Shallow geophysical exploration of the Upper Kama Potash Salt Deposit von Sanfirov, I. A., Stepanov, Yu. I., Fat’kin, K. B., Gerasimova, I. Yu, Nikiforova, A. I.

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A genomic mutational constraint map using variation in 76,156 human genomes von Chen, Siwei, Francioli, Laurent C., Goodrich, Julia K., Collins, Ryan L., Kanai, Masahiro, Wang, Qingbo, Alföldi, Jessica, Watts, Nicholas A., Vittal, Christopher, Gauthier, Laura D., Poterba, Timothy, Wilson, Michael W., Tarasova, Yekaterina, Phu, William, Grant, Riley, Yohannes, Mary T., Koenig, Zan, Farjoun, Yossi, Banks, Eric, Donnelly, Stacey, Gabriel, Stacey, Gupta, Namrata, Ferriera, Steven, Tolonen, Charlotte, Novod, Sam, Bergelson, Louis, Roazen, David, Ruano-Rubio, Valentin, Covarrubias, Miguel, Llanwarne, Christopher, Petrillo, Nikelle, Wade, Gordon, Jeandet, Thibault, Munshi, Ruchi, Tibbetts, Kathleen, O’Donnell-Luria, Anne, Solomonson, Matthew, Seed, Cotton, Martin, Alicia R., Talkowski, Michael E., Rehm, Heidi L., Daly, Mark J., Tiao, Grace, Neale, Benjamin M., MacArthur, Daniel G., Karczewski, Konrad J.

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Inferring compound heterozygosity from large-scale exome sequencing data von Guo, Michael H., Francioli, Laurent C., Stenton, Sarah L., Goodrich, Julia K., Watts, Nicholas A., Singer-Berk, Moriel, Groopman, Emily, Darnowsky, Philip W., Solomonson, Matthew, Baxter, Samantha, Tiao, Grace, Neale, Benjamin M., Hirschhorn, Joel N., Rehm, Heidi L., Daly, Mark J., O’Donnell-Luria, Anne, Karczewski, Konrad J., MacArthur, Daniel G., Samocha, Kaitlin E.

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Phenotypic Expression, Natural History, and Risk Stratification of Cardiomyopathy Caused by Filamin C Truncating Variants von Gigli, Marta, Stolfo, Davide, Graw, Sharon L., Merlo, Marco, Gregorio, Caterina, Nee Chen, Suet, Dal Ferro, Matteo, PaldinoMD, Alessia, De Angelis, Giulia, Brun, Francesca, Jirikowic, Jean, Salcedo, Ernesto E., Turja, Sylvia, Fatkin, Diane, Johnson, Renee, van Tintelen, J. Peter, Te Riele, Anneline S.J.M., Wilde, Arthur A.M., Lakdawala, Neal K., Picard, Kermshlise, Miani, Daniela, Muser, Daniele, Maria Severini, Giovanni, Calkins, Hugh, James, Cynthia A., Murray, Brittney, Tichnell, Crystal, Parikh, Victoria N., Ashley, Euan A., Reuter, Chloe, Song, Jiangping, Judge, Daniel P., McKenna, William J., Taylor, Matthew R.G., Sinagra, Gianfranco, Mestroni, Luisa

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Author Correction: A genomic mutational constraint map using variation in 76,156 human genomes von Chen, Siwei, Francioli, Laurent C., Goodrich, Julia K., Collins, Ryan L., Kanai, Masahiro, Wang, Qingbo, Alföldi, Jessica, Watts, Nicholas A., Vittal, Christopher, Gauthier, Laura D., Poterba, Timothy, Wilson, Michael W., Tarasova, Yekaterina, Phu, William, Grant, Riley, Yohannes, Mary T., Koenig, Zan, Farjoun, Yossi, Banks, Eric, Donnelly, Stacey, Gabriel, Stacey, Gupta, Namrata, Ferriera, Steven, Tolonen, Charlotte, Novod, Sam, Bergelson, Louis, Roazen, David, Ruano-Rubio, Valentin, Covarrubias, Miguel, Llanwarne, Christopher, Petrillo, Nikelle, Wade, Gordon, Jeandet, Thibault, Munshi, Ruchi, Tibbetts, Kathleen, O’Donnell-Luria, Anne, Solomonson, Matthew, Seed, Cotton, Martin, Alicia R., Talkowski, Michael E., Rehm, Heidi L., Daly, Mark J., Tiao, Grace, Neale, Benjamin M., MacArthur, Daniel G., Karczewski, Konrad J.

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Mutation of the LUNATIC FRINGE Gene in Humans Causes Spondylocostal Dysostosis with a Severe Vertebral Phenotype von Sparrow, D.B., Chapman, G., Wouters, M.A., Whittock, N.V., Ellard, S., Fatkin, D., Turnpenny, P.D., Kusumi, K., Sillence, D., Dunwoodie, S.L.

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Influence of sex on cardiovascular outcomes in RBM20 variant carriers von Cannie, D, Protonotarios, A, Syrris, P, Sengupta, A, Bilinska, Z, Arana Achaga, X, Barriales-Villa, R, Garcia-Pavia, P, Gimeno, J, Merlo, M, Wahbi, K, Fatkin, D, Mogensen, J, Rasmussen, T B, Elliott, P

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Effects of a trauma‐informed mindful recovery program on comorbid pain, anxiety, and substance use during primary care buprenorphine treatment: A proof‐of‐concept study von Schuman‐Olivier, Zev, Fatkin, Thomas, Creedon, Timothy B., Samawi, Farah, Moore, Sarah K., Okst, Kayley, Fredericksen, Alaine (Kiera), Oxnard, Alexandra (Sasha), Roll, David, Smith, Lydia, Cook, Benjamin Lê, Weiss, Roger D.

