Whole genome sequences discriminate hereditary hemorrhagic telangiectasia phenotypes by non-HHT deleterious DNA variants von Joyce, KE, Onabanjo, E, Brownlow, S, Nur, F, Olupona, K, Fakayode, K, Sroya, M, Thomas, GA, Ferguson, T, Redhead, J, Millar, CM, Cooper, N, Layton, DM, Boardman-Pretty, F, Caulfield, MJ, Genomics England Research Consortium, GE, Shovlin, CL

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A Nest of the Arctic Three-Toed Woodpecker von England, E. G.

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Mutational signature in colorectal cancer caused by genotoxic pks+E. coli von Pleguezuelos-Manzano, Cayetano, Puschhof, Jens, Rosendahl Huber, Axel, van Hoeck, Arne, Wood, Henry M., Nomburg, Jason, Gurjao, Carino, Manders, Freek, Dalmasso, Guillaume, Stege, Paul B., Paganelli, Fernanda L., Geurts, Maarten H., Beumer, Joep, Mizutani, Tomohiro, Miao, Yi, van der Linden, Reinier, van der Elst, Stefan, Garcia, K. Christopher, Top, Janetta, Willems, Rob J. L., Giannakis, Marios, Bonnet, Richard, Quirke, Phil, Meyerson, Matthew, Cuppen, Edwin, van Boxtel, Ruben, Clevers, Hans

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Demonstration of electron acceleration in a laser-driven dielectric microstructure von Peralta, E. A., Soong, K., England, R. J., Colby, E. R., Wu, Z., Montazeri, B., McGuinness, C., McNeur, J., Leedle, K. J., Walz, D., Sozer, E. B., Cowan, B., Schwartz, B., Travish, G., Byer, R. L.

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From Field and Study von Miller, Loye, Taber, Wendell, Stager, Kenneth E., Lee, LeVon, Brooks, Allan, Neff, Johnson A., England, E. G., Pitelka, Frank A., May, Richard H., Munro, J. A., Christensen, Glen, Trelease, Thomas, Gadd, Samuel W., Moore, Robert T., Gladding, Hope M.

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From Field and Study von Munro, J. A., England, E. G., Cottam, Clarence, Hanna, Wilson C., Neff, Johnson A., Alcorn, J. R., Hawbecker, Albert C., Russell, Ward C., Adams, Lowell, Webster, J. Dan, Sooter, Clarence A., Stone, Ned W.

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High-efficiency acceleration of an electron beam in a plasma wakefield accelerator von Litos, M., Adli, E., An, W., Clarke, C. I., Clayton, C. E., Corde, S., Delahaye, J. P., England, R. J., Fisher, A. S., Frederico, J., Gessner, S., Green, S. Z., Hogan, M. J., Joshi, C., Lu, W., Marsh, K. A., Mori, W. B., Muggli, P., Vafaei-Najafabadi, N., Walz, D., White, G., Wu, Z., Yakimenko, V., Yocky, G.

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Normal and pathogenic variation of RFC1 repeat expansions: implications for clinical diagnosis von Dominik, Natalia, Magri, Stefania, Currò, Riccardo, Abati, Elena, Facchini, Stefano, Corbetta, Marinella, Macpherson, Hannah, Di Bella, Daniela, Sarto, Elisa, Stevanovski, Igor, Chintalaphani, Sanjog R, Akcimen, Fulya, Manini, Arianna, Vegezzi, Elisa, Quartesan, Ilaria, Montgomery, Kylie-Ann, Pirota, Valentina, Crespan, Emmanuele, Perini, Cecilia, Grupelli, Glenda Paola, Tomaselli, Pedro J, Marques, Wilson, Shaw, Joseph, Polke, James, Salsano, Ettore, Fenu, Silvia, Pareyson, Davide, Pisciotta, Chiara, Tofaris, George K, Nemeth, Andrea H, Ealing, John, Radunovic, Aleksandar, Kearney, Seamus, Kumar, Kishore R, Vucic, Steve, Kennerson, Marina, Reilly, Mary M, Houlden, Henry, Deveson, Ira, Tucci, Arianna, Taroni, Franco, Cortese, Andrea

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Nuclear-mitochondrial DNA segments resemble paternally inherited mitochondrial DNA in humans von Wei, Wei, Pagnamenta, Alistair T., Gleadall, Nicholas, Sanchis-Juan, Alba, Stephens, Jonathan, Broxholme, John, Tuna, Salih, Odhams, Christopher A., Fratter, Carl, Turro, Ernest, Caulfield, Mark J., Taylor, Jenny C., Rahman, Shamima, Chinnery, Patrick F.

