All Stories

  1. Microdeletions ofELP4Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation

    Article • Human Mutation, June 2015, Wiley

    Dr Laura Addis

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

    Article • Bioinformatics, April 2014, Oxford University Press (OUP)

    Dr Laura Addis

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

    Article • Genes Brain & Behavior, December 2013, Wiley

    Dr Laura Addis

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

    Article • Developmental Medicine & Child Neurology, October 2013, Wiley

    Dr Laura Addis

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

    Article • Nature Genetics, August 2013, Springer Science + Business Media

    Dr Laura Addis

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

    Article • Nature Genetics, August 2013, Springer Science + Business Media

    Dr Laura Addis

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

    Article • Epilepsy & Behavior, March 2013, Elsevier

    Dr Laura Addis

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

    Article • PLoS ONE, July 2012, PLOS

    Dr Laura Addis

  9. Identification and Characterization of the Integrin  2 1 Binding Motif in Chondroadherin Mediating Cell Attachment

    Article • Journal of Biological Chemistry, December 2010, American Society for Biochemistry & Molecular Biology (ASBMB)

    Dr Laura Addis

  10. CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment

    Article • The American Journal of Human Genetics, August 2009, Elsevier

    Dr Laura Addis

  11. A Whole-Genome Scan and Fine-Mapping Linkage Study of Auditory-Visual Synesthesia Reveals Evidence of Linkage to Chromosomes 2q24, 5q33, 6p12, and 12p12

    Article • The American Journal of Human Genetics, February 2009, Elsevier

    Dr Laura Addis

  12. Purification, crystallization and preliminary X-ray diffraction analysis of human chondroadherin

    Article • Acta Crystallographica Section F Structural Biology and Crystallization Communications, May 2008, International Union of Crystallography

    Dr Laura Addis