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  • Colin Palmer
2019

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Romagnoni, A., Jégou, S., Van Steen, K., Wainrib, G. & Hugot, J-P., 17 Jul 2019, In : Scientific Reports. 9, 1, p. 1-18 18 p., 10351.

Research output: Contribution to journalArticle

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

Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease

Veluchamy, A., Ballerini, L., Vitart, V., Schraut, K. E., Kirin, M., Campbell, H., Joshi, P. K., Relan, D., Harris, S., Vaidya, S. S. ., Dhillon, B., Zhou, K., Pearson, E., Hayward, C., Polašek, O., Deary, I. J., MacGillivray, T. J., Wilson, J. F., Trucco, M., Palmer, C. & 1 others, Doney, A., Dec 2019, In : Arteriosclerosis, Thrombosis, and Vascular Biology. 39, 12, p. 2542-2552 11 p.

Research output: Contribution to journalArticle

Open Access
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1 Citation (Scopus)
105 Downloads (Pure)
2015

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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723 Citations (Scopus)
1139 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
File
34 Citations (Scopus)
208 Downloads (Pure)
2013

Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjects

Saunders, S. P., Goh, C. S. M., Brown, S. J., Palmer, C. N. A., Porter, R. M., Cole, C., Campbell, L. E., Gierlinski, M., Barton, G. J., Schneider, G., Balmain, A., Prescott, A. R., Weidinger, S., Baurecht, H., Kabesch, M., Gieger, C., Lee, Y-A., Tavendale, R., Mukhopadhyay, S., Turner, S. W. & 14 others, Madhok, V. B., Sullivan, F. M., Relton, C., Burn, J., Meggitt, S., Smith, C. H., Allen, M. A., Barker, J. N. W. N., Reynolds, N. J., Cordell, H. J., Irvine, A. D., McLean, W. H. I., Sandilands, A. & Fallon, P. G., Nov 2013, In : Journal of Allergy and Clinical Immunology. 132, 5, p. 1121-1129 9 p.

Research output: Contribution to journalArticle

81 Citations (Scopus)
2018

Systematic review and meta-analysis of genetic risk factors for neuropathic pain

Veluchamy, A., Hébert, H. L., Meng, W., Palmer, C. N. A. & Smith, B. H., May 2018, In : Pain. 159, 5, p. 825-848 24 p.

Research output: Contribution to journalReview article

Open Access
File
14 Citations (Scopus)
261 Downloads (Pure)
2016

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
File
7 Citations (Scopus)
173 Downloads (Pure)
2018

Pharmacogenetics of inhaled long-acting beta2-agonists in asthma: a systematic review

Slob, E. M. A., Vijverberg, S. J. H., Palmer, C. N. A., Zazuli, Z., Farzan, N., Oliveri, N. M. B., Pijnenburg, M. W., Koppelman, G. H. & Maitland van der Zee, A. H., Nov 2018, In : Pediatric Allergy and Immunology. 29, 7, p. 705-714 10 p.

Research output: Contribution to journalArticle

Open Access
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9 Citations (Scopus)
204 Downloads (Pure)
2020
Open Access
File
3 Citations (Scopus)
5 Downloads (Pure)
2017

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
File
12 Citations (Scopus)
151 Downloads (Pure)
2018

Lp-PLA2 activity is associated with increased risk of diabetic retinopathy: a longitudinal disease progression study

Siddiqui, M. K., Kennedy, G., Carr, F., Doney, A., Pearson, E., Morris, A., Johnson, T., McLaughlin, M. M., Williams, R. E. & Palmer, C., Jun 2018, In : Diabetologia. 61, 6, p. 1344-1353 10 p.

Research output: Contribution to journalArticle

Open Access
File
6 Citations (Scopus)
189 Downloads (Pure)
2016
2015

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

2020

Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment

Rasmussen, E. R., Hallberg, P., Baranova, E. V., Eriksson, N., Karawajczyk, M., Johansson, C., Cavalli, M., Maroteau, C., Veluchamy, A., Islander, G., Hugosson, S., Terreehorst, I., Asselbergs, F. W., Norling, P., Johansson, H-E., Kohnke, H., Syvänen, A-C., Siddiqui, M. K., Lang, C., Magnusson, P. K. E. & 8 others, Yue, Q-Y., Wadelius, C., von Buchwald, C., Bygum, A., Alfirevic, A., Maitland-van der Zee, A. H., Palmer, C. N. A. & Wadelius, M., 21 Feb 2020, In : Pharmacogenomics Journal. 14 p.

