Related references
Note: Only part of the references are listed.Executive function as measured by the Behavior Rating Inventory of Executive Function-2: children and adolescents with Williams syndrome
C. Greiner de Magalhaes et al.
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH (2022)
Epigenetics of childhood trauma: Long term sequelae and potential for treatment
Kristina M. Thumfart et al.
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS (2022)
Genome-wide DNA methylation of the liver reveals delayed effects of early-life exposure to 17-alpha-ethinylestradiol in the self-fertilizing mangrove rivulus
Anne-Sophie Voisin et al.
EPIGENETICS (2022)
Altered White Matter and microRNA Expression in a Murine Model Related to Williams Syndrome Suggests That miR-34b/c Affects Brain Development via Ptpru and Dcx Modulation
Meitar Grad et al.
CELLS (2022)
An optimized protocol for total RNA isolation from archive d formalin-fixe d paraffin-emb e dde d tissues to identify the long non-coding RNA in oral squamous cell carcinomas
Kiran Kumar et al.
METHODSX (2022)
White matter alterations in Williams syndrome related to behavioral and motor impairments
Ariel Nir et al.
GLIA (2021)
Cognitive profile of young children with Williams syndrome
D. Miezah et al.
JOURNAL OF INTELLECTUAL DISABILITY RESEARCH (2021)
Role of the multifunctional transcription factor TFII-I in DNA damage repair
Ananda L. Roy
DNA REPAIR (2021)
Tubulin glycylation controls axonemal dynein activity, flagellar beat, and male fertility
Sudarshan Gadadhar et al.
SCIENCE (2021)
Differential DNA Methylation Landscape in Skin Fibroblasts from African Americans with Systemic Sclerosis
DeAnna Baker Frost et al.
GENES (2021)
The social dilemma: prefrontal control of mammalian sociability
Ofer Yizhar et al.
CURRENT OPINION IN NEUROBIOLOGY (2021)
Williams syndrome
Beth A. Kozel et al.
NATURE REVIEWS DISEASE PRIMERS (2021)
Methods for mapping 3D chromosome architecture
Rieke Kempfer et al.
NATURE REVIEWS GENETICS (2020)
Health Care Supervision for Children With Williams Syndrome
Colleen A. Morris et al.
PEDIATRICS (2020)
Integrated DNA methylation analysis reveals a potential role for ANKRD30B in Williams syndrome
Ryo Kimura et al.
NEUROPSYCHOPHARMACOLOGY (2020)
LINGO family receptors are differentially expressed in the mouse brain and form native multimeric complexes
Anthony Guillemain et al.
FASEB JOURNAL (2020)
Gestational arsenic exposure induces site-specific DNA hypomethylation in active retrotransposon subfamilies in offspring sperm in mice
Keiko Nohara et al.
EPIGENETICS & CHROMATIN (2020)
Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug
Boaz Barak et al.
NATURE NEUROSCIENCE (2019)
Long-term cardiovascular outcome of Williams syndrome
Seul Gi Cha et al.
CONGENITAL HEART DISEASE (2019)
The diverse roles of DNA methylation in mammalian development and disease
Maxim V. C. Greenberg et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2019)
Epigenetic Delay in the Neurodevelopmental Trajectory of DNA Methylation States in Autism Spectrum Disorders
Michael J. Corley et al.
FRONTIERS IN GENETICS (2019)
DNA methylation analysis for screening and diagnostic testing in neurodevelopmental disorders
David E. Godler et al.
DNA METHYLATION (2019)
Dynamics of social representation in the mouse prefrontal cortex
Dana Rubi Levy et al.
NATURE NEUROSCIENCE (2019)
Brain cell type-specific enhancer-promoter interactome maps and disease-risk association
Alexi Nott et al.
SCIENCE (2019)
Detecting multiple differentially methylated CpG sites and regions related to dimensional psychopathology in youths
Leticia M. Spindola et al.
CLINICAL EPIGENETICS (2019)
Integrated DNA methylation and gene expression profiling across multiple brain regions implicate novel genes in Alzheimer's disease
Stephen A. Semick et al.
ACTA NEUROPATHOLOGICA (2019)
Dosage analysis of the 7q11.23 Williams region identifies BAZ1B as a major human gene patterning the modern human face and underlying self-domestication
Matteo Zanella et al.
