Epigenomic and transcriptomic signatures of a Klinefelter syndrome (47,XXY) karyotype in the brain

Microduplication of 15q13.3 and Xq21.31 in a family with tourette syndrome and comorbidities

(2013) Linea Melchior et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

The XY gene hypothesis of psychosis: Origins and current status

(2013) Timothy J. Crow   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

A data-driven approach to preprocessing Illumina 450K methylation array data

(2013) Ruth Pidsley et al.   BMC GENOMICS

Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray

(2013) Yi-an Chen et al.   Epigenetics

Genomic Imprinting Effects of the X Chromosome on Brain Morphology

(2013) J.-F. Lepage et al.   JOURNAL OF NEUROSCIENCE

Constitutional trisomy 8 mosaicism as a model for epigenetic studies of aneuploidy

(2013) Josef Davidsson et al.   Epigenetics & Chromatin

Brain morphological abnormalities in 49,XXXXY syndrome: A pediatric magnetic resonance imaging study

(2013) Jonathan D. Blumenthal et al.   NeuroImage-Clinical

Neuroanatomical correlates of Klinefelter syndrome studied in relation to the neuropsychological profile

(2013) Anne Skakkebæk et al.   NeuroImage-Clinical

Comb-p: software for combining, analyzing, grouping and correcting spatially correlated P-values

(2012) B. S. Pedersen et al.   BIOINFORMATICS

The sva package for removing batch effects and other unwanted variation in high-throughput experiments

(2012) Jeffrey T. Leek et al.   BIOINFORMATICS

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder

(2012) Dianne F Newbury et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Methylation-Specific PCR Allows for Fast Diagnosis of X Chromosome Disomy and Reveals Skewed Inactivation of the X Chromosome in Men With Klinefelter Syndrome

(2012) A. Mehta et al.   JOURNAL OF ANDROLOGY

Genetic evidence for association between NOTCH4 and schizophrenia supported by a GWAS follow-up study in a Japanese population

(2012) M Ikeda et al.   MOLECULAR PSYCHIATRY

Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood

(2012) Matthew N Davies et al.   GENOME BIOLOGY

Protective Roles for Potassium SK/KCa2 Channels in Microglia and Neurons

(2012) Amalia M. Dolga et al.   Frontiers in Pharmacology

Expression of selected genes escaping from X inactivation in the 41, XXY* mouse model for Klinefelter’s syndrome

(2011) Steffi Werler et al.   ACTA PAEDIATRICA

Klinefelter syndrome

(2011) Anne M. Wikström et al.   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

DNA methylation in repetitive elements and Alzheimer disease

(2011) V. Bollati et al.   BRAIN BEHAVIOR AND IMMUNITY

Blood leukocyte Alu and LINE-1 methylation and gastric cancer risk in the Shanghai Women's Health Study

(2011) Y Gao et al.   BRITISH JOURNAL OF CANCER

Methylation of L1Hs promoters is lower on the inactive X, has a tendency of being higher on autosomes in smaller genomes and shows inter-individual variability at some loci

(2011) Heike Singer et al.   HUMAN MOLECULAR GENETICS

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

(2011) L Priebe et al.   MOLECULAR PSYCHIATRY

Miwi catalysis is required for piRNA amplification-independent LINE1 transposon silencing

(2011) Michael Reuter et al.   NATURE

A Longitudinal Twin Study of Skewed X Chromosome-Inactivation

(2011) Chloe Chung Yi Wong et al.   PLoS One

Chromosomal Variants in Klinefelter Syndrome

(2011) A. Frühmesser et al.   Sexual Development

The Parent-of-Origin of the Extra X Chromosome May Differentially Affect Psychopathology in Klinefelter Syndrome

(2010) Hilgo Bruining et al.   BIOLOGICAL PSYCHIATRY

Altered DNA Methylation in Leukocytes with Trisomy 21

(2010) Kristi Kerkel et al.   PLoS Genetics

The cognitive phenotype in Klinefelter syndrome: A review of the literature including genetic and hormonal factors

(2009) Richard Boada et al.   Developmental Disabilities Research Reviews

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

(2009) J Elia et al.   MOLECULAR PSYCHIATRY

EphB2 and EphA4 receptors regulate formation of the principal inter-hemispheric tracts of the mammalian forebrain

(2009) S.K.Y. Ho et al.   NEUROSCIENCE

The influence of sex chromosome aneuploidy on brain asymmetry

(2008) Roozbeh Rezaie et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

lumi: a pipeline for processing Illumina microarray

(2008) P. Du et al.   BIOINFORMATICS

Strong association of de novo copy number mutations with sporadic schizophrenia

(2008) Bin Xu et al.   NATURE GENETICS

Large-Scale Population Study of Human Cell Lines Indicates that Dosage Compensation Is Virtually Complete

(2008) Colette M. Johnston et al.   PLoS Genetics

Differential methylation of the X-chromosome is a possible source of discordance for bipolar disorder female monozygotic twins

(2007) Araceli Rosa et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS