gunawardana, Jay, Jenkins, Catherine E., Cochrane, Chris, Ben-Neriah, Susana, Tan, King, Morin, Ryan D., Opat, Stephen, Sehn, Laurie H., Connors, Joseph M., Marra, Marco A., Weng, Andrew P., Steidl, Christian, Gascoyne, Randy D.

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Recurrent somatic mutations of PTPN1 in primary mediastinal B cell lymphoma and Hodgkin lymphoma von Gunawardana, Jay, Chan, Fong Chun, Telenius, Adèle, Woolcock, Bruce, Kridel, Robert, Tan, King L, Ben-Neriah, Susana, Mottok, Anja, Lim, Raymond S, Boyle, Merrill, Rogic, Sanja, Rimsza, Lisa M, Guiter, Chrystelle, Leroy, Karen, Gaulard, Philippe, Haioun, Corinne, Marra, Marco A, Savage, Kerry J, Connors, Joseph M, Shah, Sohrab P, Gascoyne, Randy D, Steidl, Christian

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The E3 ubiquitin ligase UBR5 is recurrently mutated in mantle cell lymphoma von Meissner, Barbara, Kridel, Robert, Lim, Raymond S., Rogic, Sanja, Tse, Kane, Scott, David W., Moore, Richard, Mungall, Andy J., Marra, Marco A., Connors, Joseph M., Steidl, Christian, Gascoyne, Randy D.

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Gene Expression–Based Model Using Formalin-Fixed Paraffin-Embedded Biopsies Predicts Overall Survival in Advanced-Stage Classical Hodgkin Lymphoma von SCOTT, David W, CHAN, Fong Chun, WOOLCOCK, Bruce W, FARINHA, Pedro, FISHER, Richard I, RIMSZA, Lisa M, BARTLETT, Nancy L, CHESON, Bruce D, SHEPHERD, Lois E, ADVANI, Ranjana H, CONNORS, Joseph M, KAHL, Brad S, FANGXIN HONG, GORDON, Leo I, HORNING, Sandra J, STEIDL, Christian, GASCOYNE, Randy D, ROGIC, Sanja, TAN, King L, MEISSNER, Barbara, BEN-NERIAH, Susana, BOYLE, Merrill, KRIDEL, Robert, TELENIUS, Adele

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TBL1XR1/TP63: a novel recurrent gene fusion in B-cell non-Hodgkin lymphoma von Scott, David W., Mungall, Karen L., Ben-Neriah, Susana, Rogic, Sanja, Morin, Ryan D., Slack, Graham W., Tan, King L., Chan, Fong Chun, Lim, Raymond S., Connors, Joseph M., Marra, Marco A., Mungall, Andrew J., Steidl, Christian, Gascoyne, Randy D.

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An RCOR1 loss–associated gene expression signature identifies a prognostically significant DLBCL subgroup von Chan, Fong Chun, Telenius, Adele, Healy, Shannon, Ben-Neriah, Susana, Mottok, Anja, Lim, Raymond, Drake, Marie, Hu, Sandy, Ding, Jiarui, Ha, Gavin, Scott, David W., Kridel, Robert, Bashashati, Ali, Rogic, Sanja, Johnson, Nathalie, Morin, Ryan D., Rimsza, Lisa M., Sehn, Laurie, Connors, Joseph M., Marra, Marco A., Gascoyne, Randy D., Shah, Sohrab P., Steidl, Christian

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Evaluation of gene-finding programs on mammalian sequences von Rogic, S, Mackworth, A K, Ouellette, F B

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Correlation between the secondary structure of pre-mRNA introns and the efficiency of splicing in Saccharomyces cerevisiae von Rogic, Sanja, Montpetit, Ben, Hoos, Holger H, Mackworth, Alan K, Ouellette, Bf Francis, Hieter, Philip

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Meta-Analysis of Gene Expression Patterns in Animal Models of Prenatal Alcohol Exposure Suggests Role for Protein Synthesis Inhibition and Chromatin Remodeling von Rogic, Sanja, Wong, Albertina, Pavlidis, Paul

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Meta-analysis of kindling-induced gene expression changes in the rat hippocampus von Rogic, Sanja, Pavlidis, Paul

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3D-QSAR-based pharmacophore determination and design of novel DPP-4 inhibitors von Rogić, Sanja, Gagić, Žarko

