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Items where Author is "Ahmadi, K"

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Mao, J, Vanderlelie, JJ, Perkins, AV, Redman, CWG, Ahmadi, KR and Rayman, MP (2016) Genetic polymorphisms. that affect selenium status and response to selenium supplementation in United Kingdom pregnant women AMERICAN JOURNAL OF CLINICAL NUTRITION, 103 (1). pp. 100-106.

Allum, F, Shao, X, Guénard, F, Simon, MM, Busche, S, Caron, M, Lambourne, J, Lessard, J, Tandre, K, Hedman, ÅK, Kwan, T, Ge, B, Rönnblom, L, McCarthy, MI, Deloukas, P, Richmond, T, Burgess, D, Spector, TD, Tchernof, A, Marceau, S, Lathrop, M, Vohl, MC, Pastinen, T, Grundberg, E, Ahmadi, KR, Ainali, C, Barrett, A, Bataille, V, Bell, JT, Buil, A, Dermitzakis, ET, Dimas, AS, Durbin, R, Glass, D, Hassanali, N, Ingle, C, Knowles, D, Krestyaninova, M, Lindgren, CM, Lowe, CE, Meduri, E, Di Meglio, P, Min, JL, Montgomery, SB, Nestle, FO, Nica, AC, Nisbet, J, O'Rahilly, S, Parts, L, Potter, S, Sandling, J, Sekowska, M, Shin, SY, Small, KS, Soranzo, N, Surdulescu, G, Travers, ME, Tsaprouni, L, Tsoka, S, Wilk, A, Yang, TP and Zondervan, KT (2015) Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants Nature Communications, 6.

Ahmadi, KR and Andrew, T (2014) Opportunism: a panacea for implementation of whole-genome sequencing studies in nutrigenomics research? GENES AND NUTRITION, 9 (2).

Cotlarciuc, I, Malik, R, Holliday, EG, Ahmadi, KR, Paré, G, Psaty, BM, Psaty, BM, Fornage, M, Hasan, N, Rinne, PE, Ikram, MA, Markus, HS, Rosand, J, Rosand, J, Rosand, J, Mitchell, BD, Mitchell, BD, Kittner, SJ, Kittner, SJ, Kittner, SJ, Meschia, JF, Van Meurs, JBJ, Uitterlinden, AG, Worrall, BB, Worrall, BB, Dichgans, M, Dichgans, M and Sharma, P (2014) Effect of genetic variants associated with plasma homocysteine levels on stroke risk Stroke, 45 (7). pp. 1920-1924.

van Meurs, JB, Pare, G, Schwartz, SM, Hazra, A, Tanaka, T, Vermeulen, SH, Cotlarciuc, I, Yuan, X, Mälarstig, A, Bandinelli, S, Bis, JC, Blom, H, Brown, MJ, Chen, C, Chen, YD, Clarke, RJ, Dehghan, A, Erdmann, J, Ferrucci, L, Hamsten, A, Hofman, A, Hunter, DJ, Goel, A, Johnson, AD, Kathiresan, S, Kampman, E, Kiel, DP, Kiemeney, LA, Chambers, JC, Kraft, P, Lindemans, J, McKnight, B, Nelson, CP, O'Donnell, CJ, Psaty, BM, Ridker, PM, Rivadeneira, F, Rose, LM, Seedorf, U, Siscovick, DS, Schunkert, H, Selhub, J, Ueland, PM, Vollenweider, P, Waeber, G, Waterworth, DM, Watkins, H, Witteman, JC, den Heijer, M, Jacques, P, Uitterlinden, AG, Kooner, JS, Rader, DJ, Reilly, MP, Mooser, V, Chasman, DI, Samani, NJ and Ahmadi, KR (2013) Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease. Am J Clin Nutr.

Andrew, T, Gill, R, Gillham-Nasenya, I and Ahmadi, KR (2013) Unravelling the basis of variability in cobalamin levels in the general population. Br J Nutr. pp. 1-8.

Rahmioglu, N, Heaton, J, Clement, G, Gill, R, Surdulescu, G, Zlobecka, K, Hodgkiss, D, Smith, NW and Ahmadi, KR (2013) Genome-wide association study reveals a complex genetic architecture underpinning-induced CYP3A4 enzyme activity. Eur J Drug Metab Pharmacokinet, 38 (1). pp. 63-67.

