Nael Nadif Kasri

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Full professor

Radboudumc

Netherlands

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About

Nael Nadif Kasri is a Full Professor at Radboudumc in the Netherlands. His research primarily focuses on neurobiology, particularly in the areas of synaptic function, DNA methylation signatures in genetic disorders, and the functionality of human pluripotent stem cell-derived astrocytes. His recent work has also explored parvalbumin interneuron plasticity and the impacts of copy number variations on neuronal maturation.

Recent Grants

Grant: Close

Hypathia Track

Open Date: 2011-01-01

Close Date: 2015-12-01

Articles (22)

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Collaborators (7)

Pierre-Luc Germain

University of Zurich

SWITZERLAND

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NICOLO' CAPORALE

University of Milan

ITALY

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Guy Shpak

Erasmus University Rotterdam

NETHERLANDS

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Dirk Schubert

Associate Professor Translational Neuroscience

Radboud Universiteit Donders Institute for Brain Cognition and Behaviour

NETHERLANDS

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Giuseppe Testa

Head

ITALY

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Sara Hijazi

University of Oxford

UNITED KINGDOM

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Bas Lendemeijer

Columbia University

UNITED STATES

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Nael Nadif Kasri

Research Interests

Explore related searches

Contact this professor

About

Recent Grants

Articles (22)

Shining light on parvalbumin interneuron plasticity

CACNA1A haploinsufficiency leads to reduced synaptic function and increased intrinsic excitability

Human Pluripotent Stem Cell-Derived Astrocyte Functionality Compares Favorably with Primary Rat Astrocytes

Multiscale modeling uncovers 7q11.23 copy number variation–dependent changes in ribosomal biogenesis and neuronal maturation and excitability

A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells

A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense <i>KANSL1</i> variants and comparison to fibroblast cells

Correction: A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells

Integrative transcriptomics and electrophysiological profiling of hiPSC-derived neurons identifies novel druggable pathways in Koolen-de Vries Syndrome

Navigating Human Astrocyte Differentiation: Direct and Rapid one-step Differentiation of Induced Pluripotent Stem Cells to Functional Astrocytes Supporting Neuronal Network development

Neural and metabolic dysregulation in PMM2-deficient human<i> in</i><i> vitro</i> neural models

Excitatory/inhibitory balance in epilepsies and neurodevelopmental disorders: Depolarizing γ-aminobutyric acid as a common mechanism.

Sialic acid biosynthesis pathway blockade disturbs neuronal network formation in human iPSC‐derived excitatory neurons

The OTUD7A-Ankyrin pathway: a newly identified disease mechanism for the 15q13.3 microdeletion disorder

A human<italic> in</italic><italic> vitro</italic> neuronal model for studying homeostatic plasticity at the network level

Generation of an induced pluripotent stem cell line carrying biallelic deletions (SCTCi019-B) in ALDH7A1 using CRISPR/Cas9

FriendlyClearMap: an optimized toolkit for mouse brain mapping and analysis

Basolateral amygdala activation enhances object recognition memory by inhibiting anterior insular cortex activity

Brunner syndrome associated MAOA mutations result in NMDAR hyperfunction and increased network activity in human dopaminergic neurons

Cadherin-13 is a critical regulator of GABAergic modulation in human stem-cell-derived neuronal networks

Following Excitation/Inhibition Ratio Homeostasis from Synapse to EEG in Monogenetic Neurodevelopmental Disorders

Generation of induced pluripotent stem cell lines carrying monoallelic (UCSFi001-A-60) or biallelic (UCSFi001-A-61; UCSFi001-A-62) frameshift variants in CACNA1A using CRISPR/Cas9

Imbalanced autophagy causes synaptic deficits in a human model for neurodevelopmental disorders.

Collaborators (7)

Pierre-Luc Germain

NICOLO' CAPORALE

Guy Shpak

Dirk Schubert

Giuseppe Testa

Sara Hijazi

Bas Lendemeijer

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