Find Research outputs

Search results

• Genetic modifications to lignin biosynthesis in field-grown poplar trees have inconsistent effects on the rate of woody trunk decomposition

  Tilston, E. L., Halpin, C. & Hopkins, D. W., Nov 2004, In: Soil Biology and Biochemistry. 36, 11, p. 1903-1906 4 p.

  Research output: Contribution to journal › Article › peer-review
  20 Citations (Scopus)

• Genetic polymorphism of cytochrome P450 2C19 in healthy Malaysian subjects

  Yang, Y. S., Wong, L. P., Lee, T. C., Mustafa, A. M., Mohamed, Z. & Lang, C. C., 2004, In: British Journal of Clinical Pharmacology. 58, 3, p. 332-5 4 p.

  Research output: Contribution to journal › Article › peer-review
  50 Citations (Scopus)

• Genetic polymorphisms in xenobiotic metabolism

  Smith, C. A. D., Smith, G. & Wolf, C. R., 1994, In: European Journal of Cancer. 30, 13, p. 1921-35 15 p.

  Research output: Contribution to journal › Article › peer-review
  93 Citations (Scopus)

• Genetic prediction of treatment response in psoriasis is still a work in progress

  Foulkes, A. & Brown, S., 18 Aug 2017, In: British Journal of Dermatology. 177, 2, p. 344-345

  Research output: Contribution to journal › Comment/debate › peer-review

  Open Access

  File
  2 Citations (Scopus)

  227 Downloads (Pure)

• Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus

  CARDIOGRAMplusC4D Steering Committee, Van Zuydam, N. R., Ladenvall, C., Voight, B. F., Strawbridge, R. J., Fernandez-Tajes, J., Rayner, N. W., Robertson, N. R., Mahajan, A., Vlachopoulou, E., Goel, A., Kleber, M. E., Nelson, C. P., Kwee, L. C., Esko, T., Mihailov, E., Mägi, R., Milani, L., Fischer, K., Kanoni, S., & 31 othersKumar, J., Song, C., Hartiala, J. A., Pedersen, N. L., Perola, M., Gieger, C., Peters, A., Qu, L., Willems, S. M., Doney, A. S. F., Morris, A. D., Zheng, Y., Sesti, G., Hu, F. B., Qi, L., Laakso, M., Thorsteinsdottir, U., Grallert, H., Van Duijn, C., Reilly, M. P., Ingelsson, E., Deloukas, P., Kathiresan, S., Metspalu, A., Shah, S. H., Sinisalo, J., Salomaa, V., Morris, A. P., Colhoun, H. M., McCarthy, M. I. & Palmer, C. N. A., Dec 2020, In: Circulation: Genomic and Precision Medicine. 13, 6, p. 640-648 9 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File
  35 Downloads (Pure)

• Genetic profiling versus drug rotation in the optimisation of antihypertensive treatment

  Mackenzie, I. S. & Brown, M. J., Sep 2002, In: Clinical Medicine. 2, 5, p. 465-473 9 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access
  6 Citations (Scopus)

• Genetic recoding to dissect the roles of site-specific protein O-GlcNAcylation

  Gorelik, A., Galan Bartual, S., Borodkin, V., Varghese, J., Ferenbach, A. & van Aalten, D., Nov 2019, In: Nature Structural & Molecular Biology. 26, 11, p. 1071-1077 7 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File
  34 Citations (Scopus)

  88 Downloads (Pure)

• Genetic recombination can generate altered restriction specificity

  Fuller-Pace, F. V., Bullas, L. R., Delius, H. & Murray, N. E., 1 Oct 1984, In: Proceedings of the National Academy of Sciences of the United States of America. 81, 19 I, p. 6095-6099 5 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access
  71 Citations (Scopus)

• Genetic regulation of aldosterone production in cardiovascular disease

  Connell, J. M., Davies, E., Mackenzie, S. & Fraser, R., Mar 2010, In: Endocrine Journal. 57, p. S272-S272 1 p.

