A global cloud free pixel- based image composite from Sentinel-2 data von Corbane, C., Politis, P., Kempeneers, P., Simonetti, D., Soille, P., Burger, A., Pesaresi, M., Sabo, F., Syrris, V., Kemper, T.

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Application of the Symbolic Machine Learning to Copernicus VHR Imagery: The European Settlement Map von Corbane, C., Sabo, F., Syrris, V., Kemper, T., Politis, P., Pesaresi, M., Soille, P., Ose, K.

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A versatile data-intensive computing platform for information retrieval from big geospatial data von Soille, P., Burger, A., De Marchi, D., Kempeneers, P., Rodriguez, D., Syrris, V., Vasilev, V.

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Classification through hierarchical clustering and dimensionality reduction von Syrris, V., Petridis, V.

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Statistical descriptors for human actions classification von Syrris, V., Petridis, V.

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Detection and identification of human actions using Predictive Modular Neural Networks von Petridis, V., Deb, B., Syrris, V.

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Application of Fuzzy Lattice Neurocomputing (FLN) for Environmental Data Estimation von Petridis, V., Theocharis, J.B., Syrris, V.

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Use of high-throughput targeted exome-sequencing to screen for copy number variation in hypertrophic cardiomyopathy von Lopes, L.R, Murphy, C, Syrris, P, Dalageorgou, C, McKenna, W.J, Elliott, P.M, Plagnol, V

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Genetic regulation of myocardial fibrosis in hypertrophic cardiomyopathy von Patel, V, Syrris, P, Coats, C, Lucena, J, Lara-Pezzi, E, Garcia-Pavia, P, Elliott, P M

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X-linked Emery-Dreifuss muscular dystrophy is associated with a high risk of malignant ventricular arrhythmia von Cannie, D, Syrris, P, Rodriguez-Palomares, J F, Marini-Bettolo, C, Mestroni, L, Parikh, V N, Barriales-Villa, R, Jiminez-Jaimez, J, Garcia-Pavia, P, Charron, P, Biagini, E, Garcia-Pinilla, J M, Savvatis, K, Wahbi, K, Elliott, P M

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A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriers von Carrick, RT, Gasperetti, A, Protonotarios, A, Murray, B, Laredo, M, Van der Schaaf, I, Dooijes, D, Syrris, P, Cannie, D, Tichnell, C, Gilotra, NA, Cappelletto, C, Medo, K, Saguner, AM, Duru, F, Hylind, RJ, Abrams, DJ, Lakdawala, NK, Cadrin-Tourigny, J, Targetti, M, Olivotto, I, Graziosi, M, Cox, M, Biagini, E, Charron, P, Compagnucci, P, Casella, M, Conte, G, Tondo, C, Yazdani, M, Ware, JS, Prasad, SK, Calò, L, Smith, ED, Helms, AS, Hespe, S, Ingles, J, Tandri, H, Ader, F, Peretto, G, Peters, S, Horton, A, Yao, J, Schulze-Bahr, E, Dittman, S, Carruth, ED, Young, K, Qureshi, M, Haggerty, C, Parikh, VN, Taylor, M, Mestroni, L, Wilde, A, Sinagra, G, Merlo, M, Gandjbakhch, E, Van Tintelen, JP, Te Riele, ASJM, Elliot, P, Calkins, H, Wu, KC, James, CA

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A Novel Myosin Essential Light Chain Mutation Causes Hypertrophic Cardiomyopathy with Late Onset and Low Expressivity von Andersen, Paal Skytt, Hedley, Paula Louise, Page, Stephen P., Syrris, Petros, Moolman-Smook, Johanna Catharina, McKenna, William John, Elliott, Perry Mark, Christiansen, Michael

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High-throughput genotyping and phenotyping reveals new genetic determinants of clinical phenotype in hypertrophic cardiomyopathy von Rocha Lopes, L., Giambartolomei, C., Syrris, P., O'Mahony, C., Dalageorgou, C., Jenkins, S., Hubank, M., Mc Kenna, W., Plagnol, V., Elliott, P.

