A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis by Norsworthy, Penny J., Thompson, Andrew G. B., Mok, Tze H., Guntoro, Fernando, Dabin, Luke C., Nihat, Akin, Paterson, Ross W., Schott, Jonathan M., Collinge, John, Mead, Simon, Viré, Emmanuelle A.

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Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans by Domin, Jan, Mangion, Jonathan, Cook, H. Terence, Petretto, Enrico, Vyse, Timothy J, Flint, Jonathan, Johnson, Michelle D, Patel, Sheetal G, Pusey, Charles D, Cook, Paul R, Evans, David J, Duda, Mark, Smith, Jennifer, Dong, Rong, Bhangal, Gurjeet, Aitman, Timothy J, Roberton-Lowe, Cheri, Sheehan-Rooney, Kelly, Marshall, Amy J, Boyle, Joseph J, Norsworthy, Penny J, Hodges, Matthew D

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Genetic analysis of the cardiac methylome at single nucleotide resolution in a model of human cardiovascular disease by Johnson, Michelle D, Mueller, Michael, Adamowicz-Brice, Martyna, Collins, Melissa J, Gellert, Pascal, Maratou, Klio, Srivastava, Prashant K, Rotival, Maxime, Butt, Shahena, Game, Laurence, Atanur, Santosh S, Silver, Nicholas, Norsworthy, Penny J, Langley, Sarah R, Petretto, Enrico, Pravenec, Michal, Aitman, Timothy J

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Genetic, physiological and comparative genomic studies of hypertension and insulin resistance in the spontaneously hypertensive rat by Coan, Philip M, Hummel, Oliver, Garcia Diaz, Ana, Barrier, Marjorie, Alfazema, Neza, Norsworthy, Penny J, Pravenec, Michal, Petretto, Enrico, Hübner, Norbert, Aitman, Timothy J

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Targeted genetic testing for familial hypercholesterolaemia using next generation sequencing: a population-based study by Norsworthy, Penny J, Vandrovcova, Jana, Thomas, Ellen R A, Campbell, Archie, Kerr, Shona M, Biggs, Jennifer, Game, Laurence, Soutar, Anne K, Smith, Blair H, Dominiczak, Anna F, Porteous, David J, Morris, Andrew D, Scotland, Generation, Aitman, Timothy J

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The use of next generation sequencing for detection of mutations in familial hypercholesterolaemia by Vandrovcova, Jana, Norsworthy, Penny J, Thomas, Ellen R.A, Biggs, Jennifer, Neuwirth, Clare, Tan, Yvonne, Game, Laurence, Campbell, Archie, Kerr, Shona M, Smith, Blair H, Dominiczak, Anna, Porteous, David, Morris, Andrew, Soutar, Anne, Aitman, Timothy J

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Identification and biochemical analysis of a novel APOB mutation that causes autosomal dominant hypercholesterolemia by Thomas, Ellen R. A., Atanur, Santosh S., Norsworthy, Penny J., Encheva, Vesela, Snijders, Ambrosius P., Game, Laurence, Vandrovcova, Jana, Siddiq, Afshan, Seed, Mary, Soutar, Anne K., Aitman, Timothy J.

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Radiation hybrid mapping of 70 rat genes from a data set of differentially expressed genes by Wallace, Caroline A, Ali, Saira, Glazier, Anne M, Norsworthy, Penny J, Carlos, Danilo C, Scott, James, Freeman, Tom C, Stanton, Lawrence W, Kwitek, Anne E, Aitman, Timothy J

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Malaria susceptibility and CD36 mutation by AITMAN, T. J, COOPER, L. D, HILL, A. V, SCOTT, J, NORSWORTHY, P. J, WAHID, F. N, GRAY, J. K, CURTIS, B. R, MCKEIGUE, P. M, KWIATKOWSKI, D, GREENWOOD, B. M, SNOW, R. W

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Genetic Analysis of the Cardiac Methylome at Single Nucleotide Resolution in a Model of Human Cardiovascular Disease: e1004813 by Johnson, Michelle D, Mueller, Michael, Adamowicz-Brice, Martyna, Collins, Melissa J, Gellert, Pascal, Maratou, Klio, Srivastava, Prashant K, Rotival, Maxime, Butt, Shahena, Game, Laurence, Atanur, Santosh S, Silver, Nicholas, Norsworthy, Penny J, Langley, Sarah R, Petretto, Enrico, Pravenec, Michal, Aitman, Timothy J

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Population genetics Malaria susceptibility and CD36 mutation by Aitman, Timothy J, Cooper, Lisa D, Norsworthy, Penny J, Wahid, Faisal N, Gray, Jennefer K, Curtis, Brian R, McKeigue, Paul M, Kwiatkowski, Dominic, Greenwood, Brian M, Snow, Robert W, Hill, Adrian V, Scott, James

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A high-resolution radiation hybrid map of the proximal region of rat chromosome 4 by al-Majali, K M, Glazier, A M, Norsworthy, P J, Wahid, F N, Cooper, L D, Wallace, C A, Scott, J, Lausen, B, Aitman, T J

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Malaria susceptibility and CD36 mutation: Population genetics by Aitman, Timothy J., Cooper, Lisa D., Norsworthy, Penny J., Wahid, Faisal N., Gray, Jennefer K., Curtis, Brian R., McKeigue, Paul M, Kwiatkowski, Dominic, Greenwood, Brian M., Snow, Robert W., Hill, Adrian V, Scott, James

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Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study by Jones, Emma, Hummerich, Holger, Viré, Emmanuelle, Uphill, James, Dimitriadis, Athanasios, Speedy, Helen, Campbell, Tracy, Norsworthy, Penny, Quinn, Liam, Whitfield, Jerome, Linehan, Jacqueline, Jaunmuktane, Zane, Brandner, Sebastian, Jat, Parmjit, Nihat, Akin, How Mok, Tze, Ahmed, Parvin, Collins, Steven, Stehmann, Christiane, Sarros, Shannon, Kovacs, Gabor G, Geschwind, Michael D, Golubjatnikov, Aili, Frontzek, Karl, Budka, Herbert, Aguzzi, Adriano, Karamujić-Čomić, Hata, van der Lee, Sven J, Ibrahim-Verbaas, Carla A, van Duijn, Cornelia M, Sikorska, Beata, Golanska, Ewa, Liberski, Pawel P, Calero, Miguel, Calero, Olga, Sanchez-Juan, Pascual, Salas, Antonio, Martinón-Torres, Federico, Bouaziz-Amar, Elodie, Haïk, Stéphane, Laplanche, Jean-Louis, Brandel, Jean-Phillipe, Amouyel, Phillipe, Lambert, Jean-Charles, Parchi, Piero, Bartoletti-Stella, Anna, Capellari, Sabina, Poleggi, Anna, Ladogana, Anna, Pocchiari, Maurizio, Aneli, Serena, Matullo, Giuseppe, Knight, Richard, Zafar, Saima, Zerr, Inga, Booth, Stephanie, Coulthart, Michael B, Jansen, Gerard H, Glisic, Katie, Blevins, Janis, Gambetti, Pierluigi, Safar, Jiri, Appleby, Brian, Collinge, John, Mead, Simon

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