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GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility

Neuron (Cambridge, Mass.), 2016-04, Vol.90 (1), p.56-69

2016

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CaMKII controls neuromodulation via neuropeptide gene expression and axonal targeting of neuropeptide vesicles

PLoS biology, 2020-08, Vol.18 (8), p.e3000826

2020

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The Wnt/Ca2+ pathway is involved in interneuronal communication mediated by tunneling nanotubes

The EMBO journal, 2019-12, Vol.38 (23), p.e101230-n/a

2019

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The intellectual disability‐associated CAMK2G p.Arg292Pro mutation acts as a pathogenic gain‐of‐function

Human mutation, 2018-12, Vol.39 (12), p.2008-2024

2018

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Non-associative potentiation of perisomatic inhibition alters the temporal coding of neocortical layer 5 pyramidal neurons

PLoS biology, 2014-07, Vol.12 (7), p.e1001903-e1001903

2014

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TAOK1 is associated with neurodevelopmental disorder and essential for neuronal maturation and cortical development

Human mutation, 2021-04, Vol.42 (4), p.445-459

2021

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A behavioral test battery for mouse models of Angelman syndrome: a powerful tool for testing drugs and novel Ube3a mutants

Molecular autism, 2018-09, Vol.9 (1), p.47-47, Article 47

2018

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CAMK2-Dependent Signaling in Neurons Is Essential for Survival

The Journal of neuroscience, 2019-07, Vol.39 (28), p.5424-5439

2019

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RHEB/mTOR hyperactivity causes cortical malformations and epileptic seizures through increased axonal connectivity

PLoS biology, 2021-05, Vol.19 (5), p.e3001279-e3001279

2021

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Netrin‐G2 dysfunction causes a Rett‐like phenotype with areflexia

Human mutation, 2020-02, Vol.41 (2), p.476-486

2020

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Loss of CAMK2G affects intrinsic and motor behavior but has minimal impact on cognitive behavior

Frontiers in neuroscience, 2023-01, Vol.16, p.1086994

2023

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Cognitive deficits in Tsc1+/−mice in the absence of cerebral lesions and seizures

Annals of neurology, 2007-12, Vol.62 (6), p.648-655

2007

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Assessing the requirements of prenatal UBE3A expression for rescue of behavioral phenotypes in a mouse model for Angelman syndrome

Molecular autism, 2020-09, Vol.11 (1), p.1-70, Article 70

2020

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Delayed loss of UBE3A reduces the expression of Angelman syndrome-associated phenotypes

Molecular autism, 2019-05, Vol.10 (1), p.23-23, Article 23

2019

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Dissociation of locomotor and cerebellar deficits in a murine Angelman syndrome model

The Journal of clinical investigation, 2015-11, Vol.125 (11), p.4305-4315

2015

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Adult Ube3a Gene Reinstatement Restores the Electrophysiological Deficits of Prefrontal Cortex Layer 5 Neurons in a Mouse Model of Angelman Syndrome

The Journal of neuroscience, 2018-09, Vol.38 (37), p.8011-8030

2018

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Case Report: Developmental Delay and Acute Neuropsychiatric Episodes Associated With a de novo Mutation in the CAMK2B Gene (c.328G>A p.Glu110Lys)

Frontiers in pharmacology, 2022-05, Vol.13, p.794008

2022

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Enhanced Transmission at the Calyx of Held Synapse in a Mouse Model for Angelman Syndrome

Frontiers in cellular neuroscience, 2018-01, Vol.11, p.418-418

2018

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Role of calcium/calmodulin-dependent kinase 2 in neurodevelopmental disorders

Brain research bulletin, 2021-06, Vol.171, p.209-220

2021

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Rheb Is Essential for Murine Development

Molecular and Cellular Biology, 2011-04, Vol.31 (8), p.1672-1678

2011

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The role of ubiquitin ligase E3A in polarized contact guidance and rescue strategies in UBE3A-deficient hippocampal neurons

Molecular autism, 2019-11, Vol.10 (1), p.41-18, Article 41

2019

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Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model

The Journal of clinical investigation, 2015-05, Vol.125 (5), p.2069-2076

2015

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The molecular, temporal and region-specific requirements of the beta isoform of Calcium/Calmodulin-dependent protein kinase type 2 (CAMK2B) in mouse locomotion

Scientific reports, 2016-05, Vol.6 (1), p.26989-26989, Article 26989

2016

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Measuring Electroencephalography: The Ups and Downs of Delta and Beta Bands as Biomarkers for 15q11-q13–Related Disorders

Biological psychiatry (1969), 2019-05, Vol.85 (9), p.e45-e46

van Woerden, Geeske M.

2019

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GABAergic Neuron-Specific Loss of Ube3a Causes Angelman Syndrome-Like EEG Abnormalities and Enhances Seizure Susceptibility

CaMKII controls neuromodulation via neuropeptide gene expression and axonal targeting of neuropeptide vesicles

The Wnt/Ca2+ pathway is involved in interneuronal communication mediated by tunneling nanotubes

The intellectual disability‐associated CAMK2G p.Arg292Pro mutation acts as a pathogenic gain‐of‐function

Non-associative potentiation of perisomatic inhibition alters the temporal coding of neocortical layer 5 pyramidal neurons

TAOK1 is associated with neurodevelopmental disorder and essential for neuronal maturation and cortical development

A behavioral test battery for mouse models of Angelman syndrome: a powerful tool for testing drugs and novel Ube3a mutants

CAMK2-Dependent Signaling in Neurons Is Essential for Survival

RHEB/mTOR hyperactivity causes cortical malformations and epileptic seizures through increased axonal connectivity

Netrin‐G2 dysfunction causes a Rett‐like phenotype with areflexia

The MAP3K7 gene: Further delineation of clinical characteristics and genotype/phenotype correlations

Loss of CAMK2G affects intrinsic and motor behavior but has minimal impact on cognitive behavior

Cognitive deficits in Tsc1+/−mice in the absence of cerebral lesions and seizures

Assessing the requirements of prenatal UBE3A expression for rescue of behavioral phenotypes in a mouse model for Angelman syndrome

Delayed loss of UBE3A reduces the expression of Angelman syndrome-associated phenotypes

Dissociation of locomotor and cerebellar deficits in a murine Angelman syndrome model

Adult Ube3a Gene Reinstatement Restores the Electrophysiological Deficits of Prefrontal Cortex Layer 5 Neurons in a Mouse Model of Angelman Syndrome

Case Report: Developmental Delay and Acute Neuropsychiatric Episodes Associated With a de novo Mutation in the CAMK2B Gene (c.328G>A p.Glu110Lys)

Enhanced Transmission at the Calyx of Held Synapse in a Mouse Model for Angelman Syndrome

Role of calcium/calmodulin-dependent kinase 2 in neurodevelopmental disorders

Rheb Is Essential for Murine Development

The role of ubiquitin ligase E3A in polarized contact guidance and rescue strategies in UBE3A-deficient hippocampal neurons

Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model

The molecular, temporal and region-specific requirements of the beta isoform of Calcium/Calmodulin-dependent protein kinase type 2 (CAMK2B) in mouse locomotion

Measuring Electroencephalography: The Ups and Downs of Delta and Beta Bands as Biomarkers for 15q11-q13–Related Disorders

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