Language Impairment and Dyslexia Genes Influence Language Skills in Children With Autism Spectrum Disorders

Association of theROBO1gene with reading disabilities in a family-based analysis

(2014) C. Tran et al.   GENES BRAIN AND BEHAVIOR

A Genome Scan for Loci Shared by Autism Spectrum Disorder and Language Impairment

(2013) Christopher W. Bartlett et al.   AMERICAN JOURNAL OF PSYCHIATRY

Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services

(2013) Jennifer L. Roberts et al.   GENE

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

(2013) Brett S Abrahams et al.   Molecular Autism

Gene × Gene Interaction in Shared Etiology of Autism and Specific Language Impairment

(2012) Christopher W. Bartlett et al.   BIOLOGICAL PSYCHIATRY

The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure

(2012) Thomas S. Scerri et al.   PLoS One

Imaging genetics of FOXP2 in dyslexia

(2011) Arndt Wilcke et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain

(2011) Sonja C. Vernes et al.   PLoS Genetics

Genetic Variance in a Component of the Language Acquisition Device: ROBO1 Polymorphisms Associated with Phonological Buffer Deficits

(2010) Timothy C. Bates et al.   BEHAVIOR GENETICS

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects

(2010) D. F. Newbury et al.   BEHAVIOR GENETICS

Overlaps Between Autism and Language Impairment: Phenomimicry or Shared Etiology?

(2010) D. V. M. Bishop   BEHAVIOR GENETICS

METAL: fast and efficient meta-analysis of genomewide association scans

(2010) C. J. Willer et al.   BIOINFORMATICS

Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population

(2010) S. Paracchini et al.   GENES BRAIN AND BEHAVIOR

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

(2010) Beate Peter et al.   Journal of Neurodevelopmental Disorders

The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors

(2010) Gerald D. Fischbach et al.   NEURON

CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment

(2009) Dianne F. Newbury et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A genome-wide linkage and association scan reveals novel loci for autism

(2009) Lauren A. Weiss et al.   NATURE

Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene

(2008) Maricela Alarcón et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genetic analyses ofRoundabout(ROBO) axon guidance receptors in autism

(2008) A. Anitha et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Relations Among Speech, Language, and Reading Disorders

(2008) Bruce F. Pennington et al.   Annual Review of Psychology

Overlap between autism and specific language impairment: comparison of Autism Diagnostic Interview and Autism Diagnostic Observation Schedule scores

(2008) Ovsanna T. Leyfer et al.   Autism Research

Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies

(2008) Klaus-Peter Lesch et al.   JOURNAL OF NEURAL TRANSMISSION

A Functional Genetic Link between Distinct Developmental Language Disorders

(2008) Sonja C. Vernes et al.   NEW ENGLAND JOURNAL OF MEDICINE