LinkedOmics: analyzing multi-omics data within and across 32 cancer types von Vasaikar, Suhas V, Straub, Peter, Wang, Jing, Zhang, Bing

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Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome von Hirbo, Jibril B, Pasutto, Francesca, Gamazon, Eric R, Evans, Patrick, Pawar, Priyanka, Berner, Daniel, Sealock, Julia, Tao, Ran, Straub, Peter S, Konkashbaev, Anuar I, Breyer, Max A, Schlötzer-Schrehardt, Ursula, Reis, André, Brantley, Jr, Milam A, Khor, Chiea C, Joos, Karen M, Cox, Nancy J

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Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease von Dennis, Jessica K, Sealock, Julia M, Straub, Peter, Lee, Younga H, Hucks, Donald, Actkins, Ky'Era, Faucon, Annika, Feng, Yen-Chen Anne, Ge, Tian, Goleva, Slavina B, Niarchou, Maria, Singh, Kritika, Morley, Theodore, Smoller, Jordan W, Ruderfer, Douglas M, Mosley, Jonathan D, Chen, Guanhua, Davis, Lea K

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Dense phenotyping from electronic health records enables machine learning-based prediction of preterm birth von Abraham, Abin, Le, Brian, Kosti, Idit, Straub, Peter, Velez-Edwards, Digna R, Davis, Lea K, Newton, J M, Muglia, Louis J, Rokas, Antonis, Bejan, Cosmin A, Sirota, Marina, Capra, John A

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Predicted expression of genes involved in the thiopurine metabolic pathway and azathioprine discontinuation due to myelotoxicity von Daniel, Laura L., Dickson, Alyson L., Zanussi, Jacy T., Miller‐Fleming, Tyne W., Straub, Peter S., Wei, Wei‐Qi, Plummer, W. Dale, Dupont, William D., Liu, Ge, Anandi, Prathima, Reese, Tyler S., Birdwell, Kelly A., Kawai, Vivian K., Hung, Adriana M., Cox, Nancy J., Feng, QiPing, Stein, C. Michael, Chung, Cecilia P.

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Fine-scale sampling uncovers the complexity of migrations in 5th–6th century Pannonia von Vyas, Deven N., Koncz, István, Modi, Alessandra, Mende, Balázs Gusztáv, Tian, Yijie, Francalacci, Paolo, Lari, Martina, Vai, Stefania, Straub, Péter, Gallina, Zsolt, Szeniczey, Tamás, Hajdu, Tamás, Pejrani Baricco, Luisella, Giostra, Caterina, Radzevičiūtė, Rita, Hofmanová, Zuzana, Évinger, Sándor, Bernert, Zsolt, Pohl, Walter, Caramelli, David, Vida, Tivadar, Geary, Patrick J., Veeramah, Krishna R.

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Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia in 106,160 Patients Across Four Health Care Systems von Zheutlin, Amanda B, Dennis, Jessica, Karlsson Linnér, Richard, Moscati, Arden, Restrepo, Nicole, Straub, Peter, Ruderfer, Douglas, Castro, Victor M, Chen, Chia-Yen, Ge, Tian, Huckins, Laura M, Charney, Alexander, Kirchner, H. Lester, Stahl, Eli A, Chabris, Christopher F, Davis, Lea K, Smoller, Jordan W

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T95. ITERATING TOWARDS PRECISION PHENOTYPING OF SCHIZOPHRENIA IN THE ELECTRONIC HEALTH RECORD von Lake, Allison M., Reddy, India A., Straub, Peter, Davis, Lea K.

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Abstract 5112: LinkedOmics: Analyzing multi-omics data within and across 32 cancer types von Vasaikar, Suhas, Straub, Peter, Wang, Jing, Zhang, Bing

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The Process Is a Process All Its Own von Straub, Peter

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Identification, recovery, and impact of ghost fishing gear in the Mullica River-Great Bay Estuary (New Jersey, USA): Stakeholder-driven restoration for smaller-scale systems von Sullivan, Mark, Evert, Steven, Straub, Peter, Reding, Melanie, Robinson, Nathan, Zimmermann, Elizabeth, Ambrose, David

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TU3. A PHENOME-WIDE ASSOCIATION STUDY OF POLYGENIC RISK FOR ATTENTION DEFICIT HYPERACTIVITY DISORDER ACROSS TWO GENETIC ANCESTRIES IN ELECTRONIC HEALTH RECORD DATA von Niarchou, Maria, Sealock, Julia, Straub, Peter, Sanchez-Roige, Sandra, Sutcliffe, James, Davis, Lea K.

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Use of the PsycheMERGE Network to Investigate the Association Between Depression Polygenic Scores and White Blood Cell Count von Sealock, Julia M, Lee, Younga H, Moscati, Arden, Venkatesh, Sanan, Voloudakis, Georgios, Straub, Peter, Singh, Kritika, Feng, Yen-Chen A, Ge, Tian, Roussos, Panos, Smoller, Jordan W, Chen, Guanhua, Davis, Lea K

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Exploring genetic risk for catatonia in a genome wide association study and polygenic risk score analysis von Wilson, Jo Ellen, Sealock, Julia, Straub, Peter, Raman, Rameela, Kipp, Aaron M, Dittus, Robert S, Heckers, Stephan, Ely, Wes, Davis, Lea K

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The Collected Short Stories of Freddie Prothero: Introduction by Törless Magnussen, PhD von Straub, Peter

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Investigating the genetic pathways of insomnia in Autism Spectrum Disorder von Niarchou, Maria, Singer, Emily V., Straub, Peter, Malow, Beth A., Davis, Lea K.

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90 INVESTIGATING THE SHARED GENETIC ARCHITECTURE BETWEEN CORONARY ARTERY DISEASE AND MAJOR DEPRESSIVE DISORDER von Singh, Kritika, Dennis, Jessica, Sealock, Julia, Scott, Timothy, Straub, Peter, Hucks, Donald, Hodges, Emily, Davis, Lea

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Neil Gaiman: An Introduction von Straub, Peter

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Genome-wide meta-analysis of myasthenia gravis uncovers new loci and provides insights into polygenic prediction von Braun, Alice, Shekhar, Sudhanshu, Levey, Daniel F., Straub, Peter, Kraft, Julia, Panagiotaropoulou, Georgia M., Heilbron, Karl, Awasthi, Swapnil, Meleka Hanna, Rafael, Hoffmann, Sarah, Stein, Maike, Lehnerer, Sophie, Mergenthaler, Philipp, Elnahas, Abdelrahman G., Topaloudi, Apostolia, Koromina, Maria, Palviainen, Teemu, Asbjornsdottir, Bergrun, Stefansson, Hreinn, Skuladóttir, Astros Th, Jónsdóttir, Ingileif, Stefansson, Kari, Reis, Kadri, Esko, Tõnu, Palotie, Aarno, Leypoldt, Frank, Stein, Murray B., Fontanillas, Pierre, Kaprio, Jaakko, Gelernter, Joel, Davis, Lea K., Paschou, Peristera, Tannemaat, Martijn R., Verschuuren, Jan J.G.M., Kuhlenbäumer, Gregor, Gregersen, Peter K., Huijbers, Maartje G., Stascheit, Frauke, Meisel, Andreas, Ripke, Stephan

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A phenome‐wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data von Niarchou, Maria, Sealock, Julia M., Straub, Peter, Sanchez‐Roige, Sandra, Sutcliffe, James S., Davis, Lea K.

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