Jillian M. Couto

Somatic instability of the expanded CTG triplet repeat in myotonic dystrophy type 1 is a heritable quantitative trait and modifier of disease severity

Fernando Morales, Jillian M. Couto, Catherine F. Higham et al. · Human Molecular Genetics · 2012 · 179 citations · Full text

Support for EKN1 as the susceptibility locus for dyslexia on 15q21

K. Wigg, Jillian M. Couto, Yu Feng et al. · Molecular Psychiatry · 2004 · 129 citations

Neuropsychology, Molecular Neuroscience, Neurophysiology +9

The KIAA0319-Like<i>(KIAA0319L)</i>Gene on Chromosome 1p34 as a Candidate for Reading Disabilities

Jillian M. Couto, Lissette Gomez, Karen Wigg et al. · Journal of Neurogenetics · 2008 · 56 citations · Full text

Reading Disabilities, Psychiatry, Genetic Disorder +15

Association of Attention-Deficit/Hyperactivity Disorder with a Candidate Region for Reading Disabilities on Chromosome 6p

Jillian M. Couto, Lissette Gomez, Karen Wigg et al. · Biological Psychiatry · 2009 · 54 citations · Full text

Adhd, Developmental Disability, Psychiatry +10

Association of reading disabilities with regions marked by acetylated H3 histones in <i>KIAA0319</i>

Jillian M. Couto, Izzy Livne‐Bar, Katherine Huang et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2009 · 53 citations · Full text

Histone Modifications, Rd Locus, Epigenetic Change +20