Jasmin Morandell

Klosterneuburg, 3400, Austria

Last Updated: 09/26/2026

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Found 10 publications

Decoding neuronal vulnerability: Multidimensional analysis of D1R- and D2R- medium-sized spiny neurons in Huntington's disease.

Decoding neuronal vulnerability: Multidimensional analysis of D1R- and D2R- medium-sized spiny neurons in Huntington's disease.

Journal: Brain pathology (Zurich, Switzerland)
Published: December 29, 2025

Circular RNAs as disease modifiers of complex neurologic disorders.

Circular RNAs as disease modifiers of complex neurologic disorders.

Journal: Frontiers in pharmacology
Published: February 15, 2025

CircHTT(2,3,4,5,6) - co-evolving with the HTT CAG-repeat tract - modulates Huntington's disease phenotypes.

CircHTT(2,3,4,5,6) - co-evolving with the HTT CAG-repeat tract - modulates Huntington's disease phenotypes.

Journal: Molecular therapy. Nucleic acids
Published: November 26, 2023

SINEUP RNA rescues molecular phenotypes associated with CHD8 suppression in autism spectrum disorder model systems.

SINEUP RNA rescues molecular phenotypes associated with CHD8 suppression in autism spectrum disorder model systems.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: July 04, 2022

CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectories.

CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectories.

Journal: Cell reports
Published: April 01, 2021

Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development.

Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development.

Journal: Nature communications
Published: August 05, 2020

Molecular mechanisms for targeted ASD treatments.

Molecular mechanisms for targeted ASD treatments.

Journal: Current opinion in genetics & development
Published: March 27, 2020

Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition.

Haploinsufficiency of the intellectual disability gene SETD5 disturbs developmental gene expression and cognition.

Journal: Nature neuroscience
Published: April 17, 2018

Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.

Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.

Journal: American journal of human genetics
Published: June 11, 2015

The Expression of Tubb2b Undergoes a Developmental Transition in Murine Cortical Neurons.

The Expression of Tubb2b Undergoes a Developmental Transition in Murine Cortical Neurons.

Journal: The Journal of comparative neurology
Published: November 18, 2014
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Last Updated: 09/26/2026