Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36

In vivo Atoh1 targetome reveals how a proneural transcription factor regulates cerebellar development

(2011) T. J. Klisch et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Rare Copy Number Variation Discovery and Cross-Disorder Comparisons Identify Risk Genes for ADHD

(2011) A. C. Lionel et al.   Science Translational Medicine

SNP Sets and Reading Ability: Testing Confirmation of a 10-SNP Set in a Population Sample

(2011) Michelle Luciano et al.   Twin Research and Human Genetics

Identification of a novel intronic enhancer responsible for the transcriptional regulation of musashi1 in neural stem/progenitor cells

(2011) Satoshi Kawase et al.   Molecular Brain

Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility

(2010) Sabina Domené et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Differential Genetic Etiology of Reading Difficulties as a Function of IQ: An Update

(2010) S. J. Wadsworth et al.   BEHAVIOR GENETICS

The Engrailed homeobox genes determine the different foliation patterns in the vermis and hemispheres of the mammalian cerebellum

(2010) Y. Cheng et al.   DEVELOPMENT

Reading Disability in Twins

(2010) Harry Bakwin   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study

(2010) M. Ribasés et al.   GENES BRAIN AND BEHAVIOR

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

(2010) M Arcos-Burgos et al.   MOLECULAR PSYCHIATRY

Lmo4 and Clim1 Progressively Delineate Cortical Projection Neuron Subtypes during Development

(2009) Eiman Azim et al.   CEREBRAL CORTEX

Family-based studies indicate association ofEngrailed 2gene with autism in an Indian population

(2009) B. Sen et al.   GENES BRAIN AND BEHAVIOR

Disturbances in the secretion of neurotransmitters in IA-2/IA-2β null mice: Changes in behavior, learning and lifespan

(2009) T. Nishimura et al.   NEUROSCIENCE

A role for PKC in mediating stress-induced prefrontal cortical structural plasticity and cognitive function

(2009) G. Chen et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Deletion of Atoh1 Disrupts Sonic Hedgehog Signaling in the Developing Cerebellum and Prevents Medulloblastoma

(2009) A. Flora et al.   SCIENCE

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

(2009) Maja Bucan et al.   PLoS Genetics

Structural Variation of Chromosomes in Autism Spectrum Disorder

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genome Scan of a Nonword Repetition Phenotype in Families with Dyslexia: Evidence for Multiple Loci

(2008) Zoran Brkanac et al.   BEHAVIOR GENETICS

Impairments in phonological processing and nonverbal intellectual function in parents of children with autism

(2008) Gwen L. Schmidt et al.   JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY

Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein

(2008) Yongsu Jeong et al.   NATURE GENETICS

Lhx2 Selector Activity Specifies Cortical Identity and Suppresses Hippocampal Organizer Fate

(2008) V. S. Mangale et al.   SCIENCE