Reprogramming of mesenchymal stem cells by the synovial sarcoma-associated oncogene SYT–SSX2 von Garcia, C B, Shaffer, C M, Alfaro, M P, Smith, A L, Sun, J, Zhao, Z, Young, P P, VanSaun, M N, Eid, J E

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A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough von Mosley, J D, Shaffer, C M, Van Driest, S L, Weeke, P E, Wells, Q S, Karnes, J H, Velez Edwards, D R, Wei, W-Q, Teixeira, P L, Bastarache, L, Crawford, D C, Li, R, Manolio, T A, Bottinger, E P, McCarty, C A, Linneman, J G, Brilliant, M H, Pacheco, J A, Thompson, W, Chisholm, R L, Jarvik, G P, Crosslin, D R, Carrell, D S, Baldwin, E, Ralston, J, Larson, E B, Grafton, J, Scrol, A, Jouni, H, Kullo, I J, Tromp, G, Borthwick, K M, Kuivaniemi, H, Carey, D J, Ritchie, M D, Bradford, Y, Verma, S S, Chute, C G, Veluchamy, A, Siddiqui, M K, Palmer, C N A, Doney, A, MahmoudPour, S H, Maitland-van der Zee, A H, Morris, A D, Denny, J C, Roden, D M

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Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes von Ramirez, A H, Shaffer, C M, Delaney, J T, Sexton, D P, Levy, S E, Rieder, M J, Nickerson, D A, George, A L, Roden, D M

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A polymorphism in HLA-G modifies statin benefit in asthma von Naidoo, D, Wu, A C, Brilliant, M H, Denny, J, Ingram, C, Kitchner, T E, Linneman, J G, McGeachie, M J, Roden, D M, Shaffer, C M, Shah, A, Weeke, P, Weiss, S T, Xu, H, Medina, M W

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Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals von Winkler, T.W., Teumer, A., Thio, C.H.L., Li, M., Yang, Q., Nutile, T., Gunther, F., Parsa, A., Vries, A.P.J. de, Zonderman, A.B., Smith, A.V., Oldehinkel, A.J., Franke, A., Metspalu, A., Hicks, A.A., Tonjes, A., Peters, A., Ponte, B., Schottker, B., Brumpton, B., Jung, B., Ning, B., Hayward, C., Hartman, C.A., Heng, C.K., Cheng, C.Y., Willer, C.J., Toniolo, D., Waterworth, D.M., Montgomery, G.W., Snieder, H., Stringham, H.M., Schmidt, H., Tzoulaki, I., Olafsson, I., Martins, J., Cook, J.P., Halbritter, J., Felix, J.F., Divers, J., Kooner, J.S., Liu, J.J., Xu, J., Arnlov, J., Kuusisto, J., Jakobsdottir, J., Chambers, J.C., Gaziano, J.M., Marten, J., Jonas, J.B., Christensen, K., Matsuda, K., Strauch, K., Hveem, K., Wallentin, L., Raffield, L.M., Phillips, L.S., Ikram, M.A., Kleber, M.E., Francescatto, M., Concas, M.P., Piratsu, M., Laakso, M., Borst, M.H. de, Kavousi, M., Waldenberger, M., Boehnke, M., Stumvoll, M., Kastarinen, M., Martin, N.G., Pirastu, N., Hutri-Kahonen, N., Raitakari, O.T., Gasparini, P., Mishra, P.P., Magnusson, P.K.E., Elliott, P., Ridker, P.M., Joshi, P.K., Pramstaller, P.P., Vollenweider, P., Sim, R.Z.H., Burkhardt, R., Schmidt, R., Mutsert, R. de, Dam, R.M. van, Felicita, S.C., Padmanabhan, S., Vaccargiu, S., Hallan, S., Bakker, S.J.L., Lim, S.C., Lucae, S., Bergmann, S., Boutin, T.S., Bergler, T., Rabelink, T.J., Haller, T., Volker, U., Vitart

