The startle disease mutation α1S270T predicts shortening of glycinergic synaptic currents von Wu, Zhiyi, Lape, Remigijus, Jopp‐Saile, Lea, O'Callaghan, Benjamin J., Greiner, Timo, Sivilotti, Lucia G.

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The startle disease mutation alpha 1S270T predicts shortening of glycinergic synaptic currents von Wu, Zhiyi, Lape, Remigijus, Jopp-Saile, Lea, O'Callaghan, Benjamin J., Greiner, Timo, Sivilotti, Lucia G.

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Pathophysiology of Dyt1-Tor1a dystonia in mice is mediated by spinal neural circuit dysfunction von Pocratsky, Amanda M, Nascimento, Filipe, Özyurt, M Görkem, White, Ian J, Sullivan, Roisin, O'Callaghan, Benjamin J, Smith, Calvin C, Surana, Sunaina, Beato, Marco, Brownstone, Robert M

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Identification of genes involved in exoprotein release using a high-throughput exoproteome screening assay in Yersinia entomophaga von Schoof, Marion, O'Callaghan, Maureen, Sheen, Campbell R, Glare, Travis R, Hurst, Mark R H

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Long-term health outcomes of people with reduced kidney function in the UK: A modelling study using population health data von Schlackow, Iryna, Simons, Claire, Oke, Jason, Feakins, Benjamin, O'Callaghan, Christopher A., Hobbs, F. D. Richard, Lasserson, Daniel, Stevens, Richard J., Perera, Rafael, Mihaylova, Borislava

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A genetics-led approach defines the drug target landscape of 30 immune-related traits von Fang, Hai, De Wolf, Hans, Knezevic, Bogdan, Burnham, Katie L., Osgood, Julie, Sanniti, Anna, Lledó Lara, Alicia, Kasela, Silva, De Cesco, Stephane, Wegner, Jörg K., Handunnetthi, Lahiru, McCann, Fiona E., Chen, Liye, Sekine, Takuya, Brennan, Paul E., Marsden, Brian D., Damerell, David, O’Callaghan, Chris A., Bountra, Chas, Bowness, Paul, Sundström, Yvonne, Milani, Lili, Berg, Louise, Göhlmann, Hinrich W., Peeters, Pieter J., Fairfax, Benjamin P., Sundström, Michael, Knight, Julian C.

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Emergence of winner-takes-all connectivity paths in random nanowire networks von Manning, Hugh G., Niosi, Fabio, da Rocha, Claudia Gomes, Bellew, Allen T., O’Callaghan, Colin, Biswas, Subhajit, Flowers, Patrick F., Wiley, Benjamin J., Holmes, Justin D., Ferreira, Mauro S., Boland, John J.

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TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study von de Vries, Petrus J, Belousova, Elena, Benedik, Mirjana P, Carter, Tom, Cottin, Vincent, Curatolo, Paolo, Dahlin, Maria, D'Amato, Lisa, d'Augères, Guillaume B, Ferreira, José C, Feucht, Martha, Fladrowski, Carla, Hertzberg, Christoph, Jozwiak, Sergiusz, Kingswood, J Chris, Lawson, John A, Macaya, Alfons, Marques, Ruben, Nabbout, Rima, O'Callaghan, Finbar, Qin, Jiong, Sander, Valentin, Sauter, Matthias, Shah, Seema, Takahashi, Yukitoshi, Touraine, Renaud, Youroukos, Sotiris, Zonnenberg, Bernard, Jansen, Anna C

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The Adelaide Score: An artificial intelligence measure of readiness for discharge after general surgery von Kovoor, Joshua G, Bacchi, Stephen, Gupta, Aashray K, Stretton, Brandon, Malycha, James, Reddi, Benjamin A, Liew, Danny, O'Callaghan, Patrick G, Beltrame, John F, Zannettino, Andrew C, Jones, Karen L, Horowitz, Michael, Dobbins, Christopher, Hewett, Peter J, Trochsler, Markus I, Maddern, Guy J

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Interactive effects of ontogeny, food ration and temperature on elemental incorporation in otoliths of a coral reef fish von Walther, Benjamin D, Kingsford, Michael J, O'Callaghan, Mark D, McCulloch, Malcolm T