  Research output: Contribution to journal › Meeting abstract › peer-review

• Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

  Lee, S. H., Ripke, S., Neale, B. M., Faraone, S. V., Purcell, S. M., Perlis, R. H., Mowry, B. J., Thapar, A., Goddard, M. E., Witte, J. S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen, O. A., Anjorin, A., Anney, R., Anttila, V., Arking, D. E., Asherson, P., & 31 othersAzevedo, M. H., Backlund, L., Badner, J. A., Bailey, A. J., Banaschewski, T., Barchas, J. D., Barnes, M. R., Barrett, T. B., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen, S. E., Berrettini, W., Betancur, C., Bettecken, T., Biederman, J., Binder, E. B., Black, D. W., Blackwood, D. H. R., Bloss, C. S., Boehnke, M., Boomsma, D. I., Breen, G., Breuer, R., Bruggeman, R., Cormican, P., Day, R., Matthews, K. & Cross-Disorder Group of the Psychiatric Genomics Consortium, 2013, In: Nature Genetics. 45, p. 984-994 11 p.

  Research output: Contribution to journal › Article › peer-review
  1579 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 othersFontaine, 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 journal › Letter › peer-review
  2017 Citations (Scopus)

• Genetic Risk and Atrial Fibrillation in Patients with Heart Failure

  Kloosterman, M., Santema, B. T., Roselli, C., Nelson, C. P., Koekemoer, A., Romaine, S. P. R., Van Gelder, I. C., Lam, C. S. P., Artola, V. A., Lang, C., Ng, L. L., Metra, M., Anker, S. D., Filippatos, G. S., Dickstein, K., Ponikowski, P., van der Harst, P., Meer, P. V. D., Van Veldhuisen, D. J., Benjamin, E. J., & 3 othersVoors, A. A., Samani, N. J. & Rienstra, M., 27 Mar 2020, In: European Journal of Heart Failure. 22, 3, p. 519-527 9 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File
  6 Citations (Scopus)

  44 Downloads (Pure)

• 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 othersReiner, 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 journal › Article › peer-review
  361 Citations (Scopus)

• Genetic Risk of Diverticular Disease Predicts Early Stoppage of Nicorandil

  Noyes, J., Mordi, I. R., Doney, A. S., Palmer, C. N. A., Pearson, E. R. & Lang, C. C., Dec 2020, In: Clinical Pharmacology & Therapeutics. 108, 6, p. 1171-1175 5 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File
  2 Citations (Scopus)

  42 Downloads (Pure)

• Genetics

  Hall, E., 2009, International encyclopedia of human geography. Kitchin, R. & Thrift, N. (eds.). Elsevier, p. 355-359 5 p.

  Research output: Chapter in Book/Report/Conference proceeding › Entry for encyclopedia/dictionary
  1 Citation (Scopus)

• Genetics, eugenics and culture: transatlantic perspectives, 1900-2000

  Simpson, M., 27 Jul 2013.

  Research output: Contribution to conference › Other › peer-review

• Genetics in Atopic Dermatitis: Historical Perspective and Future Prospects

  Brown, S. J., Elias, M. S. & Bradley, M., 9 Jun 2020, In: Acta Dermato-Venereologica. 100, 100-year theme: Atopic dermatitis, p. 349-357 9 p., adv00163.

  Research output: Contribution to journal › Review article › peer-review

  Open Access

  File
  8 Citations (Scopus)

  108 Downloads (Pure)

• Genetics of Atopic Dermatitis: From DNA Sequence to Clinical Relevance

  Løset, M., Brown, S. J., Saunes, M. & Hveem, K., Aug 2019, In: Dermatology . 235, 5, p. 355-364 10 p.

  Research output: Contribution to journal › Review article › peer-review

  Open Access

  File
  37 Citations (Scopus)

  101 Downloads (Pure)

• Genetics of Drug Response in Diabetes

  Pearson, E. R. & Florez, J. C., 2014, In: Frontiers in Diabetes. 23, p. 158-172 15 p.

  Research output: Contribution to journal › Article › peer-review

• Genetics of gastric cancer

  McLean, M. H. & El-Omar, E. M., Nov 2014, In: Nature Reviews Gastroenterology and Hepatology. 11, 11, p. 664-674 11 p.

