Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy von Mazzarotto, Francesco, Tayal, Upasana, Buchan, Rachel J., Midwinter, William, Wilk, Alicja, Whiffin, Nicola, Govind, Risha, Mazaika, Erica, de Marvao, Antonio, Dawes, Timothy J.W., Felkin, Leanne E., Ahmad, Mian, Theotokis, Pantazis I., Edwards, Elizabeth, Ing, Alexander Y., Thomson, Kate L., Chan, Laura L.H., Sim, David, Baksi, A. John, Pantazis, Antonis, Roberts, Angharad M., Watkins, Hugh, Funke, Birgit, O’Regan, Declan P., Olivotto, Iacopo, Barton, Paul J.R., Prasad, Sanjay K., Cook, Stuart A., Ware, James S., Walsh, Roddy

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Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies von Mazzarotto, Francesco, Hawley, Megan H., Beltrami, Matteo, Beekman, Leander, de Marvao, Antonio, McGurk, Kathryn A., Statton, Ben, Boschi, Beatrice, Girolami, Francesca, Roberts, Angharad M., Lodder, Elisabeth M., Allouba, Mona, Romeih, Soha, Aguib, Yasmine, Baksi, A. John, Pantazis, Antonis, Prasad, Sanjay K., Cerbai, Elisabetta, Yacoub, Magdi H., O’Regan, Declan P., Cook, Stuart A., Ware, James S., Funke, Birgit, Olivotto, Iacopo, Bezzina, Connie R., Barton, Paul J. R., Walsh, Roddy

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Cardiomyopathies in 100,000 genomes project: interval evaluation improves diagnostic yield and informs strategies for ongoing gene discovery von Josephs, Katherine S, Seaby, Eleanor G, May, Philippa, Theotokis, Pantazis, Yu, Jing, Andreou, Avgi, Sinclair, Hannah, Morris-Rosendahl, Deborah, Thomas, Ellen R A, Ennis, Sarah, Roberts, Angharad M, Ware, James S

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Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac condition... von Josephs, Katherine S, Roberts, Angharad M, Theotokis, Pantazis, Walsh, Roddy, Ostrowski, Philip J, Edwards, Matthew, Fleming, Andrew, Thaxton, Courtney, Roberts, Jason D, Care, Melanie, Zareba, Wojciech, Adler, Arnon, Sturm, Amy C, Tadros, Rafik, Novelli, Valeria, Owens, Emma, Bronicki, Lucas, Jarinova, Olga, Callewaert, Bert, Peters, Stacey, Lumbers, Tom, Jordan, Elizabeth, Asatryan, Babken, Krishnan, Neesha, Hershberger, Ray E, Chahal, C Anwar A, Landstrom, Andrew P, James, Cynthia, McNally, Elizabeth M, Judge, Daniel P, van Tintelen, Peter, Wilde, Arthur, Gollob, Michael, Ingles, Jodie, Ware, James S

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Direct and indirect effect of the COVID-19 pandemic on patients with cardiomyopathy von Hammersley, Daniel J, Buchan, Rachel J, Lota, Amrit S, Mach, Lukas, Jones, Richard E, Halliday, Brian P, Tayal, Upasana, Meena, Devendra, Dehghan, Abbas, Tzoulaki, Ioanna, Baksi, A John, Pantazis, Antonis, Roberts, Angharad M, Prasad, Sanjay K, Ware, James S

