Caroline Stanasiuk - Concepedia

Author

Caroline Stanasiuk

Heart and Diabetes Center North Rhine-Westphalia ORCID

Also Known As

C. Stanasiuk, Caroline Stanasiuk

Publications

597

Citations

H-Index

Concepts

All Affiliations

Heart and Diabetes Center North Rhine-Westphalia Ruhr University Bochum Universitätsklinikum Würzburg National Research Center for Preventive Medicine National Medical Research Center of Cardiology

About

Caroline Stanasiuk is an author at Heart and Diabetes Center North Rhine-Westphalia specializing in medicine, cardiology, and cardiovascular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	349
2	Cell Biology	3	3	270
3	Natural Sciences	2	2	48
4	Biochemistry	1	1	14
5	Biomedical Engineering	1	1	36

Caroline Stanasiuk

Publications

583

Citations

H-Index

Page 1

	Year	Citations
Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies Daniel Reichart, Eric L. Lindberg, Henrike Maatz, Science Cardiac MuscleHeart FailureGeneticsCardiac Progenitor CellsCongenital Heart Anomaly	2022	222
Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect Andreas Brodehl, Seyed Ahmad Pour Hakimi, Caroline Stanasiuk, Genes	2019	66
The Novel Desmin Variant p.Leu115Ile Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy Alexandros Protonotarios, Andreas Brodehl, Angeliki Asimaki, Canadian Journal of Cardiology CardiomyopathyHeart FailureCardiovascular DiseaseBiventricular Arrhythmogenic CardiomyopathyPathology	2020	43
Desminopathy: Novel Desmin Variants, a New Cardiac Phenotype, and Further Evidence for Secondary Mitochondrial Dysfunction Miloš Kubánek, Tereza Schimerová, Lenka Piherová, Journal of Clinical Medicine	2020	40
A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy Andreas Brodehl, Jana Davina Debus, Caroline Stanasiuk, Journal of Molecular and Cellular Cardiology	2020	38
The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy Andreas Brodehl, R. P. Myasnikov, Caroline Stanasiuk, Genes	2021	38
Noncompaction cardiomyopathy is caused by a novel in‐frame desmin ( <i>DES</i> ) deletion mutation within the 1A coiled‐coil rod segment leading to a severe filament assembly defect Andrey V. Marakhonov, Andreas Brodehl, R. P. Myasnikov, Human Mutation Cardiac MuscleHeart FailureGeneticsCardiac Progenitor CellsPathology	2019	36
Cardiomyopathy‐associated mutations in the RS domain affect nuclear localization of RBM20 Anna Gaertner, Baerbel Klauke, Elina Felski, Human Mutation Cardiac MuscleCardiomyopathyFunctional GenomicsCardiac ReprogrammingRbm20 Mutations	2020	34
Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset Andreas Brodehl, R. P. Myasnikov, Bärbel Klauke, International Journal of Molecular Sciences	2021	28
Incorporation of desmocollin‐2 into the plasma membrane requires <i>N</i>‐glycosylation at multiple sites Andreas Brodehl, Caroline Stanasiuk, Dario Anselmetti, FEBS Open Bio Proteinlipid InteractionCell AdhesionGlycobiologyMolecular BiologyDesmosomal Protein	2019	14

Page 1