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An abnormal Ca2+ response in mutant sarcomere protein–mediated familial hypertrophic cardiomyopathy von Fatkin, Diane, McConnell, Bradley K., Mudd, James O., Semsarian, Christopher, Moskowitz, Ivan G.P., Schoen, Frederick J., Giewat, Michael, Seidman, Christine E., Seidman, J.G.

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Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis von Liang, Bo, Soka, Magdalena, Christensen, Alex Horby, Olesen, Morten S, Larsen, Anders P, Knop, Filip K, Wang, Fan, Nielsen, Jonas B, Andersen, Martin N, Humphreys, David, Mann, Stefan A, Huttner, Inken G, Vandenberg, Jamie I, Svendsen, Jesper H, Haunsø, Stig, Preiss, Thomas, Seebohm, Guiscard, Olesen, Søren-Peter, Schmitt, Nicole, Fatkin, Diane

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Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice von McConnell, B K, Jones, K A, Fatkin, D, Arroyo, L H, Lee, R T, Aristizabal, O, Turnbull, D H, Georgakopoulos, D, Kass, D, Bond, M, Niimura, H, Schoen, F J, Conner, D, Fischman, D A, Seidman, C E, Seidman, J G, Fischman, D H

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Spontaneous Coronary Artery Dissection (SCAD) and a Family History of Aortic Artery Dissection—A Case Series von McGrath-Cadell, L., Hesselson, S., Tarr, I., Iismaa, S., Bax, M., Junday, K., Dunwoodie, S., Fatkin, D., Kovacic, J., Muller, D., Giannoulatou, E., Graham, B.

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An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy von Fatkin, D, McConnell, B K, Mudd, J O, Semsarian, C, Moskowitz, I G, Schoen, F J, Giewat, M, Seidman, C E, Seidman, J G

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Comparison of Two Murine Models of Familial Hypertrophic Cardiomyopathy von McConnell, Bradley K, Fatkin, Diane, Semsarian, Christopher, Jones, Karen A, Georgakopoulos, Dimitrios, Maguire, Colin T, Healey, Michael J, Mudd, James O, Moskowitz, Ivan P.G, Conner, David A, Giewat, Michael, Wakimoto, Hiroko, Berul, Charles I, Schoen, Frederick J, Kass, David A, Seidman, Christine E, Seidman, J.G

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Contribution of noncanonical splice variants to TTN truncating variants cardiomyopathy von Patel, PN, Ito, K, Willcox, JAL, Haghighi, A, Jang, MY, Gorham, JM, DePalma, SR, Lam, L, McDonough, B, Johnson, R, Lakdawala, NK, Roberts, A, Barton, PJR, Cook, SA, Fatkin, D, Seidman, CE, Seidman, JG

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Feasibility and acceptability of mindful recovery opioid use care continuum (M-ROCC): A concurrent mixed methods study von Fatkin, Thomas, Moore, Sarah K., Okst, Kayley, Creedon, Timothy B, Samawi, Farah, Fredericksen, Alaine Kiera, Roll, David, Oxnard, Alexandra, Lê Cook, Benjamin, Schuman-Olivier, Zev

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Exclusion of atrial thrombus by transesophageal echocardiography does not preclude embolism after cardioversion of atrial fibrillation : a multicenter study von BLACK, I. W, FATKIN, D, VERHORST, P. M. J, KLEIN, A. L, SAGAR, K. B, KHANDHERIA, B. K, LEUNG, D. Y, GALLOWAY, J. M, FENELEY, M. P, WALSH, W. F, GRIMM, R. A, STOLLBERGER, C

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TASK-1 potassium channel mutations in atrial fibrillation von Olesen, M., Liang, B., Soka, M., Larsen, A. P., Knop, F. K., Wang, F., Nielsen, J. B., Andersen, M. N., Humphreys, D., Mann, S. A., Vandenberg, J. I., Svendsen, J. H., Haunso, S., Preiss, T., Seebohm, G., Olesen, S.- P., Schmitt, N., Fatkin, D.

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Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene von Fatkin, D, Christe, M E, Aristizabal, O, McConnell, B K, Srinivasan, S, Schoen, F J, Seidman, C E, Turnbull, D H, Seidman, J G

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Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease von Roberts, AM, Ware, JS, Herman, DS, Schafer, S, Baksi, J, Bick, AG, Buchan, RJ, Walsh, R, John, S, Wilkinson, S, Mazzarotto, F, Felkin, LE, Gong, S, L MacArthur, JA, Cunningham, F, Flannick, J, Gabriel, SB, Altshuler, DM, Macdonald, PS, Heinig, M, Keogh, AM, Hayward, CS, Banner, NR, Pennell, DJ, O'Regan, DP, San, TR, De Marvao, A, W Dawes, TJ, Gulati, A, Birks, EJ, Yacoub, MH, Radke, M, Gotthardt, M, Wilson, JG, O'Donnell, CJ, Prasad, SK, Barton, PJ, Fatkin, D, Hubner, N, Seidman, JG, Seidman, CE, Cook, SA

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