Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms
Developmental dyslexia (DD) is a complex neurodevelopmental deficit characterized by
impaired reading acquisition, in spite of adequate neurological and sensorial conditions …
impaired reading acquisition, in spite of adequate neurological and sensorial conditions …
Molecular genetics of dyslexia: an overview
Dyslexia is a highly heritable learning disorder with a complex underlying genetic
architecture. Over the past decade, researchers have pinpointed a number of candidate …
architecture. Over the past decade, researchers have pinpointed a number of candidate …
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Attention deficit/hyperactivity disorder (ADHD) is a highly heritable childhood behavioral
disorder affecting 5% of children and 2.5% of adults. Common genetic variants contribute …
disorder affecting 5% of children and 2.5% of adults. Common genetic variants contribute …
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
A Gialluisi, TFM Andlauer, N Mirza-Schreiber… - Translational …, 2019 - nature.com
Developmental dyslexia (DD) is one of the most prevalent learning disorders, with high
impact on school and psychosocial development and high comorbidity with conditions like …
impact on school and psychosocial development and high comorbidity with conditions like …
FOXP transcription factors in vertebrate brain development, function, and disorders
M Co, AG Anderson, G Konopka - Wiley Interdisciplinary …, 2020 - Wiley Online Library
FOXP transcription factors are an evolutionarily ancient protein subfamily coordinating the
development of several organ systems in the vertebrate body. Association of their genes …
development of several organ systems in the vertebrate body. Association of their genes …
Neurogenetics and auditory processing in developmental dyslexia
Dyslexia is a polygenic developmental reading disorder characterized by an
auditory/phonological deficit. Based on the latest genetic and neurophysiological studies …
auditory/phonological deficit. Based on the latest genetic and neurophysiological studies …
Genome‐wide association study of shared components of reading disability and language impairment
JD Eicher, NR Powers, LL Miller… - Genes, Brain and …, 2013 - Wiley Online Library
Written and verbal languages are neurobehavioral traits vital to the development of
communication skills. Unfortunately, disorders involving these traits—specifically reading …
communication skills. Unfortunately, disorders involving these traits—specifically reading …
Therapeutic modulation of JAK-STAT, mTOR, and PPAR-γ signaling in neurological dysfunctions
The cytokine-activated Janus kinase (JAK)–signal transducer and activator of transcription
(STAT) cascade is a pleiotropic pathway that involves receptor subunit multimerization. The …
(STAT) cascade is a pleiotropic pathway that involves receptor subunit multimerization. The …
The genetics of reading disabilities: from phenotypes to candidate genes
This article provides an overview of (a) issues in definition and diagnosis of specific reading
disabilities at the behavioral level that may occur in different constellations of developmental …
disabilities at the behavioral level that may occur in different constellations of developmental …
NRSN1 associated grey matter volume of the visual word form area reveals dyslexia before school
Literacy learning depends on the flexibility of the human brain to reconfigure itself in
response to environmental influences. At the same time, literacy and disorders of literacy …
response to environmental influences. At the same time, literacy and disorders of literacy …