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A Touchscreen Motivation Assessment Evaluated in Huntington's Disease Patients and R6/1 Model Mice von Heath, Christopher J, O'Callaghan, Claire, Mason, Sarah L, Phillips, Benjamin U, Saksida, Lisa M, Robbins, Trevor W, Barker, Roger A, Bussey, Timothy J, Sahakian, Barbara J

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AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders von Salpietro, Vincenzo, Dixon, Christine L., Guo, Hui, Bello, Oscar D., Vandrovcova, Jana, Efthymiou, Stephanie, Maroofian, Reza, Heimer, Gali, Burglen, Lydie, Valence, Stephanie, Torti, Erin, Hacke, Moritz, Rankin, Julia, Tariq, Huma, Colin, Estelle, Procaccio, Vincent, Striano, Pasquale, Mankad, Kshitij, Lieb, Andreas, Chen, Sharon, Pisani, Laura, Bettencourt, Conceicao, Männikkö, Roope, Manole, Andreea, Brusco, Alfredo, Grosso, Enrico, Ferrero, Giovanni Battista, Armstrong-Moron, Judith, Gueden, Sophie, Bar-Yosef, Omer, Tzadok, Michal, Monaghan, Kristin G., Santiago-Sim, Teresa, Person, Richard E., Cho, Megan T., Willaert, Rebecca, Yoo, Yongjin, Chae, Jong-Hee, Quan, Yingting, Wu, Huidan, Wang, Tianyun, Bernier, Raphael A., Xia, Kun, Blesson, Alyssa, Jain, Mahim, Motazacker, Mohammad M., Jaeger, Bregje, Schneider, Amy L., Boysen, Katja, Muir, Alison M., Myers, Candace T., Gavrilova, Ralitza H., Gunderson, Lauren, Schultz-Rogers, Laura, Klee, Eric W., Dyment, David, Osmond, Matthew, Parellada, Mara, Llorente, Cloe, Gonzalez-Peñas, Javier, Carracedo, Angel, Van Haeringen, Arie, Ruivenkamp, Claudia, Nava, Caroline, Heron, Delphine, Nardello, Rosaria, Iacomino, Michele, Minetti, Carlo, Skabar, Aldo, Fabretto, Antonella, Raspall-Chaure, Miquel, Chez, Michael, Tsai, Anne, Fassi, Emily, Shinawi, Marwan, Constantino, John N., De Zorzi, Rita, Fortuna, Sara, Kok, Fernando, Keren, Boris, Bonneau, Dominique, Choi, Murim, Benzeev, Bruria, Zara, Federico, Mefford, Heather C., Scheffer, Ingrid E., Clayton-Smith, Jill, Macaya, Alfons, Rothman, James E., Eichler, Evan E., Kullmann, Dimitri M., Houlden, Henry

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Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 loci von Soutar, Marc P M, Melandri, Daniela, O'Callaghan, Benjamin, Annuario, Emily, Monaghan, Amy E, Welsh, Natalie J, D'Sa, Karishma, Guelfi, Sebastian, Zhang, David, Pittman, Alan, Trabzuni, Daniah, Verboven, Anouk H A, Pan, Kylie S, Kia, Demis A, Bictash, Magda, Gandhi, Sonia, Houlden, Henry, Cookson, Mark R, Kasri, Nael Nadif, Wood, Nicholas W, Singleton, Andrew B, Hardy, John, Whiting, Paul J, Blauwendraat, Cornelis, Whitworth, Alexander J, Manzoni, Claudia, Ryten, Mina, Lewis, Patrick A, Plun-Favreau, Hélène

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Statistical models for the deterioration of kidney function in a primary care population: A retrospective database analysis [version 2; peer review: 2 approved] von Oke, Jason L, Feakins, Benjamin G, Schlackow, Iryna, Mihaylova, Borislava, Simons, Claire, O'Callaghan, Chris A, Lasserson, Daniel S, Hobbs, F D Richard, Stevens, Richard J, Perera, Rafael

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International Guideline for Idiopathic Inflammatory Myopathy-Associated Cancer Screening: an International Myositis Assessment and Clinical Studies Group (IMACS) initiative von Oldroyd, Alexander G. S., Callen, Jeffrey P., Chinoy, Hector, Chung, Lorinda, Fiorentino, David, Gordon, Patrick, Machado, Pedro M., McHugh, Neil, Selva-O’Callaghan, Albert, Schmidt, Jens, Tansley, Sarah L., Vleugels, Ruth Ann, Werth, Victoria P., Aggarwal, Rohit

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The resistance of Cu nanowire–nanowire junctions and electro-optical modeling of Cu nanowire networks von Manning, Hugh G., Flowers, Patrick F., Cruz, Mutya A., Rocha, Claudia Gomes da, Callaghan, Colin O', Ferreira, Mauro S., Wiley, Benjamin J., Boland, John J.