SCIENCE ADVANCES (2019)
GAD1 alternative transcripts and DNA methylation in human prefrontal cortex and hippocampus in brain development, schizophrenia
R. Tao et al.
MOLECULAR PSYCHIATRY (2018)
Genomic DNA Methylation Signatures Enable Concurrent Diagnosis and Clinical Genetic Variant Classification in Neurodevelopmental Syndromes
Erfan Aref-Eshghi et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
Cardiovascular disease in Williams syndrome
R. Thomas Collins
CURRENT OPINION IN PEDIATRICS (2018)
Williams syndrome deletions and duplications: Genetic windows to understanding anxiety, sociality, autism, and schizophrenia
Bernard J. Crespi et al.
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS (2017)
Oxytocin and vasopressin neural networks: Implications for social behavioral diversity and translational neuroscience
Zachary V. Johnson et al.
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS (2017)
The Transcription Factor Sp3 Cooperates with HDAC2 to Regulate Synaptic Function and Plasticity in Neurons
Hidekuni Yamakawa et al.
CELL REPORTS (2017)
CpG and Non-CpG Methylation in Epigenetic Gene Regulation and Brain Function
Hyun Sik Jang et al.
GENES (2017)
Low-input Capture-C: A Chromosome Conformation Capture Assay to Analyze Chromatin Architecture in Small Numbers of Cells
A. Marieke Oudelaar et al.
BIO-PROTOCOL (2017)
metilene: fast and sensitive calling of differentially methylated regions from bisulfite sequencing data
Frank Juehling et al.
GENOME RESEARCH (2016)
The nuclear receptor Tlx regulates motor, cognitive and anxiety-related behaviours during adolescence and adulthood
James D. O'Leary et al.
BEHAVIOURAL BRAIN RESEARCH (2016)
Epigenetic control of oligodendrocyte development: adding new players to old keepers
Jia Liu et al.
CURRENT OPINION IN NEUROBIOLOGY (2016)
A human neurodevelopmental model for Williams syndrome
Thanathom Chailangkarn et al.
NATURE (2016)
Neurobiology of social behavior abnormalities in autism and Williams syndrome
Boaz Barak et al.
NATURE NEUROSCIENCE (2016)
Spatial genome organization and cognition
Prashanth Rajarajan et al.
NATURE REVIEWS NEUROSCIENCE (2016)
Epigenetic mechanisms in neurogenesis
Bing Yao et al.
NATURE REVIEWS NEUROSCIENCE (2016)
Epigenetic Basis of Mental Illness
Eric J. Nestler et al.
NEUROSCIENTIST (2016)
DNA methylation dynamics in neurogenesis
Zhiqin Wang et al.
EPIGENOMICS (2016)
The Orphan Nuclear Receptor TLX/NR2E1 in Neural Stem Cells and Diseases
Tao Wang et al.
NEUROSCIENCE BULLETIN (2016)
Functional Characterization of DNA Methylation in the Oligodendrocyte Lineage
Sarah Moyon et al.
CELL REPORTS (2016)
Williams-Beuren syndrome: pitfalls for diagnosis in limited resources setting
Aime Lumaka et al.
CLINICAL CASE REPORTS (2016)
Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23
Emma Strong et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2015)
DNA Methylation and Its Implications and Accessibility for Neuropsychiatric Therapeutics
Jeremy J. Day et al.
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, VOL 55 (2015)
Plasticity of DNA methylation in a nerve injury model of pain
Meike Goelzenleuchter et al.
EPIGENETICS (2015)
Chromatin Landscape Defined by Repressive Histone Methylation during Oligodendrocyte Differentiation
Jia Liu et al.
JOURNAL OF NEUROSCIENCE (2015)
What are super-enhancers?
Sebastian Pott et al.
NATURE GENETICS (2015)
Genome-wide targeting of the epigenetic regulatory protein CTCF to gene promoters by the transcription factor TFII-I
Rodrigo Pena-Hernandez et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
Osteogenesis and neurogenesis: a robust link also for language evolution
Cedric Boeckx et al.
FRONTIERS IN CELLULAR NEUROSCIENCE (2015)
Methylation of ribosomal RNA by NSUN5 is a conserved mechanism modulating organismal lifespan
Markus Schosserer et al.
