Comparative and Functional Genomic Resource for Mechanistic Studies of Human Blood Pressure–Associated Single Nucleotide Polymorphisms by Mishra, Manoj K., Liang, Eugene Y., Geurts, Aron M., Auer, Paul W.L., Liu, Pengyuan, Rao, Sridhar, Greene, Andrew S., Liang, Mingyu, Liu, Yong

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Loss of Nuclear Localized Parathyroid Hormone-Related Protein in Primary Breast Cancer Predicts Poor Clinical Outcome and Correlates with Suppressed Stat5 Signaling by Tran, Thai H, Utama, Fransiscus E, Sato, Takahiro, Peck, Amy R, Langenheim, John F, Udhane, Sameer S, Sun, Yunguang, Liu, Chengbao, Girondo, Melanie A, Kovatich, Albert J, Hooke, Jeffrey A, Shriver, Craig D, Hu, Hai, Palazzo, Juan P, Bibbo, Marluce, Auer, Paul W, Flister, Michael J, Hyslop, Terry, Mitchell, Edith P, Chervoneva, Inna, Rui, Hallgeir

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Abstract 040: Comparative Genomic Analysis and Functional Insights for Blood Pressure-Associated Single Nucleotide Polymorphisms by Liu, Yong, Mishra, Manoj, Liang, Eugene, Geurts, Aron, Auer, Paul W., Liu, Pengyuan, Rao, Sridhar, Greene, Andrew, Liang, Mingyu

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Abstract P2-09-01: Population-based risk estimates of clinical subtypes of breast cancer among carriers of germline pathogenic variants in cancer predisposition genes by Yadav, Siddhartha, Hu, Chunling, Boddicker, Nicholas J., Polley, Eric, Hart, Steven, Gnanaolivu, Rohan, Huang, Hongyan, Yao, Song, Vachon, Celine M., Teras, Lauren, Taylor, Jack A., Sandler, Dale P., Palmer, Julie R., Olson, Janet E., Neuhausen, Susan, Martinez, Elena, Lindstroem, Sara, Le Marchand, Loic, Kooperberg, Charles, Haiman, Christopher, Gaudet, Mia M., Lacey, James V., Bertrand, Kimberly A., Bernstein, Leslie, Auer, Paul W., Ambrosone, Christine, Weitzel, Jeffrey N., Kraft, Peter, Goldgar, David E., Nathanson, Katherine L., Domchek, Susan M., Couch, Fergus J.

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Abstract PR3: Framework for post-GWAS functional annotation of regulatory regions associated with susceptibility loci for colorectal cancer by Rosse, Stephanie A., T. Chen, Christina, J. Kahsai, Orsalem, S. Zebari, Ahmad, W. Livermore Auer, Paul, Casey, Graham, Peters, Ulrike, S. Carlson, Christopher

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fate of duplicated genes in a polyploid plant genome by Roulin, Anne, Auer, Paul L, Libault, Marc, Schlueter, Jessica, Farmer, Andrew, May, Greg, Stacey, Gary, Doerge, Rebecca W, Jackson, Scott A

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Statistical design and analysis of RNA sequencing data by Auer, Paul L, Doerge, R W

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Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results by Tabor, Holly K., Auer, Paul L., Jamal, Seema M., Chong, Jessica X., Yu, Joon-Ho, Gordon, Adam S., Graubert, Timothy A., O’Donnell, Christopher J., Rich, Stephen S., Nickerson, Deborah A., Bamshad, Michael J.

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Multi-centre reproducibility of diffusion MRI parameters for clinical sequences in the brain by Grech-Sollars, Matthew, Hales, Patrick W., Miyazaki, Keiko, Raschke, Felix, Rodriguez, Daniel, Wilson, Martin, Gill, Simrandip K., Banks, Tina, Saunders, Dawn E., Clayden, Jonathan D., Gwilliam, Matt N., Barrick, Thomas R., Morgan, Paul S., Davies, Nigel P., Rossiter, James, Auer, Dorothee P., Grundy, Richard, Leach, Martin O., Howe, Franklyn A., Peet, Andrew C., Clark, Chris A.

