CTNND2—a candidate gene for reading problems and mild intellectual disability

Amelioration of the typical cognitive phenotype in a patient with the 5pter deletion associated with Cri-du-chat syndrome in addition to a partial duplication ofCTNND2

(2014) Jennifer M. Sardina et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Intragenic duplication-A novel causative mechanism for SATB2-associated syndrome

(2014) Agne Liedén et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The molecular genetics and neurobiology of developmental dyslexia as model of a complex phenotype

(2014) Juha Kere   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment

(2014) R. Nudel et al.   GENES BRAIN AND BEHAVIOR

Genome-wide screening for DNA variants associated with reading and language traits

(2014) A. Gialluisi et al.   GENES BRAIN AND BEHAVIOR

The clinical significance of small copy number variants in neurodevelopmental disorders

(2014) Reza Asadollahi et al.   JOURNAL OF MEDICAL GENETICS

Genome sequencing identifies major causes of severe intellectual disability

(2014) Christian Gilissen et al.   NATURE

Reaching a CNV milestone

(2014) Arthur L Beaudet   NATURE GENETICS

Palmitoylation of δ-catenin by DHHC5 mediates activity-induced synapse plasticity

(2014) G Stefano Brigidi et al.   NATURE NEUROSCIENCE

Isl1 Directly Controls a Cholinergic Neuronal Identity in the Developing Forebrain and Spinal Cord by Forming Cell Type-Specific Complexes

(2014) Hyong-Ho Cho et al.   PLoS Genetics

Genome-wide association study of shared components of reading disability and language impairment

(2013) J. D. Eicher et al.   GENES BRAIN AND BEHAVIOR

The integrated landscape of driver genomic alterations in glioblastoma

(2013) Veronique Frattini et al.   NATURE GENETICS

Replicative mechanisms for CNV formation are error prone

(2013) Claudia M B Carvalho et al.   NATURE GENETICS

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development

(2013) Silvia Cappello et al.   NATURE GENETICS

Embryonic disruption of the candidate dyslexia susceptibility gene homolog Kiaa0319-like results in neuronal migration disorders

(2013) M.P. Platt et al.   NEUROSCIENCE

Three Dyslexia Susceptibility Genes, DYX1C1, DCDC2, and KIAA0319, Affect Temporo-Parietal White Matter Structure

(2012) Fahimeh Darki et al.   BIOLOGICAL PSYCHIATRY

Molecular Networks of DYX1C1 Gene Show Connection to Neuronal Migration Genes and Cytoskeletal Proteins

(2012) Kristiina Tammimies et al.   BIOLOGICAL PSYCHIATRY

A tractography study in dyslexia: neuroanatomic correlates of orthographic, phonological and speech processing

(2012) M. Vandermosten et al.   BRAIN

Sequencing Chromosomal Abnormalities Reveals Neurodevelopmental Loci that Confer Risk across Diagnostic Boundaries

(2012) Michael E. Talkowski et al.   CELL

Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration

(2012) Colby Chiang et al.   NATURE GENETICS

Clinical Diagnosis by Whole-Genome Sequencing of a Prenatal Sample

(2012) Michael E. Talkowski et al.   NEW ENGLAND JOURNAL OF MEDICINE

Structural Variation in the Human Genome and its Role in Disease

(2010) Paweł Stankiewicz et al.   Annual Review of Medicine

Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGH

(2010) A Lindstrand et al.   CLINICAL GENETICS

Mutation spectrum revealed by breakpoint sequencing of human germline CNVs

(2010) Donald F Conrad et al.   NATURE GENETICS

The Sequence Alignment/Map format and SAMtools

(2009) H. Li et al.   BIOINFORMATICS

Circos: An information aesthetic for comparative genomics

(2009) M. Krzywinski et al.   GENOME RESEARCH

S100B Protein Regulates Astrocyte Shape and Migration via Interaction with Src Kinase

(2009) Flora Brozzi et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

 -Catenin Regulates Spine and Synapse Morphogenesis and Function in Hippocampal Neurons during Development

(2009) J. Arikkath et al.   JOURNAL OF NEUROSCIENCE

δ-Catenin Is Required for the Maintenance of Neural Structure and Function in Mature Cortex In Vivo

(2009) Cheryl Matter et al.   NEURON

Cadherins as Targets for Genetic Diseases

(2009) A. El-Amraoui et al.   Cold Spring Harbor Perspectives in Biology

A Microhomology-Mediated Break-Induced Replication Model for the Origin of Human Copy Number Variation

(2009) P. J. Hastings et al.   PLoS Genetics

Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

(2008) Peter J Campbell et al.   NATURE GENETICS

High-resolution in situ hybridization to whole-mount zebrafish embryos

(2007) Christine Thisse et al.   Nature Protocols