Current Search:  Research Repository (x) » * (x) » Citation (x) » Shukla, P. (x) » Grigorenko, Elena L (x)

Search results

  • CSV Spreadsheet
(1 - 29 of 29)
Spelling well despite developmental language disorder
Teaching children with autism to read for meaning
Lexical processing deficits in children with developmental language disorder
Reading and a diffusion model analysis of reaction time.
In search of the perfect phenotype
Identifying learning patterns of children at risk for Specific Reading Disability.
Lexical decision as an endophenotype for reading comprehension
Gender and agreement processing in children with developmental language disorder.
Gene expression in the human brain
Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.
application of the elastic net for an endophenotype analysis.
balanced t(10;15) translocation in a male patient with developmental language disorder.
Education in Juvenile Detention Facilities in the State of Connecticut
Cross-informant symptoms from CBCL, TRF, and YSR
BDNF Val66Met Polymorphism Influences Reading Ability and Patterns of Neural Activation in Children.
At the height of fashion
Attentional but not pre-attentive neural measures of auditory discrimination are atypical in children with developmental language disorder.
Age-related changes of gene expression in the neocortex
Academic Achievement Among Juvenile Detainees.
Dynamic assessment and response to intervention
Comparison of whole-genome DNA methylation patterns in whole blood, saliva, and lymphoblastoid cell lines.
COMT Val/Met polymorphism is associated with reading-related skills and consistent patterns of functional neural activation.
Childhood adversity and DNA methylation of genes involved in the hypothalamus-pituitary-adrenal axis and immune system
Behavior, brain, and genome in genomic disorders
BDNF ValMet polymorphism is associated with structural neuroanatomical differences in young children.
Same or different? Insights into the etiology of phonological awareness and rapid naming.
Sources of Cognitive Exploration
Schooling and variation in the COMT gene
Searching for Potocki-Lupski syndrome phenotype