Research output: Contribution to journalArticle

Open Access
File
1 Citation (Scopus)
34 Downloads (Pure)
2012

Paradoxical lower serum triglyceride levels and higher type 2 diabetes mellitus susceptibility in obese individuals with the PNPLA3 148M variant

Palmer, C. N. A., Maglio, C., Pirazzi, C., Burza, M. A., Adiels, M., Burch, L., Donnelly, L. A., Colhoun, H., Doney, A. S., Dillon, J. F., Pearson, E. R., McCarthy, M., Hattersley, A. T., Frayling, T., Morris, A. D., Peltonen, M., Svensson, P-A., Jacobson, P., Borén, J., Sjöström, L. & 2 others, Carlsson, L. M. S. & Romeo, S., 2012, In : PLoS ONE. 7, 6, e39362.

Research output: Contribution to journalArticle

60 Citations (Scopus)
2014

Quality control and conduct of genome-wide association meta-analyses

Winkler, T. W., Day, F. R., Croteau-Chonka, D. C., Wood, A. R., Locke, A. E., Mägi, R., Ferreira, T., Fall, T., Graff, M., Justice, A. E., Luan, J., Gustafsson, S., Randall, J. C., Vedantam, S., Workalemahu, T., Kilpeläinen, T. O., Scherag, A., Esko, T., Kutalik, Z., Heid, I. M. & 2 others, Loos, R. J. F. & Genetic Investigation of ANthropometric Traits (GIANT) Consortium, May 2014, In : Nature Protocols. 9, 5, p. 1192-1212 21 p.

Research output: Contribution to journalArticle

157 Citations (Scopus)
2020

The effect of LRRK2 loss-of-function variants in humans

Whiffin, N., Armean, I. M., Kleinman, A., Marshall, J. L., Minikel, E. V., Goodrich, J. K., Quaife, N. M., Cole, J. B., Wang, Q., Karczewski, K. J., Cummings, B. B., Francioli, L., Laricchia, K., Guan, A., Alipanahi, B., Morrison, P., Baptista, M. A. S., Merchant, K. M., Ware, J. S., Havulinna, A. S. & 18 others, Iliadou, B., Lee, J-J., Nadkarni, G. N., Whiteman, C., 23andMe Research Team, Daly, M., Esko, T., Hultman, C., Loos, R. J. F., Milani, L., Palotie, A., Pato, C., Pato, M., Saleheen, D., Sullivan, P. F., Alföldi, J., Cannon, P. & MacArthur, D. G., 27 May 2020, In : Nature Medicine. 21 p.

Research output: Contribution to journalArticle

Open Access
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4 Citations (Scopus)
20 Downloads (Pure)
2014

Leveraging cross-species transcription factor binding site patterns: from diabetes risk loci to disease mechanisms

Claussnitzer, M., Dankel, S. N., Klocke, B., Grallert, H., Glunk, V., Berulava, T., Lee, H., Oskolkov, N., Fadista, J., Ehlers, K., Wahl, S., Hoffmann, C., Qian, K., Rönn, T., Riess, H., Müller-Nurasyid, M., Bretschneider, N., Schroeder, T., Skurk, T., Horsthemke, B. & 18 others, DIAGRAM+Consortium, Spieler, D., Klingenspor, M., Seifert, M., Kern, M. J., Mejhert, N., Dahlman, I., Hansson, O., Hauck, S. M., Blüher, M., Arner, P., Groop, L., Illig, T., Suhre, K., Hsu, Y-H., Mellgren, G., Hauner, H. & Laumen, H., 16 Jan 2014, In : Cell. 156, 1-2, p. 343-358 16 p.