NATURE COMMUNICATIONS (2015)
Oxytocin, vasopressin, and Williams syndrome: epigenetic effects on abnormal social behavior
Brian W. Haas et al.
FRONTIERS IN GENETICS (2015)
Mammalian SWI/SNF chromatin remodeling complexes and cancer: Mechanistic insights gained from human genomics
Cigall Kadoch et al.
SCIENCE ADVANCES (2015)
DNMT3L interacts with transcription factors to target DNMT3L/DNMT3B to specific DNA sequences: Role of the DNMT3L/DNMT3B/p65-NFκB complex in the (de-)methylation of TRAF1
Romain Pacaud et al.
BIOCHIMIE (2014)
Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia
Jennifer Gladys Mulle et al.
BIOLOGICAL PSYCHIATRY (2014)
A Highly Conserved Program of Neuronal Microexons Is Misregulated in Autistic Brains
Manuel Irimia et al.
CELL (2014)
The Methyltransferase WBSCR22/Merm1 Enhances Glucocorticoid Receptor Function and Is Regulated in Lung Inflammation and Cancer
Maryam Jangani et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
Common DNA methylation alterations in multiple brain regions in autism
C. Ladd-Acosta et al.
MOLECULAR PSYCHIATRY (2014)
The DNA methylation landscape of human early embryos
Hongshan Guo et al.
NATURE (2014)
MECHANISMS REGULATING THE DEVELOPMENT OF OLIGODENDROCYTES AND CENTRAL NERVOUS SYSTEM MYELIN
S. Mitew et al.
NEUROSCIENCE (2014)
DNA methylation changes in the postmortem dorsolateral prefrontal cortex of patients with schizophrenia
Shusuke Numata et al.
FRONTIERS IN GENETICS (2014)
Challenges in Clinical Diagnosis of Williams-Beuren Syndrome in Sub-Saharan Africans: Case Reports from Cameroon
Cedrik Tekendo-Ngongang et al.
MOLECULAR SYNDROMOLOGY (2014)
DNA methylome profiling of human tissues identifies global and tissue-specific methylation patterns
Kaie Lokk et al.
GENOME BIOLOGY (2014)
ChIP-Chip Identifies SEC23A, CFDP1, and NSD1 as TFII-I Target Genes in Human Neural Crest Progenitor Cells
Aleksandr V. Makeyev et al.
CLEFT PALATE-CRANIOFACIAL JOURNAL (2013)
Myelin inhibits oligodendroglial maturation and regulates oligodendrocytic transcription factor expression
Jason R. Plemel et al.
GLIA (2013)
DNA methylation: roles in mammalian development
Zachary D. Smith et al.
NATURE REVIEWS GENETICS (2013)
What role does TFII-I have to play in epigenetic modulation during embryogenesis?
Dashzeveg Bayarsaihan
EPIGENOMICS (2013)
Genetic association of the EGR2 gene with bipolar disorder in Korea
Se Hyun Kim et al.
EXPERIMENTAL AND MOLECULAR MEDICINE (2012)
The contributions of oxytocin and vasopressin pathway genes to human behavior
Richard P. Ebstein et al.
HORMONES AND BEHAVIOR (2012)
The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders
Claire Bacon et al.
HUMAN GENETICS (2012)
Genome-wide Studies of CCCTC-binding Factor (CTCF) and Cohesin Provide Insight into Chromatin Structure and Regulation
Bum-Kyu Lee et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
Epigenetic modulation by TFII-I during embryonic stem cell differentiation
Dashzeveg Bayarsaihan et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2012)
Extracellular signal-regulated kinase 1/2 signaling promotes oligodendrocyte myelination in vitro
Junhua Xiao et al.
JOURNAL OF NEUROCHEMISTRY (2012)
Reduced insulin secretion correlates with decreased expression of exocytotic genes in pancreatic islets from patients with type 2 diabetes
Sofia A. Andersson et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY (2012)
Oxytocin and Vasopressin Are Dysregulated in Williams Syndrome, a Genetic Disorder Affecting Social Behavior
Li Dai et al.
PLOS ONE (2012)
Diversity and Complexity in Chromatin Recognition by TFII-I Transcription Factors in Pluripotent Embryonic Stem Cells and Embryonic Tissues
Aleksandr V. Makeyev et al.