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Meta-Analysis of Gene Expression in Autism Spectrum Disorder von Ch'ng, Carolyn, Kwok, Willie, Rogic, Sanja, Pavlidis, Paul

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Concurrent Expression of MYC and BCL2 in Diffuse Large B-Cell Lymphoma Treated With Rituximab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone von JOHNSON, Nathalie A, SLACK, Graham W, CHAN, Wing C, IQBAL, Javeed, MEYER, Paul N, LENZ, Georg, WRIGHT, George, RIMSZA, Lisa M, VALENTINO, Carlo, BRUNHOEBER, Patrick, GROGAN, Thomas M, BRAZIEL, Rita M, SAVAGE, Kerry J, COOK, James R, TUBBS, Raymond R, WEISENBURGER, Dennis D, CAMPO, Elias, ROSENWALD, Andreas, OTT, German, DELABIE, Jan, HOLCROFT, Christina, JAFFE, Elaine S, STAUDT, Louis M, CONNORS, Joseph M, GASCOYNE, Randy D, BEN-NERIAH, Susana, ROGIC, Sanja, SCOTT, David W, TAN, King L, STEIDL, Christian, SEHN, Laurie H

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T74. HIGH YIELD OF DEEP PHENOTYPING AND LONG READ WHOLE GENOME SEQUENCING IN TREATMENT-RESISTANT PSYCHOSIS von Singh, Gagan, Rajan-Babu, Indhu-Shree, Carrion, Prescilla, Rowell, William, Rogic, Sanja, Pour, Mohadeseh Gharib, Guron, Mike, MacIsaac, Julie, Minor, Agata, Hrynchak, Monica, White, Randall, Honer, William, Sullivan, Patrick, Pavlidis, Paul, Stowe, Robert

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VariCarta: A Comprehensive Database of Harmonized Genomic Variants Found in Autism Spectrum Disorder Sequencing Studies von Belmadani, Manuel, Jacobson, Matthew, Holmes, Nathan, Phan, Minh, Nguyen, Tue, Pavlidis, Paul, Rogic, Sanja

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Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencing von Morin, Ryan D., Mungall, Karen, Pleasance, Erin, Mungall, Andrew J., Goya, Rodrigo, Huff, Ryan D., Scott, David W., Ding, Jiarui, Roth, Andrew, Chiu, Readman, Corbett, Richard D., Chan, Fong Chun, Mendez-Lago, Maria, Trinh, Diane L., Bolger-Munro, Madison, Taylor, Greg, Hadj Khodabakhshi, Alireza, Ben-Neriah, Susana, Pon, Julia, Meissner, Barbara, Woolcock, Bruce, Farnoud, Noushin, Rogic, Sanja, Lim, Emilia L., Johnson, Nathalie A., Shah, Sohrab, Jones, Steven, Steidl, Christian, Holt, Robert, Birol, Inanc, Moore, Richard, Connors, Joseph M., Gascoyne, Randy D., Marra, Marco A.

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Multi-parametric analysis of 57 SYNGAP1 variants reveal impacts on GTPase signaling, localization, and protein stability von Meili, Fabian, Wei, William J., Sin, Wun-Chey, Meyers, Warren M., Dascalu, Iulia, Callaghan, Daniel B., Rogic, Sanja, Pavlidis, Paul, Haas, Kurt

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ModelMatcher: A scientist‐centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research von Harnish, J. Michael, Li, Lucian, Rogic, Sanja, Poirier‐Morency, Guillaume, Kim, Seon‐Young, Boycott, Kym M., Wangler, Michael F., Bellen, Hugo J., Hieter, Philip, Pavlidis, Paul, Liu, Zhandong, Yamamoto, Shinya

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ASSESSING THE UTILITY OF PHARMACOGENETIC TESTING IN A COHORT WITH TREATMENT-RESISTANT SCHIZOPHRENIA OR SCHIZOAFFECTIVE DISORDER von Verzosa, Natasha, Williams, Hilary, Rafizadeh, Reza, Narang, Ankita, Carrion, Prescilla, Procyshyn, Ric, White, Randall, Poirier-Morency, Guillaume, Rogic, Sanja, Mungall, Andrew, Sullivan, Patrick, Honer, William, Pavlidis, Paul, Stowe, Robert, Bousman, Chad

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