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B. Stallmeyer · SciRah

Researcher profile · Semantic Scholar

B. Stallmeyer

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B. Stallmeyer — researcher profile on SciRah

h-index: 30
Works: 76
Citations: 4,093

Most-cited papers

Large and sustained induction of chemokines during impaired wound healing in the genetically diabetic mouse: prolonged persistence of neutrophils and macrophages during the late phase of repair.
C. Wetzler, Heiko Kämpfer, B. Stallmeyer, J. Pfeilschifter +1 more
2000Journal of Investigative Dermatology604 citations Open access
Semantic Scholar
Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I.
M. Kruse, E. Schulze-Bahr, V. Corfield, A. Beckmann +6 more
2009Journal of Clinical Investigation335 citations Open access
Semantic Scholar
Leptin enhances wound re-epithelialization and constitutes a direct function of leptin in skin repair.
S. Frank, B. Stallmeyer, Heiko Kämpfer, Nicole Kolb +1 more
2000Journal of Clinical Investigation330 citations Open access
Semantic Scholar
Nitric oxide triggers enhanced induction of vascular endothelial growth factor expression in cultured keratinocytes (HaCaT) and during cutaneous wound repair
S. Frank, B. Stallmeyer, Heiko Kämpfer, Nicole Kolb +1 more
1999The FASEB Journal245 citations Open access
Semantic Scholar
A Large Candidate Gene Survey Identifies the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes
S. Kääb, Dana C. Crawford, Moritz F. Sinner, Elijah R. Behr +36 more
2011Circulation: Cardiovascular Genetics169 citations Open access
Semantic Scholar
Mutational spectrum in the Ca2+‐activated cation channel gene TRPM4 in patients with cardiac conductance disturbances
B. Stallmeyer, S. Zumhagen, I. Denjoy, G. Duthoit +8 more
2012Human Mutation167 citations Open access
Semantic Scholar
The neurotransmitter receptor-anchoring protein gephyrin reconstitutes molybdenum cofactor biosynthesis in bacteria, plants, and mammalian cells.
B. Stallmeyer, G. Schwarz, J. Schulze, A. Nerlich +3 more
1999Proceedings of the National Academy of Sciences of the United States of America152 citations Open access
Semantic Scholar
Genome-wide association analyses identify novel Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
J. Barc, R. Tadros, C. Glinge, David Y. Chiang +152 more
2022Nature Genetics114 citations Open access
Semantic Scholar
Mutations in a polycistronic nuclear gene associated with molybdenum cofactor deficiency
J. Reiss, N. Cohen, C. Dorche, H. Mandel +4 more
1998Nature Genetics106 citations
Semantic Scholar
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
N. Lahrouchi, R. Tadros, L. Crotti, Y. Mizusawa +102 more
2020Circulation105 citations Open access
Semantic Scholar
Human iPS cell model of type 3 long QT syndrome recapitulates drug-based phenotype correction
D. Malan, Miao Zhang, B. Stallmeyer, Jovanca Müller +4 more
2016Basic Research in Cardiology94 citations Open access
Semantic Scholar
Human molybdopterin synthase gene: identification of a bicistronic transcript with overlapping reading frames.
B. Stallmeyer, G. Drugeon, Jochen Reiss, A. Haenni +1 more
1999American Journal of Human Genetics94 citations Open access
Semantic Scholar
Molybdenum co-factor biosynthesis: the Arabidopsis thaliana cDNA cnx1 encodes a multifunctional two-domain protein homologous to a mammalian neuroprotein, the insect protein Cinnamon and three Escherichia coli proteins.
B. Stallmeyer, A. Nerlich, J. Schiemann, H. Brinkmann +1 more
1995The Plant Journal93 citations Open access
Semantic Scholar
Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome.
Konstantin Wemhöner, C. Friedrich, B. Stallmeyer, A. Coffey +8 more
2015Journal of Molecular and Cellular Cardiology84 citations
Semantic Scholar
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
R. Walsh, N. Lahrouchi, R. Tadros, F. Kyndt +126 more
2020Genetics in Medicine82 citations Open access
