Direct-to-consumer raw genetic data and third-party interpretation services: more burden than bargain? von Moscarello, Tia, Murray, Brittney, Reuter, Chloe M., Demo, Erin

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Assessing and attending to psychosocial concerns in genetic counseling: Proposing the BATHE method von Moscarello, Tia, Higgs, Emily, Pollard, Elizabeth, Monroe, Mattie, Nguyen, Thuy-Mi P, Campion, MaryAnn, Reuter, Chloe M

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Genome Sequencing in Hypertrophic Cardiomyopathy von Ashley, Euan A., Reuter, Chloe M., Wheeler, Matthew T.

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The genetic architecture of Plakophilin 2 cardiomyopathy von Dries, Annika M., Kirillova, Anna, Reuter, Chloe M., Garcia, John, Zouk, Hana, Hawley, Megan, Murray, Brittney, Tichnell, Crystal, Pilichou, Kalliopi, Protonotarios, Alexandros, Medeiros-Domingo, Argelia, Kelly, Melissa A., Baras, Aris, Ingles, Jodie, Semsarian, Christopher, Bauce, Barbara, Celeghin, Rudy, Basso, Cristina, Jongbloed, Jan D.H., Nussbaum, Robert L., Funke, Birgit, Cerrone, Marina, Mestroni, Luisa, Taylor, Matthew R.G., Sinagra, Gianfranco, Merlo, Marco, Saguner, Ardan M., Elliott, Perry M., Syrris, Petros, van Tintelen, J. Peter, James, Cynthia A., Haggerty, Christopher M., Parikh, Victoria N.

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Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing von Reuter, Chloe M., Kohler, Jennefer N., Bonner, Devon, Zastrow, Diane, Fernandez, Liliana, Dries, Annika, Marwaha, Shruti, Davidson, Jean, Brokamp, Elly, Herzog, Matthew, Hong, Joyce, Macnamara, Ellen, Rosenfeld, Jill A., Schoch, Kelly, Spillmann, Rebecca, Loscalzo, Joseph, Krier, Joel, Stoler, Joan, Sweetser, David, Palmer, Christina G.S., Phillips, John A., Shashi, Vandana, Adams, David A., Yang, Yaping, Ashley, Euan A., Fisher, Paul G., Mulvihill, John J., Bernstein, Jonathan A., Wheeler, Matthew T.

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Arrhythmogenic Cardiomyopathy: Mechanisms, Genetics, and Their Clinical Implications von Reuter, Chloe M., Dries, Annika M., Parikh, Victoria N.

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A New Approach to Rare Diseases of Children: The Undiagnosed Diseases Network von Reuter, Chloe M., Brimble, Elise, DeFilippo, Colette, Dries, Annika M., Enns, Gregory M., Ashley, Euan A., Bernstein, Jonathan A., Fisher, Paul Graham, Wheeler, Matthew T.

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Patient experiences with clinical confirmatory genetic testing after using direct-to-consumer raw DNA and third-party genetic interpretation services von Dolphyn, Tiffany T. Nguyen, Ormond, Kelly E, Weissman, Scott M, Kim, Helen J, Reuter, Chloe M

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Correction to: The genetic architecture of Plakophilin 2 cardiomyopathy von Dries, Annika M., Kirillova, Anna, Reuter, Chloe M., Garcia, John, Zouk, Hana, Hawley, Megan, Murray, Brittney, Tichnell, Crystal, Pilichou, Kalliopi, Protonotarios, Alexandros, Medeiros-Domingo, Argelia, Kelly, Melissa A., Baras, Aris, Ingles, Jodie, Semsarian, Christopher, Bauce, Barbara, Celeghin, Rudy, Basso, Cristina, Jongbloed, Jan D.H., Nussbaum, Robert L., Funke, Birgit, Cerrone, Marina, Mestroni, Luisa, Taylor, Matthew R.G., Sinagra, Gianfranco, Merlo, Marco, Saguner, Ardan M., Elliott, Perry M., Syrris, Petros, van Tintelen, J. Peter, James, Cynthia A., Haggerty, Christopher M., Parikh, Victoria N.

