Jeanette Holden

Affiliations: 
 
Google:
"Jeanette Holden"
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Lackner C, Sabbagh MA, Hallinan E, et al. (2012) Dopamine receptor D4 gene variation predicts preschoolers' developing theory of mind. Developmental Science. 15: 272-80
Malenfant P, Liu X, Hudson ML, et al. (2012) Association of GTF2i in the Williams-Beuren syndrome critical region with autism spectrum disorders. Journal of Autism and Developmental Disorders. 42: 1459-69
Feldman MA, Ward RA, Savona D, et al. (2012) Development and initial validation of a parent report measure of the behavioral development of infants at risk for autism spectrum disorders. Journal of Autism and Developmental Disorders. 42: 13-22
Malisza KL, Clancy C, Shiloff D, et al. (2011) Functional magnetic resonance imaging of facial information processing in children with autistic disorder, attention deficit hyperactivity disorder and typically developing controls. International Journal of Adolescent Medicine and Health. 23: 269-77
Harvard C, Strong E, Mercier E, et al. (2011) Understanding the impact of 1q21.1 copy number variant. Orphanet Journal of Rare Diseases. 6: 54
Liu X, Malenfant P, Reesor C, et al. (2011) 2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders. European Journal of Human Genetics : Ejhg. 19: 1264-70
Liu X, Solehdin F, Cohen IL, et al. (2011) Population- and family-based studies associate the MTHFR gene with idiopathic autism in simplex families. Journal of Autism and Developmental Disorders. 41: 938-44
Malisza KL, Clancy C, Shiloff D, et al. (2011) Functional evaluation of hidden figures object analysis in children with autistic disorder. Journal of Autism and Developmental Disorders. 41: 13-22
Noor A, Whibley A, Marshall CR, et al. (2010) Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability. Science Translational Medicine. 2: 49ra68
Qiao Y, Liu X, Harvard C, et al. (2007) Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis. Bmc Genomics. 8: 167
See more...