Grundberg, E, Small, KS, Hedman, Å, Nica, AC, Buil, A, Keildson, S, Bell, JT, Yang, TP, Meduri, E, Barrett, A, Nisbett, J, Sekowska, M, Wilk, A, Shin, SY, Glass, D, Travers, M, Min, JL, Ring, S, Ho, K, Thorleifsson, G, Kong, A, Thorsteindottir, U, Ainali, C, Dimas, AS, Hassanali, N, Ingle, C, Knowles, D, Krestyaninova, M, Lowe, CE, Di Meglio, P, Montgomery, SB, Parts, L, Potter, S, Surdulescu, G, Tsaprouni, L, Tsoka, S, Bataille, V, Durbin, R, Nestle, FO, O'Rahilly, S, Soranzo, N, Lindgren, CM, Zondervan, KT, Ahmadi, KR, Schadt, EE, Stefansson, K, Smith, GD, McCarthy, MI, Deloukas, P, Dermitzakis, ET, Spector, TD and Multiple Tissue Human Expression Resource (MuTHER) Consortium, (2012) Mapping cis- and trans-regulatory effects across multiple tissues in twins. Nat Genet, 44 (10). pp. 1084-1089.

Chambers, JC, Zhang, W, Sehmi, J, Li, X, Wass, MN, Van der Harst, P, Holm, H, Sanna, S, Kavousi, M, Baumeister, SE, Coin, LJ, Deng, G, Gieger, C, Heard-Costa, NL, Hottenga, JJ, Kühnel, B, Kumar, V, Lagou, V, Liang, L, Luan, J, Vidal, PM, Mateo Leach, I, O'Reilly, PF, Peden, JF, Rahmioglu, N, Soininen, P, Speliotes, EK, Yuan, X, Thorleifsson, G, Alizadeh, BZ, Atwood, LD, Borecki, IB, Brown, MJ, Charoen, P, Cucca, F, Das, D, de Geus, EJ, Dixon, AL, Döring, A, Ehret, G, Eyjolfsson, GI, Farrall, M, Forouhi, NG, Friedrich, N, Goessling, W, Gudbjartsson, DF, Harris, TB, Hartikainen, AL, Heath, S, Hirschfield, GM, Hofman, A, Homuth, G, Hyppönen, E, Janssen, HL, Johnson, T, Kangas, AJ, Kema, IP, Kühn, JP, Lai, S, Lathrop, M, Lerch, MM, Li, Y, Liang, TJ, Lin, JP, Loos, RJ, Martin, NG, Moffatt, MF, Montgomery, GW, Munroe, PB, Musunuru, K, Nakamura, Y, O'Donnell, CJ, Olafsson, I, Penninx, BW, Pouta, A, Prins, BP, Prokopenko, I, Puls, R, Ruokonen, A, Savolainen, MJ, Schlessinger, D, Schouten, JN, Seedorf, U, Sen-Chowdhry, S, Siminovitch, KA, Smit, JH, Spector, TD, Tan, W, Teslovich, TM, Tukiainen, T, Uitterlinden, AG, Van der Klauw, MM, Vasan, RS, Wallace, C, Wallaschofski, H, Wichmann, HE, Willemsen, G, Würtz, P, Xu, C, Yerges-Armstrong, LM, Alcohol Genome-wide Association (AlcGen) Consortium, , Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study, , Genetic Investigation of Anthropometric Traits (GIANT) Consortiu, , Global Lipids Genetics Consortium, , Genetics of Liver Disease (GOLD) Consortium, , International Consortium for Blood Pressure (ICBP-GWAS), , Meta-analyses of Glucose and Insulin-Related Traits Consortium (, , Abecasis, GR, Ahmadi, KR, Boomsma, DI, Caulfield, M, Cookson, WO, van Duijn, CM, Froguel, P, Matsuda, K, McCarthy, MI, Meisinger, C, Mooser, V, Pietiläinen, KH, Schumann, G, Snieder, H, Sternberg, MJ, Stolk, RP, Thomas, HC, Thorsteinsdottir, U, Uda, M, Waeber, G, Wareham, NJ, Waterworth, DM, Watkins, H, Whitfield, JB, Witteman, JC, Wolffenbuttel, BH, Fox, CS, Ala-Korpela, M, Stefansson, K, Vollenweider, P, Völzke, H, Schadt, EE, Scott, J, Järvelin, MR, Elliott, P and Kooner, JS (2011) Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Nat Genet, 43 (11). pp. 1131-1138.

