Common Creatine Kinase gene mutation results in falsely reassuring CK levels in muscle disorders

Por Wallace, B., Siddiqui, M.K., Palmer, C.N.A., George, J.
Publicado no QJM (2016)

Members of the nuclear receptor superfamily regulate transcription from the hepatitis B virus nucleocapsid promoter.

Por Raney, A K, Johnson, J L, Palmer, C N, McLachlan, A
Publicado em 1997

Arginine‐16 β(2) adrenoceptor genotype predisposes to exacerbations in young asthmatics taking regular salmeterol

Por Palmer, C N A, Lipworth, B J, Lee, S, Ismail, T, Macgregor, D F, Mukhopadhyay, S
Publicado em 2006

Investigation of known estimated glomerular filtration rate loci in patients with Type 2 diabetes

Por Deshmukh, H A, Palmer, C N A, Morris, A D, Colhoun, H M
Publicado em 2013

Fatty acid signals in Bacillus megaterium are attenuated by cytochrome P-450-mediated hydroxylation.

Por English, N, Palmer, C N, Alworth, W L, Kang, L, Hughes, V, Wolf, C R
Publicado em 1997

A genome‐wide association study suggests that MAPK14 is associated with diabetic foot ulcers

Por Meng, W., Veluchamy, A., Hébert, H.L., Campbell, A., Colhoun, H.M., Palmer, C.N.A.
Publicado no Br J Dermatol (2017)

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

Por Meng, W., Deshmukh, H.A., van Zuydam, N.R., Liu, Y., Donnelly, L.A., Zhou, K., Morris, A.D., Colhoun, H.M., Palmer, C.N.A., Smith, B.H.
Publicado no Eur J Pain (2015)

Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes

Por Rafiq, S., Melzer, D., Weedon, M. N., Lango, H., Saxena, R., Scott, L. J., Palmer, C. N. A., Morris, A. D., McCarthy, M. I., Ferrucci, L., Hattersley, A. T., Zeggini, E., Frayling, T. M.
Publicado em 2008

Phenotype Standardization of Angioedema in the Head and Neck Region Caused by Agents Acting on the Angiotensin System

Por Wadelius, M, Marshall, S E, Islander, G, Nordang, L, Karawajczyk, M, Yue, Q-Y, Terreehorst, I, Baranova, E V, Hugosson, S, Sköldefors, K, Pirmohamed, M, Maitland-van der Zee, A-H, Alfirevic, A, Hallberg, P, Palmer, C N A
Publicado em 2014

Phenotype Standardization for Statin-Induced Myotoxicity

Por Alfirevic, A, Neely, D, Armitage, J, Chinoy, H, Cooper, R G, Laaksonen, R, Carr, D F, Bloch, K M, Fahy, J, Hanson, A, Yue, Q-Y, Wadelius, M, Maitland-van Der Zee, A H, Voora, D, Psaty, B M, Palmer, C N A, Pirmohamed, M
Publicado em 2014

A role for coding functional variants in HNF4A in Type 2 Diabetes susceptibility

Por 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, Palmer, C N A, Frayling, T M, Gloyn, A L, McCarthy, M I
Publicado em 2010

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

Por 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., Dekker, J. M., ’t Hart, L. M., Pearson, E. R.
Publicado em 2012

Genetic association analysis of LARS2 with type 2 diabetes

Por Reiling, E., Jafar-Mohammadi, B., van ’t Riet, E., Weedon, M. N., van Vliet-Ostaptchouk, J. V., Hansen, T., Saxena, R., van Haeften, T. W., Arp, P. A., Das, S., Nijpels, G., Groenewoud, M. J., van Hove, E. C., Uitterlinden, A. G., Smit, J. W. A., Morris, A. D., Doney, A. S. F., Palmer, C. N. A., Guiducci, C., Hattersley, A. T., Frayling, T. M., Pedersen, O., Slagboom, P. E., Altshuler, D. M., Groop, L., Romijn, J. A., Maassen, J. A., Hofker, M. H., Dekker, J. M., McCarthy, M. I., ’t Hart, L. M.
Publicado em 2009

