Svenja Schneider - Concepedia

Author

Svenja Schneider

University of Cologne ORCID

Also Known As

S Schneider, Svenja M. Schneider, Svenja Schneider, Svenja Schneider, MD

Publications

472

Citations

H-Index

Concepts

All Affiliations

University of Cologne Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases Ionis Pharmaceuticals (United States)University Hospital Cologne

About

Svenja Schneider is an author at University of Cologne specializing in medicine, spinal cord injury, and surgery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	355
2	Health Sciences	1	1	15
3	Natural Sciences	1	1	56
4	Anatomy	1	1	15
5	Cell Biology	1	1	56

Svenja Schneider

Publications

410

Citations

H-Index

Page 1

	Year	Citations
Neurocalcin Delta Suppression Protects against Spinal Muscular Atrophy in Humans and across Species by Restoring Impaired Endocytosis Anna Kaczmarek, Svenja Schneider, Kathryn J. Swoboda, The American Journal of Human Genetics NeuroregenerationSpinal Cord InjuryPhysiologyDegenerative DiseaseSpinal Muscular Atrophy	2017	215
CHP1 reduction ameliorates spinal muscular atrophy pathology by restoring calcineurin activity and endocytosis Eva Janzen, Natalia Mendoza-Ferreira, Seyyedmohsen Hosseinibarkooie, Brain Spinal Cord InjuryChp1 KnockdownChp1 LevelsSkeletal MuscleMedicine	2018	56
Accuracy of Balancing at Total Knee Surgery Using an Instrumented Tibial Trial Patrick Meere, Svenja Schneider, Peter S. Walker The Journal of Arthroplasty Instrumented Tibial TrialTotal Knee SurgerySurgeryJoint ReplacementArthroscopic Technique	2016	37
Neurocalcin Delta Knockout Impairs Adult Neurogenesis Whereas Half Reduction Is Not Pathological Aaradhita Upadhyay, Seyyedmohsen Hosseinibarkooie, Svenja Schneider, Frontiers in Molecular Neuroscience	2019	34
NCALD Antisense Oligonucleotide Therapy in Addition to Nusinersen further Ameliorates Spinal Muscular Atrophy in Mice Laura Torres‐Benito, Svenja Schneider, Roman Rombo, The American Journal of Human Genetics Spinal Cord InjuryMedicineDegenerative DiseaseSpinal Muscular AtrophyNeurology	2019	32
Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function Natalia Mendoza-Ferreira, Marie Coutelier, Eva Janzen, Neurology Genetics	2018	21
[The use of the T-Scan system in occlusal diagnosis]. A Dees, Peter Proff, Svenja Schneider PubMed T-scan SystemFunctional DiagnosticsGross AnatomyIntraoral ScannerHealth Sciences	1992	15

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