Semantic Scholar
Human molybdopterin synthase gene: genomic structure and mutations in molybdenum cofactor deficiency type B.
Jochen Reiss, Claude Dorche, B. Stallmeyer, R. Mendel +2 more
1999American Journal of Human Genetics82 citations Open access
Semantic Scholar
Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorder
C. Friedrich, S. Rinné, S. Zumhagen, Aytuğ K. Kiper +5 more
2014EMBO Molecular Medicine74 citations Open access
Semantic Scholar
Regulation of eNOS in normal and diabetes-impaired skin repair: implications for tissue regeneration.
B. Stallmeyer, Manuel Anhold, C. Wetzler, Kornelija Kahlina +2 more
2002Nitric oxide70 citations
Semantic Scholar
Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2
I. Kolder, M. Tanck, P. Postema, J. Barc +18 more
2015Circulation: Cardiovascular Genetics69 citations Open access
Semantic Scholar
Genetic Architecture of Azoospermia-Time to Advance the Standard of Care.
M. J. Wyrwoll, Nils Köckerling, M. Vockel, Ann-Kristin Dicke +18 more
2022European Urology68 citations
Semantic Scholar
Sodium permeable and “hypersensitive” TREK‐1 channels cause ventricular tachycardia
Niels Decher, Beatriz Ortiz-Bonnin, C. Friedrich, Marcus Schewe +13 more
2017EMBO Molecular Medicine67 citations Open access
Semantic Scholar
Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking.
L. Anneken, S. Baumann, Patrick Vigneault, P. Biliczki +14 more
2016European Heart Journal61 citations Open access
Semantic Scholar
Overlapping Cardiac Phenotype Associated with a Familial Mutation in the Voltage Sensor of the KCNQ1 Channel
Ulrike Henrion, S. Zumhagen, Katja Steinke, N. Strutz‐Seebohm +4 more
2012Cellular Physiology and Biochemistry60 citations Open access
Semantic Scholar
Tpeak-Tend interval and Tpeak-Tend/QT ratio in patients with Brugada syndrome.
S. Zumhagen, E. M. Zeidler, B. Stallmeyer, Mark Ernsting +2 more
2016Europace56 citations
Semantic Scholar
Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy.
D. Frank, Ashraf Yusuf Rangrez, C. Friedrich, S. Dittmann +15 more
2019Circulation Genomic and Precision Medicine54 citations Open access
Semantic Scholar
A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction
B. Stallmeyer, J. Kuß, S. Kotthoff, S. Zumhagen +9 more
2017Circulation Research50 citations Open access
Semantic Scholar
A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease
A. Neu, M. Eiselt, M. Paul, Kathrin Sauter +3 more
2010Human Mutation44 citations Open access
Semantic Scholar
Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K+ Channel) Channel Function
J. Kuß, B. Stallmeyer, Matthias Goldstein, S. Rinné +7 more
2019Circulation Genomic and Precision Medicine38 citations
Semantic Scholar
An International Multi-Center Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition
Jason D. Roberts, S. Asaki, Andrea Mazzanti, J. Bos +55 more
2020Circulation36 citations Open access
Semantic Scholar
DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermia
Ann-Kristin Dicke, A. Pilatz, M. J. Wyrwoll, M. Punab +10 more
2023Communications Biology34 citations Open access
Semantic Scholar
A Heterozygous Deletion Mutation in the Cardiac Sodium Channel Gene SCN5A with Loss- and Gain-of-Function Characteristics Manifests as Isolated Conduction Disease, without Signs of Brugada or Long QT Syndrome
S. Zumhagen, M. Veldkamp, B. Stallmeyer, A. Baartscheer +6 more
2013PLoS ONE29 citations Open access
Semantic Scholar
Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction
H. Itoh, M. Berthet, V. Fressart, I. Denjoy +13 more
2015European Journal of Human Genetics26 citations Open access
Semantic Scholar
New Cav1.2 Channelopathy with High-Functioning Autism, Affective Disorder, Severe Dental Enamel Defects, a Short QT Interval, and a Novel CACNA1C Loss-of-Function Mutation
D. Endres, Niels Decher, Isabell Röhr, Kirsty S. Vowinkel +13 more
2020International Journal of Molecular Sciences25 citations Open access
