Approach to epigenetic analysis in language disorders

GATES: A Rapid and Powerful Gene-Based Association Test Using Extended Simes Procedure

(2011) Miao-Xin Li et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genetic Variation in the KIAA0319 5′ Region as a Possible Contributor to Dyslexia

(2011) Adrienne Elbert et al.   BEHAVIOR GENETICS

Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children

(2011) Cadmon KP Lim et al.   Behavioral and Brain Functions

DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits

(2011) Tom S. Scerri et al.   BIOLOGICAL PSYCHIATRY

15q11.2–13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain

(2011) Dag H. Yasui et al.   HUMAN MOLECULAR GENETICS

Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder

(2011) Emma L. Dempster et al.   HUMAN MOLECULAR GENETICS

Mapping and analysis of chromatin state dynamics in nine human cell types

(2011) Jason Ernst et al.   NATURE

Epigenetic Mechanisms in Cognition

(2011) Jeremy J. Day et al.   NEURON

The Use of Genomic Information to Optimize Cancer Chemotherapy

(2011) Federico Innocenti et al.   SEMINARS IN ONCOLOGY

Epigenetic Regulation of Learning and Memory by Drosophila EHMT/G9a

(2011) Jamie M. Kramer et al.   PLOS BIOLOGY

Gene-Based Tests of Association

(2011) Hailiang Huang 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

Pleiotropic Effects of DCDC2 and DYX1C1 Genes on Language and Mathematics Traits in Nuclear Families of Developmental Dyslexia

(2010) Cecilia Marino 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

A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression

(2010) Haiying Meng et al.   BEHAVIOR GENETICS

The Language of Histone Crosstalk

(2010) Jung-Shin Lee et al.   CELL

Hippocampus development and function: role of epigenetic factors and implications for cognitive disease

(2010) PS Lagali et al.   CLINICAL GENETICS

Epigenetics, Copy Number Variation, and Other Molecular Mechanisms Underlying Neurodevelopmental Disabilities: New Insights and Diagnostic Approaches

(2010) Andrea L. Gropman et al.   JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS

A theoretical molecular network for dyslexia: integrating available genetic findings

(2010) G Poelmans et al.   MOLECULAR PSYCHIATRY

Epigenetic modifications as therapeutic targets

(2010) Theresa K Kelly et al.   NATURE BIOTECHNOLOGY

Epigenetic modifications and human disease

(2010) Anna Portela et al.   NATURE BIOTECHNOLOGY

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Altered Histone Acetylation Is Associated with Age-Dependent Memory Impairment in Mice

(2010) S. Peleg et al.   SCIENCE

The study of eQTL variations by RNA-seq: from SNPs to phenotypes

(2010) Jacek Majewski et al.   TRENDS IN GENETICS

Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319

(2009) Jillian M. Couto et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Association of Attention-Deficit/Hyperactivity Disorder with a Candidate Region for Reading Disabilities on Chromosome 6p

(2009) Jillian M. Couto et al.   BIOLOGICAL PSYCHIATRY

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

(2009) Simon G Gregory et al.   BMC Medicine

Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia

(2009) Satu Massinen et al.   HUMAN MOLECULAR GENETICS

Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype

(2009) T Kleefstra et al.   JOURNAL OF MEDICAL GENETICS

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

Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation

(2009) T C Bates et al.   MOLECULAR PSYCHIATRY

Finding the missing heritability of complex diseases

(2009) Teri A. Manolio et al.   NATURE

HDAC2 negatively regulates memory formation and synaptic plasticity

(2009) Ji-Song Guan et al.   NATURE

Progress towards a cellular neurobiology of reading disability

(2009) Lisa A. Gabel et al.   NEUROBIOLOGY OF DISEASE

Further evidence for DYX1C1 as a susceptibility factor for dyslexia

(2009) Faten Dahdouh et al.   PSYCHIATRIC GENETICS

A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene

(2009) Megan Y. Dennis et al.   PLoS Genetics

Association of theKIAA0319Dyslexia Susceptibility Gene With Reading Skills in the General Population

(2008) Silvia Paracchini et al.   AMERICAN JOURNAL OF PSYCHIATRY

The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia

(2008) Isabel Tapia-Páez et al.   FASEB JOURNAL

Epigenetic Regulation of bdnf Gene Transcription in the Consolidation of Fear Memory

(2008) F. D. Lubin et al.   JOURNAL OF NEUROSCIENCE

A Functional Genetic Link between Distinct Developmental Language Disorders

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

Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample

(2008) Kerstin U. Ludwig et al.   PSYCHIATRIC GENETICS

Heritability of specific language impairment depends on diagnostic criteria

(2007) D. V. M. Bishop et al.   GENES BRAIN AND BEHAVIOR