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The Gene Curation Coalition: A global effort to harmonize gene–disease evidence resources von DiStefano, Marina T., Goehringer, Scott, Babb, Lawrence, Alkuraya, Fowzan S., Amberger, Joanna, Amin, Mutaz, Austin-Tse, Christina, Balzotti, Marie, Berg, Jonathan S., Birney, Ewan, Bocchini, Carol, Bruford, Elspeth A., Coffey, Alison J., Collins, Heather, Cunningham, Fiona, Daugherty, Louise C., Einhorn, Yaron, Firth, Helen V., Fitzpatrick, David R., Foulger, Rebecca E., Goldstein, Jennifer, Hamosh, Ada, Hurles, Matthew R., Leigh, Sarah E., Leong, Ivone U.S., Maddirevula, Sateesh, Martin, Christa L., McDonagh, Ellen M., Olry, Annie, Puzriakova, Arina, Radtke, Kelly, Ramos, Erin M., Rath, Ana, Riggs, Erin Rooney, Roberts, Angharad M., Rodwell, Charlotte, Snow, Catherine, Stark, Zornitza, Tahiliani, Jackie, Tweedie, Susan, Ware, James S., Weller, Phillip, Williams, Eleanor, Wright, Caroline F., Yates, Thabo Michael, Rehm, Heidi L.

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Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations von Domínguez, Fernando, Cuenca, Sofía, Bilińska, Zofia, Toro, Rocío, Villard, Eric, Barriales-Villa, Roberto, Ochoa, Juan Pablo, Asselbergs, Folkert, Sammani, Arjan, Franaszczyk, Maria, Akhtar, Mohammed, Coronado-Albi, Maria José, Rangel-Sousa, Diego, Rodriguez-Palomares, Jose F., Jiménez-Jáimez, Juan, Garcia-Pinilla, José Manuel, Ripoll-Vera, Tomás, Mogollón-Jiménez, Maria Victoria, Fontalba-Romero, Ana, Garcia-Medina, Dolores, Palomino-Doza, Julian, de Gonzalo-Calvo, David, Cicerchia, Marcos, Salazar-Mendiguchia, Joel, Salas, Clara, Pankuweit, Sabine, Hey, Thomas Morris, Mogensen, Jens, Barton, Paul J., Charron, Philippe, Elliott, Perry, Garcia-Pavia, Pablo, Eiskjær, Hans, Barriales, Roberto, Fernández Fernández, Xusto, Cicerchia, Marcos, Monserrat, Lorenzo, Ochoa, Juan Pablo, Salazar-Mendiguchia, Joel, Mogollón, Maria Victoria, Ripoll, Tomás, Charron, Philippe, Richard, Pascale, Villard, Eric, Palomino Doza, Julian, Fontalba, Ana, Alonso-Pulpón, Luis, Cobo-Marcos, Marta, Domínguez, Fernando, Garcia-Pavia, Pablo, Gómez-Bueno, Manuel, González-López, Esther, Hernández-Hernández, Aitor, Hernández-Pérez, Francisco José, López-Sainz, Ángela, Restrepo-Córdoba, Alejandra, Segovia-Cubero, Javier, Toro, Rocio, de Gonzalo-Calvo, David, Rosa Longobardo, Félix, Limeres, Javier, Rodriguez-Palomares, Jose F., Garcia-Pinilla, Jose Manuel, López-Garrido, Miguel A., Jiménez-Jaimez, Juan, Garcia-Medina, Dolores, Rangel Sousa, Diego, Peña, Maria Luisa, Mogensen, Jens, Morris-Hey, Thomas, Barton, Paul J., Cook, Stuart A., Midwinter, William, Roberts, Angharad M., Ware, James S., Walsh, Roddy, Akhtar, Mohammed, Elliott, Perry M., Rocha-Lopes, Luis, Savvatis, Konstantinos, Syrris, Petros, Michalak, Ewa, Ploski, Rafal, Sobieszczanska-Malek, Malgorzata, Bilińska, Zofia, Pankuweit, Sabine, Asselbergs, Folkert, Baas, Annette, Dooijes, Dennis, Sammani, Arjan

