Edinburgh Research Explorer

Centre for Genomic and Experimental Medicine

Organisational unit: Research Centre

  1. Chapter (peer-reviewed) › Research › Peer-reviewed
  2. Adhesion molecules in bone remodelling

    Hughes, D. E. & Salter, D., 16 May 1997, Adhesion Molecules in Health and Disease. Paul, L. & Issekutz, T. (eds.). Marcel Dekker Inc., p. 427-444

    Research output: Chapter in Book/Report/Conference proceedingChapter (peer-reviewed)

  3. Connective Tissue Responses to Mechanical Stresses

    Salter, D., 8 Nov 2010, Rheumatology. Hochberg, M., Silman, A., Smolen, J., Weinblatt, M. & Weisman, M. (eds.). 5 ed. Elsevier - Health Sciences Division

    Research output: Chapter in Book/Report/Conference proceedingChapter (peer-reviewed)

  4. Connective Tissue Responses to Mechanical Stresses

    Salter, D., 13 Jun 2014, Rheumatology. Hochberg, M. C., Silman, A. J., Smolen, J. S., Weinblatt, M. & Weisman, M. (eds.). 6 ed. Elsevier - Health Sciences Division

    Research output: Chapter in Book/Report/Conference proceedingChapter (peer-reviewed)

  5. Data integration in eHealth: a domain/disease specific roadmap

    Ure, J., Procter, R., Martone, M., Porteous, D., Lloyd, S., Lawrie, S., Job, D., Baldock, R., Philp, A., Liewald, D., Rakebrandt, F., Blaikie, A., McKay, C., Anderson, S., Ainsworth, J., van Hemert, J., Blanquer, I., Sinnott, R., Barillot, C., Gibaud, F. B. & 17 others, Williams, A., Hartswood, M., Watson, P., Smith, L., Burger, A., Kennedy, J., Gonzalez-Velez, H., Stevens, R., Corcho, O., Morton, R., Linksted, P., Deschenes, M., McGilchrist, M., Johnson, P., Voss, A., Gertz, R. & Wardlaw, J., 2007, From Genes to Personalized HealthCare: Grid Solutions for the Life Sciences. Vol. 126. p. 144-53 10 p.

    Research output: Chapter in Book/Report/Conference proceedingChapter (peer-reviewed)

  6. Disease-associated sequence variations in factor H: A structural biology approach

    Herbert, A. P., Soares, D. C., Pangburn, M. K. & Barlow, P. N., 2006, Current Topics in Complement. Springer-Verlag GmbH, Vol. 586. p. 313-327 15 p. (Advances in Experimental Medicine and Biology ).

    Research output: Chapter in Book/Report/Conference proceedingChapter (peer-reviewed)

  7. Genetics of Paget's disease of bone

    Albagha, O., 2013, Genetics of bone biology and skeletal disease. USA: Academic Press, p. 295-308

    Research output: Chapter in Book/Report/Conference proceedingChapter (peer-reviewed)

  8. Optimisation of quantitative real-time PCR conditions for studies in cartilage mechanobiology

    Salter, D. & Chowdhury, T., 2 Nov 2010, 3D Cell Culture Methods and Protocols . Haycock, J. (ed.). 1 ed. HUMANA PRESS INC, Vol. 695. (Methods in Molecular Biology).

    Research output: Chapter in Book/Report/Conference proceedingChapter (peer-reviewed)

  9. Pathology and Pathogenesis of Osteoarthritis

    Aigner, T., Schmitz, N. & Salter, D., 13 Jun 2014, Rheumatology . Hochberg, M., Silman, A., Smolen, J., Weinblatt, M. & Weisman, M. (eds.). 6 ed. Elsevier - Health Sciences Division

    Research output: Chapter in Book/Report/Conference proceedingChapter (peer-reviewed)

  10. The impact of mechanical stress on the pathophysiology of Osteoarthritis.

    Nuki, G. & Salter, D., 2007, Osteoarthritis : A Companion to Rheumatology . Sharma, L. & Berenbaum, F. (eds.). Elsevier Health Sciences

    Research output: Chapter in Book/Report/Conference proceedingChapter (peer-reviewed)

  11. Paper › Research › Not peer-reviewed
  12. Prediction of major depressive disorder within the Generation Scotland cohort

    Bermingham, M., 30 Oct 2015, (Unpublished).

    Research output: Contribution to conferencePaper

  13. Paper › Research › Peer-reviewed
  14. Effect of missing data and sample size on the performance of genotype-environment association methods

    Xuereb, A., Stahlke, A., Bermingham, M., Brown, M., Nonaka, E., Razgour, O., Pavinato, V., Andrews, K. R., Joost, S., Landguth, E. L., Manel, S. & Forester, B. R., 12 Apr 2017.

    Research output: Contribution to conferencePaper

  15. Machine learning can improve prediction of depression in Generation Scotland

    Bermingham, M., 23 Nov 2015.

    Research output: Contribution to conferencePaper

  16. Poster › Research › Not peer-reviewed
  17. Poster › Research › Peer-reviewed
  18. Abstract › Research › Peer-reviewed
  19. QuPath: Digital Pathology for Everyone

    Bankhead, P., 2019, (Unpublished).

    Research output: Contribution to conferenceAbstract

  20. Other › Research › Not peer-reviewed
  21. Other › Research › Peer-reviewed
  22. Characterisation of atherosclerotic plaque by spectral analysis of 30 MHz intravascular ultrasound radio frequency data

    Spencer, T., Ramo, M. P., Salter, D., Sutherland, G., Fox, K. A. & Mcdicken, W. N., 1997, p. 1073-1076.

