[HTML][HTML] How the visual aspects can be crucial in reading acquisition: The intriguing case of crowding and developmental dyslexia
S Gori, A Facoetti - Journal of vision, 2015 - iovs.arvojournals.org
Developmental dyslexia (DD) is the most common neurodevelopmental disorder (about
10% of children across cultures) characterized by severe difficulties in learning to read …
10% of children across cultures) characterized by severe difficulties in learning to read …
[HTML][HTML] 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 …
The interface between genetics and psychology: lessons from developmental dyslexia
DVM Bishop - Proceedings of the Royal Society B …, 2015 - royalsocietypublishing.org
Developmental dyslexia runs in families, and twin studies have confirmed that there is a
substantial genetic contribution to poor reading. The way in which discoveries in molecular …
substantial genetic contribution to poor reading. The way in which discoveries in molecular …
Gray matter features of reading disability: a combined meta-analytic and direct analysis approach
Meta-analysis of voxel-based morphometry dyslexia studies and direct analysis of 293
reading disability and control cases from six different research sites were performed to …
reading disability and control cases from six different research sites were performed to …
A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation
M Grati, I Chakchouk, Q Ma, M Bensaid… - Human molecular …, 2015 - academic.oup.com
Hearing loss is the most common sensory deficit in humans. We show that a point mutation
in DCDC2 (DCDC2a), a member of doublecortin domain-containing protein superfamily …
in DCDC2 (DCDC2a), a member of doublecortin domain-containing protein superfamily …
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 …
[HTML][HTML] The polygenic nature and complex genetic architecture of specific learning disorder
Specific Learning Disorder (SLD) is a multifactorial, neurodevelopmental disorder which
may involve persistent difficulties in reading (dyslexia), written expression and/or …
may involve persistent difficulties in reading (dyslexia), written expression and/or …
Early Childhood Educators' Perceptions of Dyslexia and Ability to Identify Students At-Risk.
M Gonzalez, TBH Brown - Journal of education and learning, 2019 - ERIC
This study primarily explored the perceptions of dyslexia held by early childhood educators
teaching in Head Start centers. A secondary purpose was to investigate how early childhood …
teaching in Head Start centers. A secondary purpose was to investigate how early childhood …
The DCDC2 Intron 2 Deletion Impairs Illusory Motion Perception Unveiling the Selective Role of Magnocellular-Dorsal Stream in Reading (Dis)ability
Developmental dyslexia (DD) is a heritable neurodevelopmental reading disorder that could
arise from auditory, visual, and cross-modal integration deficits. A deletion in intron 2 of the …
arise from auditory, visual, and cross-modal integration deficits. A deletion in intron 2 of the …