Emotional experience in patients with clinically isolated syndrome and early multiple sclerosis von Hälbig, T. D., Wüstenberg, T., Giess, R. M., Kunte, H., Bellmann‐Strobl, J., Ruprecht, K., Paul, F.

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Epstein-Barr virus antibodies in serum and DNA load in saliva are not associated with radiological or clinical disease activity in patients with early multiple sclerosis von Gieß, René M, Pfuhl, Catherina, Behrens, Janina R, Rasche, Ludwig, Freitag, Erik, Khalighy, Nima, Otto, Carolin, Wuerfel, Jens, Brandt, Alexander U, Hofmann, Jörg, Eberspächer, Bettina, Bellmann-Strobl, Judith, Paul, Friedemann, Ruprecht, Klemens

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Intrathecal IgM production is a strong risk factor for early conversion to multiple sclerosis von Pfuhl, Catherina, Grittner, Ulrike, Gieß, René M, Scheel, Michael, Behrens, Janina R, Rasche, Ludwig, Pache, Florence C, Wenzel, Rüdiger, Brandt, Alexander U, Bellmann-Strobl, Judith, Paul, Friedemann, Ruprecht, Klemens, Oechtering, Johanna

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Multi-parameter immune profiling of peripheral blood mononuclear cells by multiplexed single-cell mass cytometry in patients with early multiple sclerosis von Böttcher, Chotima, Fernández-Zapata, Camila, Schlickeiser, Stephan, Kunkel, Desiree, Schulz, Axel R., Mei, Henrik E., Weidinger, Carl, Gieß, René M., Asseyer, Susanna, Siegmund, Britta, Paul, Friedemann, Ruprecht, Klemens, Priller, Josef

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Low 25-hydroxyvitamin D, but not the bioavailable fraction of 25-hydroxyvitamin D, is a risk factor for multiple sclerosis von Behrens, Janina R., Rasche, Ludwig, Gieß, Rene M., Pfuhl, Catherina, Wakonig, Katharina, Freitag, Erik, Deuschle, Katrin, Bellmann-Strobl, Judith, Paul, Friedemann, Ruprecht, Klemens, Dörr, Jan

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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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Genetic parameter estimates for feet and leg traits in Red Angus cattle von Giess, Lane K., Jensen, Brady R., Bormann, Jennifer M., Rolf, Megan M., Weaber, Robert L.

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475P Optimising genomic testing for patients with central nervous system (CNS) tumours using oxford nanopore technology von Sosinsky, A.A., Howell, R., Freeman, T., Giess, A., Tanguy, M., Elgar, G.

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Genome sequencing of an extended series of NDM-producing Klebsiella pneumoniae isolates from neonatal infections in a Nepali hospital characterizes the extent of community- versus... von Stoesser, N, Giess, A, Batty, E M, Sheppard, A E, Walker, A S, Wilson, D J, Didelot, X, Bashir, A, Sebra, R, Kasarskis, A, Sthapit, B, Shakya, M, Kelly, D, Pollard, A J, Peto, T E A, Crook, D W, Donnelly, P, Thorson, S, Amatya, P, Joshi, S

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Extensive Within-Host Diversity in Fecally Carried Extended-Spectrum-Beta-Lactamase-Producing Escherichia coli Isolates: Implications for Transmission Analyses von Stoesser, N, Sheppard, A E, Moore, C E, Golubchik, T, Parry, C M, Nget, P, Saroeun, M, Day, N P J, Giess, A, Johnson, J R, Peto, T E A, Crook, D W, Walker, A S

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Next-generation sequencing identifies altered whole blood microRNAs in neuromyelitis optica spectrum disorder which may permit discrimination from multiple sclerosis von Keller, Andreas, Leidinger, Petra, Meese, Eckart, Haas, Jan, Backes, Christina, Rasche, Ludwig, Behrens, Janina R, Pfuhl, Catherina, Wakonig, Katharina, Gieß, René M, Jarius, Sven, Meder, Benjamin, Bellmann-Strobl, Judith, Paul, Friedemann, Pache, Florence C, Ruprecht, Klemens

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CNTF is a major protective factor in demyelinating CNS disease: A neurotrophic cytokine as modulator in neuroinflammation von Gold, Ralf, Linker, Ralf A, Mäurer, Mathias, Gaupp, Stefanie, Martini, Rudolf, Holtmann, Bettina, Giess, Ralf, Rieckmann, Peter, Lassmann, Hans, Toyka, Klaus V, Sendtner, Michael

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The Protein-Tethered Lipid Bilayer: A Novel Mimic of the Biological Membrane von Giess, Frank, Friedrich, Marcel G., Heberle, Joachim, Naumann, Renate L., Knoll, Wolfgang

