[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 …

Genetics of developmental dyslexia

TS Scerri, G Schulte-Körne - European child & adolescent psychiatry, 2010 - Springer
Developmental dyslexia is a highly heritable disorder with a prevalence of at least 5% in
school-aged children. Linkage studies have identified numerous loci throughout the genome …

[图书][B] Developmental disorders of language learning and cognition

C Hulme, MJ Snowling - 2013 - books.google.com
This important new text is a comprehensive survey of current thinking and research on a
wide range of developmental disorders. Highlights key research on normal and typical …

[图书][B] Diagnosing learning disorders: A neuropsychological framework

BF Pennington - 2008 - books.google.com
Page 1 Diagnosing Learning Disorders A Neuropsychological Framework Bruce F. Pennington
Page 2 DIAGNOSING LEARNING DISORDERS Page 3 Page 4 Diagnosing Learning …

Investigation of dyslexia and SLI risk variants in reading-and language-impaired subjects

DF Newbury, S Paracchini, TS Scerri, L Winchester… - Behavior genetics, 2011 - Springer
Dyslexia (or reading disability) and specific language impairment (or SLI) are common
childhood disorders that show considerable co-morbidity and diagnostic overlaps and have …

Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms

S Mascheretti, A De Luca, V Trezzi, D Peruzzo… - Translational …, 2017 - nature.com
Developmental dyslexia (DD) is a complex neurodevelopmental deficit characterized by
impaired reading acquisition, in spite of adequate neurological and sensorial conditions …

Molecular genetics of dyslexia: an overview

A Carrion‐Castillo, B Franke, SE Fisher - Dyslexia, 2013 - Wiley Online Library
Dyslexia is a highly heritable learning disorder with a complex underlying genetic
architecture. Over the past decade, researchers have pinpointed a number of candidate …

[HTML][HTML] DCDC2, KIAA0319 and CMIP are associated with reading-related traits

TS Scerri, AP Morris, LL Buckingham, DF Newbury… - Biological …, 2011 - Elsevier
BACKGROUND: Several susceptibility genes have been proposed for dyslexia (reading
disability; RD) and specific language impairment (SLI). RD and SLI show comorbidity, but it …

Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions

P Pinel, F Fauchereau, A Moreno, A Barbot… - Journal of …, 2012 - Soc Neuroscience
Recent advances have been made in the genetics of two human communication skills:
speaking and reading. Mutations of the FOXP2 gene cause a severe form of language …

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 …