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The Ionospheric Connection Explorer Mission: Mission Goals and Design von Immel, T. J., England, S. L., Mende, S. B., Heelis, R. A., Englert, C. R., Edelstein, J., Frey, H. U., Korpela, E. J., Taylor, E. R., Craig, W. W., Harris, S. E., Bester, M., Bust, G. S., Crowley, G., Forbes, J. M., Gérard, J.-C., Harlander, J. M., Huba, J. D., Hubert, B., Kamalabadi, F., Makela, J. J., Maute, A. I., Meier, R. R., Raftery, C., Rochus, P., Siegmund, O. H. W., Stephan, A. W., Swenson, G. R., Frey, S., Hysell, D. L., Saito, A., Rider, K. A., Sirk, M. M.

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Initial Observations by the GOLD Mission von Eastes, R. W., McClintock, W. E., Burns, A. G., Anderson, D. N., Andersson, L., Aryal, S., Budzien, S. A., Cai, X., Codrescu, M. V., Correira, J. T., Daniell, R. E., Dymond, K. F., England, S. L., Eparvier, F. G., Evans, J. S., Foroosh, H., Gan, Q., Greer, K. R., Karan, D. K., Krywonos, A., Laskar, F. I., Lumpe, J. D., Martinis, C. R., McPhate, J. B., Oberheide, J., Siegmund, O. H., Solomon, S. C., Veibel, V., Woods, T. N.

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Practice Parameter update: The care of the patient with amyotrophic lateral sclerosis: Multidisciplinary care, symptom management, and cognitive/behavioral impairment (an evidence-... von MILLER, Rg, JACKSON, C. E, SHOESMITH, C, STRONG, M. J, WOOLLEY, S. C, KASARSKIS, E. J, ENGLAND, J. D, FORSHEW, D, JOHNSTON, W, KALRA, S, KATZ, J. S, MITSUMOTO, H, ROSENFELD, J

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Global‐Scale Observations of the Equatorial Ionization Anomaly von Eastes, R. W., Solomon, S. C., Daniell, R. E., Anderson, D. N., Burns, A. G., England, S. L., Martinis, C. R., McClintock, W. E.

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The Global-Scale Observations of the Limb and Disk (GOLD) Mission von Eastes, R. W., McClintock, W. E., Burns, A. G., Anderson, D. N., Andersson, L., Codrescu, M., Correira, J. T., Daniell, R. E., England, S. L., Evans, J. S., Harvey, J., Krywonos, A., Lumpe, J. D., Richmond, A. D., Rusch, D. W., Siegmund, O., Solomon, S. C., Strickland, D. J., Woods, T. N., Aksnes, A., Budzien, S. A., Dymond, K. F., Eparvier, F. G., Martinis, C. R., Oberheide, J.

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DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration von Vig, Anjali, Poulter, James A., Ottaviani, Daniele, Tavares, Erika, Toropova, Katerina, Tracewska, Anna Maria, Mollica, Antonio, Kang, Jasmine, Kehelwathugoda, Oshini, Paton, Tara, Maynes, Jason T., Wheway, Gabrielle, Arno, Gavin, Khan, Kamron N., McKibbin, Martin, Toomes, Carmel, Ali, Manir, Di Scipio, Matteo, Li, Shuning, Ellingford, Jamie, Black, Graeme, Webster, Andrew, Rydzanicz, Małgorzata, Stawiński, Piotr, Płoski, Rafał, Vincent, Ajoy, Cheetham, Michael E., Inglehearn, Chris F., Roberts, Anthony, Heon, Elise

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Human and mouse essentiality screens as a resource for disease gene discovery von Cacheiro, Pilar, Muñoz-Fuentes, Violeta, Murray, Stephen A., Dickinson, Mary E., Bucan, Maja, Nutter, Lauryl M. J., Peterson, Kevin A., Haselimashhadi, Hamed, Flenniken, Ann M., Morgan, Hugh, Westerberg, Henrik, Konopka, Tomasz, Hsu, Chih-Wei, Christiansen, Audrey, Lanza, Denise G., Beaudet, Arthur L., Heaney, Jason D., Fuchs, Helmut, Gailus-Durner, Valerie, Sorg, Tania, Prochazka, Jan, Novosadova, Vendula, Lelliott, Christopher J., Wardle-Jones, Hannah, Wells, Sara, Teboul, Lydia, Cater, Heather, Stewart, Michelle, Hough, Tertius, Wurst, Wolfgang, Sedlacek, Radislav, Adams, David J., Seavitt, John R., Tocchini-Valentini, Glauco, Mammano, Fabio, Braun, Robert E., McKerlie, Colin, Herault, Yann, de Angelis, Martin Hrabě, Mallon, Ann-Marie, Lloyd, K. C.  Kent, Brown, Steve D. M., Parkinson, Helen, Meehan, Terrence F., Smedley, Damian

