Bärbel Klauke - Concepedia

Author

Bärbel Klauke

Heart and Diabetes Center North Rhine-Westphalia

Also Known As

B. Klauke, Bärbel Klauke

Publications

554

Citations

H-Index

Concepts

All Affiliations

Heart and Diabetes Center North Rhine-Westphalia Ruhr University Bochum Bielefeld University Libin Cardiovascular Institute of Alberta University of Calgary

About

Bärbel Klauke is an author at Heart and Diabetes Center North Rhine-Westphalia specializing in medicine, molecular biology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	246
2	Molecular Biology	4	4	211
3	Natural Sciences	1	1	61
4	Cell Biology	1	1	61
5	Cellular Physiology	1	1	61

Bärbel Klauke

Publications

531

Citations

H-Index

Page 1

	Year	Citations
The novel αB‐crystallin ( <i>CRYAB</i> ) mutation p.D109G causes restrictive cardiomyopathy Andreas Brodehl, Anna Gaertner, Bärbel Klauke, Human Mutation Novel Rcm GeneCardiac MuscleHeart FailureGeneticsMolecular Biology	2017	77
The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus Hendrik Milting, Bärbel Klauke, Alex Hørby Christensen, European Heart Journal	2014	76
The Novel Desmin Mutant p.A120D Impairs Filament Formation, Prevents Intercalated Disk Localization, and Causes Sudden Cardiac Death Andreas Brodehl, Mareike Dieding, Bärbel Klauke, Circulation Cardiovascular Genetics	2013	66
Dual Color Photoactivation Localization Microscopy of Cardiomyopathy-associated Desmin Mutants Andreas Brodehl, Per Niklas Hedde, Mareike Dieding, Journal of Biological Chemistry Desmin Filament StructuresCardiac MuscleMolecular BiologyCytoskeletonOptogenetics	2012	61
Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect Andreas Brodehl, Mareike Dieding, Niklas Biere, Journal of Molecular and Cellular Cardiology Cardiac MuscleCardiomyopathyGenetic DisorderGeneticsMolecular Biology	2015	47
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
Molecular autopsy of sudden unexplained deaths reveals genetic predispositions for cardiac diseases among young forensic cases Nicole Hellenthal, Anna Gaertner, Bärbel Klauke, EP Europace	2016	36
No Association Between Single Nucleotide Polymorphisms and the Development of Nephrotoxicity After Orthotopic Heart Transplantation Bärbel Klauke, Andreas Wirth, Armin Zittermann, The Journal of Heart and Lung Transplantation Transplantation SurgeryTransplantationCardiorenal SyndromesCardiovascular DiseaseGenetics	2008	35
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
A novel desmin (<i>DES</i>) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathy Ilona Schirmer, Mareike Dieding, Bärbel Klauke, Molecular Genetics & Genomic Medicine	2017	26

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