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TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data by Huang, Le, Rosen, Jonathan D., Sun, Quan, Chen, Jiawen, Wheeler, Marsha M., Zhou, Ying, Min, Yuan-I, Kooperberg, Charles, Conomos, Matthew P., Stilp, Adrienne M., Rich, Stephen S., Rotter, Jerome I., Manichaikul, Ani, Loos, Ruth J.F., Kenny, Eimear E., Blackwell, Thomas W., Smith, Albert V., Jun, Goo, Sedlazeck, Fritz J., Metcalf, Ginger, Boerwinkle, Eric, Raffield, Laura M., Reiner, Alex P., Auer, Paul L., Li, Yun

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Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project by Johnsen, Jill M., Auer, Paul L., Morrison, Alanna C., Jiao, Shuo, Wei, Peng, Haessler, Jeffrey, Fox, Keolu, McGee, Sean R., Smith, Joshua D., Carlson, Christopher S., Smith, Nicholas, Boerwinkle, Eric, Kooperberg, Charles, Nickerson, Deborah A., Rich, Stephen S., Green, David, Peters, Ulrike, Cushman, Mary, Reiner, Alex P.

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The Cooperative Activities of CSLD2, CSLD3, and CSLD5 Are Required for Normal Arabidopsis Development by Yin, Lan, Verhertbruggen, Yves, Oikawa, Ai, Manisseri, Chithra, Knierim, Bernhard, Prak, Lina, Jensen, Jacob Krüger, Knox, J. Paul, Auer, Manfred, Willats, William G.T., Scheller, Henrik Vibe

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Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset by Gordon, Adam S, Tabor, Holly K, Johnson, Andrew D, Snively, Beverly M, Assimes, Themistocles L, Auer, Paul L, Ioannidis, John P A, Peters, Ulrike, Robinson, Jennifer G, Sucheston, Lara E, Wang, Danxin, Sotoodehnia, Nona, Rotter, Jerome I, Psaty, Bruce M, Jackson, Rebecca D, Herrington, David M, O'Donnell, Christopher J, Reiner, Alexander P, Rich, Stephen S, Rieder, Mark J, Bamshad, Michael J, Nickerson, Deborah A

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Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixe... by Kowalski, Madeline H, Qian, Huijun, Hou, Ziyi, Rosen, Jonathan D, Tapia, Amanda L, Shan, Yue, Jain, Deepti, Argos, Maria, Arnett, Donna K, Avery, Christy, Barnes, Kathleen C, Becker, Lewis C, Bien, Stephanie A, Bis, Joshua C, Blangero, John, Boerwinkle, Eric, Bowden, Donald W, Buyske, Steve, Cai, Jianwen, Cho, Michael H, Choi, Seung Hoan, Choquet, Hélène, Cupples, L Adrienne, Cushman, Mary, Daya, Michelle, de Vries, Paul S, Ellinor, Patrick T, Faraday, Nauder, Fornage, Myriam, Gabriel, Stacey, Ganesh, Santhi K, Graff, Misa, Gupta, Namrata, He, Jiang, Heckbert, Susan R, Hidalgo, Bertha, Hodonsky, Chani J, Irvin, Marguerite R, Johnson, Andrew D, Jorgenson, Eric, Kaplan, Robert, Kardia, Sharon L R, Kelly, Tanika N, Kooperberg, Charles, Lasky-Su, Jessica A, Loos, Ruth J F, Lubitz, Steven A, Mathias, Rasika A, McHugh, Caitlin P, Montgomery, Courtney, Moon, Jee-Young, Morrison, Alanna C, Palmer, Nicholette D, Pankratz, Nathan, Papanicolaou, George J, Peralta, Juan M, Peyser, Patricia A, Rich, Stephen S, Rotter, Jerome I, Silverman, Edwin K, Smith, Jennifer A, Smith, Nicholas L, Taylor, Kent D, Thornton, Timothy A, Tiwari, Hemant K, Tracy, Russell P, Wang, Tao, Weiss, Scott T, Weng, Lu-Chen, Wiggins, Kerri L, Wilson, James G, Yanek, Lisa R, Zöllner, Sebastian, North, Kari E, Auer, Paul L, Raffield, Laura M, Reiner, Alexander P, Li, Yun