    Research output: Contribution to conferenceOther

  23. Article › Research › Not peer-reviewed
  24. Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

    Davies, G., Lam, M., Harris, S. E., Trampush, J. W., Luciano, M., Hill, W. D., Hagenaars, S. P., Ritchie, S. J., Marioni, R. E., Fawns-Ritchie, C., Liewald, D. C. M., Okely, J. A., Ahola-Olli, A. V., Barnes, C. L. K., Bertram, L., Bis, J. C., Burdick, K. E., Christoforou, A., DeRosse, P., Djurovic, S. & 202 others, Espeseth, T., Giakoumaki, S., Giddaluru, S., Gustavson, D. E., Hayward, C., Hofer, E., Ikram, M. A., Karlsson, R., Knowles, E., Lahti, J., Leber, M., Li, S., Mather, K. A., Melle, I., Morris, D., Oldmeadow, C., Palviainen, T., Payton, A., Pazoki, R., Petrovic, K., Reynolds, C. A., Sargurupremraj, M., Scholz, M., Smith, J. A., Smith, A. V., Terzikhan, N., Thalamuthu, A., Trompet, S., van der Lee, S. J., Ware, E. B., Windham, B. G., Wright, M. J., Yang, J., Yu, J., Ames, D., Amin, N., Amouyel, P., Andreassen, O. A., Armstrong, N. J., Assareh, A. A., Attia, J. R., Attix, D., Avramopoulos, D., Bennett, D. A., Böhmer, A. C., Boyle, P. A., Brodaty, H., Campbell, H., Cannon, T. D., Cirulli, E. T., Congdon, E., Conley, E. D., Corley, J., Cox, S. R., Dale, A. M., Dehghan, A., Dick, D., Dickinson, D., Eriksson, J. G., Evangelou, E., Faul, J. D., Ford, I., Freimer, N. A., Gao, H., Giegling, I., Gillespie, N. A., Gordon, S. D., Gottesman, R. F., Griswold, M. E., Gudnason, V., Harris, T. B., Hartmann, A. M., Hatzimanolis, A., Heiss, G., Holliday, E. G., Joshi, P. K., Kähönen, M., Kardia, S. L. R., Karlsson, I., Kleineidam, L., Knopman, D. S., Kochan, N. A., Konte, B., Kwok, J. B., Le Hellard, S., Lee, T., Lehtimäki, T., Li, S-C., Lill, C. M., Liu, T., Koini, M., London, E., Longstreth, W. T., Lopez, O. L., Loukola, A., Luck, T., Lundervold, A. J., Lundquist, A., Lyytikäinen, L-P., Martin, N. G., Montgomery, G. W., Murray, A. D., Need, A. C., Noordam, R., Nyberg, L., Ollier, W., Papenberg, G., Pattie, A., Polasek, O., Poldrack, R. A., Psaty, B. M., Reppermund, S., Riedel-Heller, S. G., Rose, R. J., Rotter, J. I., Roussos, P., Rovio, S. P., Saba, Y., Sabb, F. W., Sachdev, P. S., Satizabal, C. L., Schmid, M., Scott, R. J., Scult, M. A., Simino, J., Slagboom, P. E., Smyrnis, N., Soumaré, A., Stefanis, N. C., Stott, D. J., Straub, R. E., Sundet, K., Taylor, A. M., Taylor, K. D., Tzoulaki, I., Tzourio, C., Uitterlinden, A., Vitart, V., Voineskos, A. N., Kaprio, J., Wagner, M., Wagner, H., Weinhold, L., Wen, K. H., Widen, E., Yang, Q., Zhao, W., Adams, H. H. H., Arking, D. E., Bilder, R. M., Bitsios, P., Boerwinkle, E., Chiba-Falek, O., Corvin, A., De Jager, P. L., Debette, S., Donohoe, G., Elliott, P., Fitzpatrick, A. L., Gill, M., Glahn, D. C., Hägg, S., Hansell, N. K., Hariri, A. R., Ikram, M. K., Jukema, J. W., Vuoksimaa, E., Keller, M. C., Kremen, W. S., Launer, L., Lindenberger, U., Palotie, A., Pedersen, N. L., Pendleton, N., Porteous, D. J., Räikkönen, K., Raitakari, O. T., Ramirez, A., Reinvang, I., Rudan, I., Dan Rujescu, Schmidt, R., Schmidt, H., Schofield, P. W., Schofield, P. R., Starr, J. M., Steen, V. M., Trollor, J. N., Turner, S. T., Van Duijn, C. M., Villringer, A., Weinberger, D. R., Weir, D. R., Wilson, J. F., Malhotra, A., McIntosh, A. M., Gale, C. R., Seshadri, S., Mosley, T. H., Bressler, J., Lencz, T. & Deary, I. J., 1 May 2019, In : Nature Communications. 10, 1, p. 2068

    Research output: Contribution to journalArticle

  25. Cohort profile for the STratifying Resilience and Depression Longitudinally (STRADL) study: A depression-focused investigation of Generation Scotland, using detailed clinical, cognitive, and neuroimaging assessments

    Habota, T., Sandu, A., Waiter, G. D., Mcneil, C. J., Steele, J. D., Macfarlane, J. A., Whalley, H. C., Valentine, R., Younie, D., Crouch, N., Hawkins, E. L., Hirose, Y., Romaniuk, L., Milburn, K., Buchan, G., Coupar, T., Stirling, M., Jagpal, B., Maclennan, B., Priba, L. & 20 others, Harris, M. A., Hafferty, J. D., Adams, M. J., Campbell, A. I., Macintyre, D. J., Pattie, A., Murphy, L., Reynolds, R. M., Elliot, R., Penton-voak, I. S., Munafò, M. R., Evans, K. L., Seckl, J. R., Wardlaw, J. M., Lawrie, S. M., Haley, C. S., Porteous, D. J., Deary, I. J., Murray, A. D. & Mcintosh, A. M., 25 Nov 2019, In : Wellcome Open Research . 4, p. 185

    Research output: Contribution to journalArticle

  26. Editorial: Early corticosteroids in ulcerative colitis

    Kennedy, N. A. & Satsangi, J., Sep 2014, In : Alimentary Pharmacology and Therapeutics. 40, 6, p. 727

    Research output: Contribution to journalArticle

  27. Genetic and environmental determinants of stressful life events and their overlap with depression and neuroticism

    Clarke, T., Zeng, Y., Navrady, L., Xia, C., Haley, C., Campbell, A., Navarro, P., Amador, C., Adams, M. J., Howard, D. M., Soler, A., Hayward, C., Thomson, P. A., Smith, B. H., Padmanabhan, S., Hocking, L. J., Hall, L. S., Porteous, D. J., Deary, I. J. & Mcintosh, A. M., 14 Feb 2018, In : Wellcome Open Research . 3, p. 11

    Research output: Contribution to journalArticle

  28. Article › Research › Peer-reviewed
  29. "Blind imagination'': Brain activation after loss of the mind's eye

    Zeman, A., McGonigle, D., Gountouna, E., Torrens, L., Della Sala, S. & Logie, R., Feb 2007, In : Journal of Neurology Neurosurgery & Psychiatry. 78, 2, p. 209-209 1 p.

    Research output: Contribution to journalArticle

  30. 11β-Hydroxysteroid Dehydrogenase Type 1, But Not Type 2, Deficiency Worsens Acute Inflammation and Experimental Arthritis in Mice

    Coutinho, A. E., Gray, M., Brownstein, D. G., Salter, D. M., Sawatzky, D. A., Clay, S., Gilmour, J. S., Seckl, J. R., Savill, J. S. & Chapman, K. E., Jan 2012, In : Endocrinology . 153, 1, p. 234-240 7 p.

