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	31	Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings Enthalten in Nature genetics Bd. 57, 24.6.2025, Nr. 7, date:7.2025: 1790-1791
	32	Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum Enthalten in Orphanet journal of rare diseases Bd. 8, 15.3.2013, Nr. 1, date:12.2013: 1-13
	33	Comprehensive assessment of of thoracic stent grafts after emergency implantation in multi trauma patients Enthalten in Journal of cardiovascular magnetic resonance Bd. 11, 28.1.2009, Nr. 1, date:1.2009: 1-316
	34	Increased S100A4 expression in the vasculature of human COPD lungs and murine model of smoke-induced emphysema Enthalten in Respiratory research Bd. 16, 20.10.2015, Nr. 1, date:12.2015: 1-12
	35	Indicating biologics for chronic rhinosinusitis with nasal polyps (CRSwNP) Enthalten in Allergo journal international Bd. 31, 28.7.2022, Nr. 6, date:9.2022: 149-160
	36	Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings Enthalten in Nature genetics Bd. 56, 22.7.2024, Nr. 8, date:8.2024: 1644-1653
	37	Regions of common inter-individual DNA methylation differences in human monocytes: genetic basis and potential function Enthalten in Epigenetics & chromatin Bd. 10, 26.7.2017, Nr. 1, date:12.2017: 1-18

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