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	1	Patients with complex and very-early-onset ATL1-related spastic paraplegia offer insights on genotype/phenotype correlations and support for autosomal recessive forms of SPG3A Enthalten in Journal of neurology Bd. 271, 13.7.2024, Nr. 9, date:9.2024: 6343-6348
	2	Reanalysis of unsolved prenatal exome sequencing for structural defects: diagnostic yield and contribution of postnatal/postmortem features Enthalten in European journal of human genetics Bd. 33, 4.4.2025, Nr. 5, date:5.2025: 675-682

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