E. Hennessy

发表

Explorer CMIP and ATP 2 C 2 Modulate Phonological Short-Term Memory in Language Impairment

Dorothy V. M. Bishop, Gillian Baird, Dianne F. Newbury, 2009 .

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

G. Baird, P. Bolton, J. Knight, 2013, Developmental Medicine & Child Neurology.

Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment

A. Hoischen, C. Francks, G. Baird, 2015, PLoS genetics.

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

William W. Cohen, Gillian Baird, A Pickles, 2015, European Journal of Human Genetics.

Genome-wide analysis identi fi es a role for common copy number variants in speci fi c language impairment

G. Baird, P. Bolton, J. Knight, 2015 .

Associations of HLA alleles with specific language impairment

G. Baird, P. Bolton, A. Monaco, 2014, Journal of Neurodevelopmental Disorders.

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment

G Baird, C. Francks, G. Baird, 2014, Genes, brain, and behavior.

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

Peter Donnelly, Gillian Baird, Simon E Fisher, 2014, European Journal of Human Genetics.

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

Dorothy V.M. Bishop, Gillian Baird, Dianne F. Newbury, 2009, American journal of human genetics.

Reply to Pembrey et al: ‘ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'

P. Donnelly, C. Francks, A. Pagnamenta, 2014, European Journal of Human Genetics.