Britta Keyser

Medizinische Hochschule Hannover — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

19h-index825citations29works0.02yr avg
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Research Topics

Connective tissue disorders research(13), Cardiac Valve Diseases and Treatments(9), Aortic Disease and Treatment Approaches(9), Metabolism and Genetic Disorders(6), Mitochondrial Function and Pathology(5)

Publications29 total

P1617Contractile imbalance as trigger for HCM pathogenesis: evidence from mutations in different sarcomeric proteins
European Heart Journal·2019· 1 cited
Myosin and Mybp-C-Mutations in Hypertrophic Cardiomyopathy: Variable Effects on Calcium Sensitivity and Contractile Imbalance from Cell to Cell
Biophysical Journal·2019Open Access
Burst-Like Transcription of Mutant and Wildtype MYH7-Alleles as Possible Origin of Cell-to-Cell Contractile Imbalance in Hypertrophic Cardiomyopathy
Frontiers in Physiology·2018· 48 citedOpen Access
Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy
Journal of Muscle Research and Cell Motility·2017· 32 citedOpen Access
Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse
IJC Heart & Vasculature·2016· 20 citedOpen Access
Clinical and genetic diagnosis of Marfan syndrome in childhood are Equal- FBN1 mutation should not influence handling of pediatric patients with confirmed Marfansyndrome
Journal of Integrative Cardiology·2016Open Access
Clinical utility gene card for: Hereditary thoracic aortic aneurysm andă dissection including next-generation sequencing-based approaches
HAL (Le Centre pour la Communication Scientifique Directe)·2016
Clinical utility gene card for: Hereditary thoracic aortic aneurysm and dissection including next-generation sequencing-based approaches
European Journal of Human Genetics·2015· 30 citedOpen Access
Blood-based microRNA signatures differentiate various forms of cardiac hypertrophy
International Journal of Cardiology·2015· 98 citedOpen Access
The main pulmonary artery in adults: a controlled multicenter study with assessment of echocardiographic reference values, and the frequency of dilatation and aneurysm in Marfan syndrome
Orphanet Journal of Rare Diseases·2014· 39 citedOpen Access
Overexpression of Gremlin-1 in Patients with Loeys-Dietz Syndrome: Implications on Pathophysiology and Early Disease Detection
PLoS ONE·2014· 17 citedOpen Access
Total Serum Transforming Growth Factor‐β1 Is Elevated in the Entire Spectrum of Genetic Aortic Syndromes
Clinical Cardiology·2014· 40 citedOpen Access
Observational Cohort Study of Ventricular Arrhythmia in Adults with Marfan Syndrome Caused by FBN1 Mutations
PLoS ONE·2013· 53 citedOpen Access
Dural ectasia in Loeys–Dietz syndrome: comprehensive study of 30 patients with a <i><scp>TGFBR1</scp></i> or <i><scp>TGFBR2</scp></i> mutation
Clinical Genetics·2013· 22 cited
Comprehensive analysis of dural ectasia in 150 patients with a causative <i><scp>FBN1</scp></i> mutation
Clinical Genetics·2013· 27 cited
FBN1 gene mutation characteristics and clinical features for the prediction of mitral valve disease progression
International Journal of Cardiology·2012· 18 cited
High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections
Molecular and Cellular Probes·2012· 9 cited
A Novel GJC2 Mutation Associated with Hypomyelination and Müllerian Agenesis Syndrome: Coincidence or a New Entity?
Neuropediatrics·2012· 7 cited
TGFBR3 variation is not a common cause of Marfan-like syndrome and Loeys-Dietz-like syndrome
Journal of Negative Results in BioMedicine·2012· 9 citedOpen Access
A simple clinical model to estimate the probability of Marfan syndrome
QJM·2012· 31 citedOpen Access
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Frequent Co-authors

Yskert Von Kodolitsch(12), Meike Rybczynski(11), Sara Sheikhzadeh(10), Peter N. Robinson(9), Thomas S. Mir(9), Stefan Blankenberg(8), Mine Arslan‐Kirchner(7), Mathias Hillebrand(7), Kurt Ullrich(5), Thomas Braulke(5), Chris Mühlhausen(5), Jürgen Berger(5), Jörg Schmidtke(5), J. Berger(5), Kerstin Kutsche(5), Manfred Stuhrmann(4), Judith Montag(4), Theresia Kraft(4), Julie De Backer(4), David M. Koeller(3)