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  • Colin Palmer

17q21 variant increases the risk of exacerbations in asthmatic children despite inhaled corticosteroids use

Farzan, N., Vijverberg, S. J., Hernandez-Pacheco, N., Bel, E. H. D., Berce, V., Bønnelykke, K., Bisgaard, H., Burchard, E. G., Canino, G., Celedón, J. C., Chew, F. T., Chiang, W. C., Cloutier, M. M., Forno, E., Francis, B., Hawcutt, D. B., Herrera-Luis, E., Kabesch, M., Karimi, L., Melén, E. & 19 others, Mukhopadhyay, S., Merid, S. K., Palmer, C. N., Pino-Yanes, M., Munir, P., Potočnik, U., Repnik, K., Schieck, M., Sevelsted, A., Yang Yie, S., Smyth, R. L., Soares, P., Söderhäll, C., Tantisira, K. G., Tavendale, R., Sze Man, T., Turner, S., Verhamme, K. M. & Maitland-van der Zee, A-H., Oct 2018, In : Allergy. 73, 10, p. 2083-2088 6 p.

Research output: Contribution to journalLetter

Open Access
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6 Citations (Scopus)
146 Downloads (Pure)

A common missense variant of LILRB5 is associated with statin intolerance: A GoDARTS study

Siddiqui, M. K., Veluchamy, A., Tavendale, R., Carr, F., Maroteau, C., Pearson, E. R., Looker, H. M., Morris, A. D., Dow, E., George, J., Doney, A. & Palmer, C. N. A., 6 Oct 2015.

Research output: Contribution to conferencePoster

A common missense variant of LILRB5 is associated with statin intolerance and myalgia

Siddiqui, M. K., Maroteau, C., Veluchamy, A., Tornio, A., Tavendale, R., Carr, F., Abelega, N-U., Carr, D., Bloch, K., Hallberg, P., Yue, Q-Y., Pearson, E. R., Colhoun, H., Morris, A. D., Dow, E., George, J., Pirmohamed, M., Ridker, P. M., Doney, A. S. F., Alfirevic, A. & 5 others, Wadelius, M., Maitland-van der Zee, A. H., Chasman, D. I., Palmer, C. N. A. & PREDICTION-ADR Consortium, 21 Dec 2017, In : European Heart Journal. 38, 48, p. 3569-3575 7 p.

Research output: Contribution to journalArticle

Open Access
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12 Citations (Scopus)
151 Downloads (Pure)

A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome

Aung, T., Ozaki, M., Mizoguchi, T., Allingham, R. R., Li, Z., Haripriya, A., Nakano, S., Uebe, S., Harder, J. M., Chan, A. S. Y., Lee, M. C., Burdon, K. P., Astakhov, Y. S., Abu-Amero, K. K., Zenteno, J. C., Nilgün, Y., Zarnowski, T., Pakravan, M., Safieh, L. A., Jia, L. & 30 others, Wang, Y. X., Williams, S., Paoli, D., Schlottmann, P. G., Huang, L., Sim, K. S., Foo, J. N., Nakano, M., Ikeda, Y., Kumar, R. S., Ueno, M., Manabe, S., Hayashi, K., Kazama, S., Ideta, R., Mori, Y., Miyata, K., Sugiyama, K., Higashide, T., Chihara, E., Inoue, K., Ishiko, S., Yoshida, A., Yanagi, M., Kiuchi, Y., Aihara, M., Ohashi, T., Sakurai, T., Sugimoto, T. & Wellcome Trust Case Control Consortium 2, Apr 2015, In : Nature Genetics. 47, 4, p. 387-392 6 p.

Research output: Contribution to journalLetter

44 Citations (Scopus)

A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease

Nikpay, M., Goel, A., Won, H-H., Hall, L. M., Willenborg, C., Kanoni, S., Saleheen, D., Kyriakou, T., Nelson, C. P., Hopewell, J. C., Webb, T. R., Zeng, L., Dehghan, A., Elver, M., Armasu, S. M., Auro, K., Bjonnes, A., Chasman, D. I., Chen, S., Ford, I. & 31 others, Franceschini, N., Gieger, C., Grace, C., Gustafsson, S., Huang, J., Hwang, S-J., Kim, Y. K., Kleber, M. E., Lau, K. W., Lu, X., Lu, Y., Lyytikäinen, L-P., Mihailov, E., Morrison, A. C., Pervjakova, N., Qu, L., Rose, L. M., Salfati, E., Saxena, R., Scholz, M., Smith, A. V., Tikkanen, E., Uitterlinden, A., Yang, X., Zhang, W., Zhao, W., de Andrade, M., de Vries, P. S., van Zuydam, N. R., Palmer, C. N. & for the CARDIoGRAMplusC4D Consortium, Oct 2015, In : Nature Genetics. 47, 10, p. 1121-1130 10 p.

Research output: Contribution to journalArticle

Open Access
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713 Citations (Scopus)
1138 Downloads (Pure)

ADRB2 haplotypes and risk of exacerbations in asthmatic children and young adults treated with long-acting beta 2-agonists: A meta-analysis in the PiCA consortium

Karimi, L., Vijverberg, S. J., Engelkes, M., Hernandez-Pacheco, N., Farzan, N., Soares, P., Francis, B. R., Pino-Yanes, M., Eng, C., Mukhopadhyay, S., Schieck, M., Kabesch, M., Burchard, E. G., Palmer, C. N. A., Turner, S. W., Janssens, H. M., Maitland-Van Der Zee, A-H. & Verhamme, K. M. C., 21 Nov 2019, In : European Respiratory Journal. 54, 63, PA5388.

Research output: Contribution to journalMeeting abstract

Age-dependent elastin degradation is enhanced in chronic obstructive pulmonary disease

the Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints (ECLIPSE) Investigators, Huang, J. T. J., Bolton, C. E., Miller, B. E., Tal-Singer, R., Rabinovich, R. A., Palmer, C. N. A., Thomson, N. C. & MacNee, W., 30 Sep 2016, In : European Respiratory Journal. 48, 4, p. 1215-1218 4 p.

Research output: Contribution to journalLetter

Open Access
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7 Citations (Scopus)
172 Downloads (Pure)

A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility

Damotte, V., Guillot-Noel, L., Patsopoulos, N. A., Madireddy, L., El Behi, M., International Multiple Sclerosis Genetics Consortium, Wellcome Trust Case Control Consortium 2, De Jager, P. L., Baranzini, S. E., Cournu-Rebeix, I. & Fontaine, B., Mar 2014, In : Genes and Immunity. 15, 2, p. 126-132 7 p.

