Nuala H. Simpson
Oxford, ENG OX26PY, United Kingdom
Last Updated: 09/26/2026
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Found 20 publications
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: August 23, 2022
Inconsistent language lateralisation - Testing the dissociable language laterality hypothesis using behaviour and lateralised cerebral blood flow.
Journal: Cortex; a journal devoted to the study of the nervous system and behavior
Published: April 02, 2022
Stage 2 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: testing the double hit hypothesis.
Journal: Wellcome open research
Published: May 21, 2021
Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: January 06, 2020
Stage 1 Registered Report: Variation in neurodevelopmental outcomes in children with sex chromosome trisomies: protocol for a test of the double hit hypothesis.
Journal: Wellcome open research
Published: February 02, 2018
Correction: Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment.
Journal: PLoS genetics
Published: June 27, 2015
Statistical modelling studies examining the dimensional structure of psychopathology experienced by adults with intellectual disabilities: Systematic review.
Journal: Research in developmental disabilities
Published: March 17, 2015
Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'.
Journal: European journal of human genetics : EJHG
Published: December 25, 2014
Lack of replication for the myosin-18B association with mathematical ability in independent cohorts.
Lack of replication for the myosin-18B association with mathematical ability in independent cohorts.
Journal: Genes, brain, and behavior
Published: December 09, 2014
Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
Journal: European journal of human genetics : EJHG
Published: July 17, 2014
Last Updated: 09/26/2026