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Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis von Dominguez, Fernando, Lopes, Luis Rocha, Ochoa, Juan Pablo, Barriales-Villa, Roberto, Climent, Vicente, Linschoten, Marijke, Tiron, Coloma, Chiriatti, Chiara, Marques, Nuno, Rasmussen, Torsten B., Espinosa, María Ángeles, Cesar, Sergi, Field, Ella, Garcia-Pinilla, Jose M., Muir, Alison R., Roberts, Angharad M., Santas, Enrique, Zorio, Esther, Peña-Peña, Maria Luisa, Navarro, Marina, Fernandez, Adrian, Palomino-Doza, Julian, Azevedo, Olga, Lorenzini, Massimiliano, García-Álvarez, Maria I., Bento, Dina, Jensen, Morten K., Méndez, Irene, Pezzoli, Laura, Sarquella-Brugada, Georgia, Campuzano, Oscar, Gonzalez-Lopez, Esther, Kaski, Juan Pablo, Brugada, Ramon, Monserrat, Lorenzo, Olivotto, Iacopo, Elliott, Perry M., Garcia-Pavia, Pablo, Rasmussen, Torsten B., Jensen, Morten K., Larrañaga-Moreira, Jose María, Alonso-García, Diego, Cárdenas-Reyes, Ivonne Johana, Cicerchia, Marcos, García-Ferro, German, García-Hernández, Soledad, Monserrat, Lorenzo, Nöel-Bröger, María, Ochoa, Juan Pablo, Ortiz, Martin, Bento, Dina, Mota, Teresa, Fernandes, Raquel, Costa, Hugo, Marques, Nuno, Climent, Vicente, García-Álvarez, Maria I., Cesar, Sergi, Sarquella-Brugada, Georgia, Muir, Alison R., Pezzoli, Laura, Quarta, Giovanni, Fernandez, Adrian, Field, Ella, Azevedo, Olga, Santas, Enrique, Chiriatti, Chiara, Brugada, Ramon, Campuzano, Oscar, Doza, Julian Palomino, Salguero-Bodes, Rafael, Valverde-Gomez, Maria, Espinosa, Maria Angeles, Mendez, Irene, Cobo-Marcos, Marta, Domínguez, Fernando, Garcia-Pavia, Pablo, González-López, Esther, Segovia-Cubero, Javier, Vilches, Silvia, Garcia-Pinilla, Jose Manuel, López-Garrido, Miguel, Abad, Victoria Doncel, Navarro, Marina, Sabater-Molina, Maria, Gimeno-Blanes, Juan Ramón, Peña-Peña, Maria Luisa, Mogensen, Jens, Barton, Paul J., Cook, Stuart A., Roberts, Angharad M., Ware, James S., Lopes, Luis Rocha, Lorenzini, Massimiliano, Syrris, Petros, Truszkowska, Grażyna, Michalak, Ewa, Asselbergs, Folkert, Baas, Annette F., Dooijes, Dennis

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Moderate excess alcohol consumption and adverse cardiac remodelling in dilated cardiomyopathy von Tayal, Upasana, Gregson, John, Buchan, Rachel, Whiffin, Nicola, Halliday, Brian P, Lota, Amrit, Roberts, Angharad M, Baksi, A John, Voges, Inga, Jarman, Julian W E, Baruah, Resham, Frenneaux, Michael, Cleland, John G F, Barton, Paul, Pennell, Dudley J, Ware, James S, Cook, Stuart A, Prasad, Sanjay K

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Toward robust clinical genome interpretation: Developing a consistent terminology to characterize Mendelian disease-gene relationships—allelic requirement, inheritance modes, and d... von Roberts, Angharad M., DiStefano, Marina T., Riggs, Erin Rooney, Josephs, Katherine S., Alkuraya, Fowzan S., Amberger, Joanna, Amin, Mutaz, Berg, Jonathan S., Cunningham, Fiona, Eilbeck, Karen, Firth, Helen V., Foreman, Julia, Hamosh, Ada, Hay, Eleanor, Leigh, Sarah, Martin, Christa L., McDonagh, Ellen M., Perrett, Daniel, Ramos, Erin M., Robinson, Peter N., Rath, Ana, Sant, David W., Stark, Zornitza, Whiffin, Nicola, Rehm, Heidi L., Ware, James S.

