King's College London

Research portal

Dr Roland Roberts

  1. Nesprin-2 epsilon: A novel nesprin isoform expressed in human ovary and Ntera-2 cells

    Lam, L. T., Boehm, S. V., Roberts, R. G. & Morris, G. E., 26 Aug 2011, In: Biochemical and Biophysical Research Communications. 412, 2, p. 291 - 295 5 p.

    Research output: Contribution to journalArticlepeer-review

  2. A CASE-BY-CASE EVOLUTIONARY ANALYSIS OF FOUR IMPRINTED RETROGENES

    McCole, R. B., Loughran, N. B., Chahal, M., Fernandes, L. P., Roberts, R. G., Fraternali, F., O'Connell, M. J. & Oakey, R. J., May 2011, In: Evolution. 65, 5, p. 1413 - 1427 15 p.

    Research output: Contribution to journalArticlepeer-review

  3. Characterisation of the FAM69 family of cysteine-rich endoplasmic reticulum proteins

    Tennant-Eyles, A. J., Moffitt, H., Whitehouse, C. A. & Roberts, R. G., 18 Mar 2011, In: Biochemical and Biophysical Research Communications. 406, 3, p. 471 - 477 7 p.

    Research output: Contribution to journalArticlepeer-review

  4. Deep Sequencing of the Nicastrin Gene in Pooled DNA, the Identification of Genetic Variants That Affect Risk of Alzheimertextquotesingles Disease

    Lupton, M. K., Proitsi, P., Danillidou, M., Tsolaki, M., Hamilton, G., Wroe, R., Pritchard, M., Lord, K., Martin, B. M., Kloszewska, I., Soininen, H., Mecocci, P., Vellas, B., Harold, D., Hollingworth, P., Lovestone, S., Powell, J. F. & Roberts, R. (ed.), 1 Feb 2011, In: PloS one. 6, 2, p. e17298

    Research output: Contribution to journalArticlepeer-review

  5. Dystrophin and the brain

    Ricotti, V., Roberts, R. G. & Muntoni, F., Jan 2011, In: Developmental Medicine and Child Neurology. 53, 1, p. 12 - 12 1 p.

    Research output: Contribution to journalEditorialpeer-review

  6. Heterozygous deletion of a 2-Mb region including the dystroglycan gene in a patient with mild myopathy, facial hypotonia, oral-motor dyspraxia and white matter abnormalities

    Frost, A. R., Böhm, S. V., Sewduth, R. N., Josifova, D., Ogilvie, C. M., Izatt, L. & Roberts, R. G., Jul 2010, In: European Journal of Human Genetics. 18, 7, p. 852 - 855 4 p.

    Research output: Contribution to journalArticlepeer-review

  7. Mutation of the RAD51C gene in a Fanconi anemia-like disorder

    Vaz, F., Hanenberg, H., Schuster, B., Barker, K., Wiek, C., Erven, V., Neveling, K., Endt, D., Kesterton, I., Autore, F., Fraternali, F., Freund, M., Hartmann, L., Grimwade, D., Roberts, R. G., Schaal, H., Mohammed, S., Rahman, N., Schindler, D. & Mathew, C. G., May 2010, In: Nature Genetics. 42, 5, p. 406 - 409 4 p.

    Research output: Contribution to journalArticlepeer-review

  8. Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease

    Prescott, N. J., Dominy, K. M., Kubo, M., Lewis, C. M., Fisher, S. A., Redon, R., Huang, N., Stranger, B. E., Blaszczyk, K., Hudspith, B., Parkes, G., Hosono, N., Yamazaki, K., Onnie, C. M., Forbes, A., Dermitzakis, E. T., Nakamura, Y., Mansfield, J. C., Sanderson, J., Hurles, M. E. & 2 others, Roberts, R. G. & Mathew, C. G., 27 Jan 2010, In: Human Molecular Genetics. 19, 9, p. 1828 - 1839 12 p., ddq041.