Research output: Contribution to journalArticle

19 Citations (Scopus)

A gene variant near ATM is significantly associated with metformin treatment response in type 2 diabetes: a replication and meta-analysis of five cohorts

van Leeuwen, N., Nijpels, G., Becker, M. L., Deshmukh, H., Zhou, K., Stricker, B. H. C., Uitterlinden, A. G., Hofman, A., van 't Riet, E., Palmer, C. N. A., Guigas, B., Slagboom, P. E., Durrington, P., Calle, R. A., Neil, A., Hitman, G., Livingstone, S. J., Colhoun, H., Holman, R. R., McCarthy, M. I. & 3 others, Dekker, J. M., 't Hart, L. M. & Pearson, E., 2012, In : Diabetologia. 55, 7, p. 1971-1977 7 p.

Research output: Contribution to journalArticle

82 Citations (Scopus)

A genome-wide association search for type 2 diabetes genes in African Americans

Palmer, N. D., McDonough, C. W., Hicks, P. J., Roh, B. H., Wing, M. R., An, S. S., Hester, J. M., Cooke, J. N., Bostrom, M. A., Rudock, M. E., Talbert, M. E., Lewis, J. P., Ferrara, A., Lu, L., Ziegler, J. T., Sale, M. M., Divers, J., Shriner, D., Adeyemo, A., Rotimi, C. N. & 6 others, Ng, M. C. Y., Langefeld, C. D., Freedman, B. I., Bowden, D. W., DIAGRAM Consortium & MAGIC Investigators, 2012, In : PLoS ONE. 7, 1, p. e29202

Research output: Contribution to journalArticle

120 Citations (Scopus)

A genome-wide association study finds genetic variants associated with neck or shoulder pain in UK Biobank

Meng, W., Chan, B. W., Harris, C., Freidin, M. B., Hebert, H., Adams, M. J., Campbell, A., Hayward, C., Zheng, H., Zhang, X., Colvin, L., Hales, T., Palmer, C., Williams, F. M. K., McIntosh, A. M. & Smith, B. H., 15 Apr 2020, In : Human Molecular Genetics. 29, 8, p. 1396-1404 9 p.

Research output: Contribution to journalArticle

Open Access
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12 Downloads (Pure)

A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough

Mosley, J. D., Shaffer, C. M., Van Driest, S. L., Weeke, P. E., Wells, Q. S., Karnes, J. H., Velez Edwards, D. R., Wei, W-Q., Teixeira, P. L., Bastarache, L., Crawford, D. C., Li, R., Manolio, T. A., Bottinger, E. P., McCarty, C. A., Linneman, J. G., Brilliant, M. H., Pacheco, J. A., Thompson, W., Chisholm, R. L. & 27 others, Jarvik, G. P., Crosslin, D. R., Carrell, D. S., Baldwin, E., Ralston, J., Larson, E. B., Grafton, J., Scrol, A., Jouni, H., Kullo, I. J., Tromp, G., Borthwick, K. M., Kuivaniemi, H., Carey, D. J., Ritchie, M. D., Bradford, Y., Verma, S. S., Chute, C. G., Veluchamy, A., Siddiqui, M., Palmer, C. N. A., Doney, A., MahmoudPour, S. H., Maitland-van der Zee, A. H., Morris, A. D., Denny, J. C. & Roden, D. M., Jun 2016, In : Pharmacogenomics Journal. 16, 3, p. 231-237 7 p.

Research output: Contribution to journalArticle

Open Access
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27 Citations (Scopus)
163 Downloads (Pure)

A genome-wide association study implicates that the TTC39C gene is associated with diabetic maculopathy with decreased visual acuity

Meng, W., Chan, B., Ezeonwumelu, C., Hebert, H., Campbell, A., Soler, V. & Palmer, C., 2 Jul 2019, In : Ophthalmic Genetics. 40, 3, p. 252-258 7 p.

Research output: Contribution to journalArticle

Open Access
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13 Downloads (Pure)

A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes

Finnish Diabetic Nephropathy Study (FinnDiane), Surrogate Markers for Micro- and Macro-Vascular Hard Endpoints for Innovative Diabetes Tools (SUMMIT) Study Group, GENIE (GEnetics of Nephropathy an International Effort) Consortium, Warren 3 and Genetics of Kidneys in Diabetes (GoKinD) Study Group, Van Zuydam, N. R., Ahlqvist, E., Sandholm, N., Deshmukh, H., Rayner, N. W., Abdalla, M., Ladenvall, C., Ziemek, D., Fauman, E., Robertson, N. R., McKeigue, P. M., Valo, E., Forsblom, C., Harjutsalo, V., Perna, A., Rurali, E. & 65 others, Marcovecchio, M. L., Igo, R. P., Salem, R. M., Perico, N., Lajer, M., Käräjämäki, A., Imamura, M., Kubo, M., Takahashi, A., Sim, X., Liu, J., Van Dam, R. M., Jiang, G., Tam, C. H. T., Luk, A. O. Y., Lee, H. M., Lim, C. K. P., Szeto, C. C., So, W. Y., Chan, J. C. N., Ang, S. F., Dorajoo, R., Wang, L., Clara, T. S. H., McKnight, A. J., Duffy, S., Pezzolesi, M. G., Marre, M., Gyorgy, B., Hadjadj, S., Hiraki, L. T., Ahluwalia, T. S., Almgren, P., Schulz, C-A., Orho-Melander, M., Linneberg, A., Christensen, C., Witte, D. R., Grarup, N., Brandslund, I., Melander, O., Paterson, A. D., Trégouët, D-A., Maxwell, A. P., Lim, S. C., Ma, R. C. W., Tai, E. S., Maeda, S., Lyssenko, V., Tuomi, T., Krolewski, A., Rich, S. S., Hirschhorn, J. N., Florez, J. C., Dunger, D., Pedersen, O., Hansen, T., Rossing, P., Remuzzi, G., Brosnan, M. J., Palmer, C. N. A., Groop, P-H., Colhoun, H. M., Groop, L. C. & McCarthy, M. I., Jul 2018, In : Diabetes. 67, 7, p. 1414-1427 14 p.

