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 …

The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on

LG Guidi, A Velayos‐Baeza… - European Journal of …, 2018 - Wiley Online Library
The capacity for language is one of the key features underlying the complexity of human
cognition and its evolution. However, little is known about the neurobiological mechanisms …

Language development and disorders: Possible genes and environment interactions

L Onnis, A Truzzi, X Ma - Research in developmental disabilities, 2018 - Elsevier
Abstract Language development requires both basic cognitive mechanisms for learning
language and a rich social context from which learning takes off. Disruptions in learning …

Primary cilia as a possible link between left-right asymmetry and neurodevelopmental diseases

A Trulioff, A Ermakov, Y Malashichev - Genes, 2017 - mdpi.com
Cilia have multiple functions in the development of the entire organism, and participate in
the development and functioning of the central nervous system. In the last decade, studies …

Knockout Mice for Dyslexia Susceptibility Gene Homologs KIAA0319 and KIAA0319L have Unaffected Neuronal Migration but Display Abnormal Auditory …

LG Guidi, J Mattley, I Martinez-Garay… - Cerebral …, 2017 - academic.oup.com
Developmental dyslexia is a neurodevelopmental disorder that affects reading ability
caused by genetic and non-genetic factors. Amongst the susceptibility genes identified to …

Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice

I Martinez-Garay, LG Guidi, ZG Holloway… - Brain Structure and …, 2017 - Springer
Developmental dyslexia is a common disorder with a strong genetic component, but the
underlying molecular mechanisms are still unknown. Several candidate dyslexia …

Animal models of developmental dyslexia: Where we are and what we are missing

V Lampis, R Ventura, M Di Segni, C Marino… - Neuroscience & …, 2021 - Elsevier
Developmental dyslexia (DD) is a complex neurodevelopmental disorder and the most
common learning disability among both school-aged children and across languages …

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

KM Price, KG Wigg, E Eising, Y Feng… - Translational …, 2022 - nature.com
Reading Disability (RD) is often characterized by difficulties in the phonology of the
language. While the molecular mechanisms underlying it are largely undetermined, loci are …

Dyslexia‐Related Hearing Loss Occurs Mainly through the Abnormal Spontaneous Electrical Activity of Spiral Ganglion Neurons

G Hong, X Fu, X Chen, L Zhang, X Han… - Advanced …, 2023 - Wiley Online Library
Dyslexia is a reading and spelling disorder due to neurodevelopmental abnormalities and is
occasionally found to be accompanied by hearing loss, but the reason for the associated …

The mediation role of dynamic multisensory processing using molecular genetic data in dyslexia

S Mascheretti, V Riva, B Feng, V Trezzi, C Andreola… - Brain sciences, 2020 - mdpi.com
Although substantial heritability has been reported and candidate genes have been
identified, we are far from understanding the etiopathogenetic pathways underlying …