Research output: Contribution to journalArticle

73 Citations (Scopus)
2015

Shared genetic basis for migraine and ischemic stroke: a genome-wide analysis of common variants

Malik, R., Freilinger, T., Winsvold, B. S., Anttila, V., Vander Heiden, J., Traylor, M., de Vries, B., Holliday, E. G., Terwindt, G. M., Sturm, J., Bis, J. C., Hopewell, J. C., Ferrari, M. D., Rannikmae, K., Wessman, M., Kallela, M., Kubisch, C., Fornage, M., Meschia, J. F., Lehtimäki, T. & 31 others, Sudlow, C., Clarke, R., Chasman, D. I., Mitchell, B. D., Maguire, J., Kaprio, J., Farrall, M., Raitakari, O. T., Kurth, T., Ikram, M. A., Reiner, A. P., Longstreth, W. T., Rothwell, P. M., Strachan, D. P., Sharma, P., Seshadri, S., Quaye, L., Cherkas, L., Schürks, M., Rosand, J., Ligthart, L., Boncoraglio, G. B., Davey Smith, G., van Duijn, C. M., Stefansson, K., Worrall, B. B., Nyholt, D. R., Markus, H. S., van den Maagdenberg, A. M. J. M., International Headache Genetics Consortium & METASTROKE Collaboration of the International Stroke Genetics Consortium, 26 May 2015, In : Neurology. 84, 21, p. 2132-2145 14 p.

Research output: Contribution to journalArticle

50 Citations (Scopus)
2011

Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergy

Brown, S. J., Asai, Y., Cordell, H. J., Campbell, L. E., Zhao, Y., Liao, H., Northstone, K., Henderson, J., Alizadehfar, R., Ben-Shoshan, M., Morgan, K., Roberts, G., Masthoff, L. J. N., Pasmans, S. G. M. A., van den Akker, P. C., Wijmenga, C., Hourihane, J. OB., Palmer, C. N. A., Lack, G., Clarke, A. & 3 others, Hull, P. R., Irvine, A. D. & McLean, W. H. I., Mar 2011, In : Journal of Allergy and Clinical Immunology. 127, 3, p. 661-667 7 p.

Research output: Contribution to journalArticle

Open Access
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265 Citations (Scopus)
163 Downloads (Pure)
2020
Open Access
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18 Downloads (Pure)
2019

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

CHD Exome+ Consortium, EPIC-CVD Consortium, ExomeBP Consortium, Global Lipids Genetic Consortium, GoT2D Genes Consortium, EPIC-InterAct Consortium, INTERVAL Study, ReproGen Consortium, T2D-Genes Consortium, The MAGIC Investigators, Understanding Society Scientific Group, Turcot, V., Lu, Y., Highland, H. M., Schurmann, C., Justice, A. E., Fine, R. S., Bradfield, J. P., Esko, T., Giri, A. & 43 others, Graff, M., Guo, X., Hendricks, A. E., Karaderi, T., Lempradl, A., Locke, A. E., Mahajan, A., Marouli, E., Sivapalaratnam, S., Young, K. L., Alfred, T., Feitosa, M. F., Masca, N. G. D., Manning, A. K., Medina-Gomez, C., Mudgal, P., Ng, M. C. Y., Reiner, A. P., Vedantam, S., Willems, S. M., Winkler, T. W., Abecasis, G., Aben, K. K., Alam, D. S., Alharthi, S. E., Allison, M., Amouyel, P., Asselbergs, F. W., Auer, P. L., Balkau, B., Bang, L. E., Campbell, P. T., Evangelou, E., Li, J., Mitchell, P., Morris, A. D., Morris, A. D., Palmer, C. N. A., Roberts, D. J., Scott, R. A., Wood, A. R., Hirschhorn, J. N. & Loos, R. J. F., 3 Jun 2019, In : Nature Genetics. 51, p. 1191-1192 2 p.

Research output: Contribution to journalArticle

2011

Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

Evans, D. M., Spencer, C. C. A., Pointon, J. J., Su, Z., Harvey, D., Kochan, G., Opperman, U., Dilthey, A., Pirinen, M., Stone, M. A., Appleton, L., Moutsianas, L., Leslie, S., Wordsworth, T., Kenna, T. J., Karaderi, T., Thomas, G. P., Ward, M. M., Weisman, M. H., Farrar, C. & 31 others, Bradbury, L. A., Danoy, P., Inman, R. D., Maksymowych, W., Gladman, D., Rahman, P., Morgan, A., Marzo-Ortega, H., Bowness, P., Gaffney, K., Gaston, J. S. H., Smith, M., Bruges-Armas, J., Couto, A-R., Sorrentino, R., Paladini, F., Ferreira, M. A., Xu, H., Liu, Y., Jiang, L., Lopez-Larrea, C., Diaz-Pena, R., Lopez-Vazquez, A., Zayats, T., Band, G., Bellenguez, C., Blackburn, H., Blackwell, J. M., Bramon, E., Palmer, C. N. A. & Wellcome Trust Case Control Consor, Australo-Anglo-Amer Spondyloarthri, Spondyloarthrit Res Consortium Can, Aug 2011, In : Nature Genetics. 43, 8, p. 761-767 7 p.

