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Copy number variation burden does not predict severity of neurodevelopmental phenotype in children with a sex chromosome trisomy.

Journal article

Mountford HS. et al, (2020), Am J Med Genet C Semin Med Genet, 184, 256 - 266

Genome-wide analysis identifies a role for common copy number variants in specific language impairment.

Journal article

Simpson NH. et al, (2015), Eur J Hum Genet, 23, 1370 - 1377

Lack of replication for the myosin-18B association with mathematical ability in independent cohorts.

Journal article

Pettigrew KA. et al, (2015), Genes Brain Behav, 14, 369 - 376

Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment.

Journal article

Ceroni F. et al, (2014), Eur J Hum Genet, 22, 1165 - 1171

Genome-wide screening for DNA variants associated with reading and language traits.

Journal article

Gialluisi A. et al, (2014), Genes Brain Behav, 13, 686 - 701

A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma.

Journal article

Ceroni F. et al, (2014), Autism Res, 7, 254 - 263

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

Journal article

Simpson NH. et al, (2014), Dev Med Child Neurol, 56, 346 - 353

Associations of HLA alleles with specific language impairment.

Journal article

Nudel R. et al, (2014), J Neurodev Disord, 6

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