Marta Ribeiro

Institute for Biotechnology and Bioengineering — Portugal

Medicine · Health Sciences

3h-index46citations16works0.82yr avg
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Research Topics

Cardiomyopathy and Myosin Studies(9), Congenital heart defects research(8), Viral Infections and Immunology Research(4), RNA Research and Splicing(3), Pluripotent Stem Cells Research(2)

Publications16 total

Alternative splicing dynamics during human cardiac development in vivo and in vitro
Stem Cell Reports·2026· 2 citedOpen Access
Emerging patterns in HIV integrase resistance
AIDS·2025Open Access
Abstract 4358220: Patient-derived iPSC-cardiomyocytes harbouring deep intronic <i>MYBPC3</i> variants show features consistent with hypertrophic cardiomyopathy
Circulation·2025
Alternative splicing dynamics during human cardiac development <i>in vivo</i> and <i>in vitro</i>
2025· 2 citedOpen Access
Hybrid next-generation sequencing protocol for testing HIV-2 drug resistance
Journal of Virological Methods·2025Open Access
Patient-derived induced pluripotent stem cells to study non-canonical splicing variants associated with Hypertrophic Cardiomyopathy
Stem Cell Research·2024· 3 citedOpen Access
Generation of induced pluripotent stem cells from an individual with early onset and severe hypertrophic cardiomyopathy linked to MYBPC3: c.772G &gt; A mutation
Human Cell·2024· 1 citedOpen Access
Establishment and characterization of induced pluripotent stem cells from an individual with familial hypertrophic cardiomyopathy carrying the MYBPC3 c.772G&amp;gt;A mutation
2024Open Access
Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying MYBPC3 nonsense mutations
Stem Cell Research·2024· 1 citedOpen Access
Contributors
Elsevier eBooks·2024Open Access
Principles of novel cellular and molecular cardiovascular therapeutics
Elsevier eBooks·2024
Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying the MYBPC3 missense c.1484G&gt;A mutation
Stem Cell Research·2023· 1 citedOpen Access
Clinical significance of genetic variation in hypertrophic cardiomyopathy: comparison of computational tools to prioritize missense variants
Frontiers in Cardiovascular Medicine·2022· 12 citedOpen Access
GENE EDITED IPSC-DERIVED CARDIOMYOCYTES REVEAL RNA SPLICING DEFECTS IN HYPERTROPHIC CARDIOMYOPATHY
2021
RNA Splicing Defects in Hypertrophic Cardiomyopathy: Implications for Diagnosis and Therapy
International Journal of Molecular Sciences·2020· 24 citedOpen Access
Two novel (1334delC and 1363G to A, G455R) mutations in exon 12 of the β‐hexosaminidase α‐chain gene in two Portuguese patients
Human Mutation·1997

Frequent Co-authors

Marta Furtado(12), Sandra Martins(11), Teresa Carvalho(11), Maria Carmo‐Fonseca(10), Simão Teixeira da Rocha(6), Joanna Jager(5), Joaquim M. S. Cabral(5), Dulce Brito(4), Perry Elliott(3), Maria Carmo-Fonseca(3), Petros Syrris(2), Luís R. Lopes(2), Beatriz Gomes-Silva(2), Henrike Maatz(2), Michael Gotthardt(2), Rosina Savisaar(2), Harm Jan Bogaard(2), Margarida Veloso(2), Joaquim Cabanas(2), Fátima Gonçalves(2)