PLOS ONE (2012)
Validation of a DNA methylation microarray for 450,000 CpG sites in the human genome
Juan Sandoval et al.
EPIGENETICS (2011)
The GPR17 Receptor in NG2 Expressing Cells: Focus on In Vivo Cell Maturation and Participation in Acute Trauma and Chronic Damage
Enrica Boda et al.
GLIA (2011)
Neocortical excitation/inhibition balance in information processing and social dysfunction
Ofer Yizhar et al.
NATURE (2011)
Integrative genomics viewer
James T. Robinson et al.
NATURE BIOTECHNOLOGY (2011)
Oxytocin and vasopressin in the human brain: social neuropeptides for translational medicine
Andreas Meyer-Lindenberg et al.
NATURE REVIEWS NEUROSCIENCE (2011)
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Stephan J. Sanders et al.
NEURON (2011)
Analysis of DNA Methylation in a Three-Generation Family Reveals Widespread Genetic Influence on Epigenetic Regulation
Jason Gertz et al.
PLOS GENETICS (2011)
High Prevalence of Diabetes and Pre-Diabetes in Adults With Williams Syndrome
B. R. Pober et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2010)
Introduction: Williams Syndrome
Colleen A. Morris
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2010)
Cognitive and Behavioral Characteristics of Children With Williams Syndrome: Implications for Intervention Approaches
Carolyn B. Mervis et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2010)
Expressing Hoxa2 across the entire endochondral skeleton alters the shape of the skeletal template in a spatially restricted fashion
Sara Tavella et al.
DIFFERENTIATION (2010)
A genome-wide map of human genetic interactions inferred from radiation hybrid genotypes
Andy Lin et al.
GENOME RESEARCH (2010)
Locus-wide identification of Egr2/Krox20 regulatory targets in myelin genes
Sung-Wook Jang et al.
JOURNAL OF NEUROCHEMISTRY (2010)
Mechanisms of Regulation of Oligodendrocyte Development by p38 Mitogen-Activated Protein Kinase
Li-Jin Chew et al.
JOURNAL OF NEUROSCIENCE (2010)
Simple Combinations of Lineage-Determining Transcription Factors Prime cis-Regulatory Elements Required for Macrophage and B Cell Identities
Sven Heinz et al.
MOLECULAR CELL (2010)
Conserved role of intragenic DNA methylation in regulating alternative promoters
Alika K. Maunakea et al.
NATURE (2010)
The NIH Roadmap Epigenomics Mapping Consortium
Bradley E. Bernstein et al.
NATURE BIOTECHNOLOGY (2010)
Defining the chromatin landscape in demyelinating disorders
Jimmy Long Huynh et al.
NEUROBIOLOGY OF DISEASE (2010)
The Challenge of Translation in Social Neuroscience: A Review of Oxytocin, Vasopressin, and Affiliative Behavior
Thomas R. Insel
NEURON (2010)
Brain-Derived Neurotrophic Factor Promotes Central Nervous System Myelination via a Direct Effect upon Oligodendrocytes
Junhua Xiao et al.
NEUROSIGNALS (2010)
MEDICAL PROGRESS Williams-Beuren Syndrome
Barbara R. Pober
NEW ENGLAND JOURNAL OF MEDICINE (2010)
Epigenetic Modifiers Are Necessary but Not Sufficient for Reprogramming Non-Myelinating Cells into Myelin Gene-Expressing Cells
Jia Liu et al.
PLOS ONE (2010)
Regulation of Oligodendrocyte Differentiation and Myelination
Ben Emery
SCIENCE (2010)
Epigenetic regulation of oligodendrocyte identity
Jia Liu et al.
TRENDS IN NEUROSCIENCES (2010)
New Findings concerning Cardiovascular Manifestations emerging from Long-term Follow-up of 150 patients with the Williams-Beuren-Beuren syndrome
Alessia Del Pasqua et al.
CARDIOLOGY IN THE YOUNG (2009)
Oxytocin, vasopressin, and human social behavior
Markus Heinrichs et al.
FRONTIERS IN NEUROENDOCRINOLOGY (2009)
An operational definition of epigenetics
Shelley L. Berger et al.
GENES & DEVELOPMENT (2009)
Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism
Susan E. Swanberg et al.
