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  • Colin Palmer
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

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)

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.

Research output: Contribution to journalArticle

124 Citations (Scopus)

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.

Research output: Contribution to journalArticle

63 Citations (Scopus)
128 Citations (Scopus)

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

303 Citations (Scopus)

Comparison of montelukast versus salmeterol in children with asthma carrying-at-risk beta(2)adrenergic receptor polymorphism: a genotype-stratified randomised controlled trial

Basu, K., Donald, H. P., Lipworth, B. J., Tavendale, R., MacGregor, D. F., Ogston, S. A., Palmer, C. N. A. & Mukhopadhyay, S., 2011, In : Journal of Allergy and Clinical Immunology. 127, 2 Supplement, p. AB212 1 p.

Research output: Contribution to journalBook/Film/Article review

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21

Spencer, C. C. A., Plagnol, V., Strange, A., Gardner, M., Paisan-Ruiz, C., Band, G., Barker, R. A., Bellenguez, C., Bhatia, K., Blackburn, H., Blackwell, J. M., Bramon, E., Brown, M. A., Brown, M. A., Burn, D., Casas, J-P., Chinnery, P. F., Clarke, C. E., Corvin, A., Craddock, N. & 31 others, Deloukas, P., Edkins, S., Evans, J., Freeman, C., Gray, E., Hardy, J., Hudson, G., Hunt, S., Jankowski, J., Langford, C., Lees, A. J., Markus, H. S., Mathew, C. G., McCarthy, M. I., Morrison, K. E., Palmer, C. N. A., Pearson, J. P., Peltonen, L., Pirinen, M., Plomin, R., Potter, S., Rautanen, A., Sawcer, S. J., Su, Z., Trembath, R. C., Viswanathan, A. C., Williams, N. W., Morris, H. R., Donnelly, P., Wood, N. W. & UK Parkinson's Disease Consortium, 2011, In : Human Molecular Genetics. 20, 2, p. 345-53 9 p.

Research output: Contribution to journalArticle

Open Access
File
160 Citations (Scopus)
144 Downloads (Pure)

FCER2 T2206C variant associated with chronic symptoms and exacerbations in steroid-treated asthmatic children

Koster, E. S., Maitland-van der Zee, A-H., Tavendale, R., Mukhopadhyay, S., Vijverberg, S. J. H., Raaijmakers, J. A. M. & Palmer, C. N. A., Dec 2011, In : Allergy. 66, 12, p. 1546-1552 7 p.

Research output: Contribution to journalArticle

44 Citations (Scopus)

FGFR2 protein expression in breast cancer: nuclear localisation and correlation with patient genotype

Martin, A. J., Grant, A., Ashfield, A. M., Palmer, C. N., Baker, L., Quinlan, P. R., Purdie, C. A., Thompson, A. M., Jordan, L. B. & Berg, J. N., 1 Jan 2011, In : BMC Research Notes. 4

Research output: Contribution to journalArticle

18 Citations (Scopus)

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Sawcer, S., Hellenthal, G., Pirinen, M., Spencer, C. C. A., Patsopoulos, N. A., Moutsianas, L., Dilthey, A., Su, Z., Freeman, C., Hunt, S. E., Edkins, S., Gray, E., Booth, D. R., Potter, S. C., Goris, A., Band, G., Oturai, A. B., Strange, A., Saarela, J., Bellenguez, C. & 31 others, Fontaine, B., Gillman, M., Hemmer, B., Gwilliam, R., Zipp, F., Jayakumar, A., Martin, R., Leslie, S., Hawkins, S., Giannoulatou, E., D'alfonso, S., Blackburn, H., Boneschi, F. M., Liddle, J., Harbo, H. F., Perez, M. L., Spurkland, A., Waller, M. J., Mycko, M. P., Ricketts, M., Comabella, M., Hammond, N., Kockum, I., McCann, O. T., Ban, M., Whittaker, P., Kemppinen, A., Weston, P., Hawkins, C., Palmer, C. N. A. & Wellcome Trust Case Control Consor, Int Multiple Sclerosis Genetics Co, 11 Aug 2011, In : Nature. 476, 7359, p. 214-219 6 p.

Research output: Contribution to journalLetter

1710 Citations (Scopus)

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

522 Citations (Scopus)

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
File
267 Citations (Scopus)
166 Downloads (Pure)

Mendelian randomization studies do not support a role for raised circulating triglyceride levels influencing type 2 diabetes, glucose levels, or insulin resistance.

De Silva, N. M. G., Freathy, R. M., Palmer, T. M., Donnelly, L. A., Luan, J., Gaunt, T., Langenberg, C., Weedon, M. N., Shields, B., Knight, B. A., Ward, K. J., Sandhu, M. S., Harbord, R. M., McCarthy, M. I., Smith, G. D., Ebrahim, S., Hattersley, A. T., Wareham, N., Lawlor, D. A., Morris, A. D. & 2 others, Palmer, C. N. A. & Frayling, T. M., Mar 2011, In : Diabetes. 60, 3, p. 1008-1018 11 p.

