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Dr Barry Coull

Research Associate

  1. 2019
  2. Published

    A rare missense mutation in GJB3 (Cx31G45E) is associated with a unique cellular phenotype resulting in necrotic cell death

    Easton, J. A., Albuloushi, A. K., Kamps, M. A. F., Brouns, G. H. M. R., Broers, J. L. V., Coull, B. J., Oji, V., van Geel, M., van Steensel, M. A. M. & Martin, P. E., 1/10/2019, In : Experimental Dermatology. 28, 10, p. 1106-1113 8 p.

    Research output: Contribution to journalJournal article

  3. Published

    Multicentric osteolytic syndromes represent a phenotypic spectrum defined by defective collagen remodeling

    de Vos, I. J. H. M., Wong, A. S. W., Welting, T. J. M., Coull, B. J. & van Steensel, M. A. M., 1/08/2019, In : American Journal of Medical Genetics, Part A. 179, 8, p. 1652-1664 13 p.

    Research output: Contribution to journalJournal article

  4. 2018
  5. Published

    Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype

    De Vos, I. J. H. M., Tao, E. Y., Ong, S. L. M., Goggi, J. L., Scerri, T., Wilson, G. R., Low, C. G. M., Wong, A. S. W., Grussu, D., Stegmann, A. P. A., Van Geel, M., Janssen, R., Amor, D. J., Bahlo, M., Dunn, N. R., Carney, T. J., Lockhart, P. J., Coull, B. J. & Van Steensel, M. A. M., 15/08/2018, In : Human Molecular Genetics. 27, 16, p. 2775-2788 14 p.

    Research output: Contribution to journalJournal article

  6. 2015
  7. FLCN and AMPK Confer Resistance to Hyperosmotic Stress via Remodeling of Glycogen Stores

    Possik, E., Ajisebutu, A., Manteghi, S., Gingras, M. C., Vijayaraghavan, T., Flamand, M., Coull, B., Schmeisser, K., Duchaine, T., van Steensel, M., Hall, D. H. & Pause, A., 1/01/2015, In : PLoS Genetics. 11, 10, 18 p., e1005520.

    Research output: Contribution to journalJournal article

  8. 2014
  9. Published

    FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation

    Dunlop, E. A., Seifan, S., Claessens, T., Behrends, C., Kamps, M. A. F., Rozycka, E., Kemp, A. J., Nookala, R. K., Blenis, J., Coull, B. J., Murray, J. T., Van Steensel, M. A. M., Wilkinson, S. & Tee, A. R., 1/10/2014, In : Autophagy. 10, 10, p. 1749-1760 12 p.

    Research output: Contribution to journalJournal article

  10. Published

    The tumor suppressor folliculin regulates AMPK-dependent metabolic transformation

    Yan, M., Gingras, M. C., Dunlop, E. A., Nouët, Y., Dupuy, F., Jalali, Z., Possik, E., Coull, B. J., Kharitidi, D., Dydensborg, A. B., Faubert, B., Kamps, M., Sabourin, S., Preston, R. S., Davies, D. M., Roughead, T., Chotard, L., Van Steensel, M. A. M., Jones, R., Tee, A. R. & 1 others, Pause, A., 2/06/2014, In : Journal of Clinical Investigation. 124, 6, p. 2640-2650 11 p.

    Research output: Contribution to journalJournal article

  11. 2013
  12. Published

    Birt-hogg-dubé syndrome is a novel ciliopathy

    Luijten, M. N. H., Basten, S. G., Claessens, T., Vernooij, M., Scott, C. L., Janssen, R., Easton, J. A., Kamps, M. A. F., Vreeburg, M., Broers, J. L. V., Geel, M. V., Menko, F. H., Harbottle, R. P., Nookala, R. K., Tee, A. R., Land, S. C., Giles, R. H., Coull, B. J. & van Steensel, M. A. M., 1/11/2013, In : Human Molecular Genetics. 22, 21, p. 4383-4397 15 p.

    Research output: Contribution to journalJournal article

  13. Published

    A de novo FLCN mutation in a patient with spontaneous pneumothorax and renal cancer; A clinical and molecular evaluation

    Menko, F. H., Johannesma, P. C., Van Moorselaar, R. J. A., Reinhard, R., Van Waesberghe, J. H., Thunnissen, E., Houweling, A. C., Leter, E. M., Waisfisz, Q., Van Doorn, M. B., Starink, T. M., Postmus, P. E., Coull, B. J., Van Steensel, M. A. M. & Gille, J. J. P., 1/09/2013, In : Familial Cancer. 12, 3, p. 373-379 7 p.

    Research output: Contribution to journalJournal article

  14. Birt-Hogg-Dubé syndrome and the skin

    Vernooij, M., Claessens, T., Luijten, M., Van Steensel, M. A. M. & Coull, B. J., 1/09/2013, In : Familial Cancer. 12, 3, p. 381-385 5 p.

    Research output: Contribution to journalJournal article

  15. 2012
  16. Published

    What's new in Birt-Hogg-Dubé syndrome?

    Claessens, T., Vernooij, M., Luijten, M., Coull, B. J. & Van Steensel, M. A., 1/12/2012, In : Expert Review of Dermatology. 7, 6, p. 521-528 8 p.

    Research output: Contribution to journalReview article

  17. 2008
  18. Published

    Distinct BRCT domains in Mcph1/Brit1 mediate ionizing radiation-induced focus formation and centrosomal localization

    Jeffers, L. J., Coull, B. J., Stack, S. J. & Morrison, C. G., 3/01/2008, In : Oncogene. 27, 1, p. 139-144 6 p.

    Research output: Contribution to journalJournal article

  19. 2005
  20. Published

    Ubiquitin-binding domains in Y-family polymerases regulate translesion synthesis

    Bienko, M., Green, C. M., Crosetto, N., Rudolf, F., Zapart, G., Coull, B., Kannouche, P., Wider, G., Peter, M., Lehmann, A. R., Hofmann, K. & Dikic, I., 16/12/2005, In : Science. 310, 5755, p. 1821-4 4 p.

    Research output: Contribution to journalJournal article

  21. 2003
  22. Published

    Localization of DNA polymerases eta and iota to the replication machinery is tightly co-ordinated in human cells

    Kannouche, P., Fernández de Henestrosa, A. R., Coull, B., Vidal, A. E., Gray, C., Zicha, D., Woodgate, R. & Lehmann, A. R., 3/03/2003, In : EMBO Journal. 21, 22, p. 1223-33 11 p.

    Research output: Contribution to journalJournal article

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