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Mrs Helen Rooks

  1. Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC)

    Brewin, J. N., Rooks, H., Gardner, K., Senior, H., Morje, M., Patel, H., Calvet, D., Bartolucci, P., Thein, S-L., Menzel, S. & Rees, D. C., 23 Dec 2020, In: Haematologica. Online ahead of print

    Research output: Contribution to journalArticlepeer-review

  2. F cell numbers are associated with an X-linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease

    Urio, F., Nkya, S., Rooks, H., Mgaya, J. A., Masamu, U., Zozimus Sangeda, R., Mmbando, B. P., Brumat, M., Mselle, T., Menzel, S., Luzzatto, L. & Makani, J., Dec 2020, In: British Journal of Haematology. 191, 5, p. 888-896 9 p.

    Research output: Contribution to journalArticlepeer-review

  3. A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia

    Adeyemo, T. A., Ojewunmi, O. O., Oyetunji, I. A., Rooks, H., Rees, D. C., Akinsulie, A. O., Akanmu, A. S., Thein, S. L. & Menzel, S., 7 Jun 2018, In: PLoS ONE. 13, 6, e0197927.

    Research output: Contribution to journalArticlepeer-review

  4. g(HbF): a genetic model of fetal hemoglobin in sickle cell disease

    Gardner, K., Fulford, T., Silver, N., Rooks, H., Angelis, N., Allman, M., Nkya, S., Makani, J., Howard, J., Kesse-Adu, R., Rees, D. C., Stuart-Smith, S., Yeghen, T., Awogbade, M., Sangeda, R. Z., Mgaya, J., Patel, H., Newhouse, S., Menzel, S. & Thein, S. L., 13 Feb 2018, In: Blood Advances. 2, 3, p. 235-239 5 p.

    Research output: Contribution to journalArticlepeer-review

  5. Beta thalassaemia intermedia due to co-inheritance of three unique alpha globin cluster duplications characterised by next generation sequencing analysis

    Clark, B., Shooter, C., Smith, F., Brawand, D., Steedman, L., Oakley, M., Rushton, P., Rooks, H., Wang, X., Drousiotou, A., Kyrri, A., Hadjigavriel, M., Will, A., Fisher, C., Higgs, D. R., Phylipsen, M., Harteveld, C., Kleanthous, M. & Thein, S. L., 29 Jul 2016, (E-pub ahead of print) In: British Journal of Haematology.

    Research output: Contribution to journalArticlepeer-review

  6. Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer

    Mtatiro, S. N., Mgaya, J., Singh, T., Mariki, H., Rooks, H., Soka, D., Mmbando, B., Thein, S. L., Barrett, J. C., Makani, J., Cox, S. E. & Menzel, S., 10 Feb 2015, In: BMC Medical Genetics. 16, 1, 4.

    Research output: Contribution to journalArticlepeer-review

  7. Next generation sequencing identifies a novel rearrangement in the HBB cluster permitting to-the-base characterization

    Shooter, C., Rooks, H., Thein, S. L. & Clark, B., 1 Jan 2015, In: Human Mutation. 36, 1, p. 142-150 9 p.

    Research output: Contribution to journalArticlepeer-review

  8. Genome wide association study of fetal hemoglobin in sickle cell Anemia in Tanzania

    Mtatiro, S. N., Singh, T., Rooks, H., Mgaya, J., Mariki, H., Soka, D., Mmbando, B., Msaki, E., Kolder, I., Thein, S. L., Menzel, S., Cox, S. E., Makani, J. & Barrett, J. C., 5 Nov 2014, In: PL o S One . 9, 11, e111464.

    Research output: Contribution to journalArticlepeer-review

  9. Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP-2

    Menzel, S., Rooks, H., Zelenika, D., Mtatiro, S. N., Gnanakulasekaran, A., Drasar, E., Cox, S., Liu, L., Masood, M., Silver, N., Garner, C., Vasavda, N., Howard, J., Makani, J., Adekile, A., Pace, B., Spector, T., Farrall, M., Lathrop, M. & Thein, S. L., 1 Nov 2014, In: Annals of Human Genetics. 78, 6, p. 434-451 18 p.

    Research output: Contribution to journalArticlepeer-review

  10. HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers

    Stadhouders, R., Aktuna, S., Thongjuea, S., Aghajanirefah, A., Pourfarzad, F., van IJcken, W., Lenhard, B., Rooks, H., Best, S., Menzel, S., Grosveld, F., Thein, S. L. & Soler, E., 1 Apr 2014, In: Journal of Clinical Investigation. 124, 4, p. 1699-1710 12 p.

    Research output: Contribution to journalArticlepeer-review

  11. Genetic determinants of haemolysis in sickle cell anaemia

    Milton, J. N., Rooks, H., Drasar, E., McCabe, E. L., Baldwin, C. T., Melista, E., Gordeuk, V. R., Nouraie, M., Kato, G. R., Minniti, C., Taylor, J., Campbell, A., Luchtman-Jones, L., Rana, S., Castro, O., Zhang, Y., Thein, S. L., Sebastiani, P., Gladwin, M. T., Steinberg, M. H. & 1 others, Walk-PHAAST Investigators, Apr 2013, In: British Journal of Haematology. 161, 2, p. 270-278 9 p.

    Research output: Contribution to journalArticlepeer-review

  12. HbA2 levels in normal adults are influenced by two distinct genetic mechanisms

    Menzel, S., Garner, C., Rooks, H., Spector, T. D. & Thein, S. L., Jan 2013, In: British Journal of Haematology. 160, 1, p. 101-105 5 p.

    Research output: Contribution to journalArticlepeer-review

  13. A novel 506 kb deletion causing epsilon gamma delta beta thalassemia

    Rooks, H., Clark, B., Best, S., Rushton, P., Oakley, M., Thein, O. S., Cuthbert, A. C., Britland, A., Ruf, A. & Thein, S. L., 15 Oct 2012, In: Blood Cells Molecules and Diseases. 49, 3-4, p. 121-127 7 p.

    Research output: Contribution to journalArticlepeer-review

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