Research output: Contribution to journalArticle

57 Citations (Scopus)

PPAR alpha and PPAR delta nuclear receptor regulation of body weight and hepatic steatosis

Garbacz, W., Higgins, L. & Palmer, C., 18 Dec 2011, In : Toxicology. 290, 2-3, p. 135-135 1 p.

Research output: Contribution to journalBook/Film/Article review

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)

β-Agonist safety and the elephant in the room?

Williamson, P. A., Short, P. M., McKinlay, L., Palmer, C. N. A. & Lipworth, B. J., Jun 2011, In : Thorax. 66, 6, p. 542 1 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)
2012

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)

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)

Clinical validity of plasma and urinary desmosine as biomarkers for chronic obstructive pulmonary disease

Huang, J. T-J., Chaudhuri, R., Albarbarawi, O., Barton, A., Grierson, C., Rauchhaus, P., Weir, C. J., Messow, M., Stevens, N., McSharry, C., Feuerstein, G., Mukhopadhyay, S., Brady, J., Palmer, C. N. A., Miller, D. & Thomson, N. C., 16 Jan 2012, In : Thorax. 67, 6, p. 502-508 7 p.

Research output: Contribution to journalArticle

Open Access
File
47 Citations (Scopus)
135 Downloads (Pure)

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

Su, Z., Gay, L. J., Strange, A., Palles, C., Band, G., Whiteman, D. C., Lescai, F., Langford, C., Nanji, M., Edkins, S., Van Der Winkel, A., Levine, D., Sasieni, P., Bellenguez, C., Howarth, K., Freeman, C., Trudgill, N., Tucker, A. T., Pirinen, M., Peppelenbosch, M. P. & 124 others, Van Der Laan, L. J. W., Kuipers, E. J., Drenth, J. P. H., Peters, W. H., Reynolds, J. V., Kelleher, D. P., McManus, R., Grabsch, H., Prenen, H., Bisschops, R., Krishnadath, K., Siersema, P. D., Van Baal, J. W. P. M., Middleton, M., Petty, R., Gillies, R., Burch, N., Bhandari, P., Paterson, S., Edwards, C., Penman, I., Vaidya, K., Ang, Y., Murray, I., Patel, P., Ye, W., Mullins, P., Wu, A. H., Bird, N. C., Dallal, H., Shaheen, N. J., Murray, L. J., Koss, K., Bernstein, L., Romero, Y., Hardie, L. J., Zhang, R., Winter, H., Corley, D. . A., Panter, S., Risch, H. A., Reid, B. J., Sargeant, I., Gammon, M. D., Smart, H., Dhar, A., McMurtry, H., Ali, H., Liu, G., Casson, A. G., Chow, W-H., Rutter, M., Tawil, A., Morris, D., Nwokolo, C., Isaacs, P., Rodgers, C., Ragunath, K., MacDonald, C., Haigh, C., Monk, D., Davies, G., Wajed, S., Johnston, D., Gibbons, M., Cullen, S., Church, N., Langley, R., Griffin, M., Alderson, D., Deloukas, P., Hunt, S. E., Gray, E., Dronov, S., Potter, S. C., Tashakkori-Ghanbaria, A., Anderson, M., Brooks, C., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N., Trynka, G., Wijmenga, C., Cazier, J-B., Atherfold, P., Nicholson, A. M., Gellatly, N. L., Glancy, D., Cooper, S. C., Cunningham, D., Lind, T., Hapeshi, J., Ferry, D., Rathbone, B., Brown, J., Love, S., Attwood, S., MacGregor, S., Watson, P., Sanders, S., Ek, W., Harrison, R. F., Moayyedi, P., De Caestecker, J., Barr, H., Stupka, E., Vaughan, T. L., Peltonen, L., Spencer, C. C. A., Tomlinson, I., Donnelly, P. & Jankowski, J. A. Z., 2012, In : Nature Genetics. 44, 10, p. 1131-1136 6 p.

Research output: Contribution to journalArticle

117 Citations (Scopus)

Conditional expression of human PPARδ and a dominant negative variant of hPPARδ in vivo

Higgins, L. G., Garbacz, W. G., Gustafsson, M. C. U., Sitheswaran, N., Ashby, P. R., Wolf, C. R. & Palmer, C. N. A., 2012, In : PPAR Research. 12 p., 216817.

Research output: Contribution to journalArticle

2 Citations (Scopus)

Deep Resequencing Unveils Genetic Architecture of ADIPOQ and Identifies a Novel Low-Frequency Variant Strongly Associated With Adiponectin Variation

Warren, L. L., Li, L., Nelson, M. R., Ehm, M. G., Shen, J., Fraser, D. J., Aponte, J. L., Nangle, K. L., Slater, A. J., Woollard, P. M., Hall, M. D., Topp, S. D., Yuan, X., Cardon, L. R., Chissoe, S. L., Mooser, V., Morris, A. D., Palmer, C. N. A., Perry, J. R., Frayling, T. M. & 2 others, Whittaker, J. C. & Waterworth, D. M., May 2012, In : Diabetes. 61, 5, p. 1297-1301 5 p.