  Research output: Contribution to journal › Review article › peer-review
  299 Citations (Scopus)

• Genetics of inflammation in the gastrointestinal tract and how it can cause cancer

  McLean, M. H. & El-Omar, E. M., 2011, Inflammation and Gastrointestinal Cancers. Jankowski, J. A. Z. (ed.). Berlin: Springer Verlag, Vol. 185. p. 173-183 11 p. (Recent Results in Cancer Research).

  Research output: Chapter in Book/Report/Conference proceeding › Chapter (peer-reviewed) › peer-review
  21 Citations (Scopus)

• Genetics of kidney tumours

  Fleming, S., 1998, In: Forum Trends in Experimental and Clinical Medicine. 8, 2, p. 176-84 9 p.

  Research output: Contribution to journal › Article › peer-review

  16 Citations (Scopus)

• Genetics of monogenic disorders of calcium and bone metabolism

  Newey, P. J., Hannan, F. M., Wilson, A. & Thakker, R. V., Oct 2022, In: Clinical Endocrinology. 97, 4, p. 483-501 19 p.

  Research output: Contribution to journal › Review article › peer-review

  Open Access

  File
  3 Citations (Scopus)

  2 Downloads (Pure)

• Genetics of renal tumours

  Fleming, S., 1997, In: Cancer and Metastasis Reviews. 16, 1-2, p. 127-40 14 p.

  Research output: Contribution to journal › Article › peer-review
  18 Citations (Scopus)

• Genetics of Skeletal Disorders

  Hannan, F. M., Newey, P. J., Whyte, M. P. & Thakker, R. V., 2020, Bone Regulators and Osteoporosis Therapy. Stern, P. H. (ed.). Switzerland: Springer , p. 325-351 27 p. (Handbook of Experimental Pharmacology; vol. 262).

  Research output: Chapter in Book/Report/Conference proceeding › Chapter (peer-reviewed) › peer-review
  1 Citation (Scopus)

• Genetic stability of microspore-derived doubled haploids of barley: A cytological, biochemical, and molecular study

  Finnie, S. J., Forster, B. P., Chalmers, K. J., Dyer, A. F., Waugh, R. & Powell, W., 1 Jan 1991, In: Genome. 34, 6, p. 923-928 6 p.

  Research output: Contribution to journal › Article › peer-review
  15 Citations (Scopus)

• Genetic structural and functional analysis of cytochrome P450s in the CYP2D gene family

  Wolf, C. R., Modi, S., Lian, L. Y., Paine, M., Smith, G. & Roberts, G. C. K., 31 Jul 1997, In: FASEB Journal. 11, 9, p. A773-A773 1 p., P25.

  Research output: Contribution to journal › Meeting abstract › peer-review

• Genetic structure among arable populations of Capsella bursa-pastoris is linked to functional traits and in-field conditions

  Begg, G. S., Wishart, J., Young, M. W., Squire, G. R. & Iannetta, P. P. M., May 2012, In: Ecography. 35, 5, p. 446-457 12 p.

  Research output: Contribution to journal › Article › peer-review
  18 Citations (Scopus)

• Genetic studies in the nigerian population implicate an MSX1 mutation in complex oral facial clefting disorders

  Butali, A., Mossey, P. A., Adeyemo, W. L., Jezewski, P. A., Onwuamah, C. K., Ogunlewe, M. O., Ugboko, V. I., Adejuyigbe, O., Adigun, A. I., Abdur-Rahman, L. O., Onah, I. I., Audu, R. A., Idigbe, E. O., Mansilla, M. A., Dragan, E. A., Petrin, A. L., Bullard, S. A., Uduezue, A. O., Akpata, O., Osaguona, A. O., & 10 othersOlasoji, H. O., Ligali, T. O., Kejeh, B. M., Iseh, K. R., Olaitan, P. B., Adebola, A. R., Efunkoya, E., Adesina, O. A., Oluwatosin, O. M. & Murray, J. C., 2011, In: Cleft Palate-Craniofacial Journal. 48, 6, p. 646-653 8 p.