    Research output: Contribution to journalArticle

  31. 5-fluorouracil steady state pharmacokinetics and outcome in patients receiving protracted venous infusion for advanced colorectal cancer

    Jodrell, D. I., Stewart, M., Aird, R., Knowles, G., Bowman, A., Wall, L., Cummings, J. & Mclean, C., 2001, In : British Journal of Cancer. 84, 5, p. 600-603

    Research output: Contribution to journalArticle

  32. 708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits

    Thomson, P. A., Parla, J. S., McRae, A. F., Kramer, M., Ramakrishnan, K., Yao, J., Soares, D. C., McCarthy, S., Morris, S. W., Cardone, L., Cass, S., Ghiban, E., Hennah, W., Evans, K. L., Rebolini, D., Millar, J. K., Harris, S. E., Starr, J. M., MacIntyre, D. J., Generation Scotland & 7 others, McIntosh, A. M., Watson, J. D., Deary, I. J., Visscher, P. M., Blackwood, D. H., McCombie, W. R. & Porteous, D. J., 1 Jun 2014, In : Molecular Psychiatry. 19, 6, p. 668-675 8 p.

    Research output: Contribution to journalArticle

  33. APOE E4 status predicts age-related cognitive decline in the ninth decade: longitudinal follow-up of the Lothian Birth Cohort 1921

    Schiepers, O. J. G., Harris, S. E., Gow, A. J., Pattie, A., Brett, C. E., Starr, J. & Deary, I. J., Mar 2012, In : Molecular Psychiatry. 17, 3, p. 315-324

    Research output: Contribution to journalArticle

  34. A 25-year old woman with recurrent episodes of collapse and loss of consciousness

    Wildman, J., Baker, M. R., Price, D. A., Tiwari, S., Kumar, H., Rice, G. I., Crow, Y. & Thomas, R. H., 1 May 2020, In : Neurology.

    Research output: Contribution to journalArticle

  35. A 29-year-old male with chest pain and haemoptysis

    Young, E. C., Mills, N. L., Henriksen, P. A., Murchison, J. T., Salter, D. M., Hayward, R. L., Newby, D. E. & Simpson, A. J., 2008, In : European Respiratory Journal. 32, 5, p. 1404-7 4 p.

    Research output: Contribution to journalArticle

  36. A 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardation

    Pickard, B. S., Hollox, E. J., Malloy, M. P., Porteous, D. J., Blackwood, D. H., Armour, J. A. & Muir, W. J., 2004, In : BMC Medical Genetics. 5, p. 21 1 p.

    Research output: Contribution to journalArticle

  37. A 5' promoter region SNP in NRG1 is associated with schizophrenia risk and type III isoform expression

    Nicodemus, K. K., Law, A. J., Luna, A., Vakkalanka, R., Straub, R. E., Kleinman, J. E. & Weinberger, D. R., Aug 2009, In : Molecular Psychiatry. 14, 8, p. 741-3 3 p.

    Research output: Contribution to journalArticle

  38. A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidate region for bipolar affective disorder

    Evans, K., Le Hellard, S., Morris, S. W., Lawson, D., Whitton, C., Semple, C., Fantes, J. A., Torrance, H. S., Malloy, M. P., Maule, J. C., Humphray, S. J., Ross, M. T., Bentley, D. R., Muir, W., Blackwood, D. & Porteous, D. J., 2001, In : Genomics. 71, 3, p. 315-23 9 p.

    Research output: Contribution to journalArticle

  39. A 700-kb physical map of a region of 16q23.2 homozygously deleted in multiple cancers and spanning the common fragile site FRA16D

    Paige, A. J., Taylor, K. J., Stewart, A., Sgouros, J. G., Gabra, H., Sellar, G. C., Smyth, J. F., Porteous, D. J. & Watson, J. E., 2000, In : Cancer Research. 60, 6, p. 1690-7 8 p.

    Research output: Contribution to journalArticle

  40. A British Society of Paediatric Gastroenterology, Hepatology and Nutrition survey of the effectiveness and safety of adalimumab in children with inflammatory bowel disease

    Russell, R. K., Wilson, M. L., Loganathan, S., Bourke, B., Kiparissi, F., Mahdi, G., Torrente, F., Rodrigues, A., Davies, I., Thomas, A., Akobeng, A. K., Fagbemi, A., Hyer, W., Spray, C., Vaish, S., Rogers, P., McGrogan, P., Heuschkel, R. B., Ayub, N., Fell, J. M. & 8 others, Afzal, N. A., Green, M., Murphy, M. S., Rao, P., Shah, N., Ho, G. -T., Naik, S. & Wilson, D. C., 15 Apr 2011, In : Alimentary Pharmacology and Therapeutics. 33, 8, p. 946-953 8 p.

    Research output: Contribution to journalArticle

  41. A Class III Semaphorin (Sema3e) Inhibits Mouse Osteoblast Migration and Decreases Osteoclast Formation In Vitro

    Hughes, A., Kleine-Albers, J., Helfrich, M. H., Ralston, S. H. & Rogers, M. J., Feb 2012, In : Calcified Tissue International. 90, 2, p. 151-162 12 p.

    Research output: Contribution to journalArticle

  42. A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway is Associated with Major Depressive Disorder

    Zeng, Y., Navarro, P., Fernandez-pujals, A. M., Hall, L. S., Clarke, T., Thomson, P. A., Smith, B. H., Hocking, L. J., Padmanabhan, S., Hayward, C., Macintyre, D. J., Wray, N. R., Deary, I., Porteous, D. J., Haley, C. S. & Mcintosh, A. M., 15 Feb 2017, In : Biological Psychiatry. 81, 4, p. 336-346

    Research output: Contribution to journalArticle

  43. A DNA methylation biomarker of alcohol consumption

    Liu, C., Marioni, R. E., Hedman, K. K., Pfeiffer, L., Tsai, P. C., Reynolds, L. M., Just, A. C., Duan, Q., Boer, C. G., Tanaka, T., Elks, C. E., Aslibekyan, S., Brody, J. A., Kühnel, B., Herder, C., Almli, L. M., Zhi, D., Wang, Y., Huan, T., Yao, C. & 53 others, Mendelson, M. M., Joehanes, R., Liang, L., Love, S. A., Guan, W., Shah, S., McRae, A. F., Kretschmer, A., Prokisch, H., Strauch, K., Peters, A., Visscher, P. M., Wray, N. R., Guo, X., Wiggins, K. L., Smith, A. K., Binder, E. B., Ressler, K. J., Irvin, M. R., Absher, D. M., Hernandez, D., Ferrucci, L., Bandinelli, S., Lohman, K., Ding, J., Trevisi, L., Gustafsson, S., Sandling, J. H., Stolk, L., Uitterlinden, A. G., Yet, I., Castillo-Fernandez, J. E., Spector, T. D., Schwartz, J. D., Vokonas, P., Lind, L., Li, Y., Fornage, M., Arnett, D. K., Wareham, N. J., Sotoodehnia, N., Ong, K. K., van Meurs, J. B. J., Conneely, K. N., Baccarelli, A. A., Deary, I. J., Bell, J. T., North, K. E., Liu, Y., Waldenberger, M., London, S. J., Ingelsson, E. & Levy, D., 15 Nov 2016, In : Molecular Psychiatry.

