Catarina Morais Seabra

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Information about journal articles, updated at 23-01-2022, from platform CIÊNCIAVITAE.

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

Sequeira, Diana B.; Oliveira, Ana Rafaela; Seabra, Catarina M.; Palma, Paulo J.; Ramos, Carlos; Figueiredo, Maria H.; Santos, Ana C.; et al, Clinical Oral Investigations. 2021. . 10.1007/s00784-021-03840-9 . published Clinical Oral Investigations

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

Franco, Lara O.; Carvalho, Mário J.; Costa, Jéssica; Ferreira, Pedro A.; Guedes, Joana R.; Sousa, Renato; Edfawy, Mohamed; et al, 2020. under revision

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

Seabra, Catarina M.; Aneichyk, Tatsiana; Erdin, Serkan; Tai, Derek J. C.; De Esch, Celine E. F.; Razaz, Parisa; An, Yu; et al, Molecular Autism. 1. 11. 2020. . 10.1186/s13229-020-00354-1 . published Molecular Autism

Effects of a New Bioceramic Material on Human Apical Papilla Cells

Sequeira, Diana; Seabra, Catarina; Palma, Paulo; Cardoso, Ana; Peça, João; Santos, João, Journal of Functional Biomaterials. 4. 9. 2018. . 10.3390/jfb9040074 . published Journal of Functional Biomaterials

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

Seabra, C.M.; Szoko, N.; Erdin, S.; Ragavendran, A.; Stortchevoi, A.; Maciel, P.; Lundberg, K.; et al, American Journal of Medical Genetics, Part A. 2478 - 2484. 9. 173. 2017. . 10.1002/ajmg.a.38327 . published American Journal of Medical Genetics, Part A

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

Redin C; Brand H; Collins RL; Kammin T; Mitchell E; Hodge JC; Hanscom C; et al, Nature Genetics. 2017. . 10.1038/ng.3720 . published Nature Genetics

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

Shaw ND; Brand H; Kupchinsky ZA; Bengani H; Plummer L; Jones TI; Erdin S; et al, Nature Genetics. 2017. . 10.1038/ng.3743 . published Nature Genetics

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

Collins RL; Brand H; Redin CE; Hanscom C; Antolik C; Stone MR; Glessner JT; et al, Genome Biology. 2017. . 10.1186/s13059-017-1158-6 . published Genome Biology

Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR.

Tai DJ; Ragavendran A; Manavalan P; Stortchevoi A; Seabra CM; Erdin S; Collins RL; et al, Nature Neuroscience. 2016. . 10.1038/nn.4235 . published Nature Neuroscience

The mutational spectrum of WT1 in male infertility.

Seabra CM; Quental S; Lima AC; Carvalho F; Gonçalves J; Fernandes S; Pereira I; et al, The Journal of Urology. 2015. . 10.1016/j.juro.2014.11.004 . published The Journal of Urology

A novel Alu-mediated microdeletion at 11p13 removes WT1 in a patient with cryptorchidism and azoospermia.

Seabra CM; Quental S; Neto AP; Carvalho F; Gonçalves J; Oliveira JP; Fernandes S; et al, Reproductive BioMedicine Online. 2014. . 10.1016/j.rbmo.2014.04.017 . published Reproductive BioMedicine Online

Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.

Lopes AM; Aston KI; Thompson E; Carvalho F; Gonçalves J; Huang N; Matthiesen R; et al, PLoS Genetics. 2013. . 10.1371/journal.pgen.1003349 . published PLoS Genetics

All projects

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Information of exclusive responsibility of the researcher 23-01-2022 , from platform CIÊNCIAVITAE.

2021 -

Disease modelling of frontotemporal dementia in human brain organoids



Universidade de Coimbra Centro de Neurociências e Biologia Celular

Funders: Fundação para a Ciência e a Tecnologia

2021 -

Exploring the Immunogenetics of FTD using advanced human brain organoids



Universidade de Coimbra Centro de Neurociências e Biologia Celular

Funders: Takeda Pharmaceuticals International AG

2019 - 2022

Syn2Psy - Synaptic Dysfunction in Neuropsychiatric Disorders




Funders: EU Framework Programme for Research and Innovation Marie Sklodowska-Curie Actions

2018/05/07 - 2020/05/06

ProTeAN - Production and Testing of Human Neurons and Brain Orgnoids




Funders: EU Framework Programme for Research and Innovation Marie Sklodowska-Curie Actions

2017/11 - 2018/04

Social Hierarchy and Early Life Stress Adversity: Optogenetic Modulation of Prefrontal Cortical Circuits and Neuroepigenetic Regulation


Integration into Research Grant Fellow


Funders: Fundação para a Ciência e a Tecnologia

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