Research output: Contribution to journalArticle

25 Citations (Scopus)

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): A meta-analysis of genome-wide association studies

Traylor, M., Farrall, M., Holliday, E. G., Sudlow, C., Hopewell, J. C., Cheng, Y-C., Fornage, M., Ikram, M. A., Malik, R., Bevan, S., Thorsteinsdottir, U., Nalls, M. A., Longstreth, W. T., Wiggins, K. L., Yadav, S., Parati, E. A., DeStefano, A. L., Worrall, B. B., Kittner, S. J., Khan, M. S. & 62 others, Reiner, A. P., Helgadottir, A., Achterberg, S., Fernandez-Cadenas, I., Abboud, S., Schmidt, R., Walters, M., Chen, W-M., Ringelstein, E. B., O'Donnell, M., Ho, W. K., Pera, J., Lemmens, R., Norrving, B., Higgins, P., Benn, M., Sale, M., Kuhlenbäumer, G., Doney, A. S. F., Vicente, A. M., Delavaran, H., Algra, A., Davies, G., Oliveira, S. A., Palmer, C. N. A., Deary, I., Schmidt, H., Pandolfo, M., Montaner, J., Carty, C., de Bakker, P. I. W., Kostulas, K., Ferro, J. M., van Zuydam, N. R., Valdimarsson, E., Nordestgaard, B. G., Lindgren, A., Thijs, V., Slowik, A., Saleheen, D., Paré, G., Berger, K., Thorleifsson, G., Hofman, A., Mosley, T. H., Mitchell, B. D., Furie, K., Clarke, R., Levi, C., Seshadri, S., Gschwendtner, A., Boncoraglio, G. B., Sharma, P., Bis, J. C., Gretarsdottir, S., Psaty, B. M., Rothwell, P. M., Rosand, J., Meschia, J. F., Stefansson, K., Dichgans, M. & Markus, H. S., 2012, In : Lancet Neurology. 11, 11, p. 951-962 12 p.

Research output: Contribution to journalArticle

306 Citations (Scopus)

Genome-wide association and functional follow-up reveals new loci for kidney function

Pattaro, C., Köttgen, A., Teumer, A., Garnaas, M., Boeger, C. A., Fuchsberger, C., Olden, M., Chen, M-H., Tin, A., Taliun, D., Li, M., Gao, X., Gorski, M., Yang, Q., Hundertmark, C., Foster, M. C., O'Seaghdha, C. M., Glazer, N., Isaacs, A., Liu, C-T. & 31 others, Smith, A. V., O'Connell, J. R., Struchalin, M., Tanaka, T., Li, G., Johnson, A. D., Gierman, H. J., Feitosa, M., Hwang, S-J., Atkinson, E. J., Lohman, K., Cornelis, M. C., Johansson, A., Toenjes, A., Dehghan, A., Chouraki, V., Holliday, E. G., Sorice, R., Kutalik, Z., Lehtimaeki, T., Esko, T., Deshmukh, H., Ulivi, S., Chu, A. Y., Murgia, F., Trompet, S., Imboden, M., Colhoun, H., Doney, A., Palmer, C. & WTCCC2, CARDIoGRAM Consortium, CARe Consortium, ICBP Consortium, 2012, In : PLoS Genetics. 8, 3, p. - 15 p., e1002584.

Research output: Contribution to journalArticle

Open Access
File
124 Citations (Scopus)
122 Downloads (Pure)

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Bellenguez, C., Bevan, S., Gschwendtner, A., Spencer, C. C. A., Burgess, A. I., Pirinen, M., Jackson, C. A., Traylor, M., Strange, A., Su, Z., Band, G., Syme, P. D., Malik, R., Pera, J., Norrving, B., Lemmens, R., Freeman, C., Schanz, R., James, T., Poole, D. & 31 others, Murphy, L., Segal, H., Cortellini, L., Cheng, Y-C., Woo, D., Nalls, M. A., Müller-Myhsok, B., Meisinger, C., Seedorf, U., Ross-Adams, H., Boonen, S., Wloch-Kopec, D., Valant, V., Slark, J., Furie, K., Delavaran, H., Langford, C., Deloukas, P., Edkins, S., Hunt, S., Gray, E., Dronov, S., Peltonen, L., Gretarsdottir, S., Thorleifsson, G., Thorsteinsdottir, U., Stefansson, K., Boncoraglio, G. B., Parati, E. A., Palmer, C. N. A. & WTCCC2, ISGC, Mar 2012, In : Nature Genetics. 44, 3, p. 328-U141 8 p.

Research output: Contribution to journalArticle

282 Citations (Scopus)

Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia

Wellcome Trust Case Control Consortium 2, 15 Oct 2012, In : Biological Psychiatry. 72, 8, p. 620-628 9 p.