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Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest von Floyd, Brendan J., Weile, Jochen, Kannankeril, Prince J., Glazer, Andrew M., Reuter, Chloe M., MacRae, Calum A., Ashley, Euan A., Roden, Dan M., Roth, Frederick P., Parikh, Victoria N.

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The genetic architecture of Plakophilin 2 cardiomyopathy von Dries, Annika M, Kirillova, Anna, Reuter, Chloe M, Garcia, John, Zouk, Hana, Hawley, Megan, Murray, Brittney, Tichnell, Crystal, Pilichou, Kalliopi, Protonotarios, Alexandros, Medeiros-Domingo, Argelia, Kelly, Melissa A, Baras, Aris, Ingles, Jodie, Semsarian, Christopher, Bauce, Barbara, Celeghin, Rudy, Basso, Cristina, Jongbloed, Jan D H, Nussbaum, Robert L, Funke, Birgit, Cerrone, Marina, Mestroni, Luisa, Taylor, Matthew R G, Sinagra, Gianfranco, Merlo, Marco, Saguner, Ardan M, Elliott, Perry M, Syrris, Petros, van Tintelen, J Peter

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Beyond the exome: what's next in diagnostic testing for Mendelian conditions von Wojcik, Monica H, Reuter, Chloe M, Marwaha, Shruti, Mahmoud, Medhat, Duyzend, Michael H, Barseghyan, Hayk, Yuan, Bo, Boone, Philip M, Groopman, Emily E, Délot, Emmanuèle C, Jain, Deepti, Sanchis-Juan, Alba, Starita, Lea M, Talkowski, Michael, Montgomery, Stephen B, Bamshad, Michael J, Chong, Jessica X, Wheeler, Matthew T, Berger, Seth I, O'Donnell-Luria, Anne, Sedlazeck, Fritz J, Miller, Danny E

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Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest von Floyd, Brendan J., Weile, Jochen, Kannankeril, Prince J., Glazer, Andrew M., Reuter, Chloe M., MacRae, Calum A., Ashley, Euan A., Roden, Dan M., Roth, Frederick P., Parikh, Victoria N.

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Beyond the exome: what's next in diagnostic testing for Mendelian conditions von Wojcik, Monica H, Reuter, Chloe M, Marwaha, Shruti, Mahmoud, Medhat, Duyzend, Michael H, Barseghyan, Hayk, Yuan, Bo, Boone, Philip M, Groopman, Emily E, Délot, Emmanuèle C, Jain, Deepti, Sanchis-Juan, Alba, Genomics Research to Elucidate the Genetics of Rare Diseases, Consortium, Starita, Lea M, Talkowski, Michael, Montgomery, Stephen B, Bamshad, Michael J, Chong, Jessica X, Wheeler, Matthew T, Berger, Seth I, O'Donnell-Luria, Anne, Sedlazeck, Fritz J, Miller, Danny E

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Beyond the exome: what's next in diagnostic testing for Mendelian conditions von Wojcik, Monica H, Reuter, Chloe M, Marwaha, Shruti, Mahmoud, Medhat, Duyzend, Michael H, Barseghyan, Hayk, Yuan, Bo, Boone, Philip M, Groopman, Emily E, Délot, Emmanuèle C, Jain, Deepti, Sanchis-Juan, Alba, Starita, Lea M, Talkowski, Michael, Montgomery, Stephen B, Bamshad, Michael J, Chong, Jessica X, Wheeler, Matthew T, Berger, Seth I, O'Donnell-Luria, Anne, Sedlazeck, Fritz J, Miller, Danny E

