Lili Senman

Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia.

Wendy Roberts, Juha Kere, Lars Feuk, 2006, American journal of human genetics.

Executive processes in appearance-reality tasks: the role of inhibition of attention and symbolic representation.

Ellen Bialystok, Lili Senman, E. Bialystok, 2004, Child development.

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2

Jessica Brian, Wendy Roberts, Lars Feuk, 2006, American journal of medical genetics. Part A.

Disruption at the Ptchd1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability Nih Public Access

Chi-Chung Hui, Andre Franke, Geraldine Dawson, 2010 .

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Thomas Bourgeron, Alberto Segre, Alberto Maria Segre, 2007, Nature Genetics.

Speech and Language Impairment and Oromotor Dyspraxia Due to Deletion of 7 q 31 That Involves FOXP 2

Stephen W. Scherer, Lucy R. Osborne, Jessica Brian, 2006 .

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.