A case of extrapyramidal side effects due to possible paliperidone: voriconazole interaction von Beilby, Louise, Arno, Lucy

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A Randomized Noninferiority Trial to Compare Enteral to Parenteral Phosphate Replacement on Biochemistry, Waste, and Environmental Impact and Healthcare Cost in Critically Ill Pati... von Nguyen, Chinh D, Panganiban, Haustine P, Fazio, Timothy, Karahalios, Amalia, Ankravs, Melissa J, MacIsaac, Christopher M, Rechnitzer, Thomas, Arno, Lucy, Tran-Duy, An, McAlister, Scott, Ali Abdelhamid, Yasmine, Deane, Adam M

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A Randomized Noninferiority Trial to Compare Enteral to Parenteral Phosphate Replacement on Biochemistry, Waste, and Environmental Impact and Healthcare Cost in Critically Ill Pati... von Nguyen, Chinh D, Panganiban, Haustine P, Fazio, Timothy, Karahalios, Amalia, Ankravs, Melissa J, MacIsaac, Christopher M, Rechnitzer, Thomas, Arno, Lucy, Tran-Duy, An, McAlister, Scott, Ali Abdelhamid, Yasmine, Deane, Adam M

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Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing von Sanchis-Juan, Alba, Stephens, Jonathan, French, Courtney E, Gleadall, Nicholas, Mégy, Karyn, Penkett, Christopher, Shamardina, Olga, Stirrups, Kathleen, Delon, Isabelle, Dewhurst, Eleanor, Dolling, Helen, Erwood, Marie, Grozeva, Detelina, Stefanucci, Luca, Arno, Gavin, Webster, Andrew R, Cole, Trevor, Austin, Topun, Branco, Ricardo Garcia, Ouwehand, Willem H, Raymond, F Lucy, Carss, Keren J

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Robustness and uncertainties in global multivariate wind-wave climate projections von Morim, Joao, Hemer, Mark, Wang, Xiaolan L., Cartwright, Nick, Trenham, Claire, Semedo, Alvaro, Young, Ian, Bricheno, Lucy, Camus, Paula, Casas-Prat, Mercè, Erikson, Li, Mentaschi, Lorenzo, Mori, Nobuhito, Shimura, Tomoya, Timmermans, Ben, Aarnes, Ole, Breivik, Øyvind, Behrens, Arno, Dobrynin, Mikhail, Menendez, Melisa, Staneva, Joanna, Wehner, Michael, Wolf, Judith, Kamranzad, Bahareh, Webb, Adrean, Stopa, Justin, Andutta, Fernando

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Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal Degeneration von Ku, Cristy A, Hull, Sarah, Arno, Gavin, Vincent, Ajoy, Carss, Keren, Kayton, Robert, Weeks, Douglas, Anderson, Glenn W, Geraets, Ryan, Parker, Camille, Pearce, David A, Michaelides, Michel, MacLaren, Robert E, Robson, Anthony G, Holder, Graham E, Heon, Elise, Raymond, F. Lucy, Moore, Anthony T, Webster, Andrew R, Pennesi, Mark E

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Mutations in CACNA2D4 Cause Distinctive Retinal Dysfunction in Humans von Ba-Abbad, Rola, MD, Arno, Gavin, PhD, Carss, Keren, PhD, Stirrups, Kathleen, PhD, Penkett, Christopher J., PhD, Moore, Anthony T., MD, Michaelides, Michel, MD, Raymond, F. Lucy, MA, DPhil, Webster, Andrew R., MD, Holder, Graham E., PhD

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Expanding the FDXR-Associated Disease Phenotype: Retinal Dystrophy Is a Recurrent Ocular Feature von Jurkute, Neringa, Shanmugarajah, Priya D, Hadjivassiliou, Marios, Higgs, Jenny, Vojcic, Miodrag, Horrocks, Iain, Nadjar, Yann, Touitou, Valerie, Lenaers, Guy, Poh, Roy, Acheson, James, Robson, Anthony G, Raymond, F Lucy, Reilly, Mary M, Yu-Wai-Man, Patrick, Moore, Anthony T, Webster, Andrew R, Arno, Gavin

