Julian Schröter

The Symptom Complex of Familial Sinus Node Dysfunction and Myocardial Noncompaction Is Associated With Mutations in the HCN4 Channel

Patrick A. Schweizer, Julian Schröter, Sebastian Greiner et al. · Journal of the American College of Cardiology · 2014 · 143 citations

Channelopathies, Cardiomyopathy, Hcn4 Channel +8

Altered HCN4 channel C-linker interaction is associated with familial tachycardia–bradycardia syndrome and atrial fibrillation

Nana Duhme, Patrick A. Schweizer, Dierk Thomas et al. · European Heart Journal · 2012 · 102 citations · Full text

Genotypic diversity and phenotypic spectrum of infantile liver failure syndrome type 1 due to variants in LARS1

Dominic Lenz, Desirée E.C. Smith, Ellen Crushell et al. · Genetics in Medicine · 2020 · 48 citations · Full text

Hepatology, Genetic Disorder, Genetics +11

Refining Genotypes and Phenotypes in KCNA2-Related Neurological Disorders

Jan Henje Döring, Julian Schröter, Jerome Jüngling et al. · International Journal of Molecular Sciences · 2021 · 34 citations · Full text

Phenotypic diversity, disease progression, and pathogenicity of <scp><i>MVK</i></scp> missense variants in mevalonic aciduria

Heiko Brennenstuhl, Mohammed Nashawi, Julian Schröter et al. · Journal of Inherited Metabolic Disease · 2021 · 28 citations · Full text