Atan, Denize - University of Bristol - School of Clinical Sciences

个人简介

Denize completed her training in Clinical Medicine and Surgery at the University of Oxford (BM BCh) after first graduating from the University of Cambridge in Medical Sciences (MA Hons).

研究领域

Neurodevelopment and vision

近期论文

查看导师最新文章（温馨提示：请注意重名现象，建议点开原文通过作者单位确认）

Márquez, A, Cordero-Coma, M, Martín-Villa, JM, Gorro?o-Echebarría, MB, Blanco, R, Valle, DD, Rio, MJD, Blanco, A, Olea, JL, Cordero, Y, Capella, MJ, Díaz-Llopis, M, Ortego-Centeno, N, Ruiz-Arruza, I, Lloren?, V, Adán, A, Fonollosa, A, Berge, JT, Atan, D, Dick, AD, De Boer, JH, Kuiper, J, Rothova, A & Martín, J, 2016, ‘New insights into the genetic component of non-infectious uveitis through an Immunochip strategy’. Journal of Medical Genetics. Jung, CC, Atan, D, Ng, D, Ploder, L, Ross, SE, Klein, M, Birch, DG, Diez, E & McInnes, RR, 2015, ‘Transcription factor PRDM8 is required for rod bipolar and type 2 OFF-cone bipolar cell survival and amacrine subtype identity’. Proceedings of the National Academy of Sciences of the United States of America, vol 112., pp. E3010-E3019 Atan, D, Heissigerova, J, Kuffová, L, Hogan, A, Kilmartin, DJ, Forrester, JV, Bidwell, JL, Dick, AD & Churchill, AJ, 2013, ‘Tumor necrosis factor polymorphisms associated with tumor necrosis factor production influence the risk of idiopathic intermediate uveitis’. Molecular Vision, vol 19., pp. 184-195 Ross, S, McCord, A, Jung, C, Atan, D, Mok, S, Hemberg, M, Kim, T, Hu, L, Cohen, S, Lin, Y, Harrar, D, McInnes, R, Greenberg, M & Salogiannis, J, 2012, ‘Bhlhb5 and Prdm8 form a repressor complex involved in neuronal circuit assembly’. Neuron, vol 73., pp. 292 - 303 Atan, D, Fraser-Bell, S, Plskova, J, Kuffova, L, Hogan, A, Tufail, A, Kilmartin, D, Forrester, J, Bidwell, J, Dick, A & Churchill, A, 2011, ‘Punctate inner choroidopathy and multifocal choroiditis with panuveitis share haplotypic associations with IL10 and TNF Loci’. Investigative Opthalmology & Visual Science, vol 52., pp. 3573 - 3581 Gill, H, Muthusamy, B, Atan, D, Williams, C & Ellis, M, 2011, ‘Joubert syndrome presenting with motor delay and oculomotor apraxia’. Case reports in pediatrics, vol 2011., pp. 262641 Atan, D, Fraser-Bell, S, Plskova, J, Kuffova, L, Hogan, A, Tufail, A, Kilmartin, D, Forrester, J, Bidwell, J, Dick, A & Churchill, A, 2010, ‘Cytokine polymorphism in noninfectious uveitis’. Investigative Opthalmology & Visual Science, vol 51., pp. 4133 - 4142 Atan, D, Foy, C & Scanlon, P, 2008, ‘Reply to ‘Evaluation of the effect of JPEG and JPEG2000 image compression on the detection of diabetic retinopathy’’. Eye (Lond), vol 22(3):471. Glover, N, Ah-Chan, J, Frith, P, Downes, S & Atan, D, 2008, ‘Unremitting sympathetic ophthalmia associated with homozygous interleukin-10-1082A single nucleotide polymorphism’. Br J Ophthalmol, vol 92(1)., pp. 155 - 156 Churchill, A, Carter, J, Lovell, H, Ramsden, C, Turner, S, Yeung, A, Escardo, J & Atan, D, 2006, ‘VEGF polymorphisms are associated with neovascular age-related macular degeneration’. Human Molecular Genetics, vol 15 (19)., pp. 2955 - 2961