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Microbial translocation is associated with extensive immune activation in dengue virus infected patients with severe disease von van de Weg, Cornelia A M, Pannuti, Cláudio S, de Araújo, Evaldo S A, van den Ham, Henk-Jan, Andeweg, Arno C, Boas, Lucy S V, Felix, Alvina C, Carvalho, Karina I, de Matos, Andreia M, Levi, José E, Romano, Camila M, Centrone, Cristiane C, de Lima Rodrigues, Celia L, Luna, Expedito, van Gorp, Eric C M, Osterhaus, Albert D M E, Martina, Byron E E, Kallas, Esper G

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Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa von de Bruijn, Suzanne E., Fiorentino, Alessia, Ottaviani, Daniele, Fanucchi, Stephanie, Melo, Uirá S., Corral-Serrano, Julio C., Mulders, Timo, Georgiou, Michalis, Rivolta, Carlo, Pontikos, Nikolas, Arno, Gavin, Roberts, Lisa, Greenberg, Jacquie, Albert, Silvia, Gilissen, Christian, Aben, Marco, Rebello, George, Mead, Simon, Raymond, F. Lucy, Corominas, Jordi, Smith, Claire E.L., Kremer, Hannie, Downes, Susan, Black, Graeme C., Webster, Andrew R., Inglehearn, Chris F., van den Born, L. Ingeborgh, Koenekoop, Robert K., Michaelides, Michel, Ramesar, Raj S., Hoyng, Carel B., Mundlos, Stefan, Mhlanga, Musa M., Cremers, Frans P.M., Cheetham, Michael E., Roosing, Susanne, Hardcastle, Alison J.

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A clinical and molecular characterisation of CRB1-associated maculopathy von Khan, Kamron N, Robson, Anthony, Mahroo, Omar A R, Arno, Gavin, Inglehearn, Chris F, Armengol, Monica, Waseem, Naushin, Holder, Graham E, Carss, Keren J, Raymond, Lucy F, Webster, Andrew R, Moore, Anthony T, McKibbin, Martin, van Genderen, Maria M, Poulter, James A, Michaelides, Michel

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Ceramide synthase TLCD3B is a novel gene associated with human recessive retinal dystrophy von Bertrand, Renae Elaine, Wang, Jun, Xiong, Kaitlyn H., Thangavel, Chinthana, Qian, Xinye, Ba-Abbad, Rola, Liang, Qingnan, Simões, Renata T., Sampaio, Shirley A. M., Carss, Keren J., Lucy Raymond, F., Robson, Anthony G., Webster, Andrew R., Arno, Gavin, Porto, Fernanda Belga Ottoni, Chen, Rui

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Unique noncoding variants upstream of PRDM13 are associated with a spectrum of developmental retinal dystrophies including progressive bifocal chorioretinal atrophy von Silva, Raquel S., Arno, Gavin, Cipriani, Valentina, Pontikos, Nikolas, Defoort‐Dhellemmes, Sabine, Kalhoro, Ambreen, Carss, Keren J., Raymond, F. Lucy, Dhaenens, Claire Marie, Jensen, Hanne, Rosenberg, Thomas, Heyningen, Veronica, Moore, Anthony T., Puech, Bernard, Webster, Andrew R.

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Phenopolis: an open platform for harmonization and analysis of genetic and phenotypic data von Pontikos, Nikolas, Yu, Jing, Moghul, Ismail, Withington, Lucy, Blanco-Kelly, Fiona, Vulliamy, Tom, Wong, Tsz Lun Ernest, Murphy, Cian, Cipriani, Valentina, Fiorentino, Alessia, Arno, Gavin, Greene, Daniel, Jacobsen, Julius O B, Clark, Tristan, Gregory, David S, Nemeth, Andrea M, Halford, Stephanie, Inglehearn, Chris F, Downes, Susan, Black, Graeme C, Webster, Andrew R, Hardcastle, Alison J, Plagnol, Vincent