Research output: Contribution to journalArticle

Open Access
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38 Citations (Scopus)
105 Downloads (Pure)

A genome-wide association study provides evidence of sex-specific involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) with diabetic neuropathic pain

Meng, W., Deshmukh, H. A., Donnelly, L. A., Wellcome Trust Case Control Consortium 2, Surrogate Markers for Micro- and Macro-Vascular Hard Endpoints for Innovative Diabetes Tools (SUMMIT) Study Group, Torrance, N., Colhoun, H. M., Palmer, C. N. A. & Smith, B. H., Oct 2015, In : EBioMedicine. 2, 10, p. 1386-1393 8 p.

Research output: Contribution to journalArticle

Open Access
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23 Citations (Scopus)
176 Downloads (Pure)

A Genome-Wide Association Study Provides New Evidence That CACNA1C Gene is Associated With Diabetic Cataract

Chang, C., Zhang, K., Veluchamy, A., Hébert, H. L., Looker, H. C., Colhoun, H. M., Palmer, C. N. A. & Meng, W., 1 Apr 2016, In : Investigative Ophthalmology & Visual Science. 57, 4, p. 2246-50 5 p.

Research output: Contribution to journalArticle

Open Access
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4 Citations (Scopus)
149 Downloads (Pure)

A genome-wide association study suggested that the mitogen-activated protein kinase 14 gene (MAPK14) is associated with diabetic foot ulcer

Meng, W., Veluchamy, A., Hebert, H., Campbell, A., Colhoun, H. M. & Palmer, C., Dec 2017, In : British Journal of Dermatology. 177, 6, p. 1664-1670 7 p.

Research output: Contribution to journalArticle

Open Access
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8 Citations (Scopus)
120 Downloads (Pure)

A genome-wide association study suggests an association of Chr8p21.3 (GFRA2) with diabetic neuropathic pain

Meng, W., Deshmukh, H. A., van Zuydam, N. R., Liu, Y., Donnelly, L. A., Zhou, K., Wellcome Trust Case Control Consortium 2, Surrogate Markers for Micro- and Macro-Vascular Hard Endpoints for Innovative Diabetes Tools (SUMMIT) Study Group, Morris, A. D., Colhoun, H. M., Palmer, C. N. A. & Smith, B. H., Mar 2015, In : European Journal of Pain. 19, 3, p. 392-399 8 p.

Research output: Contribution to journalArticle

Open Access
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34 Citations (Scopus)
207 Downloads (Pure)

A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes

Wellcome Trust Case Control Consortium 2, Surrogate Markers for Micro- and Macro-Vascular Hard Endpoints for Innovative Diabetes Tools (SUMMIT) Study Group, Meng, W., Shah, K. P., Pollack, S., Toppila, L., Hebert, H. L., McCarthy, M. I., Groop, L. C., Ahlqvist, E., Lyssenko, V., Argardh, E., Daniell, M., Kaidonis, G., Craig, J. E., Mitchell, P., Liew, G., Kifley, A., Wang, J. J., Jensen, R. A. & 21 others, Penman, A., Hancock, H., Chen, C. J., Correa, A., Kuo, J. Z., Li, X., Chen, Y-D. I., Rotter, J. I., Klein, R., Klein, B. E., Wong, T. Y., Morris, A. D., Doney, A. S. F., Colhoun, H. M., Price, A. L., Burdon, K. P., Groop, P-H., Sandholm, N., Grassi, M. A., Sobrin, L. & Palmer, C. N. A., Nov 2018, In : Acta Ophthalmologica. 96, 7, p. e811-e819 9 p.

Research output: Contribution to journalArticle

Open Access
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15 Citations (Scopus)
142 Downloads (Pure)

A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk

Manning, A., Highland, H. M., Gasser, J., Sim, X., Tukiainen, T., Fontanillas, P., Grarup, N., Rivas, M. A., Mahajan, A., Locke, A. E., Cingolani, P., Pers, T. H., Viñuela, A., Brown, A. A., Wu, Y., Flannick, J., Fuchsberger, C., Gamazon, E. R., Gaulton, K. J., Im, H. K. & 242 others, Teslovich, T. M., Blackwell, T. W., Bork-Jensen, J., Burtt, N. P., Chen, Y., Green, T., Hartl, C., Kang, H. M., Kumar, A., Ladenvall, C., Ma, C., Moutsianas, L., Pearson, R. D., Perry, J. R. B., Rayner, N. W., Robertson, N. R., Scott, L. J., van de Bunt, M., Eriksson, J. G., Jula, A., Koskinen, S., Lehtimäki, T., Palotie, A., Raitakari, O. T., Jacobs, S. B., Wessel, J., Chu, A. Y., Scott, R. A., Goodarzi, M. O., Blancher, C., Buck, G., Buck, D., Chines, P. S., Gabriel, S., Gjesing, A. P., Groves, C. J., Hollensted, M., Huyghe, J. R., Jackson, A. U., Jun, G., Justesen, J. M., Mangino, M., Murphy, J., Neville, M., Onofrio, R., Small, K. S., Stringham, H. M., Trakalo, J., Banks, E., Carey, J., Carneiro, M. O., DePristo, M., Farjoun, Y., Fennell, T., Goldstein, J. I., Grant, G., Hrabé de Angelis, M., Maguire, J., Neale, B. M., Poplin, R., Purcell, S., Schwarzmayr, T., Shakir, K., Smith, J. D., Strom, T. M., Wieland, T., Lindstrom, J., Brandslund, I., Christensen, C., Surdulescu, G. L., Lakka, T. A., Doney, A. S. F., Nilsson, P., Wareham, N. J., Langenberg, C., Varga, T. V., Franks, P. W., Rolandsson, O., Rosengren, A. H., Farook, V. S., Thameem, F., Puppala, S., Kumar, S., Lehman, D. M., Jenkinson, C. P., Curran, J. E., Fowler, S. P., Arya, R., DeFronzo, R. A., Abboud, H. E., Syvänen, A-C., Hicks, P. J., Palmer, N. D., Ng, M. C. Y., Bowden, D. W., Freedman, B. I., Esko, T., Mägi, R., Milani, L., Mihailov, E., Metspalu, A., Narisu, N., Kinnunen, L., Bonnycastle, L. L., Swift, A., Pasko, D., Wood, A. R., Fadista, J., Pollin, T. I., Barzilai, N., Atzmon, G., Glaser, B., Thorand, B., Strauch, K., Peters, A., Roden, M., Müller-Nurasyid, M., Liang, L., Kriebel, J., Illig, T., Grallert, H., Gieger, C., Meisinger, C., Lannfelt, L., Musani, S. K., Griswold, M., Taylor, H. A., Wilson, G., Correa, A., Oksa, H., Scott, W. R., Afzal, U., Tan, S-T., Loh, M., Chambers, J. C., Sehmi, J., Kooner, J. S., Lehne, B., Cho, Y. S., Lee, J-Y., Han, B-G., Käräjämäki, A., Qi, Q., Qi, L., Huang, J., Hu, F. B., Melander, O., Orho-Melander, M., Below, J. E., Aguilar, D., Wong, T. Y., Liu, J., Khor, C-C., Chia, K. S., Lim, W. Y., Cheng, C-Y., Chan, E., Tai, E. S., Aung, T., Linneberg, A., Isomaa, B., Meitinger, T., Tuomi, T., Hakaste, L., Kravic, J., Jørgensen, M. E., Lauritzen, T., Deloukas, P., Stirrups, K. E., Owen, K. R., Farmer, A. J., Frayling, T. M., O'Rahilly, S. P., Walker, M., Levy, J. C., Hodgkiss, D., Hattersley, A. T., Kuulasmaa, T., Stančáková, A., Barroso, I., Bharadwaj, D., Chan, J., Chandak, G. R., Daly, M. J., Donnelly, P. J., Ebrahim, S. B., Elliott, P., Fingerlin, T., Froguel, P., Hu, C., Jia, W., Ma, R. C. W., McVean, G., Park, T., Prabhakaran, D., Sandhu, M., Scott, J., Sladek, R., Tandon, N., Teo, Y. Y., Zeggini, E., Watanabe, R. M., Koistinen, H. A., Kesaniemi, Y. A., Uusitupa, M., Spector, T. D., Salomaa, V., Rauramaa, R., Palmer, C. N. A., Prokopenko, I., Morris, A. D., Bergman, R. N., Collins, F. S., Lind, L., Ingelsson, E., Tuomilehto, J., Karpe, F., Groop, L., Jørgensen, T., Hansen, T., Pedersen, O., Kuusisto, J., Abecasis, G., Bell, G. I., Blangero, J., Cox, N. J., Duggirala, R., Seielstad, M., Wilson, J. G., Dupuis, J., Ripatti, S., Hanis, C. L., Florez, J. C., Mohlke, K. L., Meigs, J. B., Laakso, M., Morris, A. P., Boehnke, M., Altshuler, D., McCarthy, M. I., Gloyn, A. L. & Lindgren, C. M., Jul 2017, In : Diabetes. 66, 7, p. 2019-2032 14 p.