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Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis von Rhodes, C.J, Batai, K, Bleda, M, Haimel, M, Southgate, L, Germain, M, Pauciulo, M.W, Hadinnapola, C, Aman, J, Girerd, B, Knight, J, Hanscombe, K.B, Karnes, J.H, Kaakinen, M, Gall, H, Ulrich, A, Harbaum, L, Cebola, I, Ferrer, J, Lutz, K, Swietlik, E.M, Ahmad, F, Amouyel, P, Archer, S.L, Argula, R, Austin, E.D, Badesch, D, Barnett, C, Benza, R, Bogaard, H.J, Burger, C.D, Church, C, Coghlan, J.G, Corris, P.A, Danesino, C, Debette, S, Elliott, C.G, Elwing, J, Eyries, M, Franke, A, Frantz, R.P, Frost, A, Ghio, S, Gibbs, J.S.R, Harley, J, Hill, N.S, Hirsch, R, Houweling, A.C, Howard, L.S, Kiely, D.G, Klinger, J, Kovacs, G, Lahm, T, Laudes, M, Machado, RD, Ross, R.V.M, Martin, L.J, Moledina, S, Montani, D, Nathan, S.D, Newnham, M, Olschewski, A, Olschewski, H, Ouwehand, W.H, Peacock, A.J, Pepke-Zaba, J, Rehman, Z, Robbins, I, Roden, D.M, Rosenzweig, E.B, Saydain, G, Scelsi, L, Schilz, R, Seeger, W, Simms, R.W, Sitbon, O, Suntharalingam, J, Tchourbanov, A.Y, Thenappan, T, Torres, F, Toshner, M.R, Treacy, C.M, Noordegraaf, A.V, Waisfisz, Q, Walsworth, A.K, Walter, R.E, Wilt, J, Lawrie, A, Humbert, M, Soubrier, F, Trégouët, D.-A, Prokopenko, I, Kittles, R, Gräf, S, Trembath, R.C, Desai, A.A, Morrell, N.W, Wilkins, M.R, UK NIHR BioResource Rare Diseases Consortium, US PAH Biobank Consortium

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Exome-wide association study of plasma lipids in > 300,000 individuals von Peloso, G.M., Yu, H., Wang, X., Saleheen, D., Emdin, C., Alam, D., Alves, A.C., Amouyel, P., Angelantonio, E. di, Auer, P.L., Ballantyne, C.M., Bis, J.C., Bottinger, E.P., Brandslund, I., Brown, M., Busonero, F., Chambers, J.C., Chasman, D.I., Chen, Y.D.I., Chu, A.Y., Cucca, F., Cupples, L.A., Damrauer, S.M., Dedoussis, G., Denny, J.C., Dominiczak, A., Ebeling, T., Eiriksdottir, G., Farmaki, A.E., Franks, P.W., Frikke-Schmidt, R., Fritsche, L.G., Gao, W., Garcia, M.E., Gieger, C., Giulianini, F., Grarup, N., Gudnason, V., Holmen, O.L., Hveem, K., Jabeen, S., Jackson, A.U., Jakobsdottir, J., Jarvelin, M.R., Jorgensen, M.E., Kamstrup, P.R., Kanoni, S., Karpe, F., Kee, F., Khera, A.V., Klarin, D., Kooner, J.S., Langsted, A., Launer, L.J., Lauritzen, T., Liewald, D.C.M., Lin, L.A., Loos, R.J.F., Lu, Y.C., Lu, X.F., Malarstig, A., Manning, A.K., Mantyselka, P., Melander, O., Muller-Nurasyid, M., Munroe, P.B., Neville, M.J., Nielsen, S.F., Orho-Melander, M., Padmanabhan, S., Palmer, C.N.A., Pasko, D., Pisinger, C., Rader, D.J., Ridker, P.M., Roden, D.M., Rotter, J.I., Rudan, I., Sanna, S., Schmidt, E.M., Sevilla, R.S., Sim, X.L., Smith, B.H., Strauch, K., Tada, H., Tall, A.R., Tang, H., Tardif, J.C., Tuomilehto, J., Varga, T.V., Waldenberger, M., Zheng, N.S., Zhou, Y., Howson, J.M.M., McCarthy, M.I., Cowan, C.A., Abecasis, G., Musunuru, K., Willer, C.J., Kathiresan, S.

