Dominic Lenz

Heidelberg University — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

16h-index1.1kcitations60works3.02yr avg
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Research Topics

Metabolism and Genetic Disorders(22), Genomics and Rare Diseases(14), RNA modifications and cancer(8), Mitochondrial Function and Pathology(7), Genetics and Neurodevelopmental Disorders(6)

Publications60 total

Genetisch determiniertes akutes Leberversagen
Die Gastroenterologie·2026
SCYL1 deficiency in CALFAN syndrome is associated with ER stress and cell death
Disease Models & Mechanisms·2025Open Access
Paediatric acute liver failure: A prospective, nationwide, population‐based surveillance study in Germany
Journal of Pediatric Gastroenterology and Nutrition·2025· 1 citedOpen Access
Hepatic Phenotype in NBAS‐Associated Disease: Clinical Course, Prognostic Factors and Outcome in 230 Patients
Liver International·2025· 3 citedOpen Access
WED-336 Studying the enterohepatic circulation in progressive familial intrahepatic cholestasis type I
Journal of Hepatology·2025
Hepatic Form of Dihydrolipoamide Dehydrogenase Deficiency (DLDD): Phenotypic Spectrum, Laboratory Findings, and Therapeutic Approaches in 52 Patients
Universität Zürich, ZORA·2025Open Access
Hepatic Form of Dihydrolipoamide Dehydrogenase Deficiency ( <scp>DLDD</scp> ): Phenotypic Spectrum, Laboratory Findings, and Therapeutic Approaches in 52 Patients
Journal of Inherited Metabolic Disease·2025· 3 citedOpen Access
Reply: The race against time in genetic testing for PALF
Hepatology·2025
Missense variants in the TRPM7 α-kinase domain are associated with recurrent pediatric acute liver failure
Hepatology Communications·2024· 1 citedOpen Access
The management of paediatric acute liver failure: results from an international multi-centre survey across Europe
Intensive Care Medicine – Paediatric and Neonatal·2024· 1 citedOpen Access
Simultaneous determination of cytosolic aminoacyl-tRNA synthetase activities by LC–MS/MS
Nucleic Acids Research·2024· 5 citedOpen Access
Therapeutischer Plasmataustausch bei amatoxingebundenem akutem Leberversagen – Ergebnisse einer Zwischenanalyse der Amanita-PEX-Studie
Zeitschrift für Gastroenterologie·2024
<scp>MRI</scp> in <scp>LARS1</scp> deficiency—Spectrum, patterns, and correlation with acute neurological deterioration
Journal of Inherited Metabolic Disease·2024· 2 citedOpen Access
TOP-346-YI Therapeutic plasma exchange in Amatoxin associated acute liver failure-results from an interim analysis of the Amanita-PEX study
Journal of Hepatology·2024
Outcomes after newborn screening for propionic and methylmalonic acidemia and homocystinurias
Journal of Inherited Metabolic Disease·2024· 10 citedOpen Access
Distinct neonatal hyperammonemia and liver synthesis dysfunction: case report of a severe MEGDHEL syndrome
Frontiers in Pediatrics·2024· 2 citedOpen Access
Disorders of vesicular trafficking presenting with recurrent acute liver failure: <scp>NBAS</scp>, <scp>RINT1</scp>, and <scp>SCYL1</scp> deficiency
Journal of Inherited Metabolic Disease·2024· 16 citedOpen Access
Impact of genetic and non-genetic factors on phenotypic diversity in NBAS-associated disease
Molecular Genetics and Metabolism·2024· 5 citedOpen Access
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome
Brain Communications·2024· 8 citedOpen Access
Genetic landscape of pediatric acute liver failure of indeterminate origin
Hepatology·2023· 26 citedOpen Access
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Frequent Co-authors

Christian Staufner(29), Holger Prokisch(20), Georg F. Hoffmann(20), Stefan Kölker(17), Matias Wagner(13), Johannes A. Mayr(11), Lea D. Schlieben(11), Robert Kopajtich(9), Peter Freisinger(9), Ivo Barić(9), Ekkehard Sturm(9), Elke Lainka(9), Sven F. Garbade(9), Felix Distelmaier(8), Robert W. Taylor(8), Saskia B. Wortmann(8), Thomas Meitinger(8), Bianca Peters(8), Alexander Fichtner(8), Kei Murayama(7)