ROBOTIC SURGERY SYSTEM von Davies, James, Cooper, Adrian Edward, Medeiros, Chace Francis, Brittain, Thomas Henry, Pflaumer, Hans Christian, Monteiro, Andre Fraser, Laakso, Aki Hannu Einari

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ROBOTIC SURGERY SYSTEM von MARINOVICH, Matthew Michael, BOONZAIER, James Angus, WOLF, Marcus Joseph, MCDIARMID, Ian, SMITHEMAN, Paul, PAWULSKI, Mark, NOAKES, Robert Ian, MONTEIRO, Andre Fraser, BRITTAIN, Thomas Henry, DAVIS, Austin Paul, BARTON, Rupert Anthony, PFLAUMER, Hans Christian, COOPER, Adrian Edward, MEDEIROS, Chace Francis, HORVATH, Jozsef, HOLMES, Brian Gregory

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ROBOTIC SURGICAL SYSTEM WITH CONTROL DRIVE ASSEMBLY FOR SINGLE PORT SURGICAL TECHNIQUES von LAAKSO, Aki Hannu Einari, MARINOVICH, Matthew Michael, COOKE, Jon, MCDIARMID, Ian, BOONZAIER, James Angus, WOLF, Marcus Joseph, SMITHEMAN, Paul, KING, Brian, MEDEIROS, Chace F, NOAKES, Robert Ian, MONTEIRO, Andre Fraser, BRITTAIN, Thomas Henry, DAVIS, Austin Paul, BARTON, Rupert Anthony, PFLAUMER, Hans Christian, COOPER, Adrian Edward, PAWULSKI, Mark J, AHUJA, Akshaya, HORVATH, Jozsef, HOLMES, Brian Gregory

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ROBOTIC SURGERY SYSTEM von MARINOVICH, Matthew Michael, BOONZAIER, James Angus, WOLF, Marcus Joseph, MCDIARMID, Ian, SMITHEMAN, Paul, PAWULSKI, Mark, NOAKES, Robert Ian, MONTEIRO, Andre Fraser, BRITTAIN, Thomas Henry, DAVIS, Austin Paul, BARTON, Rupert Anthony, PFLAUMER, Hans Christian, COOPER, Adrian Edward, MEDEIROS, Chace Francis, HORVATH, Jozsef, HOLMES, Brian Gregory

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Specialist multidisciplinary input maximises rare disease diagnoses from whole genome sequencing von Macken, William L., Falabella, Micol, McKittrick, Caroline, Pizzamiglio, Chiara, Ellmers, Rebecca, Eggleton, Kelly, Woodward, Cathy E., Patel, Yogen, Labrum, Robyn, Phadke, Rahul, Reilly, Mary M., DeVile, Catherine, Sarkozy, Anna, Footitt, Emma, Davison, James, Rahman, Shamima, Houlden, Henry, Bugiardini, Enrico, Quinlivan, Rosaline, Hanna, Michael G., Vandrovcova, Jana, Pitceathly, Robert D. S.

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Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders von Gracia-Diaz, Carolina, Zhou, Yijing, Yang, Qian, Maroofian, Reza, Espana-Bonilla, Paula, Lee, Chul-Hwan, Zhang, Shuo, Padilla, Natàlia, Fueyo, Raquel, Waxman, Elisa A., Lei, Sunyimeng, Otrimski, Garrett, Li, Dong, Sheppard, Sarah E., Mark, Paul, Harr, Margaret H., Hakonarson, Hakon, Rodan, Lance, Jackson, Adam, Vasudevan, Pradeep, Powel, Corrina, Mohammed, Shehla, Maddirevula, Sateesh, Alzaidan, Hamad, Faqeih, Eissa A., Efthymiou, Stephanie, Turchetti, Valentina, Rahman, Fatima, Maqbool, Shazia, Salpietro, Vincenzo, Ibrahim, Shahnaz H., di Rosa, Gabriella, Houlden, Henry, Alharbi, Maha Nasser, Al-Sannaa, Nouriya Abbas, Bauer, Peter, Zifarelli, Giovanni, Estaras, Conchi, Hurst, Anna C. E., Thompson, Michelle L., Chassevent, Anna, Smith-Hicks, Constance L., de la Cruz, Xavier, Holtz, Alexander M., Elloumi, Houda Zghal, Hajianpour, M J, Rieubland, Claudine, Braun, Dominique, Banka, Siddharth, French, Deborah L., Heller, Elizabeth A., Saade, Murielle, Song, Hongjun, Ming, Guo-li, Alkuraya, Fowzan S., Agrawal, Pankaj B., Reinberg, Danny, Bhoj, Elizabeth J., Martínez-Balbás, Marian A., Akizu, Naiara

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Neuronal intranuclear inclusion disease is genetically heterogeneous von Chen, Zhongbo, Yan Yau, Wai, Jaunmuktane, Zane, Tucci, Arianna, Sivakumar, Prasanth, Gagliano Taliun, Sarah A., Turner, Chris, Efthymiou, Stephanie, Ibáñez, Kristina, Sullivan, Roisin, Bibi, Farah, Athanasiou‐Fragkouli, Alkyoni, Bourinaris, Thomas, Zhang, David, Revesz, Tamas, Lashley, Tammaryn, DeTure, Michael, Dickson, Dennis W., Josephs, Keith A., Gelpi, Ellen, Kovacs, Gabor G., Halliday, Glenda, Rowe, Dominic B., Blair, Ian, Tienari, Pentti J., Suomalainen, Anu, Fox, Nick C., Wood, Nicholas W., Lees, Andrew J., Haltia, Matti J., Hardy, John, Ryten, Mina, Vandrovcova, Jana, Houlden, Henry

