Dosage-sensitivity of imprinted genes expressed in the brain: 15q11–q13 and neuropsychiatric illness: Figure 1

Overexpression of Chromosome 15q11-q13 Gene Products: A Risk Factor for Schizophrenia and Associated Psychoses?

(2012) Erik Boot et al.   AMERICAN JOURNAL OF PSYCHIATRY

Enhanced appetitive learning and reversal learning in a mouse model for Prader-Willi syndrome.

(2012) Dinko Relkovic et al.   BEHAVIORAL NEUROSCIENCE

Maternal Control of Nutrient Allocation in Plant Seeds by Genomic Imprinting

(2012) Liliana M. Costa et al.   CURRENT BIOLOGY

New insights into establishment and maintenance of DNA methylation imprints in mammals

(2012) G. Kelsey et al.   PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES

H3K9me2 attracts PGC7 in the zygote to prevent Tet3-mediated oxidation of 5-methylcytosine

(2012) P. E. Szabo et al.   Journal of Molecular Cell Biology

Critical Evaluation of Imprinted Gene Expression by RNA–Seq: A New Perspective

(2012) Brian DeVeale et al.   PLoS Genetics

Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness

(2011) Andrés Ingason et al.   AMERICAN JOURNAL OF PSYCHIATRY

Genomic imprinting; the cost of mother's care

(2011) Anthony R. Isles   BIOESSAYS

High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy

(2011) Larissa R Stewart et al.   BMC Medical Genetics

Behavioural and cognitive profiles of mouse models for Prader–Willi syndrome

(2011) Dinko Relkovic et al.   BRAIN RESEARCH BULLETIN

Epigenetic and genetic disturbance of the imprinted 11p15 region in Beckwith-Wiedemann and Silver-Russell syndromes

(2011) J Demars et al.   CLINICAL GENETICS

Genomic imprinting: recognition and marking of imprinted loci

(2011) Lara K Abramowitz et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Developmental regulation of somatic imprints

(2011) Rosalind M. John et al.   DIFFERENTIATION

Fetal overgrowth in the Cdkn1c mouse model of Beckwith-Wiedemann syndrome

(2011) S. J. Tunster et al.   Disease Models & Mechanisms

Genomic imprinting as an adaptative model of developmental plasticity

(2011) Elizabeth J. Radford et al.   FEBS LETTERS

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

Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome

(2011) Makiko Meguro-Horike et al.   HUMAN MOLECULAR GENETICS

Distinct physiological and behavioural functions for parental alleles of imprinted Grb10

(2011) Alastair S. Garfield et al.   NATURE

Postnatal loss of Dlk1 imprinting in stem cells and niche astrocytes regulates neurogenesis

(2011) Sacri R. Ferrón et al.   NATURE

Dynamic CpG island methylation landscape in oocytes and preimplantation embryos

(2011) Sébastien A Smallwood et al.   NATURE GENETICS

Genomic imprinting: the emergence of an epigenetic paradigm

(2011) Anne C. Ferguson-Smith   NATURE REVIEWS GENETICS

Increased Gene Dosage of Ube3a Results in Autism Traits and Decreased Glutamate Synaptic Transmission in Mice

(2011) S. E. P. Smith et al.   Science Translational Medicine

Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples

(2011) Haley A Scoles et al.   Molecular Autism

The Kraepelinian dichotomy – going, going … but still not gone

(2010) Nick Craddock et al.   BRITISH JOURNAL OF PSYCHIATRY

The Angelman Syndrome Protein Ube3A Regulates Synapse Development by Ubiquitinating Arc

(2010) Paul L. Greer et al.   CELL

Further refinement of the critical minimal genetic region for the imprinting disorder 6q24 transient neonatal diabetes

(2010) L. E. Docherty et al.   DIABETOLOGIA

Angelman Syndrome, a Genomic Imprinting Disorder of the Brain

(2010) S. J. Chamberlain et al.   JOURNAL OF NEUROSCIENCE

Independent evidence for the selective influence of GABAA receptors on one component of the bipolar disorder phenotype

(2010) R Breuer et al.   MOLECULAR PSYCHIATRY

High-Resolution Analysis of Parent-of-Origin Allelic Expression in the Mouse Brain

(2010) C. Gregg et al.   SCIENCE

The Importance of Imprinting in the Human Placenta

(2010) Jennifer M. Frost et al.   PLoS Genetics

Increased apoptosis during neonatal brain development underlies the adult behavioral deficits seen in mice lacking a functionalpaternally expressed gene 3(Peg3)

(2009) Kevin D. Broad et al.   Developmental Neurobiology

Behavioural and cognitive abnormalities in an imprinting centre deletion mouse model for Prader–Willi syndrome

(2009) Dinko Relkovic et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour

(2009) Christine M. Doe et al.   HUMAN MOLECULAR GENETICS

Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype

(2009) N Craddock et al.   MOLECULAR PSYCHIATRY

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

(2009) Joseph T. Glessner et al.   NATURE

Gene Dosage Effects of the Imprinted Delta-Like Homologue 1 (Dlk1/Pref1) in Development: Implications for the Evolution of Imprinting

(2009) Simao Teixeira da Rocha et al.   PLoS Genetics

In search of the psychosis gene in people with Prader-Willi syndrome

(2008) Tessa Webb et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A Maternal-Zygotic Effect Gene, Zfp57, Maintains Both Maternal and Paternal Imprints

(2008) Xiajun Li et al.   DEVELOPMENTAL CELL

Failure of neuronal homeostasis results in common neuropsychiatric phenotypes

(2008) Melissa B. Ramocki et al.   NATURE

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

(2008) Amber Hogart et al.   NEUROBIOLOGY OF DISEASE