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Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease von Splinter, Kimberly, Adams, David R, Bacino, Carlos A, Bellen, Hugo J, Bernstein, Jonathan A, Cheatle-Jarvela, Alys M, Eng, Christine M, Esteves, Cecilia, Gahl, William A, Hamid, Rizwan, Jacob, Howard J, Kikani, Bijal, Koeller, David M, Kohane, Isaac S, Lee, Brendan H, Loscalzo, Joseph, Luo, Xi, McCray, Alexa T, Metz, Thomas O, Mulvihill, John J, Nelson, Stanley F, Palmer, Christina G.S, Phillips, John A, Pick, Leslie, Postlethwait, John H, Reuter, Chloe, Shashi, Vandana, Sweetser, David A, Tifft, Cynthia J, Walley, Nicole M, Wangler, Michael F, Westerfield, Monte, Wheeler, Matthew T, Wise, Anastasia L, Worthey, Elizabeth A, Yamamoto, Shinya, Ashley, Euan A

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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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G3BPs tether the TSC complex to lysosomes and suppress mTORC1 signaling von Prentzell, Mirja Tamara, Rehbein, Ulrike, Cadena Sandoval, Marti, De Meulemeester, Ann-Sofie, Baumeister, Ralf, Brohée, Laura, Berdel, Bianca, Bockwoldt, Mathias, Carroll, Bernadette, Chowdhury, Suvagata Roy, von Deimling, Andreas, Demetriades, Constantinos, Figlia, Gianluca, de Araujo, Mariana Eca Guimaraes, Heberle, Alexander M., Heiland, Ines, Holzwarth, Birgit, Huber, Lukas A., Jaworski, Jacek, Kedra, Magdalena, Kern, Katharina, Kopach, Andrii, Korolchuk, Viktor I., van 't Land-Kuper, Ineke, Macias, Matylda, Nellist, Mark, Palm, Wilhelm, Pusch, Stefan, Ramos Pittol, Jose Miguel, Reil, Michèle, Reintjes, Anja, Reuter, Friederike, Sampson, Julian R., Scheldeman, Chloë, Siekierska, Aleksandra, Stefan, Eduard, Teleman, Aurelio A., Thomas, Laura E., Torres-Quesada, Omar, Trump, Saskia, West, Hannah D., de Witte, Peter, Woltering, Sandra, Yordanov, Teodor E., Zmorzynska, Justyna, Opitz, Christiane A., Thedieck, Kathrin

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Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy von Parikh, Victoria N, Caleshu, Colleen, Reuter, Chloe, Lazzeroni, Laura C, Ingles, Jodie, Garcia, John, McCaleb, Kristen, Adesiyun, Tolulope, Sedaghat-Hamedani, Farbod, Kumar, Saurabh, Graw, Sharon, Gigli, Marta, Stolfo, Davide, Dal Ferro, Matteo, Ing, Alexander Y, Nussbaum, Robert, Funke, Birgit, Wheeler, Matthew T, Hershberger, Ray E, Cook, Stuart, Steinmetz, Lars M, Lakdawala, Neal K, Taylor, Matthew R G, Mestroni, Luisa, Merlo, Marco, Sinagra, Gianfranco, Semsarian, Christopher, Meder, Benjamin, Judge, Daniel P, Ashley, Euan

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Emery–Dreifuss muscular dystrophy Type 1 is associated with a high risk of malignant ventricular arrhythmias and end-stage heart failure von Cannie, Douglas E, Syrris, Petros, Protonotarios, Alexandros, Bakalakos, Athanasios, Pruny, Jean-François, Ditaranto, Raffaello, Martinez-Veira, Cristina, Larrañaga-Moreira, Jose M, Medo, Kristen, Bermúdez-Jiménez, Francisco José, Ben Yaou, Rabah, Leturcq, France, Mezcua, Ainhoa Robles, Marini-Bettolo, Chiara, Cabrera, Eva, Reuter, Chloe, Limeres Freire, Javier, Rodríguez-Palomares, José F, Mestroni, Luisa, Taylor, Matthew R G, Parikh, Victoria N, Ashley, Euan A, Barriales-Villa, Roberto, Jiménez-Jáimez, Juan, Garcia-Pavia, Pablo, Charron, Philippe, Biagini, Elena, García Pinilla, José M, Bourke, John, Savvatis, Konstantinos, Wahbi, Karim, Elliott, Perry M

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