12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech

Genetics of Speech and Language Disorders

(2011) Changsoo Kang et al.   Annual Review of Genomics and Human Genetics

Rab6, Rab8, and MICAL3 Cooperate in Controlling Docking and Fusion of Exocytotic Carriers

(2011) Ilya Grigoriev et al.   CURRENT BIOLOGY

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

(2011) Brian J O'Roak et al.   NATURE GENETICS

Mosaic 7q31 Deletion Involving FOXP2 Gene Associated With Language Impairment

(2011) C. Palka et al.   PEDIATRICS

De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment

(2010) Fadi F. Hamdan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Delineation of 15q13.3 microdeletions

(2010) A Masurel-Paulet et al.   CLINICAL GENETICS

Chiari I malformation, delayed gross motor skills, severe speech delay and epileptiform discharges in a child with FOXP1 haploinsufficiency

(2010) Christopher W Carr et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

1.39 Mb inherited interstitial deletion in 12p13.33 associated with developmental delay

(2010) Ahmed T. Abdelmoity et al.   European Journal of Medical Genetics

CAST and ELKS proteins: structural and functional determinants of the presynaptic active zone

(2010) Y. Hida et al.   JOURNAL OF BIOCHEMISTRY

SynArfGEF is a guanine nucleotide exchange factor for Arf6 and localizes preferentially at post-synaptic specializations of inhibitory synapses

(2010) Masahiro Fukaya et al.   JOURNAL OF NEUROCHEMISTRY

Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients

(2010) Ester Saus et al.   JOURNAL OF PSYCHIATRIC RESEARCH

Which Neurodevelopmental Disorders Get Researched and Why?

(2010) Dorothy V. M. Bishop   PLoS One

2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate gene

(2009) Caroline Rooryck et al.   European Journal of Medical Genetics

A 785kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis

(2009) Mitchel J. Pariani et al.   European Journal of Medical Genetics

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

(2009) E K Green et al.   MOLECULAR PSYCHIATRY

FOXP2 as a molecular window into speech and language

(2009) Simon E. Fisher et al.   TRENDS IN GENETICS

A Functional Genetic Link between Distinct Developmental Language Disorders

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