3D Bayesian cluster analysis of super-resolution data reveals LAT recruitment to the T cell synapse von Griffié, Juliette, Shlomovich, Leigh, Williamson, David J., Shannon, Michael, Aaron, Jesse, Khuon, Satya, L. Burn, Garth, Boelen, Lies, Peters, Ruby, Cope, Andrew P., Cohen, Edward A. K., Rubin-Delanchy, Patrick, Owen, Dylan M.

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Machine learning for cluster analysis of localization microscopy data von Williamson, David J., Burn, Garth L., Simoncelli, Sabrina, Griffié, Juliette, Peters, Ruby, Davis, Daniel M., Owen, Dylan M.

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Why is PTPN22 a good candidate susceptibility gene for autoimmune disease? von Burn, Garth L., Svensson, Lena, Sanchez-Blanco, Cristina, Saini, Manoj, Cope, Andrew P.

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Bayesian cluster identification in single-molecule localization microscopy data von Rubin-Delanchy, Patrick, Burn, Garth L, Griffié, Juliette, Williamson, David J, Heard, Nicholas A, Cope, Andrew P, Owen, Dylan M

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A switch-variant model integrates the functions of an autoimmune variant of the phosphatase PTPN22 von Vang, Torkel, Nielsen, Jimmi, Burn, Garth L

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Quantitative fibre analysis of single-molecule localization microscopy data von Peters, Ruby, Griffié, Juliette, Burn, Garth L., Williamson, David J., Owen, Dylan M.

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A Bayesian cluster analysis method for single-molecule localization microscopy data von Griffié, Juliette, Shannon, Michael, Bromley, Claire L, Boelen, Lies, Burn, Garth L, Williamson, David J, Heard, Nicholas A, Cope, Andrew P, Owen, Dylan M, Rubin-Delanchy, Patrick

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Live-Cell Super-resolution Reveals F-Actin and Plasma Membrane Dynamics at the T Cell Synapse von Ashdown, George W., Burn, Garth L., Williamson, David J., Pandžić, Elvis, Peters, Ruby, Holden, Michael, Ewers, Helge, Shao, Lin, Wiseman, Paul W., Owen, Dylan M.

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Superresolution imaging of the cytoplasmic phosphatase PTPN22 links integrin-mediated T cell adhesion with autoimmunity von Burn, Garth L, Cornish, Georgina H, Potrzebowska, Katarzyna, Samuelsson, Malin, Griffié, Juliette, Minoughan, Sophie, Yates, Mark, Ashdown, George, Pernodet, Nicolas, Morrison, Vicky L, Sanchez-Blanco, Cristina, Purvis, Harriet, Clarke, Fiona, Brownlie, Rebecca J, Vyse, Timothy J, Zamoyska, Rose, Owen, Dylan M, Svensson, Lena M, Cope, Andrew P

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Membrane lipid order of sub‐synaptic T cell vesicles correlates with their dynamics and function von Ashdown, George W., Williamson, David J., Soh, Gary H.M., Day, Nathan, Burn, Garth L., Owen, Dylan M.

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Dynamic Bayesian Cluster Analysis of Live‐Cell Single Molecule Localization Microscopy Datasets von Griffié, Juliette, Burn, Garth L., Williamson, David J., Peters, Ruby, Rubin‐Delanchy, Patrick, Owen, Dylan M.

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Prehospital Tranexamic Acid for Severe Trauma von Gruen, Russell L, Mitra, Biswadev, Bernard, Stephen A, McArthur, Colin J, Burns, Brian, Gantner, Dashiell C, Maegele, Marc, Cameron, Peter A, Dicker, Bridget, Forbes, Andrew B, Hurford, Sally, Martin, Catherine A, Mazur, Stefan M, Medcalf, Robert L, Murray, Lynnette J, Myles, Paul S, Ng, Sze J, Pitt, Veronica, Rashford, Stephen, Reade, Michael C, Swain, Andrew H, Trapani, Tony, Young, Paul J

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The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study von Latourelle, Jeanne C, Sun, Mei, Lew, Mark F, Suchowersky, Oksana, Klein, Christine, Golbe, Lawrence I, Mark, Margery H, Growdon, John H, Wooten, G Frederick, Watts, Ray L, Guttman, Mark, Racette, Brad A, Perlmutter, Joel S, Ahmed, Anwar, Shill, Holly A, Singer, Carlos, Goldwurm, Stefano, Pezzoli, Gianni, Zini, Michela, Saint-Hilaire, Marie H, Hendricks, Audrey E, Williamson, Sally, Nagle, Michael W, Wilk, Jemma B, Massood, Tiffany, Huskey, Karen W, Laramie, Jason M, DeStefano, Anita L, Baker, Kenneth B, Itin, Ilia, Litvan, Irene, Nicholson, Garth, Corbett, Alastair, Nance, Martha, Drasby, Edward, Isaacson, Stuart, Burn, David J, Chinnery, Patrick F, Pramstaller, Peter P, Al-hinti, Jomana, Moller, Anette T, Ostergaard, Karen, Sherman, Scott J, Roxburgh, Richard, Snow, Barry, Slevin, John T, Cambi, Franca, Gusella, James F, Myers, Richard H