  Research output: Contribution to journal › Article › peer-review
  32 Citations (Scopus)

• Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration

  Wilman, H. R., Parisinos, C. A., Atabaki-Pasdar, N., Kelly, M., Thomas, E. L., Neubauer, S., IMI DIRECT Consortium, Mahajan, A., Hingorani, A. D., Patel, R. S., Hemingway, H., Franks, P. W., Bell, J. D., Banerjee, R. & Yaghootkar, H., Sep 2019, In: Journal of Hepatology. 71, 3, p. 594-602 9 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File
  14 Citations (Scopus)

  73 Downloads (Pure)

• Genetic studies of body mass index yield new insights for obesity biology

  Locke, A. E., Kahali, B., Berndt, S. I., Justice, A. E., Pers, T. H., Day, F. R., Powell, C., Vedantam, S., Buchkovich, M. L., Yang, J., Croteau-Chonka, D. C., Esko, T., Fall, T., Ferreira, T., Gustafsson, S., Kutalik, Z., Luan, J., Mägi, R., Randall, J. C., Winkler, T. W., & 31 othersWood, A. R., Workalemahu, T., Faul, J. D., Smith, J. A., Hua Zhao, J., Zhao, W., Chen, J., Fehrmann, R., Hedman, Å. K., Karjalainen, J., Schmidt, E. M., Absher, D., Amin, N., Anderson, D., Beekman, M., Bolton, J. L., Bragg-Gresham, J. L., Buyske, S., Demirkan, A., Deng, G., Ehret, G. B., Feenstra, B., Feitosa, M. F., Fischer, K., Goel, A., Gong, J., Jackson, A. U., Doney, A. S. F., Morris, A. D., Palmer, C. N. A. & LifeLines Cohort Study, 12 Feb 2015, In: Nature. 518, 7538, p. 197-206 10 p.

  Research output: Contribution to journal › Article › peer-review
  2627 Citations (Scopus)

• Genetic susceptibility to psoriasis and psoriatic arthritis: Implications for therapy

  Hébert, H. L., Ali, F. R., Bowes, J., Griffiths, C. E. M., Barton, A. & Warren, R. B., Mar 2012, In: British Journal of Dermatology. 166, 3, p. 474-482 9 p.

  Research output: Contribution to journal › Review article › peer-review
  60 Citations (Scopus)

• Genetic testing for Familial Hypercholesterolemia: utility beyond diagnosis

  Bigossi, M. & Siddiqui, M. K., 10 Nov 2022, (E-pub ahead of print) In: European Journal of Preventive Cardiology. 3 p.

  Research output: Contribution to journal › Editorial › peer-review

• Genetic Transformation of Candida auris via Homology-Directed Repair Using a Standard Lithium Acetate Protocol

  Bravo Ruiz, G. & Lorenz, A., 9 Jun 2022, Candida auris: Methods and Protocols. Lorenz, A. (ed.). 1 ed. Springer , p. 95-110 16 p. (Methods in Molecular Biology; vol. 2517).

  Research output: Chapter in Book/Report/Conference proceeding › Chapter (peer-reviewed) › peer-review

• Genetic validation of Aspergillus fumigatus phosphoglucomutase as a viable therapeutic target in invasive aspergillosis

  Yan, K., Stanley, M., Kowalski, B., Raimi, O., Ferenbach, A., Wei, P., Fang, W. & van Aalten, D., Jun 2022, In: Journal of Biological Chemistry. 298, 6, 20 p., 102003.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File
  19 Downloads (Pure)

• Genetic variability of Arthurdendyus triangulatus (Dendy, 1894), a non-native invasive land planarian

  Roberts, D. M., Boag, B., Hunter, F., Tarlton, J., Mackenzie, K. & Neilson, R., 1 Jul 2020, In: Zootaxa. 4808, 1, p. 38-50 13 p.