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Substitution mutational signatures in whole-genome-sequenced cancers in the UK population von Degasperi, Andrea, Zou, Xueqing, Amarante, Tauanne Dias, Martinez-Martinez, Andrea, Koh, Gene Ching Chiek, Dias, João M L, Heskin, Laura, Chmelova, Lucia, Rinaldi, Giuseppe, Wang, Valerie Ya Wen, Nanda, Arjun S, Bernstein, Aaron, Momen, Sophie E, Young, Jamie, Perez-Gil, Daniel, Memari, Yasin, Badja, Cherif, Shooter, Scott, Czarnecki, Jan, Brown, Matthew A, Davies, Helen R, Nik-Zainal, Serena

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De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas von Tolchin, Dara, Yeager, Jessica P., Prasad, Priya, Dorrani, Naghmeh, Russi, Alvaro Serrano, Martinez-Agosto, Julian A., Haseeb, Abdul, Santen, G.W.E., Ruivenkamp, Claudia, Mercimek-Andrews, Saadet, Depienne, Christel, Kuechler, Alma, Mikat, Barbara, Ludecke, Hermann-Josef, Bilan, Frederic, Le Guyader, Gwenael, Gilbert-Dussardier, Brigitte, Keren, Boris, Heide, Solveig, Haye, Damien, Van Esch, Hilde, Keldermans, Liesbeth, Lancaster, Emily, Krantz, Ian D., Krock, Bryan L., DeChene, Elizabeth T., Melistaccio, Giada, Suri, Mohnish, Foulds, Nicola, Bleda, M., Boardman-Pretty, F., Boissiere, J.M., Boustred, C.R., Caulfield, M.J., Chan, G.C., Craig, C.E.H., Daugherty, L.C., Devereau, A., Elgar, G., Foulger, R.E., Fowler, T., Furió-Tarí, P., Hackett, J.M., Halai, D., Holman, J.E., Hubbard, T.J.P., Lahnstein, L., Lawson, K., Leigh, S.E.A., Leong, I.U.S., Maleady-Crowe, F., Mason, J., McDonagh, E.M., Need, A.C., Odhams, C.A., Perez-Gil, D., Polychronopoulos, D., Pullinger, J., Rahim, T., Rendon, A., Rogers, T., Ryten, M., Savage, K., Scott, R.H., Siddiq, A., Sieghart, A., Smedley, D., Smith, K.R., Sosinsky, A., Spooner, W., Stevens, H.E., Stuckey, A., Thomas, E.R.A., Thompson, S.R., Tregidgo, C., Tucci, A., Walsh, E., Welland, M.J., Williams, E., Witkowska, K., Wood, S.M., Zarowiecki, M., Begtrup, Amber, Henderson, Lindsay B., Forster, Cara, Reed, Patrick, McDonald, Marie T., McConkie-Rosell, Allyn, Thevenon, Julien, Le Tanno, Pauline, Coutton, Charles, Stewart, Sarah, Maver, Ales, Gorazd, Rudolf, Pichon, Olivier, Nizon, Mathilde, Cogné, Benjamin, Isidor, Bertrand, Stoeva, Radka, Le Caignec, Cédric

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Cardiac Investigations in Sudden Unexpected Death in DEPDC5-Related Epilepsy von Bacq, Alexandre, Roussel, Delphine, Bonduelle, Thomas, Zagaglia, Sara, Maletic, Marina, Ribierre, Théo, Adle-Biassette, Homa, Marchal, Cécile, Jennesson, Mélanie, An, Isabelle, Picard, Fabienne, Navarro, Vincent, Sisodiya, Sanjay M, Baulac, Stéphanie

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Opportunities and Challenges for Molecular Understanding of Ciliopathies-The 100,000 Genomes Project von Wheway, Gabrielle, Mitchison, Hannah M

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