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Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes von Ramirez, A.H, Shaffer, C.M, Delaney, J.T, Sexton, D.P, Levy, S.E, Rieder, M.J, Nickerson, D.A, George, Jr., A.L, Roden, D.M

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A polymorphism in HLA-G modifies statin benefit in asthma von Naidoo, D, Wu, A.C, Brilliant, M.H, Denny, J, Ingram, C, Kitchner, T.E, Linneman, J.G, McGeachie, M.J, Roden, D.M, Shaffer, C.M, Shah, A, Weeke, P, Weiss, S.T, Xu, H, Medina, M.W

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Reprogramming of mesenchymal stem cells by the synovial sarcoma-associated oncogene SYT-SSX2 von Garcia, C.B, Shaffer, C.M, Alfaro, M.P, Smith, A.L, Sun, J, Zhao, Z, Young, P.P, VanSaun, M.N, Eid, J.E

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A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough von Mosley, J.D, Shaffer, C.M, Van Driest, S.L, Weeke, P.E, Wells, Q.S, Karnes, J.H, Edwards, D.R. Velez, Wei, W.-Q, Teixeira, P.L, Bastarache, L, Crawford, D.C, Li, R, Manolio, T.A, Bottinger, E.P, McCarty, C.A, Linneman, J.G, Brilliant, M.H, Pacheco, J.A, Thompson, W, Chisholm, R.L, Jarvik, G.P, Crosslin, D.R, Carrell, D.S, Baldwin, E, Ralston, J, Larson, E.B, Grafton, J, Scrol, A, Jouni, H, Kullo, I.J, Tromp, G, Borthwick, K.M, Kuivaniemi, H, Carey, D.J, Ritchie, M.D, Bradford, Y, Verma, S.S, Chute, C.G, Veluchamy, A, Siddiqui, M.K, Palmer, C.N.A, Doney, A, MahmoudPour, S.H, Maitland-van der Zee, A.H, Morris, A.D, Denny, J.C, Roden, D.M

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The National Landscape of Living Kidney Donor Follow‐Up in the United States von Henderson, M. L., Thomas, A. G., Shaffer, A., Massie, A. B., Luo, X., Holscher, C. M., Purnell, T. S., Lentine, K. L., Segev, D. L.

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GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos von Sanders, A.E., Jain, D., Sofer, T., Kerr, K.F., Laurie, C.C., Shaffer, J.R., Marazita, M.L., Kaste, L.M., Slade, G.D., Fillingim, R.B., Ohrbach, R., Maixner, W., Kocher, T., Bernhardt, O., Teumer, A., Schwahn, C., Sipilä, K., Lähdesmäki, R., Männikkö, M., Pesonen, P., Järvelin, M., Rizzatti-Barbosa, C.M., Meloto, C.B., Ribeiro-Dasilva, M., Diatchenko, L., Serrano, P., Smith, S.B.

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OA19.03 Exportin 1 Inhibition Constraints Lineage Plasticity and Histological Transformation through Downregulation of SOX2 von Quintanal-Villalonga, A., Durani, V., Sabet, A., Redin, E., Kawasaki, K., Shaffer, M., Manoj, P., Sridhar, H., Haffner, M.C., Sawyers, C.L., Rudin, C.M.

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Trends in Renal Function Prior to and after LVAD Placement and Association with Post LVAD Mortality von Maharaj, V., Masotti, M., Schultz, J., Martin, C.M., John, R., Alexy, T., Thenappan, T., Knoper, R., Shaffer, A., Cogswell, R.

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Correlation between Body Mass Index and Renal Function before and after LVAD: Evidence for Overestimation of Renal Function Using Creatinine in the Advanced Heart Failure Populatio... von Cogswell, R., Masotti, M., Schultz, J., Martin, C.M., Pritzker, M., Kamdar, F., Knoper, R., Shaffer, A., John, R.

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Trends in Body Mass Index before and after Left Ventricular Assist Device and Association with Pectoralis Muscle Measures: Evidence for Progressive Sarcopenia Prior to LVAD Implant... von Schultz, J., Hoeg, A., Masotti, M., Teigen, L., John, R., Shaffer, A., Martin, C.M., Alexy, T., Cogswell, R.

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Smoking and IPMN malignant progression von Carr, R.A, Roch, A.M, Shaffer, K, Aboudi, S, Schmidt, C.M, DeWitt, J, Ceppa, E.P, House, M.G, Zyromski, N.J, Nakeeb, A

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Surgical Outcomes of HeartMate2 to HeartMate3 Pump Exchange: A Single Center Experience von Shaffer, A., Goodwin, K., Cogswell, R., Shah, H., Schultz, J.M., Martin, C.M., John, R.M.

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Risk Factors and Clinical Significance of Vasoplegia after LVAD Implantation von El Rafei, A., Schultz, J., Masotti, M., Maharaj, V., Fraser, M., Mutschler, M., Martin, C.M., Alexy, T., Kamdar, F., Knoper, R., Shaffer, A., John, R., Cogswell, R.

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