Research output: Contribution to journalArticle

Open Access
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22 Citations (Scopus)
21 Downloads (Pure)

A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies

Bodea, C. A., Neale, B. M., Ripke, S., International IBD Genetics Consortium, Daly, M. J., Devlin, B. & Roeder, K., 5 May 2016, In : American Journal of Human Genetics. 98, 5, p. 857-868 12 p.

Research output: Contribution to journalArticle

6 Citations (Scopus)

A multigenic model to predict risk of ischemic stroke in subjects with type 2 diabetes

Pola, R., Kimber, C. H., Giarretta, I., Doney, A., Morris, A. M., Gaetani, E. & Palmer, C. N., Jun 2011, In : Atherosclerosis. Supplements. 12, 1, p. 127-127 1 p.

Research output: Contribution to journalArticle

Analysis with the exome array identifies multiple new independent variants in lipid loci

Kanoni, S., Masca, N. G. D., Stirrups, K. E., Varga, T. V., Warren, H. R., Scott, R. A., Southam, L., Zhang, W., Yaghootkar, H., Müller-Nurasyid, M., Couto Alves, A., Strawbridge, R. J., Lataniotis, L., Hashim, N. A., Besse, C., Boland, A., Braund, P. S., Connell, J. M., Dominiczak, A., Farmaki, A-E. & 31 others, Franks, S., Grallert, H., Jansson, J-H., Karaleftheri, M., Keinänen-Kiukaanniemi, S., Matchan, A., Pasko, D., Peters, A., Poulter, N., Rayner, N. W., Renström, F., Rolandsson, O., Sabater-Lleal, M., Sennblad, B., Sever, P., Shields, D., Silveira, A., Stanton, A. V., Strauch, K., Tomaszewski, M., Tsafantakis, E., Waldenberger, M., Blakemore, A. I. F., Dedoussis, G., Escher, S. A., Kooner, J. S., McCarthy, M. I., Palmer, C. N. A., Wellcome Trust Case Control Consortium, Hamsten, A. & Caulfield, M. J., 27 Jul 2016, In : Human Molecular Genetics. 25, 18, p. 4094-4106 13 p.

Research output: Contribution to journalArticle

Open Access
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8 Citations (Scopus)
157 Downloads (Pure)

Ancestral haplotype 8.1 and lung disease severity in European cystic fibrosis patients

Corvol, H., Beucher, J., Boelle, P-Y., Busson, P-F., Muselet-Charlier, C., Clement, A., Ratjen, F., Grasemann, H., Laki, J., Palmer, C. N. A., Elborn, J. S. & Mehta, A., Jan 2012, In : Journal of Cystic Fibrosis. 11, 1, p. 63-67 5 p.

Research output: Contribution to journalArticle

18 Citations (Scopus)

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

Scott, R. A., Scott, L. J., Maegi, R., Marullo, L., Gaulton, K. J., Kaakinen, M., Pervjakova, N., Pers, T. H., Johnson, A. D., Eicher, J. D., Jackson, A. U., Ferreira, T., Lee, Y., Ma, C., Steinthorsdottir, V., Thorleifsson, G., Qi, L., Van Zuydam, N. R., Mahajan, A., Chen, H. & 31 others, Almgren, P., Voight, B. F., Grallert, H., Mueller-Nurasyid, M., Ried, J. S., Rayner, N. W., Robertson, N., Karssen, L. C., Van Leeuwen, E. M., Willems, S. M., Fuchsberger, C., Kwan, P., Teslovich, T. M., Chanda, P., Li, M., Lu, Y., Dina, C., Thuillier, D., Yengo, L., Jiang, L., Sparso, T., Kestler, H. A., Chheda, H., Eisele, L., Gustafsson, S., Franberg, M., Strawbridge, R. J., Benediktsson, R., Morris, A. D., Palmer, C. N. A. & for the DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium, Nov 2017, In : Diabetes. 66, 11, p. 2888-2902 15 p.