Small, KS, Hedman, AK, Grundberg, E, Nica, AC, Thorleifsson, G, Kong, A, Thorsteindottir, U, Shin, SY, Richards, HB, Soranzo, N, Ahmadi, KR, Lindgren, CM, Stefansson, K, Dermitzakis, ET, Deloukas, P, Spector, TD and McCarthy, MI (2011) Erratum: Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes (Nature Genetics (2011) 43 (561-564)) Nature Genetics, 43 (10).

Rahmioglu, N, Heaton, J, Clement, G, Gill, R, Surdulescu, G, Zlobecka, K, Hodgkiss, D, Ma, Y, Hider, RC, Smith, NW and Ahmadi, KR (2011) Genetic epidemiology of induced CYP3A4 activity. Pharmacogenet Genomics, 21 (10). pp. 642-651.

Nicholson, G, Rantalainen, M, Li, JV, Maher, AD, Malmodin, D, Ahmadi, KR, Faber, JH, Barrett, A, Min, JL, Rayner, NW, Toft, H, Krestyaninova, M, Viksna, J, Neogi, SG, Dumas, ME, Sarkans, U, MolPAGE Consortium, , Donnelly, P, Illig, T, Adamski, J, Suhre, K, Allen, M, Zondervan, KT, Spector, TD, Nicholson, JK, Lindon, JC, Baunsgaard, D, Holmes, E, McCarthy, MI and Holmes, CC (2011) A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection. PLoS Genet, 7 (9).

Rahmioglu, N, Le Gall, G, Heaton, J, Kay, KL, Smith, NW, Colquhoun, IJ, Ahmadi, KR and Kemsley, EK (2011) Prediction of variability in CYP3A4 induction using a combined 1H NMR metabonomics and targeted UPLC-MS approach. J Proteome Res, 10 (6). pp. 2807-2816.

Heaton, J, Rahmioglu, N, Ahmadi, KR, Legido-Quigley, C and Smith, NW (2011) Rapid quantification of quinine and its major metabolite (3S)-3-hydroxyquinine in diluted urine by UPLC-MS/MS. J Pharm Biomed Anal, 55 (3). pp. 494-499.

Small, KS, Hedman, AK, Grundberg, E, Nica, AC, Thorleifsson, G, Kong, A, Thorsteindottir, U, Shin, SY, Richards, HB, GIANT Consortium, , MAGIC Investigators, , DIAGRAM Consortium, , Soranzo, N, Ahmadi, KR, Lindgren, CM, Stefansson, K, Dermitzakis, ET, Deloukas, P, Spector, TD, McCarthy, MI and MuTHER Consortium, (2011) Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes. Nat Genet, 43 (6). pp. 561-564.

Ahmadi, KR (2011) Role of common genetic variants on the risk of Stevens-Johnson syndrome and toxic epidermal necrolysis. Pharmacogenomics, 12 (6). pp. 761-764.

Nicholson, G, Rantalainen, M, Hallgrímsdóttir, IB, Silverman, BW, Donnelly, P, Holmes, CC, Maher, AD, Li, JV, Dumas, M-E, Nicholson, JK, Lindon, JC, Holmes, E, Malmodin, D, Faber, JH, Toft, H, Baunsgaard, D, Ahmadi, KR, Spector, TD, Barrett, A, Allen, M, McCarthy, MI, Krestyaninova, M, Sarkans, U, Viksna, J, Neogi, SG, Maher, AD, Silverman, BW, Donnelly, P, Zondervan, KT and McCarthy, MI (2011) Human metabolic profiles are stably controlled by genetic and environmental variation Molecular Systems Biology, 7.

Cotlarciuc, I, Andrew, T, Dew, T, Clement, G, Gill, R, Surdulescu, G, Sherwood, R and Ahmadi, KR (2011) The basis of differential responses to folic acid supplementation. J Nutrigenet Nutrigenomics, 4 (2). pp. 99-109.

Min, JL, Taylor, JM, Richards, JB, Watts, T, Pettersson, FH, Broxholme, J, Ahmadi, KR, Surdulescu, GL, Lowy, E, Gieger, C, Newton-Cheh, C, Perola, M, Soranzo, N, Surakka, I, Lindgren, CM, Ragoussis, J, Morris, AP, Cardon, LR, Spector, TD and Zondervan, KT (2011) The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traits. PLoS One, 6 (7).