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Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project by Hu, Yao, Haessler, Jeffrey W., Manansala, Regina, Wiggins, Kerri L., Moscati, Arden, Beiser, Alexa, Heard-Costa, Nancy L., Sarnowski, Chloe, Raffield, Laura M., Chung, Jaeyoon, Marini, Sandro, Anderson, Christopher D., Rosand, Jonathan, Xu, Huichun, Sun, Xiao, Kelly, Tanika N., Wong, Quenna, Lange, Leslie A., Rotter, Jerome I., Correa, Adolfo, Vasan, Ramachandran S., Seshadri, Sudha, Rich, Stephen S., Do, Ron, Loos, Ruth J.F., Longstreth, William T., Bis, Joshua C., Psaty, Bruce M., Tirschwell, David L., Assimes, Themistocles L., Silver, Brian, Liu, Simin, Jackson, Rebecca, Wassertheil-Smoller, Sylvia, Mitchell, Braxton D., Fornage, Myriam, Auer, Paul L., Reiner, Alex P., Kooperberg, Charles

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Differences in the Circulating Proteome in Individuals with versus without Sickle Cell Trait by Cai, Yanwei, Franceschini, Nora, Surapaneni, Aditya, Garrett, Melanie E, Tahir, Usman A, Hsu, Li, Telen, Marilyn J, Yu, Bing, Tang, Hua, Li, Yun, Liu, Simin, Gerszten, Robert E, Coresh, Josef, Manson, JoAnn E, Wojcik, Genevieve L, Kooperberg, Charles, Auer, Paul L, Foster, Matthew W, Grams, Morgan E, Ashley-Koch, Allison E, Raffield, Laura M, Reiner, Alex P

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Clonal haematopoiesis and risk of chronic liver disease by Wong, Waihay J., Emdin, Connor, Bick, Alexander G., Zekavat, Seyedeh M., Niroula, Abhishek, Pirruccello, James P., Dichtel, Laura, Griffin, Gabriel, Uddin, Md Mesbah, Gibson, Christopher J., Kovalcik, Veronica, Lin, Amy E., McConkey, Marie E., Vromman, Amelie, Sellar, Rob S., Kim, Peter G., Agrawal, Mridul, Weinstock, Joshua, Long, Michelle T., Yu, Bing, Banerjee, Rajarshi, Nicholls, Rowan C., Dennis, Andrea, Kelly, Matt, Loh, Po-Ru, McCarroll, Steve, Boerwinkle, Eric, Vasan, Ramachandran S., Jaiswal, Siddhartha, Johnson, Andrew D., Chung, Raymond T., Corey, Kathleen, Levy, Daniel, Ballantyne, Christie, Ebert, Benjamin L., Natarajan, Pradeep

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Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture by Forgetta, Vincenzo, Estrada, Karol, Leo, Paul J., Dahia, Chitra L., Liu, Ching‐Ti, Uggla, Charlotta, Evans, Daniel S., Walter, Klaudia, Pettersson‐Kymmer, Ulrika, McCarthy, Shane, Kwan, Tony, Jhamai, Mila, Trajanoska, Katerina, Huang, Jie, Danecek, Petr, Wilmot, Beth, Li, Rui, Moayyeri, Alireza, Claussnitzer, Melina, Cheng, Chia‐Ho, Cheung, Warren, Ge, Bing, Chen, Shu‐Huang, Choi, Kwangbom, Oei, Ling, Fraser, James, Hibbs, Matthew A., Gregson, Celia L., Paquette, Denis, Wibom, Carl, Tranah, Gregory J., Marshall, Mhairi, Gardiner, Brooke B., Cremin, Katie, Auer, Paul, Hsu, Li, Thorleifsson, Gudmar, Enneman, Anke W., de Groot, Lisette C. P. G. M., Melin, Beatrice, Christiansen, Claus, Sayers, Adrian, Zhou, Yanhua, Calderari, Sophie, van Rooij, Jeroen, Carlson, Chris, Peters, Ulrike, Uitterlinden, Andre G., Williams, Stephen R., Farber, Charles, Grinberg, Daniel, Chasman, Daniel I., Giulianini, Franco, Ridker, Paul M., Eisman, John A., Nguyen, Tuan V., Center, Jacqueline R., Garcia‐Giralt, Natalia, Mellström, Dan, Vandenput, Liesbeth, Amin, Najaf, van Duijn, Cornelia M., Karlsson, Magnus K., Svensson, Olle, Rousseau, François, Bussière, Johanne, Koromani, Fjorda, Langdahl, Bente L., Jensen, Jens‐Erik B., Kaptoge, Stephen, Khaw, Kay‐Tee, Reeve, Jonathan, Xuereb‐Anastasi, Angela, Åkesson, Kristina, Olmos, Jose M., Zarrabeitia, Maria T., Riancho, Jose A., Alonso, Nerea, Jiang, Xi, Goltzman, David, Grundberg, Elin, Gauguier, Dominique, Orwoll, Eric S., Karasik, David, Davey‐Smith, George, Smith, Albert V., Harris, Tamara B., Carola Zillikens, M., Thorsteinsdottir, Unnur, Soranzo, Nicole, Durbin, Richard, Brown, Matthew A., Spector, Tim, Adrienne Cupples, L., Greenwood, Celia M. T., Jackson, Rebecca D., Rowe, David W., Loomis, Cynthia A., Ackert‐Bicknell, Cheryl L., Kiel, Douglas P.

