King's College London

Research portal

Dr Laura Addis

  1. Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures

    EuroEPINOMICS RES Consortium, 1 May 2020, In : Epilepsia. 61, 5, p. 995-1007 13 p.

    Research output: Contribution to journalArticle

  2. Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses

    Addis, L., Sproviero, W., Thomas, S. V., Caraballo, R. H., Newhouse, S. J., Gomez, K., Hughes, E., Kinali, M., McCormick, D., Hannan, S., Cossu, S., Taylor, J., Akman, C. I., Wolf, S. M., Mandelbaum, D. E., Gupta, R., Van Der Spek, R. A., Pruna, D. & Pal, D. K., Sep 2018, In : Journal of Medical Genetics. 55, 9

    Research output: Contribution to journalArticle

  3. Idiopathic focal epilepsies: The lost tribe

    Pal, D. K., Ferrie, C., Addis, L., Akiyama, T., Capovilla, G., Caraballo, R., De Saint-Martin, A., Fejerman, N., Guerrini, R., Hamandi, K., Helbig, I., Ioannides, A. A., Kobayashi, K., Lal, D., Lesca, G., Muhle, H., Neubauer, B. A., Pisano, T., Rudolf, G., Seegmuller, C. & 8 others, Shibata, T., Smith, A., Striano, P., Strug, L. J., Szepetowski, P., Valeta, T., Yoshinaga, H. & Koutroumanidis, M., 3 Sep 2016, In : EPILEPTIC DISORDERS. 18, 3, p. 252-288 37 p.

    Research output: Contribution to journalArticle

  4. Analysis of rare copy number variation in absence epilepsies

    Addis, L., Rosch, R. E., Valentin, A., Makoff, A., Robinson, R., Everett, K. V., Nashef, L. & Pal, D. K., Apr 2016, In : Neurology. Genetics. 2, 2, e56.

    Research output: Contribution to journalArticle

  5. Accepted/In press

    A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy

    Panjwani, N., Wilson, M., Addis, L., Crosbie, J., Wirrell, E., Auvin, S., Caraballo, R., Kinali, M., McCormick, D., Oren, C., Taylor, J., Trounce, J., Clarke, T., Akman, C., Kugler, S., Mandelbaum, D., McGoldrick, P., Wolf, S., Arnold, P., Schachar, R. & 2 others, Pal, D. K. & Strug, L., 2016, (Accepted/In press) In : Annals of Clinical and Translational Neurology.

    Research output: Contribution to journalArticle

  6. Microdeletions of ELP4 are Associated with Language Impairment, Autism Spectrum Disorder and Mental Retardation

    Addis, L., Ahn, J. W., Dobson, R. J. B., Dixit, A., Ogilvie, C. M., Pinto, D., Vaags, A. K., Coon, H., Chaste, P., Wilson, S., Parr, J. R., Andrieux, J., Lenne, B., Tumer, Z., Leuzzi, V., Aubell, K., Koillinen, H., Curran, S. R., Marshall, C. R., Scherer, S. W. & 3 others, Strug, L. J., Collier, D. A. & Pal, D. K., 1 Sep 2015, In : Human Mutation. 36, 9

    Research output: Contribution to journalArticle

  7. Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic

    Derkach, A., Chiang, T., Gong, J., Addis, L., Dobbins, S., Tomlinson, I., Houlston, R., Pal, D. K. & Strug, L. J., 1 Aug 2014, In : Bioinformatics (Oxford, England). 30, 15, p. 2179-2188 10 p.

    Research output: Contribution to journalArticle

  8. Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

    Simpson, N. H., Addis, L., Brandler, W. M., Slonims, V., Clark, A., Watson, J., Scerri, T. S., Hennessy, E. R., Bolton, P. F., Conti-Ramsden, G., Fairfax, B. P., Knight, J. C., Stein, J., Talcott, J. B., O'Hare, A., Baird, G., Paracchini, S., Fisher, S. E., Newbury, D. F. & SLI Consortium, Apr 2014, In : Developmental Medicine and Child Neurology. 56, 4, p. 346-353 8 p.

