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Items where Author is "Rahman, S"

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Number of items: 9.

Article

Breedon, JR, Marshall, CR, Giovannoni, G, van Heel, DA, Akhtar, S, Anwar, M, Arciero, E, Asgar, O, Ashraf, S, Breen, G, Chung, R, Curtis, CJ, Chaudhary, S, Chowdhury, M, Colligan, G, Deloukas, P, Durham, C, Durrani, F, Eto, F, Finer, S , Garcia, AA, Griffiths, C, Harvey, J, Heng, T, Huang, QQ, Hurles, M, Hunt, KA, Hussain, S, Islam, K, Jacobs, BM, Khan, A, Khan, A, Lavery, C, Lee, SH, Lerner, R, MacArthur, D, Malawsky, D, Martin, H, Mason, D, Mazid, MB, McDermott, J, McSweeney, S, Miah, S, Munir, S, Newman, B, Owor, E, Qureshi, A, Rahman, S, Safa, N, Solly, J, Tahmasebi, F, Trembath, RC, Tricker, K, Uddin, N, van Heel, DA, Winckley, C, Wright, J, Dobson, R and Jacobs, BM (2023) Polygenic risk score prediction of multiple sclerosis in individuals of South Asian ancestry. Brain Communications, 5 (2).

Ward, RJ, Rahman, S, Wuerger, S and Marshall, A (2022) Predicting the crossmodal correspondences of odors using an electronic nose. Heliyon, 8 (4). ISSN 2405-8440

Horga, A, Woodward, CE, Mills, A, Pare├ęs, I, Hargreaves, IP, Brown, RM, Bugiardini, E, Brooks, T, Manole, A, Remzova, E, Rahman, S, Reilly, MM, Houlden, H, Sweeney, MG, Brown, GK, Polke, JM, Gago, F, Parton, MJ, Pitceathly, RDS and Hanna, MG (2019) Differential phenotypic expression of a novel PDHA1 mutation in a female monozygotic twin pair. Human Genetics, 138 (11-12). pp. 1313-1322. ISSN 0340-6717

Othman, NAF, Rahman, S, Wan Muhamad Hatta, S, Soin, N, Benbakhti, B and Duffy, S (2019) Design Optimization of the graded AlGaN/GaN HEMT device performance based on material and physical dimensions. Microelectronics International, 36 (2). pp. 73-82. ISSN 1356-5362

McKiernan, P, Ball, S, Santra, S, Foster, K, Fratter, C, Poulton, J, Craig, K, McFarland, R, Rahman, S, Hargreaves, IP, Gupte, G, Sharif, K and Taylor, RW (2016) Incidence of Primary Mitochondrial Disease in Children Younger Than 2 Years Presenting With Acute Liver Failure. Journal of Pediatric Gastroenterology and Nutrition, 63 (6). pp. 592-597. ISSN 0277-2116

Ferdinandusse, S, Waterham, HR, Heales, SJR, Brown, GK, Hargreaves, IP, Taanman, J-W, Gunny, R, Abulhoul, L, Wanders, RJA, Clayton, PT, Leonard, JV and Rahman, S (2013) HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase. Orphanet Journal of Rare Diseases, 188. ISSN 1750-1172

Foley, AR, Menezes, MP, Pandraud, A, Gonzalez, MA, Al-Odaib, A, Abrams, AJ, Sugano, K, Yonezawa, A, Manzur, AY, Burns, J, Hughes, I, McCullagh, BG, Jungbluth, H, Lim, MJ, Lin, J-P, Megarbane, A, Urtizberea, JA, Shah, AH, Antony, J, Webster, R , Broomfield, A, Ng, J, Mathew, AA, O'Byrne, JJ, Forman, E, Scoto, M, Prasad, M, O'Brien, K, Olpin, S, Oppenheim, M, Hargreaves, IP, Land, JM, Wang, MX, Carpenter, K, Horvath, R, Straub, V, Lek, M, Gold, W, Farrell, MO, Brandner, S, Phadke, R, Matsubara, K, McGarvey, ML, Scherer, SS, Baxter, PS, King, MD, Clayton, P, Rahman, S, Reilly, MM, Ouvrier, RA, Christodoulou, J, Zuechner, S, Muntoni, F and Houlden, H (2013) Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2. Brain, 137 (1). pp. 44-56. ISSN 1460-2156

Uusimaa, J, Evans, J, Smith, C, Butterworth, A, Craig, K, Ashley, N, Liao, C, Carver, J, Diot, A, Macleod, L, Hargreaves, IP, Al-Hussaini, A, Faqeih, E, Asery, A, Al Balwi, M, Eyaid, W, Al-Sunaid, A, Kelly, D, van Mourik, I, Ball, S , Jarvis, J, Mulay, A, Hadzic, N, Samyn, M, Baker, A, Rahman, S, Stewart, H, Morris, AAM, Seller, A, Fratter, C, Taylor, RW and Poulton, J (2013) Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene. European Journal of Human Genetics, 22 (2). pp. 184-191. ISSN 1018-4813

Conference or Workshop Item

Ward, R, Rahman, S, Wuerger, S and Marshall, A (2021) Predicting the colour associated with odours using an electronic nose. In: Proceedings of the 1st Workshop on Multisensory Experiences - SensoryX'21 . (ACM International Conference on Interactive Media Experience, June 21-23, 2021, NY, USA).

This list was generated on Thu Jun 20 19:36:51 2024 UTC.