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Research Outputs

  1. 2017
  2. Stimulating thought: a functional MRI study of transcranial direct current stimulation in schizophrenia

    Orlov, N. D., O’daly, O., Tracy, D. K., Daniju, Y., Hodsoll, J., Valdearenas, L., Rothwell, J. & Shergill, S. S., Sep 2017, In : Brain. 140, 9, p. 2490-2497

    Research output: Contribution to journalArticle

  3. Revealing the inner workings of organoids

    Dias, C. & Guillemot, F., 15 May 2017, In : The EMBO journal. 36, p. 1299-1301

    Research output: Contribution to journalReview article

  4. Interaction of language, auditory and memory brain networks in auditory verbal hallucinations

    Ćurčić-Blake, B., Ford, J. M., Hubl, D., Orlov, N. D., Sommer, I. E., Waters, F., Allen, P., Jardri, R., Woodruff, P. W., David, O., Mulert, C., Woodward, T. S. & Aleman, A., 1 Jan 2017, In : Progress in Neurobiology. 148, p. 1-20 20 p.

    Research output: Contribution to journalArticle

  5. Obesity-associated gene TMEM18 has a role in the central control of appetite and body weight regulation.

    Larder, R., Sim, M. F. M., Gulati, P., Antrobus, R., Tung, Y. C. L., Rimmington, D., Ayuso, E., Polex-Wolf, J., Lam, B. Y. H., Dias, C., Logan, D. W., Virtue, S., Bosch, F., Yeo, G. S. H., Saudek, V., O'Rahilly, S. & Coll, A. P., 2017, In : Proceedings of the National Academy of Sciences of the United States of America. 114, 25, p. 9421 9426 p.

    Research output: Contribution to journalArticle

  6. 2016
  7. BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription

    Dias, C., Estruch, S. B., Graham, S. A., McRae, J., Sawiak, S. J., Hurst, J. A., Joss, S. K., Holder, S. E., Morton, J. E. V., Turner, C., Thevenon, J., Mellul, K., Sánchez-Andrade, G., Ibarra-Soria, X., Deriziotis, P., Santos, R. F., Lee, S-C., Faivre, L., Kleefstra, T., Liu, P. & 4 others, Hurles, M. E., DDD Study, Fisher, S. E. & Logan, D. W., 4 Aug 2016, In : American Journal of Human Genetics. 99, 2, p. 253-274 22 p.

    Research output: Contribution to journalArticle

  8. Efeito da estimulação transcraniana por corrente contínua (ETCC) sobre o córtex pré-frontal combinada a treinamento cognitivo para o tratamento da esquizofrenia: Ensaio clínico randomizado simulação controlado

    Shiozawa, P., Gomes, J. S., Ducos, D. V., Akiba, H. T., Dias, Á. M., Trevizol, A. P., Uchida, R. R., Orlov, N. & Cordeiro, Q., 1 Jul 2016, In : Trends in Psychiatry and Psychotherapy. 38, 3, p. 175-177 3 p.

    Research output: Contribution to journalArticle

  9. 2014
  10. Neuroimaging effects of 1 Hz right temporoparietal rTMS on normal auditory processing: Implications for clinical hallucination treatment paradigms

    Tracy, D. K., De Sousa De Abreu, M., Nalesnik, N., Mao, L., Lage, C. & Shergill, S. S., 12 Dec 2014, In : Journal of Clinical Neurophysiology. 31, 6, p. 541-546 6 p.

    Research output: Contribution to journalArticle

  11. Desmosterolosis: An illustration of diagnostic ambiguity of cholesterol synthesis disorders

    Dias, C., Rupps, R., Millar, B., Choi, K., Marra, M., Demos, M., Kratz, L. E. & Boerkoel, C. F., 25 Jun 2014, In : Orphanet Journal of Rare Diseases. 9, 1, 94.

    Research output: Contribution to journalArticle

  12. Unheard voices: outcomes of tertiary care for treatment-refractory psychosis

    Sarker, S. N., Tracy, D. K., Mateos Fernandez, M-J., Nalesnik, N., Dhillon, G., Onwumere, J., Prins, A-M., Schepman, K., Collier, T., White, T. P., Patel, A., Gaughran, F. & Shergill, S., 1 Apr 2014, In : BJPsych Bulletin. 38, 2, p. 71-74 4 p.

    Research output: Contribution to journalArticle

  13. 2013
  14. Co-segregation of trichorhinophalangeal syndrome with a t(8;13)(q23.3;q21.31) familial translocation that appears to increase TRPS1 gene expression

    David, D., Marques, B., Ferreira, C., Araújo, C., Vieira, L., Soares, G., Dias, C. & Pinto, M., 1 Nov 2013, In : Human Genetics. 132, 11, p. 1287-1299 13 p.

    Research output: Contribution to journalArticle

  15. Novel mutations in FA2H-associated neurodegeneration: An underrecognized condition?

    Rupps, R., Hukin, J., Balicki, M., Mercimek-Mahmutoglu, S., Rolfs, A. & Dias, C., 1 Nov 2013, In : Journal of Child Neurology. 28, 11, p. 1500-1504 5 p.

    Research output: Contribution to journalArticle

  16. Recurrent subacute post-viral onset of ataxia associated with a PRF1 mutation

    Dias, C., McDonald, A., Sincan, M., Rupps, R., Markello, T., Salvarinova, R., Santos, R. F., Menghrajani, K., Ahaghotu, C., Sutherland, D. P., Fortuno, E. S., Kollmann, T. R., Demos, M., Friedman, J. M., Speert, D. P., Gahl, W. A. & Boerkoel, C. F., 1 Nov 2013, In : European Journal of Human Genetics. 21, 11, p. 1232-1239 8 p.