Semantic Scholar
Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Desmosomal Variants Are Rarely De Novo: Segregation and Haplotype Analysis of a Multinational Cohort.
F. V. van Lint, B. Murray, C. Tichnell, R. Zwart +14 more
2019Circulation Genomic and Precision Medicine25 citations Open access
Semantic Scholar
The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans
M. J. Wyrwoll, Channah M Gaasbeek, Ieva Golubickaitė, Rytis Stakaitis +23 more
2022American Journal of Human Genetics24 citations Open access
Semantic Scholar
Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype
M. M. Limberg, S. Zumhagen, Michael F. Netter, A. Coffey +7 more
2013Basic Research in Cardiology24 citations
Semantic Scholar
Identification of Novel Mutations in LMNA Associated with Familial Forms of Dilated Cardiomyopathy
B. Stallmeyer, M. Koopmann, E. Schulze-Bahr
2012Genetic Testing and Molecular Biomarkers24 citations
Semantic Scholar
PKC δ-induced activation of MAPK pathway is required for bFGF-stimulated proliferation of coronary smooth muscle cells
A. Skaletz-Rorowski, H. Eschert, J. Leng, B. Stallmeyer +3 more
200524 citations Open access
Semantic Scholar
Genes Causing Inherited Forms of Cardiomyopathies
M. Paul, S. Zumhagen, B. Stallmeyer, M. Koopmann +2 more
2009Herz Kardiovaskuläre Erkrankungen23 citations
Semantic Scholar
POPDC2 a novel susceptibility gene for conduction disorders.
S. Rinné, Beatriz Ortiz-Bonnin, B. Stallmeyer, Aytuğ K. Kiper +16 more
2020Journal of Molecular and Cellular Cardiology22 citations Open access
Semantic Scholar
Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac death.
B. Fischer, S. Dittmann, A. Brodehl, A. Unger +8 more
2020International Journal of Cardiology21 citations
Semantic Scholar
Early repolarization pattern: a marker of increased risk in patients with catecholaminergic polymorphic ventricular tachycardia.
E. Tülümen, E. Schulze-Bahr, S. Zumhagen, B. Stallmeyer +10 more
2016Europace21 citations
Semantic Scholar
Whole Exome Sequencing Identifies a Heterozygous Variant in the Cav1.3 Gene CACNA1D Associated with Familial Sinus Node Dysfunction and Focal Idiopathic Epilepsy
S. Rinné, B. Stallmeyer, Alexandra Pinggera, Michael F. Netter +8 more
2022International Journal of Molecular Sciences17 citations Open access
Semantic Scholar
PKC delta-induced activation of MAPK pathway is required for bFGF-stimulated proliferation of coronary smooth muscle cells.
A. Skaletz-Rorowski, H. Eschert, J. Leng, B. Stallmeyer +3 more
2005Cardiovascular Research17 citations
Semantic Scholar
Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes.
M. J. Wyrwoll, E. V. van Walree, G. Hamer, N. Rotte +16 more
2021Human Reproduction16 citations Open access
Semantic Scholar
Inherited long QT syndrome
S. Zumhagen, B. Stallmeyer, C. Friedrich, L. Eckardt +2 more
2012Herzschrittmachertherapie & Elektrophysiologie15 citations
Semantic Scholar
Bi-allelic variants in INSL3 and RXFP2 cause bilateral cryptorchidism and male infertility.
Ann-Kristin Dicke, J. Albrethsen, Bradley L. Hoare, M. J. Wyrwoll +10 more
2023Human Reproduction14 citations Open access
Semantic Scholar
Scrutinizing the human TEX genes in the context of human male infertility
Marie H. Sieper, A. Gaikwad, Marion Fros, P. Weber +7 more
2023Andrology13 citations Open access
Semantic Scholar
(Tpeak - Tend)/QRS and (Tpeak - Tend)/(QT × QRS) as risk markers in Brugada syndrome: authors' reply.
S. Zumhagen, B. Stallmeyer, L. Eckardt, E. Schulze-Bahr
2017Europace13 citations Open access
Semantic Scholar
Functional assessment of DMRT1 variants and their pathogenicity for isolated male infertility.
J. Emich, Avinash Gaikwad, B. Stallmeyer, D. Fietz +6 more
2022Fertility and Sterility9 citations Open access
Semantic Scholar

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E. Schulze-Bahr — researcher profile on SciRah
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