    Research output: Contribution to journalArticle

  9. Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci

    Addis, L., Chiang, T., Clarke, T., Hardison, H., Kugler, S., Mandelbaum, D. E., Novotny, E., Wolf, S., Strug, L. J. & Pal, D. K., Mar 2014, In : Genes, brain, and behavior. 13, 3, p. 333-340 8 p.

    Research output: Contribution to journalArticle

  10. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

    Lemke, J. R., Lal, D., Reinthaler, E. M., Steiner, I., Nothnagel, M., Alber, M., Geider, K., Laube, B., Schwake, M., Finsterwalder, K., Franke, A., Schilhabel, M., Jähn, J. A., Muhle, H., Boor, R., Van Paesschen, W., Caraballo, R., Fejerman, N., Weckhuysen, S., De Jonghe, P. & 51 others, Larsen, J., Møller, R. S., Hjalgrim, H., Addis, L., Tang, S., Hughes, E., Pal, D. K., Veri, K., Vaher, U., Talvik, T., Dimova, P., Guerrero López, R., Serratosa, J. M., Linnankivi, T., Lehesjoki, A-E., Ruf, S., Wolff, M., Buerki, S., Wohlrab, G., Kroell, J., Datta, A. N., Fiedler, B., Kurlemann, G., Kluger, G., Hahn, A., Haberlandt, D. E., Kutzer, C., Sperner, J., Becker, F., Weber, Y. G., Feucht, M., Steinböck, H., Neophythou, B., Ronen, G. M., Gruber-Sedlmayr, U., Geldner, J., Harvey, R. J., Hoffmann, P., Herms, S., Altmüller, J., Toliat, M. R., Thiele, H., Nürnberg, P., Wilhelm, C., Stephani, U., Helbig, I., Lerche, H., Zimprich, F., Neubauer, B. A., Biskup, S. & von Spiczak, S., Sep 2013, In : Nature Genetics. 45, 9, p. 1067-1072 6 p.

    Research output: Contribution to journalArticle

  11. GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction

    Lesca, G., Rudolf, G., Bruneau, N., Lozovaya, N., Labalme, A., Boutry-Kryza, N., Salmi, M., Tsintsadze, T., Addis, L., Motte, J., Wright, S., Tsintsadze, V., Michel, A., Doummar, D., Lascelles, K., Strug, L., Waters, P., de Bellescize, J., Vrielynck, P., de Saint Martin, A. & 9 others, Ville, D., Ryvlin, P., Arzimanoglou, A., Hirsch, E., Vincent, A., Pal, D., Burnashev, N., Sanlaville, D. & Szepetowski, P., 28 Aug 2013, In : Nature Genetics. 45, 9, p. 1061-1066 6 p.

    Research output: Contribution to journalLetter

  12. Imaging and genetics of language and cognition in pediatric epilepsy

    Addis, L., Lin, J. J., Pal, D. K., Hermann, B. & Caplan, R., Mar 2013, In : Epilepsy & Behavior. 26, 3, p. 303-312 10 p.

    Research output: Contribution to journalLiterature review

  13. The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy

    Strug, L. J., Addis, L., Chiang, T., Baskurt, Z., Li, W., Clarke, T., Hardison, H., Kugler, S. L., Mandelbaum, D. E., Novotny, E. J., Wolf, S. M. & Pal, D. K., 18 Jul 2012, In : PL o S One . 7, 7, p. - 7 p., e40696.

    Research output: Contribution to journalArticle

  14. Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects

    Newbury, D. F., Paracchini, S., Scerri, T. S., Winchester, L., Addis, L., Richardson, A. J., Walter, J., Stein, J. F., Talcott, J. B. & Monaco, A. P., Jan 2011, In : Behavior Genetics. 41, 1, p. 90 - 104 15 p.

    Research output: Contribution to journalArticle

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

Full text

Full text

Meeting and poster abstracts

Meeting and poster abstracts

Authors

© 2018 King's College London | Strand | London WC2R 2LS | England | United Kingdom | Tel +44 (0)20 7836 5454