A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13

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

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

Genome-Wide Association Study of Receptive Language Ability of 12-Year-Olds

(2014) Nicole Harlaar et al.   JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH

Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence

(2014) Beate St Pourcain et al.   Molecular Autism

TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities

(2013) Wojciech Wiszniewski et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria

(2013) Samantha J Turner et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A combined study of genetic association and brain imaging on theDAOAgene in schizophrenia

(2013) Jun Chen et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

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

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

A genome-wide association study for reading and language abilities in two population cohorts

(2013) M. Luciano et al.   GENES BRAIN AND BEHAVIOR

Meta-analysis of genetic association studies on bipolar disorder

(2012) Fayaz Seifuddin et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Association between the DAOA/G72 gene and bipolar disorder and meta-analyses in bipolar disorder and schizophrenia

(2011) Daniel J Müller et al.   BIPOLAR DISORDERS

Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population

(2011) Pia Villanueva et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A balanced t(10;15) translocation in a male patient with developmental language disorder

(2011) A. Gulhan Ercan-Sencicek et al.   European Journal of Medical Genetics

CNTNAP2variants affect early language development in the general population

(2011) A. J. O. Whitehouse et al.   GENES BRAIN AND BEHAVIOR

Spoiling the Whole Bunch: Quality Control Aimed at Preserving the Integrity of High-Throughput Genotyping

(2010) Anna Pluzhnikov et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

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

Ordered Subset Analysis Identifies Loci Influencing Lung Cancer Risk on Chromosomes 6q and 12q

(2010) S. Fang et al.   CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION

An extended Family with a Dominantly Inherited Speech Disorder

(2010) J. A. Hurst et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3

(2010) L. Addis et al.   GENES BRAIN AND BEHAVIOR

Association of D16S515 Microsatellite with Specific Language Impairment on Robinson Crusoe Island, an Isolated Chilean Population: A Possible Key to Understanding Language Development

(2010) Pia Villanueva et al.   HUMAN BIOLOGY

Genetic variation in G72 correlates with brain activation in the right middle temporal gyrus in a verbal fluency task in healthy individuals

(2010) Axel Krug et al.   HUMAN BRAIN MAPPING

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

Identification of Clinical Markers of Specific Language Impairment in Adults

(2010) Gerard H. Poll et al.   JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH

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

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

Genetic variation in the G72 (DAOA) gene affects temporal lobe and amygdala structure in subjects affected by bipolar disorder

(2009) Riccardo Zuliani et al.   BIPOLAR DISORDERS

Genome-Wide Scan for Linkage to Type 1 Diabetes in 2,496 Multiplex Families From the Type 1 Diabetes Genetics Consortium

(2009) P. Concannon et al.   DIABETES

Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment

(2009) Mabel L. Rice et al.   Journal of Neurodevelopmental Disorders

A putative high risk diplotype of the G72 gene is in healthy individuals associated with better performance in working memory functions and altered brain activity in the medial temporal lobe

(2009) Andreas Jansen et al.   NEUROIMAGE

Dynamic Microtubules Regulate Dendritic Spine Morphology and Synaptic Plasticity

(2009) Jacek Jaworski et al.   NEURON

CPEB3 is associated with human episodic memory

(2009) Christian Vogler   Frontiers in Behavioral Neuroscience

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

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

Genetic Variation in the DAOA (G72) Gene Modulates Hippocampal Function in Subjects at High Risk of Schizophrenia

(2008) Jeremy Hall et al.   BIOLOGICAL PSYCHIATRY

Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits

(2008) Matthias Groszer et al.   CURRENT BIOLOGY

A Functional Genetic Link between Distinct Developmental Language Disorders

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

Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment

(2007) M. Falcaro et al.   GENES BRAIN AND BEHAVIOR