    Research output: Contribution to journalArticlepeer-review

  9. Characterisation of the interaction between syndecan-2, neurofibromin and CASK: Dependence of interaction on syndecan dimerization

    Volta, M., Calza, S., Roberts, A. M. & Roberts, R. G., 8 Jan 2010, In: Biochemical and Biophysical Research Communications. 391, 2, p. 1216 - 1221 6 p.

    Research output: Contribution to journalArticlepeer-review

  10. The relationship between syntrophins and syntrophin-binding sites (SBSs) in the dystrophins and dystrobrevins

    Bohm, S. V., Sewduth, R. N., Zhuo, L. L., Constantinou, P. & Roberts, R. G., 2010, In: Neuromuscular Disorders. 20, p. S11 - S11

    Research output: Contribution to journalMeeting abstract

  11. Profound human/mouse differences in alpha-dystrobrevin isoforms: a novel syntrophin-binding site and promoter missing in mouse and rat

    Boehm, S. V., Constantinou, P., Tan, S., Jin, H. & Roberts, R. G., 4 Dec 2009, In: BMC Biology. 7, 85.

    Research output: Contribution to journalArticlepeer-review

  12. A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case report.

    Mackie Ogilvie, C., Ahn, JW., Mann, K., Roberts, RG. & Flinter, F., 2009, In: Molecular Cytogenetics. 2, 1, 9.

    Research output: Contribution to journalArticlepeer-review

  13. Expression of Members of the Dystrophin, Dystrobrevin, and Dystrotelin Superfamily

    Boehm, S. V. & Roberts, R. G., 2009, In: Critical Reviews in Eukaryotic Gene Expression. 19, 2, p. 89 - 108 20 p.

    Research output: Contribution to journalLiterature reviewpeer-review

  14. Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart

    Gill, H. K., Parsons, S. R., Spalluto, C., Davies, A. F., Knorz, V. J., Burlinson, C. E. G., Ng, B. L., Carter, N. P., Ogilvie, C. M., Wilson, D. I. & Roberts, R. G., 2009, In: European Journal of Human Genetics. 17, 11, p. 1423 - 1431 9 p.

    Research output: Contribution to journalArticlepeer-review

  15. Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation

    Bagnall, R. D., Roberts, R. G., Mirza, M. M., Torigoe, T., Prescott, N. J. & Mathew, C. G., May 2008, In: European Journal of Human Genetics. 16, 5, p. 619 - 625 7 p.

    Research output: Contribution to journalArticlepeer-review

  16. Dystrobrevin and dystrophin family gene expression in zebrafish

    Boehm, S., Jin, H., Hughes, S. M., Roberts, R. G. & Hinits, Y., Jan 2008, In: Gene Expression Patterns. 8, 2, p. 71 - 78 8 p.

    Research output: Contribution to journalArticlepeer-review

  17. A third syntrophin binding site: Higher isoform diversity of alpha-dystrobrevin in non-rodents

    Boehm, S. V., Jin, H. & Roberts, R. G., 2008, In: Neuromuscular Disorders. 18, 9-10, p. 778 - 779 2 p.

    Research output: Contribution to journalMeeting abstract

  18. Association of a promoter variant and copy number polymorphisms at the IRGM locus with Crohn's disease

    Prescott, N., Fisher, S. A., Dominy, K. M., Blaszczyk, K., Redon, R., Huang, N., Onnie, C. M., Lewis, C. M., Sanderson, J., Forbes, A., Mansfield, J. C., Hurles, M. E., Roberts, R. G. & Mathew, C. G., 2008, In: Journal of Medical Genetics. 45, p. S23 - S23

    Research output: Contribution to journalMeeting abstract

  19. Content-dependent slpicing of two novel 5 prime untranslated exons contributes to the complex regulation of NOD2 protein expression in intestinal inflammation.