Research output: Contribution to journalArticle

521 Citations (Scopus)

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.

Research output: Contribution to journalArticle

22 Citations (Scopus)
2012

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)
2017

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)

Discovery of novel heart rate-associated loci using the Exome Chip

van den Berg, M. E., Warren, H. R., Cabrera, C. P., Verweij, N., Mifsud, B., Haessler, J., Bihlmeyer, N. A., Fu, Y-P., Weiss, S., Lin, H. J., Grarup, N., Li-Gao, R., Pistis, G., Shah, N., Brody, J. A., Müller-Nurasyid, M., Lin, H., Mei, H., Smith, A. V., Lyytikäinen, L-P. & 101 others, Hall, L. M., van Setten, J., Trompet, S., Prins, B. P., Isaacs, A., Radmanesh, F., Marten, J., Entwistle, A., Kors, J. A., Silva, C. T., Alonso, A., Bis, J. C., de Boer, R. A., de Haan, H. G., de Mutsert, R., Dedoussis, G., Dominiczak, A. F., Doney, A. S. F., Ellinor, P. T., Eppinga, R. N., Felix, S. B., Guo, X., Hagemeijer, Y., Hansen, T., Harris, T. B., Heckbert, S. R., Huang, P. L., Hwang, S-J., Kähönen, M., Kanters, J. K., Kolcic, I., Launer, L. J., Li, M., Yao, J., Linneberg, A., Liu, S., Macfarlane, P. W., Mangino, M., Morris, A. D., Mulas, A., Murray, A. D., Nelson, C. P., Orrú, M., Padmanabhan, S., Peters, A., Porteous, D. J., Poulter, N. R., Psaty, B. M., Qi, L., Raitakari, O. T., Rivadeneira, F., Roselli, C., Rudan, I., Sattar, N., Sever, P., Sinner, M. F., Soliman, E. Z., Spector, T. D., Stanton, A. V., Stirrups, K. E., Taylor, K. D., Tobin, M. D., Uitterlinden, A. G., Vaartjes, I., Hoes, A. W., van der Meer, P., Völker, U., Waldenberger, M., Xie, Z., Zoledziewska, M., Tinker, A., Polasek, O., Rosand, J., Jamshidi, Y., van Duijn, C. M., Zeggini, E., Wouter Jukema, J., Asselbergs, F. W., Samani, N. J., Lehtimäki, T., Gudnason, V., Wilson, J., Lubitz, S. A., Kääb, S., Sotoodehnia, N., Caulfield, M. J., Palmer, C. N. A., Sanna, S., Mook-Kanamori, D. O., Deloukas, P., Pedersen, O., Rotter, J. I., Dörr, M., O'Donnell, C. J., Hayward, C., Arking, D. E., Kooperberg, C., van der Harst, P., Eijgelsheim, M., Stricker, B. H. C. & Munroe, P. B., 15 Jun 2017, In : Human Molecular Genetics. 26, 12, p. 2346-2363 18 p.

Research output: Contribution to journalArticle

Open Access
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10 Citations (Scopus)
138 Downloads (Pure)

Quantifying the extent to which index event biases influence large genetic association studies

Yaghootkar, H., Bancks, M. P., Jones, S. E., McDaid, A., Beaumont, R., Donnelly, L., Wood, A. R., Campbell, A., Tyrrell, J., Hocking, L. J., Tuke, M. A., Ruth, K. S., Pearson, E. R., Murray, A., Freathy, R. M., Munroe, P. B., Hayward, C., Palmer, C., Weedon, M. N., Pankow, J. S. & 2 others, Frayling, T. M. & Kutalik, Z., 1 Jun 2017, In : Human Molecular Genetics. 26, 5, p. 1018-1030 13 p.

