Fréderike W. Riemslagh

Medicine · Health Sciences

9h-index251citations21works2.02yr avg
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Research Topics

Amyotrophic Lateral Sclerosis Research(7), Congenital heart defects research(6), Genetic Neurodegenerative Diseases(4), Zebrafish Biomedical Research Applications(4), Neurogenetic and Muscular Disorders Research(3)

Publications21 total

eScience Center Training Report 2024
Zenodo (CERN European Organization for Nuclear Research)·2026Open Access
eScience Center Training Report 2024
Zenodo (CERN European Organization for Nuclear Research)·2026Open Access
The pericardium forms as a distinct structure during heart formation
Nature Communications·2025· 3 citedOpen Access
The pericardium forms as a distinct structure during heart formation
2024· 5 citedOpen Access
eScience Center Training Report 2020-2022
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
Cover Image
Developmental Dynamics·2022Open Access
Endothelial versus pronephron fate decision is modulated by the transcription factors Cloche/Npas4l, Tal1, and Lmo2
Science Advances·2022· 21 citedOpen Access
Heterogeneity and genomic loci of ubiquitous transgenic Cre reporter lines in zebrafish
Developmental Dynamics·2022· 12 citedOpen Access
Heterogeneity and genomic loci of ubiquitous Cre reporter transgenes in zebrafish
2021· 1 citedOpen Access
Reduction of oxidative stress suppresses poly-GR-mediated toxicity in zebrafish embryos
Disease Models & Mechanisms·2021· 11 citedOpen Access
From Stripes to a Beating Heart: Early Cardiac Development in Zebrafish
Journal of Cardiovascular Development and Disease·2021· 59 citedOpen Access
Inducible expression of human <i>C9ORF72</i> 36× G4C2 hexanucleotide repeats is sufficient to cause RAN translation and rapid muscular atrophy in mice
Disease Models & Mechanisms·2021· 18 citedOpen Access
Inducible expression of human <i>C9ORF72</i> 36x G <sub>4</sub> C <sub>2</sub> hexanucleotide repeats is sufficient to cause RAN translation and rapid muscular atrophy in mice
2020
Faculty Opinions recommendation of Single-cell chromatin accessibility maps reveal regulatory programs driving early mouse organogenesis.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature·2020
Faculty Opinions recommendation of Severe head dysgenesis resulting from imbalance between anterior and posterior ontogenetic programs.
Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature·2019
Molecular Mechanisms of C9ORF72-linked Frontotemporal Dementia and Amyotrophic Lateral Sclerosis : Moleculaire mechanismen van C9ORF72 geassocieerde frontotemporale dementie en amyotrofische laterale sclerose
Data Archiving and Networked Services (DANS)·2019Open Access
HR23B pathology preferentially co-localizes with p62, pTDP-43 and poly-GA in C9ORF72-linked frontotemporal dementia and amyotrophic lateral sclerosis
Acta Neuropathologica Communications·2019· 17 citedOpen Access
Retraction Note to: A new inducible transgenic mouse model for C9orf72-associated GGGGCC repeat expansion supports a gain-of-function mechanism in C9orf72-associated ALS and FTD
Acta Neuropathologica Communications·2016Open Access
Intact neuronal function in Rheb1 mutant mice: implications for TORC1-based treatments
Human Molecular Genetics·2015· 20 citedOpen Access
RETRACTED ARTICLE: A new inducible transgenic mouse model for C9orf72-associated GGGGCC repeat expansion supports a gain-of-function mechanism in C9orf72-associated ALS and FTD
Acta Neuropathologica Communications·2014· 26 citedOpen Access
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Frequent Co-authors

Christian Mosimann(9), Hannah R. Moran(6), Rob Willemsen(6), Alexa Burger(6), Cassie L. Kemmler(4), Renate K. Hukema(4), Alex Maas(4), Shamiram Melhem(3), Herma C. van der Linde(3), John C. van Swieten(3), Esmay C. van der Toorn(3), Rob F. M. Verhagen(3), Robert L. Lalonde(3), Andrew J. Aman(3), Jelena Kresoja‐Rakic(3), Susan Nieuwenhuize(3), David M. Parichy(3), Lies‐Anne Severijnen(2), Dieter Edbauer(2), Nicolas Charlet‐Berguerand(2)