Research output: Contribution to journalArticle

101 Citations (Scopus)

HBA1C and mortality in diabetic individuals with heart failure: an observational cohort study

Elder, D. H. J., Donnelly, L., Wong, A., Szwejkowski, B. R., Pauriah, M., Lim, T. K., Pringle, S. D., Choy, A., Pearson, E., Morris, A., George, J., Struthers, A., Palmer, C., Doney, A. & Lang, C., 2012, In : Heart. 98, Suppl. 1, p. A9-A10 6 p.

Research output: Contribution to journalMeeting abstract

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Genetic Anal Psoriasis Consortium, Wellcome Trust Case Control, 1 Dec 2012, In : Nature Genetics. 44, 12, p. 1341-1348 8 p.

Research output: Contribution to journalArticle

556 Citations (Scopus)

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

Chasman, D. I., Fuchsberger, C., Pattaro, C., Teumer, A., Boeger, C. A., Endlich, K., Olden, M., Chen, M-H., Tin, A., Taliun, D., Li, M., Gao, X., Gorski, M., Yang, Q., Hundertmark, C., Foster, M. C., O'Seaghdha, C. M., Glazer, N., Isaacs, A., Liu, C-T. & 34 others, Smith, A. V., O'Connell, J. R., Struchalin, M., Tanaka, T., Li, G., Johnson, A. D., Gierman, H. J., Feitosa, M. F., Hwang, S-J., Atkinson, E. J., Lohman, K., Cornelis, M. C., Johansson, A., Toenjes, A., Dehghan, A., Lambert, J-C., Holliday, E. G., Sorice, R., Kutalik, Z., Lehtimaeki, T., Esko, T., Deshmukh, H., Ulivi, S., Chu, A. Y., Murgia, F., Trompet, S., Imboden, M., Colhoun, H., Doney, A., Palmer, C., CARDIoGRAM Consortium, ICBP Consortium, CARe Consortium & WTCCC2, 15 Dec 2012, In : Human Molecular Genetics. 21, 24, p. 5329-5343 15 p.

Research output: Contribution to journalArticle

45 Citations (Scopus)

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

Scott, R. A., Lagou, V., Welch, R. P., Wheeler, E., Montasser, M. E., Luan, J., MäGi, R., Strawbridge, R. J., Rehnberg, E., Gustafsson, S., Kanoni, S., Rasmussen-Torvik, L. J., Yengo, L., Lecoeur, C., Shungin, D., Sanna, S., Sidore, C., Johnson, P. C. D., Jukema, J. W., Johnson, T. & 193 others, Mahajan, A., Verweij, N., Thorleifsson, G., Hottenga, J. J., Shah, S., Smith, A. V., Sennblad, B., Gieger, C., Salo, P., Perola, M., Timpson, N. J., Evans, D. M., St Pourcain, B., Wu, Y., Andrews, J. S., Hui, J., Bielak, L. F., Zhao, W., Horikoshi, M., Navarro, P., Isaacs, A., O'Connell, J. R., Stirrups, K., Vitart, V., Hayward, C., Esko, T., Mihailov, E., Fraser, R. M., Fall, T., Voight, B. F., Raychaudhuri, S., Chen, H., Lindgren, C. M., Morris, A. P., Rayner, N. W., Robertson, N., Rybin, D., Liu, C-T., Beckmann, J. S., Willems, S. M., Chines, P. S., Jackson, A. U., Kang, H. M., Stringham, H. M., Song, K., Tanaka, T., Peden, J. F., Goel, A., Hicks, A. A., An, P., Muller-Nurasyid, M., Franco-Cereceda, A., Folkersen, L., Marullo, L., Jansen, H., Oldehinkel, A. J., Bruinenberg, M., Pankow, J. S., North, K. E., Forouhi, N. G., Loos, R. J. F., Edkins, S., Varga, T. V., Hallmans, G., Oksa, H., Mulas, A., Nagaraja, R., Trompet, S., Ford, I., Small, K., Miljkovic, I., Liu, Y., Atalay, M., Kiess, W., James, A. L., Rivadeneira, F., Uitterlinden, A. G., Palmer, C. N. A., Doney, A. S. F., Willemsen, G., Smit, J. H., Campbell, S., Polasek, O., Bonnycastle, L. L., Hercberg, S., Dimitriou, M., Bolton, J. L., Fowkes, G. R., Kovacs, P., Lindström, J., Zemunik, T., Bandinelli, S., Wild, S. H., Basart, H. V., Rathmann, W., Grallert, H., Maerz, W., Kleber, M. E., Boehm, B. O., Peters, A., Pramstaller, P. P., Province, M. A., Borecki, I. B., Hastie, N. D., Rudan, I., Campbell, H., Watkins, H., Farrall, M., Stumvoll, M., Ferrucci, L., Waterworth, D. M., Bergman, R. N., Collins, F. S., Watanabe, R. M., Pedersen, N. L., Sattar, N., Harris, T. B., Cucca, F., Ripatti, S., Salomaa, V., Mohlke, K. L., Balkau, B., Froguel, P., Pouta, A., Jarvelin, M-R., Wareham, N. J., Bouatia-Naji, N., McCarthy, M. I., Franks, P. W., Meigs, J. B., Teslovich, T. M., Florez, J. C., Tuomilehto, J., de Geus, E. J. C., Penninx, B. W., Hofman, A., Oostra, B. A., Psaty, B. M., Vollenweider, P., Wilson, J. F., Hovingh, G. K., Wright, A. F., Metspalu, A., Uusitupa, M., Magnusson, P. K. E., Kyvik, K. O., Kaprio, J., Price, J. F., Dedoussis, G. V., Deloukas, P., Meneton, P., Lind, L., Boehnke, M., Shuldiner, A. R., van Duijn, C. M., Morris, A. D., Toenjes, A., Peyser, P. A., Beilby, J. P., Korner, A., Kuusisto, J., Langenberg, C., Ingelsson, E., Laakso, M., Bornstein, S. R., Schwarz, P. E. H., Lakka, T. A., Rauramaa, R., Adair, L. S., Smith, G. D., Spector, T. D., Illig, T., de Faire, U., Hamsten, A., Gudnason, V., Kivimaki, M., Hingorani, A., Keinanen-Kiukaanniemi, S. M., Saaristo, T. E., Boomsma, D. I., van der Harst, P., Dupuis, J., Bakker, S. J. L., Kong, A., Gigante, B., Kumari, M., Herder, C., Munroe, P. B., Caulfield, M., Jula, A., Mangino, M., Prokopenko, I. & Barroso, I., 2012, In : Nature Genetics. 44, 9, p. 991-1005 15 p.