    Research output: Contribution to journalArticle

  44. A DNA nanoswitch incorporating the fluorescent base analogue 2-aminopurine detects single nucleotide mismatches in unlabelled targets

    Campbell, C. J., Mountford, C. P., Stoquert, H. C., Buck, A. H., Dickinson, P., Ferapontova, E., Terry, J. G., Beattie, J. S., Walton, A. J., Crain, J., Ghazal, P. & Mount, A. R., 2009, In : Analyst. 134, 9, p. 1873-1879 7 p.

    Research output: Contribution to journalArticle

  45. A Dominantly Inherited 5' UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer

    Evans, D. G. R., van Veen, E. M., Byers, H. J., Wallace, A. J., Ellingford, J. M., Beaman, G., Santoyo-Lopez, J., Aitman, T. J., Eccles, D. M., Lalloo, F. I., Smith, M. J. & Newman, W. G., 2 Aug 2018, In : American Journal of Human Genetics. 103, 2, p. 213-220 8 p.

    Research output: Contribution to journalArticle

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

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

    Research output: Contribution to journalArticle

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

    van Zuydam, N. R., Ahlqvist, E., Sandholm, N., Deshmukh, H., Rayner, N. W., Abdalla, M., Ladenvall, C., Ziemek, D., Fauman, E., Robertson, N. R., McKeigue, P. M., Valo, E., Forsblom, C., Harjutsalo, V., Perna, A., Rurali, E., Marcovecchio, M. L., Igo, R. P., Salem, R. M., Perico, N. & 31 others, Lajer, M., Käräjämäki, A., Imamura, M., Kubo, M., Takahashi, A., Sim, X., Liu, J., van Dam, R. M., Jiang, G., Tam, C. H. T., Luk, A. O. Y., Lee, H. M., Lim, C. K. P., Szeto, C. C., So, W. Y., Chan, J. C. N., Ang, S. F., Dorajoo, R., Wang, L., Hua Clara, T. S., McKnight, A-J., Duffy, S., Pezzolesi, M. G., Consortium, G., Marre, M., Gyorgy, B., Hadjadj, S., Hiraki, L. T., Ahluwalia, T. S., Colhoun, H. M. & FINNDIANE Study centres, 1 Jul 2018, In : Diabetes .

    Research output: Contribution to journalArticle

  48. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

    Sung, Y. J., Winkler, T. W., de Las Fuentes, L., Bentley, A. R., Brown, M. R., Kraja, A. T., Schwander, K., Ntalla, I., Guo, X., Franceschini, N., Lu, Y., Cheng, Y-C., Sim, X., Vojinovic, D., Marten, J., Musani, S. K., Li, C., Feitosa, M. F., Kilpeläinen, T. O., Richard, M. A. & 31 others, Noordam, R., Aslibekyan, S., Aschard, H., Bartz, T. M., Dorajoo, R., Liu, Y., Manning, A. K., Rankinen, T., Smith, A. V., Tajuddin, S. M., Tayo, B. O., Warren, H. R., Zhao, W., Zhou, Y., Matoba, N., Sofer, T., Alver, M., Amini, M., Boissel, M., Chai, J. F., Chen, X., Divers, J., Harris, S. E., Campbell, A., Hagenaars, S. P., Polasek, O., Rudan, I., Starr, J. M., Deary, I. J., Hayward, C. & CHARGE Neurology Working Group, Mar 2018, In : American Journal of Human Genetics. 102, 3

    Research output: Contribution to journalArticle

  49. A Multi-Cohort Study of Polymorphisms in the GH/IGF Axis and Physical Capability: The HALCyon Programme

    Alfred, T., Ben-Shlomo, Y., Cooper, R., Hardy, R., Cooper, C., Deary, I. J., Gaunt, T. R., Gunnell, D., Harris, S. E., Kumari, M., Martin, R. M., Sayer, A. A., Starr, J. M., Kuh, D., Day, I. N. M. & HALCyon Study Team, 10 Jan 2012, In : PLoS ONE. 7, 1, p. 186-195 10 p., e29883.

    Research output: Contribution to journalArticle

  50. A Novel Urinary Peptidomic Classifier Predicts Incident Heart Failure

    Zhang, Z., Ravassa, S., Nkuipou-Kenfack, E., Yang, W. Y., Kerr, S., Koeck, T., Campbell, A., Kuznetsova, T., Mischak, H., Padmanabhan, S., Dominiczak, A. F., Delles, C. & Staessen, J. A., 7 Aug 2017, In : Journal of the American Heart Association. 6, 8, 12 p.

    Research output: Contribution to journalArticle

  51. A POT1 mutation implicates defective telomere end fill-in and telomere truncations in Coats plus

    Takai, H., Jenkinson, E., Kabir, S., Babul-hirji, R., Najm-tehrani, N., Chitayat, D. A., Crow, Y. J. & De Lange, T., 1 Apr 2016, In : Genes & Development. 30, 7, p. 812-826

    Research output: Contribution to journalArticle

  52. A Phase I/IIa Safety and Efficacy Study of Nebulized Liposome-mediated Gene Therapy for Cystic Fibrosis Supports a Multidose Trial

    Alton, E. W. F. W., Boyd, A. C., Porteous, D. J., Davies, G., Davies, J. C., Griesenbach, U., Higgins, T. E., Gill, D. R., Hyde, S. C., Innes, J. A. & UK Cystic Fibrosis Gene Therapy Consortium *, 1 Dec 2015, In : American Journal of Respiratory and Critical Care Medicine. 192, 11, p. 1389-92 4 p.

    Research output: Contribution to journalArticle

  53. A Quantitative Chloride Channel Conductance Assay for Efficacy Testing of AAV.BEST1

    Wood, S. R., McClements, M. E., Martinez-Fernandez de la Camara, C., Patrício, M. I., Uggenti, C., Sekaran, S., Barnard, A. R., Manson, F. D. & MacLaren, R. E., Apr 2019, In : Human gene therapy methods. 30, 2, p. 44-52 9 p.