Research output: Contribution to journalArticle

Open Access
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13 Citations (Scopus)
134 Downloads (Pure)
2013

Tailored second-line therapy in asthmatic children with the Arg16 genotype

Lipworth, B. J., Basu, K., Donald, H. P., Tavendale, R., MacGregor, D. F., Ogston, S. A., Palmer, C. N. A. & Mukhopadhyay, S., Apr 2013, In : Clinical Science. 124, 8, p. 521-528 8 p.

Research output: Contribution to journalArticle

53 Citations (Scopus)
2011

The CHI3L1 rs4950928 polymorphism is associated with asthma-related hospital admissions in children and young adults

Cunningham, J., Basu, K., Tavendale, R., Palmer, C. N. A., Smith, H. & Mukhopadhyay, S., May 2011, In : Annals of Allergy, Asthma & Immunology. 106, 5, p. 381-386 6 p.

Research output: Contribution to journalArticle

16 Citations (Scopus)
2013

Metformin pharmacogenetics and SLC2A2: genome-wide association study and 2-stage replication in GoDARTS and UKPDS

Zhou, K., Bennett, A., Coleman, R., Groves, R., Holman, R., McCarthy, M., Palmer, C. & Pearson, E., Mar 2013, In : Diabetic Medicine. 30, Suppl. 1, p. 52-52 1 p., P79.

Research output: Contribution to journalMeeting abstract

10 Citations (Scopus)
2020

PheGWAS: A new dimension to visualize GWAS across multiple phenotypes

George, G., Gan, S., Huang, Y., Appleby, P., Nar, A. S., Venkatesan, R., Mohan, V., Palmer, C. N. A. & Doney, A. S. F., 15 Apr 2020, In : Bioinformatics. 36, 8, p. 2500-2505 6 p.

Research output: Contribution to journalArticle

Open Access
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62 Downloads (Pure)
2019

Serum kidney injury molecule 1 and β2-microglobulin perform as well as larger biomarker panels for prediction of rapid decline in renal function in type 2 diabetes

Colombo, M., Looker, H. C., Farran, B., Hess, S., Groop, L., Palmer, C. N. A., Brosnan, M. J., Dalton, R. N., Wong, M., Turner, C., Ahlqvist, E., Dunger, D., Agakov, F., Durrington, P., Livingstone, S., Betteridge, D. J., McKeigue, P. M. & Colhoun, H. M., 1 Jan 2019, In : Diabetologia. 62, 1, p. 156-168 13 p.

Research output: Contribution to journalArticle

Open Access
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17 Citations (Scopus)
146 Downloads (Pure)
2017

Early life antibiotic use and the risk of asthma and asthma exacerbations in children

Ahmadizar, F., Vijverberg, S. J. H., Arets, H. G. M., de Boer, A., Turner, S., Devereux, G., Arabkhazaeli, A., Soares, P., Mukhopadhyay, S., Garssen, J., Palmer, C. N. A., de Jongste, J. C., Jaddoe, V. W. V., Duijts, L., van Meel, E. R., Kraneveld, A. D. & Maitland-van der Zee, A. H., Aug 2017, In : Pediatric Allergy and Immunology. 28, 5, p. 430-437 8 p.

Research output: Contribution to journalArticle

Open Access
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32 Citations (Scopus)
200 Downloads (Pure)
2013
24 Citations (Scopus)
2014

Inactivating mutations in NPC1L1 and protection from coronary heart disease

Stitziel, N. O., Won, H-H., Morrison, A. C., Peloso, G. M., Do, R., Lange, L. A., Fontanillas, P., Gupta, N., Duga, S., Goel, A., Farrall, M., Saleheen, D., Ferrario, P., König, I., Asselta, R., Merlini, P. A., Marziliano, N., Notarangelo, M. F., Schick, U., Auer, P. & 57 others, Assimes, T. L., Reilly, M., Wilensky, R., Rader, D. J., Hovingh, G. K., Meitinger, T., Kessler, T., Kastrati, A., Laugwitz, K-L., Siscovick, D., Rotter, J. I., Hazen, S. L., Tracy, R., Cresci, S., Spertus, J., Jackson, R., Schwartz, S. M., Natarajan, P., Crosby, J., Muzny, D., Ballantyne, C., Rich, S. S., O'Donnell, C. J., Abecasis, G., Sunyaev, S., Nickerson, D. A., Buring, J. E., Ridker, P. M., Chasman, D. I., Austin, E., Ye, Z., Kullo, I. J., Weeke, P. E., Shaffer, C. M., Bastarache, L. A., Denny, J. C., Roden, D. M., Palmer, C., Deloukas, P., Lin, D-Y., Tang, Z., Erdmann, J., Schunkert, H., Danesh, J., Marrugat, J., Elosua, R., Ardissino, D., McPherson, R., Watkins, H., Reiner, A. P., Wilson, J. G., Altshuler, D., Gibbs, R. A., Lander, E. S., Boerwinkle, E., Gabriel, S. & Kathiresan, S., 27 Nov 2014, In : New England Journal of Medicine. 371, 22, p. 2072-2082 11 p.