    Rosenstiel, PC., Huse, K., Franke, A., Hampe, J., Roberts, R., Mathew, C., Platzer, M. & Schreiber, S., 2008, In: Gastroenterology. 134, 4, p. A514 - A514

    Research output: Contribution to journalMeeting abstract

  20. Copy Number Variation at the Crohn's disease susceptibility locus, IRGM

    Dominy, K., Prescott, N. J., Fisher, S. A., Blaszczyk, K., Redon, R., Huang, N., Onnie, C. M., Lewis, C. M., Sanderson, J., Forbes, A., Mansfield, J. C., Hurles, M. E., Roberts, R. G. & Mathew, C. G., 2008, In: Journal of Medical Genetics. 45, p. S77 - S77

    Research output: Contribution to journalMeeting abstract

  21. Dystrotelins and the core function of dystrophins and dystrobrevins

    Roberts, R. G., 2008, In: Neuromuscular Disorders. 18, 9-10, p. 778 - 778 1 p.

    Research output: Contribution to journalMeeting abstract

  22. Patterns of evolutionary conservation in the nesprin genes highlight probable functionally important protein domains and isoforms

    Simpson, J. G. & Roberts, R. G., 2008, In: Biochemical Society Transactions. 36, 6, p. 1359 - 1367 9 p.

    Research output: Contribution to journalArticlepeer-review

  23. Functional characterization of two novel 5 ' untranslated exons reveals a complex regulation of NOD2 protein expression

    Rosenstiel, P., Huse, K., Franke, A., Hampe, J., Reichwald, K., Platzer, C., Roberts, R. G., Mathew, C. G., Platzer, M. & Schreiber, S., 20 Dec 2007, In: BMC GENOMICS. 8, 472.

    Research output: Contribution to journalArticlepeer-review

  24. Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity

    Zhang, Q., Bethmann, C., Worth, N. F., Davies, J. D., Wasner, C., Feuer, A., Ragnauth, C. D., Yi, Q., Mellad, J. A., Warren, D. T., Wheeler, M. A., Ellis, J. A., Skepper, J. N., Vorgerd, M., Schlotter-Weigel, B., Weissberg, P. L., Roberts, R. G., Wehnert, M. & Shanahan, C. M., 1 Dec 2007, In: Human Molecular Genetics. 16, 23, p. 2816-2833 18 p.

    Research output: Contribution to journalArticlepeer-review

  25. Schistosome dystrophin and dystrobrevin proteins contain large insertions

    Tan, S., Johnston, DA. & Roberts, RG., 26 Oct 2007, In: Biochemical and Biophysical Research Communications. 362, 3, p. 700 - 706 7 p.

    Research output: Contribution to journalArticlepeer-review

  26. Identification, evolution and association studies of a novel promoter and first exon of the human NOD2 (CARD15) gene.

    King, K., Bagnall, R., Fisher, SA., Sheikh, F., Cuthbert, A., Tan, S., Mundy, NI., Rosenstiel, P., Schreiber, S., Mathew, CG. & Roberts, RG., Oct 2007, In: Genomics. 90, 4, p. 493 - 501 9 p.

    Research output: Contribution to journalArticlepeer-review

  27. Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

    Parkes, M., Barrett, J. C., Prescott, N. J., Tremelling, M., Anderson, C. A., Fisher, S. A., Roberts, R. G., Nimmo, E. R., Cummings, F. R., Soars, D., Drummond, H., Lees, C. W., Khawaja, S. A., Bagnall, R., Burke, D. A., Todhunter, C. E., Ahmad, T., Onnie, C. M., McArdle, W., Strachan, D. & 11 others, Bethel, G., Bryan, C., Lewis, C. M., Deloukas, P., Forbes, A., Sanderson, J., Jewell, D. P., Satsangi, J., Mansfield, J. C., Cardon, L. & Mathew, C. G., Jul 2007, In: Nature Genetics. 39, 7, p. 830 - 832 3 p.