    Research output: Contribution to journalArticle

  54. A Rare Haplotype in the Upstream Regulatory Region of COL1A1 Is Associated With Reduced Bone Quality and Hip Fracture

    Jin, H., Stewart, T. L., Van't Hof, R., Reid, D. M., Aspden, R. M. & Ralston, S., Mar 2009, In : Journal of Bone and Mineral Research. 24, 3, p. 448-454 7 p.

    Research output: Contribution to journalArticle

  55. A Role for the Nonsense-Mediated mRNA Decay Pathway in Maintaining Genome Stability in Caenorhabditis elegans

    González-Huici, V., Wang, B. & Gartner, A., 20 Jun 2017, In : Genetics. 206, 4, p. 1853-1864 12 p.

    Research output: Contribution to journalArticle

  56. A Schizosaccharomyces pombe artificial chromosome large DNA cloning system

    Young, D. J., Nimmo, E. R. & Allshire, R. C., 1998, In : Nucleic Acids Research. 26, 22, p. 5052-60 9 p.

    Research output: Contribution to journalArticle

  57. A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome

    Rutsch, F., Macdougall, M., Lu, C., Buers, I., Mamaeva, O., Nitschke, Y., Rice, G., Erlandsen, H., Kehl, H., Thiele, H., Nürnberg, P., Höhne, W., Crow, Y., Feigenbaum, A. & Hennekam, R., 1 Feb 2015, In : American Journal of Human Genetics. 96, 2, p. 275-282

    Research output: Contribution to journalArticle

  58. A Systematic Review of the Role of Vitamin D on Neuromuscular Remodelling Following Exercise and Injury

    Minshull, C., Biant, L. C., Ralston, S. H. & Gleeson, N., 1 May 2016, In : Calcified Tissue International. 98, 5, p. 426-437 12 p.

    Research output: Contribution to journalArticle

  59. A Variant in MCF2L Is Associated with Osteoarthritis

    Day-Williams, A. G., Southam, L., Panoutsopoulou, K., Rayner, N. W., Esko, T., Estrada, K., Helgadottir, H. T., Hofman, A., Ingvarsson, T., Jonsson, H., Keis, A., Kerkhof, H. J. M., Thorleifsson, G., Arden, N. K., Carr, A., Chapman, K., Deloukas, P., Loughlin, J., McCaskie, A., Ollier, W. E. R. & 26 others, Ralston, S. H., Spector, T. D., Wallis, G. A., Wilkinson, J. M., Aslam, N., Birell, F., Carluke, I., Joseph, J., Rai, A., Reed, M., Walker, K., Doherty, S. A., Jonsdottir, I., Maciewicz, R. A., Muir, K. R., Metspalu, A., Rivadeneira, F., Stefansson, K., Styrkarsdottir, U., Uitterlinden, A. G., van Meurs, J. B. J., Zhang, W., Valdes, A. M., Doherty, M., Zeggini, E. & ArcOGEN Consortium, 9 Sep 2011, In : American Journal of Human Genetics. 89, 3, p. 446-450 5 p.

    Research output: Contribution to journalArticle

  60. A case of hypocomplementaemic urticarial vasculitis with cardiac valve involvement successfully treated with cyclophosphamide and high-dose glucocorticoids

    Hauser, B., McRorie, E., McKay, N., Brenn, T. & Amft, N., 5 Apr 2014, In : International journal of rheumatic diseases.

    Research output: Contribution to journalArticle

  61. A case-control association study and family-based expression analysis of the bipolar disorder candidate gene PI4K2B

    Houlihan, L., Christoforou, A., Arbuckle, M. I., Torrance, H. S., Anderson, S. M., Muir, W., Porteous, D. J., Blackwood, D. H. & Evans, K. L., Dec 2009, In : Journal of Psychiatric Research. 43, 16, p. 1272-1277 6 p.

    Research output: Contribution to journalArticle

  62. A case-control association study on the NPAS3 gene

    Pickard, B., Christoforou, A., Thomson, P., Evans, K., Morris, S., Porteous, D., Blackwood, D. & Muir, W., 2006, In : American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 141B, 7, p. 761 1 p.

    Research output: Contribution to journalArticle

  63. A case-control study in an Orcadian population investigating the relationship between human plasma N-glycans and metabolic syndrome.

    McLachlan, F., Timofeeva, M., Bermingham, M., Wild, S., Rudan, I., Lauc, G., Wang, W., Campbell, H., Wilson, J. & Theodoratou, E., 8 Oct 2016, In : Journal of glycomics & Lipidomics.

    Research output: Contribution to journalArticle

  64. A clinical study assessing the tolerability and biological effects of infliximab, a TNF-alpha inhibitor, in patients with advanced cancer

    Brown, E. R., Charles, K. A., Hoare, S. A., Rye, R. L., Jodrell, D. I., Aird, R. E., Vora, R., Prabhakar, U., Nakada, M., Corringham, R. E., DeWitte, M., Sturgeon, C., Propper, D., Balkwill, F. R. & Smyth, J. F., Jul 2008, In : Annals of oncology. 19, 7, p. 1340-1346 7 p.

    Research output: Contribution to journalArticle

  65. A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence

    Hill, W. D., Marioni, R., Maghzian, O., Ritchie, S. J., Hagenaars, S. P., McIntosh, A., Gale, C., Davies, G. & Deary, I., Feb 2019, In : Molecular Psychiatry. 24, 2, p. 169-181

    Research output: Contribution to journalArticle

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

    K Siddiqui, M., 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. M., 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, 29 Aug 2017, In : European Heart Journal.

    Research output: Contribution to journalArticle

  67. A common variant in the 3'UTR of the GRIK4 glutamate receptor gene affects transcript abundance and protects against bipolar disorder

    Pickard, B. S., Knight, H. M., Hamilton, R. S., Soares, D. C., Walker, R., Boyd, J. K. F., Machell, J., Maclean, A., McGhee, K. A., Condie, A., Porteous, D. J., Clair, D. S., Davis, I., Blackwood, D. H. R. & Muir, W. J., 30 Sep 2008, In : Proceedings of the National Academy of Sciences. 105, 39, p. 14940-14945 6 p.

    Research output: Contribution to journalArticle

  68. A contiguous clone map over 3 Mb on the long arm of chromosome 11 across a balanced translocation associated with schizophrenia

    Evans, K. L., Brown, J., Shibasaki, Y., Devon, R. S., He, L., Arveiler, B., Christie, S., Maule, J. C., Baillie, D. & Slorach, E. M., 10 Aug 1995, In : Genomics. 28, 3, p. 420-8 9 p.