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Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy von Tucci, Arianna, Cipriani, Valentina, Demidov, German, Rocca, Clarissa, Senderek, Jan, Butryn, Michaela, Lam, Tanya, Cali, Elisa, Vestito, Letizia, Maroofian, Reza, Deininger, Natalie, Rautenberg, Maren, Admard, Jakob, Bartels, Claudius, Horvath, Rita, Chinnery, Patrick F., Tiet, May Yung, Hewamadduma, Channa, Tofaris, George K., Ambrose, J.C., Arumugam, P., Baple, E.L., Bleda, M., Boardman-Pretty, F., Boissiere, J.M., Boustred, C.R., Brittain, H., Caulfield, M.J., Craig, C.E.H., Daugherty, L.C., Devereau, A., Elgar, G., Foulger, R.E., Fowler, T., Furió-Tarí, P., Hackett, J.M., Halai, D., Hamblin, A., Henderson, S., Holman, J.E., Ibáñez, K., Jackson, R., Jones, L.J., Kasperaviciute, D., Kayikci, M., Lahnstein, L., Lawson, K., Leigh, S.E.A., Leong, I.U.S., Maleady-Crowe, F., Mason, J., McDonagh, E.M., Moutsianas, L., Mueller, M., Odhams, C.A., Patch, C., Perez-Gil, D., Pullinger, J., Rahim, T., Riesgo-Ferreiro, P., Rogers, T., Ryten, M., Sawant, K., Scott, R.H., Siddiq, A., Sieghart, A., Smedley, D., Smith, K.R., Spooner, W., Stevens, H.E., Stuckey, A., Sultana, R., Thomas, E.R.A., Tucci, A., Watters, S.A., Welland, M.J., Williams, E., Zarowiecki, M., Wood, Nicholas W., Hayer, Stefanie N., Bender, Friedemann, Menden, Benita, Cordts, Isabell, Klein, Katrin, Krauss, Joachim K., Blahak, Christian, Strom, Tim M., Sturm, Marc, van de Warrenburg, Bart, Lerche, Holger, Maček, Boris, Ossowski, Stephan, Timmann, Dagmar, Wolf, Marc E., Smedley, Damian, Riess, Olaf, Schöls, Ludger, Houlden, Henry, Haack, Tobias B., Hengel, Holger

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Repeat expansions in NOP56 are a cause of spinocerebellar ataxia Type 36 in the British population von Lam, Tanya, Rocca, Clarissa, Ibanez, Kristina, Dalmia, Anupriya, Tallman, Samuel, Hadjivassiliou, Marios, Hensiek, Anke, Nemeth, Andrea, Facchini, Stefano, Wood, Nicholas, Cortese, Andrea, Houlden, Henry, Tucci, Arianna

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Crystal structure of an ADP-ribosylated protein with a cytidine deaminase-like fold, but unknown function (TM1506), from Thermotoga maritima at 2.70 Å resolution von Xu, Qingping, Kozbial, Piotr, McMullan, Daniel, Sri Krishna, S., Brittain, Scott M., Ficarro, Scott B., DiDonato, Michael, Miller, Mitchell D., Abdubek, Polat, Axelrod, Herbert L., Chiu, Hsiu-Ju, Clayton, Thomas, Duan, Lian, Elsliger, Marc-André, Feuerhelm, Julie, Grzechnik, Slawomir K., Hale, Joanna, Han, Gye Won, Jaroszewski, Lukasz, Klock, Heath E., Morse, Andrew T., Nigoghossian, Edward, Paulsen, Jessica, Reyes, Ron, Rife, Christopher L., van den Bedem, Henry, White, Aprilfawn, Hodgson, Keith O., Wooley, John, Deacon, Ashley M., Godzik, Adam, Lesley, Scott A., Wilson, Ian A.

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Structure of a tryptophanyl-tRNA synthetase containing an iron-sulfur cluster von Han, Gye Won, Yang, Xiang-Lei, McMullan, Daniel, Chong, Yeeting E., Krishna, S. Sri, Rife, Christopher L., Weekes, Dana, Brittain, Scott M., Abdubek, Polat, Ambing, Eileen, Astakhova, Tamara, Axelrod, Herbert L., Carlton, Dennis, Caruthers, Jonathan, Chiu, Hsiu-Ju, Clayton, Thomas, Duan, Lian, Feuerhelm, Julie, Grant, Joanna C., Grzechnik, Slawomir K., Jaroszewski, Lukasz, Jin, Kevin K., Klock, Heath E., Knuth, Mark W., Kumar, Abhinav, Marciano, David, Miller, Mitchell D., Morse, Andrew T., Nigoghossian, Edward, Okach, Linda, Paulsen, Jessica, Reyes, Ron, Van Den Bedem, Henry, White, Aprilfawn, Wolf, Guenter, Xu, Qingping, Hodgson, Keith O., Wooley, John, Deacon, Ashley M., Godzik, Adam, Lesley, Scott A., Elsliger, Marc-André, Schimmel, Paul, Wilson, Ian A.

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Identifying effects of accelerometers on the swimming performance of juvenile lemon sharks von Nugent, Thomas, Baker, Brian, Piersiak, Dean, Swain, Henry, Siegert, Gavin, Paget-Brown, Heather, ElizaSchmidt, Bouyoucos, Ian, Brittain, Candice

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