Research output: Contribution to journalArticle

268 Citations (Scopus)
2011

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

Zhou, K., Bellenguez, C., Spencer, C. C. A., Bennett, A. J., Coleman, R. L., Tavendale, R., Hawley, S. A., Donnelly, L. A., Schofield, C., Groves, C. J., Burch, L., Carr, F., Strange, A., Freeman, C., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Craddock, N. & 31 others, Deloukas, P., Dronov, S., Duncanson, A., Edkins, S., Gray, E., Hunt, S., Jankowski, J., Langford, C., Markus, H. S., Mathew, C. G., Plomin, R., Rautanen, A., Sawcer, S. J., Samani, N. J., Trembath, R., Viswanathan, A. C., Wood, N. W., Harries, L. W., Hattersley, A. T., Doney, A. S. F., Colhoun, H., Morris, A. D., Sutherland, C., Hardie, D. G., Peltonen, L., McCarthy, M. I., Holman, R. R., Palmer, C. N. A., Donnelly, P., Pearson, E. R. & Wellcome Trust Case Control Consor, GoDARTS UKPDS Diabet Pharmacogenet, MAGIC Investigators, Feb 2011, In : Nature Genetics. 43, 2, p. 117-120 4 p.

Research output: Contribution to journalLetter

302 Citations (Scopus)
2017

Utility of Population-Level DNA Sequence Data in the Diagnosis of Hereditary Endocrine Disease

Newey, P. J., Berg, J. N., Zhou, K., Palmer, C. N. A. & Thakker, R. V., 1 Dec 2017, In : Journal of the Endocrine Society. 1, 12, p. 1507-1526 20 p.

Research output: Contribution to journalArticle

Open Access
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8 Citations (Scopus)
165 Downloads (Pure)
2013

Genetic variants predicting left ventricular hypertrophy in a diabetic population: a Go-DARTS study including meta-analysis

Parry, H. M., Donnelly, L. A., Van Zuydam, N., Doney, A. S. F., Elder, D. H. J., Morris, A. D., Struthers, A. D., Palmer, C. N. A., Lang, C. C. & Wellcome Trust Case Control Consortium 2, 23 Jul 2013, In : Cardiovascular Diabetology. 12, 109.

Research output: Contribution to journalArticle

Open Access
12 Citations (Scopus)
2014

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium, Mahajan, A., Go, M. J., Zhang, W., Below, J. E., Gaulton, K. J., Ferreira, T., Horikoshi, M., Johnson, A. D., Ng, M. C. Y., Prokopenko, I., Saleheen, D., Wang, X., Zeggini, E., Abecasis, G. R., Adair, L. S., Almgren, P., Atalay, M., Aung, T., Baldassarre, D. & 30 others, Balkau, B., Bao, Y., Barnett, A. H., Barroso, I., Basit, A., Been, L. F., Beilby, J., Bell, G. I., Benediktsson, R., Bergman, R. N., OBoehm, B., Boerwinkle, E., Bonnycastle, L. L., Burtt, N., Cai, Q., Campbell, H., Carey, J., Cauchi, S., Caulfield, M., Doney, A. S. F., Donnelly, P. J., James, A., Matthews, D. R., Morris, A. D., Palmer, C. N. A., Scott, J., Scott, L. J., Shah, N., Wood, A. R. & Zhang, F., 9 Feb 2014, In : Nature Genetics. 46, 3, p. 234-244 11 p.

Research output: Contribution to journalArticle

596 Citations (Scopus)
2016

Factors associated with quality of life in children with asthma living in Scotland

Taminskiene, V., Mukhopadhyay, S., Palmer, C., Mehta, A., Ayres, J., Valiulis, A. & Turner, S. W., May 2016, In : Pediatric Pulmonology. 51, 5, p. 484-490 7 p.