    Research output: Contribution to journalArticle

  69. A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression

    Knight, H. M., Pickard, B. S., Maclean, A., Malloy, M. P., Soares, D. C., McRae, A. F., Condie, A., White, A., Hawkins, W., McGhee, K., van Beck, M., MacIntyre, D. J., Starr, J., Deary, I. J., Visscher, P. M., Porteous, D. J., Cannon, R. E., St Clair, D., Muir, W. J. & Blackwood, D. H., Dec 2009, In : American Journal of Human Genetics. 85, 6, p. 833-846 14 p.

    Research output: Contribution to journalArticle

  70. A demonstration using mouse models that successful gene therapy for cystic fibrosis requires only partial gene correction

    Dorin, J. R., Farley, R., Webb, S., Smith, S. N., Farini, E., Delaney, S. J., Wainwright, B. J., Alton, E. W. & Porteous, D. J., 1996, In : Gene Therapy. 3, 9, p. 797-801 5 p.

    Research output: Contribution to journalArticle

  71. A dominant role for the methyl-CpG-binding protein Mbd2 in controlling Th2 induction by dendritic cells

    Cook, P. C., Owen, H., Deaton, A. M., Borger, J. G., Brown, S. L., Clouaire, T., Jones, G. R., Jones, L., Lundie, R. J., Marley, A. K., Morrison, V. L., Phythian-Adams, A. T., Wachter, E., Webb, L. M., Sutherland, T. E., Thomas, G. D., Grainger, J. R., Selfridge, J., McKenzie, A. N. J., Allen, J. E. & 5 others, Fagerholm, S. C., Maizels, R. M., Ivens, A. C., Bird, A. & Macdonald, A. S., 24 Apr 2015, In : Nature Communications. 6, 6920.

    Research output: Contribution to journalArticle

  72. A framework for the development of guidelines for the management of glucocorticoid-induced osteoporosis

    Lekamwasam, S., Adachi, J. D., Agnusdei, D., Bilezikian, J., Boonen, S., Borgstrom, F., Cooper, C., Diez Perez, A., Eastell, R., Hofbauer, L. C., Kanis, J. A., Langdahl, B. L., Lesnyak, O., Lorenc, R., McCloskey, E., Messina, O. D., Napoli, N., Obermayer-Pietsch, B., Ralston, S. H., Sambrook, P. N. & 7 others, Silverman, S., Sosa, M., Stepan, J., Suppan, G., Wahl, D. A., Compston, J. E. & Joint IOF-ECTS GIO Guidelines Work, Sep 2012, In : Osteoporosis international. 23, 9, p. 2257-2276 20 p.

    Research output: Contribution to journalArticle

  73. A functional polymorphism under positive evolutionary selection in ADRB2 is associated with human intelligence with opposite effects in the young and the elderly.

    Bochdanovits, Z., Gosso, F. M., Berg, L., Rizzu, P., Polderman, T. J. C., Pardo, L. M., Houlihan, L., Luciano, M., Starr, J., Harris, S. E., Deary, I. J., Geus, E. J. C., Boomsma, D. I., Heutink, P. & Posthuma, D., 1 Jan 2009, In : Behavior Genetics. 39, 1, p. 15-23

    Research output: Contribution to journalArticle

  74. A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition

    Harris, S. E., Fox, H., Wright, A. F., Hayward, C., Starr, J., Whalley, L. J. & Deary, I. J., 2 Jul 2007, In : BMC Genetics. 8, p. - 18 p., 43.

    Research output: Contribution to journalArticle

  75. A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42

    Macgregor, S., Visscher, P. M., Knott, S. A., Thomson, P., Porteous, D. J., Millar, J. K., Devon, R. S., Blackwood, D. & Muir, W. J., 2004, In : Molecular Psychiatry. 9, 12, p. 1083-1090 8 p.

    Research output: Contribution to journalArticle

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

    Meng, W., Chan, B. W., Harris, C., Freidin, M. B., Hebert, H. L., Adams, M. J., Campbell, A., Hayward, C., Zheng, H., Zhang, X., Colvin, L. A., Hales, T. G., Palmer, C. N. A., Williams, F. M. K., Mcintosh, A. & Smith, B. H., 3 Apr 2020, In : Human Molecular Genetics.

    Research output: Contribution to journalArticle

  77. A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing

    Davies, G., Harris, S., Reynolds, C. A., Payton, A., Knight, H. M., Liewald, D. C., Lopez, L. M., Luciano, M., Gow, A. J., Henderson, R., Murray, C., Pattie, A., Fox, H. C., Redmond, P., Lutz, M. W., Chiba-Falek, O., Linnertz, C., Saith, S., Haggarty, P., McNeill, G. & 15 others, Ke, X., Ollier, W., Horan, M., Roses, A. D., Ponting, C. P., Porteous, D. J., Tenesa, A., Corley, J., Pickles, A., Starr, J. M., Whalley, L. J., Pedersen, N. L., Pendleton, N., Visscher, P. M. & Deary, I. J., Jan 2014, In : Molecular Psychiatry. 19, 1, p. 76-87 12 p.

    Research output: Contribution to journalArticle

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

    Meng, W., Veluchamy, A., Hébert, H. L., Campbell, A., Colhoun, H. M. & Palmer, C. N. A., 3 Jul 2017, In : British journal of dermatology.

    Research output: Contribution to journalArticle

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

    Wellcome Trust Case Control Consortium 2 (WTCCC2), Surrogate markers for Micro- and Macro-vascular hard endpoints for Innovative diabetes Tools (SUMMIT) study group, 1 Nov 2018, In : Acta Ophthalmologica.

    Research output: Contribution to journalArticle

  80. A genome-wide search for genetic influences and biological pathways related to the brain's white matter integrity

    Lopez, L., Bastin, M. E., Munoz-Maniega, S., Penke, L., Davies, G., Christoforou, A., Valdes Hernandez, M., Royle, N. A., Tenesa, A., Starr, J. M., Porteous, D. J., Wardlaw, J. M. & Deary, I. J., Aug 2012, In : Neurobiology of Aging. 33, 8, p. 1847.e1–1847.e14 14 p.

    Research output: Contribution to journalArticle

  81. A genome-wide search for linkage in a large bipolar family: comparison of genotyping accuracy using di- and tetranucleotide repeat microsatellite markers

    He, L., Morris, S., Lennon, A., St Clair, D. M., Porteous, D. J., Wright, A. F., Muir, W. & Blackwood, D., 1996, In : Psychiatric Genetics. 6, 3, p. 123-9 7 p.

