Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation by Choi, Seung Hoan, Weng, Lu-Chen, Roselli, Carolina, Lin, Honghuang, Haggerty, Christopher M, Shoemaker, M. Benjamin, Barnard, John, Arking, Dan E, Chasman, Daniel I, Albert, Christine M, Chaffin, Mark, Tucker, Nathan R, Smith, Jonathan D, Gupta, Namrata, Gabriel, Stacey, Margolin, Lauren, Shea, Marisa A, Shaffer, Christian M, Yoneda, Zachary T, Boerwinkle, Eric, Smith, Nicholas L, Silverman, Edwin K, Redline, Susan, Vasan, Ramachandran S, Burchard, Esteban G, Gogarten, Stephanie M, Laurie, Cecelia, Blackwell, Thomas W, Abecasis, Gonçalo, Carey, David J, Fornwalt, Brandon K, Smelser, Diane T, Baras, Aris, Dewey, Frederick E, Jaquish, Cashell E, Papanicolaou, George J, Sotoodehnia, Nona, Van Wagoner, David R, Psaty, Bruce M, Kathiresan, Sekar, Darbar, Dawood, Alonso, Alvaro, Heckbert, Susan R, Chung, Mina K, Roden, Dan M, Benjamin, Emelia J, Murray, Michael F, Lunetta, Kathryn L, Lubitz, Steven A, Ellinor, Patrick T

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Genome-first approach of the prevalence and cancer phenotypes of pathogenic or likely pathogenic germline TP53 variants by de Andrade, Kelvin C., Strande, Natasha T., Kim, Jung, Haley, Jeremy S., Hatton, Jessica N., Frone, Megan N., Khincha, Payal P., Thone, Gretchen M., Mirshahi, Uyenlinh L., Schneider, Cynthia, Desai, Heena, Dove, James T., Smelser, Diane T., Levine, Arnold J., Maxwell, Kara N., Stewart, Douglas R., Carey, David J., Savage, Sharon A.

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Genetic-based prediction of disease traits: prediction is very difficult, especially about the future by Schrodi, Steven J, Mukherjee, Shubhabrata, Shan, Ying, Tromp, Gerard, Sninsky, John J, Callear, Amy P, Carter, Tonia C, Ye, Zhan, Haines, Jonathan L, Brilliant, Murray H, Crane, Paul K, Smelser, Diane T, Elston, Robert C, Weeks, Daniel E

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Familial Hypocalciuric Hypercalcemia Type 1 and Autosomal-Dominant Hypocalcemia Type 1: Prevalence in a Large Healthcare Population by Dershem, Ridge, Gorvin, Caroline M., Metpally, Raghu P.R., Krishnamurthy, Sarathbabu, Smelser, Diane T., Hannan, Fadil M., Carey, David J., Thakker, Rajesh V., Breitwieser, Gerda E.

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Population risk factor estimates for abdominal aortic aneurysm from electronic medical records: a case control study by Smelser, Diane T, Tromp, Gerard, Elmore, James R, Kuivaniemi, Helena, Franklin, David P, Kirchner, H Lester, Carey, David J

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Genomics-First Evaluation of Heart Disease Associated With Titin-Truncating Variants by Haggerty, Christopher M, Damrauer, Scott M, Levin, Michael G, Birtwell, David, Carey, David J, Golden, Alicia M, Hartzel, Dustin N, Hu, Yirui, Judy, Renae, Kelly, Melissa A, Kember, Rachel L, Lester Kirchner, H, Leader, Joseph B, Liang, Lusha, McDermott-Roe, Chris, Babu, Apoorva, Morley, Michael, Nealy, Zachariah, Person, Thomas N, Pulenthiran, Arichanah, Small, Aeron, Smelser, Diane T, Stahl, Richard C, Sturm, Amy C, Williams, Heather, Baras, Aris, Margulies, Kenneth B, Cappola, Thomas P, Dewey, Frederick E, Verma, Anurag, Zhang, Xinyuang, Correa, Adolfo, Hall, Michael E, Wilson, James G, Ritchie, Marylyn D, Rader, Daniel J, Murray, Michael F, Fornwalt, Brandon K, Arany, Zoltan

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Update on Abdominal Aortic Aneurysm Research: From Clinical to Genetic Studies by Smelser, Diane T., Hinterseher, Irene, Elmore, James R., Ryer, Evan J., Kuivaniemi, Helena, Tromp, Gerard