Chambers, JC, Zhang, W, Lord, GM, van der Harst, P, Lawlor, DA, Sehmi, JS, Gale, DP, Wass, MN, Ahmadi, KR, Bakker, SJL, Beckmann, J, Bilo, HJG, Bochud, M, Brown, MJ, Caulfield, MJ, Connell, JMC, Cook, HT, Cotlarciuc, I, Smith, GD, de Silva, R, Deng, G, Devuyst, O, Dikkeschei, LD, Dimkovic, N, Dockrell, M, Dominiczak, A, Ebrahim, S, Eggermann, T, Farrall, M, Ferrucci, L, Floege, J, Forouhi, NG, Gansevoort, RT, Han, X, Hedblad, B, van der Heide, JJH, Hepkema, BG, Hernandez-Fuentes, M, Hypponen, E, Johnson, T, de Jong, PE, Kleefstra, N, Lagou, V, Lapsley, M, Li, Y, Loos, RJF, Luan, J, Luttropp, K, Marechal, C, Melander, O, Munroe, PB, Nordfors, L, Parsa, A, Peltonen, L, Penninx, BW, Perucha, E, Pouta, A, Prokopenko, I, Roderick, PJ, Ruokonen, A, Samani, NJ, Sanna, S, Schalling, M, Schlessinger, D, Schlieper, G, Seelen, MAJ, Shuldiner, AR, Sjogren, M, Smit, JH, Snieder, H, Soranzo, N, Spector, TD, Stenvinkel, P, Sternberg, MJE, Swaminathan, R, Tanaka, T, Ubink-Veltmaat, LJ, Uda, M, Vollenweider, P, Wallace, C, Waterworth, D, Zerres, K, Waeber, G, Wareham, NJ, Maxwell, PH, McCarthy, MI, Jarvelin, M-R, Mooser, V, Abecasis, GR, Lightstone, L, Scott, J, Navis, G, Elliott, P and Kooner, JS (2010) Genetic loci influencing kidney function and chronic kidney disease NATURE GENETICS, 42 (5). pp. 373-375.

Rahmioğlu, N and Ahmadi, KR (2010) Classical twin design in modern pharmacogenomics studies. Pharmacogenomics, 11 (2). pp. 215-226.

McEvoy, BP, Montgomery, GW, McRae, AF, Ripatti, S, Perola, M, Spector, TD, Cherkas, L, Ahmadi, KR, Boomsma, D, Willemsen, G, Hottenga, JJ, Pedersen, NL, Magnusson, PK, Kyvik, KO, Christensen, K, Kaprio, J, Heikkilä, K, Palotie, A, Widen, E, Muilu, J, Syvänen, AC, Liljedahl, U, Hardiman, O, Cronin, S, Peltonen, L, Martin, NG and Visscher, PM (2009) Geographical structure and differential natural selection among North European populations. Genome Res, 19 (5). pp. 804-814.

Soranzo, N, Rivadeneira, F, Chinappen-Horsley, U, Malkina, I, Richards, JB, Hammond, N, Stolk, L, Nica, A, Inouye, M, Hofman, A, Stephens, J, Wheeler, E, Arp, P, Gwilliam, R, Jhamai, PM, Potter, S, Chaney, A, Ghori, MJ, Ravindrarajah, R, Ermakov, S, Estrada, K, Pols, HA, Williams, FM, McArdle, WL, van Meurs, JB, Loos, RJ, Dermitzakis, ET, Ahmadi, KR, Hart, DJ, Ouwehand, WH, Wareham, NJ, Barroso, I, Sandhu, MS, Strachan, DP, Livshits, G, Spector, TD, Uitterlinden, AG and Deloukas, P (2009) Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. PLoS Genet, 5 (4).

Rahmioglu, N, Andrew, T, Cherkas, L, Surdulescu, G, Swaminathan, R, Spector, T and Ahmadi, KR (2009) Epidemiology and genetic epidemiology of the liver function test proteins. PLoS One, 4 (2).

Crockford, DJ, Maher, AD, Ahmadi, KR, Barrett, A, Plumb, RS, Wilson, ID and Nicholson, JK (2008) 1H NMR and UPLC-MSE statistical heterospectroscopy: Characterization of drug metabolites (Xenometabolome) in epidemiological studies (Analytical Chemistry (2008) 80, (6835-6844)) Analytical Chemistry, 80 (21).