    Research output: Contribution to journalArticle

  82. A guide to out of programme training and experience in Australia

    Kennedy, N. A. & Cock, C., 2011, In : British journal of hospital medicine. 72, 9, p. M141-4

    Research output: Contribution to journalArticle

  83. A linkage map for the hybridising toads Bombina bombina and B. variegata (Anura: Discoglossidae): Discoglossidae)

    Nürnberger, B., Hofman, S., Förg-Brey, B., Praetzel, G., Maclean, A., Szymura, J. M., Abbott, C. M. & Barton, N. H., 1 Aug 2003, In : Heredity. 91, 2, p. 136-142 7 p.

    Research output: Contribution to journalArticle

  84. A locus for bipolar affective disorder on chromosome 4p

    Blackwood, D. H., He, L., Morris, S. W., McLean, A., Whitton, C., Thomson, M., Walker, M. T., Woodburn, K., Sharp, C. M., Wright, A. F., Shibasaki, Y., St Clair, D. M., Porteous, D. J. & Muir, W. J., 1996, In : Nature Genetics. 12, 4, p. 427-430 4 p.

    Research output: Contribution to journalArticle

  85. A long-range restriction map across 3 Mb of the chromosome 11 breakpoint region of a translocation linked to schizophrenia: localization of the breakpoint and the search for neighbouring genes

    Millar, K., Brown, J., Maule, J. C., Shibasaki, Y., Christie, S., Lawson, D., Anderson, S., Wilson-Annan, J. C., Devon, R., St Clair, D. M., Blackwood, D., Muir, W. & Porteous, D. J., 1998, In : Psychiatric Genetics. 8, 3, p. 175-81 7 p.

    Research output: Contribution to journalArticle

  86. A major role for common genetic variation in anxiety disorders

    Purves, K. L., Coleman, J. R. I., Meier, S. M., Rayner, C., Davis, K. A. S., Cheesman, R., Bækvad-hansen, M., Børglum, A. D., Wan Cho, S., Jürgen Deckert, J., Gaspar, H. A., Bybjerg-grauholm, J., Hettema, J. M., Hotopf, M., Hougaard, D., Hübel, C., Kan, C., Mcintosh, A. M., Mors, O., Bo Mortensen, P. & 6 others, Nordentoft, M., Werge, T., Nicodemus, K. K., Mattheisen, M., Breen, G. & Eley, T. C., 20 Nov 2019, In : Molecular Psychiatry.

    Research output: Contribution to journalArticle

  87. A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration

    de Vries, P. S., Chasman, D. I., Sabater-Lleal, M., Chen, M-H., Huffman, J. E., Steri, M., Tang, W., Teumer, A., Marioni, R. E., Grossmann, V., Hottenga, J. J., Trompet, S., Müller-Nurasyid, M., Zhao, J. H., Brody, J. A., Kleber, M. E., Guo, X., Wang, J. J., Auer, P. L., Attia, J. R. & 111 others, Yanek, L. R., Ahluwalia, T. S., Lahti, J., Venturini, C., Tanaka, T., Bielak, L. F., Joshi, P. K., Rocanin-Arjo, A., Kolcic, I., Navarro, P., Rose, L. M., Oldmeadow, C., Riess, H., Mazur, J., Basu, S., Goel, A., Yang, Q., Ghanbari, M., Willemsen, G., Rumley, A., Fiorillo, E., de Craen, A. J. M., Grotevendt, A., Scott, R., Taylor, K. D., Delgado, G. E., Yao, J., Kifley, A., Kooperberg, C., Qayyum, R., Lopez, L. M., Berentzen, T. L., Räikkönen, K., Mangino, M., Bandinelli, S., Peyser, P. A., Wild, S., Trégouët, D-A., Wright, A. F., Marten, J., Zemunik, T., Morrison, A. C., Sennblad, B., Tofler, G., de Maat, M. P. M., de Geus, E. J. C., Lowe, G. D., Zoledziewska, M., Sattar, N., Binder, H., Völker, U., Waldenberger, M., Khaw, K-T., McKnight, B., Huang, J., Jenny, N. S., Holliday, E. G., Qi, L., McEvoy, M. G., Becker, D. M., Starr, J. M., Sarin, A-P., Hysi, P. G., Hernandez, D. G., Jhun, M. A., Campbell, H., Hamsten, A., Rivadeneira, F., McArdle, W. L., Slagboom, P. E., Zeller, T., Koenig, W., Psaty, B. M., Haritunians, T., Liu, J., Palotie, A., Uitterlinden, A. G., Stott, D. J., Hofman, A., Franco, O. H., Polasek, O., Rudan, I., Morange, P-E., Wilson, J. F., Kardia, S. L. R., Ferrucci, L., Spector, T. D., Eriksson, J. G., Hansen, T., Deary, I. J., Becker, L. C., Scott, R. J., Mitchell, R., März, W., Wareham, N. J., Peters, A., Greinacher, A., Wild, P. S., Jukema, J. W., Boomsma, D. I., Hayward, C., Cucca, F., Tracy, R., Watkins, H., Reiner, A. P., Folsom, A. R., Ridker, P. M., O'Donnell, C. J., Smith, N. L., Strachan, D. P. & Dehghan, A., 10 Nov 2015, In : Human Molecular Genetics.

    Research output: Contribution to journalArticle

  88. A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip

    Evangelou, E., Kerkhof, H. J., Styrkarsdottir, U., Ntzani, E. E., Bos, S. D., Esko, T., Evans, D. S., Metrustry, S., Panoutsopoulou, K., Ramos, Y. F. M., Thorleifsson, G., Tsilidis, K. K., Arden, N., Aslam, N., Bellamy, N., Birrell, F., Blanco, F. J., Carr, A., Chapman, K., Day-Williams, A. G. & 31 others, Deloukas, P., Doherty, M., Engstrom, G., Helgadottir, H. T., Hofman, A., Ingvarsson, T., Jonsson, H., Keis, A., Keurentjes, J. C., Kloppenburg, M., Lind, P. A., McCaskie, A., Martin, N. G., Milani, L., Montgomery, G. W., Nelissen, R. G. H. H., Nevitt, M. C., Nilsson, P. M., Ollier, W. E. R., Parimi, N., Rai, A., Ralston, S. H., Reed, M. R., Riancho, J. A., Rivadeneira, F., Rodriguez-Fontenla, C., Southam, L., Thorsteinsdottir, U., Tsezou, A., AWallis, G. & ArcOGEN Consortium, Dec 2014, In : Annals of the Rheumatic Diseases. 73, 12, p. 2130-2136 7 p.

