The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
C Bacon, GA Rappold - Human genetics, 2012 - Springer
Rare disruptions of FOXP2 have been strongly implicated in deficits in language
development. Research over the past decade has suggested a role in the formation of …
development. Research over the past decade has suggested a role in the formation of …
Evo-devo, deep homology and FoxP2: implications for the evolution of speech and language
C Scharff, J Petri - … Transactions of the Royal Society B …, 2011 - royalsocietypublishing.org
The evolution of novel morphological features, such as feathers, involves the modification of
developmental processes regulated by gene networks. The fact that genetic novelty …
developmental processes regulated by gene networks. The fact that genetic novelty …
Modeling autistic features in animals
PH Patterson - Pediatric research, 2011 - nature.com
A variety of features of autism can be simulated in rodents, including the core behavioral
hallmarks of stereotyped and repetitive behaviors, and deficits in social interaction and …
hallmarks of stereotyped and repetitive behaviors, and deficits in social interaction and …
Genome‐wide screening for DNA variants associated with reading and language traits
A Gialluisi, DF Newbury, EG Wilcutt… - Genes, Brain and …, 2014 - Wiley Online Library
Reading and language abilities are heritable traits that are likely to share some genetic
influences with each other. To identify pleiotropic genetic variants affecting these traits, we …
influences with each other. To identify pleiotropic genetic variants affecting these traits, we …
Decoding the genetics of speech and language
SA Graham, SE Fisher - Current opinion in neurobiology, 2013 - Elsevier
Researchers are beginning to uncover the neurogenetic pathways that underlie our
unparalleled capacity for spoken language. Initial clues come from identification of genetic …
unparalleled capacity for spoken language. Initial clues come from identification of genetic …
Autism-associated promoter variant in MET impacts functional and structural brain networks
As genes that confer increased risk for autism spectrum disorder (ASD) are identified, a
crucial next step is to determine how these risk factors impact brain structure and function …
crucial next step is to determine how these risk factors impact brain structure and function …
Genes, cognition, and communication: insights from neurodevelopmental disorders
DVM Bishop - Annals of the New York Academy of Sciences, 2009 - Wiley Online Library
Twin and family studies have demonstrated that most cognitive traits are moderately to
highly heritable. Neurodevelopmental disorders such as dyslexia, autism, and specific …
highly heritable. Neurodevelopmental disorders such as dyslexia, autism, and specific …
Theory of mind in children with specific language impairment: A systematic review and meta‐analysis
KK Nilsson, KJ de Lopez - Child development, 2016 - Wiley Online Library
The relation between language and theory of mind (ToM) has been debated for more than
two decades. In a similar vein, ToM has been examined in children with specific language …
two decades. In a similar vein, ToM has been examined in children with specific language …
Genetic advances in autism: heterogeneity and convergence on shared pathways
BR Bill, DH Geschwind - Current opinion in genetics & development, 2009 - Elsevier
The autism spectrum disorders (ASD) are a heterogeneous set of developmental disorders
characterized at their core by deficits in social interaction and communication. Current …
characterized at their core by deficits in social interaction and communication. Current …
Regulation of neuronal migration, an emerging topic in autism spectrum disorders
Autism spectrum disorders (ASD) encompass a group of neurodevelopmental diseases that
demonstrate strong heritability, however, the inheritance is not simple and many genes have …
demonstrate strong heritability, however, the inheritance is not simple and many genes have …