Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
Journal Article
Overview
publication date
- February 11, 2019
has subject area
- Adolescent
- Adult
- Child
- Cognition
- Disease Attributes - Genetic Predisposition to Disease
- Environment and Public Health - Cohort Studies
- Environment and Public Health - Genome-Wide Association Study
- Environment and Public Health - Genome-Wide Association Study
- Female
- Genetic Association Studies - Genome-Wide Association Study
- Genetic Techniques - Genome-Wide Association Study
- Genotype
- Genotype - Genetic Predisposition to Disease
- Health Care Evaluation Mechanisms - Cohort Studies
- Humans
- Investigative Techniques - Cohort Studies
- Investigative Techniques - Genome-Wide Association Study
- Investigative Techniques - Genome-Wide Association Study
- Male
- Multifactorial Inheritance
- Nervous System Diseases - Dyslexia
- Nervous System Diseases - Dyslexia
- Neurodevelopmental Disorders - Dyslexia
- Polymorphism, Single Nucleotide
- Sequence Analysis - Genome-Wide Association Study
- Signs and Symptoms - Dyslexia
- Signs and Symptoms - Dyslexia
- Young Adult
has restriction
- gold
Date in CU Experts
- February 20, 2019 9:14 AM
Full Author List
- Gialluisi A; Andlauer TFM; Mirza-Schreiber N; Moll K; Becker J; Hoffmann P; Ludwig KU; Czamara D; St Pourcain B; Brandler W
author count
- 45
citation count
- 60
published in
- Translational Psychiatry Journal
Other Profiles
International Standard Serial Number (ISSN)
- 2158-3188
Digital Object Identifier (DOI)
Additional Document Info
volume
- 9
number
- ARTN 77