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Carolin Mattausch

Observed name: Mattausch, Carolin
ORCID: 0009-0002-4981-0576
Observed ORCID: 0009-0002-4981-0576
OpenAlex ID: A5094337808
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies
2025 · Elsa Leitão, Amandine Santini, et al. · medRxiv · 9
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Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies
2026 · Elsa Leitão, Amandine Santini, et al. · Nature Genetics · 7
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RBMX functional retrocopy safeguards brain development in a species-dependent context
2026 · Pierre Tilliole, Carolin Mattausch, et al. · Brain
RBMX functional retrocopy safeguards brain development
2025 · Pierre Tilliole, Carolin Mattausch, et al. · medRxiv
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies
2025 · Leitão, Elsa, Santini, Amandine, et al. · RWTH Publications (RWTH Aachen)
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies
2025 · Leitão, Elsa, Santini, Amandine, et al. · RWTH Publications (RWTH Aachen)
Supplementary tables master's thesis Carolin Mattausch 2023
2023 · Mattausch, Carolin · Zenodo (CERN European Organization for Nuclear Research)
Works count: 7
Citation count: 16
H-index: 2
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