Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.

Show other versions (1)

Dyslexia is one of the most common childhood disorders with a prevalence of around 5-10% in school-age children. Although an important genetic component is known to have a role in the aetiology of dyslexia, we are far from understanding the molecular mechanisms leading to the disorder. Several candi...

Deskribapen osoa

Xehetasun bibliografikoak
Egile Nagusiak:	Becker, J, Czamara, D, Scerri, T, Ramus, F, Csépe, V, Talcott, J, Stein, J, Morris, A, Ludwig, K, Hoffmann, P, Honbolygó, F, Tóth, D, Fauchereau, F, Bogliotti, C, Iannuzzi, S, Chaix, Y, Valdois, S, Billard, C, George, F, Soares-Boucaud, I, Gérard, C, van der Mark, S, Schulz, E, Vaessen, A, Maurer, U
Formatua:	Journal article
Hizkuntza:	English
Argitaratua:	2014

Antzeko izenburuak

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
nork: Becker, J, et al.
Argitaratua: (2014)

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
nork: Gialluisi, A, et al.
Argitaratua: (2019)

PCSK6 is associated with handedness in individuals with dyslexia
nork: Richardson, A, et al.
Argitaratua: (2011)

PCSK6 is associated with handedness in individuals with dyslexia.
nork: Scerri, T, et al.
Argitaratua: (2011)

Dys-topian dys-languages. Orwell, Huxley and Bradbury
nork: Diana Thermes
Argitaratua: (2016-12-01)

Results of a collaborative study of the EDNAP group regarding the reproducibility and robustness of the Y-chromosome STRs DYS19, DYS389 I and II, DYS390 and DYS393 in a PCR pentaplex format.
nork: Carracedo, A, et al.
Argitaratua: (2001)

DysDiTect: Dyslexia Identification Using CNN-Positional-LSTM-Attention Modeling with Chinese Dictation Task
nork: Hey Wing Liu, et al.
Argitaratua: (2024-04-01)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
nork: Newbury, D, et al.
Argitaratua: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
nork: Newbury, D, et al.
Argitaratua: (2011)

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects
nork: Newbury, D, et al.
Argitaratua: (2011)

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language- Impaired Subjects
nork: Richardson, A, et al.
Argitaratua: (2011)

The genetic lexicon of dyslexia.
nork: Paracchini, S, et al.
Argitaratua: (2007)

The DCDC2 deletion is not a risk factor for dyslexia
nork: Scerri, T, et al.
Argitaratua: (2017)

Correction: identification of candidate genes for dyslexia susceptibility on chromosome 18.
nork: Scerri, T, et al.
Argitaratua: (2010)

Identification of candidate genes for dyslexia susceptibility on chromosome 18
nork: Richardson, A, et al.
Argitaratua: (2010)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
nork: Scerri, T, et al.
Argitaratua: (2010)

Phylogenetic evidence for multiple independent duplication events at the DYS19 locus.
nork: Capelli, C, et al.
Argitaratua: (2007)

Identification of candidate genes for dyslexia susceptibility on chromosome 18.
nork: Thomas S Scerri, et al.
Argitaratua: (2010-10-01)

ERP Correlates of Altered Orthographic-Phonological Processing in Dyslexia
nork: Vera Varga, et al.
Argitaratua: (2021-10-01)

Cerebellar morphology in developmental dyslexia.
nork: Rae, C, et al.
Argitaratua: (2002)

Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18.
nork: Thomas S. Scerri, et al.
Argitaratua: (2010-01-01)

The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structure
nork: Scerri, T, et al.
Argitaratua: (2012)

The perception of "sine-wave speech" by adults with developmental dyslexia.
nork: Rosner, B, et al.
Argitaratua: (2003)

Multivariate multipoint linkage analysis of QTL in dyslexia
nork: Marlow, A, et al.
Argitaratua: (2002)

Molecular characterisation and population genetics of the DYS458 .2 allelic variant
nork: Ferri, G, et al.
Argitaratua: (2008)

Investigating the role of visual and auditory search in reading and developmental dyslexia
nork: Marie eLallier, et al.
Argitaratua: (2013-09-01)

Remediation of Allophonic Perception and Visual Attention Span in Developmental Dyslexia: A Joint Assay
nork: Rachel Zoubrinetzky, et al.
Argitaratua: (2019-07-01)

Gene expression profiling studies on Caenorhabditis elegans dystrophin mutants dys-1(cx-35) and dys-1(cx18).
nork: Towers, P, et al.
Argitaratua: (2006)

Pronounced dys-autonomic symptoms announcing a primary Sjögren’s syndrome
nork: F. Masini, et al.
Argitaratua: (2020-07-01)

Lack of asymmetry characterises the cerebellum in developmental dyslexia
nork: Harasty, J, et al.
Argitaratua: (2001)

Loss of Y Chromosome Amelogenin Y, DYS570, and DYS576 in Males: A Case Report
Argitaratua: (2021-06-01)

Heme (dys)homeostasis and liver disease
nork: Tiago L. Duarte, et al.
Argitaratua: (2024-07-01)

Sexual (Dys)function after Urethroplasty
nork: Luís Xambre
Argitaratua: (2016-01-01)

Histone acetylation in neuronal (dys)function
nork: Bonnaud Emilie M., et al.
Argitaratua: (2016-05-01)

The phonological and visual basis of developmental dyslexia in Brazilian Portuguese reading children.
nork: Giseli Donadon Germano, et al.
Argitaratua: (2014-10-01)

Machine learning and dyslexia: Classification of individual structural neuro-imaging scans of students with and without dyslexia
nork: P. Tamboer, et al.
Argitaratua: (2016-01-01)

The cerebellum and dyslexia.
nork: Stoodley, C, et al.
Argitaratua: (2011)

(Nie)bezpieczna rodzina – kalejdoskop (dys)funkcji
nork: Beata Maria Nowak
Argitaratua: (2019-12-01)

Editorial: Probabilistic Perspectives on Brain (Dys)function
nork: Thomas Parr, et al.
Argitaratua: (2021-06-01)

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
nork: Simpson, N, et al.
Argitaratua: (2014)