Research output: Contribution to journalArticle

491 Citations (Scopus)

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium, Wellcome Trust Case Control Consortium, MAGIC Investigators, GIANT Consortium, Morris, A. P., Voight, B. F., Teslovich, T. M., Ferreira, T., Segre, A. V., Steinthorsdottir, V., Strawbridge, R. J., Khan, H., Grallert, H., Mahajan, A., Prokopenko, I., Kang, H. M., Dina, C., Esko, T., Fraser, R. M., Kanoni, S. & 35 others, Kumar, A., Lagou, V., Langenberg, C., Luan, J., Lindgren, C. M., Mueller-Nurasyid, M., Pechlivanis, S., Rayner, N. W., Scott, L. J., Wiltshire, S., Yengo, L., Kinnunen, L., Rossin, E. J., Raychaudhuri, S., Johnson, A. D., Dimas, A. S., Loos, R. J. F., Vedantam, S., Chen, H., Florez, J. C., Fox, C., Liu, C-T., Rybin, D., Couper, D. J., Kao, W. H. L., Li, M., Cornelis, M. C., Kraft, P., Sun, Q., van Dam, R. M., Stringham, H. M., Doney, A. S. F., Palmer, C. N. A., Morris, A. D. & South Asian Type 2 Diabetes SAT2D Consortium, Sep 2012, In : Nature Genetics. 44, 9, p. 981-990 12 p.

Research output: Contribution to journalArticle

1162 Citations (Scopus)

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

Dastani, Z., Hivert, M-F., Timpson, N., Perry, J. R. B., Yuan, X., Scott, R. A., Henneman, P., Heid, I. M., Kizer, J. R., Lyytikäinen, L-P., Fuchsberger, C., Tanaka, T., Morris, A. P., Small, K., Isaacs, A., Beekman, M., Coassin, S., Lohman, K., Qi, L., Kanoni, S. & 31 others, Pankow, J. S., Uh, H-W., Wu, Y., Bidulescu, A., Rasmussen-Torvik, L. J., Greenwood, C. M. T., Ladouceur, M., Grimsby, J., Manning, A. K., Liu, C-T., Kooner, J., Mooser, V. E., Vollenweider, P., Kapur, K. A., Chambers, J., Wareham, N. J., Langenberg, C., Frants, R., Willems-Vandijk, K., Oostra, B. A., Willems, S. M., Lamina, C., Winkler, T. W., Psaty, B. M., Tracy, R. P., Brody, J., Chen, I., Doney, A. S. F., Morris, A. D., Palmer, C. N. A. & DIAGRAM+ Consortium, 29 Mar 2012, In : PLoS Genetics. 8, 3, p. e1002607

Research output: Contribution to journalArticle

258 Citations (Scopus)

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)

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)

Skin-targeted inhibition of PPAR β/δ by selective antagonists to treat PPAR β/δ-mediated psoriasis-like skin disease in vivo

Hack, K., Reilly, L., Palmer, C., Read, K., Norval, S., Kime, R., Booth, K. & Foerster, J., May 2012, In : PLoS ONE. 7, 5

Research output: Contribution to journalArticle

Open Access
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24 Citations (Scopus)
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Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