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Anti-PL-7 (Anti-Threonyl-tRNA Synthetase) Antisynthetase Syndrome: Clinical Manifestations in a Series of Patients From a European Multicenter Study (EUMYONET) and Review of the Li... von Labirua-Iturburu, Ane, Selva-O’Callaghan, Albert, Vincze, Melinda, Dankó, Katalin, Vencovsky, Jiri, Fisher, Benjamin, Charles, Peter, Dastmalchi, Maryam, Lundberg, Ingrid E.

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Rehabilitation versus surgical reconstruction for non-acute anterior cruciate ligament injury (ACL SNNAP): a pragmatic randomised controlled trial von Davies, Loretta, Stokes, Jamie, Fletcher, Heidi, Bottomley, Nicholas, Paez, Arsenio, Lythe, Vanessa, Carr, Andrew, O'Leary, Sean, Haddad, Fares, Price, Andrew, Campbell, Marion, Howell, Tessa, Davies, Jackie, Vertue, Mark, Bray, Rachel, Kiszely, Alastair, Manara, Jon, Pai, Vishai, Putnis, Sven, Theodorides, Anthony, Vetharajan, Niraj, Young, Lucy, Bullock, Susan, Kent, Benjamin, Kincaid, Robin, Lazizi, Mohamed, Powell, Tim, Riddlestone, Peter, Hall, Andrew, Jeffrey, Helen, Thonse, Raghuram, Dunne, Debra, Shah, Feisal, Teuke, Joanna, Croucher, Andrea, Hawkes-Blackburn, Catherine, Kadunyi, Joyce, Anand, Sanjeev, Cowen, Laura, Davis, Jack, Houchen-Wolloff, Linzy, Varachia, Husein, Wood, Richard, Gray, Glaxy, Nichols, Jessica, Panes, Alice, Triggs, David, Buckley, Sarah, Adcode, Megan, Cottingham, Megan, Foster, Eliza, Williams, James, Jayachandran, Jayadeep, Deakin, Marc, Hynes, Samantha, McKenna, David, Scott-Dempster, Clare, Sykes, Adam, Wood, Simon, Modi, Nishil, Parker, Nicola, Pecheva, Mira, Rumonovic, Rowan, McLoughlin, Emma, Wright, Daniel, Baker, Simon, Lewis, Alison, Campbell, Terence, Hazlerigg, Alexandra, Parsons, Georgie, Montaser, Rugaia, Templeton-Ward, Oliver, Diment, Sarah, Vachtsevanos, Leonidas, Ollerenshaw, Joanna, Sutton, Paul, Chikate, Albert, Daniel, Diane, Finnigan, Tom, McGowan, Angela, Sands Johnson, David, Smith, Lara, Allsop, Lynne, Desai, Vikram, Gill, Mandy, Heeley, Cheryl, Lovegrove, Wayne, Slack, Katie, Satish, Venkat, Thelwall, Claire, Areirobulos, Miltiades, de Feyter, Pascal, Ditchfield, Lisa, Massey, Daniel, Stables, Gareth, Cable, Sarah, Da Rocha, Joana, Mohammed, Haadiya, Joshi, Yogesh, Morgan, Tania

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Computed tomographic parenchymal lung findings in premature infants with pulmonary vein stenosis von O’Callaghan, Barry, Zablah, Jenny E., Weinman, Jason P., Englund, Erin K., Morgan, Gareth J., Ivy, D. Dunbar, Frank, Benjamin S., Mong, David Andrew, Malone, LaDonna J., Browne, Lorna P.

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ANGPTL6 Genetic Variants Are an Underlying Cause of Familial Intracranial Aneurysms von Hostettler, Isabel C., O'Callaghan, Benjamin, Bugiardini, Enrico, O'Connor, Emer, Vandrovcova, Jana, Davagnanam, Indran, Alg, Varinder, Bonner, Stephen, Walsh, Daniel, Bulters, Diederik, Kitchen, Neil, Brown, Martin M., Grieve, Joan, Werring, David J., Houlden, Henry

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