Julian Schröter - Concepedia

Author

Julian Schröter

Heidelberg University ORCID

Also Known As

J Schröter, J. Schroter, J. Schröter, Julian Schröter, Schröter, Julian

Publications

582

Citations

H-Index

Concepts

All Affiliations

Heidelberg University University Hospital Heidelberg Radboud University Nijmegen Radboud University Medical Center University Medical Center Freiburg

About

Julian Schröter is an author at Heidelberg University specializing in medicine, genetics, and inherited metabolic disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	238
2	Engineering	1	1	13
3	Health Sciences	1	1	14
4	Social Sciences	1	1	20
5	Biomedical Engineering	1	1	13

Julian Schröter

Publications

549

Citations

H-Index

Page 1

	Year	Citations
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, Journal of the American College of Cardiology ChannelopathiesCardiomyopathyHcn4 ChannelPhysiologyGenetic Epidemiology	2014	143
Altered HCN4 channel C-linker interaction is associated with familial tachycardia–bradycardia syndrome and atrial fibrillation Nana Duhme, Patrick A. Schweizer, Dierk Thomas, European Heart Journal	2012	102
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, Genetics in Medicine HepatologyGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic Epidemiology	2020	48
Refining Genotypes and Phenotypes in KCNA2-Related Neurological Disorders Jan Henje Döring, Julian Schröter, Jerome Jüngling, International Journal of Molecular Sciences	2021	34
Phenotypic diversity, disease progression, and pathogenicity of <scp><i>MVK</i></scp> missense variants in mevalonic aciduria Heiko Brennenstuhl, Mohammed Nashawi, Julian Schröter, Journal of Inherited Metabolic Disease	2021	28
Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies Julian Schröter, Bernt Popp, Heiko Brennenstuhl, European Journal of Human Genetics	2022	23
Cross-sectional quantitative analysis of the natural history of TUBA1A and TUBB2B tubulinopathies Julian Schröter, Jan Henje Döring, Sven F. Garbade, Genetics in Medicine	2020	22
Further evidence for <i>de novo</i> variants in <i>SYNCRIP</i> as the cause of a neurodevelopmental disorder Francesca Semino, Julian Schröter, Marjolein H. Willemsen, Human Mutation NeurogenomicsBrain DevelopmentGeneticsNeurodevelopmentDisease Gene Identification	2021	20
Exploring genotype–phenotype correlations in glutaric aciduria type 1 Imke M. E. Schuurmans, Bianca Dimitrov, Julian Schröter, Journal of Inherited Metabolic Disease	2023	20
Quantitative retrospective natural history modeling of <i>WDR45</i>-related developmental and epileptic encephalopathy – a systematic cross-sectional analysis of 160 published cases Afshin Saffari, Julian Schröter, Sven F. Garbade, Autophagy	2021	18

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