Catarina M. Seabra

Coimbra, Portugal

Last Updated: 09/26/2026

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Found 15 publications

CASPR2 Autoimmune Antibodies Induce Neuronal Hyperactivity in Human Brain Organoids.

CASPR2 Autoimmune Antibodies Induce Neuronal Hyperactivity in Human Brain Organoids.

Journal: Journal of neurochemistry

Published: August 19, 2025

A Novel Genetic Variant in MBD5 Associated with Severe Epilepsy and Intellectual Disability: Potential Implications on Neural Primary Cilia.

A Novel Genetic Variant in MBD5 Associated with Severe Epilepsy and Intellectual Disability: Potential Implications on Neural Primary Cilia.

Journal: International journal of molecular sciences

Published: July 14, 2023

Regeneration of pulp-dentin complex using human stem cells of the apical papilla: in vivo interaction with two bioactive materials.

Regeneration of pulp-dentin complex using human stem cells of the apical papilla: in vivo interaction with two bioactive materials.

Journal: Clinical oral investigations

Published: December 16, 2020

Social subordination induced by early life adversity rewires inhibitory control of the prefrontal cortex via enhanced Npy1r signaling.

Social subordination induced by early life adversity rewires inhibitory control of the prefrontal cortex via enhanced Npy1r signaling.

Journal: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology

Published: January 30, 2020

Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons.

Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons.

Journal: Molecular autism

Published: November 04, 2019

Effects of a New Bioceramic Material on Human Apical Papilla Cells.

Effects of a New Bioceramic Material on Human Apical Papilla Cells.

Journal: Journal of functional biomaterials

Published: November 22, 2018

Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

Journal: Nature genetics

Published: May 27, 2017

A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings.

A novel microduplication of ARID1B: Clinical, genetic, and proteomic findings.

Journal: American journal of medical genetics. Part A

Published: November 28, 2016

Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome.

Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome.

Journal: Genome biology

Published: September 27, 2016

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

Journal: Nature genetics

Published: June 15, 2016

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.

Journal: Nature genetics

Published: April 04, 2016

Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR.

Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR.

Journal: Nature neuroscience

Published: May 08, 2015

Showing 1-12 of 15

Last Updated: 09/26/2026