    Research output: Contribution to journalArticlepeer-review

  28. The dystrotelin, dystrophin and dystrobrevin superfamily: new paralogues and old isoforms

    Jin, H., Tan, S., Hermanowski, J., Bohm, S., Pacheco, S., McCauley, J. M., Greener, M. J., Hinits, Y., Hughes, S. M., Sharpe, P. T. & Roberts, R. G., 17 Jan 2007, In: BMC GENOMICS. 8, 20 p., 19.

    Research output: Contribution to journalArticlepeer-review

  29. A screen for retrotransposed imprinted genes reveals an association between X chromosome homology and maternal germ-line methylation.

    Wood, AJ., Roberts, RG., Monk, D., Moore, GE., Schulz, R. & Oakey, RJ., 2007, In: PL o S Genetics. 3, 2, p. 192 - 203 12 p., e20.

    Research output: Contribution to journalArticlepeer-review

  30. Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31

    Onnie, C., Fisher, S. A., King, K., Mirza, M., Roberts, R., Forbes, A., Sanderson, J., Lewis, C. M. & Mathew, C. G., Jul 2006, In: GENES AND IMMUNITY. 7, 5, p. 359 - 365 7 p.

    Research output: Contribution to journalArticlepeer-review

  31. Mutation, selection, and evolution of the Crohn disease susceptibility gene CARD15.

    King, K., Sheikh, M. E., Cuthbert, A. P., Fisher, S. A., Onnie, C. M., Mirza, M. M., Pattni, R. C., Sanderson, J., Forbes, A., Mansfield, J., Lewis, C. M., Roberts, R. G. & Mathew, C. G., Jan 2006, In: Human Mutation. 27, 1, p. 44 - 54 11 p.

    Research output: Contribution to journalArticlepeer-review

  32. Novel members of the dystrophin/dystrobrevin family.

    Jin, H., Tan, S., Hermanoski, J. & Roberts, RG., 2006, In: Journal of Muscle Research and Cell Motility. 27, 5-7, p. 530 - 530 1 p.

    Research output: Contribution to journalMeeting abstract

  33. Studies of the nesprin family in vertebrates and flies.

    Simpson, JG., Shanahan, CM., Tear, G. & Roberts, RG., 2006, In: Journal of Muscle Research and Cell Motility. 27, 5-7, p. 509 - 510 2 p.

    Research output: Contribution to journalPoster abstract

  34. The evolution of the dystrophin/dystrobrevin family.

    Tan, S., Jin, H. & Roberts, RG., 2006, In: Journal of Muscle Research and Cell Motility. 27, 5-7, p. 534 - 535 2 p.

    Research output: Contribution to journalPoster abstract

  35. Bax/Bak-dependent release of DDP/TIMM8a promotes Drp-1-mediated mitochondrial fission and mitoptosis during programmed cell death.

    Arnoult, D., Rismanchi, N., Grodet, A., Roberts, R. G., Seeburg, D. P., Estaquier, J., Sheng, M. & Blackstone, C., 6 Dec 2005, In: Current Biology. 15, 23, p. 2112 - 2118 7 p.

    Research output: Contribution to journalArticlepeer-review

  36. Nesprin-2 is a multi-isomeric protein that binds lamin and emerin at the nuclear envelope and forms a subcellular network in skeletal muscle

    Zhang, Q., Ragnauth, C. D., Skepper, J. N., Worth, N. F., Warren, D. T., Roberts, R. G., Weissberg, P. L., Ellis, J. A. & Shanahan, C. M., 15 Feb 2005, In: Journal of Cell Science. 118, 4, p. 673 - 687 15 p.

    Research output: Contribution to journalArticlepeer-review

  37. Structural evolution of the BRCA1 genomic region in primates

    Jin, H., Selfe, J., Whitehouse, C., Morris, J. R., Solomon, E. & Roberts, R. G., Dec 2004, In: Genomics. 84, 6, p. 1071 - 1082 12 p.

