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O'Neill, Adam C., Kyrousi, Christina, Klaus, Johannes, Leventer, Richard J., Kirk, Edwin P., Fry, Andrew, Pilz, Daniela T., Morgan, Tim, Jenkins, Zandra A., Drukker, Micha, Berkovic, Samuel F., Scheffer, Ingrid E., Guerrini, Renzo, Markie, David M., Götz, Magdalena, Cappello, Silvia and Robertson, Stephen P.
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Fry, Andrew E., Fawcett, Katherine A., Zelnik, Nathanel, Yuan, Hongjie, Thompson, Belinda A. N., Shemer-Meiri, Lilach, Cushion, Thomas D., Mugalaasi, Hood, Sims, David, Stoodley, Neil, Chung, Seo-Kyung, Rees, Mark I., Patel, Chirag V., Brueton, Louise A., Layet, Valérie, Giuliano, Fabienne, Kerr, Michael P., Banne, Ehud, Meiner, Vardiella, Lerman-Sagie, Tally, Helbig, Katherine L., Kofman, Laura H., Knight, Kristin M., Chen, Wenjuan, Kannan, Varun, Hu, Chun, Kusumoto, Hirofumi, Zhang, Jin, Swanger, Sharon A., Shaulsky, Gil H., Mirzaa, Ghayda M., Muir, Alison M., Mefford, Heather C., Dobyns, William B., Mackenzie, Amanda B., Mullins, Jonathan G. L., Lemke, Johannes R., Bahi-Buisson, Nadia, Traynelis, Stephen F., Iago, Heledd F. and Pilz, Daniela T.
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Urquhart, J.E., Beaman, G., Byers, H., Roberts, N.A., Chervinsky, E., O'Sullivan, J., Pilz, Daniela, Fry, Andrew, Williams, S.G., Bhaskar, S.S., Khayat, M., Simanovsky, N., Shachar, I.B., Shalev, S.A. and Newman, W.G. 2016. DMRTA2 (DMRT5) is mutated in a novel cortical brain malformation. Clinical Genetics 89 (6) , pp. 724-727. 10.1111/cge.12734 |
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Mirzaa, Ghayda M., Parry, David A., Fry, Andrew E., Giamanco, Kristin A., Schwartzentruber, Jeremy, Vanstone, Megan, Logan, Clare V., Roberts, Nicola, Johnson, Colin A., Singh, Shawn, Kholmanskikh, Stanislav S., Adams, Carissa, Hodge, Rebecca D., Hevner, Robert F., Bonthron, David T., Braun, Kees P. J., Faivre, Laurence, Rivière, Jean-Baptiste, St-Onge, Judith, Gripp, Karen W., Mancini, Grazia M. S., Pang, Ki, Sweeney, Elizabeth, van Esch, Hilde, Verbeek, Nienke, Wieczorek, Dagmar, Steinraths, Michelle, Majewski, Jacek, Boycott, Kym M., Pilz, Daniela T., Ross, M. Elizabeth, Dobyns, William B. and Sheridan, Eamonn G.
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Cushion, Thomas D., Dobyns, William B., Mullins, Jonathan G. L., Stoodley, Neil, Chung, Seo-Kyung, Fry, Andrew Evan, Hehr, Ute, Gunny, Roxana, Aylsworth, Arthur S., Prabhakar, Prab, Uyanik, Gokhan, Rankin, Julia, Rees, Mark I. and Pilz, Daniela T. 2013. Overlapping cortical malformations and mutations in TUBB2B and TUBA1A. Brain 136 (2) , pp. 536-548. 10.1093/brain/aws338 |
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Fry, Andrew Evan, Kerr, Michael Patrick, Gibbon, Frances, Turnpenny, Peter D., Hamandi, Khalid, Stoodley, Neil, Robertson, Stephen and Pilz, Daniela T. 2013. Neuropsychiatric disease in patients with periventricular heterotopia. The Journal of Neuropsychiatry & Clinical Neurosciences 25 (1) , pp. 26-31. 10.1176/appi.neuropsych.11110336 |
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Fry, Andrew Evan, Ghansa, Anita, Small, Kerrin S., Palma, Alejandro, Auburn, Sarah, Diakite, Mahamadou, Green, Angela, Campino, Susana, Teoh, Yin Yoong Jimmy, Clark, Taane G., Jeffreys, Anna E., Wilson, Jonathan, Jallow, Muminatou, Sisay-Joof, Fatou, Pinder, Margaret, Griffiths, Michael J., Peshu, Norbert, Williams, Thomas N., Newton, Charles R., Marsh, Kevin, Molyneux, Malcolm E., Taylor, Terrie E., Koram, Kwadwo, Oduro, Abraham R., Rogers, William O., Rockett, Kirk A., Sabeti, Pardis C. and Kwiatkowski, Dominic P. 2009. Positive selection of a CD36 nonsense variant in sub-Saharan Africa, but no association with severe malaria phenotypes. Human Molecular Genetics 18 (14) , pp. 2683-2692. 10.1093/hmg/ddp192 |
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Teoh, Yin Yoong Jimmy, Fry, Andrew Evan, Bhattacharya, Kanishka, Small, Kerrin S., Kwiatkowski, Dominic P. and Clark, Taane G. 2009. Genome-wide comparisons of variation in linkage disequilibrium. Genome Research 19 (10) , pp. 1849-1860. 10.1101/gr.092189.109 |
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Wei, Christina, Fry, Andrew Evan, Gregory, John Welbourn, Procter, Annie M. and Warner, Justin T. 2008. Central precocious puberty in a patient with adrenal hypoplasia congenita [Poster presentation abstract]. Hormone Research 70 (S1) 10.1159/000157533 |
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Fry, Andrew Evan, Griffiths, Michael J., Auburn, Sarah, Diakite, Mahamadou, Forton, Julian T., Green, Angela, Richardson, Anna, Wilson, Jonathan, Jallow, Muminatou, Sisay-Joof, Fatou, Pinder, Margaret, Peshu, Norbert, Williams, Thomas N., Marsh, Kevin, Molyneux, Malcolm E., Taylor, Terrie E., Rockett, Kirk A. and Kwiatkowski, Dominic P. 2007. Common variation in the ABO glycosyltransferase is associated with susceptibility to severe 'Plasmodium falciparum' malaria. Human Molecular Genetics 17 (4) , pp. 567-576. 10.1093/hmg/ddm331 |
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