  Research output: Contribution to journal › Article › peer-review
  1 Citation (Scopus)

• Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D

  Viñuela, A., Varshney, A., van de Bunt, M., Prasad, R. B., Asplund, O., Bennett, A., Boehnke, M., Brown, A. A., Erdos, M. R., Fadista, J., Hansson, O., Hatem, G., Howald, C., Iyengar, A. K., Johnson, P., Krus, U., MacDonald, P. E., Mahajan, A., Manning Fox, J. E., Narisu, N., & 16 othersNylander, V., Orchard, P., Oskolkov, N., Panousis, N. I., Payne, A., Stitzel, M. L., Vadlamudi, S., Welch, R., Collins, F. S., Mohlke, K. L., Gloyn, A. L., Scott, L. J., Dermitzakis, E. T., Groop, L., Parker, S. C. J. & McCarthy, M. I., 30 Sep 2020, In: Nature Communications. 11, 14 p., 4912.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File
  43 Citations (Scopus)

  56 Downloads (Pure)

• Genetic Variants in CPA6 and PRPF31 are Associated with Variation in Response to Metformin in Individuals with Type 2 Diabetes

  Rotroff, D. M., Yee, S. W., Zhou, K., Marvel, S. W., Shah, H. S., Jack, J. R., Havener, T. M., Hedderson, M. M., Kubo, M., Herman, M. A., Gao, H., Mychaleckyi, J. C., McLeod, H. L., Doria, A., Giacomini, K. M., Pearson, E. R., Wagner, M. J., Buse, J. B., Motsinger-Reif, A. A. & MetGen Investigators and the ACCORD/ACCORDion Investigators, Jul 2018, In: Diabetes. 67, 7, p. 1428-1440 13 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File
  23 Citations (Scopus)

  137 Downloads (Pure)

• Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

  Ehret, G. B., Munroe, P. B., Rice, K. M., Bochud, M., Johnson, A. D., Chasman, D. I., Smith, A. V., Tobin, M. D., Verwoert, G. C., Hwang, S-J., Pihur, V., Vollenweider, P., O'Reilly, P. F., Amin, N., Bragg-Gresham, J. L., Teumer, A., Glazer, N. L., Launer, L., Zhao, J. H., Aulchenko, Y., & 31 othersHeath, S., Sober, S., Parsa, A., Luan, J., Arora, P., Dehghan, A., Zhang, F., Lucas, G., Hicks, A. A., Jackson, A. U., Peden, J. F., Tanaka, T., Wild, S. H., Rudan, I., Igl, W., Milaneschi, Y., Parker, A. N., Fava, C., Chambers, J. C., Fox, E. R., Kumari, M., Go, M. J., van der Harst, P., Kao, W. H. L., Sjogren, M., Vinay, D. G., Alexander, M., Tabara, Y., Shaw-Hawkins, S., Connell, J. M. & CARDIoGRAM Consortium, KidneyGen Consortium, EchoGen Consortium, CKDGen Consortium, Int Consortium Blood Pressure Geno, CHARGE-HF Consortium, 6 Oct 2011, In: Nature. 478, 7367, p. 103-109 7 p.

  Research output: Contribution to journal › Article › peer-review
  1561 Citations (Scopus)

• Genetic Variants in XRCC2: New Insights Into Colorectal Cancer Tumorigenesis

  Curtin, K., Lin, W-Y., George, R., Katory, M., Shorto, J., Cannon-Albright, L. A., Smith, G., Bishop, D. T., Cox, A., Camp, N. J. & Colorectal Canc Study Grp, Sep 2009, In: Cancer Epidemiology, Biomarkers and Prevention. 18, 9, p. 2476-2484 9 p.

  Research output: Contribution to journal › Article › peer-review
  36 Citations (Scopus)

• Genetic variants linked to education predict longevity

  22 Nov 2016, In: Proceedings of the National Academy of Sciences of the United States of America. 113, 47, p. 13366-13371 6 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File
  44 Citations (Scopus)

  112 Downloads (Pure)

• 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 journal › Article › peer-review

  Open Access
  13 Citations (Scopus)

• 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 journal › Meeting abstract › peer-review

• Genetic variation at fibrinogen loci and plasma fibrinogen levels

  Connor, J. M., Fowkes, F. G. R., Wood, J., Smith, F. B., Donnan, P. T. & Lowe, G. D. O., Jul 1992, In: Journal of Medical Genetics. 29, 7, p. 480-482 3 p.