HUMAN MOLECULAR GENETICS (2009)
Post-translational modifications of tubulin in the nervous system
Nobuyuki Fukushima et al.
JOURNAL OF NEUROCHEMISTRY (2009)
The oligodendrocyte-specific G protein-coupled receptor GPR17 is a cell-intrinsic timer of myelination
Ying Chen et al.
NATURE NEUROSCIENCE (2009)
Initial association of NR2E1 with bipolar disorder and identification of candidate mutations in bipolar disorder, schizophrenia, and aggression through resequencing
Ravinesh A. Kumar et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS (2008)
Determination and functional analysis of the consensus binding site for TFII-I family member BEN, implicated in Williams-Beuren Syndrome
Maria B. Lazebnik et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Active gene repression by the Egr2•NAB complex during peripheral nerve myelination
Gennifer M. Mager et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Research Review: Williams syndrome: a critical review of the cognitive, behavioral, and neuroanatomical phenotype
Marilee A. Martens et al.
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY (2008)
A role for adult TLX-positive neural stem cells in learning and behaviour
Chun-Li Zhang et al.
NATURE (2008)
Induction of Olig2+ Precursors by FGF Involves BMP Signalling Blockade at the Smad Level
Bilada Bilican et al.
PLOS ONE (2008)
Recruitment of coregulator complexes to the β-globin gene locus by TFII-I and upstream stimulatory factor
Valerie J. Crusselle-Davis et al.
FEBS JOURNAL (2007)
LINGO-1 antagonist promotes spinal cord remyelination and axonal integrity in MOG-induced experimental autoimmune encephalomyelitis
Sha Mi et al.
NATURE MEDICINE (2007)
GAD1 mRNA Expression and DNA Methylation in Prefrontal Cortex of Subjects with Schizophrenia
Hsien-Sung Huang et al.
PLOS ONE (2007)
Epigenetic regulation in psychiatric disorders
Nadia Tsankova et al.
NATURE REVIEWS NEUROSCIENCE (2007)
Neuron-glia communication in the control of oligodendrocyte function and myelin biogenesis
Mikael Simons et al.
JOURNAL OF CELL SCIENCE (2006)
Multiple roles of Id4 in developmental myelination: Predicted outcomes and unexpected findings
Mireya Marin-Husstege et al.
GLIA (2006)
Gene expression analyses reveal molecular relationships among 20 regions of the human CNS
RB Roth et al.
NEUROGENETICS (2006)
Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour
A Meyer-Lindenberg et al.
NATURE REVIEWS NEUROSCIENCE (2006)
Direct regulation of myelin protein zero expression by the Egr2 transactivator
SE LeBlanc et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Temporal requirement of Hoxa2 in cranial neural crest skeletal morphogenesis
F Santagati et al.
DEVELOPMENT (2005)
Nab proteins are essential for peripheral nervous system myelination
N Le et al.
NATURE NEUROSCIENCE (2005)
LINGO-1 negatively regulates myelination by oligodendrocytes
S Mi et al.
NATURE NEUROSCIENCE (2005)
Axonal neuregulin-1 regulates myelin sheath thickness
GV Michailov et al.
SCIENCE (2004)
LINGO-1 is a component of the Nogo-66 receptor/p75 signaling complex
S Mi et al.
NATURE NEUROSCIENCE (2004)
Vasopressin and oxytocin release within the brain: a dynamic concept of multiple and variable modes of neuropeptide communication
R Landgraf et al.
FRONTIERS IN NEUROENDOCRINOLOGY (2004)
Signaling from integrins to Fyn to Rho family GTPases regulates morphologic differentiation of oligodendrocytes
XQ Liang et al.
JOURNAL OF NEUROSCIENCE (2004)
Advances in chromatin remodeling and human disease
KS Cho et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2004)
A candidate X-linked mental retardation gene is a component of a new family of histone deacetylase-containing complexes
MA Hakimi et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Neuroscience - New insights into neuron-glia communication
RD Fields et al.
SCIENCE (2002)
Physical and functional interactions of histone deacetylase 3 with TFII-I family proteins and PIASαβ
MI Tussié-Luna et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
The Id4 HLH protein and the timing of oligodendrocyte differentiation
T Kondo et al.
EMBO JOURNAL (2000)