Search results

• 2015

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

  Malik, R., Freilinger, T., Winsvold, B. S., Anttila, V., Vander Heiden, J., Traylor, M., De Vries, B., Holliday, E. G., Terwindt, G. M., Sturm, J., Bis, J. C., Hopewell, J. C., Ferrari, M. D., Rannikmae, K., Wessman, M., Kallela, M., Kubisch, C., Fornage, M., Meschia, J. F. & Lehtimaki, T. & 105 others, Sudlow, C., Clarke, R., Chasman, D. I., Mitchell, B. D., Maguire, J., Kaprio, J., Farrall, M., Raitakari, O. T., Kurth, T., Ikram, M. A., Reiner, A. P., Longstreth, W. T., Rothwell, P. M., Strachan, D. P., Sharma, P., Seshadri, S., Quaye, L., Cherkas, L., Schurks, M., Rosand, J., Ligthart, L., Boncoraglio, G. B., Davey Smith, G., Van Duijn, C. M., Stefansson, K., Worrall, B. B., Nyholt, D. R., Markus, H. S., Van Den Maagdenberg, A. M. J. M., Cotsapas, C., Zwart, J. A., Palotie, A., Dichgans, M., Thorsteinsdottir, U., Destefano, A. L., Levi, C., Gretarsdottir, S., Donnelly, P., Barroso, I., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath F, R. C., Viswanathan, A. C., Wood, N. W., Spencer, C. C., Band, G., Bellengues, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Langford, C., Hunt, S. E., Edkind, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronv, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Rickette, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Gormley, P., Bettella, F., Mcmahon, G., Todt, U., Palta, P., Hamalainen, E., Steinberg, S., Stefansson, H., Farkkila, M., Artto, V., Kaunisto, M. A., Schoenen, J., Frants, R. R., Borck, G., Gobel, H., Heinze, A., Heinze-kuhn, K. & Muller-myhsok, B., 26 May 2015, In: Neurology. 84, 21, p. 2132-2145 14 p., 21 .

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

  • Auras 100%
  92 Citations (Scopus)

• The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis

  Robinson, P. C., Leo, P. J., Pointon, J. J., Cremin, K., Bradbury, L. A., Donnelly (chair), P., Barroso (deputy Chair), I., M Blackwell, J., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N., Plomin, R. & Rautanen, A. & 59 others, Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Spencer, C. C., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Donnelly, P., Langford, C., Hunt, S. E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Barroso, I., Deloukas, P., Mathew (chair), C. G., Blackwell, J. M., Brown, M. A., Corvin, A., Spencer, C. C. A., Mccloskey, E., Eisman, J., Jones, G., Nicholson, G., Eastell, R., Sambrook, P., Prince, R., Dennison, E., Reid, I., Wark, J., Stebbings, S., Harrison, A. A., Evans, D. M., Duncan, E. L., Wordsworth, B. P. & Brown, M. A., 26 Nov 2015, (E-pub ahead of print) In: GENES AND IMMUNITY. 17, 1, p. 46-51

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

  • Genetics 100%
  • Protein 100%
  • Zinc Finger 100%
  • Genetic Determinism 50%
  • Major Histocompatibility Complex 50%
  33 Citations (Scopus)
• 2014

  A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation

  Bramon, E., Pirinen, M., Strange, A., Lin, K., Freeman, C., Bellenguez, C., Su, Z., Band, G., Pearson, R., Vukcevic, D., Langford, C., Deloukas, P., Hunt, S., Gray, E., Dronov, S., Potter, S. C., Tashakkori-Ghanbaria, A., Edkins, S., Bumpstead, S. J. & Arranz, M. J. & 31 others, Bakker, S., Bender, S., Bruggeman, R., Cahn, W., Chandler, D., Collier, D. A., Crespo-Facorro, B., Dazzan, P., de Haan, L., Di Forti, M., Dragović, M., Giegling, I., Hall, J., Iyegbe, C., Jablensky, A., Kravariti, E., Mata, I., McDonald, C., Pariante, C. M., Picchioni, M., Shaikh, M., Toulopoulou, T., Van Os, J., Walshe, M., Mathew, C. G., Plomin, R., Trembath, R. C., Lewis, C. M., Murray, R. M., Powell, J. & Psychosis Endophenotypes International Consortium, 1 Mar 2014, In: Biological psychiatry. 75, 5, p. 386-397 12 p.

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

  • Single Nucleotide Polymorphism 100%
  • Genome Wide Association Study 100%
  • Bipolar Disorder 33%
  • Genomics 25%
  40 Citations (Scopus)

• Genome-wide estimates of inbreeding in unrelated individuals and their association with cognitive ability

  Power, R., Nagoshi, C., Defries, J. C., Donnelly, P., Barroso, I., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N., Rautanen, A., Sawcer, S. J., Trembath, R. C. & Viswanathan, A. C. & 41 others, Wood, N. W., Spencer, C. C. A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Donnelly, P., Langford, C., Hunt, S. E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Barroso, I., Deloukas, P., Mathew, C. G., Blackwell, J. M., Brown, M. A., Corvin, A., Spencer, C. C. A. & Plomin, R., Mar 2014, In: European Journal of Human Genetics. 22, 3, p. 386-390 5 p.

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

  • Inbreeding 100%
  • Single Nucleotide Polymorphism 72%
  • Molecular Genetics 9%
  • Minor Allele Frequency 9%
  • Genetic Procedures 9%
  18 Citations (Scopus)
• 2013

  Genome-wide association analysis identifies 13 new risk loci for schizophrenia

  Ripke, S., O'dushlaine, C., Chambert, K., Moran, J. L., K??hler, A. K., Akterin, S., Bergen, S. E., Collins, A. L., Crowley, J. J., Fromer, M., Kim, Y., Lee, S. H., Magnusson, P. K. E., Sanchez, N., Stahl, E. A., Williams, S., Wray, N. R., Xia, K., Bettella, F. & Borglum, A. D. & 15 others, Bulik-sullivan, B. K., Cormican, P., Craddock, N., De Leeuw, C., Durmishi, N., Gill, M., Lin, K., Neale, B. M., Powell, J., Riley, B. P., Walters, J. T., Multicenter Genetic Studies of Schizophrenia Consortium, Psychosis Endophenotypes International Consortium, Wellcome Trust Case Consortium 2 & Purcell, S., Oct 2013, In: Nature Genetics. 45, 10, p. 1150-1159 10 p.

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

  • Single Nucleotide Polymorphism 100%
  • Genome Wide Association Study 100%
  • Candidate Gene 33%
  • Genetic Divergence 33%
  • Genomics 33%
  1217 Citations (Scopus)

• Loss of c-Jun N-terminal kinase-interacting protein-1 does not affect axonal transport of the amyloid precursor protein or Aβ production

  Vagnoni, A., Glennon, E. B. C., Perkinton, M. S., Gray, E. H., Noble, W. & Miller, C. C. J., 15 Nov 2013, In: Human Molecular Genetics. 22, 22, p. 4646-52 7 p.

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

  Open Access

  • N-Terminus 100%
  • Nerve Fiber Transport 100%
  • Kinesin 25%
  • Posttranslational Modification 16%
  • Transport Protein 16%
• 1982

  Presynaptic microtubules: organisation and assembly/disassembly

  Gordon-Weeks, P. R., Burgoyne, R. D. & Gray, E. G., Mar 1982, In: Neuroscience. 7, 3, p. 739-749 11 p.

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

  • Microtubules 100%
  • Synapse 45%
  • Coil 36%
  • Mitochondrion 18%
  • Presynaptic Terminal 18%
  47 Citations (Scopus)