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Inflammation gene variants and susceptibility to albuminuria in the U.S. population: analysis in the Third National Health and Nutrition Examination Survey (NHANES III), 1991-1994 by Ned, Renée M, Yesupriya, Ajay, Imperatore, Giuseppina, Smelser, Diane T, Moonesinghe, Ramal, Chang, Man-Huei, Dowling, Nicole F

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Rare-variant pathogenicity triage and inclusion of synonymous variants improves analysis of disease associations of orphan G protein–coupled receptors by Dershem, Ridge, Metpally, Raghu P.R., Jeffreys, Kirk, Krishnamurthy, Sarathbabu, Smelser, Diane T., Hershfinkel, Michal, Carey, David J., Robishaw, Janet D., Breitwieser, Gerda E.

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Association of varicose veins with rare protein-truncating variants in PIEZO1 identified by exome sequencing of a large clinical population by Smelser, Diane T., Haley, Jeremy S., Ryer, Evan J., Elmore, James R., Cook, Adam M., Carey, David J.

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Do Hernias Contribute to Increased Severity of Aneurysmal Disease among Abdominal Aortic Aneurysm Patients? by Hinterseher, Irene, Miszczuk, Milena, Corvinus, Florian, Zimmermann, Carolin, Estrelinha, Mariana, Smelser, Diane T., Kuivaniemi, Helena

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Genetic Basis of Thoracic Aortic Aneurysms in a Large Unselected Clinical Population by Mirshahi, Hannah S., Haley, Jeremy S., Smelser, Diane T., Ryer, Evan J., Elmore, James R., Carey, David J.

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Genetic risk models: Influence of model size on risk estimates and precision by Shan, Ying, Tromp, Gerard, Kuivaniemi, Helena, Smelser, Diane T., Verma, Shefali S., Ritchie, Marylyn D., Elmore, James R., Carey, David J., Conley, Yvette P., Gorin, Michael B., Weeks, Daniel E.

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The ACE I/D Polymorphism in US Adults: Limited Evidence of Association With Hypertension-Related Traits and Sex-Specific Effects by Race/Ethnicity by Ned, Renée M., Yesupriya, Ajay, Imperatore, Giuseppina, Smelser, Diane T., Moonesinghe, Ramal, Chang, Man-Huei, Dowling, Nicole F.

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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure by Henry, Albert, Roselli, Carolina, Sveinbjörnsson, Garðar, Fatemifar, Ghazaleh, Hedman, Åsa K., Morley, Michael P., Helgadottir, Anna, Verweij, Niek, Dehghan, Abbas, Almgren, Peter, Andersson, Charlotte, Backman, Joshua D., Biggs, Mary L., Brandimarto, Jeffrey, Buckbinder, Leonard, Carey, David J., Chasman, Daniel I., Chen, Xu, Chung, Jonathan, Cook, James P., Delgado, Graciela E., Denaxas, Spiros, Dörr, Marcus, Dudley, Samuel C., Esko, Tõnu, Finan, Chris, Gottdiener, John S., Gross, Stefan, Guðbjartsson, Daníel F., Gutmann, Rebecca, Haggerty, Christopher M., Hyde, Craig L., Ingelsson, Erik, Jukema, J. Wouter, Kavousi, Maryam, Khaw, Kay-Tee, Kleber, Marcus E., Køber, Lars, Koekemoer, Andrea, Langenberg, Claudia, Lind, Lars, Lotta, Luca A., Luan, Jian’an, März, Winfried, Melander, Olle, Mordi, Ify R., Morgan, Thomas, Morris, Andrew D., Morris, Andrew P., Morrison, Alanna C., Nelson, Christopher P., Niessner, Alexander, Niiranen, Teemu, O’Donoghue, Michelle L., Owens, Anjali T., Parry, Helen M., Perola, Markus, Rice, Kenneth M., Ridker, Paul M., Rotter, Jerome I., Salo, Perttu, Salomaa, Veikko, Smelser, Diane T., Stender, Steen, Stott, David J., Tammesoo, Mari-Liis, Taylor, Kent D., Teder-Laving, Maris, Thorsteinsdottir, Unnur, Torp-Pedersen, Christian, Trompet, Stella, Tyl, Benoit, Uitterlinden, Andre G., Veluchamy, Abirami, Völker, Uwe, Voors, Adriaan A., Wareham, Nicholas J., Waterworth, Dawn, Weiss, Raul, Wiggins, Kerri L., Yerges-Armstrong, Laura M., Yu, Bing, Zannad, Faiez, Zhao, Jing Hua, Hemingway, Harry, McMurray, John J. V., Yang, Jian, Visscher, Peter M., Malarstig, Anders, Holm, Hilma, Sattar, Naveed, Holmes, Michael V., Cappola, Thomas P., Hingorani, Aroon D., Kuchenbaecker, Karoline, Ellinor, Patrick T., Smith, J. Gustav, Vasan, Ramachandran S., Swerdlow, Daniel I., Lumbers, R. Thomas