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Comparison of Proteomic Assessment Methods in Multiple Cohort Studies by Raffield, Laura M., Dang, Hong, Pratte, Katherine A., Jacobson, Sean, Gillenwater, Lucas A., Ampleford, Elizabeth, Barjaktarevic, Igor, Basta, Patricia, Clish, Clary B., Comellas, Alejandro P., Cornell, Elaine, Curtis, Jeffrey L., Doerschuk, Claire, Durda, Peter, Emson, Claire, Freeman, Christine M., Guo, Xiuqing, Hastie, Annette T., Hawkins, Gregory A., Herrera, Julio, Johnson, W. Craig, Labaki, Wassim W., Liu, Yongmei, Masters, Brett, Miller, Michael, Ortega, Victor E., Papanicolaou, George, Peters, Stephen, Taylor, Kent D., Rich, Stephen S., Rotter, Jerome I., Auer, Paul, Reiner, Alex P., Tracy, Russell P., Ngo, Debby, Gerszten, Robert E., O'Neal, Wanda K., Bowler, Russell P.

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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction by Do, Ron, Stitziel, Nathan O., Won, Hong-Hee, Jørgensen, Anders Berg, Duga, Stefano, Angelica Merlini, Pier, Kiezun, Adam, Farrall, Martin, Goel, Anuj, Zuk, Or, Guella, Illaria, Asselta, Rosanna, Lange, Leslie A., Peloso, Gina M., Auer, Paul L., Girelli, Domenico, Martinelli, Nicola, Farlow, Deborah N., DePristo, Mark A., Roberts, Robert, Stewart, Alexander F. R., Saleheen, Danish, Danesh, John, Epstein, Stephen E., Sivapalaratnam, Suthesh, Kees Hovingh, G., Kastelein, John J., Samani, Nilesh J., Schunkert, Heribert, Erdmann, Jeanette, Shah, Svati H., Kraus, William E., Davies, Robert, Nikpay, Majid, Johansen, Christopher T., Wang, Jian, Hegele, Robert A., Hechter, Eliana, Marz, Winfried, Kleber, Marcus E., Huang, Jie, Johnson, Andrew D., Li, Mingyao, Burke, Greg L., Gross, Myron, Liu, Yongmei, Assimes, Themistocles L., Heiss, Gerardo, Lange, Ethan M., Folsom, Aaron R., Taylor, Herman A., Olivieri, Oliviero, Hamsten, Anders, Clarke, Robert, Reilly, Dermot F., Yin, Wu, Rivas, Manuel A., Donnelly, Peter, Rossouw, Jacques E., Psaty, Bruce M., Herrington, David M., Wilson, James G., Rich, Stephen S., Bamshad, Michael J., Tracy, Russell P., Adrienne Cupples, L., Rader, Daniel J., Reilly, Muredach P., Spertus, John A., Cresci, Sharon, Hartiala, Jaana, Wilson Tang, W. H., Hazen, Stanley L., Allayee, Hooman, Reiner, Alex P., Carlson, Christopher S., Kooperberg, Charles, Jackson, Rebecca D., Boerwinkle, Eric, Lander, Eric S., Schwartz, Stephen M., Siscovick, David S., McPherson, Ruth, Tybjaerg-Hansen, Anne, Abecasis, Goncalo R., Watkins, Hugh, Nickerson, Deborah A., Ardissino, Diego, Sunyaev, Shamil R., O'Donnell, Christopher J., Altshuler, David, Gabriel, Stacey, Kathiresan, Sekar

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