  Research output: Contribution to journal › Article › peer-review

  46 Citations (Scopus)

• Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

  Saxena, R., Hivert, M-F., Langenberg, C., Tanaka, T., Pankow, J. S., Vollenweider, P., Lyssenko, V., Bouatia-Naji, N., Dupuis, J., Jackson, A. U., Kao, W. H. L., Li, M., Glazer, N. L., Manning, A. K., Luan, J., Stringham, H. M., Prokopenko, I., Johnson, T., Grarup, N., Boesgaard, T. W., & 31 othersLecoeur, C., Shrader, P., O'Connell, J., Ingelsson, E., Couper, D. J., Rice, K., Song, K., Andreasen, C. H., Dina, C., Köttgen, A., Le Bacquer, O., Pattou, F., Taneera, J., Steinthorsdottir, V., Rybin, D., Ardlie, K., Sampson, M., Qi, L., van Hoek, M., Weedon, M. N., Aulchenko, Y. S., Voight, B. F., Grallert, H., Balkau, B., Bergman, R. N., Bielinski, S. J., Bonnefond, A., Doney, A., Palmer, C. N. A., Morris, A. D. & GIANT Consortium, MAGIC Investigators, Feb 2010, In: Nature Genetics. 42, 2, p. 142-148 7 p.

  Research output: Contribution to journal › Article › peer-review
  503 Citations (Scopus)

• Genetic variation in hepatic glucose-6-phosphatase system genes in cases of sudden infant death syndrome

  Forsyth, L., Scott, H. M., Howatson, A. ., Busuttil, A., Hume, R. & Burchell, A., May 2007, In: Journal of Pathology. 212, 1, p. 112-120 9 p.

  Research output: Contribution to journal › Article › peer-review
  10 Citations (Scopus)

• Genetic variation in hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depression

  McIntosh, A. M., Simen, A. A., Evans, K. L., Hall, J., MacIntyre, D. J., Blackwood, D., Morris, A. D., Smith, B. H., Dominiczak, A., Porteous, D., Deary, I. J. & Thomson, P. A., 2012, In: Frontiers in Genetics. 3, 00116.

  Research output: Contribution to journal › Article › peer-review
  8 Citations (Scopus)

• Genetic variation in Kruppel like factor 15 is associated with left ventricular hypertrophy in patients with type 2 diabetes: discovery and replication cohorts

  Patel, S. K., Wai, B., Lang, C. C., Levin, D., Palmer, C. N. A., Parry, H. M., Velkoska, E., Harrap, S. B., Srivastava, P. M. & Burrell, L. M., Apr 2017, In: EBioMedicine. 18, p. 171-178 8 p.

  Research output: Contribution to journal › Article › peer-review

  Open Access

  File
  13 Citations (Scopus)

  85 Downloads (Pure)

• Genetic variation in the beta2-adrenergic receptor but not catecholamine-O-methyltransferase predisposes to chronic pain: results from the 1958 British Birth Cohort Study

  Hocking, L. J., Smith, B. H., Jones, G. T., Reid, D. M., Strachan, D. P. & Macfarlane, G. J., Apr 2010, In: Pain. 149, 1, p. 143-151 9 p.

  Research output: Contribution to journal › Article › peer-review
  78 Citations (Scopus)

• Genetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformations in hereditary hemorrhagic telangiectasia 1 (HHT1) and may influence expression of PTPN14

  Letteboer, T. G. W., Benzinou, M., Merrick, C., Quigley, D., Zhau, K., Kim, I. J., To, M. D., Jablons, D., Van Amstel, J. K. P., Westermann, C., Giraud, S., Dupuis-Girod, S., Lesca, G., Berg, J., Balmain, A. & Akhurst, R. J., 12 Mar 2015, In: Frontiers in Genetics. 6, 9 p., 67.

  Research output: Contribution to journal › Article › peer-review
  14 Citations (Scopus)