Perry, J. R. B., Voight, B. F., Yengo, L., Amin, N., Dupuis, J., Ganser, M., Grallert, H., Navarro, P., Li, M., Qi, L., Steinthorsdottir, V., Scott, R. A., Almgren, P., Arking, D. E., Aulchenko, Y., Balkau, B., Benediktsson, R., Bergman, R. N., Boerwinkle, E., Bonnycastle, L. & 31 others, Burtt, N. P., Campbell, H., Charpentier, G., Collins, F. S., Gieger, C., Green, T., Hadjadj, S., Hattersley, A. T., Herder, C., Hofman, A., Johnson, A. D., Kottgen, A., Kraft, P., Labrune, Y., Langenberg, C., Manning, A. K., Mohlke, K. L., Morris, A. P., Oostra, B., Pankow, J., Petersen, A-K., Pramstaller, P. P., Prokopenko, I., Rathmann, W., Rayner, W., Roden, M., Rudan, I., Rybin, D., Morris, A. D., Palmer, C. N. A. & GIANT Consortium, DIAGRAM Consortium, MAGIC, 2012, In : PLoS Genetics. 8, 5, p. - 14 p., e1002741.

Research output: Contribution to journalArticle

135 Citations (Scopus)

The role of ATM in response to metformin treatment and activation of AMPK reply

Zhou, K., Bellenguez, C., Sutherland, C., Hardie, G., Palmer, C., Donnelly, P. & Pearson, E., Apr 2012, In : Nature Genetics. 44, 4, p. 361-362 2 p.

Research output: Contribution to journalLetter

15 Citations (Scopus)
2013

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.

Research output: Contribution to journalArticle

199 Citations (Scopus)

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)

Clinical predictors of rate of progression of type 2 diabetes: an extreme case-control study

Donnelly, L. A., Zhou, K., Palmer, C. N. A., Doney, A. S. F., Morris, A. D. & Pearson, E. R., Mar 2013, In : Diabetic Medicine. 30, Suppl. 1, p. 94-94 1 p., P213.

Research output: Contribution to journalMeeting abstract

Cohort profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness

Smith, B. H., Campbell, A., Linksted, P., Fitzpatrick, B., Jackson, C., Kerr, S. M., Deary, I. J., Macintyre, D. J., Campbell, H., McGilchrist, M., Hocking, L. J., Wisely, L., Ford, I., Lindsay, R. S., Morton, R., Palmer, C. N. A., Dominiczak, A. F., Porteous, D. J. & Morris, A. D., Jun 2013, In : International Journal of Epidemiology. 42, 3, p. 689-700 12 p.

Research output: Contribution to journalArticle

126 Citations (Scopus)

Common Polymorphisms in the CYP11B1 and CYP11B2 Genes: Evidence for a Digenic Influence on Hypertension

Alvarez-Madrazo, S., MacKenzie, S. M., Davies, E., Fraser, R., Lee, W-K., Brown, M., Caulfield, M. J., Dominiczak, A. F., Farrall, M., Lathrop, M., Hedner, T., Melander, O., Munroe, P. B., Samani, N., Stewart, P. M., Wahlstrand, B., Webster, J., Palmer, C. N. A., Padmanabhan, S. & Connell, J. M., 2013, In : Hypertension. 61, 1, p. 232-239 8 p.

Research output: Contribution to journalArticle

20 Citations (Scopus)

Common variants associated with plasma triglycerides and risk for coronary artery disease