    Research output: Contribution to journalArticle

  17. 2012
  18. An analysis of exome sequencing for diagnostic testing of the genes associated with muscle disease and spastic paraplegia

    Dias, C., Sincan, M., Cherukuri, P. F., Rupps, R., Huang, Y., Briemberg, H., Selby, K., Mullikin, J. C., Markello, T. C., Adams, D. R., Gahl, W. A. & Boerkoel, C. F., 1 Apr 2012, In : Human Mutation. 33, 4, p. 614-626 13 p.

    Research output: Contribution to journalArticle

  19. Clinical, biochemical and molecular characterization of Cystinuria in a cohort of 12 patients

    Barbosa, M., Lopes, A., Mota, C., Martins, E., Oliveira, J., Alves, S., de Bonis, P., do Céu Mota, M., Dias, C., Rodrigues-Santos, P., Fortuna, A. M., Quelhas, D., Lacerda, L., Bisceglia, L. & Cardoso, M. L., 1 Jan 2012, In : Clinical Genetics. 81, 1, p. 47-55 9 p.

    Research output: Contribution to journalArticle

  20. 2011
  21. An fMRI study of prefrontal dysfunction and symptomatic recovery in schizophrenia

    Smee, C., Krabbendam, L., O'Daly, O., Prins, A. -M., Nalesnik, N., Morley, L., Samson, G. & Shergill, S., Jun 2011, In : Acta Psychiatrica Scandinavica. 123, 6, p. 440-450 11 p.

    Research output: Contribution to journalArticle

  22. New insights into the pathogenesis of autosomal-dominant cutis laxa with report of five ELN mutations

    Callewaert, B., Renard, M., Hucthagowder, V., Albrecht, B., Hausser, I., Blair, E., Dias, C., Albino, A., Wachi, H., Sato, F., Mecham, R. P., Loeys, B., Coucke, P. J., De Paepe, A. & Urban, Z., 1 Apr 2011, In : Human Mutation. 32, 4, p. 445-455 11 p.

    Research output: Contribution to journalArticle

  23. 2010
  24. Development of NIPBL Locus-Specific Database Using LOVD: From Novel Mutations to Further Genotype-Phenotype Correlations in Cornelia de Lange Syndrome

    Oliveira, J., Dias, C., Redeker, E., Costa, E., Silva, J., Reis Lima, M., Den Dunnen, J. T. & Santos, R., 1 Nov 2010, In : Human Mutation. 31, 11, p. 1216-1222 7 p.

    Research output: Contribution to journalArticle

  25. A nonsense porcn mutation in severe focal dermal hypoplasia with natal teeth

    Dias, C., Basto, J., Pinho, O., Barbêdo, C., Mártins, M., Bornholdt, D., Fortuna, A., Grzeschik, K. H. & Lima, M., 1 Aug 2010, In : Fetal and Pediatric Pathology. 29, 5, p. 305-313 9 p.

    Research output: Contribution to journalArticle

  26. Private dysferlin exon skipping mutation (c.5492G > A) with a founder effect reveals further alternative splicing involving exons 49-51

    Santos, R., Oliveira, J., Vieira, E., Coelho, T., Carneiro, A. L., Evangelista, T., Dias, C., Fortuna, A., Geraldo, A., Negro, L., Guimares, A. & Bronze-Da-Rocha, E., 1 Aug 2010, In : Journal of Human Genetics. 55, 8, p. 546-549 4 p.

    Research output: Contribution to journalArticle

  27. 2009
  28. Sudden death in spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type

    Dias, C., Cairns, R. & Patel, M., 1 Jan 2009, In : Clinical Dysmorphology. 18, 1, p. 25-29 5 p.

    Research output: Contribution to journalArticle

  29. 2008
  30. Infantile neuroaxonal dystrophy: What's most important for the diagnosis?

    Carrilho, I., Santos, M., Guimarães, A., Teixeira, J., Chorão, R., Martins, M., Dias, C., Gregory, A., Westaway, S., Nguyen, T., Hayflick, S. & Barbot, C., 1 Nov 2008, In : European Journal of Paediatric Neurology. 12, 6, p. 491-500 10 p.

    Research output: Contribution to journalArticle

  31. Neurodegeneration associated with genetic defects in phospholipase A2

    Gregory, A., Westaway, S. K., Holm, I. E., Kotzbauer, P. T., Hogarth, P., Sonek, S., Coryell, J. C., Nguyen, T. M., Nardocci, N., Zorzi, G., Rodriguez, D., Desguerre, I., Bertini, E., Simonati, A., Levinson, B., Dias, C., Barbot, C., Carrilho, I., Santos, M., Malik, I. & 2 others, Gitschier, J. & Hayflick, S. J., 28 Oct 2008, In : Neurology. 71, 18, p. 1402-1409 8 p.

    Research output: Contribution to journalArticle

  32. 2007
  33. Aplicação dos critérios de diagnóstico de síndrome de Angelman actualizados aos doentes da consulta de neuropediatria

    Dias, C., Santos, M., Ribeiro, A., Carrilho, I., Lima, M. R., Barbot, C. & Chorão, R., 1 May 2007, In : Sinapse. 7, 1, p. 10-17 8 p.

    Research output: Contribution to journalArticle

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