Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart von Hertz, C. L., Christiansen, S. L., Ferrero-Miliani, L., Dahl, M., Weeke, P. E., Ottesen, G. L., Frank-Hansen, R., Bundgaard, H., Morling, N.

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Common and Rare Variants in SCN10A Modulate the Risk of Atrial Fibrillation von Jabbari, Javad, Olesen, Morten S, Yuan, Lei, Nielsen, Jonas B, Liang, Bo, Macri, Vincenzo, Christophersen, Ingrid E, Nielsen, Nikolaj, Sajadieh, Ahmad, Ellinor, Patrick T, Grunnet, Morten, Haunsø, Stig, Holst, Anders G, Svendsen, Jesper H, Jespersen, Thomas

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Prevalence of the HOXB13 G84E mutation in Danish men undergoing radical prostatectomy and its correlations with prostate cancer risk and aggressiveness von Storebjerg, Tine M., Høyer, Søren, Kirkegaard, Pia, Bro, Flemming, Ørntoft, Torben F., Borre, Michael, Sørensen, Karina D.

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Genetic investigation of 100 heart genes in sudden unexplained death victims in a forensic setting von Christiansen, Sofie Lindgren, Hertz, Christin Løth, Ferrero-Miliani, Laura, Dahl, Morten, Weeke, Peter Ejvin, LuCamp, Ottesen, Gyda Lolk, Frank-Hansen, Rune, Bundgaard, Henning, Morling, Niels

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Dominant optic atrophy in Denmark - report of 15 novel mutations in OPA1, using a strategy with a detection rate of 90 von Almind, Gitte J, Ek, Jakob, Rosenberg, Thomas, Eiberg, Hans, Larsen, Michael, Lucamp, Lucamp, Brøndum-Nielsen, Karen, Grønskov, Karen

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A novel heterozygous nonsense mutation of the OPTN gene segregating in a Danish family with ALS von Tümer, Zeynep, Bertelsen, Birgitte, Gredal, Ole, Magyari, Melinda, Nielsen, Karen Cecilie, LuCamp, Grønskov, Karen, Brøndum-Nielsen, Karen

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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls von Mercader, Josep M., Udler, Miriam S., Mahajan, Anubha, Caulkins, Lizz, Barajas-Olmos, Francisco, Blackwell, Thomas W., Boerwinkle, Eric, Brody, Jennifer A., Chen, Siying, Contreras-Cubas, Cecilia, Córdova, Emilio, Correa, Adolfo, Cortes, Maria, Dolan, Lawrence, Drews, Kimberly L., Gabriel, Stacey, Garay-Sevilla, Maria Eugenia, García-Ortiz, Humberto, Gross, Myron, Heard-Costa, Nancy L., Jackson, Anne U., Jørgensen, Marit E., Kang, Hyun Min, Kim, Bong-Jo, Lyssenko, Valeriya, Manning, Alisa K., Marcketta, Anthony, Martínez-Hernández, Angélica, Matsuo, Karen, Mayer-Davis, Elizabeth, Mohlke, Karen L., Morrison, Alanna C., Ndungu, Anne, Ng, Maggie C. Y., O’Dushlaine, Colm, Payne, Anthony J., Pihoker, Catherine, Preuss, Michael, Psaty, Bruce M., Reiner, Alexander P., Robertson, Neil R., Santoro, Nicola, Schurmann, Claudia, So, Wing Yee, Soberón, Xavier, Thameem, Farook, Tomlinson, Brian, van Dam, Rob M., Vujkovic, Marijana, Witte, Daniel R., Barzilai, Nir, Bonnycastle, Lori L., Bowden, Donald W., Chambers, John C., Cheng, Ching-Yu, de Vries, Paul S., Glaser, Benjamin, Groop, Leif, Kooner, Jaspal Singh, Kwak, Soo Heon, Lehman, Donna M., Spector, Timothy D., Tai, E. Shyong, Tuomilehto, Jaakko, Wilson, James G., Burke, Brian, Carey, David J., Chan, Juliana C. N., Dupuis, Josée, Frossard, Philippe, Heckbert, Susan R., Hwang, Mi Yeong, Kim, Young Jin, Kirchner, H. Lester, Lee, Jong-Young, Lee, Juyoung, Loos, Ruth J. F., Ma, Ronald C. W., O’Donnell, Christopher J., Park, Kyong Soo, Rasheed, Asif, Saleheen, Danish, Sim, Xueling, Hanis, Craig L., Orozco, Lorena, Dewey, Frederick E., Baras, Aris, Gieger, Christian, Meitinger, Thomas, Strauch, Konstantin, Lange, Leslie, Hansen, Torben, Pedersen, Oluf, Dabelea, Dana, Bell, Graeme I., Sladek, Rob, Rich, Steve S., Rotter, Jerome I., Altshuler, David, Boehnke, Michael