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The UK10K project identifies rare variants in health and disease von Walter, K, Min, JL, Huang, J, Crooks, L, McCarthy, S, Xu, C, Futema, M, Lawson, D, Iotchkova, V, Schiffels, S, Danecek, P, Wain, LV, Humphries, SE, Barrett, JC, Plagnol, V, Richards, JB, Soranzo, N, Bala, S, Cox, T, Du, Y, Ellis, P, Flicek, P, Huang, L, Keane, T, Li, Y, Liang, J, Maslen, J, Muddyman, D, Tian, J, Wang, G, Wang, J, Wong, K, Zhang, P, Boustred, C, Chen, L, Clement, G, Cocca, M, Geihs, M, Howie, B, Jamshidi, Y, Karczewski, KJ, Kemp, JP, Lopes, M, Mathieson, I, Metrustry, S, Quaye, L, Shin, S-Y, Small, KS, Artigas, MS, Spector, TD, St Pourcain, B, Tachmazidou, I, Valdes, AM, Yang, J, Craddock, N, Curtis, D, Gallagher, L, Geschwind, D, Gurling, H, Lee, I, McGuffin, P, McKechanie, AG, O'Donovan, MC, Pietilainen, O, Rehnstrom, K, Skuse, D, Bochukova, E, Farooqi, IS, Keogh, J, Wheeler, E, Al Turki, S, Anderson, CA, Beales, P, Carss, K, Cirak, S, Foley, AR, Franklin, CS, Grozeva, D, Roberts, N, Schmidts, M, Spasic-Boskovic, O, Stevens, E, Van Kogelenberg, M, Vijayarangakannan, P, Whyte, T, Oualkacha, K, Kent, A, Khawaja, F, Lopes, LR, Migone, N, Pollitt, RC, Scott, RH, Chambers, JC, Dedoussis, G, Gasparini, P, Isaacs, A, Langenberg, C, Luan, J, Benn, M, Toniolo, D

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YOUNG INVESTIGATORS COMPETITION, HRC 2013 von Phan, T. T., Khan, S., Dewhurst, M., Lee, D., James, S., de Belder, M., Linker, N. J., Thornley, A., Turley, A. J., Ahmed, F. Z., Arumugam, P., Allen, S., Daniels, K., Clarke, B., Mamas, M., James, J., Zaidi, A. M., Ullah, W., Hunter, R., Lovell, M., Dhinoja, M., Earley, M., Sporton, S., Schilling, R., Raju, H., Hedley, P., Arno, G., Ware, J., Jeffery, S., Cook, S., Christiansen, M., Behr, E. R., Sohal, M., Chen, Z., Sammut, E., Jackson, T., Child, N., Wright, M., O'Neill, M., Cooklin, M., Gill, J., Carr-White, G., Razavi, R., Rinaldi, C. A., Nunn, L. M., Lopes, L., Syrris, P., Plagnol, V., Firman, E., Dalageorgou, C., Domingo, D., Zorio, E., Murday, V., Findlay, I., Duncan, A., Fynn, S., White, A., Goddard, M., Robert, L., Bueser, T., Langman, C., Bundgaard, H., Ferrero-Miliani, L., Wheeldon, N., O'Beirne, A., Suvarna, S. K., Lowe, M. D., McKenna, W. J., Elliott, P. M., Lambiase, P. D.

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Lack of c-kit mutation in familial urticaria pigmentosa von Rosbotham, J L, Malik, N M, Syrris, P, Jeffery, S, Bedlow, A, Gharraie, S, Murday, V A, Holden, C A, Carter, N D

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Genetic regulation of myocardial fibrosis in hypertrophic cardiomyopathy von Patel, V, Syrris, P, Coats, C, Lucena, J, Lara-Pezzi, E, Garcia-Pavia, P, Elliott, PM

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A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients von Nagyova, E, Hoorntje, ET, Rijdt, WPT, Bosman, LP, Syrris, P, Protonotarios, A, Elliott, PM, Tsatsopoulou, A, Mestroni, L, Taylor, MRG, Sinagra, G, Merlo, M, Wada, Y, Horie, M, Mogensen, J, Christensen, AH, Gerull, B, Song, L, Yao, Y, Fan, S, Saguner, AM, Duru, F, Koskenvuo, JW, Cruz Marino, T, Tichnell, C, Judge, DP, Dooijes, D, Lekanne Deprez, RH, Basso, C, Pilichou, K, Bauce, B, Wilde, AAM, Charron, P, Fressart, V, van der Heijden, JF, van den Berg, MP, Asselbergs, FW, James, CA, Jongbloed, JDH, Harakalova, M, van Tintelen, JP

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Cardiac myosin binding protein-C variants in paediatric-onset hypertrophic cardiomyopathy: natural history and clinical outcomes von Field, E, Norrish, G, Acquaah, V, Dady, K, Cicerchia, M, Ochoa, JP, Syrris, P, McLeod, K, McGowan, R, Fell, H, Lopes, L, Cervi, E, Kaski, JP

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The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy von Protonotarios, A, Brodehl, A, Asimaki, A, Jager, J, Quinn, E, Stanasiuk, C, Ratnavadivel, S, Futema, M, Akhtar, MM, Gossios, TD, Ashworth, M, Savvatis, K, Walhorn, V, Anselmetti, D, Elliott, PM, Syrris, P, Milting, H, Lopes, LR

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