Research output: Contribution to journalArticle

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208 Citations (Scopus)
505 Downloads (Pure)

Application of pharmacogenomics and bioinformatics to exemplify the utility of human ex vivo organoculture models in the field of precision medicine

Cowan, K., MacLuskie, G., Finch, M., Palmer, C. N. A., Hair, J., Bylesjo, M., Lynagh, S., Brankin, P., McNeil, M., Low, C., Mallinson, D., Gourlay, E. M., Child, H., Cheyne, L. & Bunton, D. C., 20 Dec 2019, In : PLoS ONE. 14, 12, p. 1-15 15 p., e0226564.

Research output: Contribution to journalArticle

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A role for coding functional variants in HNF4A in type 2 diabetes susceptibility

Jafar-Mohammadi, B., Groves, C. J., Gjesing, A. P., Herrera, B. M., Winckler, W., Stringham, H. M., Morris, A. P., Lauritzen, T., Doney, A. S. F., Morris, A. D., Weedon, M. N., Swift, A. J., Kuusisto, J., Laakso, M., Altshuler, D., Hattersley, A. T., Collins, F. S., Boehnke, M., Hansen, T., Pedersen, O. & 5 others, Palmer, C. N. A., Frayling, T. M., Gloyn, A. L., McCarthy, M. I. & DIAGRAM Consortium, Jan 2011, In : Diabetologia. 54, 1, p. 111-119 9 p.

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22 Citations (Scopus)

Association analyses based on false discovery rate implicate new loci for coronary artery disease

Nelson, C. P., Goel, A., Butterworth, A. S., Kanoni, S., Webb, T. R., Marouli, E., Zeng, L., Ntalla, I., Lai, F. Y., Hopewell, J. C., Giannakopoulou, O., Jiang, T., Hamby, S. E., Di Angelantonio, E., Assimes, T. L., Bottinger, E. P., Chambers, J. C., Clarke, R., Palmer, C. N. A., Cubbon, R. M. & 31 others, Ellinor, P. T., Ermel, R., Evangelou, E., Franks, P. W., Grace, C., Gu, D., Hingorani, A. D., Howson, J. M. M., Ingelsson, E., Kastrati, A., Kessler, T., Kyriakou, T., Lehtimäki, T., Lu, X., Lu, Y., März, W., McPherson, R., Metspalu, A., Pujades-Rodriguez, M., Ruusalepp, A., Schadt, E. E., Schmidt, A. F., Sweeting, M. J., Zalloua, P. A., AlGhalayini, K., Keavney, B. D., Kooner, J. S., Loos, R. J. F., Patel, R. S., Rutter, M. K. & EPIC-CVD Consortium, CARDIoGRAMplusC4D, The UK Biobank CardioMetabolic Consortium CHD working group , Sep 2017, In : Nature Genetics. 49, 9, p. 1385-1391 6 p.

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168 Citations (Scopus)

Association analysis of 29,956 individuals confirms that a low-frequency variant at CCND2 halves the risk of type 2 diabetes by enhancing insulin secretion

Yaghootkar, H., Stancáková, A., Freathy, R. M., Vangipurapu, J., Weedon, M. N., Xie, W., Wood, A. R., Ferrannini, E., Mari, A., Ring, S. M., Lawlor, D. A., Davey Smith, G., Jørgensen, T., Hansen, T., Pedersen, O., Steinthorsdottir, V., Guðbjartsson, D. F., Thorleifsson, G., Thorsteinsdottir, U., Stefansson, K. & 7 others, Hattersley, A. T., Walker, M., Morris, A. D., McCarthy, M. I., Palmer, C. N. A., Laakso, M. & Frayling, T. M., Jun 2015, In : Diabetes. 64, 6, p. 2279-2285 7 p.

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17 Citations (Scopus)

Association between Common Variation at the FTO Locus and Changes in Body Mass Index from Infancy to Late Childhood: The Complex Nature of Genetic Association through Growth and Development

Sovio, U., Mook-Kanamori, D. O., Warrington, N. M., Lawrence, R., Briollais, L., Palmer, C. N. A., Cecil, J., Sandling, J. K., Syvanen, A-C., Kaakinen, M., Beilin, L. J., Millwood, I. Y., Bennett, A. J., Laitinen, J., Pouta, A., Molitor, J., Smith, G. D., Ben-Shlomo, Y., Jaddoe, V. W. V., Palmer, L. J. & 6 others, Pennell, C. E., Cole, T. J., McCarthy, M. I., Jarvelin, M-R., Timpson, N. J. & Early Growth Genetics Consortium, Feb 2011, In : PLoS Genetics. 7, 2, p. - 13 p., e1001307.

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123 Citations (Scopus)

Association of Chromosome 9p21 with Subsequent Coronary Heart Disease events: A GENIUS-CHD study of individual participant data

CARDIoGRAMplusC4D Consortium, Patel, R. S., Schmidt, A. F., Tragante, V., McCubrey, R. O., Holmes, M. V., Howe, L. J., Direk, K., Åkerblom, A., Leander, K., Virani, S. S., Kaminski, K. A., Muehlschlegel, J. D., Dubé, M. P., Allayee, H., Almgren, P., Alver, M., Baranova, E. V., Behlouli, H., Boeckx, B. & 31 others, Braund, P. S., Breitling, L. P., Delgado, G., Duarte, N. E., Dufresne, L., Eriksson, N., Foco, L., Gijsberts, C. M., Gong, Y., Hartiala, J., Heydarpour, M., Hubacek, J. A., Kleber, M., Kofink, D., Kuukasjärvi, P., Lee, V. V., Leiherer, A., Lenzini, P. A., Levin, D., Lyytikäinen, L. P., Martinelli, N., Mons, U., Nelson, C. P., Nikus, K., Pilbrow, A. P., Ploski, R., Sun, Y. V., Tanck, M. W. T., Mordi, I. R., Palmer, C. N. & Lang, C. C., Apr 2019, In : Circulation: Genomic and Precision Medicine. 12, 4, p. 161-172 12 p.