    Research output: Contribution to journalArticle

  89. A meta-analysis of genome-wide association studies of epigenetic age acceleration

    Gibson, J., Russ, T., Clarke, T-K., Howard, D., Hillary, R., Evans, K. L., Walker, R., Bermingham, M., Morris, S., Campbell, A., Hayward, C., Murray, A., Porteous, D. J., Horvath, S., Lu, A. T., McIntosh, A., Whalley, H. & Marioni, R. E., 18 Nov 2019, In : PLoS Genetics. 15, 11, 53 p., e1008104.

    Research output: Contribution to journalArticle

  90. A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

    Porcu, E., Medici, M., Pistis, G., Volpato, C. B., Wilson, S. G., Cappola, A. R., Bos, S. D., Deelen, J., den Heijer, M., Freathy, R. M., Lahti, J., Liu, C., Lopez, L. M., Nolte, I. M., O'Connell, J. R., Tanaka, T., Trompet, S., Arnold, A., Bandinelli, S., Beekman, M. & 74 others, Bohringer, S., Brown, S. J., Buckley, B. M., Camaschella, C., de Craen, A. J. M., Davies, G., de Visser, M. C. H., Ford, I., Forsen, T., Frayling, T. M., Fugazzola, L., Goegele, M., Hattersley, A. T., Hermus, A. R., Hofman, A., Houwing-Duistermaat, J. J., Jensen, R. A., Kajantie, E., Kloppenburg, M., Lim, E. M., Masciullo, C., Mariotti, S., Minelli, C., Mitchell, B. D., Nagaraja, R., Netea-Maier, R. T., Palotie, A., Persani, L., Piras, M. G., Psaty, B. M., Raikkonen, K., Richards, J. B., Rivadeneira, F., Sala, C., Sabra, M. M., Sattar, N., Shields, B. M., Soranzo, N., Starr, J. M., Stott, D. J., Sweep, F. C. G. J., Usala, G., van der Klauw, M. M., van Heemst, D., van Mullem, A., Vermeulen, S. H., Visser, W. E., Walsh, J. P., Westendorp, R. G. J., Widen, E., Zhai, G., Cucca, F., Deary, I. J., Eriksson, J. G., Ferrucci, L., Fox, C. S., Jukema, J. W., Kiemeney, L. A., Pramstaller, P. P., Schlessinger, D., Shuldiner, A. R., Slagboom, E. P., Uitterlinden, A. G., Vaidya, B., Visser, T. J., Wolffenbuttel, B. H. R., Meulenbelt, I., Rotter, J. I., Spector, T. D., Hicks, A. A., Toniolo, D., Sanna, S., Peeters, R. P. & Naitza, S., 7 Feb 2013, In : PLoS Genetics. 9, 2, 20 p., 1003266.

    Research output: Contribution to journalArticle

  91. A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

    LifeLines Cohort Study, 10 Apr 2019, In : Human Molecular Genetics.

    Research output: Contribution to journalArticle

  92. A new yeast artificial chromosome vector designed for gene transfer into mammalian cells

    Ripoll, P. J., Cowper, A., Salmeron, S., Dickinson, P., Porteous, D. & Arveiler, B., 1998, In : Gene. 210, 1, p. 163-72 10 p.

    Research output: Contribution to journalArticle

  93. A novel 30 bp deletion in the FOXL2 gene in a phenotypically normal woman with primary amenorrhoea: Case report

    Gersak, K., Harris, S. E., Smale, W. J. & Shelling, A. N., Dec 2004, In : Human Reproduction. 19, 12, p. 2767-2770 4 p.

    Research output: Contribution to journalArticle

  94. A novel CCCH-zinc finger protein family regulates proinflammatory activation of macrophages

    Liang, J., Wang, J., Azfer, A., Song, W., Tromp, G., Kolattukudy, P. E. & Fu, M., 2008, In : Journal of Biological Chemistry. 283, 10, p. 6337-46 10 p.

    Research output: Contribution to journalArticle

  95. A pilot study of urinary peptides as biomarkers for intelligence in old age

    Lopez, L. M., Mullen, W., Zürbig, P., Harris, S. E., Gow, A. J., Starr, J., Porteous, D. J., Mischak, H. & Deary, I. J., 1 Jan 2011, In : Intelligence. 39, 1, p. 46-53

    Research output: Contribution to journalArticle

  96. A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice

    Daroszewska, A., van 't Hof, R. J., Rojas, J. A., Layfield, R., Landao-Basonga, E., Rose, L., Rose, K. & Ralston, S. H., Jul 2011, In : Human Molecular Genetics. 20, 14, p. 2734-2744 11 p.

    Research output: Contribution to journalArticle

  97. A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis

    Rivas, M. A., Graham, D., Sulem, P., Stevens, C., Desch, A. N., Goyette, P., Gudbjartsson, D., Jonsdottir, I., Thorsteinsdottir, U., Degenhardt, F., Mucha, S., Kurki, M. I., Li, D., D'Amato, M., Annese, V., Vermeire, S., Weersma, R. K., Halfvarson, J., Paavola-Sakki, P., Lappalainen, M. & 70 others, Lek, M., Cummings, B., Tukiainen, T., Haritunians, T., Halme, L., Koskinen, L. L. E., Ananthakrishnan, A. N., Luo, Y., Heap, G. A., Visschedijk, M. C., MacArthur, D. G., Neale, B. M., Ahmad, T., Anderson, C. A., Brant, S. R., Duerr, R. H., Silverberg, M. S., Cho, J. H., Palotie, A., Saavalainen, P., Kontula, K., Färkkilä, M., McGovern, D. P. B., Franke, A., Stefansson, K., Rioux, J. D., Xavier, R. J., Daly, M. J., Barrett, J., De Lane, K., Edwards, C., Hart, A., Hawkey, C., Jostins, L., Kennedy, N., Lamb, C., Lee, J., Lees, C., Mansfield, J., Mathew, C., Mowatt, C., Newman, B., Nimmo, E., Parkes, M., Pollard, M., Prescott, N., Randall, J., Rice, D., Satsangi, J., Simmons, A., Tremelling, M., Uhlig, H., Wilson, D., Abraham, C., Achkar, J. P., Bitton, A., Boucher, G., Croitoru, K., Fleshner, P., Glas, J., Kugathasan, S., Limbergen, J. V., Milgrom, R., Proctor, D., Regueiro, M., Schumm, P. L., Sharma, Y., Stempak, J. M., Targan, S. R. & Wang, M. H., 9 Aug 2016, In : Nature Communications. 7, 12342.

    Research output: Contribution to journalArticle

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