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Lyp/PTPN22 is a negative regulator of integrin mediated T cell adhesion and migration; the disease associated PTPN22 allelic variant is a loss of function mutant that perturbs T ce... von Svensson, Lena, Burn, Garth, Sanchez-Blanco, Cristina, Zamoyska, Rose, Cope, Andrew

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Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: The GenePD study von McNicoll, Christopher F., Latourelle, Jeanne C., MacDonald, Marcy E., Lew, Mark F., Suchowersky, Oksana, Klein, Christine, Golbe, Lawrence I., Mark, Margery H., Growdon, John H., Wooten, G. Frederick, Watts, Ray L., Guttman, Mark, Racette, Brad A., Perlmutter, Joel S., Ahmed, Anwar, Shill, Holly A., Singer, Carlos, Saint-Hilaire, Marie H., Massood, Tiffany, Huskey, Karen W., DeStefano, Anita L., Gillis, Tammy, Mysore, Jayalakshmi, Goldwurm, Stefano, Pezzoli, Gianni, Baker, Kenneth B., Itin, Ilia, Litvan, Irene, Nicholson, Garth, Corbett, Alastair, Nance, Martha, Drasby, Edward, Isaacson, Stuart, Burn, David J., Chinnery, Patrick F., Pramstaller, Peter P., Al-Hinti, Jomana, Moller, Anette T., Ostergaard, Karen, Sherman, Scott J., Roxburgh, Richard, Snow, Barry, Slevin, John T., Cambi, Franca, Gusella, James F., Myers, Richard H.

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Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: The Gene PD study von McNicoll, Christopher F., Latourelle, Jeanne C., MacDonald, Marcy E., Lew, Mark F., Suchowersky, Oksana, Klein, Christine, Golbe, Lawrence I., Mark, Margery H., Growdon, John H., Wooten, G. Frederick, Watts, Ray L., Guttman, Mark, Racette, Brad A., Perlmutter, Joel S., Ahmed, Anwar, Shill, Holly A., Singer, Carlos, Saint‐Hilaire, Marie H., Massood, Tiffany, Huskey, Karen W., DeStefano, Anita L., Gillis, Tammy, Mysore, Jayalakshmi, Goldwurm, Stefano, Pezzoli, Gianni, Baker, Kenneth B., Itin, Ilia, Litvan, Irene, Nicholson, Garth, Corbett, Alastair, Nance, Martha, Drasby, Edward, Isaacson, Stuart, Burn, David J., Chinnery, Patrick F., Pramstaller, Peter P., Al‐Hinti, Jomana, Moller, Anette T., Ostergaard, Karen, Sherman, Scott J., Roxburgh, Richard, Snow, Barry, Slevin, John T., Cambi, Franca, Gusella, James F., Myers, Richard H.

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The Gly2019Ser mutation in LRRK2is not fully penetrant in familial Parkinson's disease: the GenePD study von Latourelle, Jeanne C, Sun, Mei, Lew, Mark F, Suchowersky, Oksana, Klein, Christine, Golbe, Lawrence I, Mark, Margery H, Growdon, John H, Wooten, G Frederick, Watts, Ray L, Guttman, Mark, Racette, Brad A, Perlmutter, Joel S, Ahmed, Anwar, Shill, Holly A, Singer, Carlos, Goldwurm, Stefano, Pezzoli, Gianni, Zini, Michela, Saint-Hilaire, Marie H, Hendricks, Audrey E, Williamson, Sally, Nagle, Michael W, Wilk, Jemma B, Massood, Tiffany, Huskey, Karen W, Laramie, Jason M, DeStefano, Anita L, Baker, Kenneth B, Itin, Ilia, Litvan, Irene, Nicholson, Garth, Corbett, Alastair, Nance, Martha, Drasby, Edward, Isaacson, Stuart, Burn, David J, Chinnery, Patrick F, Pramstaller, Peter P, Al-hinti, Jomana, Moller, Anette T, Ostergaard, Karen, Sherman, Scott J, Roxburgh, Richard, Snow, Barry, Slevin, John T, Cambi, Franca, Gusella, James F, Myers, Richard H

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The Gly2019Ser Mutation in LRRK2 is not Fully Penetrant in Familial Parkinson's Disease: The GenePD Study von Latourelle, Jeanne C, Lew, Mark F, Suchowersky, Oksana, Klein, Christine, Golbe, Lawrence I, Mark, Margery H, Wooten, G Frederick, Watts, Ray L, Guttman, Mark, Racette, Brad A, Perlmutter, Joel S, Ahmed, Anwar, Shill, Holly A, Singer, Carlos, Goldwurm, Stefano, Pezzoli, Gianni, Zini, Michela, Saint-Hilaire, Marie H, Hendricks, Audrey E, Williamson, Sally, Nagle, Michael W, Wilk, Jemma B, Massood, Tiffany, Huskey, Karen W, Laramie, Jason M, DeStefano, Anita L, Baker, Kenneth B, Itin, Ilia, Litvan, Irene, Nicholson, Garth, Corbett, Alastair, Nance, Martha, Drasby, Edward, Isaacson, Stuart, Burn, David J, Chinnery, Patrick F, Pramstaller, Peter P, Al-hinti, Jomana, Moller, Anette T, Ostergaard, Karen, Roxburgh, Richard, Snow, Barry, Slevin, John T, Cambi, Franca, Growdon, John Herbert, Gusella, James Francis, Sun, Mei, Sherman, Scott J, Myers, Richard Hepworth

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