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Association of Factor V Leiden with Subsequent Atherothrombotic Events: A GENIUS-CHD Study of Individual Participant Data

Mahmoodi, B. K., Tragante, V., Kleber, M. E., Holmes, M. V., Schmidt, A. F., McCubrey, R. O., Howe, L. J., Direk, K., Allayee, H., Baranova, E. V., Braund, P. S., Delgado, G. E., Eriksson, N., Gijsberts, C. M., Gong, Y., Hartiala, J., Heydarpour, M., Pasterkamp, G., Kotti, S., Kuukasjärvi, P. & 64 others, Lenzini, P. A., Levin, D., Lyytikäinen, L-P., Muehlschlegel, J. D., Nelson, C. P., Nikus, K., Pilbrow, A. P., Tang, W. H. W., van der Laan, S. W., van Setten, J., Vilmundarson, R. O., Deanfield, J., Deloukas, P., Dudbridge, F., James, S., Mordi, I. R., Teren, A., Bergmeijer, T. O., Body, S. C., Bots, M., Burkhardt, R., Cooper-DeHoff, R. M., Cresci, S., Danchin, N., Doughty, R. N., Grobbee, D. E., Hagström, E., Hazen, S. L., Held, C., Hoefer, I. E., Hovingh, G. K., Johnson, J. A., Kaczor, M. P., Kähönen, M., Klungel, O. H., Laurikka, J. O., Lehtimäki, T., Maitland-van der Zee, A. H., McPherson, R., Palmer, C. N., Kraaijeveld, A. O., Pepine, C. J., Sanak, M., Sattar, N., Scholz, M., Simon, T., Spertus, J. A., Stewart, A. F. R., Szczeklik, W., Thiery, J., Visseren, F. L. J., Waltenberger, J., Richards, A. M., Lang, C. C., Cameron, V. A., Åkerblom, A., Pare, G., März, W., Samani, N. J., Hingorani, A. D., Ten Berg, J. M., Wallentin, L., Asselbergs, F. W. & Patel, R., 11 Aug 2020, In : Circulation. 142, 6, p. 546-555 10 p.

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Association of organic cation transporter 1 with intolerance to metformin in Type 2 diabetes: a GoDARTS study

Dujic, T., Zhou, K., Donnelly, L. A., Tavendale, R., Palmer, C. N. A. & Pearson, E. R., May 2015, In : Diabetes. 64, 5, p. 1786-1793 8 p.

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97 Citations (Scopus)