    Research output: Contribution to journalArticlepeer-review

  38. Multiplex ligation-dependent probe amplification using a completely synthetic probe set

    Stern, R. F., Roberts, R. G., Mann, K., Yau, S. C., Berg, J. & Mackie Ogilvie, C., Sep 2004, In: Biotechniques. 37, 3, p. 399 - 405 7 p.

    Research output: Contribution to journalArticlepeer-review

  39. Characterisation of chromosomal deletions involving 3q26--> 3q28 using a novel method for multiplex ligation-dependent probe amplification, and relation of deletion position to clinical phenotype.

    Stern, A. J., Mackie Ogilvie, C., Male, A., Bonneau, D., Guichet, A., Roberts, R. & Berg, J., 2004, 54th Annual Meeting of the American Society of Human Genetics. Unknown Publisher, p. 150 1 p.

    Research output: Chapter in Book/Report/Conference proceedingMeeting abstract

  40. Identification of genes involved in the pathogenesi of haemangiomas using suppression subtractive hybridization.

    Scott, A. J., Robertson, K., Crawford, R., Smith, A., Marchuk, D., North, P., Pearson, J., Roberts, R. & Berg, J. N., 2004, 54th Annual Meeting of the American Society of Human Genetics. Unknown Publisher, p. 244 1 p.

    Research output: Chapter in Book/Report/Conference proceedingMeeting abstract

  41. Molecular characterisation of a translocation associated with hypoplastic left heart.

    Gill, H., Davies, A., Sharland, G., Ng, B., Carter, N., Splitt, M., Simpson, J., Mackie Ogilvie, C. & Roberts, R., 2004, 54th Annual Meeting of the American Society of Human Genetics. Unknown Publisher, p. 170 1 p.

    Research output: Chapter in Book/Report/Conference proceedingMeeting abstract

  42. Mutation selection and evolution of the Crohn's disease susceptibility gene, CARD15

    King, K., Sheikh, M., Cuthbert, A. P., Fisher, S. A., Onnie, C. M., Mirza, M. M., Sanderson, J., Forbes, A., Mansfield, J., Lewis, C. M., Roberts, R. G. & Mathew, C. G., 2004, 54th Annual Meeting of the American Society of Human Genetics. Unknown Publisher, p. 413 - 413 1 p.

    Research output: Chapter in Book/Report/Conference proceedingMeeting abstract

  43. The evolutionary history of the dystrophins and dystrobrevins.

    Roberts, R. G., Tan, S., Jin, H. & Greener, M. J., 2004, 54th Annual Meeting of the American Society of Human Genetics: Abstracts. Unknown Publisher, p. 233 1 p.

    Research output: Chapter in Book/Report/Conference proceedingMeeting abstract

  44. Loss of a single amino acid from dystrophin resulting in Duchenne muscular dystrophy with retention of dystrophin protein

    Becker, K., Robb, S. A., Hatton, Z., Yau, S. C., Abbs, S. & Roberts, R. G., Jun 2003, In: Human Mutation. 21, 6, p. 651 - 651 1 p.

    Research output: Contribution to journalArticlepeer-review

  45. Interaction of the deafness-dystonia protein DDP/TIMM8a with the signal transduction adaptor molecule STAM1

    Blackstone, C., Roberts, R. G., Seeburg, D. P. & Sheng, M., 30 May 2003, In: Biochemical and Biophysical Research Communications. 305, 2, p. 345 - 352 8 p.

    Research output: Contribution to journalArticlepeer-review

Previous 1 2 Next

Export:RIS BibTex Word PDF - will at most contain 500 items

Search within the list

Refine results

Type

Type

Language

Language

Publication year

Publication year

Meeting and poster abstracts

Meeting and poster abstracts

Open Access Status

Open Access Status

© 2020 King's College London | Strand | London WC2R 2LS | England | United Kingdom | Tel +44 (0)20 7836 5454