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Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides von Sangermano, Riccardo, Garanto, Alejandro, Khan, Mubeen, Runhart, Esmee H., Bauwens, Miriam, Bax, Nathalie M., van den Born, L. Ingeborgh, Khan, Muhammad Imran, Cornelis, Stéphanie S., Verheij, Joke B. G. M., Pott, Jan-Willem R., Thiadens, Alberta A. H. J., Klaver, Caroline C. W., Puech, Bernard, Meunier, Isabelle, Naessens, Sarah, Arno, Gavin, Fakin, Ana, Carss, Keren J., Raymond, F. Lucy, Webster, Andrew R., Dhaenens, Claire-Marie, Stöhr, Heidi, Grassmann, Felix, Weber, Bernhard H. F., Hoyng, Carel B., De Baere, Elfride, Albert, Silvia, Collin, Rob W. J., Cremers, Frans P. M.

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SSBP1-Disease Update: Expanding the Genetic and Clinical Spectrum, Reporting Variable Penetrance and Confirming Recessive Inheritance von Jurkute, Neringa, D'Esposito, Fabiana, Robson, Anthony G, Pitceathly, Robert D S, Cordeiro, Francesca, Raymond, F Lucy, Moore, Anthony T, Michaelides, Michel, Yu-Wai-Man, Patrick, Webster, Andrew R, Arno, Gavin

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Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa von Arno, Gavin, Agrawal, Smriti A., Eblimit, Aiden, Bellingham, James, Xu, Mingchu, Wang, Feng, Chakarova, Christina, Parfitt, David A., Lane, Amelia, Burgoyne, Thomas, Hull, Sarah, Carss, Keren J., Fiorentino, Alessia, Hayes, Matthew J., Munro, Peter M., Nicols, Ralph, Pontikos, Nikolas, Holder, Graham E., Black, Graeme, Hall, Georgina, Ingram, Stuart, Gillespie, Rachel, Manson, Forbes, Sergouniotis, Panagiotis, Inglehearn, Chris, Toomes, Carmel, Ali, Manir, McKibbin, Martin, Poulter, James, Khan, Kamron, Lord, Emma, Nemeth, Andrea, Downes, Susan, Yu, Jing, Lise, Stefano, Arno, Gavin, Fiorentino, Alessia, Ponitkos, Nikos, Plagnol, Vincent, Michaelides, Michel, Hardcastle, Alison J., Cheetham, Michael E., Webster, Andrew R., van Heyningen, Veronica, Asomugha, Chinwe, Raymond, F. Lucy, Moore, Anthony T., Plagnol, Vincent, Michaelides, Michel, Hardcastle, Alison J., Li, Yumei, Cukras, Catherine, Webster, Andrew R., Cheetham, Michael E., Chen, Rui

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Delineating the expanding phenotype associated with SCAPER gene mutation von Fasham, James, Arno, Gavin, Lin, Siying, Xu, Mingchu, Carss, Keren J., Hull, Sarah, Lane, Amelia, Robson, Anthony G., Wenger, Olivia, Self, Jay E., Harlalka, Gaurav V., Salter, Claire G., Schema, Lynn, Moss, Timothy J., Cheetham, Michael E., Moore, Anthony T., Raymond, F. Lucy, Chen, Rui, Baple, Emma L., Webster, Andrew R., Crosby, Andrew H.

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The effect of prior hysterosalpingo-foam sonography or hysterosalpingography on tubal patency: a secondary analysis of a randomized controlled trial von Kamphuis, Danah, van Welie, Nienke, van Rijswijk, Joukje, van Hooff, Marcel H A, de Bruin, Jan-Peter, Verhoeve, Harold R, Mol, Femke, van Baal, Wilhelmina M, Lambalk, Cornelis B, Stoker, Jaap, van Wely, Madelon, Bossuyt, Patrick M M, Mol, Ben Willem J, Dreyer, Kim, Mijatovic, Velja

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Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis Pigmentosa von Hull, Sarah, Attanasio, Marcella, Arno, Gavin, Carss, Keren, Robson, Anthony G, Thompson, Dorothy A, Plagnol, Vincent, Michaelides, Michel, Holder, Graham E, Henderson, Robert H, Raymond, F. Lucy, Moore, Anthony T, Webster, Andrew R

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