Bent Muller
Leipzig, SN 04103, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Journal: Molecular psychiatry
Published: November 29, 2019
Dyslexia risk variant rs600753 is linked with dyslexia-specific differential allelic expression of DYX1C1.
Journal: Genetics and molecular biology
Published: May 31, 2017
Dyslexia risk gene relates to representation of sound in the auditory brainstem.
Journal: Developmental cognitive neuroscience
Published: September 26, 2016
ATP2C2 and DYX1C1 are putative modulators of dyslexia-related MMR.
Journal: Brain and behavior
Published: May 30, 2016
NRSN1 associated grey matter volume of the visual word form area reveals dyslexia before school.
Journal: Brain : a journal of neurology
Published: November 19, 2015
Association, characterisation and meta-analysis of SNPs linked to general reading ability in a German dyslexia case-control cohort.
Journal: Scientific reports
Published: October 22, 2015
Cortical differences in preliterate children at familiar risk of dyslexia are similar to those observed in dyslexic readers.
Journal: Brain : a journal of neurology
Published: February 22, 2015
High acceptance of an early dyslexia screening test involving genetic analyses in Germany.
Journal: European journal of human genetics : EJHG
Published: September 24, 2014
Last Updated: 09/26/2026