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Next generation sequencing for clinical diagnostics and personalised medicine: implications for the next generation cardiologist von Ware, James S, Roberts, Angharad M, Cook, Stuart A

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A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy von Horvat, Claire, Johnson, Renee, Lam, Lien, Munro, Jacob, Mazzarotto, Francesco, Roberts, Angharad M., Herman, Daniel S., Parfenov, Michael, Haghighi, Alireza, McDonough, Barbara, DePalma, Steven R., Keogh, Anne M., Macdonald, Peter S., Hayward, Christopher S., Roberts, Amy, Barton, Paul J.R., Felkin, Leanne E., Giannoulatou, Eleni, Cook, Stuart A., Seidman, J.G., Seidman, Christine E., Fatkin, Diane

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Using High-Resolution Variant Frequencies Empowers Clinical Genome Interpretation and Enables Investigation of Genetic Architecture von Whiffin, Nicola, Roberts, Angharad M., Minikel, Eric, Zappala, Zach, Walsh, Roddy, O’Donnell-Luria, Anne H., Karczewski, Konrad J., Harrison, Steven M., Thomson, Kate L., Sage, Helen, Ing, Alexander Y., Barton, Paul J.R., Funke, Birgit, Cook, Stuart A., MacArthur, Daniel G., Ware, James S.

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Sex Differences in the Clinical Presentation and Natural History of Dilated Cardiomyopathy von Owen, Ruth, Buchan, Rachel, Frenneaux, Michael, Jarman, Julian W.E., Baruah, Resham, Lota, Amrit S., Halliday, Brian P., Roberts, Angharad M., Izgi, Cemil, Van Spall, Harriette G.C., Michos, Erin D., McMurray, John J.V., Januzzi, James L., Pennell, Dudley J., Cook, Stuart A., Ware, James S., Barton, Paul J., Gregson, John, Prasad, Sanjay K., Tayal, Upasana

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Noncompaction Cardiomyopathy, Sick Sinus Disease, and Aortic Dilatation: Too Much for a Single Diagnosis? von Brunet-Garcia, Laia, Odori, Alessia, Fell, Hannah, Field, Ella, Roberts, Angharad M, Starling, Luke, Kaski, Juan Pablo, Cervi, Elena

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16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2 von Barber, John C K, Hall, Victoria, Maloney, Viv K, Huang, Shuwen, Roberts, Angharad M, Brady, Angela F, Foulds, Nicki, Bewes, Beverley, Volleth, Marianne, Liehr, Thomas, Mehnert, Karl, Bateman, Mark, White, Helen

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Titin truncating mutations: A rare cause of dilated cardiomyopathy in the young von Fatkin, Diane, Lam, Lien, Herman, Daniel S, Benson, Craig C, Felkin, Leanne E, Barton, Paul J.R, Walsh, Roddy, Candan, Sukru, Ware, James S, Roberts, Angharad M, Chung, Wendy K, Smoot, Leslie, Bornaun, Helen, Keogh, Anne M, Macdonald, Peter S, Hayward, Christopher S, Seidman, J.G, Roberts, Amy E, Cook, Stuart A, Seidman, Christine E

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Republished review: Next generation sequencing for clinical diagnostics and personalised medicine: implications for the next generation cardiologist von Ware, James S, Roberts, Angharad M, Cook, Stuart A

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Next Generation Diagnostics in Inherited Arrhythmia Syndromes: A Comparison of Two Approaches von Ware, James S., John, Shibu, Roberts, Angharad M., Buchan, Rachel, Gong, Sungsam, Peters, Nicholas S., Robinson, David O., Lucassen, Anneke, Behr, Elijah R., Cook, Stuart A.

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Titin: a phenotype-genotype descriptive comparison of dilated cardiomyopathy von Baksi, Arun J, Roberts, Angharad M, Ware, James S, Gulati, Ankur, Buchan, Rachel J, Walsh, Roddy, John, Shibu, Wilkinson, Samuel, Ali, Aamir, Assomull, Ravi G, Barton, Paul J, Prasad, Sanjay K, Pennell, Dudley J, Cook, Stuart A

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