Do, R., Willer, C. J., Schmidt, E. M., Sengupta, S., Gao, C., Peloso, G. M., Gustafsson, S., Kanoni, S., Ganna, A., Chen, J., Buchkovich, M. L., Mora, S., Beckmann, J. S., Bragg-Gresham, J. L., Chang, H-Y., Demirkan, A., Den Hertog, H. M., Donnelly, L. A., Ehret, G. B., Esko, T. & 243 others, Feitosa, M. F., Ferreira, T., Fischer, K., Fontanillas, P., Fraser, R. M., Freitag, D. F., Gurdasani, D., Heikkilä, K., Hyppönen, E., Isaacs, A., Jackson, A. U., Johansson, A., Johnson, T., Kaakinen, M., Kettunen, J., Kleber, M. E., Li, X., Luan, J., Lyytikäinen, L-P., Magnusson, P. K. E., Mangino, M., Mihailov, E., Montasser, M. E., Müller-Nurasyid, M., Nolte, I. M., O'Connell, J. R., Palmer, C. D., Perola, M., Petersen, A-K., Sanna, S., Saxena, R., Service, S. K., Shah, S., Shungin, D., Sidore, C., Song, C., Strawbridge, R. J., Surakka, I., Tanaka, T., Teslovich, T. M., Thorleifsson, G., Van den Herik, E. G., Voight, B. F., Volcik, K. A., Waite, L. L., Wong, A., Wu, Y., Zhang, W., Absher, D., Asiki, G., Barroso, I., Been, L. F., Bolton, J. L., Bonnycastle, L. L., Brambilla, P., Burnett, M. S., Cesana, G., Dimitriou, M., Doney, A. S. F., Döring, A., Elliott, P., Epstein, S. E., Eyjolfsson, G. I., Gigante, B., Goodarzi, M. O., Grallert, H., Gravito, M. L., Groves, C. J., Hallmans, G., Hartikainen, A-L., Hayward, C., Hernandez, D., Hicks, A. A., Holm, H., Hung, Y-J., Illig, T., Jones, M. R., Kaleebu, P., Kastelein, J. J. P., Khaw, K-T., Kim, E., Klopp, N., Komulainen, P., Kumari, M., Langenberg, C., Lehtimäki, T., Lin, S-Y., Lindström, J., Loos, R. J. F., Mach, F., McArdle, W. L., Meisinger, C., Mitchell, B. D., Müller, G., Nagaraja, R., Narisu, N., Nieminen, T. V. M., Nsubuga, R. N., Olafsson, I., Ong, K. K., Palotie, A., Papamarkou, T., Pomilla, C., Pouta, A., Rader, D. J., Reilly, M. P., Ridker, P. M., Rivadeneira, F., Rudan, I., Ruokonen, A., Samani, N., Scharnagl, H., Seeley, J., Silander, K., Stančáková, A., Stirrups, K., Swift, A. J., Tiret, L., Uitterlinden, A. G., van Pelt, L. J., Vedantam, S., Wainwright, N., Wijmenga, C., Wild, S. H., Willemsen, G., Wilsgaard, T., Wilson, J. F., Young, E. H., Zhao, J. H., Adair, L. S., Arveiler, D., Assimes, T. L., Bandinelli, S., Bennett, F., Bochud, M., Boehm, B. O., Boomsma, D. I., Borecki, I. B., Bornstein, S. R., Bovet, P., Burnier, M., Campbell, H., Chakravarti, A., Chambers, J. C., Chen, Y-D. I., Collins, F. S., Cooper, R. S., Danesh, J., Dedoussis, G., de Faire, U., Feranil, A. B., Ferrières, J., Ferrucci, L., Freimer, N. B., Gieger, C., Groop, L. C., Gudnason, V., Gyllensten, U., Hamsten, A., Harris, T. B., Hingorani, A., Hirschhorn, J. N., Hofman, A., Hovingh, G. K., Hsiung, C. A., Humphries, S. E., Hunt, S. C., Hveem, K., Iribarren, C., Järvelin, M-R., Jula, A., Kähönen, M., Kaprio, J., Kesäniemi, A., Kivimaki, M., Kooner, J. S., Koudstaal, P. J., Krauss, R. M., Kuh, D., Kuusisto, J., Kyvik, K. O., Laakso, M., Lakka, T. A., Lind, L., Lindgren, C. M., Martin, N. G., März, W., McCarthy, M. I., McKenzie, C. A., Meneton, P., Metspalu, A., Moilanen, L., Morris, A. D., Munroe, P. B., Njølstad, I., Pedersen, N. L., Power, C., Pramstaller, P. P., Price, J. F., Psaty, B. M., Quertermous, T., Rauramaa, R., Saleheen, D., Salomaa, V., Sanghera, D. K., Saramies, J., Schwarz, P. E. H., Sheu, W. H-H., Shuldiner, A. R., Siegbahn, A., Spector, T. D., Stefansson, K., Strachan, D. P., Tayo, B. O., Tremoli, E., Tuomilehto, J., Uusitupa, M., van Duijn, C. M., Vollenweider, P., Wallentin, L., Wareham, N. J., Whitfield, J. B., Wolffenbuttel, B. H. R., Altshuler, D., Ordovas, J. M., Boerwinkle, E., Palmer, C. N. A., Thorsteinsdottir, U., Chasman, D. I., Rotter, J. I., Franks, P. W., Ripatti, S., Cupples, L. A., Sandhu, M. S., Rich, S. S., Boehnke, M., Deloukas, P., Mohlke, K. L., Ingelsson, E., Abecasis, G. R., Daly, M. J., Neale, B. M. & Kathiresan, S., 2013, In : Nature Genetics. 45, 11, p. 1345-1352 8 p.

Research output: Contribution to journalLetter

458 Citations (Scopus)

Common variants in Mendelian kidney disease genes and their association with renal function