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Common and rare variants in SCN10A modulate the risk of atrial fibrillation von Jabbari, Javad, Olesen, Morten S, Yuan, Lei, Nielsen, Jonas B, Liang, Bo, Macri, Vincenzo, Christophersen, Ingrid E, Nielsen, Nikolaj, Sajadieh, Ahmad, Ellinor, Patrick T, Grunnet, Morten, Haunsø, Stig, Holst, Anders G, Svendsen, Jesper H, Jespersen, Thomas

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SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillation von Savio-Galimberti, Eleonora, Weeke, Peter, Muhammad, Raafia, Blair, Marcia, Ansari, Sami, Short, Laura, Atack, Thomas C, Kor, Kaylen, Vanoye, Carlos G, Olesen, Morten Salling, LuCamp, Yang, Tao, George, Jr, Alfred L, Roden, Dan M, Darbar, Dawood

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Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes von Andreasen, Laura, Ahlberg, Gustav, Tang, Chuyi, Andreasen, Charlotte, Hartmann, Jacob P, Tfelt-Hansen, Jacob, Behr, Elijah R, Pehrson, Steen, Haunsø, Stig, LuCamp, Weeke, Peter E, Jespersen, Thomas, Olesen, Morten S, Svendsen, Jesper H

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Association study between CDH2 and Gilles de la Tourette syndrome in a Danish cohort von Nazaryan, Lusine, Bertelsen, Birgitte, Padmanabhuni, Shanmukha Sampath, Debes, Nanette Mol, LuCamp, Have, Christian Theil, Tümer, Zeynep

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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls von Flannick, J, Mercader, JM, Fuchsberger, C, Udler, MS, Teslovich, TM, Caulkins, L, Blackwell, TW, Brody, JA, Chen, L, Córdova, E, Dolan, L, Elliott, A, Floyd, JS, Gabriel, S, Garay-Sevilla, ME, García-Ortiz, H, Gross, M, Han, S, Heard-Costa, NL, Jackson, AU, Kelsey, M, Kim, B-J, Koistinen, HA, Leader, JB, Liu, C-T, Lyssenko, V, Marcketta, A, Malacara-Hernandez, JM, Matsuo, K, Mayer-Davis, E, Mendoza-Caamal, E, Ng, MCY, O'Dushlaine, C, Post, WS, Psaty, BM, Vasan, RS, Revilla-Monsalve, C, Robertson, NR, Santoro, N, Strom, TM, Tam, CHT, Thameem, F, Tomlinson, B, Torres, JM, Van Dam, RM, Vujkovic, M, Wang, S, Witte, DR, Barzilai, N, Blangero, J, Bowden, DW, Chan, E, Collins, FS, De Vries, PS, Glaser, B, Groop, L, Kooner, JS, Laakso, M, Lehman, DM, Nilsson, P, Tuomi, T, Aguilar-Salinas, CA, Bottinger, E, Chan, JCN, Dupuis, J, Frossard, P, Kim, YJ, Lee, J-Y, Loos, RJF, Ma, RCW, Morris, AD, Pankow, J, Saleheen, D, Sim, X, Small, KS, Haiman, C, Orozco, L, Tusié-Luna, T, Gieger, C, Meitinger, T, Strauch, K, Hansen, T, Zeitler, P, Dabelea, D, Abecasis, G, Bell, GI, Cox, NJ, Seielstad, M, Meigs, JB, Rich, SS, Rotter, JI, DiscovEHR Collaboration, CHARGE, GoT2D, SIGMA-T2D, T2D-GENES, Altshuler, D, Burtt, NP, Morris, AP, Florez, JC

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