Associations of autozygosity with a broad range of human phenotypes

Clark, D. W., Okada, Y., Moore, K. H. S., Mason, D., Pirastu, N., Gandin, I., Mattsson, H., Barnes, C. L. K., Lin, K., Zhao, J. H., Deelen, P., Rohde, R., Schurmann, C., Guo, X., Giulianini, F., Zhang, W., Medina-Gomez, C., Karlsson, R., Bao, Y., Bartz, T. M. & 416 others, Baumbach, C., Biino, G., Bixley, M. J., Brumat, M., Chai, J-F., Corre, T., Cousminer, D. L., Dekker, A. M., Eccles, D. A., van Eijk, K. R., Fuchsberger, C., Gao, H., Germain, M., Gordon, S. D., de Haan, H. G., Harris, S. E., Hofer, E., Huerta-Chagoya, A., Igartua, C., Jansen, I. E., Jia, Y., Kacprowski, T., Karlsson, T., Kleber, M. E., Li, S. A., Li-Gao, R., Mahajan, A., Matsuda, K., Meidtner, K., Meng, W., Montasser, M. E., van der Most, P. J., Munz, M., Nutile, T., Palviainen, T., Prasad, G., Prasad, R. B., Priyanka, T. D. S., Rizzi, F., Salvi, E., Sapkota, B. R., Shriner, D., Skotte, L., Smart, M. C., Smith, A. V., van der Spek, A., Spracklen, C. N., Strawbridge, R. J., Tajuddin, S. M., Trompet, S., Turman, C., Verweij, N., Viberti, C., Wang, L., Warren, H. R., Wootton, R. E., Yanek, L. R., Yao, J., Yousri, N. A., Zhao, W., Adeyemo, A. A., Afaq, S., Aguilar-Salinas, C. A., Akiyama, M., Albert, M. L., Allison, M. A., Alver, M., Aung, T., Azizi, F., Bentley, A. R., Boeing, H., Boerwinkle, E., Borja, J. B., de Borst, G. J., Bottinger, E. P., Broer, L., Campbell, H., Chanock, S., Chee, M-L., Chen, G., Chen, Y-D. I., Chen, Z., Chiu, Y-F., Cocca, M., Collins, F. S., Concas, M. P., Corley, J., Cugliari, G., van Dam, R. M., Damulina, A., Daneshpour, M. S., Day, F. R., Delgado, G. E., Dhana, K., Doney, A. S. F., Dörr, M., Doumatey, A. P., Dzimiri, N., Ebenesersdóttir, S. S., Elliott, J., Elliott, P., Ewert, R., Felix, J. F., Fischer, K., Freedman, B. I., Girotto, G., Goel, A., Gögele, M., Goodarzi, M. O., Graff, M., Granot-Hershkovitz, E., Grodstein, F., Guarrera, S., Gudbjartsson, D. F., Guity, K., Gunnarsson, B., Guo, Y., Hagenaars, S. P., Haiman, C. A., Halevy, A., Harris, T. B., Hedayati, M., van Heel, D. A., Hirata, M., Höfer, I., Hsiung, C. A., Huang, J., Hung, Y-J., Ikram, M. A., Jagadeesan, A., Jousilahti, P., Kamatani, Y., Kanai, M., Kerrison, N. D., Kessler, T., Khaw, K-T., Khor, C. C., de Kleijn, D. P. V., Koh, W-P., Kolcic, I., Kraft, P., Krämer, B. K., Kutalik, Z., Kuusisto, J., Langenberg, C., Launer, L. J., Lawlor, D. A., Lee, I-T., Lee, W-J., Lerch, M. M., Li, L., Liu, J., Loh, M., London, S. J., Loomis, S., Lu, Y., Luan, J., Mägi, R., Manichaikul, A. W., Manunta, P., Másson, G., Matoba, N., Mei, X. W., Meisinger, C., Meitinger, T., Mezzavilla, M., Milani, L., Millwood, I. Y., Momozawa, Y., Moore, A., Morange, P-E., Moreno-Macías, H., Mori, T. A., Morrison, A. C., Muka, T., Murakami, Y., Murray, A. D., de Mutsert, R., Mychaleckyj, J. C., Nalls, M. A., Nauck, M., Neville, M. J., Nolte, I. M., Ong, K. K., Orozco, L., Padmanabhan, S., Pálsson, G., Pankow, J. S., Pattaro, C., Pattie, A., Polasek, O., Poulter, N., Pramstaller, P. P., Quintana-Murci, L., Räikkönen, K., Ralhan, S., Rao, D. C., van Rheenen, W., Rich, S. S., Ridker, P. M., Rietveld, C. A., Robino, A., van Rooij, F. J. A., Ruggiero, D., Saba, Y., Sabanayagam, C., Sabater-Lleal, M., Sala, C. F., Salomaa, V., Sandow, K., Schmidt, H., Scott, L. J., Scott, W. R., Sedaghati-Khayat, B., Sennblad, B., van Setten, J., Sever, P. J., Sheu, W. H-H., Shi, Y., Shrestha, S., Shukla, S. R., Sigurdsson, J. K., Sikka, T. T., Singh, J. R., Smith, B. H., Stančáková, A., Stanton, A., Starr, J. M., Stefansdottir, L., Straker, L., Sulem, P., Sveinbjornsson, G., Swertz, M. A., Taylor, A. M., Taylor, K. D., Terzikhan, N., Tham, Y-C., Thorleifsson, G., Thorsteinsdottir, U., Tillander, A., Tracy, R. P., Tusié-Luna, T., Tzoulaki, I., Vaccargiu, S., Vangipurapu, J., Veldink, J. H., Vitart, V., Völker, U., Vuoksimaa, E., Wakil, S. M., Waldenberger, M., Wander, G. S., Wang, Y. X., Wareham, N. J., Wild, S., Yajnik, C. S., Yuan, J-M., Zeng, L., Zhang, L., Zhou, J., Amin, N., Asselbergs, F. W., Bakker, S. J. L., Becker, D. M., Lehne, B., Bennett, D. A., van den Berg, L. H., Berndt, S. I., Bharadwaj, D., Bielak, L. F., Bochud, M., Boehnke, M., Bouchard, C., Bradfield, J. P., Brody, J. A., Campbell, A., Carmi, S., Caulfield, M. J., Cesarini, D., Chambers, J. C., Chandak, G. R., Cheng, C-Y., Ciullo, M., Cornelis, M., Cusi, D., Smith, G. D., Deary, I. J., Dorajoo, R., van Duijn, C. M., Ellinghaus, D., Erdmann, J., Eriksson, J. G., Evangelou, E., Evans, M. K., Faul, J. D., Feenstra, B., Feitosa, M., Foisy, S., Franke, A., Friedlander, Y., Gasparini, P., Gieger, C., Gonzalez, C., Goyette, P., Grant, S. F. A., Griffiths, L. R., Groop, L., Gudnason, V., Gyllensten, U., Hakonarson, H., Hamsten, A., van der Harst, P., Heng, C-K., Hicks, A. A., Hochner, H., Huikuri, H., Hunt, S. C., Jaddoe, V. W. V., De Jager, P. L., Johannesson, M., Johansson, Å., Jonas, J. B., Jukema, J. W., Junttila, J., Kaprio, J., Kardia, S. L. R., Karpe, F., Kumari, M., Laakso, M., van der Laan, S. W., Lahti, J., Laudes, M., Lea, R. A., Lieb, W., Lumley, T., Martin, N. G., März, W., Matullo, G., McCarthy, M. I., Medland, S. E., Merriman, T. R., Metspalu, A., Meyer, B. F., Mohlke, K. L., Montgomery, G. W., Mook-Kanamori, D., Munroe, P. B., North, K. E., Nyholt, D. R., O'connell, J. R., Ober, C., Oldehinkel, A. J., Palmas, W., Palmer, C., Pasterkamp, G. G., Patin, E., Pennell, C. E., Perusse, L., Peyser, P. A., Pirastu, M., Polderman, T. J. C., Porteous, D. J., Posthuma, D., Psaty, B. M., Rioux, J. D., Rivadeneira, F., Rotimi, C., Rotter, J. I., Rudan, I., Den Ruijter, H. M., Sanghera, D. K., Sattar, N., Schmidt, R., Schulze, M. B., Schunkert, H., Scott, R. A., Shuldiner, A. R., Sim, X., Small, N., Smith, J. A., Sotoodehnia, N., Tai, E-S., Teumer, A., Timpson, N. J., Toniolo, D., Tregouet, D-A., Tuomi, T., Vollenweider, P., Wang, C. A., Weir, D. R., Whitfield, J. B., Wijmenga, C., Wong, T-Y., Wright, J., Yang, J., Yu, L., Zemel, B. S., Zonderman, A. B., Perola, M., Magnusson, P. K. E., Uitterlinden, A. G., Kooner, J. S., Chasman, D. I., Loos, R. J. F., Franceschini, N., Franke, L., Haley, C. S., Hayward, C., Walters, R. G., Perry, J. R. B., Esko, T., Helgason, A., Stefansson, K., Joshi, P. K., Kubo, M. & Wilson, J. F., 31 Oct 2019, In : Nature Communications. 10, 1, p. 1-17 17 p., 4957.

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A Type 1 Diabetes Genetic Risk Score Can Identify Patients With GAD65 Autoantibody-Positive Type 2 Diabetes Who Rapidly Progress to Insulin Therapy

Grubb, A. L., McDonald, T. J., Rutters, F., Donnelly, L., Hattersley, A. T., Oram, R. A., Palmer, C., van der Heijden, A. A., Carr, F., Elders, P. J. M., Weedon, M., Slieker, R. C., 't Hart, L. M., Pearson, E., Shields, B. M. & Jones, A. G., 1 Feb 2019, In : Diabetes Care. 42, 2, p. 208-214 7 p.

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Author Correction: Genome-wide association study of knee pain identifies associations with GDF5 and COL27A1 in UK Biobank

Meng, W., Adams, M. J., Palmer, C. N. A., 23andMe Research Team, Shi, J., Auton, A., Ryan, K. A., Jordan, J. M., Mitchell, B. D., Jackson, R. D., Yau, M. S., McIntosh, A. M. & Smith, B. H., 26 Mar 2020, In : Communications Biology. 3, 1, 1 p., 149.

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Biological interpretation of genome-wide association studies using predicted gene functions

Pers, T. H., Karjalainen, J. M., Chan, Y., Westra, H-J., Wood, A. R., Yang, J., Lui, J. C., Vedantam, S., Gustafsson, S., Esko, T., Frayling, T., Speliotes, E. K., Genetic Investigation of ANthropometric Traits (GIANT) Consortium, Boehnke, M., Raychaudhuri, S., Fehrmann, R. S. N., Hirschhorn, J. N. & Franke, L., 19 Jan 2015, In : Nature Communications. 6, p. 1-9 9 p., 5890.