Parsa, A., Fuchsberger, C., Köttgen, A., O'Seaghdha, C. M., Pattaro, C., de Andrade, M., Chasman, D. I., Teumer, A., Endlich, K., Olden, M., Chen, M-H., Tin, A., Kim, Y. J., Taliun, D., Li, M., Feitosa, M., Gorski, M., Yang, Q., Hundertmark, C., Foster, M. C. & 139 others, Glazer, N., Isaacs, A., Rao, M., Smith, A. V., O'Connell, J. R., Struchalin, M., Tanaka, T., Li, G., Hwang, S-J., Atkinson, E. J., Lohman, K., Cornelis, M. C., Johansson, A., Tönjes, A., Dehghan, A., Couraki, V., Holliday, E. G., Sorice, R., Kutalik, Z., Lehtimäki, T., Esko, T., Deshmukh, H., Ulivi, S., Chu, A. Y., Murgia, F., Trompet, S., Imboden, M., Kollerits, B., Pistis, G., Harris, T. B., Launer, L. J., Aspelund, T., Eiriksdottir, G., Mitchell, B. D., Boerwinkle, E., Schmidt, H., Hofer, E., Hu, F., Demirkan, A., Oostra, B. A., Turner, S. T., Ding, J., Andrews, J. S., Freedman, B. I., Giulianini, F., Koenig, W., Illig, T., Döring, A., Wichmann, H. -E., Zgaga, L., Zemunik, T., Boban, M., Minelli, C., Wheeler, H. E., Igl, W., Zaboli, G., Wild, S. H., Wright, A. F., Campbell, H., Ellinghaus, D., Nöthlings, U., Jacobs, G., Biffar, R., Ernst, F., Homuth, G., Kroemer, H. K., Nauck, M., Stracke, S., Völker, U., Völzke, H., Kovacs, P., Stumvoll, M., Mägi, R., Hofman, A., Uitterlinden, A. G., Rivadeneira, F., Aulchenko, Y. S., Polasek, O., Hastie, N., Vitart, V., Helmer, C., Wang, J. J., Stengel, B., Ruggiero, D., Bergmann, S., Kähönen, M., Viikari, J., Nikopensius, T., Province, M., Colhoun, H., Doney, A., Robino, A., Krämer, B. K., Portas, L., Ford, I., Buckley, B. M., Adam, M., Thun, G-A., Paulweber, B., Haun, M., Sala, C., Mitchell, P., Ciullo, M., Vollenweider, P., Raitakari, O., Metspalu, A., Palmer, C., Gasparini, P., Pirastu, M., Jukema, J. W., Probst-Hensch, N. M., Kronenberg, F., Toniolo, D., Gudnason, V., Shuldiner, A. R., Coresh, J., Schmidt, R., Ferrucci, L., van Duijn, C. M., Borecki, I., Kardia, S. L. R., Liu, Y., Curhan, G. C., Rudan, I., Gyllensten, U., Wilson, J. F., Franke, A., Pramstaller, P. P., Rettig, R., Prokopenko, I., Witteman, J., Hayward, C., Ridker, P. M., Bochud, M., Heid, I. M., Siscovick, D. S., Fox, C. S., Kao, W. L. & Böger, C. A., Dec 2013, In : Journal of the American Society of Nephrology. 24, 12, p. 2105-2117 13 p.

Research output: Contribution to journalArticle

22 Citations (Scopus)

Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

Fakiola, M., Strange, A., Cordell, H. J., Miller, E. N., Pirinen, M., Su, Z., Mishra, A., Mehrotra, S., Monteiro, G. R., Band, G., Bellenguez, C., Dronov, S., Edkins, S., Freeman, C., Giannoulatou, E., Gray, E., Hunt, S. E., Lacerda, H. G., Langford, C., Pearson, R. & 32 others, Pontes, N. N., Rai, M., Singh, S. P., Smith, L., Sousa, O., Vukcevic, D., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Wilson, M. E., Deloukas, P., Peltonen, L., Christiansen, F., Witt, C., Jeronimo, S. M. B., Sundar, S., Spencer, C. C. A., Blackwell, J. M., LeishGEN Consortium & Wellcome Trust Case Control, 2013, In : Nature Genetics. 45, 2, p. 208-213 6 p.

Research output: Contribution to journalLetter

69 Citations (Scopus)

Discovery and refinement of loci associated with lipid levels

Global Lipids Genetics Consortium, 2013, In : Nature Genetics. 45, 11, p. 1274-1283 10 p.

Research output: Contribution to journalArticle

1293 Citations (Scopus)

Genetic Loci for retinal arteriolar microcirculation

Sim, X., Jensen, R. A., Ikram, M. K., Cotch, M. F., Li, X., MacGregor, S., Xie, J., Smith, A. V., Boerwinkle, E., Mitchell, P., Klein, R., Klein, B. E. K., Glazer, N. L., Lumley, T., McKnight, B., Psaty, B. M., de Jong, P. T. V. M., Hofman, A., Rivadeneira, F., Uitterlinden, A. G. & 32 others, van Duijn, C. M., Aspelund, T., Eiriksdottir, G., Harris, T. B., Jonasson, F., Launer, L. J., Wellcome Trust Case Control Consortium 2, Attia, J., Baird, P. N., Harrap, S., Holliday, E. G., Inouye, M., Rochtchina, E., Scott, R. J., Viswanathan, A., Global BPgen Consortium, Li, G., Smith, N. L., Wiggins, K. L., Kuo, J. Z., Taylor, K. D., Hewitt, A. W., Martin, N. G., Montgomery, G. W., Sun, C., Young, T. L., Mackey, D. A., van Zuydam, N. R., Doney, A. S. F., Palmer, C. N. A., Morris, A. D. & Rotter, J. I., Jun 2013, In : PLoS ONE. 8, 6, e65804.

Research output: Contribution to journalArticle

10 Citations (Scopus)