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Association of serum Epstein–Barr nuclear antigen-1 antibodies and intrathecal immunoglobulin synthesis in early multiple sclerosis von Pfuhl, Catherina, Oechtering, Johanna, Rasche, Ludwig, Gieß, René M, Behrens, Janina R, Wakonig, Katharina, Freitag, Erik, Pache, Florence C, Otto, Carolin, Hofmann, Jörg, Eberspächer, Bettina, Bellmann-Strobl, Judith, Paul, Friedemann, Ruprecht, Klemens

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Comparison of in silico strategies to prioritize rare genomic variants impacting RNA splicing for the diagnosis of genomic disorders von Rowlands, Charlie, Thomas, Huw B., Lord, Jenny, Wai, Htoo A., Arno, Gavin, Beaman, Glenda, Sergouniotis, Panagiotis, Gomes-Silva, Beatriz, Campbell, Christopher, Gossan, Nicole, Hardcastle, Claire, Webb, Kevin, O’Callaghan, Christopher, Hirst, Robert A., Ramsden, Simon, Jones, Elizabeth, Clayton-Smith, Jill, Webster, Andrew R., Douglas, Andrew G. L., O’Keefe, Raymond T., Newman, William G., Baralle, Diana, Black, Graeme C. M., Ellingford, Jamie M.

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The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer von Trotman, Jamie, Armstrong, Ruth, Firth, Helen, Trayers, Claire, Watkins, James, Allinson, Kieren, Jacques, Thomas S., Nicholson, James C., Burke, G. A. Amos, Behjati, Sam, Murray, Matthew J., Hook, Catherine E., Tarpey, Patrick

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Prevalence and significance of DDX41 gene variants in the general population von Cheloor Kovilakam, Sruthi, Gu, Muxin, Dunn, William G., Marando, Ludovica, Barcena, Clea, Ambrose, J. C., Arumugam, P., Bevers, R., Bleda, M., Boardman-Pretty, F., Boustred, C. R., Brittain, H., Brown, M. A., Caulfield, M. J., Chan, G. C., Giess, A., Griffin, J. N., Hamblin, A., Henderson, S., Hubbard, T. J. P., Jackson, R., Jones, L. J., Kasperaviciute, D., Kayikci, M., Kousathanas, A., Lahnstein, L., Lakey, A., Leigh, S. E. A., Leong, I. U. S., Lopez, F. J., Maleady-Crowe, F., McEntagart, M., Minneci, F., Mitchell, J., Moutsianas, L., Mueller, M., Murugaesu, N., Need, A. C., O‘Donovan, P., Odhams, C. A., Patch, C., Perez-Gil, D., Pereira, M. B., Pullinger, J., Rahim, T., Rendon, A., Rogers, T., Savage, K., Sawant, K., Scott, R. H., Siddiq, A., Sieghart, A., Smith, S. C., Sosinsky, A., Stuckey, A., Tanguy, M., Taylor Tavares, A. L., Thomas, E. R. A., Thompson, S. R., Tucci, A., Welland, M. J., Williams, E., Witkowska, K., Wood, S. M., Zarowiecki, M., Nik-Zainal, Serena, Mohorianu, Irina, Kar, Siddhartha P., Fabre, Margarete A., Quiros, Pedro M., Vassiliou, George S.

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Origins and impact of extrachromosomal DNA von Bailey, Chris, Pich, Oriol, Thol, Kerstin, Watkins, Thomas B. K., Luebeck, Jens, Rowan, Andrew, Stavrou, Georgia, Weiser, Natasha E., Dameracharla, Bhargavi, Bentham, Robert, Lu, Wei-Ting, Kittel, Jeanette, Yang, S. Y. Cindy, Howitt, Brooke E., Sharma, Natasha, Litovchenko, Maria, Salgado, Roberto, Hung, King L., Cornish, Alex J., Moore, David A., Houlston, Richard S., Bafna, Vineet, Chang, Howard Y., Nik-Zainal, Serena, Kanu, Nnennaya, McGranahan, Nicholas, Flanagan, Adrienne M., Mischel, Paul S., Jamal-Hanjani, Mariam, Swanton, Charles

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Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update von McGuigan, Anthony, Whitworth, James, Andreou, Avgi, Hearn, Timothy, Tischkowitz, Marc, Maher, Eamonn R

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Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy von Parry, David A., Martin, Carol-Anne, Greene, Philip, Marsh, Joseph A., Blyth, Moira, Cox, Helen, Donnelly, Deirdre, Greenhalgh, Lynn, Greville-Heygate, Stephanie, Harrison, Victoria, Lachlan, Katherine, McKenna, Caoimhe, Quigley, Alan J., Rea, Gillian, Robertson, Lisa, Suri, Mohnish, Jackson, Andrew P.

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