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301 Citations (Scopus)

Biomarkers for type 2 diabetes and impaired fasting glucose using a non-targeted metabolomics approach

Menni, C., Fauman, E., Erte, I., Perry, J. R. B., Kastenmüller, G., Shin, S-Y., Petersen, A-K., Hyde, C., Psatha, M., Ward, K. J., Yuan, W., Milburn, M., Palmer, C. N. A., Frayling, T. M., Trimmer, J., Bell, J. T., Gieger, C., Mohney, R., Brosnan, M. J., Suhre, K. & 2 others, Soranzo, N. & Spector, T. D., 2013, In : Diabetes.

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199 Citations (Scopus)

Biomarkers of rapid chronic kidney disease progression in type 2 diabetes

Looker, H. C., Colombo, M., Hess, S., Brosnan, M. J., Farran, B., Dalton, R. N., Wong, M. C., Turner, C., Palmer, C. N. A., Nogoceke, E., Groop, L., Salomaa, V., Dunger, D. B., Agakov, F., McKeigue, P. M., Colhoun, H. M. & on behalf of the SUMMIT Investigators, Oct 2015, In : Kidney International. 88, 4, p. 888-896 9 p.

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Both high and low HbA1c predict incident heart failure in type 2 diabetes mellitus

Parry, H. M., Desmukh, H., Levin, D., Van Zuydam, N., Elder, D. H. J., Morris, A. D., Struthers, A. D., Palmer, C. N. A., Doney, A. S. F. & Lang, C. C., Mar 2015, In : Circulation: Heart Failure. 8, 2, p. 236-242 7 p.

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Candidate Gene Association Study for Diabetic Retinopathy in Persons with Type 2 Diabetes: The Candidate Gene Association Resource (CARe)

Sobrin, L., Green, T., Sim, X., Jensen, R. A., Tai, E. S., Tay, W. T., Wang, J. J., Mitchell, P., Sandholm, N., Liu, Y., Hietala, K., Iyengar, S. K., Brooks, M., Buraczynska, M., Van Zuydam, N., Smith, A. V., Gudnason, V., Doney, A. S. F., Morris, A. D., Leese, G. P. & 17 others, Palmer, C. N. A., Swaroop, A., Taylor, H. A., Wilson, J. G., Penman, A., Chen, C. J., Groop, P-H., Saw, S-M., Aung, T., Klein, B. E., Rotter, J. I., Siscovick, D. S., Cotch, M. F., Klein, R., Daly, M. J., Wong, T. Y. & Wellcome Trust Case Control Consor, Family Invest Nephropathy Diabet-E, Sep 2011, In : Investigative Ophthalmology & Visual Science. 52, 10, p. 7593-7602 10 p.

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63 Citations (Scopus)

Candidate long-range regulatory sites acting on the IL17-pathway genes TRAF3IP2 and IL17RA are associated with psoriasis

Nititham, J., Fergusson, C., Palmer, C., Liao, W. & Foerster, J., 4 Aug 2018, In : Experimental Dermatology. 27, 11, p. 1294-1297 4 p.

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Characterization and validation of an isotope-dilution LC-MS/MS method for quantification of total desmosine and isodesmosine in plasma and serum

Albarbarawi, O., Barton, A., Miller, D., McSharry, C., Chaudhuri, R., Thomson, N. C., Palmer, C. N. A., Devereux, G. & Huang, J. T-J., Aug 2013, In : Bioanalysis. 5, 16, p. 1991-2001 11 p.

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17 Citations (Scopus)

Childhood asthma exacerbations and the Arg16 β2-receptor polymorphism: A meta-analysis stratified by treatment

Turner, S., Francis, B., Vijverberg, S., Pino-Yanes, M., Maitland-van der Zee, A. H., Basu, K., Bignell, L., Mukhopadhyay, S., Tavendale, R., Palmer, C., Hawcutt, D., Pirmohamed, M., Burchard, E. G. & Lipworth, B., Jul 2016, In : Journal of Allergy and Clinical Immunology. 138, 1, p. 107-113 7 p.

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Childhood obesity in relation to poor asthma control and exacerbation: a meta-analysis

Ahmadizar, F., Vijverberg, S. J. H., Arets, H. G. M., de Boer, A., Lang, J. E., Kattan, M., Palmer, C. N. A., Mukhopadhyay, S., Turner, S. & Maitland-van der Zee, A. H., 30 Sep 2016, In : European Respiratory Journal. 48, 4, p. 1063-1073 11 p.

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Cholesteryl ester transfer protein polymorphisms, statin use, and their impact on cholesterol levels and cardiovascular events

Leusink, M., Onland-Moret, N. C., Asselbergs, F. W., Ding, B., Kotti, S., van Zuydam, N. R., Papp, A. C., Danchin, N., Donnelly, L., Morris, A. D., Chasman, D. I., Doevendans, P. A. F. M., Klungel, O. H., Ridker, P. M., van Gilst, W. H., Simon, T., Nyberg, F., Palmer, C. N. A., Sadee, W., van der Harst, P. & 4 others, de Bakker, P. I. W., de Boer, A., Verstuyft, C. & Maitland-van der Zee, A. H., Mar 2014, In : Clinical Pharmacology & Therapeutics. 95, 3, p. 314-320 7 p.

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CKM Glu83Gly Is Associated With Blunted Creatine Kinase Variation, but Not With Myalgia

Siddiqui, M. K., Veluchamy, A., Maroteau, C., Tavendale, R., Carr, F., Pearson, E., Colhoun, H., Morris, A. D., George, J., Doney, A., Pirmohamed, M., Alfirevic, A., Wadelius, M., Maitland-van der Zee, A. H., Ridker, P. M., Chasman, D. I., Palmer, C. N. A. & PREDICTION-ADR Consortium, Aug 2017, In : Circulation: Cardiovascular Genetics. 10, 4, e001737 .

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3 Citations (Scopus)

Clinical and genetic determinants of progression of type 2 diabetes: A DIRECT Study

Zhou, K., Donnelly, L. A., Morris, A. D., Franks, P. W., Jennison, C., Palmer, C. N. A. & Pearson, E. R., 1 Mar 2014, In : Diabetes Care. 37, 3, p. 718-724

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24 Citations (Scopus)