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Molecular Characterisation of Novel Klotho Variants Identified in Patients with Ca2+ Disturbances: FR-PO293 by Grigore, Teodora, Bayliss, Asha, Stevenson, Mark, Zuidscherwoude, Malou, Carey, David J., Haley, Jeremy S., Smelser, Diane T., Olauson, Hannes, Hoenderop, Joost, Thakker, Rajesh V.

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Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci by Tromp, Gerard, Gretarsdottir, Solveig, Baas, Annette F, Giusti, Betti, Strauss, Ewa, van‘t Hof, Femke N.G, Webb, Thomas R, Erdman, Robert, Ritchie, Marylyn D, Elmore, James R, Verma, Anurag, Pendergrass, Sarah, Kullo, Iftikhar J, Peissig, Peggy L, Verma, Shefali S, Malinowski, Jennifer, Rasmussen-Torvik, Laura J, Borthwick, Kenneth M, Smelser, Diane T, Crosslin, David R, de Andrade, Mariza, Ryer, Evan J, McCarty, Catherine A, Böttinger, Erwin P, Pacheco, Jennifer A, Carrell, David S, Franklin, David P, Phillips, Victoria L, Williams, Michael J.A, Wei, Wenhua, Blair, Ross, Hill, Andrew A, Vasudevan, Thodor M, Lewis, David R, Thomson, Ian A, Krysa, Jo, Hill, Geraldine B, Roake, Justin, Merriman, Tony R, Oszkinis, Grzegorz, Galora, Silvia, Saracini, Claudia, Abbate, Rosanna, Pulli, Raffaele, Saratzis, Athanasios, Verissimo, Ana R, Bumpstead, Suzannah, Badger, Stephen A, Clough, Rachel E, Cockerill, Gillian, Hafez, Hany, Scott, D. Julian A, Futers, T Simon, Romaine, Simon P.R, Griffin, Kathryn J, Bailey, Marc A, Smith, Alberto, van Bockxmeer, Frank M, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Blankensteijn, Jan D, Teijink, Joep A.W, de Graaf, Jacqueline, Kiemeney, Lambertus A, Lindholt, Jes S, Hughes, Anne, Bradley, Declan T, Stirrups, Kathleen, Golledge, Jonathan, Norman, Paul E, Powell, Janet T, Humphries, Steve E, Goodall, Alison H, Nelson, Christopher P, Sakalihasan, Natzi, Courtois, Audrey, Ferrell, Robert E, Eriksson, Per, Folkersen, Lasse, Franco-Cereceda, Anders, Eicher, John D, Johnson, Andrew D, Betsholtz, Christer, Ruusalepp, Arno, Franzén, Oscar, Schadt, Eric E, Lipovich, Leonard, Verhoeven, Eric L, Zeebregts, Clark J, Geelkerken, Robert H, van Sambeek, Marc R, van Sterkenburg, Steven M, de Vries, Jean-Paul, Stefansson, Kari, de Bakker, Paul I.W, Deloukas, Panos, Harrison, Seamus C, van Rij, Andre M, Samani, Nilesh J, Bown, Matthew J

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C-B3-03: Association of Epidemiologic and Genetic Factors With Abdominal Aortic Aneurysm (AAA) by Smelser, D. T, Golden, A., Masker, K., Elmore, J. R, Carey, D. J

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Effect of the CEP72 Genotype and CYP3A5-Mediated Metabolism in Predicting Vincristine-Associated Peripheral Neuropathy by Agrawal, Vaibhav, Smelser, Diane T., Carey, David J., Vadakara, Joseph J., Khan, Sharif S.

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Efficacy of 90Y-Ibritumomab Tiuxetan in the Older Population with Non-Hodgkin Lymphoma Pre-Treated with Rituximab-Based Regimens: A Single-Institution Experience by Agrawal, Vaibhav, Diane, Smelser T., Castillo, Jose I., Raup, Kelly, Treanna, Girton D., Collins, Scotty R., Brady, James O., Khan, Sharif S.

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