Research output: Contribution to journalArticle

7 Citations (Scopus)
2015
9 Citations (Scopus)
2013

Genetic variants predicting left ventricular hypertrophy in a diabetic population

Parry, H., Donnelly, L., Van Zuydam, N., Doney, A., Elder, D., Morris, A., Struthers, A. D., Palmer, C. & Lang, C., 2013, In : Journal of the American College of Cardiology. 61, 10 Supplement, p. E598 1 p.

Research output: Contribution to journalMeeting abstract

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.

Research output: Contribution to journalArticle

17 Citations (Scopus)
2019

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.

Research output: Contribution to journalArticle

Open Access
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6 Citations (Scopus)
10 Downloads (Pure)
2013

Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits

Randall, J. C., Winkler, T. W., Kutalik, Z., Berndt, S. I., Jackson, A. U., Monda, K. L., Kilpeläinen, T. O., Esko, T., Mägi, R., Li, S., Workalemahu, T., Feitosa, M. F., Croteau-Chonka, D. C., Day, F. R., Fall, T., Ferreira, T., Gustafsson, S., Locke, A. E., Mathieson, I., Scherag, A. & 32 others, Vedantam, S., Wood, A. R., Liang, L., Steinthorsdottir, V., Thorleifsson, G., Dermitzakis, E. T., Dimas, A. S., Karpe, F., Min, J. L., Nicholson, G., Clegg, D. J., Person, T., Krohn, J. P., Bauer, S., Buechler, C., Eisinger, K., DIAGRAM Consortium, Bonnefond, A., Froguel, P., MAGIC Investigators, Hottenga, J-J., Prokopenko, I., Waite, L. L., Harris, T. B., Smith, A. V., Shuldiner, A. R., McArdle, W. L., Caulfield, M. J., Munroe, P. B., Grönberg, H., Morris, A. D. & Palmer, C. N. A., Jun 2013, In : PLoS Genetics. 9, 6, p. e1003500

Research output: Contribution to journalArticle

204 Citations (Scopus)
2019

Investigating the Relationship Between Type 2 Diabetes and Dementia Using Electronic Medical Records in the GoDARTS Bioresource

Doney, A. S. F., Bonney, W., Jefferson, E., Walesby, K. E., Bittern, R., Trucco, E., Connelly, P., McCrimmon, R. J. & Palmer, C. N. A., Oct 2019, In : Diabetes Care. 42, 10, p. 1973-1980 8 p.

Research output: Contribution to journalArticle

2011

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

2019

Scientific Business Abstracts of the 113th Annual Meeting of the Association of Physicians of Great Britain and Ireland

Deciphering Developmental Disorders (DDD) Study, Cacciottolo, T. M., Perikari, A., van der Klaauw, A., Henning, E., Stadler, L. K. J., Keogh, J., Farooqi, I. S., Tenin, G., Keavney, B., Ryan, E., Budd, R., Bewley, M., Coelho, P., Rumsey, W., Sanchez, Y., McCafferty, J., Dockrell, D., Walmsley, S., Whyte, M. & 31 others, Liu, Y., Choy, M-K., Tenin, G., Abraham, S., Black, G., Keavney, B., Watkins, S., Robertson, K., Collison, D., Rush, C., Marshall, J., McGowan, R., Fraser, R., Gandhi, S., Cooper, C., Howden, A., Hukelmann, J. L., Cantrell, D. A., Mordi, I., Forteath, C., Wong, A., Mohan, M., Palmer, C., Doney, A., Rena, G., Lang, C., Gray, E. H., Williams, R., Williams, S., Hughes, J. & Davies, J., 5 Sep 2019, In : QJM : an International Journal of Medicine. 112, 9, p. 724-729 6 p., 9.

Research output: Contribution to journalMeeting abstract

2012

Obesity and eating behaviour in children and adolescents: contribution of common gene polymorphisms

Cecil, J., Dalton, M., Finlayson, G., Blundell, J., Hetherington, M. & Palmer, C., 2012, In : International Review of Psychiatry. 24, 3, p. 200-210 11 p.

Research output: Contribution to journalArticle

26 Citations (Scopus)