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

Por 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., Mukhopadhyay, S., Merid, S. K., Palmer, C. N., Pino‐Yanes, M., Pirmohamed, M., Potočnik, U., Repnik, K., Schieck, M., Sevelsted, A., Sio, Y. Y., Smyth, R. L., Soares, P., Söderhäll, C., Tantisira, K. G., Tavendale, R., Tse, S. M., Turner, S., Verhamme, K. M., Maitland‐van der Zee, A.‐H.
Publicado no Allergy (2018)

Genetically Determined Height and Coronary Artery Disease

Por Nelson, C.P., Hamby, S.E., Saleheen, D., Hopewell, J.C., Zeng, L., Assimes, T.L., Kanoni, S., Willenborg, C., Burgess, S., Amouyel, P., Anand, S., Blankenberg, S., Boehm, B.O., Clarke, R.J., Collins, R., Dedoussis, G., Farrall, M., Franks, P.W., Groop, L., Hall, A.S., Hamsten, A., Hengstenberg, C., Hovingh, G. Kees, Ingelsson, E., Kathiresan, S., Kee, F., König, I.R., Kooner, J., Lehtimäki, T., März, W., McPherson, R., Metspalu, A., Nieminen, M.S., O’Donnell, C.J., Palmer, C.N.A., Peters, A., Perola, M., Reilly, M.P., Ripatti, S., Roberts, R., Salomaa, V., Shah, S.H., Schreiber, S., Siegbahn, A., Thorsteinsdottir, U., Veronesi, G., Wareham, N., Willer, C.J., Zalloua, P.A., Erdmann, J., Deloukas, P., Watkins, H., Schunkert, H., Danesh, J., Thompson, J.R., Samani, N.J.
Publicado no N Engl J Med (2015)

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

Por 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, 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 K, Palmer, C N A, Doney, A, MahmoudPour, S H, Maitland-van der Zee, A H, Morris, A D, Denny, J C, Roden, D M
Publicado no Pharmacogenomics J (2016)

Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes

Por Albrechtsen, A., Grarup, N., Li, Y., Sparsø, T., Tian, G., Cao, H., Jiang, T., Kim, S. Y., Korneliussen, T., Li, Q., Nie, C., Wu, R., Skotte, L., Morris, A. P., Ladenvall, C., Cauchi, S., Stančáková, A., Andersen, G., Astrup, A., Banasik, K., Bennett, A. J., Bolund, L., Charpentier, G., Chen, Y., Dekker, J. M., Doney, A. S. F., Dorkhan, M., Forsen, T., Frayling, T. M., Groves, C. J., Gui, Y., Hallmans, G., Hattersley, A. T., He, K., Hitman, G. A., Holmkvist, J., Huang, S., Jiang, H., Jin, X., Justesen, J. M., Kristiansen, K., Kuusisto, J., Lajer, M., Lantieri, O., Li, W., Liang, H., Liao, Q., Liu, X., Ma, T., Ma, X., Manijak, M. P., Marre, M., Mokrosiński, J., Morris, A. D., Mu, B., Nielsen, A. A., Nijpels, G., Nilsson, P., Palmer, C. N. A., Rayner, N. W., Renström, F., Ribel-Madsen, R., Robertson, N., Rolandsson, O., Rossing, P., Schwartz, T. W., Slagboom, P. E., Sterner, M., Tang, M., Tarnow, L., Tuomi, T., van’t Riet, E., van Leeuwen, N., Varga, T. V., Vestmar, M. A., Walker, M., Wang, B., Wang, Y., Wu, H., Xi, F., Yengo, L., Yu, C., Zhang, X., Zhang, J., Zhang, Q., Zhang, W., Zheng, H., Zhou, Y., Altshuler, D., ‘t Hart, L. M., Franks, P. W., Balkau, B., Froguel, P., McCarthy, M. I., Laakso, M., Groop, L., Christensen, C., Brandslund, I., Lauritzen, T., Witte, D. R., Linneberg, A., Jørgensen, T., Hansen, T., Wang, J., Nielsen, R., Pedersen, O.
Publicado em 2012