Family-Based Analysis Using a Dense Single-Nucleotide Polymorphism–Based Map Defines Genetic Variation at PSORS1, the Major Psoriasis-Susceptibility Locus

由 Veal, Colin D., Capon, Francesca, Allen, Michael H., Heath, Emma K., Evans, Julie C., Jones, Andrew, Patel, Shanta, Burden, David, Tillman, David, Barker, Jonathan N. W. N., Trembath, Richard C.
出版 2002

Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes

由 Macfarlane, Wendy M., Frayling, Timothy M., Ellard, Sian, Evans, Julie C., Allen, Lisa I.S., Bulman, Michael P., Ayres, Susan, Shepherd, Maggie, Clark, Penny, Millward, Ann, Demaine, Andrew, Wilkin, Terence, Docherty, Kevin, Hattersley, Andrew T.
出版 1999

NTNG1 Mutations are a Rare Cause of Rett Syndrome

由 Archer, Hayler L., Evans, Julie C., Millar, David S., Thompson, Peter W., Kerr, Alison M., Leonard, Helen, Christodoulou, John, Ravine, David, Lazarou, Lazarus, Grove, Lucy, Verity, Christopher, Whatley, Sharon D., Pilz, Daniela T., Sampson, Julian R., Clarke, Angus J.
出版 2006

Studies of Association between the Gene for Calpain-10 and Type 2 Diabetes Mellitus in the United Kingdom

由 Evans, Julie C., Frayling, Timothy M., Cassell, Paul G., Saker, Philip J., Hitman, Graham A., Walker, Mark, Levy, Jonathan C., O’Rahilly, Stephen, Rao, Pamidighantam V. Subba, Bennett, Amanda J., Jones, Elizabeth C., Menzel, Stephan, Prestwich, Philip, Simecek, Nikol, Wishart, Marie, Dhillon, Ranjit, Fletcher, Chris, Millward, Ann, Demaine, Andrew, Wilkin, Terence, Horikawa, Yukio, Cox, Nancy J., Bell, Graeme I., Ellard, Sian, McCarthy, Mark I., Hattersley, Andrew T.
出版 2001

Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics

由 Pitceathly, Robert D. S., Smith, Conrad, Fratter, Carl, Alston, Charlotte L., He, Langping, Craig, Kate, Blakely, Emma L., Evans, Julie C., Taylor, John, Shabbir, Zarfishan, Deschauer, Marcus, Pohl, Ute, Roberts, Mark E., Jackson, Matthew C., Halfpenny, Christopher A., Turnpenny, Peter D., Lunt, Peter W., Hanna, Michael G., Schaefer, Andrew M., McFarland, Robert, Horvath, Rita, Chinnery, Patrick F., Turnbull, Douglass M., Poulton, Joanna, Taylor, Robert W., Gorman, Gráinne S.
出版 2012

Retrospective natural history of thymidine kinase 2 deficiency

由 Garone, Caterina, Taylor, Robert W, Nascimento, Andrés, Poulton, Joanna, Fratter, Carl, Domínguez-González, Cristina, Evans, Julie C, Loos, Mariana, Isohanni, Pirjo, Suomalainen, Anu, Ram, Dipak, Hughes, M Imelda, McFarland, Robert, Barca, Emanuele, Lopez Gomez, Carlos, Jayawant, Sandeep, Thomas, Neil D, Manzur, Adnan Y, Kleinsteuber, Karin, Martin, Miguel A, Kerr, Timothy, Gorman, Grainne S, Sommerville, Ewen W, Chinnery, Patrick F, Hofer, Monika, Karch, Christoph, Ralph, Jeffrey, Cámara, Yolanda, Madruga-Garrido, Marcos, Domínguez-Carral, Jana, Ortez, Carlos, Emperador, Sonia, Montoya, Julio, Chakrapani, Anupam, Kriger, Joshua F, Schoenaker, Robert, Levin, Bruce, Thompson, John L P, Long, Yuelin, Rahman, Shamima, Donati, Maria Alice, DiMauro, Salvatore, Hirano, Michio
發表在 J Med Genet (2018)