Crockford, DJ, Maher, AD, Ahmadi, KR, Barrett, A, Plumb, RS, Wilson, ID and Nicholson, JK (2008) 1H NMR and UPLC-MS(E) statistical heterospectroscopy: characterization of drug metabolites (xenometabolome) in epidemiological studies. Anal Chem, 80 (18). pp. 6835-6844.

Richards, JB, Rivadeneira, F, Inouye, M, Pastinen, TM, Soranzo, N, Wilson, SG, Andrew, T, Falchi, M, Gwilliam, R, Ahmadi, KR, Valdes, AM, Arp, P, Whittaker, P, Verlaan, DJ, Jhamai, M, Kumanduri, V, Moorhouse, M, van Meurs, JB, Hofman, A, Pols, HA, Hart, D, Zhai, G, Kato, BS, Mullin, BH, Zhang, F, Deloukas, P, Uitterlinden, AG and Spector, TD (2008) Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study. Lancet, 371 (9623). pp. 1505-1512.

Chinappen-Horsley, U, Blake, GM, Fogelman, I, Kato, B, Ahmadi, KR and Spector, TD (2008) Quantitative trait loci for bone lengths on chromosome 5 using dual energy X-Ray absorptiometry imaging in the Twins UK cohort. PLoS One, 3 (3).

Zhang, F, Kato, BS, Gardner, JP, Kimura, M, Spector, TD and Ahmadi, KR (2007) Lack of association between leukocyte telomere length and genetic variants in two ageing-related candidate genes. Mech Ageing Dev, 128 (7-8). pp. 415-422.

Zhang, F, Zhai, G, Kato, BS, Hart, DJ, Hunter, D, Spector, TD and Ahmadi, KR (2007) Association between KLOTHO gene and hand osteoarthritis in a female Caucasian population. Osteoarthritis Cartilage, 15 (6). pp. 624-629.

Healy, DG, Abou-Sleiman, PM, Ahmadi, KR, Gandhi, S, Muqit, MM, Bhatia, KP, Quinn, NP, Lees, AJ, Holton, JL, Revesz, T and Wood, NW (2006) NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach. Mov Disord, 21 (11). pp. 1960-1963.

Spector, TD, Ahmadi, KR and Valdes, AM (2006) Reply [7] Arthritis and Rheumatism, 54 (9). pp. 3064-3065.

Need, AC, Ahmadi, KR, Spector, TD and Goldstein, DB (2006) Obesity is associated with genetic variants that alter dopamine availability. Ann Hum Genet, 70 (Pt 3). pp. 293-303.

Healy, DG, Abou-Sleiman, PM, Casas, JP, Ahmadi, KR, Lynch, T, Gandhi, S, Muqit, MM, Foltynie, T, Barker, R, Bhatia, KP, Quinn, NP, Lees, AJ, Gibson, JM, Holton, JL, Revesz, T, Goldstein, DB and Wood, NW (2006) UCHL-1 is not a Parkinson's disease susceptibility gene. Ann Neurol, 59 (4). pp. 627-633.

Spector, TD, Ahmadi, KR and Valdes, AM (2006) When is a replication not a replication? Or how to spot a good genetic association study. Arthritis Rheum, 54 (4). pp. 1051-1054.

Ozawa, T, Healy, DG, Abou-Sleiman, PM, Ahmadi, KR, Quinn, N, Lees, AJ, Shaw, K, Wullner, U, Berciano, J, Moller, JC, Kamm, C, Burk, K, Josephs, KA, Barone, P, Tolosa, E, Goldstein, DB, Wenning, G, Geser, F, Holton, JL, Gasser, T, Revesz, T, Wood, NW and European MSA study group, (2006) The alpha-synuclein gene in multiple system atrophy. J Neurol Neurosurg Psychiatry, 77 (4). pp. 464-467.

Shah, PR, Ahmad-Annuar, A, Ahmadi, KR, Russ, C, Sapp, PC, Horvitz, HR, Brown, RH, Goldstein, DB and Fisher, EMC (2006) No association of DYNC1H1 with sporadic ALS in a case-control study of a northern European derived population: A tagging SNP approach Amyotrophic Lateral Sclerosis, 7 (1). pp. 46-56.

Shah, PR, Ahmad-Annuar, A, Ahmadi, KR, Russ, C, Sapp, PC, Horvitz, HR, Brown, RH, Goldstein, DB and Fisher, EM (2006) No association of DYNC1H1 with sporadic ALS in a case-control study of a northern European derived population: a tagging SNP approach. Amyotroph Lateral Scler, 7 (1). pp. 46-56.

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